Year: 2025
Type: article
Study design: Case Report
Abstract: Background. Amyloidosis cutis dyschromica (ACD) is a rare subtype of primary cutaneous amyloidosis. It is characterized by four diagnostic criteria: hyperpigmented patches, little to no pruritus, onset prior to puberty, and focal papillary amyloid deposition. Case report. A 58-year-old Acehnese woman presented with progressive itching and skin darkening for about twenty years, with onset later than typically seen in ACD. On physical examination, diffuse reticulate hyperpigmented patches and patchy hypopigmented macules were observed on both legs. Conclusion. Tangential excision using a dermatome in ACD achieved good results, providing stable depth of skin removal and satisfactory wound healing.
Source: Romanian Medical Journal
Authors: Budiman, Syamsul Rizal, Wahyu Lestari, Fitri Dewi Ismida, Muhammad Zulfikar Rahmandani
Institution: Universitas Syiah Kuala
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $192
Funder: Universitas Syiah Kuala
OpenAlex ID: W4414145377
