Urinary Bladder Cavernous Hemangioma in a 3-year-old: A 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.

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Embryonal rhabdomyosarcoma of oral cavity with extensive osteolysis of the mandible – A rare case report

Journal of Pierre Fauchard Academy (India Section) ◽

10.1016/j.jpfa.2016.09.002 ◽

2016 ◽

Vol 30 (2) ◽

pp. 57-61

Author(s):

Vidya Jayaram ◽

S. Jayachandran ◽

Y. Hemavathy Bhaskar

Keyword(s):

Case Report ◽

Oral Cavity ◽

Rare Case ◽

Embryonal Rhabdomyosarcoma ◽

Rare Case Report

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Malignant Urothelial Carcinoma of Urinary Bladder in a Young Child: A Rare Case Report

Urology ◽

10.1016/j.urology.2012.12.016 ◽

2013 ◽

Vol 81 (4) ◽

pp. 888-890 ◽

Cited By ~ 13

Author(s):

Sujoy Neogi ◽

Piaray Lal Kariholu ◽

Gaurav Dhakre ◽

Vishal Gupta ◽

Neema Agarwal ◽

...

Keyword(s):

Case Report ◽

Young Child ◽

Urinary Bladder ◽

Urothelial Carcinoma ◽

Rare Case ◽

Rare Case Report

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Cavernous Hemangioma of the Tongue: A Rare Case Report

Indian Journal of Public Health Research & Development ◽

10.5958/0976-5506.2019.03594.0 ◽

2019 ◽

Vol 10 (11) ◽

pp. 842

Author(s):

Neeta Mohanty ◽

Shubhangi Pareek

Keyword(s):

Case Report ◽

Cavernous Hemangioma ◽

Rare Case ◽

Rare Case Report

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A Rare Case Report of Parotid Cavernous Hemangioma in an Adult

British Journal of Medicine and Medical Research ◽

10.9734/bjmmr/2017/30899 ◽

2017 ◽

Vol 19 (5) ◽

pp. 1-5

Author(s):

Suwal Rubina ◽

Guan Jian ◽

Wang Yu ◽

Khatri Singh ◽

Nyimi Fidele

Keyword(s):

Case Report ◽

Cavernous Hemangioma ◽

Rare Case ◽

Rare Case Report

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Benign Pleural Multicystic Mesothelioma: A Rare Case Report

10.21203/rs.3.rs-165790/v1 ◽

2021 ◽

Author(s):

Alireza Rezvani ◽

SeyedehMaryam Pishva ◽

Amirhossein Erfani ◽

Ahmad Monabati ◽

Bizhan Ziaian ◽

...

Keyword(s):

Case Report ◽

Chronic Cough ◽

Rare Case ◽

Pleural Mesothelioma ◽

Case Presentation ◽

Rare Case Report ◽

History Of ◽

The Right ◽

Lateral Thoracotomy ◽

Pleural Involvement

Abstract Background: Fewer than 200 benign multicystic peritoneal mesothelioma cases were reported worldwide till 2017, while its pleural involvement has rarely been reported. Case presentation: We report a 70-year-old man who presented with three months history of chronic cough. Surgical resection was performed, and the pathology confirmed benign multicystic pleural mesothelioma. The patient underwent right lateral thoracotomy, wedges resection of the right upper lobe, and parietal pleurectomy and was discharged with an uneventful postop course.Conclusion: Based on published literature to date, this is the second reported case of pleural involvement of this disease.

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A RARE CASE REPORT OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT

Pakistan Armed Forces Medical Journal ◽

10.51253/pafmj.v71i2.4743 ◽

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.

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