485 results on '"vaskulitis"'
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152. 33-jährige Patientin mit thorako-abdominellen Schmerzen und Blutdruckdifferenz.
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Hanses, F., Müller-Ladner, U., Schölmerich, J., and Schäffler, A.
- Abstract
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- Published
- 2004
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153. Morbus Wegener im Kopf-Hals-Bereich.
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Gottschlich, S., Ambrosch, P., Gross, W., and Hellmich, B.
- Abstract
Copyright of HNO is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2004
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154. Alergijski angiitis i granulomatoza.
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Trifunovic, Gordana, Plavec, Goran, Tomic, Ilija, Popovic, Lidija, and Stefanovic, Dusan
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GRANULOMA , *CHURG-Strauss syndrome , *ASTHMA , *HEART failure , *GLUCOCORTICOIDS - Abstract
Allergic granulomatous angiitis (AGA) - Churg-Strauss syndrome, is a rare auto-immune disease characterized by three distinct clinical phases: prodromal, eosinophilic, and vasculitic, and most of respiratory symptoms and signs begin in the first two phases of the disease. Two female patients of different age, who fulfilled the diagnostic criteria for AGA, and were in different phases and with the different duration of the disease are presented. The first patient (24 years of age) was admitted to the hospital due to aggravation of asthma, heart failure, and polyneuropathy. The second one (45 years of age) was also hospitalized due to the worsening of asthma, polyneuropathy, and fever. Both were treated continuously with glucocorticoids. The older patient also received a total of six pulse doses of cyclophosphamide. Satisfactory response to such a treatment was achieved in both cases. [ABSTRACT FROM AUTHOR]
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- 2004
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155. Vitreoretinales Traktionssyndrom bei multipler Sklerose.
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Hochwarter, A., Prainer, C., Binder, S., and Stolba, U.
- Abstract
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- Published
- 2004
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156. Humorale Vaskulitisdiagnostik bei peripherer arterieller Verschlusskrankheit.
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Kroeger, Knut and Kreuzfelder, Ernst
- Abstract
Copyright of Herz is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2004
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157. Therapie der primär systemischen Vaskulitiden.
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Groot, K., Gross, W., and Hellmich, B.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2003
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158. Influenza-Schutzimpfung und Dermatosen – Koinzidenz oder kausale Assoziation?
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Hehn, Jennifer, Hartmann, Klaus, Bröcker, Eva-Bettina, and Goebeler, Matthias
- Abstract
Copyright of Journal der Deutschen Dermatologischen Gesellschaft is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2003
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159. Das Kawasaki-Syndrom Plötzlicher und unerwarteter Tod eines Säuglings.
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Zinka, B., Rauch, E., Büttner, A., Amberg, R., and Penning, R.
- Abstract
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- Published
- 2002
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160. Umschriebene Vaskulitis mit Posteriorinfarkt bei Hashimoto-Enzephalopathie.
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Becker, H., Hofmann, M., von Einsiedel, H., Conrad, B., and Sander, D.
- Abstract
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- Published
- 2002
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161. Unklares Fieber, Kopf- und Muskelschmerzen, Hämoptoe, Hepatosplenomegalie und Ikterus Zwei Fallbeispiele.
- Author
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Locher, S., Büchel, B., Kohler, H. P., and Nohl, F.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2002
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162. Das Churg-Strauss-Syndrom.
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Gross, W. L.
- Abstract
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- Published
- 2001
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163. Die primäre Angiitis des ZNS (PACNS).
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Rollnik, J. D., Brandis, A., Dehghani, K., Bufler, J., Lorenz, M., Heidenreich, F., and Donnerstag, F.
- Abstract
Copyright of Der Nervenarzt is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2001
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164. Nierenbeteiligung bei hypokomplementären Urtikaria-Vaskulitis-Syndrom – einer Spielart des systemischen Lupus erythematodes.
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Brass, Horst, Uppenkamp, Michael, and Voigtländer, Volker
- Abstract
Copyright of Medizinische Klinik (Urban & Vogel) is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2001
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165. Immunpathogenetische Vorstellungen bei entzündlich-rheumatischen Erkrankungen.
- Author
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Sieper, J., Burkhardt, H., and Gross, W.L.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2001
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166. Magnetresonanz-Angiographie bei entzündlichen Hirnerkrankungen.
