Immunological Functions of the Human Prepuce

Sexually Transmitted Infections (London), Volume 74, Issue 5: Pages 364-367, October 1998.

University of Southern California Medical Center, Los Angeles, California, USA. P M Fleiss

Wellcome Unit for the History of Medicine, University of Oxford OX2 6PE. F M Hodges

Medical College of Wisconsin, Milwaukee, Wisconsin, USA. R S Van Howe

Correspondence to: Dr. Fleiss, 1824 North Hillhurst Avenue, Los Angeles, CA 90027, USA

Accepted for publication: 5 March 1998.

P M Fleiss, F M Hodges, R S Van Howe

The demonisation of the human male prepuce has been an unscientific process, even though some research, on the surface, might seem to support it. In the late 19th century, when male circumcision came into vogue in medicine in the United States, there was near universal acceptance among American medical professionals that circumcision was an effective treatment for such "diseases" as masturbation, headache, insanity, epilepsy, paralysis, strabismus, rectal prolapse, hydrocephalus, and clubfoot.1 Leading medical journals published thousands of case reports demonstrating these and other miraculous therapeutic benefits from preputial amputation. The notion that circumcision improves hygiene and prevents sexually transmitted diseases (STDs) originated at the same time in the context of the discourse over racial and moral hygiene. The peculiar American phenomenon of mass newborn (that is, involuntary) circumcision was a product of the cold war era. United States doctors readily embraced the concept of mass, involuntary circumcision just as they had embraced involuntary sterilisation and other eugenic measures--practices rejected by almost all other Western nations. Mass circumcision peaked in the 1970s, when almost 90% of male neonates in the United States were circumcised. Since then, the rate has declined but circumcision industry spokesman have added to the list of diseases that circumcision allegedly prevents and cures.

Historically, the most common reason given for circumcision has been that it prevents masturbation. Today, the most common reason given is that it inhibits the transmission of STDs, even though rigorously controlled studies have consistently shown that circumcised males are at greater risk for all major STDs than males whose penises are intact.2-6 Circumcision advocates are now claiming that circumcision prevents AIDS.

A review of the scientific literature, however, reveals that the actual effect of circumcision is the destruction of the clinically-demonstated hygienic and immunological properties of the prepuce and intact penis.

The sphincter action of the preputial orifice functions like a one way valve, blocking the entry of contaminants while allowing the passage of urine.7,8 Ectopic sebaceous glands concentrated near the frenulum produce smegma.9-12 This natural emollient contains prostatic and seminal secretions, desquamated epithelial cells, and the mucin content of the urethral glands of LittrÉ.13,14 It protects and lubricates the glans and inner lamella of the prepuce, facilitating erection, preputial eversion, and penetration during sexual intercourse.

The inner prepuce contains apocrine glands,15 which secrete cathepsin B, lysozyme, chymotrypsin, neutrophil elastase,16 cytokine (a non-antibody protein that generates an immune response on contact with specific antigens),17 and pheromones such as androsterone.18 Lysozyme, which is also found in tears, human milk, and other body fluids destroys bacterial cell walls.

The natural composition of preputial bacterial flora is age dependent and similar to that of the eyes, mouth, skin, and female genitals.19 Washing the preputial sac was once thought to aid hygiene. Washing a stallion's preputial sack with soap, however, encourages the growth of pathogenic organisms.20 Washing the human prepuce with soap is a common cause of balanoposthitis.21

Fussell et al have claimed that the prepuce is predisposed to colonisation by pathogenic bacteria, but they did not measure naturally occuring bacterial flora in living cohorts with undisturbed preputial microenvironments.22 They measured bacterial rates in dead, amputated, chemically treated prepuces inoculated with virulent strains of pathogenic bacteria--conditions that represent no known biological or behavioural reality.

