Results 81 to 90 of about 1,949 (196)

A clinical and molecular project on gonadoblastoma needs international collaboration

Rare Tumors, 2009
No abstract available.
Nicolas Kalfa, Olivier Maillet, Charles Sultan   +2 more
doaj   +1 more source

An uncommon case of gonadoblastoma.

European journal of gynaecological oncology, 1983
Gonadoblastoma occurs almost entirely in patients with pure mixed gonadal dysgenesis or in male pseudohermaphrodites. A report of a patient with monolateral gonadoblastoma who sought consultation for primary amenorrhea is presented. Telarche and adrenarche occurred spontaneously at age 12. No signs of clitoromegaly or hirsutism were present. Endoscopic
NAPPI, CARMINE, Mastrantonio P, Mercorio F, Trezza G, Donofrio V.   +4 more
openaire   +2 more sources

Gonadoblastoma bilateral en una niña con síndrome de Turner: reporte de un caso

, 2007
A case of bilateral gonadoblastoma in a yearold girl with Tumer's syndrome and positive SRY antigen is presented. As the kariotype showed 45 X / 46 XY mosaicism, bilateral gonadal biopsy by laparoscopy was done.
Corimanya, José A., Pereyra, S., Urbina, Claudia   +2 more
core  

Current controversies in turner syndrome: Genetic testing, assisted reproduction, and cardiovascular risks

Journal of Clinical & Translational Endocrinology, 2014
Patients with Turner syndrome (TS) require close medical follow-up and management for cardiac abnormalities, growth and reproductive issues. This review summarizes current controversies in this condition, including: 1) the optimal genetic testing for ...
Amanda Ackermann, Vaneeta Bamba
doaj   +1 more source

Gonadoblastoma [PDF]

, 2020
openaire   +3 more sources

Breast cancer, ovarian gonadoblastoma and cervical cancer in a patient with Peutz-Jeghers Syndrome

, 2008
Background Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant disorder characterized by gastrointestinal hamartomatous polyps and mucocutaneous pigmentation.
Yuce, M. Ali, Kilic-Okman, Tulay, Yardim, Turgut, Altaner, Semsi, Gucer, Fatih, Tulay Kilic-Okman, Şemsi Altaner, Turgut Yardım, M. Ali Yüce, Fatih Güçer   +9 more
core   +1 more source

Immunohistochemical expression of testosterone, Mullerian-inhibiting substance, p53, Inhibin, and WT1 in the cells of gonadoblastoma, dysgerminoma and, seminoma

, 2002
O Gonadoblastoma (Gb), um tumor misto de celulas germinativas e de celulas tipo cordoessexuais do estroma, e uma forma comum de tumor em pacientes com disgenesia gonadal e influencia de material do cromossomo Y (Ychm).
Costa, Judite Rodrigues Tavares Mendes [UNIFESP]
core  

Virilization and feminization in an adolescent boy with 45X/46XY DSD due to bilateral gonadoblastomas: A case report

Journal of Pediatric Surgery Case Reports
Introduction: Children with 45X/46XY difference/disorder of sex development (DSD) have varying internal/external genitalia/gonads, Turner-like features, and increased risk of gonadal malignancy.
Thabitha J. Hoole, Shamaali Gunawardana, Sureshi Nandani Tennekoon, Malik Samarasinghe, Sumudu Nimali Seneviratne   +4 more
doaj   +1 more source

Early development of a gonadal tumor in a patient with mixed gonadal dysgenesis

Archives of Endocrinology and Metabolism
SUMMARY A gonadal tumor was diagnosed in the first months of life in a patient with genital ambiguity, a 45,X/46,XY karyotype, and mixed gonadal dysgenesis.
Sarah Crestian Cunha, Juliana Gabriel Ribeiro de Andrade, Camila Matsunaga de Angelis, Athanase Billis, Joaquim Murray Bustorff-Silva, Andréa Trevas Maciel-Guerra, Márcio Lopes Miranda, Gil Guerra-Júnior   +7 more
doaj   +1 more source

Dysgerminoma and gonadoblastoma in a girl with a 46 XY chromosome pattern [Dişi fenotipinde XY kromozomuna sahip bir çocukta gonadoblastoma ve disgerminoma]

, 2003
Twelve-year-old girl presented with severe abdominal pains for 3 months and was operated for acute appendixitis. Unfortunately during the operation, the appendix was found to be normal and and an enlarged left ovary was detected.
Zorludemir S., Tanyeli A., Tuncer R., Süleymanova S., Bayram I., Canan O., Karaoglan A.   +6 more
core   +1 more source