- Author
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Felber, S., Auer, A., and Schmutzhard, E.
- Abstract
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- Published
- 2000
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167. Thrombangiitis Obliterans.
- Author
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Franke, W., Schulte, K. W., Ruzicka, T., and Krutmann, J.
- Abstract
Copyright of Der Hautarzt is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2000
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168. Plötzlicher Herztod beim Sport infolge einer Koronariitis.
- Author
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Bilkenroth, B. and Wegmann, W.
- Abstract
Copyright of Der Pathologe is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2000
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169. Pneumokokkenmeningitis nach Zahnextraktion: Wertigkeit der MRT zur Früherkennung von Komplikationen.
- Author
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Friese, Sigrid, Gleichmann, Marc, Mader, Irina, Bühring, Udo, and Küker, Wilhelm
- Abstract
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- Published
- 2000
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170. Sneddon-Syndrom: Vaskulitis oder thrombotische Vaskulopathie?
- Author
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Zipper, Stephan G., Lambert, Sybille, Seemann, Wolf-Rainer, Baer, Ulrike, and Schlißke, Klaus
- Abstract
Copyright of Medizinische Klinik (Urban & Vogel) is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2000
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171. [Rheumatological emergency on the edge of intensive care medicine]
- Author
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Peter, Härle
- Subjects
Vasculitis ,Emergency Medical Services ,Critical Care ,Nebenniereninsuffizienz ,Immunsuppressive Therapie ,Medikamenteninduzierte Hypersensitivitätssyndrome ,Immunosuppressive treatment ,Drug-induced hypersensitivity syndrome ,Rheumatic Diseases ,Leitthema ,Humans ,Infection complications ,Vaskulitis ,Infektionskomplikationen ,Immunosuppressive Agents ,Adrenal insufficiency - Abstract
Zusammenfassung In der rheumatologischen Praxis treten immer wieder Situationen auf, die eine umgehende Entscheidung des Rheumatologen erfordern, um bleibende Schäden vom Patienten abzuwenden. Insbesondere handelt es sich um fulminant verlaufende entzündliche Erkrankungen, schwere Nebenwirkungen durch zahlreiche Medikamente oder auch Infektionskomplikationen unter einer immunsuppressiven Therapie.
- Published
- 2019
172. [What are the indications for rescue procedures? : Systemic rheumatic diseases in the intensive care unit]
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B, Hellmich and C, Löffler
- Subjects
Vasculitis ,Respiratory Distress Syndrome ,Extracorporeal membrane oxygenation ,Anti-Glomerular Basement Membrane Disease ,Intravenöse Immunglobuline ,Intravenous immunoglobulins ,Kollagenose ,Plasmapheresis ,Intensive Care Units ,Extrakorporale Membranoxygenierung ,Plasmapherese ,Rheumatic Diseases ,Leitthema ,Collagen vascular diseases ,Humans ,Vaskulitis - Abstract
Zusammenfassung Schwere, organ- oder lebensbedrohliche Manifestationen entzündlicher rheumatischer Erkrankungen, wie z. B. eine diffuse alveoläre Hämorrhagie im Rahmen einer Kleingefäßvaskulitis, sprechen nicht immer ausreichend oder mit zeitlicher Verzögerung auf eine immunsuppressive Therapie an. Bei einem drohenden oder bereits eingetretenen Organversagen besteht dann nicht selten die Notwendigkeit, die immunsuppressive Therapie auf der Intensivstation um rasch wirksame Rescue-Therapieverfahren zu ergänzen. Aufgrund der Seltenheit vieler rheumatischer Erkrankungen ist die Evidenz zum Einsatz von Rescue-Therapieverfahren wie der Plasmapherese, der extrakorporalen Membranoxygenierung (ECMO) oder der Gabe von intravenösen Immunglobulinen (IVIG) für viele Indikationen eher gering. Der Einsatz der Plasmapherese wird bei einer akuten Anti-GBM(glomeruläre Basalmembran)-Erkrankung (Goodpasture Syndrom) oder einem katastrophalen Antiphospholipidantikörpersyndrom (CAPS) als sinnvoll angesehen. Eine ECMO-Therapie kann bei persistierender respiratorischer Insuffizienz trotz mechanischer Beatmung als Folge einer diffusen alveolären Hämorrhagie oder eines Acute-Respiratory-Distress-Syndroms (ARDS) anderer Ursache erwogen werden. Eine Gabe von IVIG ist bei einer akuten kardialen Beteiligung im Rahmen einer Kawasaki-Erkrankung indiziert und kann beim CAPS sowie bei therapierefraktären Myositiden erwogen werden.
