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Crush Cytologic Findings of a Cerebral Granular Cell Astrocytoma

Authors
Kang, MyungheeKim, Na RaeChung, Dong HaeYoo, Chan Jong
Issue Date
Sep-2012
Publisher
KARGER
Keywords
Granular cell astrocytoma; Crush cytology; Immunohistochemistry
Citation
ACTA CYTOLOGICA, v.56, no.5, pp.571 - 575
Journal Title
ACTA CYTOLOGICA
Volume
56
Number
5
Start Page
571
End Page
575
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/17580
DOI
10.1159/000338392
ISSN
0001-5547
Abstract
Background: Granular cell astrocytoma (GCA) is a rare variant of astrocytoma, characterized by an aggressive prognosis compared to conventional astrocytomas of the same World Health Organization grade. Intraoperative smears provide useful clues in diagnosing neuropathology, especially in rarely encountered central nervous system tumors. Case: The patient was a 53-year-old man who presented with a huge mass at the left temporal lobe with peritumoral edema on MRI. The crush smears revealed singly-scattered, large eosinophilic cells with eccentrically located nuclei as well as plump, finely-granular cytoplasm with distinct borders. Mild cellular atypia and absence of mitotic activity were noted. These cells were admixed with small mature lymphoid cells. Histology showed scattered large granular cells which were positive for glial fibrillary acidic protein. Conclusion: The most helpful imprint cytologic findings of GCA were as follows: (1) large cells containing eosinophilic granular cytoplasm rather than the foamy or bubbly cytoplasm associated with macrophages or renal cell carcinomas; (2) distinct granular cell borders in contrast to the ruffled membrane of macrophages, and (3) markedly large-sized granular cells, ranging from 60 to 100 mu m in diameter. Copyright (c) 2012 S. Karger AG, Basel
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