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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2005-7-26
pubmed:abstractText
We report a case of embryonal tumor with novel inclusion bodies occurring in the cerebellum of a 12-year-old girl. The tumor was histopathologically composed of small undifferentiated cells intermingled with a small number of rhabdoid cells, which had an ultrastructural feature of intermediate filament whorls. Immunohistochemically, the neoplasm showed a polyphenotype, including glial fibrillary acidic protein (GFAP), S-100, synaptophysin, chromogranin A, cytokeratin, vimentin, smooth muscle actin, and desmin. However, epithelial membrane antigen (EMA) immunoreactivity was absent. The MIB-1 labeling index was high (25.6%). Ultrastructurally, there was no evidence of neuronal or myogenic differentiation. The small neoplastic cells contained numerous small intracytoplasmic inclusions stained pink by eosin and red by Masson's trichrome stain. The inclusion body was a densely packed, granulovesicular structure at the electron microscopic level, and was immunoreactive for vimentin, GFAP, desmin, and actin. Reverse transcription-PCR and immunohistochemistry showed the expression of INI1 at the RNA and protein levels, respectively. In conclusion, this tumor was differentiated from atypical teratoid/rhabdoid tumor by the absence of EMA and the presence of INI1 mRNA and protein, and diagnosed as an unclassified, embryonal tumor. Eosinophilic, granulovesicular inclusions of the tumor cells are novel cytoplasmic inclusions in the brain tumor.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0001-6322
pubmed:author
pubmed:issnType
Print
pubmed:volume
110
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
69-76
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:15965700-Cerebellar Neoplasms, pubmed-meshheading:15965700-Child, pubmed-meshheading:15965700-Chromosomal Proteins, Non-Histone, pubmed-meshheading:15965700-DNA-Binding Proteins, pubmed-meshheading:15965700-Diagnosis, Differential, pubmed-meshheading:15965700-Female, pubmed-meshheading:15965700-Humans, pubmed-meshheading:15965700-Immunohistochemistry, pubmed-meshheading:15965700-Inclusion Bodies, pubmed-meshheading:15965700-Magnetic Resonance Imaging, pubmed-meshheading:15965700-Microscopy, Electron, Transmission, pubmed-meshheading:15965700-Mucin-1, pubmed-meshheading:15965700-Neoplasm Recurrence, Local, pubmed-meshheading:15965700-Neoplasms, Germ Cell and Embryonal, pubmed-meshheading:15965700-RNA, Messenger, pubmed-meshheading:15965700-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:15965700-Rhabdoid Tumor, pubmed-meshheading:15965700-Teratoma, pubmed-meshheading:15965700-Transcription Factors, pubmed-meshheading:15965700-Tumor Markers, Biological
pubmed:year
2005
pubmed:articleTitle
Pediatric embryonal tumor of the cerebellum with rhabdoid cells and novel intracytoplasmic inclusions: distinction from atypical teratoid/rhabdoid tumor.
pubmed:affiliation
Department of Human Pathology, Gunma University Graduate School of Medicine, Maebashi, Japan. achie@med.gunma-u.ac.jp
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't