Seminoma in a Male Phenotype 46XX True Hermaphrodite
نویسندگان
چکیده
منابع مشابه
True Hermaphrodite: A Case Report
True hermaphrodite is one of the rarest variety of disorders of sexual differentiation (DSD) and represents only 5% cases of all. A 3-year-old child presented with left sided undescended testis and penoscrotal hypospadias. Chordee correction was performed 18 months back, elsewhere. At laparotomy Mullerian structures were present on left side. On right side testis was normally descended into the...
متن کاملPrimary infertility in a phenotypic male with 46XX chromosomal constitution.
The case of a 32 year old male with normal male adrenarchal hair pattern, bilateral gynaecomastia, a small phallus, hypospadias and bilateral poorly developed testes presenting with primary infertility secondary to azoospermia and a pelvic cyst is described. Repeated chromosomal analysis showed 46XX chromosomal constitution. Laparotomy revealed a simple cyst between the urinary bladder and the ...
متن کاملA Case of True Hermaphrodite Presenting as Cyclical Hematuria
True hermaphrodite (also known as ovotesticular disorder of sexual development or ovotesticular-DSD), is one of the rare varieties of disorder of sexual development. It is characterized by histologically confirmed both ovarian and testicular tissue in one individual. Here we report the case of a16-year-old phenotypic male with 46, XX genotype(true hermaphrodite) presenting with cyclical hematur...
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Caenorhabditis elegans male mating provides an excellent opportunity to determine how sensory perception regulates behavior and motor programs. The male-specific nervous system and muscles are superimposed over the general nervous system and musculature. Genetic screens and genomic approaches have identified male-specific and male-enriched genes as well as non-sex specific molecules specialized...
متن کاملUnilateral true hermaphrodite with 46,XX/46,XY dispermic chimerism.
A 13 year old female presented with ambiguous external genitalia, right inguinal ovotestis, left ovary, apparently normal Mullerian system, and absent Wolffian system. Cultured lymphocytes showed a 46,XX/46,XY karyotype. Histopathology of the gonads confirmed true hermaphroditism. The presence of two genetically different erythrocyte populations was observed. The findings suggested that the pat...
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ژورنال
عنوان ژورنال: Asian Journal of Surgery
سال: 2007
ISSN: 1015-9584
DOI: 10.1016/s1015-9584(09)60136-6