Cryptorchidism Rapid Fire Session: Update Course 2015
Educational content from recorded physician discussions — not medical advice. Talk to your (or your child's) care team about your situation.
More about cryptorchidism
same diagnosisOnly a few other public items share this diagnosis — nothing to add yet.
Video
Pediatric Surgical Oncology Research Collaborative (PSORC): Studying Rare Pediatric Tumors
56 s · Published May 2026
Video
Update Course Rewind 2025: Hirschsprung + ARM: Rare but Real
1 min · Published May 2026
Video
Update Course Rewind 2025: Hirschsprung + ARM: Rare but Real
1 min · Published May 2026
Video
Pooling Patients to Study Rare Pediatric Tumors: An Introduction to PSORC
56 s · Published May 2026
Video
The fetal frontier: A review of current and emerging fetal therapies for genetic diseases
44 s · Published May 2026
Video
Indocyanine green assists with sentinel lymph node mapping in pediatric and adolescent patients
1 min · Published May 2026
What the experts said
Cryptorchidism is one of the most common pediatric disorders of the male endocrine glands and the most common genital disorder identified at birth.
There are two types of cryptorchidism: congenital (found at birth) and acquired (testicles previously descended but can no longer be brought down without discomfort).
Treatment of cryptorchidism reduces risks including impaired fertility, testicular malignancy, risk of torsion, and treats associated inguinal hernia.
The actual mechanism of action of hormonal therapy agents for cryptorchidism is unknown.
Published studies on hormonal therapy included multiple treatment strategies with different doses and intervals, none showing good response rates or demonstrable long-term benefits.
Hormonal therapy should not be used to induce testicular descent due to low response rates and lack of evidence for long-term efficacy.
70% of undescended testicles are palpable, though they may not be palpable during examination while the child is awake but are usually palpable under anesthesia.
Ultrasound has a sensitivity of only 45% and specificity of only 78% in determining testicle location and size.
Most of the time the testes can be brought down without needing to divide the testicular vessels.
Ultrasound cannot identify intra-abdominal testicles.
For prepubertal patients (e.g., 10 years old), orchiopexy should be attempted; for pubertal patients (e.g., 14 years old), orchiectomy is preferred; 12 years old is a difficult decision point.
The teaching is that if the patient is prepubertal, orchiopexy can be attempted, but if going through puberty, orchiectomy should be performed.
Other imaging modalities are expensive, require anesthesia, or irradiate tissues, and no radiologic test is 100% accurate to determine whether a testicle is absent.
Surgical exploration (diagnostic laparoscopy or open exploration) must be performed on all non-palpable unilateral and many bilateral cryptorchid patients.
There is no apparent advantage of one-stage versus two-stage Fowler-Stevens procedure when testicular vessels cannot be spared.
Orchiectomy may be prudent in the presence of a normal contralateral descended testicle.
Imaging should not be performed for cryptorchidism as it is not helpful and can actually delay treatment.
There is no advantage for laparoscopic versus open exploration for intra-abdominal testicles.
For salvageable intra-abdominal testicles, three surgical options exist: primary orchiopexy, one-stage Fowler-Stevens, or two-stage Fowler-Stevens.
The decision tree for intra-abdominal testicles prioritizes sparing testicular vessels if possible.