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Treating complications of circumcision. Pediatr Emerg Care 1996; 12: 62-68. Cansever G. Psychological effects of circumcision. Brit J Med Psychol 1965; 38: 321-331. Christensen-Szalamski JJ, Boyce WT, Harrell H, Gardner MM. Circumcision and informed consent. Is more always better? Med Care 1987; 25: 856-867. Goepel M, P Rathert. Leitlinie zur Phimose. Urologe A, 1998; 37: 664-665. Griffiths DM, Atwell JD, Freeman NV. A prospective study of the indications and morbidity of circumcision in children. Eur Urol 1985; 11:184-187. Maxwell LG, Vaster M. Analgesia for neonatal circumcision: no more studies, just do it [editorial comment]. Arch Pediatr Adolesc Med 1999; 153: 444-445. Moses S, Bailey RC, Ronald AR. Male circumcision: assessment of health benefits and risks. Sex Transm Infect 1998; 74: 368-373. Niku SD, Stock JA, Kaplan GW. Neonatal circumcision. Urol Clin North Am 1995; 22: 57-65. Preston EN. Whither the foreskin? JAMA 1970; 213: 1853-1858. Schoen EJ. The status of circumcision of newborns. New Engl J Med 1990; 322: 1308-1312. Schoen EJ. Advantages and disadvantages of neonatal circumcision [letter]. JAMA 1997; 278: 201. Taylor JR, Lockwood AP, Taylor AJ. The prepuce: specialized mucosa of the penis and its loss to circumcision. Br J Urol 1996; 77: 291-295. To T, Agaha M, Dick PT, Feldman W. Cohort study on circumcision of newborn boys and subsequent risk of urinary tract infection. Lancet 1998; 352: 1813-1816. 16. Upadhyay V, Hammodat HM, Pease PH. Van Howe RS. Cost-effective treatment of phimosis. Pediatrics 1998; 102: E43. Wallerstein E. Circumcision. The uniquely American medical enigma. Urol Clin North Am 1985; 12: 123-132. Williams N, Kapila L. Complications of circumcision. Br J Surg 1993; 80: 1231-1236. Wiswell ТЕ, Geschke DW. Risks from circumcision during the first month of life compared with those for uncircumcised boys. Pediatrics 1989; 83: 1011-1015. 21. Wiswell ТЕ, Tencer HL, Welch CA, Chamberlain JL Circumcision in children beyond the neonatal period. Pediatrics 1993; 92: 791-793. CRYPTORCHIDISM BACKGROUND The incidence of maldescensus testis after the first year of life is 1.8-2%. A distinction is made between abdominal, inguinal or prescrotal testis retention and epifascial, femoral or penodorsal testis ectopy. Sliding and pendulous (retractile) testes are particular variations of cryptorchidism. Sliding testis with a too short spermatic cord relocates into its non-physiological position when pulled into the scrotum and then released. Pendulous (retractile) testis with hypertrophic cremaster muscle fibres is associated with an intermittent retraction of the usually orthotopic testis. DIAGNOSIS Maldescensus testis is diagnosed by clinical examination and sonography. Sonography and magnetic resonance imaging (MRI) may help in localizing the impalpable testis; the accuracy of the latter is 90% for intra-abdominal testis. Once abdominal retention is suspected, laparoscopy has been established as a diagnostic and therapeutic procedure. In this procedure, the testis can be localized in its abdominal position and placed scrotally using the technique appropriate to the anatomical conditions. A human chorionic gonadotrophin (HCG) stimulation test, as evidence of testosterone-producing testis tissue, should precede operative exploration for bilaterally impalpable testes. TREATMENT The objective of treatment is to achieve an orthotopic scrotal position of the testis, before the child's second birthday, in order to prevent irreversible damage of spermatogenesis in the affected testis. Hormone therapy (optional) is applied for testis retention only. It is ineffective for ectopy, but can be helpful for preparation of local tissue: HCG as an intramuscular injection (9000-30,000 III in different protocols) or luteinizing hormone releasing hormone (LHRH) as a nasal spray (400 ug, three times daily). Both methods are effective in about 20-30% of cases. Follow-up is important because the benefits may fail after a period of time. Surgical orchidofuniculolysis and orchidopexy are first-line treatment options. Pendulous (retractile) testes are not indicated for surgical repair. Absolute indications for a primary surgical approach are testis retention after failed hormone therapy or after previous inguinal surgery, testis ectopy and all maldescended testes with associated pathology (hernia and/or open processus vaginalis). Inguinal access of the spermatic cord is gained after opening the inguinal canal. Associated pathological conditions (open processus vaginalis, inguinal hernia) are dealt with in the same session. After the spermatic chord and testis have been freed of connective tissue and cremaster fibres have been resected, the testis is relocated tension free by pexis in the scrotum. If no testis or spermatic funicle tissue can be found during exploration of the inguinal canal, opening of the peritoneum and intraperitoneal orchidofuniculolysis is performed. If the spermatic funicle is too short, the Fowler-Stephens technique (ligation and dissection of the spermatic vessels) can be applied. Pre-conditions are intact deferent duct and epididymis vessels; these are tested by a temporary clamping of the testicular artery. In rare cases, auto-transplantation by microsurgical anastomosis of the testis vessels with the epigastric vasculature can be considered. Table 1: Management of cryptorchidism CRYPTORCHIDISM Physical examination sonography Detectable Unilateral undetectable Bilateral undetectable
MRI (optional) HCG stimulation
v Therapy Laparoscopy Intersex? REFERENCES Alaish SM, Stylianos S. Diagnostic laparoscoy. Curr Opin Pediatr 1998; 10: 323-327
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