scholarly journals Mesenteric Fibromatosis Presenting as a Diagnostic Dilemma: A Rare Differential Diagnosis of Right Iliac Fossa Mass in an Eleven Year Old—A Rare Case Report

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Abhinav Mahajan ◽  
Mohinder Singh ◽  
Anoop Varma ◽  
Gunjeet Singh Sandhu ◽  
Malwinder Singh ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Iliac Fossa ◽  
Diagnostic Dilemma ◽  
Mesenteric Fibromatosis ◽  
Rare Differential Diagnosis ◽  
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

Rare Case Report Of Mesenteric Fibromatosis

2015 ◽  
Vol 87 (9) ◽  
Author(s):  
Radhika Vidyasagar ◽  
Sudarshan ◽  
Sreedhar ◽  
Subramanya ◽  
Vidya Bhat
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Histopathological Examination ◽  
Mesenteric Tumor ◽  
Mesenteric Fibromatosis ◽  
Rare Case Report

AbstractMesenteric fibromatosis is a part of the clinical-pathologic spectrum of deep fibromatoses. We report this rare case of primary mesenteric tumor that was diagnosed to be a mesenteric fibromatosis on histopathological examination.In majority of patients it may remain asymptomatic and the management of these tumors depends on histopathological examination. Postoperatively, patient was well and subsequent follow up showed normal recovery.

Intraoral Schwannoma: A Rare Case Report

2016 ◽  
Vol 1 (1) ◽  
pp. 20-22
Author(s):  
Ranjan Agrawal ◽  
Prashant Bhardwaj ◽  
Abhinav Srivastava
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Rare Entity ◽  
Rare Occurrence ◽  
Floor Of The Mouth ◽  
Nerve Sheath ◽  
Rare Case Report ◽  
Sheath Cells

ABSTRACT Schwannomas or neurilemmomas are benign, encapsulated tumor arising from nerve sheath cells. Intracranial Schwannomas are most common with rare occurrence in the extracranial region. It rarely occurs in the floor of the mouth with very few cases reported. We present a rare case report of Schwannoma of the floor of the mouth, thereby highlighting the consideration of this rare entity as one of the differential diagnosis in cases who present to us with swelling of the floor of the mouth and also the importance of immunohistochemistry in coming to the diagnosis. How to cite this article Srivastava A, Mohan C, Bhardwaj P, Agrawal R. Intraoral Schwannoma: A Rare Case Report. Int J Adv Integ Med Sci 2016;1(1):20-22.

scholarly journals A rare case report of pyogenic granuloma of nasopharynx

2019 ◽  
Vol 5 (4) ◽  
pp. 1091
Author(s):  
Kholood S. Assiri ◽  
Mohammad S. Al-Ahmari
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Nasal Cavity ◽  
Granulation Tissue ◽  
Rare Case ◽  
Pyogenic Granuloma ◽  
Adjacent Structures ◽  
Rare Case Report ◽  
Nasal Bleeding ◽  
Radiological Studies

<p class="abstract">The etiology of pyogenic granuloma (PG) is unclear; it is a reactive tumor-like lesion arising by various stimuli. This study aims to report a rare case of PG of the nasopharynx in a 47 years old Saudi female patient. On October 15th, 2018, a 47-years old Saudi female presented with nasal obstruction for one month. The patient's complaint was associated with on/off epistaxis, headache and allergic symptoms. On examination, she had pedunculated nasopharyngeal lesion. Radiological studies revealed a right nasal cavity mass, a lesion in the nasopharynx without extension to the adjacent structures. Removal of the lesion by nasoscope and cauterization of the base were done. Histopathology revealed vascularized granulation tissue with ulcerated epithelium and fibrinous exudates. Nasopharyngeal pyogenic granuloma is rare. It is one of the differential diagnosis of nasal bleeding.</p>

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