Animal experiments reveal that in the presence of hydrogen peroxide and halide or pseudohalides, soluble peroxidase in the prepuce has an antimicrobial activity.23 Plasma cells in the mucosal lining of the bovine prepuce secrete immunoglobulin under the epidermis into the preputial cavity. In response to pathogenic bacterial infection, preputial plasma cells increase.24 Antibodies in breast milk are ingested, then excreted in the urine where they prevent Escherichia coli from adhering to the urinary tract and inner lining of the prepuce25 An 8 year prospective study that controlled for genitourinary abnormalities found no difference in the rate of upper urinary tract infections between circumcised and intact boys.26

There are no histological studies that validate the claim that the sclerotic keratinisation of the epithelium of the surgically externalized dessicated glans penis, meatus, or scar of the circumcised penis creates a barrier against infection. The higher rate of STDs in circumcised males might well be the result of the loss of preputial immunoprotective structures. The loss of the protective, self-lubricating, mobile, double-layered prepuce exposes the glans penis and meatus to direct friction, abrasion, and trauma. Eyes without eyelids would not be cleaner. Neither is a glans without its prepuce. The surgically externalized and unprotected glans and meatus of the circumcised penis are constantly exposed to abrasion and dirt, making the circumcised penis less hygienic.27 The circumcised penis is more prone to infection in the first years of life than the intact penis.28-30

The prepuce is a specific erogenous zone.31 It contains a rich, complex network of nerves and an abundance of mucocutaneous end organs sensitive to motion, touch, temperature, and erogenous stimulation.32-37 Both the inner and outer folds of he prepuce have denser distribution of nerve networks than the rest of the penile skin.33 The rich innervation of the inner prepuce contrasts sharply with the limited sensory investment of the glans penis, which is characterized primarily by free nerve endings, which feel only deep pressure and pain.39 The double layered prepuce provides the skin necessary to accommodate the expanded erect organ and to allow the penile skin to slide freely, smoothly, and pleasurably over the shaft and glans. One function of the prepuce is to facilitate smooth, gentle movement between the mucosal surface of the two partners during intercourse. The prepuce enables the penis to slip in and out of the vagina non-abrasively inside its own sheath of self-lubricating, movable skin. The female is thus stimulated by moving pressure rather than by friction only, as when the male's prepuce is missing.

Circumcision radically desensitises the penis and immobilises whatever skin remains.40 The loss of preputial mobility, primary sensory structures, orgasm triggering nerve endings, and the inevitable desensitisation of the glans may necessitate more vigorous and prolonged thrusting to achieve orgasm. For this reason a circumcised penis may be more likely than an intact penis to cause the breaks, tears, microfissures, abrasions, and lacerations in a vagina (or rectum) through which HIV in the thrusting partner's semen could enter the receiving partner's blood stream.

The prepuce is also richly vascular.37,41,42 The most vascular parts of the body are those least vulnerableto infection.

These factors may explain why circumcised males are more likely than their genitally intact peers to engage in high risk sexual behaviours (such an anal intercourse and active and passive homosexual oral sex) that lead to HIV and other STD infections.45

Epithelial Langerhans cells (ELCs), a component of the immune system, help the body recognise and process antigens, directing them to lymphocytes or macrophages. Weiss et al noted an abundance of ELCs in the outer surface of the neonate prepuce comparable with the general density of ELCs found in adult skin.44 They suggest that the relative paucity of ELCs in the inner mucosal surface of the neonatal prepuce results in a reduced immune response to cutaneous antigens and recommend universal neonatal circumcision to prevent HIV infection. This recommendation is untenable because the prepuce of virtually all neonates is fused to the glans, sealing the undeveloped preputial pouch from external contact.45,46 Furthermore, the newborn has just emerged from a sterile environment, where no ELCs are needed. There is no documentation of the comparable density of ELC in the mucous membranes of the surgically externalised glans penis, meatus, or the circumcision scar of the sexually active adult.47

Although a study of primates found that Langerhans-like cells in the lamina propria, not the epithelium, appeared to be infected with simian immunodeficiency virus,48 it is unclear whether this observation can be extrapolated to the Langerhans cells in the epithelium of the human prepuce. If Langerhans cells are a factor, the ethical response would be to promote the use of condoms, not excise normal tissue laden with immunoprotective cells.

