Primary Systemic Amyloidosis Presenting as Extensive Cutaneous Ulceration

Author:

Alhaddab Mohammed1,Srolovitz Herbert1,Rosen Nathan1

Affiliation:

1. From the Departments of Dermatology and Pathology, McGill University Health Centre, Montreal, QC

Abstract

Background: We report a case of primary systemic amyloidosis in a 78-year-old Caucasian woman presented as a nonhealing ulcer on the right thigh for 3 months. Histopathology of the skin revealed widely thickened walls of middermal and subcutaneous vessels from deposition of amorphous eosinophilic material that stained positively with Congo red and crystal violet. Objective: This case represents a very unusual presentation of primary systemic amyloidosis, one in which the cutaneous manifestations provided the first signs of a devastatingly widespread multiorgan infiltration of amyloid protein. Conclusion: This presentation of the disease may signify an advanced stage with a grave prognosis as our patient passed away 3 months after development of the cutaneous ulceration.

Publisher

SAGE Publications

Subject

Dermatology,Surgery

Cited by 9 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. Cutaneous Amyloidosis;Current Clinical Pathology;2015

2. Cutaneous Deposits;The American Journal of Dermatopathology;2014-01

3. Significant association between renal function and amyloid-positive area in renal biopsy specimens in AL amyloidosis;BMC Nephrology;2012-09-24

4. Cutaneous Amyloidosis: A Concept Review;The American Journal of Dermatopathology;2012-02

5. The blue man: a novel cutaneous manifestation of systemic amyloidosis;Amyloid;2011-04-20

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