Primary Systemic Amyloidosis Presenting as Skin Vegetations: A Case Report

Introduction:. Primary systemic amyloidosis is characterized by clonal plasma cell disorder, and its signs and symptoms are various and complex, damage to the skin and mucous membrane is often more likely to attract attention.Here we reported a case of a 61-year-old male patient who presented with t...

Full description

Bibliographic Details
Main Authors: Meng-Hua Li, Li-Ming Wu
Format: Article
Language:English
Published: Wolters Kluwer Health 2022-09-01
Series:International Journal of Dermatology and Venerology
Online Access:http://journals.lww.com/10.1097/JD9.0000000000000182
_version_ 1797991557262999552
author Meng-Hua Li
Li-Ming Wu
author_facet Meng-Hua Li
Li-Ming Wu
author_sort Meng-Hua Li
collection DOAJ
description Introduction:. Primary systemic amyloidosis is characterized by clonal plasma cell disorder, and its signs and symptoms are various and complex, damage to the skin and mucous membrane is often more likely to attract attention.Here we reported a case of a 61-year-old male patient who presented with topical mucocutaneous lesion, as well unusual skin vegetations. Case presentation:. A 61-year-old man was hospitalized due to repeated burning sensation on his back, multiple ecchymosis, and skin vegetations. Through a series of examinations (mainly including skin histopathology, bone marrow cytology, bone marrow flow cytometry, immunofixation electrophoresis), Primary systemic amyloidosis was diagnosed, but multiple myeloma could not be diagnosed. Subsequently, he received chemotherapy. In the half-year follow-up, there was no significant change in his symptoms and signs. Discussion:. In this case, in addition to the typical skin damage of primary amyloidosis, the multiple skin vegetations in the buttocks, abdomen, and arms are particularly noteworthy. According to the histopathology and Immunohistochemistry of the skin vegetation, we infer that the formation mechanism of these skin vegetation is lymphatic obstruction caused by amyloid, which leads to lymphatic dilatation, lymph leakage, and dermal edema. Conclusion:. Primary systemic amyloidosis is a rare disease, which is often difficult to diagnose. We should be alert to those atypical skin features so as not to delay diagnosis.
first_indexed 2024-04-11T08:54:13Z
format Article
id doaj.art-a1df272a45b84a579f2b0ab90d4b9f75
institution Directory Open Access Journal
issn 2096-5540
language English
last_indexed 2024-04-11T08:54:13Z
publishDate 2022-09-01
publisher Wolters Kluwer Health
record_format Article
series International Journal of Dermatology and Venerology
spelling doaj.art-a1df272a45b84a579f2b0ab90d4b9f752022-12-22T04:33:20ZengWolters Kluwer HealthInternational Journal of Dermatology and Venerology2096-55402022-09-015317818010.1097/JD9.0000000000000182202209000-00011Primary Systemic Amyloidosis Presenting as Skin Vegetations: A Case ReportMeng-Hua Li0Li-Ming Wu1Department of Dermatology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310006, China.Department of Dermatology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310006, China.Introduction:. Primary systemic amyloidosis is characterized by clonal plasma cell disorder, and its signs and symptoms are various and complex, damage to the skin and mucous membrane is often more likely to attract attention.Here we reported a case of a 61-year-old male patient who presented with topical mucocutaneous lesion, as well unusual skin vegetations. Case presentation:. A 61-year-old man was hospitalized due to repeated burning sensation on his back, multiple ecchymosis, and skin vegetations. Through a series of examinations (mainly including skin histopathology, bone marrow cytology, bone marrow flow cytometry, immunofixation electrophoresis), Primary systemic amyloidosis was diagnosed, but multiple myeloma could not be diagnosed. Subsequently, he received chemotherapy. In the half-year follow-up, there was no significant change in his symptoms and signs. Discussion:. In this case, in addition to the typical skin damage of primary amyloidosis, the multiple skin vegetations in the buttocks, abdomen, and arms are particularly noteworthy. According to the histopathology and Immunohistochemistry of the skin vegetation, we infer that the formation mechanism of these skin vegetation is lymphatic obstruction caused by amyloid, which leads to lymphatic dilatation, lymph leakage, and dermal edema. Conclusion:. Primary systemic amyloidosis is a rare disease, which is often difficult to diagnose. We should be alert to those atypical skin features so as not to delay diagnosis.http://journals.lww.com/10.1097/JD9.0000000000000182
spellingShingle Meng-Hua Li
Li-Ming Wu
Primary Systemic Amyloidosis Presenting as Skin Vegetations: A Case Report
International Journal of Dermatology and Venerology
title Primary Systemic Amyloidosis Presenting as Skin Vegetations: A Case Report
title_full Primary Systemic Amyloidosis Presenting as Skin Vegetations: A Case Report
title_fullStr Primary Systemic Amyloidosis Presenting as Skin Vegetations: A Case Report
title_full_unstemmed Primary Systemic Amyloidosis Presenting as Skin Vegetations: A Case Report
title_short Primary Systemic Amyloidosis Presenting as Skin Vegetations: A Case Report
title_sort primary systemic amyloidosis presenting as skin vegetations a case report
url http://journals.lww.com/10.1097/JD9.0000000000000182
work_keys_str_mv AT menghuali primarysystemicamyloidosispresentingasskinvegetationsacasereport
AT limingwu primarysystemicamyloidosispresentingasskinvegetationsacasereport