Intramedullary Subependymoma of the Cervical Spinal Cord: A Case Report and Review of the Literature

Subependymoma is a rare tumor of the central nervous system, representing 0.2 to 0.7% of all intracranial tumors. They are usually found in the fourth ventricle or in the walls of the lateral ventricles, often remaining asymptomatic. Subependymomas occur rarely in the cervical or thoracic spinal cor...

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Main Authors: Eiralí Guadalupe García Chapa, Juana Elizabeth Tadeo González, Mauricio Delgado Morquecho, José Armando Díaz Martínez, Mariana Mercado Flores, Ángel Martínez Ponce De León, Oralia Barboza Quintana, Rodolfo Franco Márquez
Format: Article
Language:English
Published: Thieme Medical and Scientific Publishers Pvt. Ltd. 2019-03-01
Series:Indian Journal of Neurosurgery
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Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0038-1676167
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author Eiralí Guadalupe García Chapa
Juana Elizabeth Tadeo González
Mauricio Delgado Morquecho
José Armando Díaz Martínez
Mariana Mercado Flores
Ángel Martínez Ponce De León
Oralia Barboza Quintana
Rodolfo Franco Márquez
author_facet Eiralí Guadalupe García Chapa
Juana Elizabeth Tadeo González
Mauricio Delgado Morquecho
José Armando Díaz Martínez
Mariana Mercado Flores
Ángel Martínez Ponce De León
Oralia Barboza Quintana
Rodolfo Franco Márquez
author_sort Eiralí Guadalupe García Chapa
collection DOAJ
description Subependymoma is a rare tumor of the central nervous system, representing 0.2 to 0.7% of all intracranial tumors. They are usually found in the fourth ventricle or in the walls of the lateral ventricles, often remaining asymptomatic. Subependymomas occur rarely in the cervical or thoracic spinal cord. Since its first description in the spinal cord by Boykin et al in 1954, only 47 cases have been reported. A 49-year-old man presented with a 4-year-long-lasting neck pain, which radiated to the upper right extremity for 4 years. It was insidious at onset and revealed gradual progression, difficulty in performing fine hand movements, and hyperalgesia. Magnetic resonance imaging revealed irregular hyperintensity of T2 and dilatation of the spinal cord from C4 to T1 with associated edema and an intramedullary lesion with central location. During the surgical event, a transoperative biopsy was performed that revealed loose fibrillary networks and groups of nuclei showing mild pleomorphism and microcystic formations. Histologically, we observed groups of cells with mild nuclear pleomorphism embedded in a dense, thin, glial fibrillar fundus, and microcystic formations. Immunohistochemical staining revealed diffuse positivity for the glial fibrillary acidic protein, and negative for the epithelial membrane antigen. Subependymoma accounts for 8.3% of all ependymal tumors. There are few descriptions of the cytologic features of the subependymoma because this neoplasm is rare and most commonly found incidentally in autopsies.
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spelling doaj-art-0cfd28b973774da3a510100653ee22462025-08-20T03:17:08ZengThieme Medical and Scientific Publishers Pvt. Ltd.Indian Journal of Neurosurgery2277-954X2277-91672019-03-01080106406810.1055/s-0038-1676167Intramedullary Subependymoma of the Cervical Spinal Cord: A Case Report and Review of the LiteratureEiralí Guadalupe García Chapa0Juana Elizabeth Tadeo González1Mauricio Delgado Morquecho2José Armando Díaz Martínez3Mariana Mercado Flores4Ángel Martínez Ponce De León5Oralia Barboza Quintana6Rodolfo Franco Márquez7Anatomic Pathology and Cytopathology Service, Universitary Hospital of Autonomous University of Nuevo León, Monterrey, MexicoAnatomic Pathology and Cytopathology Service, Universitary Hospital of Autonomous University of Nuevo León, Monterrey, MexicoAnatomic Pathology and Cytopathology Service, Universitary Hospital of Autonomous University of Nuevo León, Monterrey, MexicoNeurosurgery and Neurological Endovascular Therapy Service, Universitary Hospital of Autonomous University of Nuevo León, Monterrey, MexicoDepartment of Radiology, Universitary Hospital of Autonomous University of Nuevo León, Monterrey, MexicoNeurosurgery and Neurological Endovascular Therapy Service, Universitary Hospital of Autonomous University of Nuevo León, Monterrey, MexicoAnatomic Pathology and Cytopathology Service, Universitary Hospital of Autonomous University of Nuevo León, Monterrey, MexicoAnatomic Pathology and Cytopathology Service, Universitary Hospital of Autonomous University of Nuevo León, Monterrey, MexicoSubependymoma is a rare tumor of the central nervous system, representing 0.2 to 0.7% of all intracranial tumors. They are usually found in the fourth ventricle or in the walls of the lateral ventricles, often remaining asymptomatic. Subependymomas occur rarely in the cervical or thoracic spinal cord. Since its first description in the spinal cord by Boykin et al in 1954, only 47 cases have been reported. A 49-year-old man presented with a 4-year-long-lasting neck pain, which radiated to the upper right extremity for 4 years. It was insidious at onset and revealed gradual progression, difficulty in performing fine hand movements, and hyperalgesia. Magnetic resonance imaging revealed irregular hyperintensity of T2 and dilatation of the spinal cord from C4 to T1 with associated edema and an intramedullary lesion with central location. During the surgical event, a transoperative biopsy was performed that revealed loose fibrillary networks and groups of nuclei showing mild pleomorphism and microcystic formations. Histologically, we observed groups of cells with mild nuclear pleomorphism embedded in a dense, thin, glial fibrillar fundus, and microcystic formations. Immunohistochemical staining revealed diffuse positivity for the glial fibrillary acidic protein, and negative for the epithelial membrane antigen. Subependymoma accounts for 8.3% of all ependymal tumors. There are few descriptions of the cytologic features of the subependymoma because this neoplasm is rare and most commonly found incidentally in autopsies.http://www.thieme-connect.de/DOI/DOI?10.1055/s-0038-1676167subependymomacervical spinal cordglial fibrillary acidic protein
spellingShingle Eiralí Guadalupe García Chapa
Juana Elizabeth Tadeo González
Mauricio Delgado Morquecho
José Armando Díaz Martínez
Mariana Mercado Flores
Ángel Martínez Ponce De León
Oralia Barboza Quintana
Rodolfo Franco Márquez
Intramedullary Subependymoma of the Cervical Spinal Cord: A Case Report and Review of the Literature
Indian Journal of Neurosurgery
subependymoma
cervical spinal cord
glial fibrillary acidic protein
title Intramedullary Subependymoma of the Cervical Spinal Cord: A Case Report and Review of the Literature
title_full Intramedullary Subependymoma of the Cervical Spinal Cord: A Case Report and Review of the Literature
title_fullStr Intramedullary Subependymoma of the Cervical Spinal Cord: A Case Report and Review of the Literature
title_full_unstemmed Intramedullary Subependymoma of the Cervical Spinal Cord: A Case Report and Review of the Literature
title_short Intramedullary Subependymoma of the Cervical Spinal Cord: A Case Report and Review of the Literature
title_sort intramedullary subependymoma of the cervical spinal cord a case report and review of the literature
topic subependymoma
cervical spinal cord
glial fibrillary acidic protein
url http://www.thieme-connect.de/DOI/DOI?10.1055/s-0038-1676167
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