scholarly journals Intradiploic meningioma- A rare osteolytic calvarial lesion: A case report and review of literature

2016 ◽  
Vol 7 (6) ◽  
pp. 103-105
Author(s):  
Sandeep B V ◽  
Kaushik Roy ◽  
Manpreet Singh Banga ◽  
Partha Ghosh
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Clinical Practice ◽  
Head Injury ◽  
Rare Case ◽  
Review Of Literature ◽  
Medical Sciences ◽  
Rare Case Report ◽  
Intracranial Neoplasm ◽  
Scalp Mass

Meningiomas are most commonest benign intracranial neoplasm which are encountered in clinical practice. One of the most uncommon variant is intradiploic meningiomas, which can present as osteoblastic or osteolytic calvarial lesion and should be considered  as differential diagnosis. We here present a rare case report of osteolytic intradiploic meningioma of skull presenting as scalp mass with a background of head injury and discuss its management.Asian Journal of Medical Sciences Vol.7(5) 2016 103-105

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 A giant retroperitoneal schwannoma in pregnancy: a rare case report and review of literature

2020 ◽  
Vol 7 (6) ◽  
pp. 2052
Author(s):  
Aditya Prasad Padhy ◽  
Prathmesh Mishra ◽  
Deepak Das ◽  
Nishant Agarwal
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Pregnant Female ◽  
Radiological Imaging ◽  
Review Of Literature ◽  
Rare Tumors ◽  
Rare Case Report ◽  
Retroperitoneal Schwannoma ◽  
In Pregnancy

Retroperitoneal schwannomas are though more common among females, are very much rare tumors arising from sheath of nerves. Also, extremely rare during pregnancy. Very few articles till date are there regarding retroperitoneal schwannomas that’s too in pregnant female. Usually these are symptomatic unless causing some compression to other intra-abdominal structures like vessels or bowel and usually malignant. As its retroperitoneal very difficult to diagnose it. So, with proper investigations and radiological imaging, first have to find out the differential diagnosis prior to planning for surgery.

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.

Intraosseous Neurofibroma of Mandible in a 5-Year-Old: A Rare Case Report and Review of Literature

2021 ◽  
Author(s):  
Arunkumar Kamalakaran ◽  
Balaji Jayaraman ◽  
Supraja Raghavendran ◽  
Rohini Thirunavukkarasu ◽  
Mariammal Ayyappan ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Review Of Literature ◽  
Rare Case Report

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.

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