scholarly journals Multiple meningiomas in different neuroaxial locations: report of a rare case

2021 ◽  
Vol 2 (2) ◽  
pp. 91-94
Author(s):  
Gopal Raman Sharma ◽  
Sameer Aryal ◽  
Ramchandra Shrestha ◽  
Alok Deo ◽  
Rakesh Pathak
Keyword(s):  
Rare Case ◽  
Spastic Paraparesis ◽  
Multiple Meningiomas ◽  
Intradural Extramedullary

We report a rare case of multiple meningiomas in a 74 year old female who was brought to the hospital with spastic paraparesis and MRI of spine and brain revealed multiple enhancing meningiomas in brain and spines. The spinal intradural extramedullary (IDEM) meningioma at C7-D1 level was excised which had caused paraparesis and postoperatively patient became symptom free. We will discuss about the incidence, symptomatology, investigations and management of multiple meningiomas in different neuroaxial compartments at the same period of time and will review the literature.

scholarly journals A rare case of multiple meningiomas with different histology

2017 ◽  
Vol 2 (2) ◽  
pp. 114-119
Author(s):  
Toma Papacocea ◽  
Andrei Mladin ◽  
Serban Papacocea
Keyword(s):  
Rare Case ◽  
Multiple Meningiomas

A rare case of intradural extramedullary Ewing's sarcoma in the cervical region

2019 ◽  
Vol 67 (6) ◽  
pp. 1543
Author(s):  
Ketan Desai ◽  
AnshuC Warade ◽  
AshishK Jha ◽  
Sanjeev Pattankar ◽  
Chitra Madiwale ◽  
...  
Keyword(s):  
Rare Case ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Cervical Region ◽  
Intradural Extramedullary

Rare case of multiple meningiomas in nonneurofibromatosis patient at unusual locations

2017 ◽  
Vol 31 (2) ◽  
pp. 240-243 ◽  
Author(s):  
Vikrant Setia ◽  
Deepashu Sachdeva ◽  
Shrinivas Odugoudar ◽  
Pravin Borde ◽  
Daljit Singh
Keyword(s):  
Posterior Fossa ◽  
Rare Case ◽  
Intracranial Lesion ◽  
Multiple Meningiomas ◽  
Intraventricular Meningioma ◽  
Intracranial Lesions ◽  
Multiple Meningioma

Abstract Multiple meningioma is a condition in which more than one intracranial lesion is seen in different location and these lesions may occur with or without signs of neurofibromatosis. Incidence of multiple meningioma range from 1 to 10% in different series. We report a case of multiple meningioma in a 33 years old female who had 14 intracranial lesions both supratentorially and infratentorially, and underwent surgery for large right lateral intraventricular meningioma. She had two meningiomas located in posterior fossa associated with supratentorial meningioma, which has been rarely reported.

scholarly journals Diagnosis and treatment of noncommunicating extradural spinal thoracolumbar arachnoid cyst

2020 ◽  
Vol 11 ◽  
pp. 405
Author(s):  
Shahidul Islam Khan ◽  
Nazmin Ahmed ◽  
Bipin Chaurasia ◽  
Kamrul Ahsan
Keyword(s):  
Subarachnoid Space ◽  
Spastic Paraparesis ◽  
Cord Compression ◽  
Arachnoid Cysts ◽  
Csf Leak ◽  
Uneventful Recovery ◽  
Congenital Defects ◽  
Surgical Removal ◽  
Intradural Extramedullary ◽  
Extradural Cyst

Background: Noncommunicating extradural spinal arachnoid cysts are extremely rare. They are believed to arise from congenital defects in the dura mater and become enlarged as a consequence of increased cerebro-spinal fluid (CSF) pressure within the subarachnoid space. Most retain a communicating pedicle through which the extradural cyst maintains connection with the subarachnoid space, and only rarely does this communication become sealed. The optimal treatment consists of complete surgical removal of the cyst with ligation of the communicating pedicle. Case Description: A 29-year-old male presented with a progressive spastic paraparesis of 6 months’ duration. The MRI showed a circumscribed intradural extramedullary cystic lesion located from D11-L2. Notably, peroperatively, the cyst appeared to be entirely extradural, without a communicating intradural pedicle. Further, no CSF leak was observed even after Valsalva maneuvers. Following surgical extirpation of the cyst, the patient sustained an uneventful recovery within 1 postoperative month. Conclusion: Noncommunicating extradural arachnoid cysts are extremely rare causes of spinal cord compression and should be fully excised.

