Unique desmoplastic cerebral tumor in a patient with complex partial seizures

被引:8
作者
Jay, V
Edwards, V
Rutka, J
Mosskin, M
Hwang, P
Resch, L
机构
[1] Univ Toronto, Hosp Sick Children, Div Pathol, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Bloorview Epilepsy Program, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Div Neurosurg, Toronto, ON M5G 1X8, Canada
[4] Univ Toronto, Div Neuroradiol, Toronto, ON M5G 1X8, Canada
[5] Univ Toronto, Div Neurol, Toronto, ON M5G 1X8, Canada
[6] Izaak Walton Killam Hosp Children, Grace Hlth Ctr, Dept Pathol, Halifax, NS B3J 3G9, Canada
关键词
brain neoplasm; desmoplastic tumor; ultrastructure; pathology;
D O I
10.1007/s100249900032
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Primary brain tumors with prominent desmoplasia include the gliofibroma, desmoplastic infantile ganglioglioma (DIG), pleomorphic xanthoastrocytoma (PXA), and desmoplastic cerebral astrocytoma. In the present report, we describe unusual pathological appearances in two successive resections of a left temporal tumor in a patient with complex partial seizures. Both tumors showed focal astroglial and very prominent neuronal differentiation. In the first resection at age 11 years, the tumor showed only focal desmoplastic areas and prominent neuronal differentiation with bizarre atypical giant cells. In the second resection at age 14 years, the morphology was dramatically different. Now the tumor showed marked desmoplasia with tumor cells coexpressing neuronal and glial markers. Electron microscopy showed prominent neuronal differentiation in both resections and presence of basal lamina around tumor cells. Our case represents a unique example of an extraordinary degree of neuronal differentiation in a desmoplastic cerebral tumor. While cellular pleomorphism in a desmoplastic tumor traditionally suggests the diagnosis of PXA, we wish to underscore that many cells exhibiting marked cytologic atypia may in fact be of neuronal rather than of glial origin as in our case.
引用
收藏
页码:234 / 242
页数:9
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