Primary Extracranial Meningioma As A Part Of Neurofibromatosis-2 In Head And Neck: A Rare Case Report

10.5580/136c ◽  
2005 ◽  
Vol 3 (2) ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 106-108
Author(s):  
Geha Raj Dahal

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.


2014 ◽  
Vol 18 (1) ◽  
pp. 137
Author(s):  
YogeshT Lakkasetty ◽  
Sangeeta Malik ◽  
Akshay Shetty ◽  
Kourosh Nakhaei

Author(s):  
Andrews Navin Kumar ◽  
Anubhav Shivpuri ◽  
Sandeep Mehta ◽  
Shanender Singh Sambyal

<p class="abstract">In this case report a bony swelling was noticed clinically which had a cystic presentation in CT imaging. After surgical removal it was sent for histopathological examination and was diagnosed as dermoid cyst. Dermoid cyst is rarely encountered lesions of head and neck region so most frequently misdiagnosed. Though this lesion is very rare but should be considered as a differential diagnosis while evaluation cystic lesions of head and neck region.</p>


2015 ◽  
Vol 10 (2) ◽  
pp. 233-236 ◽  
Author(s):  
Ningombam Jiten Singh ◽  
Nishikanta Tripathy ◽  
Paromita Roy ◽  
Kapila Manikantan ◽  
Pattatheyil Arun

2012 ◽  
Vol 2012 ◽  
pp. 1-3
Author(s):  
Saman Vegari ◽  
Alireza Hemati ◽  
Hosein Baybordi ◽  
Leila Davarimajd ◽  
Ghasem Chatrbahr

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.


2021 ◽  
Vol 2 (6) ◽  
Author(s):  
Djoko Supriyandono ◽  
Marjono Dwi Wibowo

Background: Schwannoma is classified as a benign, encapsulated tumor, derived from the perineural cells which are classified as neural cell membranes. About 10% of Schwannomas has occurred in the head and neck and the incidence of Schwannoma arising from the Cervical C2 nerve roots is extremely rare. Aims of study: This case report aims to provide a rare case report on Schwannoma located in cervical cervices (C2& C3). Case presentation: A 37-year-old female patient with a lump in the left neck for 4 years ago, the first lump appeared as a larger (increasingly large 1×1 cm) marbles with no pain in the lump but over the past 4 months the patient felt his legs and arms are weak. Patients have a history of surgical removal of tumors in the back of the neckline by the end of 2016. At first, we estimated the lump that appeared on the left neck of the patient stands alone in the sense that it was not related to the history of the first lump surgery, but when further examination, the tumor was apparently related to the lump that appeared previously who had surgery. Conclusion: The extracranial Schwannoma in the head and neck areas is a rare neoplasm. The extracranial Schwannoma case is a case that is difficult to diagnose, in addition to good clinical examination, imaging examination, such as CT scan and MRI are an indispensable way of ensuring the diagnosis of an extracranial Schwannoma.


2014 ◽  
Vol 5 (7) ◽  
pp. 488 ◽  
Author(s):  
Hemavathi Umeshappa ◽  
Chandrashekhar M ◽  
Ashok M Shenoy ◽  
Dinesh Kumar GR

2021 ◽  
Vol Volume 14 ◽  
pp. 53-64
Author(s):  
Caterina Giannitto ◽  
Giuseppe Mercante ◽  
Giuseppe Spriano ◽  
Rossella Natoli ◽  
Francesca Gaino ◽  
...  

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