Cryptorchidism or testicular maldescent is a very common anomaly in pediatric boys and is even more common in premature infants. It occurs when the testicle does not reach its normal position in the scrotal sac during pregnancy. It is identified because the scrotal sac on that side is empty. In up to 30% of cases, cryptorchidism can affect both sides.
During the first 6 months of life the testicle can spontaneously descend into the scrotal sac without intervention, unless there is an inguinal hernia associated with cryptorchidism.
If the testicle does not reach its physiological position, it is important that the child be evaluated by a specialist in pediatric surgery, who will explore the inguinal and pelvic region if necessary, to determine the position and characteristics of the testicle and the need or not for surgical treatment. He will also determine the presence or not of associated anomalies, which may require a genetic or endocrine study as a priority.
It is important to emphasize that this consultation should not be delayed, since the testicle needs specific conditions for its normal development that it will not have if it is, for example, in an intra-abdominal location.
Cryptorchid testicles can be divided into palpable and non-palpable, this classification being fundamental to decide the treatment.
Palpable testes include:
The non-palpable testes are:
In the diagnosis of cryptorchidism, the clinical history is very important. It is important to know the maternal history of medication consumption (corticosteroids), possible pregnancy problems, family history of unexplained neonatal deaths, genital anomalies, etc.
An examination by a pediatric surgeon will also be performed to rule out possible associated anomalies and to make sure that the cremasteric reflex, so exacerbated in some children, does not mask the true location of the testicle.
Imaging studies such as ultrasound are not usually necessary, as ultrasound has limited sensitivity in identifying ectopic testes, but may be indicated in some patients to identify associated abnormalities.
Currently, the treatment of cryptorchidism is surgical and is performed from 12-18 months of age so that the testicle can develop normally, since the chances of spontaneous descent after that age are very low.
Depending on the location and whether or not it is a palpable testicle, a laparoscopic approach or an inguinal incision will be chosen .
During this procedure, the surgeon makes four incisions, one to insert the camera, two other working trocars and a scrotal incision to fix the teste in the pouch.
It is possible that the hospital stay may be slightly longer for this type of intervention, but rarely more than a day.