Kwon Ji Hyun, Min Soo Kee, Shin Mi Kyung, Lee Yong Seong, Lee Young-Goo, Ko Young Hyeh
Department of Pathology, Hallym University Kangdong Sacred Heart Hospital, Seoul, Korea.
Korean J Pathol. 2012 Feb;46(1):79-82. doi: 10.4132/KoreanJPathol.2012.46.1.79. Epub 2012 Feb 23.
Castleman disease is a rare lymphoproliferative lesion that is predominantly found in the mediastinum. Retroperitoneal and pararenal localizations are very rare. We describe a 36-year-old man with a hyaline vascular type of Castleman disease involving renal parenchyma and a paraaortic lymph node. Most reported renal Castleman disease was plasma cell type with systemic symptoms. Herein, we report the first Korean case of the hyaline vascular type of Castleman disease involving the renal parenchyma and the paraaortic lymph node simultaneously.
卡斯特曼病是一种罕见的淋巴增生性病变,主要见于纵隔。腹膜后和肾旁部位非常罕见。我们描述了一名36岁男性,患有透明血管型卡斯特曼病,累及肾实质和主动脉旁淋巴结。大多数报道的肾卡斯特曼病为伴有全身症状的浆细胞型。在此,我们报告首例韩国人同时发生累及肾实质和主动脉旁淋巴结的透明血管型卡斯特曼病病例。