Zobrazeno 1 - 10
of 134
pro vyhledávání: '"PROBABLE WOLFFIAN ORIGIN"'
Akademický článek
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Autor:
Gibbard, Evan a, b, Cochrane, Dawn R. b, Pors, Jennifer c, Negri, Gian Luca c, d, Colborne, Shane d, Cheng, Angela S. e, Chow, Christine e, Farnell, David c, Tessier-Cloutier, Basile c, McAlpine, Jessica N. f, Morin, Gregg B. a, d, Schmidt, Dietmar g, Kommoss, Stefan h, Kommoss, Friedrich i, Keul, Jacqueline j, Gilks, Blake c, e, k, Huntsman, David G. a, b, c, e, Hoang, Lynn c, e, k, ∗
Publikováno v:
In Human Pathology February 2021 108:1-11
Autor:
Maria de Pilar Estevez-Diz, Renata Colombo Bonadio, Filomena Marino Carvalho, Jesus Paula Carvalho
Publikováno v:
Gynecologic Oncology Reports, Vol 37, Iss , Pp 100838- (2021)
Female adnexal tumor of probable Wolffian origin (FATWO) are a rare type of cancer that originates from Wolffian duct remnants. Due to its rarity, no standard systemic treatment is established for cases of recurrent or metastatic disease. Previous li
Externí odkaz:
https://doaj.org/article/8d89df450f8d4d688a810dd5966a046d
Publikováno v:
Gynecologic Oncology Reports, Vol 36, Iss , Pp 100726- (2021)
Externí odkaz:
https://doaj.org/article/e12b584ef1ee4afba457d1ee3a06dbad
Publikováno v:
In Human Pathology: Case Reports June 2016 4:46-49
Publikováno v:
Human Pathology: Case Reports, Vol 4, Iss C, Pp 46-49 (2016)
Female Adnexal Tumor of Probable Wolffian Origin (FATWO) is believed to be derived from the mesonephric (Wolffian) remnants commonly located in the broad ligament. Here we report a case of FATWO with unique histologic growth pattern. The tumor has a
Externí odkaz:
https://doaj.org/article/f978fccd8fe7484a912ce34f39e1afed
Autor:
Brooke E. Howitt, Emily E. Meserve, Loes F. S. Kooreman, Britta Weigelt, Sabrina Croce, Sofia Westbom-Fremer, Mona El-Bahrawy, Gian Franco Zannoni, Pankhuri Wanjari, Eduardo Benzi, Thomas Krausz, Jennifer A. Bennett, Arnaud Da Cruz Paula, Esther Oliva, Lauren L. Ritterhouse, Ninad M Patil, Chaojie Zhen, Robert H. Young, J. Kenneth Schoolmeester, W. Glenn McCluggage
Publikováno v:
Am J Surg Pathol
American Journal of Surgical Pathology, 45(8), 1061-1074. LIPPINCOTT WILLIAMS & WILKINS
American Journal of Surgical Pathology, 45(8), 1061-1074. LIPPINCOTT WILLIAMS & WILKINS
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 (median 39) years and the tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c77ddd19c279757e2ecb9b580442ac08
https://doi.org/10.1097/pas.0000000000001677
https://doi.org/10.1097/pas.0000000000001677
Akademický článek
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Autor:
Kaori Kuriyama, Yuichiro Kanie, Kozue Morioka, Hisataka Ito, Akihito Mitsumori, Takashi Koyama, Masashi Kusakabe, Sakiko Kageyama, Moto Nakaya
Publikováno v:
Japanese Journal of Radiology
Abstarct Purpose The purpose of this study is to describe the characteristic MRI, CT, and 18F-fluorodeoxyglucose-positron emission tomography/computed tomography (FDG-PET/CT) findings of Wolffian tumor. Methods We reviewed preoperative images in four
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::166bdab36ad85f76141caae6d405cce0
http://europepmc.org/articles/PMC8490215
http://europepmc.org/articles/PMC8490215
Autor:
Michal, Michal a, ⁎, Kazakov, Dmitry V. a, Kacerovska, Denisa a, Kuroda, Naoto b, Lovric, Eva c, Wachter, David L. d, Agaimy, Abbas d, Hes, Ondrej a
Publikováno v:
In Annals of Diagnostic Pathology April 2013 17(2):151-158