Jang Sihyeok, Kim In Su, Youn Sang Woong
Department of Dermatology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.
Ann Dermatol. 2016 Feb;28(1):90-3. doi: 10.5021/ad.2016.28.1.90. Epub 2016 Jan 28.
Graft-versus-host disease (GVHD) is a common complication of bone marrow transplantation (BMT) that can be classified as acute or chronic. Chronic GVHD, which usually occurs more than 3 months after BMT, includes typical lichenoid or sclerodermatous lesions. Psoriasiform eruption is a rare clinical manifestation of chronic GVHD, and there have been no reports of psoriasiform chronic GVHD associated with hemophagocytic lymphohistiocytosis. A 33-year-old woman who was diagnosed with hemophagocytic lymphohistiocytosis 10 years ago visited our outpatient clinic with psoriasiform eruption over her entire body. She underwent allogeneic BMT 7 months previously from her sibling. Skin biopsy was performed on the lesion, and the histological features suggested GVHD. The psoriasiform lesions improved with narrow-band ultraviolet B phototherapy, with secondary vitiligo remaining on the corresponding locations.
移植物抗宿主病(GVHD)是骨髓移植(BMT)的一种常见并发症,可分为急性或慢性。慢性GVHD通常发生在BMT后3个月以上,包括典型的苔藓样或硬皮病样病变。银屑病样皮疹是慢性GVHD的一种罕见临床表现,目前尚无银屑病样慢性GVHD与噬血细胞性淋巴组织细胞增生症相关的报道。一名10年前被诊断为噬血细胞性淋巴组织细胞增生症的33岁女性因全身出现银屑病样皮疹前来我院门诊就诊。她7个月前接受了来自其同胞的异基因BMT。对病变部位进行了皮肤活检,组织学特征提示为GVHD。银屑病样病变经窄谱中波紫外线光疗后改善,相应部位遗留继发性白癜风。