成人骨髓增生异常综合征患者多发黄色肉芽肿。

Q3 Medicine Case Reports in Dermatological Medicine Pub Date : 2020-12-07 eCollection Date: 2020-01-01 DOI:10.1155/2020/8826715
Marta Martínez-García, Nicolás Silvestre-Torner, Antonio Aguilar-Martínez, Fernando Burgos-Lázaro
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引用次数: 1

摘要

成人多发黄色肉芽肿(XG)是一种罕见的迟发性少年XG。其特征是丘疹或结节的外观,最好位于躯干上。一例54岁男性骨髓增生异常综合征患者,因出现多发棕色丘疹,主要分布于躯干而就诊。到目前为止,文献中仅报道了22例这种临床形式,其中9例与恶性血液学过程有关。我们强调这个实体的重要性,作为一个可能的皮肤标记的血液失调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Multiple Xanthogranulomas in an Adult Patient with Myelodysplastic Syndrome.

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.

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CiteScore
1.50
自引率
0.00%
发文量
24
审稿时长
15 weeks
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