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Ependymoma with "granular cell" features: Report of two cases
被引:4
|作者:
Shintaku, Masayuki
[1
]
Yoshida, Makiko
[2
]
Ikarashi, Toshihiko
[3
]
Arakawa, Yasuaki
[4
]
Nagashima, Tatsuya
机构:
[1] Osaka Red Cross Hosp, Dept Pathol, Tennoji Ku, Osaka 5438555, Japan
[2] Hyogo Prefectural Kobe Childrens Hosp, Dept Pathol, Kobe, Hyogo, Japan
[3] Nagaoka Cent Gen Hosp, Dept Pathol, Nagaoka, Niigata, Japan
[4] Joetsu Gen Hosp, Dept Neurosurg, Joetsu, Niigata, Japan
关键词:
ependymoma;
granular cell;
immunohistochemistry;
karyotype;
ultrastructure;
EOSINOPHILIC HYALINE DROPLETS;
CYTOPLASMIC INCLUSIONS;
TUMORS;
GLIOBLASTOMA;
NERVE;
ASTROCYTOMAS;
NEOPLASM;
PROTEIN;
D O I:
10.1111/j.1440-1789.2012.01298.x
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
We report two cases of ependymoma which showed prominent granular cell changes of the cytoplasm. The patients were a 7-year-old boy with a tumor in the cerebellum (case 1) and a 70-year-old man with a tumor in the frontal lobe (case 2). The tumor of case 1 showed a histopathological appearance of ependymoma containing many focal aggregates of large polygonal cells in which the cytoplasm was stuffed with numerous eosinophilic granules. The tumor of case 2 predominantly showed the features of papillary ependymoma, and some tumor cells were swollen and contained similar eosinophilic granules. Intracytoplasmic granules in both tumors were immunoreactive for GFAP and ubiquitin, but not for epithelial membrane antigen, CD68 or mitochondria. Ultrastructurally, they were found as aggregates of membrane-bound, electron-dense, globular structures. Karyotypic analysis of the tumor in case 1 demonstrated 2, 11 and 12 trisomies. Intracytoplasmic eosinophilic granules occasionally occur in astrocytic and oligodendroglial neoplasms, but an appearance of similar granules is very rare in ependymoma. The two cases presented here may represent a new histopathological variant of ependymoma, and the term granular cell ependymoma is appropriate for them.
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页码:654 / 661
页数:8
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