Onkologie. 2019:13(4):184-186 | DOI: 10.36290/xon.2019.035

A rare case of adult emybryonal rhabdomyosarcoma

Katarína Balážová, Imrich Beer, Peter Čunderlík, Jana Poláková-Mištinová
Oddelenie všeobecnej kardiológie, Stredoslovenský ústav srdcových a cievnych chorôb, a. s. Banská Bystrica
Kardiochirurgické oddelenie, Stredoslovenský ústav srdcových a cievnych chorôb, a. s. Banská Bystrica
Patológia, s. r. o. Diagnostické centrum Banská Bystrica
Pracovisko MRI, Ružomberok

The case report describes a rare case of embryonal rhabdomyosarcoma in adult a 39-year-old male. March 2016 right upper limb amputation in mid-arm for malignant tumor – histology mesenchial tumor with traits v.s. fibrous monophasic synovial sarcoma. Subsequently, two years after the operation, the patient developed heart failure. Echocardiographically a tumor was found around the free wall of the left ventricle (LV) deploying on the LV wall and oppressing the free wall of LV. The finding was also confirmed by the magnetic resonance of the heart. After evaluating the heart team the patient was indicated for cardiac surgery-tumor extirpation. This has been successfully implemented. However, the patient developed severe heart failure in the early post-operative period followed by multiorgan failure and fifth post-operative day patient died. On the basis of complex histomorphological, immunohistochemical and molecular-genetic examination it is embryonal rhabdomyosarcoma (spindle cell subtype high – grade).

Keywords: rhabdomyosarcoma, metastasis, immunohistochemistry, heart failure

Published: September 15, 2019  Show citation

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Balážová K, Beer I, Čunderlík P, Poláková-Mištinová J. A rare case of adult emybryonal rhabdomyosarcoma. Onkologie. 2019;13(4):184-186. doi: 10.36290/xon.2019.035.
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