Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/30470
Title: Natural Course of Myxopapillary Ependymoma: Unusual Case Report and Review of Literature
Authors: Pusat, Serhat
Erbaş, Yahya Cem
Göçmen, Selçuk
Kocaoğlu, Murat
Erdoğan, Ersin
Keywords: Intradural
Magnetic resonance imaging
Myxopapillary ependymoma
Spinal cord tumor
gadolinium
adult
Article
backache
case report
clinical article
contrast enhancement
disease course
ependyma cell
ependymoma
feces incontinence
female
histopathology
human
human tissue
laminectomy
medical literature
nerve cell differentiation
nuclear magnetic resonance imaging
paraplegia
rare disease
spinal cord tumor
treatment refusal
urine incontinence
complication
diagnostic imaging
differential diagnosis
disease exacerbation
pathology
sacrum
thoracic vertebra
Adult
Back Pain
Diagnosis, Differential
Disease Progression
Ependymoma
Female
Humans
Magnetic Resonance Imaging
Paraparesis
Sacrum
Spinal Cord Neoplasms
Thoracic Vertebrae
Publisher: Elsevier Inc.
Abstract: Background: Spinal cord ependymomas are the most frequent primary intramedullary tumors of the cord in middle age (40–60 years of age). Myxopapillary ependymomas are low-incidence tumors and occur in the cauda equina and conus medullaris. They are typically described as fleshy, sausage-shaped, vascular lesions. Case Description: In this report, we present a 36-year-old woman who was seen in another hospital with complaints of back pain radiating into both legs 5 years ago. Magnetic resonance imaging (MRI) examinations revealed a lesion releated to the spinal cord. At that point, the patient refused the proposed surgical treatment. Five years later, the patient was referred to our clinic with advancement of the complaint to paraparesis. The new MRI showed an intradural mass at the level of T11 and S1. We performed a total intradural tumor resection. Histopathologic examination revealed a myxopapillary ependymoma. Conclusions: Myxopapillary ependymomas grow slowly and are well defined by MRI. Advancements in radiologic technology and surgical equipment have allowed this tumor type to be treated successfully. Unfortunately, if untreated, these lesions have poor prognosis and result in clinical symptoms such as paraparesis. Surgical treatment of these lesions using total resection was performed total resection and was associated with an excellent postoperative outcome. We highlight the natural course of myxopapillary ependymomas. © 2018
URI: https://hdl.handle.net/11499/30470
https://doi.org/10.1016/j.wneu.2018.10.028
ISSN: 1878-8750
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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