Cardiomyopathy in a Case of Crow-Fukase Syndrome

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概要

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• Crow-Fukase syndrome or POEMS syndrome is a variant of plasma cell dyscrasia that is characterized by polyneuropathy, organomegaly, endocrinopathy, the presence of M-protein in serum, and dermatological changes. A 60-year-old man presented with features of Crow-Fukase syndrome, such as the presence of M-protein in serum, dermatological changes, and osteosclerotic changes, but did not have polyneuropathy. To our knowledge, this is the first case of Crow-Fukase syndrome in which the presence of hypertrophic cardiomyopathy has been confirmed by a left endomyocardial biopsy. The findings suggest that hypertrophic cardiomyopathy may be a manifestation of organomegaly in patients with Crow-Fukase syndrome.

著者

• Marumo Fumiaki

  Second Department Of Internal Medicine Faculty Of Medicine Tokyo Medical And Dental University

• Shimizu Noritaka

  Second Department of Internal Medicine

• KOIKE AKIRA

  Second Department of Internal Medicine,Tokyo Medical and Dental University

• Ito Hiroshi

  Second Department Of Internal Medicine Tokyo Medical And Dental University

• Hiroe Michiaki

  Second Department Of Internal Medicine

• NOGAMI Akihiko

  Second Department of Internal Medicine, School of Medicine

• GOYA Masahiko

  Second Department of Internal Medicine, Tokyo Medical and Dental University

• NOGAMI Akihiko

  Second Department of Internal Medicine, Tokyo Medical and Dental University

• SHIMIZU Noritaka

  Second Department of Internal Medicine, Tokyo Medical and Dental University

• AKIMOTO Hajime

  Second Department of Internal Medicine, Tokyo Medical and Dental University

• KOIKE Akira

  Second Department of Internal Medicine, Tokyo Medical and Dental University

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