39 results on '"Delashaw, Johnny B Jr"'
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2. Timing of surgery and bevacizumab therapy in neurosurgical patients with recurrent high grade glioma
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Abrams, Daniela Alexandru, Hanson, Joseph A., Brown, Justin M., Hsu, Frank P.K., Delashaw, Johnny B., Jr., and Bota, Daniela A.
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- 2015
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3. Orbitosphenoid Meningiomas
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Sincoff, Eric H., Delashaw, Johnny B., Jr., and Lee, Joung H., editor
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- 2009
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4. A Multicenter, Single-Blind, Prospective Randomized Trial to Evaluate the Safety of a Polyethylene Glycol Hydrogel (Duraseal Dural Sealant System) as a Dural Sealant in Cranial Surgery
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Osbun, Joshua W., Ellenbogen, Richard G., Chesnut, Randall M., Chin, Lawrence S., Connolly, Patrick J., Cosgrove, G. Rees, Delashaw, Johnny B., Jr., Golfinos, John G., Greenlee, Jeremy D.W., Haines, Stephen J., Jallo, Jack, Muizelaar, J. Paul, Nanda, Anil, Shaffrey, Mark, Shah, Mitesh V., Tew, John M., Jr., van Loveren, Harry R., Weinand, Martin E., White, Jonathan A., and Wilberger, James E.
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- 2012
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5. Normal Hypothalamic-Pituitary-Adrenal Axis by High-Dose Cosyntropin Testing in Patients with Abnormal Response to Low-Dose Cosyntropin Stimulation: A Retrospective Review
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Fleseriu, Maria, Gassner, Marika, Yedinak, Christine, Chicea, Liana, Delashaw, Johnny B., Jr, and Loriaux, D. Lynn
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- 2010
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6. Modified orbitozygomatic craniotomy for large medial sphenoid wing meningiomas
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Cheng, Cheng-Mao, Chang, Cheng-Fu, Ma, Hsin-I, Chiang, Yung-Hsiao, McMenomey, Sean O., and Delashaw, Johnny B., Jr.
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- 2009
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7. Management of Complications in Neurotology
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Liu, James K., Saedi, Targol, Delashaw, Johnny B., Jr., and McMenomey, Sean O.
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- 2007
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8. Indications for Cerebrospinal Fluid Drainage and Avoidance of Complications
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Moza, Kapil, McMenomey, Sean O., and Delashaw, Johnny B., Jr.
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- 2005
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9. Chapter 140 - Chordomas and Chondrosarcomas
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Cetas, Justin S., Hughes, Samuel A., and Delashaw, Johnny B., Jr
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- 2011
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10. Use of frameless stereotactic computed tomography venography for intraoperative localization of dural arterial venous fistulas: case report
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Carlson, Jonathan D., Liu, James K., Dogan, Aclan, Sincoff, Eric, Anderson, Gregory J., and Delashaw, Johnny B., Jr
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- 2008
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11. Spontaneous middle fossa encephalocele and cerebrospinal fluid leakage: diagnosis and management.
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Gubbels, Samuel P., Selden, Nathan R., Delashaw Jr, Johnny B., Mcmenomey, Sean O., and Delashaw, Johnny B Jr
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- 2007
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12. Contributors
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Aarabi, Bizhan, Abbott, Rick, Abdulrauf, Saleem I., Acosta, Frank L., Jr, Adler, John R., Jr, Agazaryan, Nzhde, Aghi, Manish, Ahn, Edward S., Alaraj, Ali, Albert, Gregory W., Albright, Leland, Albuquerque, Felipe C., Alden, Tord D., Alexander, Michael J., Alexandrov, Andrei V., Al-Mefty, Ossama, Alterman, Ron L., Álvarez, Lázaro, Amankulor, Nduka M., Amenta, Peter S., Ames, Christopher P., Amin-Hanjani, Sepideh, Ammirati, Mario, Anderson, Carryn, Anderson, Richard C.E., Anderson, William S., Angevine, Peter D., Arif, Hiba, Arle, Jeffrey E., Armonda, Rocco, Arnold, Paul M., Asadi-Moghaddam, Kaveh, Asghar, Ferhan A., Ashley, William W., Jr, Aydin, Sabri, Aygun, Nafi, Baehring, Joachim M., Bagley, Jacob H., Bahgat, Diaa, Bailes, Julian E., Ball, Jonathon R., Baltuch, Gordon H., Bambakidis, Nicholas C., Baraban, Scott C., Barani, Igor J., Barbaro, Nicholas M., Barker, Frederick G., II, Barnett, Gene H., Barnwell, Stanley L., Barone, Constance M., Barrow, Daniel L., Bartolomei, Fabrice, Bartolomei, Juan, Batchelor, Tracy T., Batjer, H. Hunt, Bauer, Andrew M., Bauman, Joel A., Baumann, Thomas K., Baumgartner, James E., Bayouth, John, Beaumont, Andrew, Bederson, Joshua B., Beisse, Rudolf, Bell, Randy S., Belzberg, Allan, Benabid, Alim Louis, Benarroch, Eduardo E., Benazzouz, Abdelhamid, Bendok, Bernard R., Benzel, Edward C., Berenstein, Alejandro, Berger, Mitchel S., Bergsneider, Marvin, Bertalanffy, Helmut, Bhalla, Tarun, Bidros, Dani S., Biller, José, Bilsky, Mark H., Binder, Devin K., Bingaman, William, Birch, Rolfe, Bishop, Allen T., Black, Peter M., Blount, Jeffrey P., Blumbergs, Peter C., Bohman, Leif-Erik, Boomsaad, Zackary E., Boop, Frederick A., Bou-Haidar, Pascal, Boué, Daniel R., Bourgeois, Blaise F.D., Bowman, Robin M., Bozinov, Oliver, Bramlett, Helen M., Brem, Henry, Brem, Steven, Britz, Gavin W., Brockmeyer, Douglas L., Brooks, David J., Browd, Samuel R., Brown, Paul D., Brown, Robert D., Jr, Bruce, Jeffrey N., Brunstrom-Hernandez, Janice E., Buatti, John, Bullock, M. Ross, Burchiel, Kim J., Burger, Peter C., Bussière, Marc R., Bydon, Mohamad, Byrne, Richard W., Calcagnotto, Maria Elisa, Campbell, Victoria A., Campbell, William, Cannon, George M., Caragine, Louis P., Jr, Carson, Benjamin S., Cascino, Gregory D., Cascio, Ethan, Castinetti, Frédéric, Cawley, C. Michael, Cetas, Justin S., Chabardès, Stéphan, Chang, Edward F., Chang, Eric C., Chang, Eric L., Chang, Steven D., Chang, Steven W., Chang, Susan M., Chao, Kevin, Chapman, Paul H., Charbel, Fady T., Chauvel, Patrick, Chen, Grace, Cheng, Boyle C., Cheng, Joseph S., Chern, Joshua J., Chiocca, E. Antonio, Choutka, Ondrej, Chowdhry, Shakeel A., Christian, Cindy W., Chuang, Kathy, Claassen, Jan, Clatterbuck, Richard E., Claus, Elizabeth B., Cleary, Daniel R., Coffey, Robert J., Cohen, Alan R., Cole, Andrew J., Connolly, E. Sander, Jr, Connolly, Patrick J., Copay, Anne G., Coppens, Jeroen