A Telangiectasia Macularis Eruptiva Perstans in a Child: A Rare Vascular Phenotype of Cutaneous Mastocytosis.

IF 0.5 Q4 PEDIATRICS
Case Reports in Pediatrics Pub Date : 2026-06-17 eCollection Date: 2026-01-01 DOI:10.1155/crpe/8849274
Bouchra Baghad, Meriem Takiddine, Farida Marnissi, Soumiya Chiheb
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引用次数: 0

Abstract

Telangiectasia macularis eruptiva perstans (TMEP) is a rare vascular phenotype of cutaneous mastocytosis predominantly reported in adults; pediatric cases are exceptional and are particularly difficult to recognize in darker skin phototypes. We report the case of a 4-year-old girl who presented with subtle brown macules and faint telangiectasias, in whom dermoscopy and histopathology confirmed TMEP despite a normal serum tryptase level. Symptomatic management with antihistamines and topical tacrolimus achieved a favorable clinical outcome. This case highlights the diagnostic challenges of TMEP in skin of color and underscores the need for structured long-term surveillance.

儿童发疹性黄斑毛细血管扩张:一种罕见的皮肤肥大细胞增多症血管表型。
持续性发疹性黄斑毛细血管扩张症(TMEP)是一种罕见的血管表型,主要发生在成人皮肤肥大细胞增多症;儿科病例是例外,尤其难以识别深色皮肤的照片类型。我们报告的情况下,一个4岁的女孩谁提出了细微的棕色斑点和微弱的毛细血管扩张,其中皮肤镜和组织病理学证实TMEP,尽管正常的血清胰蛋白酶水平。用抗组胺药和局部他克莫司对症治疗取得了良好的临床结果。该病例突出了有色皮肤TMEP的诊断挑战,并强调了有组织的长期监测的必要性。
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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来源期刊
自引率
11.10%
发文量
48
审稿时长
13 weeks
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