Results 21 to 30 of about 2,046,767 (198)

Dysgerminoma in three patients with Swyer syndrome

World Journal of Surgical Oncology, 2007
Background Dysgerminoma is the most common malignant germ cell tumor of the ovary. This malignancy can be associated with pure gonadal dysgenesis or Swyer syndrome, mixed gonadal dysgenesis and partial gonadal dysgenesis.
Karimi Zarchi Mojgan, Behtash Nadereh
doaj   +1 more source

Disorders of Sexual Development-Pathological Profile of 45 Cases at a Tertiary Care Centre [PDF]

Journal of Clinical and Diagnostic Research, 2022
Disorders of Sexual Development (DSD) are rare syndromes, which show congenital discordance between chromosomal, gonadal and phenotypic sex. A retrospective analysis was performed to analyse the histopathological profile and spectrum of a large number of
Gwendolyn Fernandes, Pooja Mhashete, Minal Desale   +2 more
doaj   +1 more source

Jacobs Syndrome Presenting With Delayed Puberty and Central Hypogonadism: A Rare Case Report. [PDF]

Clin Case Rep
ABSTRACT In some rare instances, patients with 47,XYY syndrome can be short in height, accompanied by hypogonadism without the characteristic tall stature. In cases where there is delayed puberty and unusual growth pattern, a complete endocrine work‐up, including GnRH and hCG stimulation tests, along with chromosome studies, is vital.
Javaid MH, Ahmad A, Ahmad A, Khamosh MA, Hanzla M.   +4 more
europepmc   +2 more sources

Gonadoblastoma-Associated Mixed Gonadal Germ Cell Tumor with Dysgerminoma and Hepatoid Yolk Sac Tumor Components in 46XY Gonadal Dysgenesis

, 2020
Background: Disorders of sex development are congenital conditions with atypical chromosomal, gonadal, or anatomical sex development. Gonadal dysgenesis in patients containing a Y chromosome have a high risk of developing germ cell tumors with potential ...
Andrade, Liliana A. L. A., Benetti-Pinto, Cristina L., Losada, Daniele M.   +2 more
core   +1 more source

Disorders of sexual differentiation: Report of two rare cases

Indian Journal of Pathology and Microbiology, 2021
Gonadal dysgenesis is a distinct variety of Disorders of Sexual Differentiation (DSD) characterised by incomplete or defective formation of the gonads due to either structural or numerical anomalies of the sex chromosomes or mutations in the genes ...
Mary Anelia Correya, Ramesh Babu, B Archana, Samson Ravirajendiran   +3 more
doaj   +1 more source

A Mixed Gonadal Dysgenesis in an 19 Year Old Girl with Ambigous Genitalia: A Case Report

Acta Medica Indonesiana, 2023
A 19-year-old girl was referred with delayed puberty and ambiguous genitalia. She had short stature with high blood pressure and Turner’s stigmata with external genitalia Prader Score 4. Ultrasound revealed hypoplastic uterus with no gonad.
Amanda Trixie Hardigaloeh, Tri Juli Edi Tarigan, Em Yunir, Kanadi Sumapradja, Feranindhya Agiananda, Yulia Ariani, Nanis S Marzuki, Irfan Wahyudi, Lisnawati Lisnawati   +8 more
doaj   +2 more sources

A case of successful repair of urethrocutaneous fistula post proximal hypospadias repair managed by Johanson’s 2 stage urethroplasty

National Board of Examinations Journal of Medical Sciences, 2023
Urethrocutaneous fistula (UCF) after hypospadias repair remain a frustrating Problem for all the practicing urologists. Furthermore, with the improvement in suture materials and surgical techniques, complications if they may arise also present with ...
Ojas Vijayanand Potdar, Prashant Sarawade, Mohammed Ayub Karamnabi Siddiqui, Kaustubh Vaidya, Vivek Shaw, Jay Bhanushali   +5 more
doaj   +1 more source

Malignant Leydig Cell Tumor in Elderly Complete Androgen Insensitivity Patient: A Case Report

Journal of Nepal Medical Association, 2019
There are various cause of Primary amenorrhea in phenotypically females such as, complete androgen insensitivity syndrome, pure gonadal dysgenesis, 17b-hydroxysteroid dehydrogenase deficiency, or mixed gonadal dysgenesis.
Sundar Shrestha, Niroj Banepali, Rakesh Sthapit, Dipesh Agrawal   +3 more
doaj   +1 more source

Diagnosis and management of 46,XY mixed gonadal dysgenesis and disorder of sexual differentiation [PDF]

, 2009
Objective. We present our experience in diagnosing, gender assignment, and surgical management of sexual ambiguity in 46,XY mixed gonadal dysgenesis. Material and methods.
Diana Mačianskytė, Rasa Verkauskienė, Francis Jaubert, Gilvydas Verkauskas, Dainius Jančiauskas, Romualdas Preikša   +5 more
core   +2 more sources

Distinctively Different Phenotypes of Two Cases with a Rare Karyotype of 45,X/47,XYY Mosaicism: Case Report and Literature Review

Journal of Pediatric Research, 2022
The 45,X/47,XYY mosaicism is an extremely rare genetic disorder with highly phenotypic manifestations such as ovotesticular disorders of sexual development, mixed gonadal dysgenesis and Turner syndrome.
Özge Köprülü, Sezer Acar, Kadri Murat Erdoğan, Özlem Nalbantoğlu, Tarık Kırkgöz, Gülçin Arslan, Beyhan Özkaya, Yaşar Bekir Kutbay, Behzat Özkan   +8 more
doaj   +1 more source