Anetoderma Schweninger-Buzzi: Two Case Reports

Author:

Wollina Uwe,Mühle Diana,Lotti Torello,Vojvodic Aleksandra

Abstract

BACKGROUND: Anetodermas are rare disorders of connective tissue with a focal loss of elastic fibres in the upper and mid dermis. Two types are separated, inflammatory and non-inflammatory. CASE REPORTS: We report two cases of acquired anetoderma Schweniger-Buzzi type. This non-inflammatory subtype is characterised by skin-coloured or whitish atrophic sac-like protrusions of trunk skin in adult males. Chronic infections and autoimmune disorders have been excluded. The diagnosis had been confirmed by characteristic histopathology. CONCLUSIONS: Anetodermas are symptomless disorders. They can be easily overlooked. The knowledge of such conditions is of importance to identify patients with a risk of thromboembolic events and underlying infections or autoimmune connective tissue diseases.

Publisher

Scientific Foundation SPIROSKI

Subject

General Medicine

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A case of primary anetoderma of Schweninger–Buzzi type;Journal of the European Academy of Dermatology and Venereology;2023-11-14

2. Herniated Sac-like Erythematous Lesions on the Trunk with Punctiform Desquamation;Clinical Cases in Exfoliative Dermatitis;2022

3. The Risk of Thrombotic Events in Anetoderma Affecting Young Patients;Journal of Interdisciplinary Medicine;2021-06-01

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