Pseudoxanthoma elasticum-like papillary dermal elastolysis; A report of two cases and a literature review.

Q3 Medicine Dermatology online journal Pub Date : 2024-10-15 DOI:10.5070/D330564429
Rand Murshidi, Salsabiela Bani Hamad, Awad Al-Tarawneh
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Abstract

Pseudoxanthoma elasticum-like papillary dermal elastolysis is a rare, benign, acquired, gradually-developing chronic elastic tissue disorder that almost exclusively affects post-menopausal women. It is essential to recognize this disease as it mimics the inherited pseudoxanthoma clinically. The pathophysiology behind this disease is multifactorial; it includes intrinsic skin aging, ultraviolet radiation exposure, and genetic components. We report two patients with pseudoxanthoma elasticum-papillary dermal elastolysis diagnosis based on clinicopathologic correlation in two post-menopausal women who presented with multiple asymptomatic papules over the neck that developed gradually without systemic involvement, and were managed conservatively. We also discuss this disease's clinical, dermoscopic, and histopathologic features.

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假黄疽弹性瘤样乳头状真皮松解症是一种罕见、良性、获得性、逐渐发展的慢性弹性组织疾病,几乎只影响绝经后妇女。这种疾病在临床上与遗传性假黄疽相似,因此识别这种疾病至关重要。这种疾病背后的病理生理学是多因素的,包括内在皮肤老化、紫外线辐射和遗传因素。我们报告了两名绝经后女性患者的临床病理相关性,她们颈部出现多个无症状丘疹,逐渐发展,无全身受累,经保守治疗后确诊为假性黄皮瘤-毛细血管真皮松解症。我们还讨论了这种疾病的临床、皮肤镜和组织病理学特征。
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来源期刊
Dermatology online journal
Dermatology online journal Medicine-Dermatology
CiteScore
1.70
自引率
0.00%
发文量
200
审稿时长
6 weeks
期刊介绍: An open-access, refereed publication intended to meet reference and education needs of the international dermatology community since 1995. Dermatology Online Journal is supported by the Department of Dermatology UC Davis, and by the Northern California Veterans Administration.
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