Results 51 to 60 of about 647,943 (150)

Persistent Mullerian Duct Syndrome with Seminoma of Cryptorchid Testis: A Rare Case of Testicular Torsion Complication

Medical Journal of Dr. D.Y. Patil Vidyapeeth
Persistent Mullerian duct syndrome (PDMS) is characterized by the presence of Mullerian duct derivatives in a phenotypically and genetically normal individual. This is a case of a male in his 40s who was being evaluated for infertility.
Sikander Purohit, Anuradha C. K. Rao, Mary Mathew, Brij M. K. Singh   +3 more
doaj   +1 more source

Persistent Mϋllerian duct syndrome presenting as bilateral cryptorchidism: a case report

African Journal of Urology, 2022
Background Persistent Mϋllerian duct syndrome is a rare condition marked by the presence of Mϋllerian duct derivatives (uterus and fallopian tubes) in males who are seemingly (phenotypically and karyotypically) normal. Diagnosis can be made with physical
Mahesh Joshi, Ramdayal Sahu, Prama Dubey, Abhishek Barala   +3 more
doaj   +1 more source

Wt1 Is Required for the Regression of Müllerian Ducts in Male Mice by Inducing Wif1 and Osx Expression

Cell Proliferation, EarlyView.
Wt1 expressed in the MD mesenchyme promotes MD regression by inducing Wif1 and Osx transcription. In male mice, mesenchyme‐specific inactivation of Wt1 results in MD retention. ABSTRACT In mammals, Müllerian ducts (MDs) are the precursors of the female reproductive tract which regress in males during embryonic development.
Min Chen, Xin Qi, Shanshan Qin, Jia Kang, Changhuo Cen, Miao Guo, Yang Gao, Mengyue Wang, Jiayi Li, Xiuhong Cui, Yanbo Wang, Lan Zhu, Fei Gao   +12 more
wiley   +1 more source

Paraurethral Endometrioid Carcinoma Arising From Ectopic Endometriosis: A Case Report

IJU Case Reports, Volume 9, Issue 6, November 2026.
ABSTRACT Introduction Malignant transformation of endometriosis is rare and most commonly involves the ovary; transformation from paraurethral endometriosis is exceedingly rare. Case Presentation A 73‐year‐old postmenopausal woman with prior ovarian endometrioma presented with dysuria and voiding difficulty.
Keita Ogasawara, Takashi Tsuyukubo, Mizuki Hisano, Hiromitsu Fujisawa, Shigekatsu Maekawa, Mitsugu Kanehira, Mitsumasa Osakabe, Naoki Yanagawa, Hiroaki Itamochi, Wataru Obara   +9 more
wiley   +1 more source

Diagnostic Discordance in Recurrent Pregnancy Loss: Hysteroscopy Resolves Ultrasound–MRI Disagreement in Septate Uterus, but Concurrent Ovulation Induction Precludes Causal Attribution of the Reproductive Outcome

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Congenital uterine anomalies are an important and potentially treatable contributor to recurrent pregnancy loss (RPL). The septate uterus is the commonest Müllerian anomaly linked to first‐trimester loss, and its differentiation from the benign arcuate uterus is essential for management, yet imaging modalities may disagree.
Iftekhar Ahmed Sakib, Ayesa Perveen, Nishad Tasnim   +2 more
wiley   +1 more source

Advanced Primary Cervical Carcinosarcoma With Ovarian and Peritoneal Metastases in a Premenopausal Woman: A Rare Case Report From Northern Tanzania

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Cervical carcinosarcoma (CCS), also known as malignant mixed Müllerian tumor (MMMT) of the cervix, is an exceptionally rare and aggressive biphasic neoplasm composed of both epithelial and mesenchymal malignant components. Due to its rarity, optimal management strategies are not well established, particularly in low‐resource settings.
John Lugata, Gidion Kategugwa, Kimberly R. Sladek, Abitalis Mayengela, Kenneth Bagandanshwa, Baraka Shao, Edrick Elias, Joseph Mlay, Bariki Mchome, Eusebious Maro, Alex Mremi, Fredrick Mbise   +11 more
wiley   +1 more source

A Case of Persistent Mullerian Duct Syndrome Diagnosed by Laparoscopic Examination for Impalpable Testis [PDF]

, 2012
Persistent mullerian duct syndrome describes a group of patients with a 46 XY karyotype and normal male external genitalia, but internal mullerian structures.
平尾, 佳彦, 後藤, 大輔, 吉田, 克法, 青木, 勝也, 大塚, 憲司, 桑田, 真臣, 藤本, 清秀   +6 more
core  

Laparoscopic removal of a persistent mullerian duct in a male: Case report

, 2000
The authors refer to the use of the laparoscopic approach in Persistent Mullerian Duct Syndrome, starting from a case of 'male vagina' with an anomally inserted left ductus deferens inside the mullerian persistent duct. This patient was operated on using
Tani G., Lima M., Morabito A., Messina P., Bertozzi M., Ng W. T., Libri M., Domini M., Lauro V., Strano C.   +9 more
core   +1 more source

Persistent mullerian duct syndrome - A case report

, 1999
BACKGROUND: Persistent mullerian duct syndrome is a rare form of male pseudohermaphroditism in which well-developed mullerian structures are present in an otherwise normal male with XY chromosomes.
Ozbay, O, Ozeren, S, Erk, A, Elcioglu, N, Vural, B   +4 more
core   +1 more source

Standardized hysteroscopic management of complete septate uterus with duplicated cervices and longitudinal vaginal septum: A single‐center experience

International Journal of Gynecology &Obstetrics, Volume 175, Issue 1, Page 292-299, October 2026.
Abstract Objective To study perioperative and postoperative complications of a standardized ultrasound‐guided hysteroscopic treatment for complete septate uterus with duplicated cervices and non‐obstructive longitudinal vaginal septum, and to evaluate operative time, symptom changes, and reproductive outcomes. Methods Between January 2021 and May 2025,
Ursula Catena, Federica Bernardini, Emma Bonetti Palermo, Federica Pozzati, Eleonora La Fera, Francesca Moro, Antonia Carla Testa   +6 more
wiley   +1 more source