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Uterine tumors with neuroectodermal differentiation. A report of 4 cases
P. Dundr, D. Fischerová, C. Povýšil, A. Berková, L. Bauerová, D. Cibula
Jazyk angličtina Země Nizozemsko
Typ dokumentu kazuistiky, časopisecké články, práce podpořená grantem
NLK
ProQuest Central
od 1997-03-01 do 2019-01-31
Nursing & Allied Health Database (ProQuest)
od 1997-03-01 do 2019-01-31
Health & Medicine (ProQuest)
od 1997-03-01 do 2019-01-31
ROAD: Directory of Open Access Scholarly Resources
od 1995
- MeSH
- buněčná diferenciace fyziologie MeSH
- genová přestavba MeSH
- imunohistochemie MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory dělohy genetika patologie MeSH
- neuroektodermové nádory genetika patologie MeSH
- proteiny vázající kalmodulin genetika MeSH
- proteiny vázající RNA genetika MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
We report four cases of uterine tumors with neuroectodermal differentiation. One tumor had neuroectodermal component only; in the three other tumors, the neuroectodermal component was admixed with another component, namely rhabdomyosarcoma (1 case), and endometrioid adenocarcinoma (2 cases). Histologically, the neuroectodermal component consisted of small to medium sized cells arranged in diffuse sheets. The tumor cells had round nuclei with stippled to coarsely granular chromatin, mostly with non-prominent nucleoli, and scant eosinophilic or amphophilic cytoplasm. Immunohistochemically, 4/4 tumors showed expression of vimentin, synaptophysin and CD56; 3/4 tumors were CD99 and NSE positive; 2/4 tumors showed focal expression of S-100 protein; and 1/4 tumors had focal dot-like cytoplasmic positivity for cytokeratin AE1/AE3. FLI-1 was negative in all cases. FISH examination was performed and none of the tumors showed rearrangement of EWSR1 gene. Uterine tumors with neuroectodermal differentiation are rare; to the best of our knowledge only 44 cases have been reported in the literature to date, referred to as Ewing sarcoma, peripheral PNET (pPNET), PNET (not otherwise specified) and uterine tumors with neuroendocrine differentiation.
Citace poskytuje Crossref.org
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- $a Dundr, Pavel $7 xx0080436 $u Department of Pathology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Studničkova 2, Prague 128 00, Czech Republic. pdundr@seznam.cz
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- $a Uterine tumors with neuroectodermal differentiation. A report of 4 cases / $c P. Dundr, D. Fischerová, C. Povýšil, A. Berková, L. Bauerová, D. Cibula
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- $a We report four cases of uterine tumors with neuroectodermal differentiation. One tumor had neuroectodermal component only; in the three other tumors, the neuroectodermal component was admixed with another component, namely rhabdomyosarcoma (1 case), and endometrioid adenocarcinoma (2 cases). Histologically, the neuroectodermal component consisted of small to medium sized cells arranged in diffuse sheets. The tumor cells had round nuclei with stippled to coarsely granular chromatin, mostly with non-prominent nucleoli, and scant eosinophilic or amphophilic cytoplasm. Immunohistochemically, 4/4 tumors showed expression of vimentin, synaptophysin and CD56; 3/4 tumors were CD99 and NSE positive; 2/4 tumors showed focal expression of S-100 protein; and 1/4 tumors had focal dot-like cytoplasmic positivity for cytokeratin AE1/AE3. FLI-1 was negative in all cases. FISH examination was performed and none of the tumors showed rearrangement of EWSR1 gene. Uterine tumors with neuroectodermal differentiation are rare; to the best of our knowledge only 44 cases have been reported in the literature to date, referred to as Ewing sarcoma, peripheral PNET (pPNET), PNET (not otherwise specified) and uterine tumors with neuroendocrine differentiation.
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