- Published
- 2019
173. Kutane Polyarteriitis nodosa.
- Author
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Jansen, T.M. and Hoff, N.-Ph.
- Abstract
Copyright of Der Hautarzt is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2015
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174. Morbus Adamantiades-Behçet bei einer 29-jährigen Patientin.
- Author
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Hausberger, Silke, Langner-Wegscheider, Beate-Julia, and Wedrich, Andreas
- Abstract
Copyright of Spektrum der Augenheilkunde is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2015
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175. Gambaran Kunjungan Pasien Rawat Jalan Endokrinologi Anak dan Remaja FK USU / RS. H. Adam Malik Medan, Tahun 2000-2004
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Hakimi Hakimi, Melda Deliana, and Charles D. Siregar
- Subjects
hipertensi ,lcsh:R ,General Engineering ,lcsh:RJ1-570 ,vaskulitis ,lcsh:Medicine ,lcsh:Pediatrics ,perdarahan intrakranial ,nefritis lupus - Abstract
Latar belakang. Masyarakat banyak yang tidak mengetahui bahwa kelainan endokrinpada anak membutuhkan penanganan yang khusus dari ahli endokrinologi anak.Tujuan penelitian. Penelitian ini bertujuan untuk mengetahui gambaran kunjunganpasien endokrinologi anak dan remaja di RS H.Adam Malik Medan tahun 2000-2004.Metoda. Penelitian ini merupakan studi deskriptif retrospektif. Data diperoleh daricatatan rekam medik pasien yang berkunjung ke Poliklinik Endokrinologi Anak danRemaja FKUSU/RS. H. Adam Malik Medan dalam kurun waktu Januari 2000-Desember2004.Hasil. Terdapat 93 pasien yang berkunjung ke Poliklinik Endokrinologi Anak danRemaja, 33 anak perempuan (35%) dan 60 anak laki-laki(65%). Sebaran umur padasaat datang pertama kali adalah 33 anak (35%) berusia 0-5 tahun, 25 anak (27%) berusia> 5-10 tahun, 25 anak (27) % > 10-15 tahun, dan 10 anak (11%) berusia >15 tahun.Keluhan utama yang paling sering muncul pada saat pasien datang berobat pertama kaliadalah alat kelamin laki-laki kecil 15 kasus (16%) dan buah zakar tidak turun 15 kasus(16%), keluhan anak pendek 13 kasus (14%), benjolan di leher 12 kasus (13 %). Diagnosisyang dijumpai adalah kriptorkismus (20%), mikropenis (16%) dan hipotiroidismekongenital (13%). Status gizi berdasarkan NCHS WHO 2000 pada pasien yangberkunjung terutama gizi baik, terdapat pada 22 kasus (23,6%).Kesimpulan. Kasus terbanyak berkunjung ke Poliklinik Endokrinologi Anak dan Remajaadalah kriptorkismus (20%), mikropenis (16%) dan hipotiroidisme kongenital (13%).Diduga masih banyak kasus endokrinologi anak dan remaja yang tidak ditangani olehahli endokrinologi anak secara komprehensif oleh karena kemungkinan banyak kasusyang tidak dirujuk.
