Neuroenteric Cyst: A Rare Lesion of the Spinal Cord

2019 ◽  
Vol 51 (03) ◽  
pp. 233-234
Author(s):  
Marta Rodrigues ◽  
Joana Osório ◽  
Carlos Pontinha ◽  
Miguel Correia ◽  
Carla Conceição
Author(s):  
Deniz Sirinoglu ◽  
Buse Sarigul ◽  
Ozan Baskurt ◽  
Mehmet Volkan Aydin

Abstract Background Primary spinal glioblastoma is a rare lesion which constitutes only 1.5% of all spinal tumors. Diagnosis is challenging due to absence of any radiological hallmark of the disease. Even though surgery combined with chemoradiotherapy is the optimal management for these tumors, prognosis is still poor. Dissemination of glioblastoma is reported several times in the literature, which is correlated with worse prognosis and outcome. This case report that we are presenting is the first case where dissemination of primary spinal glioblastoma dissemination is limited only to spinal cord, without intracranial invasion, and regression was achieved with chemoradiotherapy. Case Report In this article, a patient with primary spinal glioblastoma who presented with paraparesia is presented. Patient underwent surgery for resection of the tumor and received adjuvant radiotherapy. However, 9 months postoperatively, dissemination was detected in epidural and subdural spaces of spinal canal, with concomitant compression of spinal cord. There was no radiographically detected lesion in cranial MRI. He underwent second session of radiotherapy, combined with chemotherapy and steroid. Five months later, regression of metastatic disseminated lesions was observed. Conclusion Primary spinal glioblastoma is a rare pathology and known to have a poor prognosis, notably with dissemination of the disease. Even though further biomolecular studies are necessary to explain the pathophysiology better, chemotherapy and radiotherapy may be effective in regression of disseminated lesions.


Author(s):  
Laxmikant Bhople ◽  
Hrushikesh Kharosekar ◽  
Nimesh Jain ◽  
Vernon Velho

AbstractIntramedullary schwanommas are rare, and most cases are reported in cervical region. Less than 20 dorsal intramedullary schwanommas have been reported till date in literature. This is due to their cell of origin, the Schwann cell, which is not normally found within the parenchyma of the brain and spinal cord; therefore it is not surprising that these lesions are rare. We report a rare solitary dorsal intramedullary schwanomma in a young adult patient who presented with paraplegia.


1972 ◽  
Vol 37 (2) ◽  
pp. 233-236 ◽  
Author(s):  
Howard Semins ◽  
G. Robert Nugent ◽  
Samuel M. Chou

✓ A dorsal laminectomy was performed on a 68-year-old woman with an intramedullary mass lesion, ultimately diagnosed as sarcoidosis. This rare lesion of the spinal cord is presented with references to similar cases.


Neurosurgery ◽  
1992 ◽  
Vol 31 (1) ◽  
pp. 121-124 ◽  
Author(s):  
Ismail H. Tekkök ◽  
Selcuk Palaoḡlu ◽  
Aykut Erbengi ◽  
Behsan Önol

1982 ◽  
Vol 56 (2) ◽  
pp. 270-274 ◽  
Author(s):  
David M. F. Kwok ◽  
Richard V. Jeffreys

✓ The authors describe a case of intramedullary enterogenous cyst of the spinal cord, and review the clinical aspects of this entity together with the histological classification. Discussions on the embryogenesis and pathogenesis of this rare lesion are reviewed and summarized.


2018 ◽  
Vol 118 ◽  
pp. 296-300 ◽  
Author(s):  
Tarek Y. El Ahmadieh ◽  
Rafael Sillero ◽  
Benjamin Kafka ◽  
Salah G. Aoun ◽  
Angela V. Price

1978 ◽  
Vol 49 (2) ◽  
pp. 292-297 ◽  
Author(s):  
Thomas J. Rosenbaum ◽  
Edward H. Soule ◽  
Burton M. Onofrio

✓ A search of the English literature revealed 46 cases of primary intraspinal teratomas, of which 22 were teratomatous cysts of the spinal cord. To clarify the confusion regarding this rare lesion, the definition, origin, presentation, and histological features of the lesion are discussed. An additional case is presented.


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