Abstract
Rhabdomyosarcoma (RMS) is the most common soft-tissue tumor in childhood, but is extremely rare in elderly. We present a rare case of cardiac RMS, which developed 1 year after the diagnosis and management of acute lymphoblastic leukemia in a 68-year-old female. The occurrence of such phenomena is intriguing, especially in an individual without prior history of malignancy at a younger age. Through the review of the existing literature, we attempt to approach the pathogenesis and clinical manifestations of this rare clinical entity.
MeSH terms
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Age of Onset
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Aged
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use
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Diagnosis, Differential
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Fatal Outcome
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Female
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Heart Neoplasms* / diagnosis
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Heart Neoplasms* / drug therapy
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Heart Neoplasms* / epidemiology
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Heart Neoplasms* / pathology
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Humans
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Neoplasms, Multiple Primary / diagnosis
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Neoplasms, Multiple Primary / etiology
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Neoplasms, Second Primary* / diagnosis
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Neoplasms, Second Primary* / drug therapy
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Neoplasms, Second Primary* / etiology
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma* / diagnosis
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma* / drug therapy
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma* / epidemiology
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma* / pathology
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Rhabdomyosarcoma* / diagnosis
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Rhabdomyosarcoma* / drug therapy
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Rhabdomyosarcoma* / epidemiology
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Rhabdomyosarcoma* / pathology
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Time Factors