A CASE OF FOAMY MYOCARDIAL TRANSFORMATION OF INFANCY

作者: Chikao YUTANI , Masami IMAKITA , Hatsue ISHIBASHI-UEDA , Tetsuro KAMIYA , Yoshio ARAGAKI

DOI: 10.1111/J.1440-1827.1985.TB01016.X

关键词: Foamy myocardial transformationElectron microscopicEtiologyEndomyocardial biopsyHyperplasiaInfantile cardiomyopathyAutopsyPathologyTachycardiaMedicine

摘要: A case of infantile cardiomyopathy in a year and four months old girl, which was clinically characterized by tachycardia resistant to any drugs marked hyperplasia mitochondria their cytoplasms on electron microscopic observation, presented. In the present light microscopical proof diagnosis obtained right endomyocardial biopsy, while most this condition has not been recognized prior autopsy. Japan newly reported, we proposed that could be designated as mitochondrial caused unknown etiology. The literatures described previously world have reviewed.

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