Scleredema with biopsy-confirmed cardiomyopathy: A case report

Author:

Nakatsuji Mei1,Ishimaru Naoto1ORCID,Ohnishi Jun1,Mizuki Shimpei1,Kanzawa Yohei1,Kawano Kei1,Nakajima Takahiro1,Kuroda Masaru2,Sano Nobuya3,Kinami Saori1

Affiliation:

1. Department of General Internal Medicine, Akashi Medical Center, Akashi, Japan

2. Department of Cardiology, Akashi Medical Center, Akashi, Japan

3. Department of Pathology, Akashi Medical Center, Akashi, Japan

Abstract

Scleredema is a rare cutaneous mucinosis characterized by diffuse swelling and non-pitting induration. A 63-year-old man reported a 5-year history of skin thickening of the trunk and a 3-week history of dyspnea. Echocardiography revealed diffuse hypokinesis. Skin biopsies obtained from the waist showed thickened dermis with mucin. Myocardial biopsies showed alcian blue-stained tissue between the muscle fibers. The patient was referred to a dermatologist for phototherapy. Cardiomyopathy should be considered in patients with scleredema. Scleredema usually has a good prognosis; however, the mortality risk could be high when accompanied by cardiomyopathy.

Publisher

SAGE Publications

Subject

Immunology,Rheumatology,Immunology and Allergy

Cited by 2 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 novel case report of isolated cardiac myxedematosus;European Heart Journal - Case Reports;2024-08-19

2. Consensus statement on the diagnosis and treatment of sclerosing diseases of the skin, Part 2: Scleromyxoedema and scleroedema;Journal of the European Academy of Dermatology and Venereology;2024-03-08

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