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噬血细胞性淋巴组织细胞增生症患者中表现为银屑病的慢性移植物抗宿主病

Chronic Graft-Versus-Host Disease Mimicking Psoriasis in a Patient with Hemophagocytic Lymphohistiocytosis.

作者信息

Jang Sihyeok, Kim In Su, Youn Sang Woong

机构信息

Department of Dermatology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.

出版信息

Ann Dermatol. 2016 Feb;28(1):90-3. doi: 10.5021/ad.2016.28.1.90. Epub 2016 Jan 28.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2eac/4737842/6a5300dea26b/ad-28-90-g001.jpg

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