Sudden death from idiopathic giant cell myocarditis

M. S. Bisharyan1, K. A. Arsenyan1, P. S. Khachatryan1, A. A. Tonoyan1
1Scientific-practical Center of Forensic Medicine of the Ministry of Health of the Republic of Armenia, Department of Forensic Medicine, Yerevan State Medical University, Yerevan, Armenia

Tóm tắt

Idiopathic giant cell myocarditis (GCM) is a rare rapidly progressing and usually fatal autoimmune disorder, which predominantly affects middle-aged people. It is usually associated with other autoimmune disorders, such as Crohn’s disease, rheumatoid arthritis, ulcerative colitis. We report an autopsy case of sudden death of a 38-year-old woman. At autopsy the heart was enlarged, with a motley appearance on sections. Microscopic examination showed abundant inflammatory infiltrates consisting of lymphocytes, leukocytes and multinucleated giant cells. Different staining methods and immunohistochemical examinations were performed for the diagnosis of GCM.

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Tài liệu tham khảo

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