Results 71 to 80 of about 7,453 (264)

Laparoscopic approach for gonadectomy in pediatric patients with intersex disorders [PDF]

, 2016
The birth of a child with a disorder of sex development (DSD) prompts a long-term management strategy that involves a myriad of professionals working with the family.
Calvo, Andres, Caprio, Maria Grazia, ESCOLINO, MARIA, ESPOSITO, CIRO, Roberti, Agnese, SETTIMI, ALESSANDRO   +5 more
core   +1 more source

Dual malignancy in adolescence: A rare case report of metachronous papillary carcinoma of thyroid following dysgerminoma of ovary

Journal of Research in Medical Sciences, 2016
Dual malignancy is rare in adolescents. Dual malignancy with the second malignancy of thyroid is rare. No association has been reported between dysgerminoma of ovary and carcinoma thyroid in medical literature. Despite a thorough PubMed search (key words
Suvadip Chakrabarti, Sanjay M Desai, Dharmendra Y Mehta, Shreyas Somanath   +3 more
doaj   +1 more source

Pure ovarian dysgerminoma in a postmenopausal patient: A case report and review of the management

Gynecologic Oncology Reports, 2022
Background: A pure ovarian dysgerminoma in a postmenopausal female is a rare phenomenon. Case: A 65-year-old female presented with a large pelvic mass. Following surgical debulking, the patient was diagnosed with FIGO Stage IIB ovarian dysgerminoma.
Jennifer Vaz, Alexandra Mulliken, Nivin Omar, Jessa Suhner, Bogna Brzezinska, Thomas Cotter, Patel Nikhil, Robert V. Higgins, Bunja Rungruang   +8 more
doaj   +1 more source

Malignant ovarian germ cell tumors in pediatric patients: The AIEOP (Associazione Italiana Ematologia Oncologia Pediatrica) study [PDF]

, 2017
Objective: Malignant ovarian germ cell tumors (MOGCT) carry an excellent prognosis, and the treatment aims to achieve results with the least possible treatment-related morbidity. The aim of this study was to assess the outcomes of pediatric patients with
Amsalem, Baranzelli, Billmire, Billmire, Billmire, Frazier, Gershenson, Gershenson, Gobel, Grimison, Hanna, Kaplan, Kollmansberger, Lhommé, Lo Curto, Lopes, Madenci, Mangili, Mangili, Mangili, Mann, Matei, Meisel, Murray, Olson, Palenzuela, Park, Parkinson, Pashankar, Patterson, Pectasides, Rescorla, Robison, Rogers, Schemper, Schenider, Solheim, Stoneham, Travis, Vicus, Zagamè   +40 more
core   +1 more source

Hypercalcemia associated with dysgerminoma and elevation of calcitriol: A case report and review of the literature

SAGE Open Medical Case Reports, 2022
We report on the case of a patient with dysgerminoma, a rare germ cell tumor, which showed hypercalcemia with an elevation of 1α,25-dihydroxycholecalciferol (calcitriol). A 27-year-old nulliparous woman presented with hypercalcemia during the examination
Natsuko Hara, Hirotsugu Suwanai, Hironori Abe, Fumiyoshi Yakou, Takuya Ishikawa, Munehiro Urayama, Takeshi Nagai, Toshitaka Nagao, Jumpei Shikuma, Takashi Miwa, Ryo Suzuki, Masato Odawara   +11 more
doaj   +1 more source

Çocukluk çağı disgerminom tedavi sonuçları

Genel Tıp Dergisi, 2021
Amaç: Over disgerminomu tanısı ile izlenen hastala­rın demografik ve klinik özellikleri ile tedavi yaklaşımlarını geriye dönük olarak incelemektir. Gereç ve Yöntem: XXXXXX Üniversitesi Tıp Fakültesi Çocuk Onkoloji Bilim Dalı’nda, 2006-2020 yılları ...
Buket Kara, Hilal Akbaş, İlhan Çiftçi, Yavuz Köksal   +3 more
doaj   +1 more source

Bilateral Ovarian Germ Cell Tumor in a 46,XX Female with Nijmegen Breakage Syndrome and Hypergonadotropic Hypogonadism

JCRPE, 2022
Nijmegen breakage syndrome (NBS) is a rare autosomal recessive disease, affecting mainly patients of Slavic origin. It is caused by a defect in the NBN gene, resulting in defective nibrin protein formation.
Malgorzata A. Krawczyk, Malgorzata Styczewska, Dorota Birkholz-Walerzak, Mariola Iliszko, Beata S. Lipska-Zietkiewicz, Wojciech Kosiak, Ninela Irga-Jaworska, Ewa Izycka-Swieszewska, Ewa Bien   +8 more
doaj   +1 more source

Diagnosis and Management of Dysgerminomas with a Brief Summary of Primitive Germ Cell Tumors

Diagnostics, 2022
Dysgerminoma represents a rare malignant tumor composed of germ cells, originally from the embryonic gonads. Regarding its incidence, we do not have precise data due to its rarity. Dysgerminoma occurs at a fertile age.
Melinda-Ildiko Mitranovici, Diana Maria Chiorean, Maria Cezara Mureșan, Corneliu-Florin Buicu, Raluca Moraru, Liviu Moraru, Titiana Cornelia Cotoi, Ovidiu Simion Cotoi, Havva Serap Toru, Adrian Apostol, Sabin Gligore Turdean, Claudiu Mărginean, Ion Petre, Ioan Emilian Oală, Zsuzsanna Simon-Szabo, Viviana Ivan, Lucian Pușcașiu   +16 more
doaj   +1 more source

Pediatric Dysgerminoma: Unveiling a Rare Ovarian Tumor

Archives of Case Reports
Background: Dysgerminomas, account for only 1% - 2% of all malignant ovarian neoplasms. Objective: This case report aims to present a rare occurrence of dysgerminoma in a pediatric patient, highlighting the clinical characteristics, diagnosis, and ...
Limaiem Faten, Saffar Khalil, Halouani Ahmed   +2 more
semanticscholar   +1 more source

Salvage resection of advanced mediastinal tumors [PDF]

, 2019
The surgical treatment of locally advanced mediastinal tumors invading the great vessels and other nearby structures still represent a tricky question, principally due to the technical complexity of the resective phase, the contingent need to carry out
Andreetti, Claudio, Ciccone, Anna Maria, D’Andrilli, Antonio, Ibrahim, Mohsen, Maurizi, Giulio, Menna, Cecilia, Poggi, Camilla, Rendina, Erino Angelo, Vanni, Camilla, Venuta, Federico   +9 more
core   +1 more source