Sarcoidosis Manifesting as Cardiac Sarcoidosis and Massive Splenomegaly

  • Kawano Sayaka
    Department of Internal Medicine, Circulatory and Body Fluid Regulation, Faculty of Medicine, University of Miyazaki, Japan
  • Kato Johji
    Frontier Science Research Center, University of Miyazaki, Japan
  • Kawano Noriaki
    Department of Internal medicine, Miyazaki Prefectural Hospital, Japan
  • Yoshimura Yuki
    Department of Cardiology, Miyazaki Prefectural Hospital, Japan
  • Masuyama Hiroyuki
    Department of Cardiology, Miyazaki Prefectural Hospital, Japan
  • Fukunaga Takashi
    Department of Cardiology, Miyazaki Prefectural Hospital, Japan
  • Shimao Yoshiya
    Department of Pathology, Miyazaki Prefectural Hospital, Japan
  • Mihara Kenroh
    Clinical Laboratory, Miyazaki Prefectural Hospital, Japan
  • Ueda Akira
    Department of Internal medicine, Miyazaki Prefectural Hospital, Japan
  • Toyoda Kiyokazu
    Department of Surgery, Miyazaki Prefectural Hospital, Japan
  • Imamura Takuroh
    Department of Internal Medicine, Circulatory and Body Fluid Regulation, Faculty of Medicine, University of Miyazaki, Japan
  • Kitamura Kazuo
    Department of Internal Medicine, Circulatory and Body Fluid Regulation, Faculty of Medicine, University of Miyazaki, Japan

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Abstract

Sarcoidosis is a multisystemic granulomatous disease of unknown etiology. We report an unusual case of sarcoidosis in a woman presenting with cardiac sarcoidosis and massive splenomegaly with a familial history of cardiac sarcoidosis. Cardiac sarcoidosis was diagnosed based on electrocardiogram, echocardiogram, 18F-fluoro-2-deoxyglucose positron emission tomography (18F-FDG-PET) and skin histological findings. We performed splenectomy to rule out malignant lymphoma, and histological findings confirmed sarcoidosis. After splenectomy, we initiated prednisolone therapy. After 20 months of diagnosis, she was symptom free. Echocardiography and 18F-FDG-PET may be a key diagnostic tool and prednisolone therapy may be safe, effective, and feasible for cardiac sarcoidosis.<br>

Journal

  • Internal Medicine

    Internal Medicine 51 (1), 65-69, 2012

    The Japanese Society of Internal Medicine

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