Ide Munenori, Asao Takayuki, Yoshida Takatomo, Hirato Junko, Shimura Tatsuo, Morinaga Nobuhiro, Shitara Yoshinori, Ishizaki Masatoshi, Kuwano Hiroyuki
Department of Surgery and.
Rare Tumors. 2010 Mar 31;2(1):e2. doi: 10.4081/rt.2010.e2.
Rosai-Dorfman disease (RDD) was formerly known as "sinus histiocytosis with massive lymphadenopathy", and cases involving the gastrointestinal tract are rare. We present a case of pure extranodal RDD, resected as a polypoid lesion in colonoscopic study. The patient was a 62-year old woman with a history of sigmoidectomy for unexplained peritonitis. Microscopic study of the polypoid lesion showed the submucosal mass with histological and immunological features of RDD. The whole body computed tomography revealed neither lymphadenopathy nor tumor-like mass.
罗萨伊-多夫曼病(RDD)以前被称为“伴有巨大淋巴结病的窦性组织细胞增生症”,累及胃肠道的病例较为罕见。我们报告一例纯结外RDD病例,在结肠镜检查中作为息肉样病变切除。患者为一名62岁女性,有因不明原因腹膜炎行乙状结肠切除术的病史。对息肉样病变的显微镜检查显示黏膜下肿块具有RDD的组织学和免疫学特征。全身计算机断层扫描未发现淋巴结病或肿瘤样肿块。