A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT

Rhabdomyosarcoma is a malignancy of mesenchymal tissue origin typically occurring in childhood and adolescence, with an incidence rate of of 4.3 patients per million population per anum. Primary rhabdomyosarcoma of para-testicular origin is an infrequent condition, making up to 7% of all the cases o...

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Autores principales:	Mussadique Ali, Chandumal ., Manzoor Khan, Jhanzeb Iftikhar, Samia Yasmeen, Umm e Kalsoom Awan
Formato:	article
Lenguaje:	EN
Publicado:	Army Medical College Rawalpindi 2021
Materias:	paratesticular remission rhabdomyosarcoma Medicine R Medicine (General) R5-920
Acceso en línea:	https://doaj.org/article/48eef3b98d3d45d99e9a296a81340b40
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spelling	oai:doaj.org-article:48eef3b98d3d45d99e9a296a81340b402021-12-02T18:44:47ZA RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT0030-96482411-884210.51253/pafmj.v71i2.4743https://doaj.org/article/48eef3b98d3d45d99e9a296a81340b402021-04-01T00:00:00Zhttps://pafmj.org/index.php/PAFMJ/article/view/4743https://doaj.org/toc/0030-9648https://doaj.org/toc/2411-8842Rhabdomyosarcoma is a malignancy of mesenchymal tissue origin typically occurring in childhood and adolescence, with an incidence rate of of 4.3 patients per million population per anum. Primary rhabdomyosarcoma of para-testicular origin is an infrequent condition, making up to 7% of all the cases of rhabdomyosarcoma tumors in children and adolescents. Here we describe a case of a 25 years old man with left paratesticular solid mass. He underwent left sided orchiectomy with histopathology revealing paratesticuler embryonal rhabdomyosarcoma. He underwent definitive chemo-radiotherapy and orchidopexy with complete remission and is on active surveillance for 4 years.Mussadique AliChandumal .Manzoor KhanJhanzeb IftikharSamia YasmeenUmm e Kalsoom AwanArmy Medical College RawalpindiarticleparatesticularremissionrhabdomyosarcomaMedicineRMedicine (General)R5-920ENPakistan Armed Forces Medical Journal, Vol 71, Iss 2, Pp 719-21 (2021)
institution	DOAJ
collection	DOAJ
language	EN
topic	paratesticular remission rhabdomyosarcoma Medicine R Medicine (General) R5-920
spellingShingle	paratesticular remission rhabdomyosarcoma Medicine R Medicine (General) R5-920 Mussadique Ali Chandumal . Manzoor Khan Jhanzeb Iftikhar Samia Yasmeen Umm e Kalsoom Awan A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT
description	Rhabdomyosarcoma is a malignancy of mesenchymal tissue origin typically occurring in childhood and adolescence, with an incidence rate of of 4.3 patients per million population per anum. Primary rhabdomyosarcoma of para-testicular origin is an infrequent condition, making up to 7% of all the cases of rhabdomyosarcoma tumors in children and adolescents. Here we describe a case of a 25 years old man with left paratesticular solid mass. He underwent left sided orchiectomy with histopathology revealing paratesticuler embryonal rhabdomyosarcoma. He underwent definitive chemo-radiotherapy and orchidopexy with complete remission and is on active surveillance for 4 years.
format	article
author	Mussadique Ali Chandumal . Manzoor Khan Jhanzeb Iftikhar Samia Yasmeen Umm e Kalsoom Awan
author_facet	Mussadique Ali Chandumal . Manzoor Khan Jhanzeb Iftikhar Samia Yasmeen Umm e Kalsoom Awan
author_sort	Mussadique Ali
title	A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT
title_short	A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT
title_full	A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT
title_fullStr	A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT
title_full_unstemmed	A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT
title_sort	rare case report of paratesticular rhabdomyosarcoma in an adult patient
publisher	Army Medical College Rawalpindi
publishDate	2021
url	https://doaj.org/article/48eef3b98d3d45d99e9a296a81340b40
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A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT

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