Pure Red Cell Aplasia를 동반한 후복막강 Castleman병 1예
Retroperitoneal Castleman’s Disease with Pure Red Cell Aplasia
장성환, 도재태, 박도중, 장명철, 노동영, 윤여규, 오승근,
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장성환 ( Chang Sung-Hwan )
서울대학교 의과대학 외과학교실
도재태 ( Doh Jae-Tae )
서울대학교 의과대학 외과학교실
박도중 ( Park Do-Joong )
서울대학교 의과대학 외과학교실
장명철 ( Chang Myung-Chul )
서울대학교 의과대학 외과학교실
노동영 ( Roh Dong-Young )
서울대학교 의과대학 외과학교실
윤여규 ( Youn Yeo-Kyu )
서울대학교 의과대학 외과학교실
오승근 ( Oh Seung-Keun )
서울대학교 의과대학 외과학교실
KMID : 0371320010610040450
Abstract
Castleman’s disease is a distinct lymphoproliferative disorder of unknown origin, which creates both a diagnostic and therapeutic dilemma for most physicians. Here, we present a case of hyaline-vascular and solitary Castleman’s disease associated
with
pure red cell aplasia. A 49-year old woman was admitted suffering from severe anemia. A bone marrow biopsy showed marked erythroid hypoplasia. A solitary retroperitoneal mass was excised and proven to be Castleman’s disease with hyaline-vascular
type
histology. Removal of the mass led to a rapid reversal of anemia. No evidence of recurrence was found 1 year after the excision.
키워드
거대 임파절 증식증; 초자질 혈관형; 고립형; Castleman’s disease; Hyaline-vascular; Solitary;
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