- Published
- 2016
176. Inflammatory diseases of the aorta
- Author
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Markus Steinbauer, Niels Zorger, and I. Töpel
- Subjects
Vasculitis ,Pathology ,medicine.medical_specialty ,Pathogenesis ,Disease ,030204 cardiovascular system & hematology ,Pathogenese ,03 medical and health sciences ,Rheumatic diseases ,0302 clinical medicine ,Aortic infection ,Large vessel vasculitis ,Medicine ,Vaskulitis ,030212 general & internal medicine ,Arteritis ,Aortitis ,business.industry ,Übersichten ,Vascular surgery ,Rheumatische Erkrankungen ,medicine.disease ,Arteriitis ,Giant cell arteritis ,Infektion der Aorta ,Etiology ,Surgery ,Cardiology and Cardiovascular Medicine ,business - Abstract
Aortitis is a term which encompasses inflammatory changes to the aortic wall from various pathogenic etiologies. Large vessel vasculitis, such as Takayasu arteritis and giant cell arteritis represent the most common entities; however, there is also an association with other rheumatological diseases. Chronic idiopathic periaortitis represents a distinct disease entity and infectious aortitis is a rare but life-threatening disease. Due to the diverse clinical pictures vascular surgeons often face a significant challenge in terms of making an accurate initial diagnosis. Treatment requires an interdisciplinary approach. This article describes the pathogenesis of the various forms of aortitis as well as the diagnostic methods and treatment approaches.Unter dem Begriff der Aortitis werden entzündliche Veränderungen der Aortenwand verschiedener pathogenetischer Ursachen zusammengefasst. Großgefäßvaskulitiden, wie die Takayasu-Arteriitis und die Riesenzellarteriitis, stellen die häufigsten Erkrankungen dar, es findet sich aber auch eine Assoziation mit anderen rheumatologischen Krankheiten. Die chronische idiopathische Periaortitis stellt eine eigene Entität dar. Eine infektiöse Aortitis ist eine seltene aber lebensbedrohliche Situation. Für den Gefäßmediziner ist es auf Grund des vielgestaltigen klinischen Bildes oft schwierig, eine exakte Erstdiagnose zu stellen. Die Behandlung erfordert eine interdisziplinäre Zusammenarbeit. Dieser Beitrag soll Ursachen, diagnostische Methoden und Therapieansätze der verschiedenen Aortitiden darstellen.
- Published
- 2016
- Full Text
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177. Nagelveränderungen bei rheumatischen Erkrankungen.
- Author
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Wollina, U., Barta, U., Uhlemann, C., Oelzner, P., and Hein, G.
- Abstract
Copyright of Der Hautarzt is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 1999
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178. Rheumatologie.
- Author
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Genth, E., Burmester, G.-R., Gross, W. L., Märker-Hermann, E., and Ringe, J. D.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 1999
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179. Associations between interleukin-1 polymorphisms and susceptibility to vasculitis: a meta-analysis
- Author
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Song, G.G., Kim, J.-H., and Lee, Y.H.
- Published
- 2016
- Full Text
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180. Skorbut: Eine seltene Differenzialdiagnose rheumatischer Erkrankungen
- Author
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Hofheinz, K., Ganzleben, I., Schliep, S., Wacker, J., Schett, G., and Manger, B.
- Published
- 2016
- Full Text
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181. Diagnostische Relevanz von histologischen Befunden bei ANCA assoziierten Vaskulitiden
- Author
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Kronfeldner, Julia
- Subjects
Biopsie ,Immunologie ,Vaskulitis ,Angiologie - Abstract
Die zytoplasmatischen-Antikörper (ANCA) assoziierte Vaskulitis ist eine diagnostische Herausforderung. Es wurde retrospektiv die Hypothese untersucht: Biopsien sind von diagnostischer Relevanz für: - die Diagnostik einer Vaskulitis, - die Diagnostik und Klassifikation einer Granulomatose mit Polyangiitis (GPA) / Mikroskopische Polyangiitis (MPA) / Eosinophile Granulomatose mit Polyangiitis (EGPA). Es wurden Patienten mit Biopsien und ANCA-assoziierter Vaskulitis aufgenommen. Die diagnostische Relevanz wurde durch Anwendung von Diagnosemethoden (Travis et al. 1991, Leavitt et al. 1990, Masi et al. 1990, DCVAS-Investigators 2017, Watts et al. 2007) untersucht. Die Patienten wurden mit und ohne Biopsien klassifiziert. Es erfolgte eine explorative Analyse der Verteilung von klinischen Parametern bei Patienten mit und ohne auffälliger Biopsie. Zur Diagnostik einer Vaskulitis nach den EULAR-Empfehlungen (Hellmich et al. 2007) war bei 8% der EGPA, 2% der GPA und 0% der MPA eine Biopsie notwendig. Durch die American College of Rheumatology (ACR) Kriterien 1990 bzw. durch die Diagnostic and Classification Criteria in Vasculitis (DCVAS)-Kriterien von 2017 werden bei der GPA 6,6% bzw. 2%, bei der EGPA 35,5% bzw. 21% und bei der MPA 0% der Patienten ohne Biopsie falsch klassifiziert. Bei Anwendung des European Medical Agency-Algorithmus werden bei der GPA 4,7%, bei der EGPA 28,8% und bei der MPA 14,6 % der Patienten ohne Biopsie falsch zugeordnet. Die Hypothese, dass Biopsien von diagnostischer Relevanz sind, bestätigte sich für GPA/MPA Patienten nicht. Bei EGPA-Patienten bestätigt sich die Hypothese. Biopsie waren vor allem im aktiven Schub, bei erhöhten Entzündungswerten und vor Therapiebeginn pathologisch. Eine Vaskulitis zeigte sich vor allem bei positivem ANCA-Status. Hierdurch kann aber noch keine klinische Empfehlung entstehen. Die Hypothese muss in weiteren prospektiven Studien bestätigt werden.
