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Year : 2003  |  Volume : 51  |  Issue : 1  |  Page : 98-99

Subependymomas in children: A report of five cases including two with osseous metaplasia

Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh-160012

Correspondence Address:
Department of Histopathology, PGIMER, Chandigarh-160012

 » Abstract 

Subependymomas are highly differentiated slow growing gliomas. They are one of the few gliomas which are biologically benign. They are extremely rare in children. However, after going through the histopathology records of our department of fourteen years (1983-1997) we found that five (20%) cases of subependymomas have been diagnosed in children out of a total of twenty-six subependymomas. Two of our cases showed the presence of osseous metaplasia, a hitherto undescribed finding.

How to cite this article:
Mallik M K, Babu N, Kakkar N, Khosla V K, Banerjee A K, Vasishta R K. Subependymomas in children: A report of five cases including two with osseous metaplasia . Neurol India 2003;51:98-9

How to cite this URL:
Mallik M K, Babu N, Kakkar N, Khosla V K, Banerjee A K, Vasishta R K. Subependymomas in children: A report of five cases including two with osseous metaplasia . Neurol India [serial online] 2003 [cited 2023 Dec 8];51:98-9. Available from:

Subependymomas are highly differentiated slow growing gliomas composed of ependymal and astrocyte-like cells. These occur in the walls of the ventricular system or rarely in the parenchyma of the spinal cord.[1] They are one of the few gliomas which are considered biologically benign. Most often, they are encountered as incidental post-mortem findings and only occasional examples are seen as surgical specimens.[2] Children are rarely affected.[1] In this article, we describe five cases of subependymomas in children who presented with neurological symptoms. The age ranged from four-and-a-half to six years. In addition, bony metaplasia, hitherto undescribed in these tumors, was seen in two cases.

  »   Case Report

After reviewing the histopathology records of the Department of Histopathology, PGIMER, Chandigarh, we found five cases of subependymomas reported over a period of fourteen years (1983-1997) among pediatric patients. Altogether twenty-six subependymomas were diagnosed during this period. The hematoxylin and eosin stained slides were reviewed and the clinical and radiological details were obtained from the hospital records. For the histopathological diagnosis, strict criteria were used and tumors where areas of both subependymoma and ependymoma were present were diagnosed as subependymomas only when the overwhelming majority of the area was subependymomatous. In three of our cases immunostaining for glial fibrillary acid protein was performed.
All the five patients were males (age range 41/2-6 years) who presented with features of raised intracranial tension for three to six months. One of them had a history of diminished vision for three months and frequent falls for five months. In two cases, there was a recurrence within one year of surgery. In one case the child expired due to postoperative complications within one week of surgery. In the remaining two cases there was no recurrence. The salient findings have been summarized in [Table - 1].
In all these cases, the tumors were received as greyish white firm fragments. In two of these cases gritty hard areas were felt on slicing. Microscopically typical histology of subependymoma was seen. A sweeping of highly fibrillar processes about clustered nuclei was noted. The nuclei were oval shaped with homogenous pale chromatin and minimal pleomorphism [Figure - 1]. The interface between the tumor and the brain was sharp. In one of our cases, small foci within the tumor showed features of ependymoma [Figure - 2]. However, because this accounted for a very small proportion of the tumor area (approx. 5%), the tumor was labeled as subependymoma. The histology did not give any indication of a higher grade in the recurrent cases. In two cases prominent osseous metaplasia associated with areas of calcification were seen [Figure - 3]. In both these lesions radiological examination had detected this change. These areas of osseous metaplasia were intimately admixed with the tumor area. Immunostaining for glial fibrillary acid protein was positive in the tumor area but not in the area of bony metaplasia.

  »   Discussion Top

Subependymomas are one of the few gliomas which are considered biologically benign.[1] They usually occur in adults.[1] Only one case report is available in the literature describing a subependymoma in a two-and-a-half year old boy.[3],[4],[5] Out of twenty-six cases of subependymomas diagnosed in our department within a period of fourteen years, five belonged to the pediatric population (approx. 20%). Our hospital series mainly consisted of the North Indian population. Whether this higher incidence is due to a geographical variation is a matter of debate.
One child expired within one week of surgery due to postoperative complications. Out of the remaining four, two cases recurred and two did not show any recurrences. The recurrences were successfully treated and the patients are doing well till date.
Two of the five cases showed osseous metaplasia. Various CNS tumors are known to show metaplastic elements like epithelial tissue, bone, cartilage and skeletal muscle.[6],[7],[8] Astrocytomas, glioblastomas, ependymomas and medulloblastomas[6],[7],[8] are some such tumors which show the presence of metaplastic elements. The most possible mechanism for the formation of such elements is the metaplasia of the supporting connective tissue.[6],[7],[8] In addition, neoplastic glial cells may also secrete substances which can lead to the formation of these elements.[8] There are reports of sarcomatous proliferation in the vasculature of subependymomas[9] and a report of rhabdomyosarcomatous differentiation.[10] However, we have not come across any report of osseous metaplasia in subependymomas. Thus the finding of bony metaplasia in two of our five cases is unusual as calcification and ossification was observed on X-Ray/CT. Since one of the most common posterior fossa SOL in children, the medulloblastoma, rarely ossifies, tumors in children with calcification and ossification as indicated by radiological examination may suggest subependymomas. 

 » References Top

1.Rosai J. Tumours of the central nervous system. Atlas of tumour pathology. 3rd series Fascicle 10. Washington DC: Armed Forces Institute of Pathology; 1994. pp.133-6.  Back to cited text no. 1    
2.Lombardi D, Scheithauer BW, Meyer FB, et al. Symptomatic subependymoma:a clinicopathological and flowcytometry study. J Neurosurg 1991;75:583-8.  Back to cited text no. 2  [PUBMED]  
3.Rea CL, Aheron RD, Rocksword CL, Smith SA. Subependymoma in a two and a half year old boy: case report. Neurosurgery 1984;14:608-11.  Back to cited text no. 3    
4.Lalitha V, Dastur DK. Neoplasm of the central nervous system-Histological types of 2237 cases. Ind J Cancer 1980;17;102-6.  Back to cited text no. 4    
5.Mathai KV. Intracranial space occupying lesion. review of 233?- cases. Neurol Ind 1978;26:157-70.  Back to cited text no. 5  [PUBMED]  
6.Kepes JJ, Fulling KH, Garcia JH. The clinical significance of adenoid formation of neoplastic astrocytes, initiating metastatic carcinomas in gliosarcomas. A review of 5 cases. Clin Neuropathol 1982;1:139-50.  Back to cited text no. 6  [PUBMED]  
7.Matthews T, Moossy J. Gliomas containing bone and cartilage. J Neuropathol Exp Neurol 1974;33:456-71  Back to cited text no. 7    
8.Rubinstein LJ, Chiang H. The role of astrocytes in the formation of cartilage in gliomas: an immunohistochemical study of 4 cases. Am J Pathol 1984;117:471­83.  Back to cited text no. 8    
9.Louis DN, Hedley-Whyte ET, Marfuja RL. Sarcomatous proliferation of the vasculature in subependymoma. Acta Neuropathol (Berl) 1989;78:332-5.  Back to cited text no. 9    
10.Tomilson FH, Scheithauer BW, Kelly PJ, Forbes GS. Subependyinoma with rhadomyosarcomatous differentiation: report of a case and literature review. Neurosurgery 1991.  Back to cited text no. 10    


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