Leiomyoma with Bizarre Nuclei: a Study of 108 Cases Focusing on Clinicopathological Features, Morphology, and Fumarate Hydratase Alterations

. 2020 Jul ; 26 (3) : 1527-1537. [epub] 20190831

Jazyk angličtina Země Švýcarsko Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid31471882

Grantová podpora
RVO 64165 Ministerstvo Zdravotnictví Ceské Republiky (CZ)
Progres Q28/LF1 Univerzita Karlova v Praze
UNCE 204065 Univerzita Karlova v Praze
SVV 260367 Univerzita Karlova v Praze
EF16_013/0001674 European Regional Development Fund
BBMRI_CZ LM2015089 European Regional Development Fund
CZ.2.16/3.1.00/24509 European Regional Development Fund

Odkazy

PubMed 31471882
DOI 10.1007/s12253-019-00739-5
PII: 10.1007/s12253-019-00739-5
Knihovny.cz E-zdroje

Leiomyoma with bizarre nuclei (LBN) is an uncommon variant of uterine smooth muscle neoplasm. Involvement of fumarate hydratase (FH) has been suggested in the pathogenesis of a subset of LBN. The goal of our study is to assess the clinicopathological, morphological, immunohistochemical and molecular findings focusing on FH in LBNs (n = 108) and compare it with the findings in usual leiomyomas (UL; n = 50) and leiomyosarcomas (LMS; n = 42). Immunohistochemically, loss of FH expression was found in 67/108 of LBN, 1/50 of UL and in no LMS. Class 4/5 FH mutations were detected in 15/53 LBN with sufficient DNA quality for molecular analysis. Pathogenic variants of the FH gene were detected in neither UL nor LMS. Local recurrence after surgery was present in 18/92 of LBN patients, 7 of which were histologically verified and 2 of which were found to be LBN. Our results confirmed that LBN behave in a benign fashion, although they may relapse. FH gene mutations were a common finding only in LBN, but not in UL and LMS. Immunohistochemistry with an antibody against FH seems to have a good sensitivity (87%) and moderate specificity (58%) with regard to predicting FH gene mutations and could be used as a screening method in tumors with features suggestive of FH alterations to identify patients who are at risk for the FH aberrations.

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