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- 2019
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182. POZVANA PREDAVANJA/USMENA PRIOPĆENJA
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Mitrović, Joško and Morović-Vergles, Jadranka
- Subjects
vaskulitis ,središnji živčani sustav - Abstract
Primarni vaskulitis središnjeg živčanog sustava (PVSŽS) rijetka je i teška bolest ograničena na središnji živčani sustav. Etiologija bolesti nije poznata, ali se smatra da uslijed interakcije između više endogenih i okolišnih čim- benika dolazi do aktivacije imunosnog sustava i upalne infiltracije stjenki malih odnosno srednje velikih krvnih žila. Kao posljedica nastaju vaskularna oštećenja koja uzrokuju ishemijske ili hemoragične promjene na mozgu. Bolest se većinom dijagnosticira kod osoba srednje životne dobi sa prisutnim neurološkim simptomima, a koje u anamnezi uglavnom nemaju rizične čimbenike za kardiovaskularne bolesti. Iako ne postoji karakteristična kli- nička slika većina bolesnika ima glavobolju i poremećaj kognitivnih funkcija. Česti su i žarišni neurološki ispadi (hemipareza, dizartrija, afazija, smetnje vida), encefalopatija ili epileptički napadaji. U rijetkim slučajevima moguća je zahvaćenost leđne moždine. Za dijagnozu bolesti važan je multidisciplinarni pristup jer je važno povezati kliničku sliku s analizom likvora i slikovnim metodama (MR angiografija ili klasična angiografija). U slučaju kliničke ili slikovne dvojbe potrebno je napraviti tkivnu biopsiju kojom se dokazuje prisustvo karakterističnih patohistoloških promjena. Laboratorij- ski nalazi kao i nalazi imunoloških pretraga najčešće su uredni. Diferencijalna dijagnostika PVSŽS je široka i uključuje različite neurološke, zarazne, vaskularne, maligne i hematološke bolesti. Kod bolesnika koji imaju sistemske simptome/znakove, povišene upalne biljege ili specifična protutijela potrebno je isključiti sekundarni oblik vaskulitisa odnosno prisustvo drugih bolesti-najčešće sistemskih bolesti vezivnog tkiva ili sistemskih vaskultisa te ih liječiti sukladno osnovnoj bolesti. Liječenje PVSŽS temelji se na primjeni imunosupresivnih lije- kova. U indukcijskoj fazi obično se koriste pulsne doze glukokortikoda i ciklofosfamid, dok se u terapiji održava- nja najčešće primjenjuju azatiopirin, metotreksat i mofetil mikofenolat. Sve je više podataka i o učinkovitosti bioloških lijekova (rituksimab, TNF alfa inhibitori).
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- 2019
183. Erythema elevatum diutinum.
- Author
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Wolff, Helmut, Maciejewski, Wojciech, and Scherer, Reiner
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- 1978
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184. Antineutrophil cytoplasmic autoantibodies: Immunobiological aspects.
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Gross, W., Csernok, E., and Schmitt, W.
