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儿童多发性隆突性皮肤纤维肉瘤伴严重联合免疫缺陷病,由腺苷脱氨酶缺乏引起。

Multicentric dermatofibrosarcoma protuberans in a child with severe combined immunodeficiency due to adenosine deaminase deficiency.

机构信息

Departments of Paediatrics, Catholic Children´s Hospital Wilhelmstift, Hamburg, Germany.

Institute of Dermatopathology, Friedrichshafen, Germany.

出版信息

Pediatr Dermatol. 2021 Jul;38(4):875-878. doi: 10.1111/pde.14597. Epub 2021 Apr 30.

Abstract

We report the case of a 4-year-old boy, post-human stem cell transplantation for severe combined immunodeficiency (SCID) due to adenosine deaminase deficiency (ADA), who developed multiple dermatofibrosarcoma protuberans (DFSP). We hypothesize a role for chimerism leading to accumulation of toxic metabolites which can cause DNA strand breaks and inhibit lymphocyte activation. Patients with ADA-SCID should remain under lifelong dermatologic surveillance as DFSP lesions can be quite inconspicuous.

摘要

我们报告了一例 4 岁男孩的病例,该男孩因腺苷脱氨酶缺乏症 (ADA) 导致严重联合免疫缺陷 (SCID) ,接受了人干细胞移植,后来发展为多发性隆凸性皮肤纤维肉瘤 (DFSP)。我们推测嵌合状态会导致有毒代谢物的积累,从而导致 DNA 链断裂并抑制淋巴细胞激活。ADA-SCID 患者应终身接受皮肤科监测,因为 DFSP 病变可能不太明显。

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