Primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report
Author:
Affiliation:
1. Department of Dermatology, Shanghai Xuhui Center Hospital , No. 966, Huaihai Road , Shanghai 200031 , China
2. Department of Scientific Research, Shanghai Xuhui Center Hospital , Shanghai 200031 , China
Abstract
Publisher
Walter de Gruyter GmbH
Subject
General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
https://www.degruyter.com/document/doi/10.1515/biol-2021-0076/pdf
Reference18 articles.
1. Ferreira ILO, Fernandes EL, Lapins J, Benini T, Silva LC, Lanzoni MA, et al. Primary localized cutaneous nodular amyloidosis on a toe: clinical presentation, histopathology, and dermoscopy findings. Dermatol Pract Concept. 2019;9(3):235–6.
2. Heng JK, Ho SA, Tan KB. Poikiloderma-like cutaneous amyloidosis – a rare presentation of primary localized cutaneous amyloidosis. Dermatol Online J. 2016 Jan 15;22(1):13030/qt20s8p7qt.
3. Heaton J, Steinhoff N, Wanner B. A review of primary cutaneous amyloidosis. JAOCD. 2017;38:46–9.
4. Caruana D, McCusker S, Harper C, Bilsland D. Curious facial plaque diagnosed as nodular primary localised cutaneous amyloidosis. BMJ Case Rep. 2019;12:e228163.
5. Ho MS, Ho J, Tan SH. Hypopigmented macular amyloidosis with or without hyperpigmentation. Clin Exp Dermatol. 2009;34(8):e547–51.
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