- Abstract
Antineutrophil cytoplasmic autoantibodies (ANCA) specific for constituents of neutrophil primary granules and monocyte lysosomes have been demonstrated in various vasculitic disorders. The staining pattern in indirect immunofluorescence microscopy using alcohol-fixed neutrophils as substrate allows distinction among 3 types of ANCA: 1) classic anti-neutrophil cytoplasmic antibody (cANCA, formerly known as ACPA); 2) a type with a perinuclear/nuclear staining pattern produced when alcohol-fixed neutrophils are used as substrate (pANCA); and 3) a mixture of both of the above types (xANCA, also described recently as pANCA). Most cANCA are directed against proteinase 3 ('Wegener's autoantigen'). Some pANCA have specificity for myeloperoxidase and are associated with idiopathic crescentic glomerulonephritis ('renal vasculitis') and other systemic vasculitides exhibiting a paucity of immune deposits in blood vessels. In addition to being a useful serological marker, ANCA appear to be directly involved in the pathogenesis of systemic vasculitis. ANCA can activate cytokine-primed granulocytes and monocytes to undergo a respiratory burst and degranulation. This effect leads to vasculitis through the attachment of these cells to the vascular endothelium primed by cytokine-induced expression of adhesion molecules (E-LAM 1) on the endothelium. Thus, the release of toxic oxygen radicals and lytic enzymes is capable of causing vascular damage. In the present paper we report on the main target antigens and on the history, nomenclature, laboratory methods, and ethiopathological implication of ANCA. Additional pathophysiological aspects of ANCA and/or autoreactive T cells and immmunoregulatory events are also discussed. [ABSTRACT FROM AUTHOR]
- Published
- 1991
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185. Immunologische Systemerkrankungen als Differentialdiagnose in der Psychiatrie.
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Lieb, Klaus, Vaith, Peter, Berger, Mathias, and Bauer, Joachim
- Abstract
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- Published
- 1997
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186. 37jähriger Patient mit Myalgien, Arthralgien, Pseudovaskulitis und Palpitationen.
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Schimpf, R., Hagendorff, A., Dettmers, C., Jung, W., Omran, H., Rockstroh, J., and Lüderitz, B.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 1998
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187. Myokardischämie bei inflammatorischer Kardiomyopathie und Myokarditis.
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Maisch, B., Funck, R. C., Hufnagel, G., and Höffken, H.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 1998
- Full Text
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188. 52jähriger Patient mit Asthma bronchiale, Eosinophilie und Hämoptoe.
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Petrides, P. E., Haegele, U., and Stein, J.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 1997
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189. Konventionelle Immunsuppression chronisch-entzündlicher Systemerkrankungen.
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Gross, W. L., Reinhold-Keller, E., and Trabandt, A.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 1997
- Full Text
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190. Vaskulitis IgA pri odraslih
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Hočevar, Alojzija and Tomšič, Matija
- Subjects
age factors ,žilne bolezni ,adult ,imunoglobulin A ,vaskulitis ,immunoglobulin A ,udc:616.13/.14-002(043.3) ,starostni dejavniki ,vasculitis ,prognoza ,indeks resnosti bolezni ,občutljivost in specifičnost ,sensitivity and specificity ,severity of illness index ,vascular diseases ,prognosis ,odrasli - Published
- 2018
191. Akutni hemoragijski edem dojenèadi.
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Premilovac, Zdenka Pleša, Pasini, Agneza Marija, Vacka, Iva Kolaèek, Pustišek, Nives, and Gagro, Alenka
- Abstract
Acute hemorrhagic edema of infancy refers to vasculitis of small blood vessels that usually occurs in children under two years of age; it is limited to the skin and has good prognosis. The aim of this paper is to present a patient with acute hemorrhagic edema of infancy with typical clinical picture and course in order to highlight uncomplicated and benign nature of the disease, which may have a dramatic clinical presentation and may cause differential diagnostic dilemmas. [ABSTRACT FROM AUTHOR]
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- 2014
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192. Therapeutisches Vorgehen bei ANCA-assoziierten Vaskulitiden
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Hellmich, B.
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- 2015
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193. Unklare akrale Nekrosen an den Fingern.
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Butsch, F., Rudolph, B.M., and Schopf, R.
