Karcinoidy gastrointestinálního traktu: význam hodnocení diferenciacních a proliferacních markerů
[Carcinoids of the gastrointestinal tract: importance of determining differentiation and proliferation markers]
Jazyk čeština Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
12874899
- MeSH
- antigen Ki-67 analýza MeSH
- antigeny CD57 analýza MeSH
- chromogranin A MeSH
- chromograniny analýza MeSH
- dospělí MeSH
- fosfopyruváthydratasa analýza MeSH
- gastrointestinální nádory chemie diagnóza MeSH
- imunohistochemie MeSH
- karcinoid chemie diagnóza MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- nádorové biomarkery analýza MeSH
- proliferační antigen buněčného jádra analýza MeSH
- senioři MeSH
- synaptofysin analýza MeSH
- tubulin analýza MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigen Ki-67 MeSH
- antigeny CD57 MeSH
- chromogranin A MeSH
- chromograniny MeSH
- fosfopyruváthydratasa MeSH
- nádorové biomarkery MeSH
- proliferační antigen buněčného jádra MeSH
- synaptofysin MeSH
- tubulin MeSH
The group of 35 carcinoid tumours obtained from 34 patients was reviewed according to recent histopathological criteria. Consequently, evaluation of the Grimelius staining and immunohistochemical detection of chromogranin A (CgA), Leu-7 (CD-57), synaptophysin, neuron-specific enolase (NSE), (beta-III tubulin, Ki-67 and proliferating cell nuclear antigen (PCNA) was performed. The majority of tumours (29, i.e. 83%) were classified as typical carcinoids composed predominantly of mixed solid and trabecular or solid and tubular growth patterns. Six tumours (17%) revealed more prominent cytological abnormalities corresponding with the diagnosis of atypical carcinoid. The majority of tumours (31, i.e. 93.9%) showed granular cytoplasmic positivity in Grimelius staining and diffuse cytoplasmic positivity of NSE (34, i.e. 97.1%). All of the 32 stained tumour samples showed positive immunoreactivity for synaptophysin. A high percentage of tumours (32, i.e. 91.4%) revealed also a positive reaction with antibody TU-20 detecting (beta-III tubulin, a marker of an early stage of neuronal differentiation. Thirty-four tumours (97.1%) showed granular cytoplasmic positivity for both markers of neuroendocrine granules (CgA and Leu-7). One tumour (2.9%) was positive only for Leu-7. Tumour cells revealed predominantly low proliferative activity evaluated by PCNA and Ki-67 immunodetection. Higher degree of proliferation was observed especially in atypical carcinoids.