Doxorubicin cardiomyopathy – case report and review of histopathologic findings (RCD code: III‐1B.5a)

Journal Title: Journal of Rare Cardiovascular Diseases - Year 2017, Vol 3, Issue 5

Abstract

The anthracycline anticancer drug Doxorubicin (Adriamycin) is an effective and frequently used chemotherapeutic agent for various malignancies. The use of doxorubicin is limited by its major adverse effect, cardiotoxicity. Doxorubicin cardiomyopathy, once developed, carries a poor prognosis with a mortality rate of over 50%. Although invasive, histopathologic analysis of myocardial tissue remains the most sensitive and specific method of diagnosing doxorubicin cardiomyopathy. Histopathologic analysis reveals not only the characteristic diagnostic features of the disease but also aids in grading the severity of doxorubicin cardiomyopathy, which guides further therapy. We report the autopsy findings of a 31-year-old man with a history of T-cell Acute Lymphoblastic Leukemia (ALL) who died of severe doxorubicin induced dilated cardiomyopathy after he was given multiple rounds of hyperfractionated Cyclophosphamide, Vincristine, Adriamycin (doxorubicin) and Dexamethasone (hyper-CVAD) over a period of six years. JRCD 2017; 3 (5): 176–179

Authors and Affiliations

Hamza Tariq, Urooj Zahra

Keywords

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JRCD in the European Heart Journal

We present to you the fourth and final issue of Journalof Rare Cardiovascular Diseases (JRCD) for 2017.

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  • EP ID EP254928
  • DOI 10.20418/jrcd.vol3no5.301
  • Views 86
  • Downloads 0

How To Cite

Hamza Tariq, Urooj Zahra (2017). Doxorubicin cardiomyopathy – case report and review of histopathologic findings (RCD code: III‐1B.5a). Journal of Rare Cardiovascular Diseases, 3(5), 176-176. https://europub.co.uk/articles/-A-254928