- Abstract
Copyright of Der Hautarzt is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 2013
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194. Progranulin-Antikörper und hyperphosphoryliertes Progranulin in Vaskulitiden, Kollagenosen und Myositiden
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Klemm, Philipp Christof Moritz and Aßmann, Gunter
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Progranulin ,Autoantikörper ,Bindegewebskrankheit ,Vaskulitis ,ddc:610 ,ddc:620 - Abstract
Autoantikörper spielen eine große Rolle in der Diagnostik und Pathogenese von Vaskulitiden und Kollagenosen. So haben antineutrophile zytoplasmatische Antikörper (ANCA) nicht nur eine Rolle in der Diagnostik der ANCA-assoziierten Vaskulitiden, sondern besitzen auch einen besonderen pathogenetischen Stellenwert. Etablierte Autoantikörper wurden oftmals per Zufall entdeckt; eine systematische Suche nach Autoantikörpern erfolgte bei Vaskulitiden bisher nicht. Unserer Arbeitsgruppe gelang es mittels Proteinarray-basierter Screeninguntersuchungen Au-toantikörper gegen Progranulin (PGRN) in Seren von Patienten mit Granulomatose mit Poly-angiitis, eosinophile Granulomatose mit Polyangiitis, Panarteriitis nodosa und Riesenzellar-teriitis zu entdecken. Progranulin ist ein natürlicher Antagonist des Tumornekrosefaktors α (TNFα). Es wirkt durch hochaffine Bindung an den Tumornekrosefaktorrezeptor-1 und -2 und Death-rezeptor 3. An den beiden ersten antagonisiert Progranulin TNFα, am letztgenannten TNF-ähnliches Molekül 1A. Aufgrund der mutmaßlich proinflammatorischen Wirkung der Progranulin-Antikörper (PGRN-Ak) wurden weitere Seren von Patienten mit rheumatologisch-autoimmunen Erkrankungen untersucht. Mittels ELISA konnten wir das Vorkommen von PGRN-Ak in Seren von Patienten mit jeweils verschiedenen Vaskulitisformen, Kollagenosen und Myositiden untersuchen: Riesenzellarteriitis/Polymyalgia rheumatica (14/65), Takayasu Arteriitis (4/13), klassischer Panarteriitis nodosa (4/10), Granulomatose mit Polyangiitis (31/ 75), eosinophiler Granulomatose mit Polyangiitis (7/23), mikroskopischer Polyangiitis (7/19), ANCA-assoziierten Vaskulitiden (3/6), Morbus Behcet (2/8), undifferenzierte Kollagenose (5/17), Sjögren Syndrom/Sicca Syndrom (9/19), CREST (2/8), systemischer Sklerose (10/31), systemischem Lupus erythematodes (39/91), Antiphospholipidsyndrom (6/15)), Dermatomyo-sitis/Polymyositis (4/33). Zusätzlich wurden zwei Kontrollgruppen (immunologische Kontroll-gruppe (6/31), nicht-immunologische Kontrollgruppe (1/30)) untersucht. Es gelang der erstmalige Nachweis von PGRN-Ak in den untersuchten Erkrankungen und die Beschreibung einer vorläufigen Prävalenz. Es konnte gezeigt werden, dass ein Zusammenhang zwischen dem Auftreten von PGRN-Ak und einer aktiven Erkrankung im Bereich der klein- und mittelkalibrigen Gefäßvaskulitiden besteht. Des Weiteren lieferte diese Arbeit erste Ergeb-nisse in der Fragestellung des molekularen Mechanismus der Entstehung von PGRN-Ak. Durch die Untersuchung mittels isoelektrischer Fokussierung zeigte sich, dass PGRN ausschließlich bei PRGN-Ak positiven Patienten in einer zusätzlichen Isoform zu finden ist. Hier konnte nach-gewiesen werden, dass es sich um eine an Serin 81 hyperphosphorylierte PGRN Isoform handelt. Je nach Phosphorylierungsstatus des PGRN zeigten sich überdies unterschiedliche Spaltmuster von PGRN in Granuline. Autoantibodies play a crucial role in the diagnostic and pathogenesis of vasculitis and connec-tive tissue disorders. Antineutrophilic cytoplasmatic antibodies (ANCA) for example are not only used diagnostically but constitute a pathogenetic role. Todays established antibodies were often discovered by chance rather than by research. A systematic search for antibodies in vas-culitis has not happened so far. We found antibodies directed against Progranulin (PGRN) by screening of sera of patients with granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis, panarteriitis nodosa and giant cell arteritis on proteinmacroarrays. PGRN is a physiologic antagonist to TNFα and TL1a. It inflicts its role by binding to TNFR-1, -2 and DR3. We screened sera of patients with different rheumatic diseases because of the presumed antiinflammatory role of PGRN-antibodies (PGRN-abs). By using ELISA we were able to identify PGRN-abs in sera of patients with vasculitis (Giant cell arteriitis/Polymyalgia rheumatica (14/65), Takayasu