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A Distinctive Adnexal (Usually Paratubal) Neoplasm Often Associated with Peutz-Jeghers Syndrome and Characterized by STK11 Alterations (STK11 Adnexal Tumor) : A Report of 22 Cases

Bennett, Jennifer A. (författare)
University of Chicago Medical Center
Young, Robert H. (författare)
Harvard University,Massachusetts General Hospital
Howitt, Brooke E. (författare)
Stanford University
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Croce, Sabrina (författare)
Institut Bergoníe
Wanjari, Pankhuri (författare)
University of Chicago Medical Center
Zhen, Chaojie (författare)
University of Chicago Medical Center
Da Cruz Paula, Arnaud (författare)
Memorial Sloan-Kettering Cancer Center
Meserve, Emily (författare)
Spectrum Healthcare Partners
Schoolmeester, J. Kenneth (författare)
Mayo Clinic Minnesota
Westbom-Fremer, Sofia (författare)
Lund University,Lunds universitet,Bröst- och ovarialcancer,Forskargrupper vid Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Breast and Ovarian Cancer Genomics,Lund University Research Groups,LUCC: Lund University Cancer Centre,Other Strong Research Environments
Benzi, Eduardo (författare)
Baylor College of Medicine
Patil, Ninad M. (författare)
Baylor College of Medicine
Kooreman, Loes (författare)
Maastricht University Medical Centre
El-Bahrawy, Mona (författare)
Imperial College London
Zannoni, Gian Franco (författare)
Catholic University of the Sacred Heart, Rome
Krausz, Thomas (författare)
University of Chicago Medical Center
McCluggage, W. Glenn (författare)
Belfast City Hospital
Weigelt, Britta (författare)
Memorial Sloan-Kettering Cancer Center
Ritterhouse, Lauren L. (författare)
Harvard University,Massachusetts General Hospital
Oliva, Esther (författare)
Harvard University,Massachusetts General Hospital
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 (creator_code:org_t)
2021
2021
Engelska.
Ingår i: American Journal of Surgical Pathology. - 0147-5185. ; 45:8, s. 1061-1074
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We describe 22 examples of a novel, usually paratubal, adnexal tumor associated with Peutz-Jeghers syndrome in nearly 50% of cases that harbored STK11 alterations in all tested (n=21). The patients ranged from 17 to 66 years (median=39 y) and the tumors from 4.5 to 25.5 cm (median=11 cm). Most (n=18) were paratubal, with metastases noted in 11/22 (50%) and recurrences in 12/15 (80%). Morphologically, they were characterized by interanastomosing cords and trabeculae of predominantly epithelioid cells, set in a variably prominent myxoid to focally edematous stroma, that often merged to form tubular, cystic, cribriform, and microacinar formations, reminiscent of salivary gland-type tumors. The tumor cells were uniformly atypical, often with prominent nucleoli and a variable mitotic index (median=9/10 HPFs). The tumors were usually positive to a variable extent for epithelial (CAM5.2, AE1/AE3, cytokeratin 7), sex cord (calretinin, inhibin, WT1), and mesothelial (calretinin, D2-40) markers, as well as hormone receptors. PAX8, SF1, and GATA-3 were rarely positive, while claudin-4, FOXL2, and TTF-1 were consistently negative. All sequenced tumors (n=21) harbored alterations in STK11, often with a loss of heterozygosity event. There were no other recurrently mutated genes. Recurrent copy number alterations included loss of 1p and 11q, and gain of 1q, 15q, and 15p. Despite an extensive morphologic, immunohistochemical, and molecular evaluation, we are unable to determine with certainty the histogenesis of this unique tumor. Wolffian, sex cord stromal, epithelial, and mesothelial origins were considered. We propose the term STK11 adnexal tumor to describe this novel entity and emphasize the importance of genetic counseling in these patients as a significant number of neoplasms occur in association with Peutz-Jeghers syndrome.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

adnexal
paratubal
Peutz-Jeghers syndrome
salivary gland-like
sex cord-like
STK11

Publikations- och innehållstyp

art (ämneskategori)
ref (ämneskategori)

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