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一名患有骨髓增生异常综合征的成年患者出现多发性黄色瘤。

Multiple Xanthogranulomas in an Adult Patient with Myelodysplastic Syndrome.

作者信息

Martínez-García Marta, Silvestre-Torner Nicolás, Aguilar-Martínez Antonio, Burgos-Lázaro Fernando

机构信息

Dermatology Service, Severo Ochoa University Hospital, Leganés, Madrid, Spain.

Pathological Anatomy Service, Severo Ochoa University Hospital, Leganés, Madrid, Spain.

出版信息

Case Rep Dermatol Med. 2020 Dec 7;2020:8826715. doi: 10.1155/2020/8826715. eCollection 2020.

Abstract

Adult multiple xanthogranuloma (XG) is a rare late-onset variant of juvenile XG. It is characterized by the appearance of papules or nodules located preferably on the trunk. A case of a 54-year-old man with myelodysplastic syndrome is presented as a history of interest, who consulted due to the appearance of multiple brownish papules distributed mainly in the trunk. So far, there are only 22 cases of this clinical form reported in the literature, 9 of them associated with malignant hematological processes. We highlight the importance of this entity as a possible cutaneous marker of blood dyscrasias.

摘要

成人多发性黄色瘤(XG)是青少年XG的一种罕见的迟发性变体。其特征是丘疹或结节的出现,最好位于躯干。本文报告一例54岁患有骨髓增生异常综合征的男性病例,该患者因躯干出现多个褐色丘疹前来就诊,此病例具有一定研究价值。迄今为止,文献中仅报道了22例这种临床类型,其中9例与恶性血液系统疾病相关。我们强调了该实体作为血液系统疾病可能的皮肤标志物的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf00/7803178/4d93fe19bcdd/CRIDM2020-8826715.001.jpg

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