R., Corbett, James J., Corcos, Daniel M., Coric, Domagoj, Cosgrove, Garth Rees, Couldwell, William T., Craig, Stirling, Crawford, Neil R., Crino, Peter B., Crowley, R. Webster, Curt, Bradford A., Czosnyka, Marek, Czosnyka, Zofia, Dadashev, Vladimir Y., Dailey, Andrew T., Danan, Deepa, Danish, Shabbar F., Dashti, Shervin R., David, Carlos A., David, David J., Day, Arthur L., De Salles, Antonio A.F., Dehdashti, Amir R., Del Brutto, Oscar H., Delashaw, Johnny B., Jr, Delman, Bradley, DeLong, Mahlon R., DeMonte, Franco, Dhall, Sanjay S., Dias, Mark S., Dickman, Curtis A., Dietrich, W. Dalton, DiLuna, Michael L., Di Meco, Francesco, Dirks, Peter, Dixon, C. Edward, Donoghue, Jacob A., Dorward, Ian G., Doshi, Amish H., Drake, James, Drzymalski, Dan, Du, Rose, Ducruet, Andrew, Duhaime, Ann-Christine, Dumont, Aaron S., Duntsch, Christopher D., Dusick, Joshua R., Dyve, Suzan, Eberwine, James, Eboli, Paula, Ecker, Robert D., Edwards, Richard J., Eichler, Marc E., Engel, Doortje C., Epstein, Nancy E., Ewend, Matthew G., Farhat, Hamad, Farrell, Christopher J., Fehlings, Michael G., Feiz-Erfan, Iman, Feldstein, Neil A., Fessler, Richard G., Figueroa, Juan J., Filler, Aaron G., Findlay, J. Max, Finn, Michael A., Fiorella, David J., Fisher, James L., Fisher, Robert S., Flamm, Eugene S., Fleck, James D., Flemming, Kelly D., Flickinger, John C., Flores-Sarnat, Laura, Follett, Kenneth A., Foote, Kelly D., Fourney, Daryl R., Fraix, Valerie, Frazier, James L., Fried, Itzhak, Friedman, Allan H., Friedman, William A., Friehs, Gerhard M., Fry, Donald E., Fuller, Gregory N., Garcia, Hector H., Gardner, Paul A., Garrett, Mark, Garton, Hugh, Gavin, Cormac G., Gean, Alisa D., Gennarelli, Thomas A., Gerganov, Venelin, Germanwala, Anand V., Gerosa, Massimo, Gerstner, Elizabeth R., Gerszten, Peter C., Ghatan, Saadi, Ghostine, Samer, Giannotta, Steven, Gigante, Paul R., Gilliam, Frank, Gilmer-Hill, Holly, Gjedde, Albert, Glick, Roberta P., Gokaslan, Ziya L., Gologorsky, Yakov, Golshani, Kiarash, Gonzalez, Nestor R., Goodrich, James Tait, Gordon, Tessa, Gorgulho, Alessandra A., Goumnerova, Liliana C., Grady, M. Sean, Grafman, Jordan, Grand, Sylvie, Grant, Gerald A., Graziano, Gregory P., Greenberg, Benjamin, Guest, James, Guha, Abhijit, Günel, Murat, Gupta, Gaurav, Gupta, Nalin, Guridi, Jorge, Guthrie, Barton L., Haddad, Georges F., Haglund, Michael M., Haid, Regis W., Jr, Haines, Stephen J., Hamani, Clement, Hamilton, Bronwyn E., Hamilton, D. Kojo, Hankinson, Todd C., Happel, Leo T., Haq, Ihtsham Ul, Haque, Raqeeb, Harbaugh, Robert E., Harraher, Ciara D., Harris, Leo, Harrop, James S., Hassaneen, Wael, Hawkins, Cynthia, Hawryluk, Gregory W.J., Haynes, Neal G., Heary, Robert F., Heimberger, Amy B., Heinricher, Mary M., Hemmen, Thomas M., Henderson, Jaimie M., Heros, Roberto C., Herrup, Karl, Hervey-Jumper, Shawn L., Heuer, Gregory G., Hirsch, Lawrence J., Hirschl, Robert, Hoh, Brian L., Hoh, Daniel J., Holland, Eric C., Holtzheimer, Paul E., Hopkins, L. Nelson, Horner, Philip J., Hovda, David A., Howard, Matthew A., III, Hsieh, Patrick, Hu, Yin C., Hua, Sherwin E., Huang, Jason H., Huang, Judy, Hughes, Samuel A., Huisman, Thierry A.G.M., Hunt, Matthew A., Hurlbert, R. John, Hurst, Robert W., Huttner, Anita, Hwang, Steven W., Isaias, Ioannis U., Iskandar, Bermans J., Jacob, Arun, Jaeckle, Kurt A., Jagannathan, Jay, Jakacki, Regina I., Jallo, George I., Jane, John A., Jr, Jane, John A., Janicki, Ryan, Janigro, Damir, Jeelani, N u Owase, Jellinger, Kurt A., Jenkins, Arthur L., III, Jernigan, Sarah, Jimenez, David F., Johanson, Conrad E., Johnson, J. Patrick, Johnson, Matthew D., Jones, G. Alexander, Jutla, Rajni K., Kainth, Koijan Singh, Kaiser, Michael G., Kakarla, U. Kumar, Kalfas, Iain H., Kalnins, Aleksandrs Uldis, Kano, Hideyuki, Kanpolat, Yucel, Kanter, Adam S., Karimi, Reza J., Kassam, Amin B., Kaufman, Bruce A., Kaufman, Christian B., Kawasaki, Hiroto, Kelley, Brian C., Kellner, Christopher P., Keong, Nicole C., Kestle, John R.W., Khalessi, Alexander A., Khan, Nadia, Khurana, Vini G., Kim, Daniel H., Kim, Dong Gyu, Kim, Dong H., Kim, Jong Hyun, Kim, Louis J., Kim, Paul K., Kim, Thomas Aquinas, Kim, Won, King, James A.J., Kitagawa, Ryan S., Kitchen, Neil D., Klimo, Paul, Jr, Kline, David G., Kobayashi, Kazutaka, Kochanek, Patrick M., Kondziolka, Douglas, Kongkham, Paul N., Koski, Tyler R., Kosztowski, Thomas, Krack, Paul, Krauss, Joachim K., Kraut, Michael A., Krayenbühl, Niklaus, Kretschmer, Thomas, Krishnaney, Ajit, Kuntz, Charles, IV, Kuo, Jeffrey V., Kwon, Brian K., Laack, Nadia N. Issa, Lad, Shivanand P., Ladha, Alim M., Ladouceur, Amos K., Lam, Arthur M., Lang, Frederick F., Lanzino, Giuseppe, Lavine, Sean D., Laws, Edward R., Jr, Lawton, Michael T., Laxton, Adrian W., Le, Tuong H., LeBas, Jean François, Lebed, Brett D., Lebow, Richard L., Lee, Amy, Lee, Ian, Lee, Seon-Kyu, Lehmann, Emily, Leiphart, James W., Lekovic, Gregory P., Lenz, Frederick A., Leonard, Jeffrey R., LeRoux, Peter D., Lévêque, Marc, Levi, Allan D., Levy, Elad I., Liau, Linda M., Liauw, Jason, Lichtenbaum, Roger, Lichtor, Terry, Limbrick, David D., Jr, Lingsma, Hester, Link, Michael J., Linskey, Mark E., Litt, Brian, Litvack, Zachary N., Liu, James K.C., Liu, Kenneth C., Loeffler, Jay S., Loftus, Christopher M., Lonser, Russell R., Louvi, Angeliki, Lozano, Andres M., Lu, Daniel C., Lukas, Rimas V., Lunsford, L. Dade, Luther, Neal, Lylyk, Pedro, Maas, Andrew I.R., Macdonald, R. Loch, Machado, Andre, Macias, Raul, Maciunas, Robert J., Maddux, Brian N., Magistretti, Pierre, Malessy, Martijn J.A., Malhotra, Neil R., Malone, Donald A., Jr, Mamelak, Adam N., Mandigo, Christopher E., Mangano, Francesco T., Maniker, Allen H., Manley, Geoffrey T., Marchac, Daniel, Marmarou, Anthony, Maroon, Joseph C., Marshall, Lawrence F., Martin, Neil A., Martin, Timothy J., Mason, Alexander M., Mathews, Marlon S., Mayberg, Helen S., McAllister, James P., II, McComb, J. Gordon, McCormick, Paul C., McCutcheon, Ian E., McDermott, Michael W., McDougall, Cameron G., McGehee, Matthew, McIntyre, Cameron C., McKhann, Guy M., II, McKisic, M. Sean, Meaney, David F., Mehta, Minesh P., Mehta, Vivek, Melega, William P., Menezes, Arnold H., Mertens, Patrick, Meyer, Fredric B., Meyer, Scott A., Meyers, Philip M., Michaelides, Costas, Michaud, Karine, Midha, Rajiv, Miele, Vincent J., Miller, Jonathan, Miller, Matthew L., Miller, Neil R., Mitrofanis, John, Miyashiro, Kevin Y., Mocco, J., Modic, Michael T., Moftakhar, Parham, Mohan, Avinash, Monteith, Stephen J., Morcos, Jacques J., Morgan, Michael, Morris, David E., Moss, S. David, Muizelaar, J. Paul, Mukhida, Karim, Mummaneni, Praveen V., Murad, Gregory J.A., Muraszko, Karin, Mussi, Antônio C.M., Najm, Imad, Nakaji, Peter, Narayanan, Sandra, Newell, David W., Nicholas, M. Kelly, Niimi, Yasunari, Nimjee, Shahid M., Niranjan, Ajay, North, Richard B., Novotny, Josef, Jr, Nurmikko, Turo, Nutt, Samuel E., Oakes, W. Jerry, Obeso, José A., Ogden, Alfred T., Ogieglo, Lissa, Ogilvy, Christopher