Gonadoblastoma: Primary Amenorrhoea with Gonadal Dysgenesis
نویسندگان
چکیده
منابع مشابه
Gonadoblastoma in a patient with 46, XY complete gonadal dysgenesis.
46, XY complete gonadal dysgenesis (Swyer syndrome) is a rare cause of 46, XY sexual development disorder. The patient presented to our clinic with absence of breast development and lack of periods at the age of 17 years. Her history and familial history involved no relevant conditions. She had Tanner stage 1 thelarche, and Tanner stage 2 pubic hair development with no axillary hair development...
متن کاملGonadoblastoma Occurring in a Patient with Familial Gonadal Dysgenesis
Recent morphologic and histogenetic studies provide a basis for the classification of testicular and ovarian tumors of germinal, mesenchymal, and sex cord origin. That gonadal tumors in the male and female are identical and homologous' 44 is attributed to totipotentiality of the cellular components that contribute to the formation of the gonad. Seminoma, embryonal carcinoma, teratoma, and chori...
متن کاملGonadoblastoma and dysgerminoma associated with 46,XY pure gonadal dysgenesis--a case report.
Gonadoblastoma and dysgerminoma developed in a 24-year-old phenotypic female patient with 46,XY pure gonadal dysgenesis. This patient presented with primary amenorrhea. Clinical characteristics showed a typical stigmata of gonadal dysgenesis: primary amenorrhea, sexual infantilism, a small uterus and bilateral streak gonads. A 46,XY karyotype was made by lymphocyte culture. The patient was coun...
متن کاملGonadal dysgenesis
Disorders of sex development (DSD), previously referred to as intersex disorders, comprise a variety of congenital diseases with anomalies of the sex chromosome, the gonads, the reproductive ducts and the genitalia. DSD is loosely classified into four groups on the basis of histological features of the gonadal tissue: XX-DSD with two ovaries (female pseudohermaphroditism), XY-DSD with two testi...
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Growth and performance Prenatal onset growth deficiency + + Psychomotor retardation + + Decreased visual responsiveness + + Hearing loss + + Craniofacies Microcephaly + + Triangular face + + Micrognathia + + Prominent nasal bridge 0 + Hypoplastic nasal alae + Eyes Ptosis + + Short palpebral fissures 0 + Epicanthal folds + + Upward slanting palpebral fissures + Ears Malformed + + Preauricular pi...
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ژورنال
عنوان ژورنال: Journal of Bangladesh College of Physicians and Surgeons
سال: 1970
ISSN: 1015-0870
DOI: 10.3329/jbcps.v26i2.4188