Results 61 to 70 of about 6,280 (170)

Surgical conservation of both ovaries in an adolescent with uterine mullerian adenosarcoma: A case report

, 2007
Fertility-sparing and minimally invasive surgeries are advancing everyday in gynecologic oncology. However, data on conservation of ovaries in uterine mullerian adenosarcoma are limited due to its very rare incidence in reproductive-aged females ...
Ozmen, Batuhan, Uzum, Nuket, Ortac, Firat, Unlu, Cihat, Ataoglu, Omur   +4 more
core   +1 more source

Comprehensive management of vulvovaginal cancers

CA: A Cancer Journal for Clinicians, Volume 75, Issue 5, Page 410-435, September/October 2025.
Abstract Vulvar and vaginal cancers represent rare malignancies, with an incidence of 2.7 per 100,000 women for vulvar cancer, predominantly affecting women older than 60 years, although rising rates are observed in younger demographics. Approximately 90% of vulvar cancers are squamous cell carcinoma and frequently are associated with human ...
Angélica Nogueira‐Rodrigues, Maaike H. M. Oonk, Domenica Lorusso, Brian Slomovitz, Mario M. Leitão Jr, Glauco Baiocchi   +5 more
wiley   +1 more source

Clinical Features, Treatment, and Surveillance of Hyperparathyroidism‐Jaw Tumor Syndrome: An Up‐to‐Date and Review of the Literature

International Journal of Endocrinology, Volume 2019, Issue 1, 2019., 2019
Hyperparathyroidism‐jaw tumor (HPT‐JT) syndrome is an autosomal dominant disorder characterized by parathyroid tumors in association with fibro‐osseous jaw tumors and uterine and renal lesions. HPT‐JT syndrome is caused by germline mutations of the cell division cycle 73 (CDC73) gene that encodes the parafibromin, a 531‐amino acid protein with ...
Francesca Torresan, Maurizio Iacobone, Vito Guarnieri   +2 more
wiley   +1 more source

Diagnostic challenges: low-grade adenosarcoma on deep endometriosis

BMC Women's Health, 2019
Background Müllerian adenosarcoma is a rare malignancy. These tumors occur mainly in the uterus, but also in extrauterine locations, usually related to endometriosis. Because of their rarity, there is limited data on optimal management strategies.
Jose Carlos Vilches Jimenez, Emilia Villegas Muñoz, Iván González Poveda, David Santos Lorente, Belinda Sanchez Pérez, Jesús S. Jimenez Lopez   +5 more
doaj   +1 more source

High grade uterine adenosarcoma with sarcomatous overgrowth in a young woman amenable to primary surgical reduction: A case study and literature review

Gynecologic Oncology Reports, 2022
Mullerian adenosarcomas are rare and often low-grade mixed tumors that typically respond well to optimal surgical resection. However, adenosarcoma with sarcomatous overgrowth (ASSO) is a high-grade mixed tumor commonly associated with invasion ...
D.D. Dowding, L.M. Wayne, A.S. Guirguis
doaj   +1 more source

Polypoid endometriosis—An exceptional subtype of endometriosis mimicking an aggressive pelvic cancer

Clinical Case Reports, Volume 12, Issue 9, September 2024.
Key Clinical Message Polypoid endometriosis is a rare manifestation of endometriosis, which may mimic pelvic cancer. This subtype commonly encountered in post‐menopausal women may be wrongly mistaken for a neoplasm on clinical, radiological, perioperative or pathologic assessments leading to inadequate treatment.
Katia Mahiou, Fara Tanjona Harizay, Morgane Lanouziere, Olivia Martz, Laurence Filipuzzi, Jean‐Marc Rousselet, Laurent Martin, Laurent Arnould, Mathilde Funes De La Vega, Anthony Bergeron   +9 more
wiley   +1 more source

Endometrioma of the Liver: A Case Report and Review of the Literature

Case Reports in Hepatology, Volume 2019, Issue 1, 2019., 2019
Hepatic endometriosis is a rare form of endometriosis first described by Finkel in 1986. A thorough review of the literature revealed 28 cases of hepatic endometriosis. This unusual condition offers several diagnostic challenges due to its variable appearance on imaging and need for histologic analysis to establish a definitive diagnosis.
Prachi Rana, Shida Haghighat, Hyosun Han, Melanie Deutsch   +3 more
wiley   +1 more source

Müllerian‐type carcinosarcoma arising in gastric endometriosis: Case report and review of the literature

Clinical Case Reports, Volume 12, Issue 3, March 2024.
Imaging findings, including (A) CT demonstrating cystic lesion emanating from the lesser curvature in the proximal stomach and (B) EUS with submucosal cystic mass measuring 10.3 cm, located 3 cm distal to gastroesophageal junction, with internal solid component; and final pathology, including (C) opened 11.0 × 7.6 × 3.8 cm cystic lesion with nodular ...
Rayne Peerenboom, Sabrina Wang, Ryan Morgan, Seth Sankary, Lindsay Yassan, Katherine Kurnit, Mitchell C. Posner   +6 more
wiley   +1 more source

Cervical Adenosarcoma with Sarcomatous Overgrowth Presenting as a Gangrenous Polyp: A Rare Case Report [PDF]

Journal of Clinical and Diagnostic Research
Cervical Müllerian adenosarcoma is a rare biphasic neoplasm, representing 2-10% of all Müllerian adenosarcomas and only 0.16% of cervical malignancies.
Reshmi Arumugam, Manjiri Dhilip Phansalkar , Sampath Karl, Moses Ambroise   +3 more
doaj   +1 more source

Management of a pure uterine corpus rhabdomyosarcoma in a postmenopausal patient: A rare case report and review of the literature

Clinical Case Reports, Volume 12, Issue 3, March 2024.
Key Clinical Message Rhabdomyosarcoma of the female genital tract often involves the vagina and cervix. It usually occurs in infants and children. Such tumors are uncommon in the uterus, especially in adults. Treatment options are based on studies of younger individuals.
John Lugata, Caleigh Smith, Onesmo Mrosso, Doris Rwenyagila, Baraka Shao, Alex Mremi   +5 more
wiley   +1 more source