Cryptorchidism, Cryptorchism

Cryptorchidism, Cryptorchism: what is it and how is it treated

Cryptorchidism, also known as cryptorchidism or sgurthorchidism, is a developmental disorder of the male reproductive organs in which one or both testicles do not descend into the scrotum but remain in the abdomen or inguinal canal.

This condition can occur in newborn boys, but in most cases the testicles will descend into the scrotum by the time of the year, although in rare cases this may take longer or not occur at all. If the testicles do not descend into the scrotum before puberty, this can lead to serious problems in the future.

One of the main negative consequences of cryptorchidism is the risk of infertility. It is believed that higher abdominal temperatures have a negative effect on sperm formation. Additionally, cryptorchidism may increase the risk of developing testicular cancer.

To treat cryptorchidism, orchidopexy surgery may be required, which involves bringing the testicle down into the scrotum. If surgery is performed before puberty, it can help ensure normal testicular development and reduce the risk of future infertility and testicular cancer.

However, like any surgery, orchidopexy may be associated with certain risks and complications, including infection, bleeding, and loss of blood supply to the testicle. Therefore, the decision to undergo surgery should be made by a medical specialist after a thorough examination and assessment of the risks and benefits.

Additionally, in some cases, cryptorchidism can be treated medically with hormone therapy, which can help trigger the descent of the testicle into the scrotum. However, this therapy is not always effective and may be associated with unwanted side effects.

In conclusion, cryptorchidism is a serious disorder that requires careful monitoring and treatment by doctors. If you suspect cryptorchidism, contact your healthcare professional for professional advice and to determine the best treatment plan.

Cryptorchidism

Cryptorchidism is a condition characterized by incomplete descent of one or both testicles from the abdominal cavity into the scrotum.

In cryptorchidism, the testicle remains in the abdomen or inguinal canal instead of descending into the scrotum. This occurs due to disruption of the normal process of testicular descent during fetal development.

Cryptorchidism is a fairly common condition, occurring in approximately 3-5% of full-term boys. The right testicle is most often affected.

If the testicle remains in the abdominal cavity, where the temperature is higher than in the scrotum, this can lead to impaired spermatogenesis and infertility. Therefore, it is important to undergo orchidopexy (surgery to move the testicle into the scrotum) before puberty. This will ensure normal testicular development and preserve fertility.

Untreated cryptorchidism is also associated with an increased risk of developing testicular cancer in the future. Therefore, timely treatment of this condition is extremely important.

Cryptorchiasis is a disorder of the development of the genital organs in the male body. The term itself is translated from Greek as “hidden eggs,” since an undescended testicle is also called “knobby.” If treatment for delayed descent is not carried out, over time it can affect the production of reproductive cells and negatively affect potency.

Genital cryptorchiasis, as this pathology is also called, can be unilateral (when one testicle descends) and bilateral (both testicles remain on the abdominal wall or in the groin area).

The disease is characterized by insufficient or complete absence of scrotal tissue and prolapse of the organ below the abdominal canaliculus. Occurs in every fifth newborn. The increase in the number of pathologies with age is explained by the fact that the period when it is necessary to move the testicles from the abdominal cavity to the scrotum area is reduced. Now 30-35% of newborns have signs of cryptogenic hypogenesis. In boys, the period of testicular displacement lasts until approximately three months of age. With bilateral cryptorasis, the lumen of the tubules becomes overgrown for about a year