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.

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 Co-Occurrence of Guillain-Barre Syndrome and Multiple Sclerosis: A Rare Case Report

2021 ◽  
pp. 1-5
Author(s):  
Amr Hassan ◽  
Alaa El-Mazny ◽  
Mohammed Saher ◽  
Ismail Ibrahim Ismail ◽  
Mohammed Almuqbil
Keyword(s):  
Multiple Sclerosis ◽  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Guillain Barre Syndrome ◽  
Guillain Barré Syndrome ◽  
Rare Case Report ◽  
Central Nervous Systems ◽  
Guillain Barré ◽  
Demyelinating Disorders

Guillain-Barre syndrome (GBS) and multiple sclerosis (MS) are autoimmune demyelinating disorders of the peripheral and central nervous systems, respectively. The co-occurrence of these 2 conditions is rare in the literature. Herein, we present a rare case of GBS and MS in a 19-year-old female who presented initially with GBS followed by MS, and we provide a literature review. Despite being rare, it should be kept in mind in the differential diagnosis of patients with atypical and usual presentation of both diseases.

scholarly journals Dysgenetic Polycystic Disease of Minor Salivary Gland: A Rare Case Report and Review of the Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
N. Srikant ◽  
Shweta Yellapurkar ◽  
Karen Boaz ◽  
Mohan Baliga ◽  
Nidhi Manaktala ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Minor Salivary Gland ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Lower Lip ◽  
Polycystic Disease ◽  
Rare Case Report

Polycystic (dysgenetic) disease of the salivary glands is a rare entity that has only recently been described in the literature. The disease is more commonly seen in females and majority of the cases have presented as bilateral parotid gland swellings. This case presenting in a 21-year-old male is the first of this unusual entity involving solely the minor salivary gland on the lower lip. This case report highlights the importance for the clinician to be aware of this differential diagnosis, when treating an innocuous lesion like a mucocele.

scholarly journals Pyogenic granuloma of tongue: A rare case report

2014 ◽  
Vol 6 (3) ◽  
pp. 84-86
Author(s):  
Sonam Sharma ◽  
Amita Sharma ◽  
Ashok Kumar ◽  
Shivani Kalhan ◽  
Jasmine Kaur
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Pyogenic Granuloma ◽  
Definitive Diagnosis ◽  
Medical Sciences ◽  
New Approaches ◽  
Rare Case Report ◽  
Chronic Irritation

Pyogenic granuloma (PG) is a kind of inflammatory hyperplasia in response to chronic irritation. Here, we report a case of 64 year old male patient with PG on midline of the dorsum of the posterior third of the tongue. Its differential diagnosis, the importance of biopsy findings in establishing definitive diagnosis and about the new approaches for its treatment is discussed. DOI: http://dx.doi.org/10.3126/ajms.v6i3.10619Asian Journal of Medical Sciences Vol.6(3) 2015 84-86

scholarly journals Omental lymphangioma: a rare case report

2020 ◽  
Vol 10 (3) ◽  
pp. 106-108
Author(s):  
Geha Raj Dahal
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Rare Case ◽  
Neck Region ◽  
Mass Effect ◽  
Complete Excision ◽  
Benign Condition ◽  
Head And Neck Region ◽  
Rare Case Report

Lymphangioma is a common pediatric problem. Most of the lymphangiomas occur in head and neck region. Lymphangioma arising from omentum is extremely rare. It is a benign condition butis locally invasive. Symptoms usually arise from its mass effect or complications. Complete excision including removal of all loculi is necessary for cure. We report such a case of omental lymphangiomain a six-year boy.

scholarly journals Botryoid rhabdomyosarcoma in mastoid and middle ear in a 4-year-old boy: A rare case report

2018 ◽  
Vol 11 (3) ◽  
pp. 130
Author(s):  
AbdelgalilAli Ragab ◽  
MouhannadMahmoud Abdulber Fakoury ◽  
Jamal Kassouma ◽  
Kamal Moustafa ◽  
FatehAl Mohamad Al Salem
Keyword(s):  
Case Report ◽  
Middle Ear ◽  
Rare Case ◽  
Rare Case Report
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