scholarly journals A rare case of intradural extramedullary Ewing's sarcoma with skip metastasis in the spine

Spinal Cord ◽  
2008 ◽  
Vol 46 (8) ◽  
pp. 582-584 ◽  
Author(s):  
K P Haresh ◽  
S K Chinikkatti ◽  
R Prabhakar ◽  
A Rishi ◽  
G K Rath ◽  
...  
Keyword(s):  
Rare Case ◽  
Ewing’S Sarcoma ◽  
Ewing's Sarcoma ◽  
Skip Metastasis ◽  
Intradural Extramedullary

scholarly journals A rare case of thoracic spinal intradural extramedullary enterogenous cyst with acute onset: case report and literature review

2019 ◽  
Vol 101 (6) ◽  
pp. e142-e146 ◽  
Author(s):  
CX Liu ◽  
B Meng ◽  
YB Li ◽  
H Bai ◽  
ZX Wu
Keyword(s):  
Rare Case ◽  
Acute Onset ◽  
Neurenteric Cyst ◽  
Enterogenous Cyst ◽  
Diagnosis And Prognosis ◽  
Thoracic Spinal ◽  
Spinal Segments ◽  
Intradural Extramedullary ◽  
Radicular Symptoms ◽  
Progressive Weakness

The intraspinal enterogenous cyst, also called an neurenteric cyst, is a rare congenital disease. It was reported to be local to the C1 to L2 spinal segments, with the majority located in the cervicothoracic region. Most patients present with symptoms of progressive focal pain, myelopathic signs or radicular symptoms. We report a rare case of thoracic spinal intradural extramedullary enterogenous cyst with rapidly progressive weakness of both lower extremities. Additionally, we analysed the literature concerning the clinical features, diagnosis and prognosis of this disease.

A Case of Upper Thoracic Intradural-Extramedullary Multiple Meningiomas

2013 ◽  
Vol 23 (3) ◽  
pp. 224-225
Author(s):  
Fatih Keskin ◽  
Erdal Kalkan ◽  
Yasar Karatas
Keyword(s):  
Multiple Meningiomas ◽  
Intradural Extramedullary ◽  
Upper Thoracic

scholarly journals Multicentric intradural extramedullary ependymoma: Report of a rare case

2015 ◽  
Vol 6 (3) ◽  
pp. 134 ◽  
Author(s):  
Raghvendra Ramdasi ◽  
Gautam Zaveri ◽  
Sunil Pandya ◽  
Atul Vats
Keyword(s):  
Rare Case ◽  
Intradural Extramedullary

scholarly journals Simultaneous trigonal and spinal meningioma with varied histology: A rare case report

2021 ◽  
Vol 12 ◽  
pp. 611
Author(s):  
H. R. Darshan ◽  
Biren Khimji Patel ◽  
Ajit Singh ◽  
Prakash Nair ◽  
Rajalakshmi Poyuran ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Rare Case ◽  
Case Description ◽  
Spinal Meningioma ◽  
Multiple Meningiomas ◽  
First Case ◽  
Rare Case Report ◽  
The Central Nervous System ◽  
Spinal Meningiomas

Background: Meningioma is one of the most common neoplasms of the central nervous system. Multiple meningiomas without neurofibromatosis are not a usual occurrence. Intraventricular meningioma with spinal meningioma is rare and not been reported in the literature. Case Description: We report a case of a 63-year-old male with the left trigonal and spinal meningioma. Both the meningiomas were resected in different settings. The histological examination of tumors revealed to be of varied histology, that is, meningothelial and atypical meningioma, respectively. Conclusion: Although various cases with multiple cranial and spinal meningiomas are described, this is the first case of an intraventricular and spinal meningioma. With varied histology, the case also reaffirms the theory of polyclonal origin of multiple meningiomas.

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