| CASE REPORT |
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| Year : 2015 | Volume
: 58
| Issue : 1 | Page : 99-101 |
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Idiopathic systemic granulomatous pathology causing sudden death due to myocarditis: A rare case report
Harpal Singh, Ramesh Kundal
Department of Pathology, Government Medical College Patiala, Patiala, Punjab, India
Correspondence Address:
Dr. Harpal Singh
Department of Pathology, Government Medical College Patiala, # 835/13 Ghuman Nagar A, Sirhind Road, Patiala - 147 001, Punjab
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0377-4929.151201
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Idiopathic granulomatous myocarditis is extremely rare, particularly since the introduction of drugs effective against tuberculosis (TB), viruses, fungi and the effective treatment of sarcoidosis. Here is a case of a 65-year-old female prisoner having history of sudden collapse and ultimately death. Autopsy findings of various viscera on histopathological examination show granulomatous pathology, that is, in spleen, liver and in the left ventricular wall of heart. Ziehl-Neelsen staining of the sections show the absence of acid fast bacilli, negative for fungal staining as most of the granulomas are noncaseating type with presence of giant cells having no asteroid body and Schuamann body, real-time polymerase chain reaction for TB is negative. Idiopathic giant cell myocarditis is a disease of relatively young adults, that is, between 3 rd and 4 th decade of life. So, this case is strongly considered to be a case of sudden death due to myocarditis as a result of idiopathic systemic granulomatous pathology, a rare case in in literature. |
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