Localized Castleman's Disease Presenting as a Vascular Right Iliac Fossa Mass

Castleman's disease is a rare lymphoproliferative disorder of unknown aetiology. The presentation is varied, diagnosis is difficult, and optimum management is still unknown. We report our experience with a case of Castleman's disease in a 34-year-old woman who presented with pallor, hepato...

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Main Authors: Khairul Abdullah Muhsein, Ngoh-Chin Liew, Abdul Rahman Hikmet Shaker, Iskandar Abdul Wahab Shahrin
Format: Article
Language:English
Published: Elsevier 2004-01-01
Series:Asian Journal of Surgery
Online Access:http://www.sciencedirect.com/science/article/pii/S1015958409602463
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spelling doaj-919d746200bc4c53a5db3d30c7fd44262020-11-25T00:59:58ZengElsevierAsian Journal of Surgery1015-95842004-01-01271545710.1016/S1015-9584(09)60246-3Localized Castleman's Disease Presenting as a Vascular Right Iliac Fossa MassKhairul Abdullah MuhseinNgoh-Chin LiewAbdul Rahman Hikmet ShakerIskandar Abdul Wahab ShahrinCastleman's disease is a rare lymphoproliferative disorder of unknown aetiology. The presentation is varied, diagnosis is difficult, and optimum management is still unknown. We report our experience with a case of Castleman's disease in a 34-year-old woman who presented with pallor, hepatosplenomegaly, and a right iliac fossa mass that was 5 cm in diameter. This was initially diagnosed as a soft tissue sarcoma and preoperative tumour embolization was planned before excision. Mesenteric arteriogram revealed that the feeder arteries arose from the superior mesenteric artery and embolization was aborted for fear of causing bowel ischaemia. On laparotomy, lymphoid enlargement was found between the leaves of the jejunal mesentery. The tumour was relatively avascular and the overlying mesenteric vessels contributed to the duplex ultrasound and computerized tomography appearance of hypervascularity. The tumour with the mesentery and the overlying segment of jejunum was excised completely. Histopathology confirmed Castleman's disease. The purpose of this report is to present this rare case that caused a diagnostic dilemma and to review the management of this disorder.http://www.sciencedirect.com/science/article/pii/S1015958409602463
collection DOAJ
language English
format Article
sources DOAJ
author Khairul Abdullah Muhsein
Ngoh-Chin Liew
Abdul Rahman Hikmet Shaker
Iskandar Abdul Wahab Shahrin
spellingShingle Khairul Abdullah Muhsein
Ngoh-Chin Liew
Abdul Rahman Hikmet Shaker
Iskandar Abdul Wahab Shahrin
Localized Castleman's Disease Presenting as a Vascular Right Iliac Fossa Mass
Asian Journal of Surgery
author_facet Khairul Abdullah Muhsein
Ngoh-Chin Liew
Abdul Rahman Hikmet Shaker
Iskandar Abdul Wahab Shahrin
author_sort Khairul Abdullah Muhsein
title Localized Castleman's Disease Presenting as a Vascular Right Iliac Fossa Mass
title_short Localized Castleman's Disease Presenting as a Vascular Right Iliac Fossa Mass
title_full Localized Castleman's Disease Presenting as a Vascular Right Iliac Fossa Mass
title_fullStr Localized Castleman's Disease Presenting as a Vascular Right Iliac Fossa Mass
title_full_unstemmed Localized Castleman's Disease Presenting as a Vascular Right Iliac Fossa Mass
title_sort localized castleman's disease presenting as a vascular right iliac fossa mass
publisher Elsevier
series Asian Journal of Surgery
issn 1015-9584
publishDate 2004-01-01
description Castleman's disease is a rare lymphoproliferative disorder of unknown aetiology. The presentation is varied, diagnosis is difficult, and optimum management is still unknown. We report our experience with a case of Castleman's disease in a 34-year-old woman who presented with pallor, hepatosplenomegaly, and a right iliac fossa mass that was 5 cm in diameter. This was initially diagnosed as a soft tissue sarcoma and preoperative tumour embolization was planned before excision. Mesenteric arteriogram revealed that the feeder arteries arose from the superior mesenteric artery and embolization was aborted for fear of causing bowel ischaemia. On laparotomy, lymphoid enlargement was found between the leaves of the jejunal mesentery. The tumour was relatively avascular and the overlying mesenteric vessels contributed to the duplex ultrasound and computerized tomography appearance of hypervascularity. The tumour with the mesentery and the overlying segment of jejunum was excised completely. Histopathology confirmed Castleman's disease. The purpose of this report is to present this rare case that caused a diagnostic dilemma and to review the management of this disorder.
url http://www.sciencedirect.com/science/article/pii/S1015958409602463
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