Intranodal "amianthoid" myofibroblastoma. Report of six cases immunohistochemical and electron microscopical study
Jazyk angličtina Země Německo Médium print
Typ dokumentu časopisecké články
PubMed
1594491
DOI
10.1016/s0344-0338(11)81179-9
PII: S0344-0338(11)81179-9
Knihovny.cz E-zdroje
- MeSH
- elektronová mikroskopie MeSH
- imunohistochemie MeSH
- leiomyom chemie patologie ultrastruktura MeSH
- lidé MeSH
- lymfatické uzliny patologie MeSH
- nádory hlavy a krku chemie patologie ultrastruktura MeSH
- nádory ze svalové tkáně chemie patologie ultrastruktura MeSH
- třísla * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Six cases of intranodal amianthoid myofibroblastomas are reported. Immunohistochemically the tumors were actin positive and S-100 protein and desmin negative. Intracytoplasmatic, actin-rich bodies, previously found to be a characteristic feature of this tumor, were identified as cytoplasmatic extensions filled with microfilaments at an ultrastructural level. Abortive vessel formation by the tumor cells and the proliferation of tumor cells centered on veins outside the capsule of the tumor in two of our cases indicated a close relationship between the intranodal palisaded myofibroblastoma and the musculature of vascular origin.
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