S., Okonkwo, David O., Okun, Michael S., Oldfield, Edward H., Olivi, Alessandro, Olvey, Stephen E., Omahen, David, O'Neill, Brent, Oskouian, Rod J., Jr, Owen, Robert, Özduman, Koray, Ozturk, Ali Kemal, Pamir, M. Necmettin, Pang, Dachling, Pardini, Jamie, Parent, Andrew D., Park, T.S., Partington, Michael D., Patel, Aman B., Patil, Parag G., Pavese, Nicola, Penn, Richard D., Perin, Noel I., Persing, John A., Petersen, Erika A., Petraglia, Anthony L., Piallat, Brigitte, Piatt, Joseph H., Pickard, John D., Piepmeier, Joseph M., Pilcher, Webster H., Pineda, José, Pinter, Joseph D., Pisculli, Mary L., Pittman, Thomas, Pollack, Ian F., Pollak, Pierre, Pollock, Bruce E., Ponce, Francisco A., Porter, Alyx B., Porter, Randall W., Post, Kalmon D., Powers, Alexander K., Proctor, Mark R., Prost, Robert W., Pugh, Jeffrey, Quiñones-Hinojosa, Alfredo, Raffel, Corey, Rajpal, Sharad, Rangel-Castilla, Leonardo, Rao, Ganesh, Raslan, Ahmed, Rasmussen, Peter A., Ray, Dibyendu K., Raza, Shaan M., Reames, Davis L., Reddy, Chandan G., Redmond, Andy J., Régis, Jean, Reilly, Peter L., Renier, Dominique, Resnick, Daniel K., Reynolds, Renee, Rezai, Ali R., Rhines, Laurence D., Rhoton, Albert L., Jr, Ribalta, Teresa, Richardson, R. Mark, Rigamonti, Daniele, Riggins, Gregory J., Riva-Cambrin, Jay, Rizzo, Paolo, Roberts, David W., Robertson, Claudia, Robinson, Lawrence, Robinson, Shenandoah, Roche, Pierre-Hugues, Rockoff, Mark A., Rodts, Gerald E., Jr, Romanelli, Pantaleo, Rosenblum, Mark L., Rosenow, Joshua M., Rosner, Michael K., Rovner, Eric S., Runge-Samuelson, Christina L., Russell, Stephen M., Rutka, James T., Sagher, Oren, St. Clair, Eric G., Samii, Madjid, Sampath, Prakash, Samudrala, Srinath, Sanai, Nader, Sanford, Robert A., Santiago, Paul, Santiago-Sim, Teresa, Sarnat, Harvey B., Sawaya, Raymond, Scheld, W. Michael, Shirzadi, Wouter I., Schiff, Nicholas D., Schirmer, Clemens M., Schlesinger, David, Schmidt, Meic H., Schouten, Joost W., Schramm, Johannes, Schuler, Thomas C., Schuster, James M., Schwartz, Theodore H., Schwartzbaum, Judith A., Schweder, Patrick M., Scott, R. Michael, Seigneuret, Eric, Selden, Nathan R., Selman, Warren R., Shaffrey, Christopher I., Shah, Manish N., Shahlaie, Kiarash, Shapiro, William R., Sharma, Deepak, Sheehan, Jason P., Sheehan, Jonas M., Sherma, Arun K., Shiflett, James M., Shih, Helen A., Shils, Jay L., Shin, Alexander Y., Shirzadi, Ali, Siddiqui, Adnan H., Sindou, Marc, Slavin, Konstantin V., Smith, Edward R., Smith, Justin S., Smith, Yoland, Smyth, Matthew D., Sneed, Penny K., Snyder, Brian J., Snyder, Kenneth V., Solomon, Robert A., Sonntag, Volker K.H., Sørensen, Leif, Soriano, Sulpicio G., Souweidane, Mark M., Spears, Julian, Spencer, David, Spencer, Dennis D., Spetzler, Robert F., Spinner, Robert J., Stacey, Brett R., Stacey, William C., Starke, Robert M., Starr, Philip A., Steinberg, Gary K., Stephens, Frederick L., Stern, Barney J., Stevenson, Charles B., Stiner, Eric, Stone, Scellig, Stroud, Nicole L., Stuart, Robert Morgan, Subach, Brian R., Sugrue, Patrick A., Suki, Dima, Sulaiman, Wale A.R., Surdell, Daniel L., Sutherling, William W., Sutton, Leslie N., Syed, Omar N., Tagliati, Michele, Takagi, Yasushi, Tamargo, Rafael J., Tan, Caroline C., Tandon, Nitin, Tatagiba, Marcos, Taylor, Michael D., Telian, Steven A., Teo, Charles, Tessier, Jeffrey M., Than, Khoi D., Thapar, Kamal, Theodore, Nicholas, Thompson, B. Gregory, Jr, Tiel, Robert, Tihan, Tarik, Tilton, Ann, Timmons, Shelly D., Toledo, Maria, Tomita, Tadanori, Tomycz, Nestor D., Torres, Napoleon, Toussaint, Charles P., Trapp, Bruce D., Traynelis, Vincent C., Tubbs, R. Shane, Tumialán, Luis M., Tunkel, Allan R., Umemura, Atsushi, Vaccaro, Alexander R., van Besien, Koen, Vitek, Jerrold L., Vives, Kenneth P., Vogel, Timothy W., Vogelbaum, Michael A., Vollmer, Dennis G., Von Allmen, Gretchen K., von Eckardstein, Kajetan L., Wackym, P. Ashley, Wainwright, Mark, Waldau, Ben, Walker, Marion L., Wallace, M. Christopher, Walsh, Brian, Wang, Huan, Wang, Michael Y., Wang, Vincent Y., Warnick, Ronald E., Webb, Sharon, Weigel, Ralf, Weil, Robert J., Weingart, Jon D., Weir, Bryce, Weiss, Martin, Weiss, Nirit, Welch, William C., Wellons, John C., III, Wen, Hung Tzu, Wess, Christian, West, G. Alexander, Wetjen, Nicholas M., Whitmore, Robert G., Whitworth, Louis A., Wichmann, Thomas, Wiemels, Joseph L., Wijdicks, Eelco F.M., Wilberger, Adam C., Wilberger, Jack, Wildrick, David M., Wilson, Jason, Winfree, Christopher J., Winn, H. Richard, Wolfla, Christopher, Wong, Eric T., Wormald, Peter J., Wrensch, Margaret, Wright, Neill M., Wright, Zachary, Yam, David, Yamada, Shinya, Yamada, Yoshiya, Yang, Isaac, Yang, Victor X.D., Yao, Tom, Yen, Chun-Po, Yeoh, H. Kwang, Yonekawa, Yasuhiro, Yoo, Alice, Yousem, David M., Yuen, Eric C., Zabramski, Joseph M., Zacest, Andrew C., Zacko, J. Christopher, Zada, Gabriel, Zafonte, Ross, Zager, Eric L., Zaidi, Hasan A., Zarzour, Hekmat, Zerris, Vasilios A., Zivin, Justin A., Zovickian, John G., Zubkov, Alexander Y., and Zwienenberg-Lee, Marike
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- 2011
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13. Commentary
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Delashaw, Johnny B., Jr.
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- 2010
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14. Diabetes Insipidus, Panhypopituitarism, and Severe Mental Status Deterioration in a Patient with Chordoid Glioma: Case Report and Literature Review
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Dziurzynski, Kristine, Delashaw, Johnny B., Jr, Gultekin, S. Humayun, Yedinak, Chris G., and Fleseriu, Maria
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- 2009
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15. Commentary
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Delashaw, Johnny B., Jr.
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- 2009
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16. Complications of Skull Base Surgery
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Nguyen, Tung T. and Delashaw, Johnny B., Jr
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- 1995
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17. In Reply: Microsurgical Clipping of an Anterior Communicating Artery Aneurysm Using a Novel Robotic Visualization Tool in Lieu of the Binocular Operating Microscope: Operative Video.
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Klinger DR, Reinard KA, Ajayi OO, and Delashaw JB Jr
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- Humans, Microsurgery, Aneurysm, Ruptured surgery, Intracranial Aneurysm surgery, Robotic Surgical Procedures
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- 2018
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18. Microsurgical Clipping of an Anterior Communicating Artery Aneurysm Using a Novel Robotic Visualization Tool in Lieu of the Binocular Operating Microscope: Operative Video.
