Evidence map›Paper›PMID 42152037›Full record

ArticleBMC research notes2026

High concordance of malignant tissue across ultrasound-guided transvaginal tru-cut biopsy cores of ovarian lesions: a prospective feasibility study.

Munachiso Iheme Ndukwe, Tatana Reslova, Jan Laco, Dominik Habes, Hana Vosmikova, Denisa Pohankova, Petra Bretova, Igor Sirak

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Article in BMC research notes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Munachiso Iheme NdukweDepartment of Oncology and Radiotherapy, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Tatana ReslovaDepartment of Obstetrics and Gynecology, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Jan LacoThe Fingerland Department of Pathology, Charles University Faculty of Medicine in Hradec Kralove, Hradec Kralove, Czech Republic.
Dominik HabesDepartment of Obstetrics and Gynecology, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic. dominik.habes2@fnhk.cz.
Hana VosmikovaThe Fingerland Department of Pathology, Charles University Faculty of Medicine in Hradec Kralove, Hradec Kralove, Czech Republic.
Denisa PohankovaDepartment of Oncology and Radiotherapy, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Petra BretovaDepartment of Obstetrics and Gynecology, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Igor SirakDepartment of Oncology and Radiotherapy, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.

Funding

Fakultní nemocnice Hradec Králové MH CZ-DRO (UHHK, 00179906)Univerzita Karlova v Praze Cooperatio programe, area DIAGUniverzita Karlova v Praze Cooperatio programe, area MATCUniverzita Karlova v Praze Cooperatio programe, area ONCOUniverzita Karlova v Praze Cooperatio programe, area ONCO + MATC
6 · The paper itself

Abstract

objectiveUltrasound-guided transvaginal tru-cut biopsy is used for histological confirmation of ovarian malignancy in selected clinical settings. Although multiple cores are routinely obtained to improve diagnostic yield, the distribution of malignant tissue across cores obtained during a single biopsy session has not been systematically evaluated. This question is particularly relevant for translational workflows, such as tissue cryopreservation, where histological verification of each individual core is impractical. We present a prospective feasibility study evaluating intra-procedural concordance of malignant tissue across ultrasound-guided transvaginal tru-cut biopsy cores of ovarian lesions.

resultsTwenty-one patients undergoing ultrasound-guided transvaginal tru-cut biopsy of ovarian lesions were included in the final analysis. Tru-cut biopsy yielded a diagnostic result in 20 of 21 procedures (95.2%; Wilson 95% confidence interval 78.1%-99.4%). In all biopsy procedures in which malignant tissue was identified in at least one core, malignant tissue was consistently present in all other evaluable cores obtained during the same session, with no discordant cases observed. When tissue fragments were present, malignant tissue was also consistently identified in fragments whenever malignant tissue was present in cores. One procedure, involving a mucinous adenocarcinoma arising in the background of a borderline tumor, yielded no malignant in any submitted material. Overall, these findings demonstrate a high degree of intra-procedural concordance of malignant tissue across biopsy cores and support the feasibility of biopsy workflows relying on confirmation of malignant tissue in a single core.

Indexed as

Image-Guided BiopsyOvarian NeoplasmsOvaryAdultAgedFeasibility StudiesFemaleHumansMiddle AgedProspective StudiesVaginaFeasibility studyMalignant tissue concordanceOvarian lesionsTissue cryopreservationTru-cut biopsyUltrasound-guided transvaginal biopsy

Identifiers

PMID42152037
PMCPMC13352936

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.