Castleman’s disease of the mesorectum: Report of a case

The Japanese journal of surgery - Tập 41 - Trang 271-275 - 2011
Mi Ri Hwang1, Hee Jin Chang1, Min Ju Kim2, Guh Jung Seo1, Sang Bum Yoo1, Ji Won Park1, Hyo Seong Choi1, Jae Hwan Oh1
1Center for Colorectal Cancer, National Cancer Center, Goyang-si, Gyeonggi-do, Republic of Korea
2Department of Radiology, Center for Clinical Service, Research Institute & Hospital, National Cancer Center, Goyang-si, Gyeonggi-do, Republic of Korea

Tóm tắt

Castleman’s disease is a benign lymphoid proliferative disorder, which most commonly presents as a solitary mass in the mediastinum, although extrathoracic sites have been reported in the neck, axilla, pelvis, mesentery, pancreas, and retroperitoneum. We report a case of asymptomatic, isolated Castleman’s disease in the mesorectum, which is extremely rare. The patient was a 34-year-old woman who underwent investigations for vaginal spotting. A presacral mass was located on the left side of the rectum, 10 cm from the anal verge. Contrast-enhanced computed tomography showed a large, well-demarcated, strongly enhancing mass with internal radiating septa in the mesorectum. The mass was well circumscribed and isointense to muscle on T1-weighted magnetic resonance imaging, appearing as a slightly hyperintense mass on T2-weighted imaging. We performed laparoscopic mesorectal mass excision, and histological examination revealed features typical of the hyaline-vascular type of Castleman’s disease. Thus, when a mesorectal mass is being investigated, Castleman’s disease should be considered in the differential diagnosis.

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