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Klinger DR, Reinard KA, Ajayi OO, and Delashaw JB Jr
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- Female, Humans, Middle Aged, Treatment Outcome, Intracranial Aneurysm surgery, Microsurgery methods, Neurosurgical Procedures methods, Robotic Surgical Procedures methods
- Abstract
Introduction: The binocular operating microscope has been the visualization instrument of choice for microsurgical clipping of intracranial aneurysms for many decades., Objective: To discuss recent technological advances that have provided novel visualization tools, which may prove to be superior to the binocular operating microscope in many regards., Methods: We present an operative video and our operative experience with the BrightMatterTM Servo System (Synaptive Medical, Toronto, Ontario, Canada) during the microsurgical clipping of an anterior communicating artery aneurysm. To the best of our knowledge, the use of this device for the microsurgical clipping of an intracranial aneurysm has never been described in the literature., Results: The BrightMatterTM Servo System (Synaptive Medical) is a surgical exoscope which avoids many of the ergonomic constraints of the binocular operating microscope, but is associated with a steep learning curve. The BrightMatterTM Servo System (Synaptive Medical) is a maneuverable surgical exoscope that is positioned with a directional aiming device and a surgeon-controlled foot pedal. While utilizing this device comes with a steep learning curve typical of any new technology, the BrightMatterTM Servo System (Synaptive Medical) has several advantages over the conventional surgical microscope, which include a relatively unobstructed surgical field, provision of high-definition images, and visualization of difficult angles/trajectories., Conclusion: This device can easily be utilized as a visualization tool for a variety of cranial and spinal procedures in lieu of the binocular operating microscope. We anticipate that this technology will soon become an integral part of the neurosurgeon's armamentarium., (Copyright © 2017 by the Congress of Neurological Surgeons)
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- 2018
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19. Quantitative Anterior and Posterior Clinoidectomy Analysis and Mobilization of the Oculomotor Nerve during Surgical Exposure of the Basilar Apex Using Frameless Stereotaxis.
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Dogan A, Cetas JS, Anderson GJ, Rekito A, and Delashaw JB Jr
- Abstract
Background Anterior and posterior clinoidectomies have been proposed to augment exposure of the basilar apex. A sequential quantitative benefit analysis offered by these maneuvers has not been reported. Methods Fourteen datasets from eight cadaveric specimens were analyzed. A modified orbitozygomatic frontotemporal craniotomy was performed. The extent of proximal control of the basilar artery was determined through the exposed opticocarotid and carotidoculomotor triangles before and after clinoidectomies and mobilization of the third nerve at the porous oculomotarius. Results Removal of the anterior and posterior clinoids significantly improved proximal basilar artery access ( p < 0.012) and increased the opticocarotid triangle and carotidoculomotor triangle areas ( p < 0.017). Surgical freedom increased inferosuperiorally in the opticocarotid triangle following anterior clinoidectomy ( p < 0.047) and in carotidoculomotor triangle following posterior clinoidectomy ( p < 0.047). Mobilization of the third nerve increased surgical freedom in the mediolateral projection of the carotidoculomotor triangle ( p < 0.047). Conclusion Anterior and posterior clinoidectomies significantly improved the area of exposure of the opticocarotid triangle, carotidoculomotor triangle, and the exposed length of the basilar artery available for proximal control. This improvement is extremely important for large or giant aneurysms of the upper basilar artery or aneurysms hidden by the posterior clinoid.
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- 2017
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20. Quantitative verification of the keyhole concept: a comparison of area of exposure in the parasellar region via supraorbital keyhole, frontotemporal pterional, and supraorbital approaches.
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Cheng CM, Noguchi A, Dogan A, Anderson GJ, Hsu FP, McMenomey SO, and Delashaw JB Jr
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- Anatomic Landmarks anatomy & histology, Cadaver, Frontal Bone anatomy & histology, Humans, Minimally Invasive Surgical Procedures methods, Orbit anatomy & histology, Sella Turcica anatomy & histology, Sella Turcica surgery, Skull Base anatomy & histology, Skull Base surgery, Stereotaxic Techniques, Surgical Flaps, Temporal Bone anatomy & histology, Anatomic Landmarks surgery, Craniotomy methods, Frontal Bone surgery, Neurosurgical Procedures methods, Orbit surgery, Temporal Bone surgery
- Abstract
Object: This study was designed to determine if the "keyhole concept," proposed by Perneczky's group, can be verified quantitatively., Methods: Fourteen (3 bilateral and 8 unilateral) sides of embalmed latex-injected cadaveric heads were dissected via 3 sequential craniotomy approaches: supraorbital keyhole, frontotemporal pterional, and supraorbital. Three-dimensional cartesian coordinates were recorded using a stereotactic localizer. The orthocenter of the ipsilateral anterior clinoid process, the posterior clinoid process, and the contralateral anterior clinoid process are expressed as a center point (the apex). Seven vectors project from the apex to their corresponding target points in a radiating manner on the parasellar skull base. Each 2 neighboring vectors border what could be considered a triangle, and the total area of the 7 triangles sharing the same apex was geometrically expressed as the area of exposure in the parasellar region., Results: Values are expressed as the mean ± SD (mm(2)). The total area of exposure was as follows: supraorbital keyhole 1733.1 ± 336.0, pterional 1699.3 ± 361.9, and supraorbital 1691.4 ± 342.4. The area of exposure on the contralateral side was as follows: supraorbital keyhole 602.2 ± 194.7, pterional 595.2 ± 228.0, and supraorbital 553.3 ± 227.2. The supraorbital keyhole skull flap was 2.0 cm(2), and the skull flap size ratio was 1:5:6.5 (supraorbital keyhole/pterional/supraorbital)., Conclusions: The area of exposure of the parasellar region through the smaller supraorbital keyhole approach is as adequate as the larger pterional and supraorbital approaches. The keyhole concept can be verified quantitatively as follows: 1) a wide area of exposure on the skull base can be obtained through a small keyhole skull opening, and 2) the side opposite the opening can also be visualized.
- Published
- 2013
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21. Single stage transcranial exposure of large dural venous sinuses for surgically-assisted direct transvenous embolization of high-grade dural arteriovenous fistulas: technical note.
- Author
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Liu JK, Choudhry OJ, Barnwell SL, Delashaw JB Jr, and Dogan A
- Subjects
- Aged, Cerebral Angiography, Female, Humans, Male, Middle Aged, Treatment Outcome, Central Nervous System Vascular Malformations surgery, Cranial Sinuses surgery, Embolization, Therapeutic methods, Neurosurgical Procedures methods, Transverse Sinuses surgery
- Abstract
Background: High-grade dural arteriovenous fistulas (DAVFs) with retrograde cortical leptomeningeal drainage are formidable lesions because of their risk for intracranial hemorrhage. Treatment is aimed at occluding venous outflow to achieve obliteration of the fistula. In DAVFs that involve a large dural venous sinus (transverse sigmoid sinus or superior sagittal sinus), occluding venous outflow can be accomplished endovascularly with transvenous embolization. However, in some cases of DAVFs with reflux into cortical leptomeningeal veins, there may be venous restrictive disease downstream, such as occlusive thrombosis, which can prohibit endovascular access via the transfemoral or transjugular routes. In these instances, a transcranial approach can be performed to expose the large dural venous sinus distal to the site of occlusion for direct catheterization of the venous outflow for transvenous embolization. This combined surgical and endovascular strategy provides direct access to the venous outflow and bypasses the site of thrombotic obstruction., Methods: In this report, we describe our technique of single stage surgically-assisted transvenous embolization in three patients with high-grade DAVFs involving a large dural sinus., Results: All patients achieved complete obliteration of their DAVFs without any venous related complications., Conclusion: Our technique of surgically-assisted direct transvenous embolization of high-grade DAVFs can be successfully performed as a single stage in the operating room with intraoperative angiography and stereotactic image guidance.
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- 2012
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22. Staged resection of large vestibular schwannomas.
