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Reflections on Historical and Other Aspects of a Remarkable Gonadal Abnormality on the 70th Anniversary of its Description by Dr Robert E. Scully.
Ulbright, Thomas M. M.D.; Young, Robert H. M.D.
doi : 10.1097/PGP.0000000000000929
Volume 42(3) pgs. 221-326 May 2023
Two Cases of Biphasic Synovial Sarcoma With Expression of PAX8 and ER: A Diagnostic Pitfall.
Zheng, Lan M.D., Ph.D.; Wang, Xiaohong I. M.D., Ph.D.; Chen, Shaoxiong M.D., Ph.D.; Moosvi, Ali Mehdi M.D.; Wan, David Q. M.D., Ph.D.; Zhang, Songlin M.D., Ph.D.
doi : 10.1097/PGP.0000000000000892
AB Synovial sarcoma (SS) is a high-grade malignant neoplasm frequently arising in the deep soft tissue of the lower and upper extremities of young adults.
Borderline With Bad Behavior: An Unusual Low-grade Serous Carcinoma With Dedifferentiation From a Serous Borderline Tumor.
Strickland, Amanda L. M.D.; Maniar, Kruti P. M.D.; Tanner, Edward M.D.; Shanes, Elisheva M.D.; Jennings, Lawrence M.D., Ph.D.; Wei, Jian-Jun M.D.
doi : 10.1097/PGP.0000000000000885
AB The pathogenesis of serous ovarian tumors has been extensively investigated, with a dualistic model dividing these cancers into 2 groups. Type I tumors, including low-grade serous carcinoma, is characteristic for concurrent presence of borderline tumors, less atypical cytology, relatively indolent biologic behavior, and molecular aberrations related to the MAPK pathway with chromosomal stability.
Endometrial, Ovarian, and Peritoneal Involvement by Endometrioid Carcinoma, Yolk Sac Tumor, and Endometriosis: Molecular Evidence for a Shared Precursor.
Halling, Geoffrey C. M.D.; Udager, Aaron M. M.D., Ph.D.; Skala, Stephanie L. M.D.
doi : 10.1097/PGP.0000000000000889
AB Recent studies have provided molecular confirmation that a subset of yolk sac tumors is somatically derived. Somatically derived yolk sac tumors are typically diagnosed in older women and are often seen adjacent to epithelial proliferations (such as endometriosis or endometrioid carcinoma) with which they share mutations.
Collision Tumor of the Ovary Involving Sertoli-Leydig Cell Tumor and High-Grade Serous Carcinoma-Report of the First Case.
Omo-Ogboi, Allen C. M.D.; Deavers, Michael T. M.D.; Schmeler, Kathleen M. M.D.; Tandon, Nidhi M.D., F.R.C.Path.
doi : 10.1097/PGP.0000000000000896
AB We report a collision tumor in the ovary of a 60-yr-old woman composed of high-grade serous carcinoma and Sertoli-Leydig cell tumor. Collision tumors in the ovary are rare and to the best of our knowledge, combination of ovarian high-grade serous carcinoma and Sertoli-Leydig cell tumor has not been described before. (C)2023International Society of Gynecological Pathologists
Cervical Adenosquamous Carcinoma: Detailed Analysis of Morphology, Immunohistochemical Profile, and Outcome in 59 Cases.
Stolnicu, Simona M.D.; Hoang, Lynn M.D.; Zhou, Qin M.A.; Iasonos, Alexia Ph.D.; Terinte, Cristina M.D.; Pesci, Anna M.D.; Aviel-Ronen, Sarit M.D.; Kiyokawa, Takako M.D.; Alvarado-Cabrero, Isabel M.D.; Oliva, Esther M.D.; Park, Kay J. M.D.; Soslow, Robert A. M.D.
doi : 10.1097/PGP.0000000000000921
AB Although both the 2014 and 2020 World Health Organization (WHO) criteria require unequivocal glandular and squamous differentiation for a diagnosis of cervical adenosquamous carcinoma (ASC), in practice, ASC diagnoses are often made in tumors that lack unequivocal squamous and/or glandular differentiation. Considering the ambiguous etiologic, morphologic, and clinical features and outcomes associated with ASCs, we sought to redefine these tumors.
Villoglandular Pattern in HPV-associated Endocervical Adenocarcinoma is Associated With Excellent Prognosis: A Reappraisal of 31 Cases Using IECC and Silva Pattern Classification.
Stolnicu, Simona M.D., Ph.D.; Brito, Maria J. M.D.; Karpathiou, Georgia M.D.; Hoang, Lynn M.D.; Felix, Ana M.D.; Mateoiu, Claudia M.D.; Fanni, Daniela M.D.; Reques, Armando M.D.; Garcia, Angel M.D.; Hardisson, David M.D.; Talu, Canan K. MD; Furtado, Antonia M.D.; Abu-Rustum, Nadeem M.D.; Soslow, Robert A. M.D.; Park, Kay J. M.D.
doi : 10.1097/PGP.0000000000000916
AB Villoglandular adenocarcinoma of the cervix is a rare histologic entity that typically develops in young women, characterized by an association with oral contraceptives and excellent prognosis, though this point is controversial.
