Congenital anorchia: Difference between revisions
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===Ultrasound=== | ===Ultrasound=== | ||
* Imaging showing absent gonadal tissue | * Imaging showing absent gonadal tissue | ||
===Other Imaging Findings=== | |||
* Low [[bone density]] | |||
==Other Diagnostic Studies== | ==Other Diagnostic Studies== |
Revision as of 15:48, 20 September 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: TRS; vanishing testes syndrome; vanishing testes; empty scrotum; testicular regression syndrome
Overview
Anorchia, is a medical condition where both testes are absent at birth. Individuals with this condition have a 46,XY chromosome constellation.
Natural History, Complications, and Prognosis
Natural History
Within a few weeks of fertilization, the embryo develops rudimentary sex organs, which are crucial to the development of the reproductive system. In the human male, if these fail to develop within eight weeks, the baby will have female genitalia (see Swyer syndrome). If the testes are lost between eight and 10 weeks, the baby will have ambiguous genitalia when it's born. However, if the testes are lost after 14 weeks, the baby will have a normal male reproductive system, other than the absence of testes.
Physical Examination
Appearance of the Patient
- Lack of secondary sex characteristics
Genitals
- Empty scrotum
Laboratory Findings
Electrolyte and Biomarker Studies
Tests and findings include:
- Low testosterone levels
- Elevated follicle stimulating hormone and luteinizing hormone levels
- X,Y karyotype
- Low anti-Mullerian hormone levels
MRI
- Imaging showing absent gonadal tissue
Ultrasound
- Imaging showing absent gonadal tissue
Other Imaging Findings
- Low bone density
Other Diagnostic Studies
- Low bone density
- Surgical exploration for evidence of male gonadal tissue
Treatment
Treatment includes psychological support.
Pharmacotherapy
Treatment includes androgen (male hormone) supplementation.
Surgery and Deviced Based Therapy
Treatment includes testicular prosthetic implantation.