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Raslan AM, Liu JK, McMenomey SO, and Delashaw JB Jr
- Subjects
- Adult, Aged, Ear, Inner surgery, Facial Nerve Injuries epidemiology, Facial Nerve Injuries etiology, Facial Nerve Injuries physiopathology, Female, Follow-Up Studies, Headache etiology, Hearing Loss, Unilateral etiology, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Neoplasm Staging, Neuroma, Acoustic complications, Postoperative Complications epidemiology, Postoperative Complications physiopathology, Retrospective Studies, Treatment Outcome, Vertigo etiology, Neuroma, Acoustic surgery, Neurosurgical Procedures methods
- Abstract
Object: Staged resection of large vestibular schwannomas (VSs) has been proposed as a strategy to improve facial nerve outcomes and morbidity. The authors report their experience with 2-stage resections of large VSs and analyze the indications, facial nerve outcomes, surgical results, and complications. The authors compare these results with those of a similar cohort of patients who underwent a single-stage resection., Methods: A retrospective review of all patients (age > 18 years) who underwent surgery from 2002 to 2010 for large (≥ 3 cm) VSs at the authors' institution with a minimum of 6 months follow-up was undertaken. A first-stage retrosigmoid approach (without meatal drilling) was performed to remove the cerebellopontine angle portion of the tumor and to decompress the brainstem. A decision to stage the operation was made intraoperatively if there was cerebellar or brainstem edema, excessive tumor adherence to the facial nerve or brainstem, a poorly stimulating facial nerve, or a thinned or splayed facial nerve. A second-stage translabyrinthine approach was performed at a later date to remove the remaining tumor. The single-stage resection consisted of a retrosigmoid approach with meatal drilling. Patient charts were evaluated for tumor size, extent of resection, tumor recurrence, House-Brackmann facial nerve function grade, and complications., Results: Twenty-eight and 19 patients underwent 2- or single-stage resection of a large VS, respectively. The average tumor size was 3.9 cm (range 3.2-7 cm) in the 2-stage group and 3.9 cm (range 3.1-5 cm) in the single-stage group. The mean follow-up was 36 ± 19 months in the 2-stage group versus 24 ± 14 months in the single-stage group. Gross-total or near-total resection was achieved in 27 (96.4%) of 28 patients in the 2-stage group and 15 (79%) of 19 patients in the single-stage group (p < 0.01). Anatomical facial nerve preservation was achieved in all but 1 patient (94.7%), and there were no recurrences on follow-up imaging in the 2-stage group. Good facial nerve functional outcome (House-Brackmann Grades I and II) at last follow-up was achieved in 23 (82%) of 28 patients in the 2-stage group and 10 (53%) of 19 patients in the single-stage group (p < 0.01). Cerebrospinal fluid leak-related complications (intracranial hypotension, blood patch, and lumboperitoneal shunt for pseudomeningocele) were more common in the 2-stage group. There were no postoperative strokes, hemorrhages, or deaths in either group., Conclusions: The authors' results suggest that staged resection of large VSs may potentially achieve better facial nerve outcomes. There does not appear to be added neurological morbidity with staged resections.
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- 2012
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23. Results of the prospective, randomized, multicenter clinical trial evaluating a biosynthesized cellulose graft for repair of dural defects.
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Rosen CL, Steinberg GK, DeMonte F, Delashaw JB Jr, Lewis SB, Shaffrey ME, Aziz K, Hantel J, and Marciano FF
- Subjects
- Adolescent, Adult, Aged, Animals, Biocompatible Materials therapeutic use, Cattle, Cellulose chemistry, Female, Humans, Male, Middle Aged, Prospective Studies, Treatment Outcome, Young Adult, Cellulose therapeutic use, Craniotomy methods, Dura Mater surgery, Membranes, Artificial, Plastic Surgery Procedures methods
- Abstract
Background: After intradural cranial surgery, a dural substitute is often required for dural closure. Although preferred, limitations of autograft include local availability and additional surgical site morbidity. Thus, allografts, xenografts, and synthetics are frequently used., Objective: To report 6-month results of a randomized, controlled trial of a biosynthesized cellulose (BSC) composed duraplasty device compared with commercially available dural replacements., Methods: A total of 99 patients (62 BSC; 37 control) were treated on protocol, using a 2:1 (BSC:control) blocked randomization schedule. Physical examinations were performed pre- and postoperatively within 10 days and at 1, 3, and 6 months. Magnetic resonance imaging was performed preoperatively and at 6 months. The primary study endpoint was the absence of pseudomeningocele and extracerebral fluid collection confirmed radiographically and the absence of cerebrospinal fluid fistula at 6 months., Results: At 6 months, the primary hypothesis, noninferiority of the BSC implant compared with the control group, was confirmed (P = .0206). Overall success was achieved by 96.6% of BSC and 97.1% of control patients. No significant difference was revealed between treatment groups for surgical site infection (P = 1.0000) or wound healing assessment (P ≥ .3685) outcomes, or radiologic endpoints (P ≥ .4061). Device strength and seal quality favored BSC., Conclusion: This randomized, controlled trial establishes BSC as noninferior to commercially available dural replacement devices. BSC offers a hypothetical advantage concerning prion and other infectious agent exposure; superior handling qualities are evident. Longer term data are necessary to identify limitations of BSC and its potential equivalence to the gold standard of pericranium.
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- 2011
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24. Wada test using secobarbital sodium (Ional) to determine language dominance.
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Yamaguchi T, Shojima M, Delashaw JB Jr, and Watanabe E
- Subjects
- Adolescent, Adult, Aged, Electroencephalography, Female, Humans, Injections, Intra-Arterial, Male, Memory physiology, Middle Aged, Treatment Outcome, Young Adult, Cerebrovascular Disorders physiopathology, Dominance, Cerebral physiology, Epilepsy physiopathology, Functional Laterality physiology, Hypnotics and Sedatives, Secobarbital
- Abstract
The intracarotid sodium amobarbital (Amytal) test, the Wada test, remains an efficient test for evaluation of language and memory function. However, due to a world shortage of amobarbital, it has become necessary to investigate the use of alternatives. We report the efficacy of the Wada test using secobarbital sodium (Ional) in determining language dominance. An accurate determination of language dominance was required in 43 patients preoperatively at our institution. Patients underwent the Wada test using secobarbital sodium, effectiveness and safety were assessed. Patients were monitored for vital signs (blood pressure, respiratory rates, heart rates and saturation of oxygen). Ten patients were further monitored for continuous intra-arterial blood pressure and monitored with scalp electroencephalography (EEG). Language dominance was determined by the Wada test with secobarbital sodium in all patients. Total volume of secobarbital sodium injected was 10-25 mg (mean 16.5 ± 3.2 mg). Changes in vital signs were minimal and any induced neurological deficits completely disappeared within 8 min. On EEG records, induced theta waves immediately appeared on the ipsilateral side of the intra-arterial injection and disappeared within 6 min. One patient described a scintillating scotoma (sensation of shimmering light in his eyes) at the moment of injection; another experienced an epileptic episode during the test and recovered after 6 min. No adverse events were observed in the remaining 41 cases. We propose secobarbital sodium as a safe and reliable alternative to sodium amobarbital used in the Wada test to determine language dominance.
- Published
- 2011
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25. Temozolomide for corticotroph pituitary adenomas refractory to standard therapy.
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Dillard TH, Gultekin SH, Delashaw JB Jr, Yedinak CG, Neuwelt EA, and Fleseriu M
- Subjects
- ACTH-Secreting Pituitary Adenoma radiotherapy, ACTH-Secreting Pituitary Adenoma surgery, Dacarbazine therapeutic use, Humans, Male, Middle Aged, Ophthalmoplegia diagnosis, Ophthalmoplegia drug therapy, Pituitary Neoplasms radiotherapy, Pituitary Neoplasms surgery, Temozolomide, ACTH-Secreting Pituitary Adenoma drug therapy, Antineoplastic Agents, Alkylating therapeutic use, Dacarbazine analogs & derivatives, Pituitary Neoplasms drug therapy
- Abstract
To highlight the potential of temozolomide (TMZ) to induce rapid tumor regression in patients with aggressive corticotroph adenomas (CA) that are refractory to surgery and radiation therapy and to review use of TMZ in other pituitary tumors. We present a case of a 56-year-old male with a 3 cm CA treated with transphenoidal surgery (TSS) and conventional radiotherapy in the same year. His hypercortisolemia recurred 11 years later with rapid tumor growth (to 4.2 × 2.5 cm) and he underwent a second TSS with good resection. The tumor recurred 6 months later with ophthalmoplegia. Over 16 months he underwent an additional three surgeries (two TSS, one craniotomy) and repeated conventional radiotherapy. Ki67 staining index on surgical specimens was 5-6%. Temozolomide is an oral alkylating agent approved for glioblastoma multiforme treatment that has only recently shown promise in treating some pituitary tumors. In this patient TMZ was started at 150 mg/m²/day, titrated to 200 mg/m²/day, taken 5 days per month. The only significant side effect was moderate nausea. After 10 weeks, the tumor showed a remarkable 60% regression with objective improvement in ophthalmoplegia. Treatment of aggressive CAs represents a therapeutic challenge and in some cases surgical debulking and radiotherapy are of limited success. Few reports of CAs responsive to TMZ have been reported in the literature. To our knowledge, this case represents the most rapid robust CA shrinkage response reported to date. Further randomized clinical trials of TMZ in the treatment of aggressive pituitary adenomas are warranted.
