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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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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AT khairulabdullahmuhsein localizedcastlemansdiseasepresentingasavascularrightiliacfossamass AT ngohchinliew localizedcastlemansdiseasepresentingasavascularrightiliacfossamass AT abdulrahmanhikmetshaker localizedcastlemansdiseasepresentingasavascularrightiliacfossamass AT iskandarabdulwahabshahrin localizedcastlemansdiseasepresentingasavascularrightiliacfossamass |
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