成人起病的胰腺血管瘤错构瘤伴下肢静脉功能不全1例报告。

IF 1.4 Q3 DERMATOLOGY
Skin Appendage Disorders Pub Date : 2025-04-01 Epub Date: 2024-11-07 DOI:10.1159/000541808
Isabela Dorado Caycedo, Juan C H López Takegami, Eduardo A Rivera Perdomo, Claudia P González Díaz
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引用次数: 0

摘要

简介:内分泌血管瘤错构瘤(Eccrine angiomatous hamartoma, EAH)是一种以内分泌腺体和血管结构增生为特征的良性肿瘤。它可以是先天性的,也可以在儿童时期出现,在成人中出现的病例很少。EAH通常表现为孤立的紫色斑块或结节,但也有多灶表现为囊胚样或节段性分布。病例介绍:我们报告了一例下肢浅静脉范围内的广泛性EAH,发生于一位年轻时被诊断为静脉功能不全的成年人,并在隐骨切除术后恶化。结论:组织病理学和超声特征提示该病例可能是EAH合并动静脉畸形的新病例。我们假设可能有共同的分子途径连接这两种情况,并且在易感患者中,隐骨切除术会加剧EAH。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adult-Onset Eccrine Angiomatous Hamartoma Associated with Lower Extremity Venous Insufficiency: A Case Report.

Introduction: Eccrine angiomatous hamartoma (EAH) is a benign tumor characterized by the proliferation of eccrine glands and vascular structures. It can be congenital or appear during childhood, with rare cases arising in adults. EAH typically presents as a solitary purplish plaque or nodule but a multifocal presentation in a blaschkoid or segmental distribution has been described.

Case presentation: We report the case of an extensive EAH following the territory of the superficial veins of the lower limbs, arising in an adult diagnosed with venous insufficiency at a young age and that worsened after saphenectomy.

Conclusion: The histopathological and ultrasonographic characteristics suggest that this case may represent a new instance of EAH associated with arteriovenous malformation. We hypothesize that there might be common molecular pathways linking both conditions and that, in predisposed patients, saphenectomy can exacerbate EAH.

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CiteScore
2.00
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