- Published
- 2011
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26. Osteoplastic pterional craniotomy revisited.
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Kim E and Delashaw JB Jr
- Subjects
- Adult, Aged, Female, Humans, Magnetic Resonance Imaging, Male, Microsurgery, Middle Aged, Prospective Studies, Surgical Flaps, Tomography, X-Ray Computed, Craniotomy methods, Intracranial Aneurysm surgery, Surgery, Plastic methods
- Abstract
Background: A standard pterional approach with a free bone flap to treat brain aneurysms was first introduced and popularized by Yaşargil., Objective: To describe a modified pterional craniotomy technique and that mobilizes part of the sphenoid wing and the pterion in a block with the temporalis muscle to enhance cosmetic results., Methods: A subperiosteal corridor is provided inferiorly by separating the temporalis muscle from the underlying bone in a retrograde dissection. Inferior chisel cuts from the front and back enter the sphenoid wing, enabling removal of part of the sphenoid wing and the pterion in 1 piece, along with the bone flap. Forty patients with aneurysms were treated in this fashion, and the cosmetic outcome was examined at 6 months postoperatively., Results: Thirty-seven patients (92.5%) demonstrated an unremarkable degree of temporalis muscle atrophy. Excellent configuration and fusion of the pterional bone flap were observed on 3-dimensional computed tomography scans., Conclusion: With the use of this muscle-preserving and bone-sparing pterional approach and with little additional labor, temporalis muscle function is preserved and improved cosmesis is obtained.
- Published
- 2011
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27. Acromegaly: a review of current medical therapy and new drugs on the horizon.
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Fleseriu M, Delashaw JB Jr, and Cook DM
- Subjects
- Acromegaly blood, Human Growth Hormone blood, Humans, Insulin-Like Growth Factor I analysis, Insulin-Like Growth Factor I metabolism, Octreotide therapeutic use, Pituitary Neoplasms blood, Radiotherapy, Adjuvant methods, Acromegaly drug therapy, Acromegaly surgery, Adenoma drug therapy, Adenoma surgery, Human Growth Hormone metabolism, Pituitary Neoplasms drug therapy, Pituitary Neoplasms surgery
- Abstract
Acromegaly is a disease that results from a growth hormone (GH)–secreting pituitary tumor. Clinically, the disease is characterized by excessive skeletal growth, soft tissue enlargement with disfigurement, and increased risk of cardiovascular death. The goals of treatment are the removal or reduction of the tumor mass via surgery and normalization of GH secretion. Another treatment goal is the preservation of normal pituitary function if possible. Transsphenoidal surgery by an experienced neurosurgeon is usually the first line of therapy, especially for small tumors. Surgeon expertise is crucial for outcome, with dedicated pituitary surgeons having better results. However, overall cure rates remain low because patients with these tumors usually present at an incurable stage. Therefore, medical therapy to control excess GH secretion plays a significant role in a large proportion of patients with acromegaly who are not cured by surgery or other forms of therapy, such as radiotherapy, and/or are awaiting the effects of radiotherapy. If surgery is not curative, lifelong monitoring and the control of excess GH is usually necessary by a care team experienced in handling this chronic disease. In the past decade major progress has occurred in the development of highly specific and selective pharmacological agents that have greatly facilitated more aggressive management of active acromegaly. Treatment approach should be individualized and take into consideration a patient's tumor size and location, symptoms, comorbid conditions, and preferences. Because a surgical cure can be difficult to achieve, all patients, even those with what seems to be a clinically and biochemically inactive disease, should undergo long-term biochemical testing and pituitary MR imaging.
- Published
- 2010
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28. Cavernous malformations of the optic pathway and hypothalamus: analysis of 65 cases in the literature.
- Author
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Liu JK, Lu Y, Raslan AM, Gultekin SH, and Delashaw JB Jr
- Subjects
- Adolescent, Adult, Cerebral Angiography, Child, Child, Preschool, Female, Hemangioma, Cavernous, Central Nervous System diagnostic imaging, Humans, Hypothalamic Neoplasms diagnostic imaging, Male, Middle Aged, Neurosurgical Procedures methods, Optic Nerve Neoplasms diagnostic imaging, Treatment Outcome, Visual Acuity, Visual Pathways diagnostic imaging, Hemangioma, Cavernous, Central Nervous System surgery, Hypothalamic Neoplasms surgery, Optic Nerve Neoplasms surgery, Visual Pathways surgery
- Abstract
Object: Cavernous malformations (CMs) of the optic pathway and hypothalamus (OPH) are extremely rare. Patients with these lesions typically present with chiasmal apoplexy, characterized by sudden visual loss, acute headaches, retroorbital pain, and nausea. Surgical removal is the recommended treatment to restore or preserve vision and to eliminate the risk of future hemorrhage. However, the anatomical location and eloquence of nearby neural structures can make these lesions difficult to access and remove. In this study, the authors review the literature for reported cases of OPH CMs to analyze clinical and radiographic presentations as well as surgical approaches and neurological outcomes., Methods: A MEDLINE/PubMed search was performed, revealing 64 cases of OPH CMs. The authors report an additional case in the study, making a total of 65 cases. Each case was analyzed for clinical presentation, lesion location, radiographic features, treatment method, and visual outcome., Results: In 65 patients with OPH CMs, the optic chiasm was affected in 54 cases, the optic nerve(s) in 35, the optic tract in 13, and the hypothalamus in 5. Loss of visual field and acuity was the most common presenting symptom (98%), followed by headache (60%). The onset of symptoms was acute in 58% of patients, subacute in 15%, and chronic progressive in 26%. Computed tomography scans revealed hyperdense suprasellar lesions, with calcification visible in 56% of cases. Magnetic resonance imaging typically demonstrated a heterogeneous lesion with mixed signal intensities suggestive of blood of different ages. The lesion was often surrounded by a peripheral rim of hypointensity on T2-weighted images in 60% of cases. Minimal or no enhancement occurred after the administration of gadolinium. Hemorrhage was reported in 82% of cases. Most patients were surgically treated (97%) using gross-total resection (60%), subtotal resection (6%), biopsy procedure alone (6%), biopsy procedure with decompression (23%), and biopsy procedure followed by radiation (2%). Those patients who underwent gross-total resection had the highest rate of visual improvement (85%). Two patients were treated conservatively, resulting in complete blindness in 1 patient and spontaneous recovery of vision in the other patient., Conclusions: Cavernous malformations of the OPH are rare and challenging lesions. Gross-total resection of these lesions is associated with favorable visual outcomes. Emergent surgery is warranted in patients presenting with chiasmal apoplexy to prevent permanent damage to the visual pathway.
- Published
- 2010
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29. Optochiasmatic cavernous hemangioma.
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Panczykowski D, Piedra MP, Cetas JS, and Delashaw JB Jr
- Subjects
- Aged, Female, Hemangioma, Cavernous radiotherapy, Hemangioma, Cavernous surgery, Hemorrhage, Humans, Optic Chiasm, Optic Nerve Glioma radiotherapy, Optic Nerve Glioma surgery, Optic Nerve Neoplasms radiotherapy, Optic Nerve Neoplasms surgery, Radionuclide Imaging, Hemangioma, Cavernous diagnostic imaging, Optic Nerve Glioma diagnostic imaging, Optic Nerve Neoplasms diagnostic imaging, Vision Disorders etiology
- Abstract
We present a case of an optochiasmatic cavernous hemangioma (OCH) treated by stereotactic radiotherapy that required subsequent surgical resection. Subtotal resection and/or radiotherapy are not curative and can lead to hemorrhage and progressive neuronal insult. We recommend complete surgical resection as the treatment of choice.
- Published
- 2010
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30. The safety and effectiveness of a dural sealant system for use with nonautologous duraplasty materials.