Primary Cutaneous Neuroendocrine Tumor of the Vulva: A Case Report.
Al-Janabi, Shaimaa M.D., Ph.D.; Kasius, Jenneke C. M.D., Ph.D.; Jaspars, Elisabeth H. M.D., Ph.D.; Snijders, Malou L.H. M.D., Ph.D.
doi : 10.1097/PGP.0000000000000919
AB Primary cutaneous neuroendocrine tumors (CNET) are extremely rare. Only a few cases have been reported so far. CNET have an indolent clinical course and usually present as a single flesh-colored nodule with a predilection for the scalp and trunk in elderly patients.
PIM1 is a Poor Prognostic Factor for and Potential Therapeutic Target in Serous Carcinoma of the Endometrium.
Takeuchi, Hodaka M.D.; Miyamoto, Tsutomu M.D., Ph.D.; Fuseya, Chiho M.D., Ph.D.; Asaka, Ryoichi M.D., Ph.D.; Ida, Koichi M.D., Ph.D.; Ono, Motoki M.D.; Tanaka, Yasuhiro M.D.; Shinagawa, Manaka M.D.; Ando, Hirofumi M.D., Ph.D.; Asaka, Shiho M.D., Ph.D.; Shiozawa, Tanri M.D., Ph.D.
doi : 10.1097/PGP.0000000000000882
AB Serous carcinoma (SC) is an aggressive histologic type of endometrial carcinoma (EMC) with a poor prognosis. The development of novel therapeutics for SC is an important issue.
Placental T-Cadherin Correlates With Trophoblastic Invasion Anomalies: Placenta Percreta and Fetal Growth Restriction.
Biyik, Ismail M.D.; Metineren, Huseyin M.D.; Ozturk, Engin M.D.; Simsek, Sercan M.D.; Oztas, Efser M.D.; Guldur, Muhammed E. M.D.; Ince, Onur M.D.
doi : 10.1097/PGP.0000000000000884
AB In this study, we compared the placental T-cadherin staining intensity of pregnant women with placenta percreta (PP) and asymmetrical fetal growth restriction (FGR) compared with healthy control pregnancies.
The Presence of the Autophagic Markers LC3B and Sequestosome 1/p62 in the Hydatidiform Mole.
Karpathiou, Georgia M.D., B.Sc., Ph.D.; Dridi, Maroa M.D.; Papoudou-Bai, Alexandra M.D., Ph.D.; Perard, Marine M.D.; Clemenson, Alix M.D.; Chauleur, Celine M.D., Ph.D.; Peoc'h, Michel M.D., Ph.D.
doi : 10.1097/PGP.0000000000000886
AB Autophagy is implicated in normal pregnancy and various pathologic pregnancy conditions. Its presence in hydatidiform moles (HM) is unknown. We immunohistochemically studied 36 HM for LC3B and p62 to precisely determine their expression in the decidua, endometrium, and villi.
Endometrioid Endometrial Carcinoma With NKX3.1 Expression in a Transgender Man: A Case Report.
Yoshida, Hiroshi M.D., Ph.D.; Uno, Masaya M.D., Ph.D.; Ogimoto, Keisuke M.D.; Kobayashi-Kato, Mayumi M.D., Ph.D.; Tanase, Yasuhito M.D., Ph.D.; Ishikawa, Mitsuya M.D., Ph.D.; Kato, Tomoyasu M.D., Ph.D.
doi : 10.1097/PGP.0000000000000869
AB Endometrial cancer in transgender men is rare, and its histopathologic features remain unknown. A 30-yr-old transgender man with an intrauterine tumor, an ovarian mass, and a 2-yr history of testosterone use was referred to us for treatment.
Inflammatory Myofibroblastic Tumor of the Placenta With Subsequent Successful Pregnancy and Benign Hysterectomy: A Case Report With 59-Month Follow-up.
Schwartz, Cooper B.A.; Gundogan, Fusun M.D.; Singh, Kamaljeet M.D.; Schoolmeester, J. Kenneth M.D.; Banet, Natalie M.D.
doi : 10.1097/PGP.0000000000000893
AB Inflammatory myofibroblastic tumors (IMT) are rare neoplasms of intermediate malignant potential which have been described in the gynecologic tract, predominantly in the myometrial wall, but also in association with the placenta.
An Unusual Benign Uterine Stromal Spindle Cell Tumor Harboring JAZF1: BCORL1 .
Rodriguez Pena, Maria D.C. M.D.; Mubeen, Aysha M.D.; Harada, Shuko M.D.; Prieto Granada, Carlos N. M.D.
doi : 10.1097/PGP.0000000000000894
AB Uterine mesenchymal lesions demonstrate various underlying genomic alterations involving MED12, JAZF1, YWHAE, BCOR, and ALK genes, among others.
CTNNB1-mutated High-grade Endometrioid Carcinoma With Extensive Squamous and Shadow Cell Differentiation Can Mimic Pilomatrix Carcinoma.
Mendoza, Rachelle M.D.; Kertowidjojo, Elizabeth M.D., Ph.D.
