Ependymomas with neuronal differentiation: a morphologic and immunohistochemical spectrum

被引:0
|
作者
Fausto J. Rodriguez
Bernd W. Scheithauer
Peter D. Robbins
Peter C. Burger
Richard B. Hessler
Arie Perry
Patrice C. Abell-Aleff
Gary W. Mierau
机构
[1] Mayo Clinic,Department of Pathology
[2] Johns Hopkins Medical Institutions,Division of Neuropathology
[3] Washington University,Department of Pathology
[4] Erlanger Medical Center,Department of Laboratory Medicine and Pathology
[5] PathCentre,undefined
[6] Children’s Hospital,undefined
[7] Mayo Clinic,undefined
来源
Acta Neuropathologica | 2007年 / 113卷
关键词
Ependymoma; Brain; Neuronal; Neuropil; Glioma; Electron microscopy; Immunohistochemistry;
D O I
暂无
中图分类号
学科分类号
摘要
The category of mixed glioneuronal tumors of the CNS is rapidly losing its definition as encompassing tumors composed of histologically distinct neuron variants and glia. We encountered five ependymomas with neuronal differentiation seen in two by histology, in two by immunohistochemistry alone, and in one by electron microscopy. Antibodies against GFAP, S-100 protein, neurofilament protein, chromogranin, synaptophysin, Neu-N, and EMA were applied. Ultrastructural studies were also performed. In addition, 33 randomly selected ependymomas of various histologic types were screened for these same antigens. Cases 1 and 2 were anaplastic and showed clearly defined neuropil islands or pale islands as in nodular desmoplastic medulloblastoma, respectively. The tumors affected a 16-year-old male and a 5-year-old female and involved the right frontoparietal lobe and fourth ventricle, respectively. The islands were positive for synaptophysin and Neu-N (cases 1 and 2), and chromogranin (case 1). Cases 3–5, as well as 7 of the 33 screened ependymomas, showed a suggestion of neuronal differentiation by immunohistochemistry alone, including immunoreactivity for Neu-N (n = 8), synaptophysin (n = 4), neurofilament protein (n = 4), and chromogranin (n = 2). Five tumors each were WHO grade II and III. Electron microscopy performed on the two cases with neuronal islands demonstrated microtubule bundles and dense core granules (case 1) and poorly differentiated cells with high nuclear/cytoplasmic ratios, with intermediate filament accumulation and rare cilia (case 2). Cases identified by immunohistochemistry or electron microscopy demonstrated dense core granules (n = 5) and aligned microtubules (n = 3). Neuronal differentiation occurs in ependymomas but is less frequently definitive (histologic, ultrastructural) than merely a limited immunohistochemical finding. The clinical significance of these observations is unknown but deserves further exploration.
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页码:313 / 324
页数:11
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