- Author
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Weinstein JS, Liu KC, Delashaw JB Jr, Burchiel KJ, van Loveren HR, Vale FL, Agazzi S, Greenberg MS, Smith DA, and Tew J Jr
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Cohort Studies, Collagen, Craniotomy adverse effects, Craniotomy instrumentation, Craniotomy methods, Elective Surgical Procedures adverse effects, Elective Surgical Procedures instrumentation, Elective Surgical Procedures methods, Equipment Safety, Female, Humans, Male, Middle Aged, Polyethylene Glycols, Retrospective Studies, Treatment Outcome, Young Adult, Biocompatible Materials therapeutic use, Dura Mater surgery, Hydrogels therapeutic use, Tissue Adhesives therapeutic use
- Abstract
Object: The DuraSeal dural sealant system, a polyethylene glycol hydrogel, has been shown to be safe and effective when used with commercial and autologous duraplasty materials. The authors report on the safety and effectiveness of this sealant when used in conjunction with nonautologous duraplasty materials., Methods: In this retrospective, nonrandomized, multicenter study, the safety and efficacy of a dural sealant system was assessed in conjunction with primarily collagen-based nonautologous duraplasty materials in a sample of 66 patients undergoing elective cranial procedures at 3 institutions. This cohort was compared with 50 well-matched patients from the DuraSeal Pivotal Trial who were treated with this sealant system and autologous duraplasty material., Results: The key end points of the study were the incidences of CSF leaks, surgical site infections, and meningitis 90 days after surgery. The incidence of postoperative CSF leakage was 7.6% in the study group (retrospective population) and 6.0% in the Pivotal Trial population. The incidence of meningitis was 0% and 4.0% in the retrospective and Pivotal Trial groups, respectively. There were no serious device-related adverse events or unanticipated adverse device effects noted for either population., Conclusions: This study demonstrates that the DuraSeal sealant system is safe and effective when used for watertight dural closure in conjunction with nonautologous duraplasty materials.
- Published
- 2010
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31. Dural arteriovenous fistula of the anterior condylar confluence and hypoglossal canal mimicking a jugular foramen tumor.
- Author
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Liu JK, Mahaney K, Barnwell SL, McMenomey SO, and Delashaw JB Jr
- Subjects
- Central Nervous System Vascular Malformations complications, Central Nervous System Vascular Malformations diagnostic imaging, Cerebral Angiography, Diagnosis, Differential, Humans, Hypoglossal Nerve Diseases diagnostic imaging, Hypoglossal Nerve Diseases etiology, Jugular Veins diagnostic imaging, Male, Middle Aged, Skull Base anatomy & histology, Skull Base Neoplasms diagnosis, Central Nervous System Vascular Malformations pathology, Hypoglossal Nerve anatomy & histology, Hypoglossal Nerve Diseases pathology, Jugular Veins pathology, Magnetic Resonance Imaging
- Abstract
The anterior condylar confluence (ACC) is located on the external orifice of the canal of the hypoglossal nerve and provides multiple connections with the dural venous sinuses of the posterior fossa, internal jugular vein, and the vertebral venous plexus. Dural arteriovenous fistulas (DAVFs) of the ACC and hypoglossal canal (anterior condylar vein) are extremely rare. The authors present a case involving an ACC DAVF and hypoglossal canal that mimicked a hypervascular jugular bulb tumor. This 53-year-old man presented with right hypoglossal nerve palsy. A right pulsatile tinnitus had resolved several months previously. Magnetic resonance imaging demonstrated an enhancing right-sided jugular foramen lesion involving the hypoglossal canal. Cerebral angiography revealed a hypervascular lesion at the jugular bulb, with early venous drainage into the extracranial vertebral venous plexus. This was thought to represent either a glomus jugulare tumor or a DAVF. The patient underwent preoperative transarterial embolization followed by surgical exploration via a far-lateral transcondylar approach. At surgery, a DAVF was identified draining into the ACC and hypoglossal canal. The fistula was surgically obliterated, and this was confirmed on postoperative angiography. The patient's hypoglossal nerve palsy resolved. Dural arteriovenous fistulas of the ACC and hypoglossal canal are rare lesions that can present with isolated hypoglossal nerve palsies. They should be included in the differential diagnosis of hypervascular jugular bulb lesions. The authors review the anatomy of the ACC and discuss the literature on DAVFs involving the hypoglossal canal.
- Published
- 2008
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32. A novel treatment approach to cholesterol granulomas. Technical note.
- Author
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Sincoff EH, Liu JK, Matsen L, Dogan A, Kim I, McMenomey SO, and Delashaw JB Jr
- Subjects
- Craniotomy methods, Humans, Male, Brain Diseases therapy, Cholesterol, Drainage methods, Granuloma, Foreign-Body therapy
- Abstract
The authors report a novel technique for the treatment of cholesterol granulomas. An extradural middle fossa approach was used to access the granuloma, with drainage through silastic tubes into the sphenoid sinus via the anteromedial triangle between V1 and V2. Cholesterol granulomas occur when the normal aeration and drainage of temporal bone air cells is occluded, resulting in vacuum formation and transudation of blood into the air cells. This process results in anaerobic breakdown of the blood with resulting cholesterol crystal formation and an inflammatory reaction. Traditional treatment of this lesion involves extensive drilling of the temporal bone to drain the granuloma cyst and establish a drainage tract into the middle ear. Such drainage procedures can be time consuming and difficult, and potentially involve structural damage to the inner ear and facial nerve. An extradural middle fossa approach provides easy access to the granuloma and anterior petrous bone entry into the granuloma for resection. Granuloma drainage is then achieved using shunt tubing in the sphenoid sinus via a small hole in the anteromedial triangle between V1 and V2. Five patients with symptomatic cholesterol granuloma were treated without complication using this novel extradural middle fossa approach. One patient required reoperation 1-year postoperatively for cyst regrowth and occlusion of the drainage tube. At the 5-year follow-up examination, no patient reported recurrent symptoms. Extradural middle fossa craniotomy and silastic tube drainage into the sphenoid sinus is a viable alternative method for treatment of cholesterol granuloma.
- Published
- 2007
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33. Posterior transpetrosal approach: less is more.
- Author
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Sincoff EH, McMenomey SO, and Delashaw JB Jr
- Subjects
- Humans, Neurosurgical Procedures methods, Skull Base surgery, Skull Base Neoplasms surgery
- Abstract
Objective: We describe our surgical posterior transpetrosal technique, particularly the transcrusal variant for lesions involving the upper and middle clivus, petroclival regions, and lesions that involve both the posterior and middle fossae., Methods: An outline of the posterior transpetrosal technique involved, particularly the transcrusal variant, is described. Important superficial landmarks are identified, and a radical mastoidectomy is performed. The antrum is identified and entered, and, upon completion of the mastoidectomy and when Trautman's triangle is defined, the temporal and suboccipital craniotomies are completed. After bone flap elevation, dura opening, and incision along the middle fossa dura, the superior petrosal sinus is ligated and cut. Tentorium cut completion is at the incisura posterior to the trochlear nerve. Watertight dural closure and standard flap replacement and skin closure complete the technique., Results: Clival exposure and the degree of temporal bone resection increase. Operative freedom also increases with increased temporal bone resection, especially when going from the retrolabyrinthine to transcrusal variants. Little is gained in terms of operative freedom and exposure of the clivus with resection of additional temporal bone beyond that of the transcrusal variant, and resection carries the cost of increasing morbidity, especially with respect to VIIth and VIIIth nerve function., Conclusion: The posterior transpetrosal approach and the transcrusal variant provide a lateral operative corridor to lesions of the upper and middle clivus. The transcrusal variant provides increased exposure and operative freedom similar to that provided by the transcochlear approach while minimizing cranial nerve morbidity.
- Published
- 2007
- Full Text
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34. Treatment options for Cushing disease after unsuccessful transsphenoidal surgery.
- Author
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Liu JK, Fleseriu M, Delashaw JB Jr, Ciric IS, and Couldwell WT
- Subjects
- Adrenalectomy, Humans, Radiosurgery, Retreatment, Sphenoid Sinus surgery, Treatment Failure, ACTH-Secreting Pituitary Adenoma surgery, Adenoma surgery, Pituitary ACTH Hypersecretion therapy
- Abstract
Cushing disease is considered an aggressive pituitary endocrinopathy because of the devastating effects from untreated hypercortisolemia. Although they are histologically benign, these adrenocorticotropic hormone (ACTH)-secreting pituitary tumors are associated with significant morbidity and premature death. Currently, transsphenoidal surgery is the primary treatment of Cushing disease associated with an ACTH-secreting pituitary tumor, resulting in remission rates ranging from about 50 to 90%. Some patients, however, will not achieve sustained remission after transsphenoidal surgery and can exhibit persistent or recurrent Cushing disease that requires multimodal treatment to achieve remission. In these patients, options for treatment include repeat transsphenoidal resection, radiation therapy (including conventional fractionated radiation therapy and stereotactic radiosurgery), and medical therapy. Despite undergoing multiple treatment modalities, some patients may ultimately require bilateral adrenalectomy for definitive treatment to eliminate hypercortisolemia associated with Cushing disease. In this article, the authors review the treatment options for patients who have persistent or recurrent Cushing disease after unsuccessful transsphenoidal surgery. The indications, current results reported in the literature, and complications of each treatment modality are discussed.