Arteri-tiis (4/13), classic Panarteriitis nodosa (4/10), granulomatosis with polyangiitis (31/ 75), eosin-ophilic granulomatosis with polyangiitis (7/23), mikroscopic polyangiitis (7/19), ANCA-assosiacted vaskulitis (3/6), Morbus Behcet (2/8)), connective tissue disorders (undifferantiated connective tissue disorder (5/17), Sjögrens syndrom/sicca syndrom (9/19), CREST (2/8), sys-temic sclerosis (10/31), systematic Lupus erythematodes (39/91), antiphospholipidsyndrom (6/15)), und myositis (dermatomyositis/polymyositis (4/33)). Additionally, two control groups were tested (autoimmune control (6/31), non-autoimmune control (1/30)). Not only were PGRN-abs firstly described in these diseases, but a first prevalance was established. Further-more, we found a significant correlation between disease activity in middle and small vessel vasculitis and PGRN-abs incidence. Also, this thesis contributed to the solution of why PGRN-abs appear. By isoelectric focusing we discovered that PGRN appears in a second isoform ex-clusively in PGRN-ab positive patients. This second isoform could be characterized as PGRN hyperphosphorylated at serine 81. Furthermore, we were able to show different cleavagepat-terns for PGRN into mature GRN based on the phosphorylationstatus of PGRN.
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- 2018
- Full Text
- View/download PDF
195. Myocardial infarction due to coronary thrombosis in a patient with Henoch-Schönlein purpura.
- Author
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Canpolat, U., Yorgun, H., Şahiner, L., and Kabakçi, G.
- Abstract
Copyright of Herz is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2012
- Full Text
- View/download PDF
196. Rasch fortschreitende Hautnekrosen.
- Author
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Creutzfeldt, R., Jansson, A., and Kurnik, K.
- Abstract
Copyright of Monatsschrift Kinderheilkunde is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2010
- Full Text
- View/download PDF
197. Immunsuppression – zu stark oder zu schwach?
- Author
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Schneidewind, A., Fleck, M., Salzberger, B., Schölmerich, J., and Ehrenstein, B.
- Abstract
Copyright of Der Internist is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2009
- Full Text
- View/download PDF
198. Isolierte Manifestation einer nekrotisierenden Vaskulitis an der Harnblase: Ein Fallbericht.
- Author
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Becker, A., Astroza, G., Quezada, N., Riaño, C., Urrutia, J., Guzman, S., and Riaño, C
- Abstract
Copyright of Der Urologe A is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2008
- Full Text
- View/download PDF
199. Pseudoangiitis bei beidseitiger okulärer Ischämie.
- Author
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Baatz, H., Lange, S., Buchner, H., and Scharioth, G.
- Abstract
Copyright of Der Ophthalmologe is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2007
- Full Text
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200. Lethal Fulminate S. aureus Sepsis in M. Behçet Overnight Cold Exposure.
- Author
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Finsterer, J. and Schmidbauer, M.
- Subjects
- *
BEHCET'S disease , *MEDICAL care - Abstract
Whether patients with Behçet's disease (BD) and immunosuppressive therapy are generally prone to acquire severe infectious diseases is unknown. A 48-year-old man under cortícosteroids and azathioprine for BD since 1995 was admitted because of a transitory ischemic attack. Between the third and fourth hospital day he was accidentally locked up, insufficiently dressed, in the hospital's chapel over night. On the following day, he developed fever and deteriorating consciousness until he became comatose. CT scans of the brain were normal and there was only a slight pleocytosis. Despite adequate therapy, the patient's condition further deteriorated such that he died. Responsible for his decline was a fulminate sepsis, diagnosed upon fever, increased C-reactive protein, thrombocyte decline, multi-organ failure, rhabdomyolysis, growth of S. aureus on blood culture, and autopsy, Patients with BD and immunosuppressive therapy, may be more vulnerable to infections and may develop lethal overwhelming sepsis already after overnight cold exposure. [ABSTRACT FROM AUTHOR]
- Published
- 2002
- Full Text
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