| 词条 | Penile agenesis and testicular agenesis |
| 释义 |
}}Penile agenesis is a birth defect in humans, occurring about once in 5–6 million male births, in which a male child is born without a penis.[1] A partner condition is testicular or gonadal agenesis. This is when a male child is born without gonads and consequently develops no testes. Penile agenesis occurs often as a consequence of Testicular agenesis, but the reverse is never the case. Most patients in both cases have no known family history and usually have an otherwise normal male anatomy. PresentationMales with penile agenesis but normal testes are of otherwise normal male appearance. Males with testicular agenesis tend not to produce the reproductive hormone 5aDHT at any stage of their lives. As a result, they tend toward prepubescent appearance, with infantile skin texture, developing little body hair particularly in the crotch area, even vellus hair. Without genitalia of either sex, the perineum is therefore left smooth. Also muscular development is retarded and testicular agenetics are of rather frail build with short limbs and small hands and feet. However certain male features are results of other male gender-marker hormones, androgens, which develop male secondary sex characteristics, among which features are the deepening of the voice and facial hair. CausesIn an embryo, the conversion of the gonads into testicles in males-to-be and into ovaries in females-to-be is the function of Leydig cells. In testicular agenesis, this process fails. Penile agenesis can be caused by testicular agenesis. Testes are the sole producer of 5-alpha dihydrotestosterone (5aDHT) in the male body. Where the gonads fail to metamorphose into testes, there is no 5aDHT. Therefore, the masculising process that builds the genital tubercle, the precursor to the penis, is stillborn. When this happens, the child is born with both penile and testicular agenesis and is known by the slang term "nullo". This combination of both conditions is estimated to occur in between 20-30 million male births. Penile agenesis can exist independently after full testicular development; in this case its cause is unknown. TreatmentA problem for people with penile agenesis is the absence of a urinary outlet. Before genital metamorphosis, the urethra runs down the anal wall, to be pulled away by the genital tubercle during male development. Without male development this does not occur. The urethra can be surgically redirected to the rim of the anus immediately after birth to enable urination and avoid consequent internal irritation from urea concentrate. In such cases, the perineum may be left devoid of any genitalia, male or female. A working penis transplant on to an agenetic patient has never been successful. Only one major penis graft was successfully completed. This occurred in China and the patient shortly rejected it on psychological grounds. However a full female or agenetic to male transplant is not yet facilitated to fulfil full reproductive functions. On March 18, 2013, it was announced that Andrew Wardle, a British man born without a penis, was going to receive a pioneering surgery to create a penis for him. The surgeons hope to "fold a large flap of skin from his arm — complete with its blood vessels and nerves — into a tube to graft onto his pubic area." [2] If the surgery goes well, the odds of starting a family are very good. Raising agenetics as femalesPeople with either penile agenesis or testicular agenesis, but not both, usually continue as males throughout their lives. Historically, people with both penile and testicular agenesis were raised as females and eventually underwent sex reassignment surgery, despite having a normal 46,XY male karyotype and no female sexual characteristics. This practice was controversial, and many individuals decided to live as males again when they reached puberty or their early twenties. The New Zealand sexologist John Money was the principal theorist who argued that boys born without an "adequate" penis, or who lost their penis in an accident, should be raised as sex reassigned girls. The book As Nature Made Him chronicles the disastrous results of the application of Money's theories in the Bruce/Brenda case. The anatomy underlying the failure of these cases is not well understood. In most males, the development of the embryo into a female is prevented by Anti-Müllerian hormones. These hormones are commonly believed to be created in the testes, but they nevertheless still appear to be produced in male embryos lacking testes. See also
References1. ^{{cite journal |last1=Bangroo |first1=A. K. |last2=Khetri |first2=Ramji |last3=Tiwari |first3=Shashi |date=Oct–Dec 2005 |title=Penile agenesis |journal=J. Indian Assoc. Pediatr. Surg. |volume=10 |issue=4 |pages=256–258 |url=http://medind.nic.in/jan/t05/i4/jant05i4p256.pdf |format=PDF}} 2. ^{{cite web|last=Moran|first=Lee|title=Man born with no penis to have miracle sex-life saving surgery from one grown on his arm |url=http://www.nydailynews.com/life-style/health/man-penis-miracle-member-surgery-article-1.1291724|work=NY Daily News|accessdate=2013-03-18}} External links{{Medical resources| DiseasesDB = | ICD10 = | ICD9 = {{ICD9|752.69}} | ICDO = | OMIM = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = }}{{Male congenital malformations of genital organs, indeterminate sex and pseudohermaphroditism}} 4 : Congenital disorders of male genital organs|Rare diseases|Human penis|Penis disorders |
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