Clinico Pathological Study of Parenchymal Lesions of Spinal Cord
DOI:
https://doi.org/10.21276/apalm.2142Keywords:
Spinal lesions, cord parenchyma, non –neoplastic, neoplasticAbstract
Background-
Spinal parenchymal lesions are rare with a wide spectrum of clinical and histological presentation. The aims and objectives was to study the incidence and histopathological features of parenchymal lesions of the spinal cord in relation to age, sex, clinical features, radiological findings and topographical distribution.
Methods –
We studied spinal lesions over a period of ten years in a tertiary care hospital. Our study comprised a total number of 241 surgical resection specimens of lesion of spinal cord out of which 73 cases of spinal cord parenchymal lesions were found. Primary vertebral tumors and paraspinal soft tissue lesions were excluded. Descriptive cross-sectional study of cases including detailed clinical data of age, sex, duration of disease, type of lesion, and radiological findings of the patients was obtained. All cases were analyzed by examining Hematoxylin and Eosin stained slides with use of special stains and immunohistochemistry, as needed.
Results - .
Male predominance was seen in spinal cord parenchymal lesions and 3rd and 4th decade age group was most commonly affected. These lesions were more common in thoracic region followed by cervical region.Neoplastic lesion of spinal cord parenchyma are more frequently encountered than nonneoplastic lesions. Astrocytomas (24.63 %) were commonest neoplastic spinal cord lesions with preponderance of low grade astrocytoma. Ependymomas and PNET accounted for 20.53 % and 4.10 % respectively
Conclusion –
The histopathological diagnosis of spinal parenchymal lesions can be extremely challenging, the difficulty exaggerated by small size of the specimen. In such situation a multidisciplinary approach including neurosurgeons, neuroradiologist and neuropathologist is highly recommended.
References
2. Brotchi J. Surgical treatment of intramedullary tumors. Experience with 316 cases. Bull Mem Acad R Med Belg. 2004; 159(5-6):335-9.
3. Craciunas SC, Gorgan MR, Cirstea CM, Aschie M. Intramedullary Tumors - Clinical, Radiological and Histological Correlations. Romanian Neurosurgery 2011 18(2):1-16.
4. Sevick RJ, Johns RD, Curry BJ. Primary spinal neuroectodermal tumour with extraneural metastasis. AJNR 1987; 8: 1151-1152.
5. Engelhard HH, Villano JL, Porter KR, Stewart AK, Barua M, Barker FG et al. Clinical presentation, histology, and treatment in 430 patients with primary tumors of the spinal cord, spinal meninges, or cauda equina. J Neurosurg Spine 2010; 13:67–77.
6. Adam Y, Benezech J, Blanquet A, Fuentes JM, Bousigue JY, Debono B et al.Intramedullary tumors. Results of a national investigation in private neurosurgery. Neurochirurgie 2010 Aug; 56(4):344-9.
7. Milano MT, Johnson MD, Sul J, Mohile NA, Korones DN, Okunieff P et al. Primary spinal cord glioma: a surveillance, epidemiology, and end results database study. J Neuro-oncol 2009 Nov: 1-10.
8. Louis DN, Ohgaki H, Wiestler OD, Cavenee KW. WHO classification of tumours of the central nervous system. 4th ed; IARC: 2007.
9. Louis DN, Ohgaki H, Wiestler OD, Cavenee KW. WHO classification of tumours of the central nervous system. 4th ed; IARC: 2007.
10. Traul DE, Shaffrey ME, Schiff D. Spinal-cord neoplasms—intradural neoplasms. Lancet oncol 2007; 8: 35–45.
11. Singh A, Gupta V, Singh H, Chand K. Nondysraphic intradural spinal lipoma.
J Pediatr Neurosci 2009 Jan-Jun; 4(1): 55–56.
12. Odebode TO, Udoffa U, Nzeh D. Cervical myelomeningocele and hydrocephalus without neurological deficit: A Case Report. American-Eurasian Journal of Scientific Research 2007; 2 (1): 60-62.
13. Odebode TO, Udoffa U, Nzeh D. Cervical myelomeningocele and hydrocephalus without neurological deficit: A Case Report. American-Eurasian Journal of Scientific Research 2007; 2 (1): 60-62.
14. Nejat F, Khotaei GT, Mamishi S. Intramedullary spinal cord abscess: Report of two cases. Iran J Ped Mar 2007; 17 (1): 69-72.
15. Thacker MM, Puri AI. Concurrent intramedullary and intracranial tuberculomas. J Postgrad Med 2004; 50: 107-109.
16. MacDonell AH, Baird RW, Bronze MS. Intramedullary tumors of the spinal cord: case report and review. Rev Infect Dis 1990; 12: 432-439.
17. Ahmad FU, Sharma BS. Treatment of intramedullary spinal cysticerco¬sis: report of 2 cases and review of literature. Surg Neurol 2007; 67: 74-77.
18. Kishor LT, Gayatri K, Naidu MR, Mateen MA, Dinakar I, Ratnakar KS. Intramedullary spinal cord cysticercosis--a case report and literature review. Indian J Pathol Microbiol 1991; 34: 219-221.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2018 Rachana Swapnil Binayke, Shantilal Mohanlalji Sisodia, Tushar Chintaman Joshi
This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access at http://opcit.eprints.org/oacitation-biblio.html).