scholarly journals A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT

2021 ◽  
Vol 71 (2) ◽  
pp. 724-26
Author(s):  
Mussadique Ali ◽  
Chandumal . ◽  
Manzoor Khan ◽  
Jhanzeb Iftikhar ◽  
Samia Yasmeen ◽  
...  
Keyword(s):  
Case Report ◽  
Complete Remission ◽  
Adult Patient ◽  
Rare Case ◽  
Embryonal Rhabdomyosarcoma ◽  
Childhood And Adolescence ◽  
Solid Mass ◽  
Mesenchymal Tissue ◽  
Rare Case Report ◽  
Tissue Origin

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.

scholarly journals Urinary Bladder Cavernous Hemangioma in a 3-year-old: A rare case report.

2021 ◽  
Author(s):  
Charles Odongo ◽  
raymond atwine ◽  
Martin Situma ◽  
ambrose okello ◽  
eugene ogwang ◽  
...  
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Cavernous Hemangioma ◽  
Rare Case ◽  
Embryonal Rhabdomyosarcoma ◽  
Bladder Tumors ◽  
Case Presentation ◽  
Rare Case Report

Introduction: Cavernous hemangioma accounts for 0.6% of bladder tumors. We present a rare case Case Presentation: A 3-year-old girl presented with intravaginal swelling, dysuria, and hematuria. She received 26 cycles of VAC for embryonal rhabdomyosarcoma. Histopathology confirmed CH. Conclusion: CH should be considered in the differentials of childhood genitourinary masses.

scholarly journals Primary intracranial peripheral primitive neuroectodermal tumor in an adult patient with aphasia: a rare case report

2021 ◽  
Author(s):  
kazem ghaemi ◽  
mahdieh rajabi-moghaddam ◽  
Hamid Abbaszadeh
Keyword(s):  
Case Report ◽  
Adult Patient ◽  
Rare Case ◽  
Primitive Neuroectodermal Tumor ◽  
Chief Complaint ◽  
Peripheral Primitive Neuroectodermal Tumor ◽  
Primitive Neuroectodermal Tumors ◽  
Neuroectodermal Tumors ◽  
Rare Case Report ◽  
First Time

Primary intracranial primitive neuroectodermal tumors (PNETs) are extremely rare malignancies, affects children and adolescents with only 10 cases has been reported over 33 years old. we present a case of PNET in a 36 years old female patient with the chief complaint of aphasia for the first time

scholarly journals A Rare Case Report: Bilateral Choanal Atresia in an Adult Patient

2020 ◽  
Vol 3 (1) ◽  
pp. 26-28
Author(s):  
Ayhan Kars ◽  
◽  
Fatih Bingol ◽  
Fatma Atalay ◽  
◽  
...  
Keyword(s):  
Case Report ◽  
Adult Patient ◽  
Rare Case ◽  
Choanal Atresia ◽  
Rare Case Report

scholarly journals Embryonal Rhabdomyosarcoma of Middle Ear and Temporal Bone: A Rare Case Report

2021 ◽  
Vol 10 (05) ◽  
pp. 426-432
Author(s):  
Gvs Rao ◽  
Laxminath Ganji ◽  
Shree Rao ◽  
Chaitanya Rao ◽  
Raja Sekhar
Keyword(s):  
Case Report ◽  
Temporal Bone ◽  
Middle Ear ◽  
Rare Case ◽  
Embryonal Rhabdomyosarcoma ◽  
Rare Case Report

scholarly journals Embryonal Rhabdomyosarcoma in Mastoid and Middle Ear in a 3-Year-Old Girl: A Rare Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-3
Author(s):  
Saman Vegari ◽  
Alireza Hemati ◽  
Hosein Baybordi ◽  
Leila Davarimajd ◽  
Ghasem Chatrbahr
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Young Children ◽  
Head And Neck ◽  
Middle Ear ◽  
Rare Case ◽  
Embryonal Rhabdomyosarcoma ◽  
Purulent Discharge ◽  
Pathologic Evaluation ◽  
Rare Case Report

Introduction. The most common sarcoma of childhood is rhabdomyosarcoma, approximately 35% of all paediatric rhabdomyosarcomas occur in the head and neck.Case Report. A 3-year-old girl referred to our clinic due to serosanguineous purulent discharge from her right ear. After paraclinical and pathologic evaluation it was diagnosed as embryonic rhabdomyosarcoma.Conclusions. In all children with mastoiditis, especially in young children, rhabdomyosarcoma should be considered as a differential diagnosis.

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