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7 results on '"Cordesmeyer, Stefanie"'

1. Multimodales chirurgisches Vorgehen zur Behandlung eines Plattenepithelkarzinoms auf dem Boden eines chronischen Druckulkus durch Hemipelvektomie und Rekonstruktion mittels Fillet-Flap

Author

Cordesmeyer, Stefanie, Kühling, August, Bausch, Dirk, Stang, Felix, Mailänder, Peter, and Kisch, Tobias

Subjects
ddc: 610, 610 Medical sciences, Medicine
Abstract

Druckulzera entstehen häufig über knöchernen Vorsprüngen und insbesondere bei immobilen Patienten wie Intensivpatienten, Betagten oder Patienten mit Hemi- bzw. Tetraplegie. In diesem Patientengut sind regelhaft eine Reihe von Komorbiditäten zu verzeichnen, welche die therapeutischen[zum vollständigen Text gelangen Sie über die oben angegebene URL], 49. Jahrestagung der Deutschen Gesellschaft der Plastischen, Rekonstruktiven und Ästhetischen Chirurgen (DGPRÄC), 23. Jahrestagung der Vereinigung der Deutschen Ästhetisch-Plastischen Chirurgen (VDÄPC)

Published
2018

2. Littoral cell angioma of the spleen in a patient with previous pulmonary sarcoidosis: a TNF-α related pathogenesis?

Author

Titze Ulf, Pützler Manfred, Cordesmeyer Stefanie, Paulus Harald, and Hoffmann Matthias W

Subjects
Splenic tumor, littoral cell angioma, visceral organ malignancies, sarcoidosis, TNF-α, Surgery, RD1-811, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract

Abstract Background Littoral cell angioma (LCA) is a rare vascular tumor of the spleen. Generally thought to be benign, additional cases of LCA with malignant features have been described. Thus, its malignant potential seems to vary and must be considered uncertain. The etiology remains unclear, but an immune dysregulation for the apparent association with malignancies of visceral organs or immune-mediated diseases has been proposed. Case Presentation We report a case of LCA in a 43-year old male patient who presented with a loss of appetite and intermittent upper abdominal pain. Computed tomography showed multiple hypoattenuating splenic lesions which were hyperechogenic on abdominal ultrasound. Lymphoma was presumed and splenectomy was performed. Pathological evaluation revealed LCA. Conclusions LCA is a rare, primary vascular neoplasm of the spleen that might etiologically be associated with immune dysregulation. In addition, it shows a striking association with synchronous or prior malignancies. With about one-third of the reported cases to date being co-existent with malignancies of visceral organs or immune-mediated diseases, this advocates for close follow-ups in all patients diagnosed with LCA. To our knowledge, this report is the first one of LCA associated with previous pulmonary sarcoidosis and hypothesizes a TNF-α related pathogenesis of this splenic tumor.

Published
2011
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3. Minimierung der Magenentleerungsstörung nach pyloruserhaltender partieller Duodenopankreatektomie (PPDP) durch einfache Modifikation der Rekonstruktionstechnik

Author

Cordesmeyer, Stefanie, Lodde, Stefanie, Buhr, Johanna, Krückemeier, Kim, Vogel, Teresa, Allemeyer, Erik, and Hoffmann, Matthias

Subjects
ddc: 610, 610 Medical sciences, Medicine
Abstract

Einleitung: Magenentleerungsstörungen (DGE) stellen neben Pankreasfisteln nach wie vor die Hauptkomplikation in der Pankreaschirurgie dar. Bezüglich der Überlegenheit der verschiedenen OP-Techniken wie distale Gastrektomie vs. PPDP, antekolische/retrokolische Rekonstruktionsverfahren[for full text, please go to the a.m. URL], 132. Kongress der Deutschen Gesellschaft für Chirurgie

Published
2015

4. Prävention verzögerter Magenentleerung nach pyloruserhaltender Pankreatoduodenektomie mittels antekolischer Rekonstruktion, einer langen Jejunumschlinge und einer Jejuno-Jejunostomie

Author

Cordesmeyer, Stefanie, Lodde, Stefanie, Fischer, Frank, and Hoffmann, Matthias

Subjects
ddc: 610, 610 Medical sciences, Medicine
Abstract

Einleitung: Die verzögerte Magenentleerung (DGE) ist eine der Hauptkomplikationen nach pyloruserhaltender Pankreaskopfresektion (PPPD). Um das Auftreten der Magenentleerungsstörungen zu reduzieren, sind die Rekonstruktionsmethoden überdacht und modifiziert worden. Ziel dieser retrospektiven[for full text, please go to the a.m. URL], 130. Kongress der Deutschen Gesellschaft für Chirurgie

Published
2013

5. Littoral cell angioma of the spleen in a patient with previous pulmonary sarcoidosis: a TNF-α related pathogenesis?

Author

Cordesmeyer, Stefanie, Pützler, Manfred, Titze, Ulf, Paulus, Harald, Hoffmann, Matthias W, and Universitäts- und Landesbibliothek Münster

Subjects
Adult, Male, genetic structures, Biopsy, Splenic tumor, littoral cell angioma, visceral organ malignancies, sarcoidosis, TNF-α, lcsh:Surgery, Case Report, lcsh:RC254-282, Diagnosis, Differential, Sarcoidosis, Pulmonary, Biomarkers, Tumor, Humans, ddc:610, Immunity, Cellular, Tumor Necrosis Factor-alpha, Splenic Neoplasms, lcsh:RD1-811, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Immunohistochemistry, eye diseases, Oncology, Medicine and health, Splenectomy, Surgery, Hemangioma, Tomography, X-Ray Computed, Spleen, Follow-Up Studies
Abstract

Background Littoral cell angioma (LCA) is a rare vascular tumor of the spleen. Generally thought to be benign, additional cases of LCA with malignant features have been described. Thus, its malignant potential seems to vary and must be considered uncertain. The etiology remains unclear, but an immune dysregulation for the apparent association with malignancies of visceral organs or immune-mediated diseases has been proposed. Case Presentation We report a case of LCA in a 43-year old male patient who presented with a loss of appetite and intermittent upper abdominal pain. Computed tomography showed multiple hypoattenuating splenic lesions which were hyperechogenic on abdominal ultrasound. Lymphoma was presumed and splenectomy was performed. Pathological evaluation revealed LCA. Conclusions LCA is a rare, primary vascular neoplasm of the spleen that might etiologically be associated with immune dysregulation. In addition, it shows a striking association with synchronous or prior malignancies. With about one-third of the reported cases to date being co-existent with malignancies of visceral organs or immune-mediated diseases, this advocates for close follow-ups in all patients diagnosed with LCA. To our knowledge, this report is the first one of LCA associated with previous pulmonary sarcoidosis and hypothesizes a TNF-α related pathogenesis of this splenic tumor.

Published
2011

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