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2015 | 86 | 7 | 337-340
Tytuł artykułu

Gigantic Solitary Fibrous Tumour of Extra-Peritoneal Space. A Case Report and Review of the Literature

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Solitary fibrous tumour (SFT) is a rare soft tissue tumour which belongs to fibroblastic/myofibroblastic group of tumours. The most often it appears in pleura, also in pericardium, internal organs, peritoneum and extraperitoenal space. SFT was first described as a new type of pleura’s tumour by Klemperer and Rabin in 1931. The histogenesis of SFT’s has been discussed for years suggesting its mesothelial origin. Recently, SFT has been classified as a mesenchymal fibroblastic tumour. We report a very rare case of 71-year old man suffering from gigantic solitary fibrous tumour of extraperitoneal space who underwent curative surgery in the Department of General, Gastroenterological and Oncologic Surgery in 2011
Słowa kluczowe
Wydawca

Rocznik
Tom
86
Numer
7
Strony
337-340
Opis fizyczny
Daty
wydano
2014-07-01
otrzymano
2013-05-08
online
2014-09-12
Twórcy
autor
  • Department of General, Gastroenterological and Oncologic Surgery, Warsaw Medical University, tomasz.guzel@wum.edu.pl
  • Department of General, Gastroenterological and Oncologic Surgery, Warsaw Medical University
  • Department of Pathomorphology, Warsaw Medical University
  • Department of General, Gastroenterological and Oncologic Surgery, Warsaw Medical University
  • Department of General, Gastroenterological and Oncologic Surgery, Warsaw Medical University
Bibliografia
  • 1. Klemperer P, Rabin CB: Primary neoplasm of the pleura: a report of five cases. Arch Pathol 1931; 11: 385-412.
  • 2. Bouhabel S, Leblanc G, Ferreira J et al.: Solitary fibrous tumour arising in the mesentery: a case report. W J Surg Oncol 2011; 9: 140.[WoS]
  • 3. Gengler C, Guillou L: Solitary fibrous tumour and haemangiopericytoma: evolution of a concept. Histopathology 2006: 48: 63-74.
  • 4. Hasegawa T, Matsuno Y, Shimodfa T et al.: Extrathoracic solitary fibrous tumours: their histological variabilityand potentially aggressive behaviour. Human Pathol 1999; 30, 12: 1464-73.[Crossref]
  • 5. Musyoki FN, Nahal A, Powell TI: Solitary fibrous tumour: an update on the spectrum of extrapleural manifestations. Skeletal Radiol 2012; 41: 5-13.[PubMed][WoS][Crossref]
  • 6. Pływaczewski R, Hawryłkeiwcz I, Langfort R i wsp.: Odosobniony guz włóknisty opłucnej u 75- letniej chorej. Pneumonol Alergol 2004; 72: 32-36.
  • 7. Nagase T, Adachi I, Yamada T et al.: Solitary fibrous tumour in the pelvic cavity with hypoglicemia: report of a case. Surg Today 2005; 35: 181-84.[Crossref]
  • 8. Yamashita S, Tochigi T, Kawamura S et al.: A case of retroperitoneal solitary fibrous tumour. Act Urol 2007; 53: 477-80.
  • 9. Cristi E, Perrone G, Battista C et al.: A rare case of solitary fibrous tumor of the pre-sacral space: morphological and immunohistochemical features. In Vivo 2005; 19: 777-80.[PubMed]
  • 10. Lau MI, Foo FJ, Sissons MC et al.: Solitary fibrous tumour of small bowel mesentery: a case report and review of the literature. Tumori 2010; 96: 1035-39.[PubMed]
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_pjs-2014-0059
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