- Published
- 2007
- Full Text
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35. Anatomical analysis of transoral surgical approaches to the clivus.
- Author
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Balasingam V, Anderson GJ, Gross ND, Cheng CM, Noguchi A, Dogan A, McMenomey SO, Delashaw JB Jr, and Andersen PE
- Subjects
- Cranial Fossa, Posterior anatomy & histology, Humans, Mandible surgery, Mouth surgery, Osteotomy, Le Fort methods, Palate surgery, Surgical Instruments, Cranial Fossa, Posterior surgery, Craniotomy methods
- Abstract
Object: The authors conducted a cadaveric anatomical study to quantify and compare the area of surgical exposure and the freedom available for instrument manipulation provided by the following four surgical approaches to the extracranial periclival region: simple transoral (STO), transoral with a palate split (TOPS), Le Fort I osteotomy (LFO), and median labioglossomandibulotomy (MLM)., Methods: Twelve unembalmed cadaveric heads with normal mouth opening capacity were serially dissected. For each approach, quantitation of extracranial periclival exposure and freedom for instrument manipulation (known here as surgical freedom) was accomplished by stereotactic localization. To quantify the extent of extracranial clival exposure obtained, anatomical measurements of the extracranial clivus were performed on 17 dry skull bases. The values (means +/- standard deviations in mm2) for periclival exposure and surgical freedom, respectively, for the surgical approaches studied were as follows: STO = 492 +/- 229 and 3164 +/- 1900; TOPS = 743 +/- 319 and 3478 +/- 2363; LFO = 689 +/- 248 and 2760 +/- 1922; and MLM 1312 +/- 384 and 8074 +/- 6451. The extent of linear midline clival exposure and the percentage of linear midline clival exposure relative to the total linear midline exposure were as follows, respectively: STO = 0.6 +/- 4.9 mm and 7.8 +/- 11%; TOPS = 8.9 +/- 5.5 mm and 24.2 +/- 16.7%; LFO = 32.9 +/- 10.2 mm and 85.0 +/- 18.7%; and MLM = 2.1 +/- 4.4 mm and 6.7 +/- 11.1%., Conclusions: The choice of approach and the resulting degree of complexity and associated morbidity depends on the location of the pathological entity. The authors found that the MLM approach, like the STO approach, provided good exposure of the craniocervical junction but limited exposure of the clivus. The TOPS approach, an approach attended by a lesser risk of morbidity, provided adequate exposure of the extracranial inferior clivus. Maximal exposure of the extracranial clivus proper was provided by the LFO approach.
- Published
- 2006
- Full Text
- View/download PDF
36. Modified osteoplastic orbitozygomatic craniotomy. Technical note.
- Author
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Balasingam V, Noguchi A, McMenomey SO, and Delashaw JB Jr
- Subjects
- Bone Transplantation, Humans, Osteogenesis, Craniotomy methods, Orbit surgery, Surgical Flaps, Zygoma surgery
- Abstract
The authors report on a surgical technique involving a one-piece osteoplastic bone flap, which incorporates the frontal, temporal, and lateral portions of the orbital rim as a technically simpler alternative to the standard orbitozygomatic (OZ) craniotomy. The orbital rim component extends just laterally from the supraorbital foramen/notch to the frontozygomatic suture. This craniotomy obviates the need for removing the zygoma and has evolved from the authors' experience in more than 200 patients with a variety of pathological lesions, both vascular and tumorous. The osteoplastic aspect of this technique was initially evaluated in 14 cadaveric sites in seven heads dissected prior to implementing this procedure clinically. The osteoplastic bone flap minimally obstructs the surgical view and provides all the advantages of a standard OZ craniotomy. Temporalis muscle atrophy leading to temporal hollowing is avoided, a bone union to the calvaria is improved, and the possibility of bone infection is decreased. The osteoplastic component of the technique adds to the improved long-term cosmesis and warrants active consideration in the art of neurosurgery.
- Published
- 2005
- Full Text
- View/download PDF
37. Extradural anterior clinoidectomy. Technical note.
- Author
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Noguchi A, Balasingam V, Shiokawa Y, McMenomey SO, and Delashaw JB Jr
- Subjects
- Brain Neoplasms surgery, Craniotomy methods, Humans, Intracranial Aneurysm surgery, Skull Base anatomy & histology, Skull Base surgery
- Abstract
The anterior clinoid process (ACP), located on the skull base, is a relatively small structure, although its removal provides enormous gain in facilitating the management of lesions--either tumors or aneurysms--in the paraclinoid region and upper basilar artery. The extensive surgical field gained contributes to safer exposure of the neurovascular elements in the vicinity while avoiding excessive and hazardous retraction of the brain. In this report the authors present a technically simpler avenue for performing an extradural anterior clinoidectomy after reviewing the anatomy of the ACP and its anatomical variations. Additionally, the original Dolenc procedure and its subseqtient derivatives are compared and contrasted to the authors' simpler and less laborious technique. Different clinical situations in which to use the procedure are described based on the authors' experience from 60 cases (40 aneurysm cases and 20 tumor cases) during a 4-year period.
- Published
- 2005
- Full Text
- View/download PDF
38. Supraorbital craniotomy for parasellar lesions. Technical note.
- Author
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Noguchi A, Balasingam V, McMenomey SO, and Delashaw JB Jr
- Subjects
- Brain Neoplasms surgery, Humans, Intracranial Aneurysm surgery, Meningioma surgery, Orbit, Craniotomy methods
- Abstract
The authors present a modification to a previously reported supraorbital craniotomy procedure that is smaller, simpler, safe, and cosmetically pleasing. Minimal brain retraction is used without compromising the surgical exposure of the orbital roof, floor of the anterior fossa, and the parasellar region to treat tumoral lesions that are located medial to the ipsilateral optic nerve as well as aneurysms of the anterior communicating artery.
- Published
- 2005
- Full Text
- View/download PDF
39. Extended middle fossa approach: quantitative analysis of petroclival exposure and surgical freedom as a function of successive temporal bone removal by using frameless stereotaxy.
- Author
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Hsu FP, Anderson GJ, Dogan A, Finizio J, Noguchi A, Liu KC, McMenomey SO, and Delashaw JB Jr
- Subjects
- Cadaver, Cochlea surgery, Ear Canal surgery, Humans, Zygoma surgery, Neurosurgical Procedures methods, Skull Base surgery, Stereotaxic Techniques
- Abstract
Object: Conventional wisdom regarding skull base surgery says that more extensive bone removal equals greater exposure. Few researchers have quantitatively examined this assertion, however. In this study the authors used a frameless stereotactic system to measure quantitatively the area of petroclival exposure and surgical freedom for manipulation of instruments with successive steps of temporal bone removal., Methods: With the aid of high-power magnification and a high-speed drill, 12 cadaveric specimens were dissected in four predetermined, successive bone removal steps: 1) removal of the Kawase triangle; 2) removal of the Glasscock triangle; 3) removal of the cochlea together with skeletonization of the anterior internal auditory canal; and 4) inferior displacement of the zygoma. Step 1 offered 62 +/- 43 mm2 of exposed petroclival area, with 84 +/- 69 mm2 of surgical freedom; Step 2, 61 +/- 22 and 76 +/- 58 mm2; Step 3, 128 +/- 47 and 109 +/- 87 mm2; and Step 4, 135 +/- 38 and 102 +/- 69 mm2, respectively., Conclusions: The middle fossa approach provided a means surgically to expose the petroclival area. When examined quantitatively by using a frameless stereotactic device, the authors determined that the removal of the cochlea and skeletonization of the anterior internal auditory canal (Step 3) provided the most significant increase in both exposure and surgical freedom. Removal of the zygoma improved neither exposure nor surgical freedom.
- Published
- 2004
- Full Text
- View/download PDF
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