It was an American circumciser in 1986 who first hypothesised that circumcision prevents HIV infection.49 In an attempt to verify this theory, others have published numerous epidemiological surveys, conducted primarily in Africa. A review of these surveys, however, does not support their assertion. Of the 36 published studies examining the relationship between the circumcised penis and HIV infection, 15 found a negative correlation50-64, four found a positive correlation,65-68 and 16 found no statistically significant difference.2,69-83

The studies that find a positive correlation are all population based. Most of the negative association studies are based on STD clinic data, have serious population bias, and must therefore be viewed with caution. For example, according to undisclosed criteria, Pépin et al counted 11% of their self reported circumcised cohort as intact. Konde-Lule et al assumed all Muslims were circumcised,77 an assumption that Urassa et al found to be true in only 68% to 92% of cases.91

Although circumcision proponents in the United States cite these studies when debating routine circumcision,84,85 African data are not applicable to developed nations.86 Circumcision status in Africa has an important but poorly understood cultural significance that proponents of circumcision have ignored. Circumcised and intact males live very different lives in the African regions investigated. Marck has shown that intact males in circumcising areas face severe discrimination in work, housing, marriage, and sexual relations. A significant percentage resort to prostitutes, increasing their risk of exposure to STDs.87 Ignoring these facts, some AIDS researchers have recommended intervening into African culture and promoting circumcision in circumcision-free regions. Implementing this recommendation would invite disaster. In many parts of Africa, circumcision causes most tetanus infections.89 The spread of tuberculosis through circumcision in developing countries is well documented.90 The risk of severe complications and death following circumcision rituals in Africa is high.91,92 The common use of dirty instruments in group circumcisions only increases the risk of HIV transmission.93 Although the risk of circumcision related complications is higher in Africa than in the United States, no level of risk is acceptable when a healthy, and often protesting, "patient" has not consented.

In addition to its long term immunological handicap, neonatal circumcision immediately compromises the immune system making the circumcised male more vulnerable to infection, often with tragic consequences.94,95 Even if the circumcisionist's studies were valid, the real and unavoidable risks of circumcision outweigh, both quantitatively and ethically, the alleged risks of intact genitalia. Amputation of the prepuce neither inhibits risky sexual behavior nor confers immunity after exposure to pathogens. This is demonstrated by the fact that the United States has both the highest number of sexually active circumcised males and the highest rates of genital cancers, STDs, and AIDS of any first world nation.96,97

Mass involuntary circumcision has failed to achieve any of the public health benefits its advocates have claimed for it; but even if it had achieved them all, there can be no scientific or ethical justification for depriving anyone of sovereignty over his own sex organs. Neonatal circumcision violates bodily integrity and imposes on an unconsenting individual a diminished penis for life. In the wake of the Nuremberg trials, it is inappropriate for doctors to persist in performing or advocating involuntary penile reduction surgery on healthy, normal individuals. The totalitarian concept of involuntary prophylactic surgery espoused by circumcision advocates has no place in modern medicine or the civilised world. The key to decreasing the transmission of STDs is education, not amputation.

Contributors: PMF, the principal investigator for this review, initiated the research and participated in the analysis and interpretation of the data. FMH participated in the design of the review and data collection, was particularly involved in the research and presentation of medicohistorical data, and wrote the first draft of the paper. RSVH is responsible for the collection, interpretation, and analysis of the HIV data, and edited the paper. PMF, FMH, and RSVH are guarantors for the scientific integrity of the paper.

Funding: None.

Conflict of Interest: None


References

  1. Hodges F. A short history of the institutionalization of involuntary sexual mutilation in the United States. In: Denniston GC, Milos MF, eds. Sexual mutilations: a human tragedy. New York. Plenum, 1997:17-40.
  2. Laumann EO, Masi CM, Zuckerman EW. Circumcision in the United States: prevalence, prophylactic effects, and sexual practice. JAMA 1997;277:1052-7.
  3. Donovan E. Bassett I, Bodsworth NJ. Male circumcision and common sexually transmitted diseases in a developed nation setting. Genitourin Med 1994;70:317-320.
  4. Smith GL, Greenup R, Takafuji ET. Circumcision as a risk factor for urethritis in racial groups. Am J Public Health 1987;77:452-454.
  5. Cook LS, Koutsky A, Holmes KK. Clinical presentation of genital warts among circumcised and uncircumcised heterosexual men attending an urban STD clinic. Genitourin Med 1993;69:62-64.
  6. Bassett I, Donovan B, Bodsworth NJ, et al. Herpes simplex virus type 2 infection of heterosexual men attending a sexual health center. Med J Aust 1994;160:697-600.
  7. Jefferson G. The peripenic muscle; some observations on the anatomy of phimosis. Surg Gynecol Obstet 1916;23:177-81.
  8. Lakshmanan S, Parkash S. Human prepuce--some aspects of structure and function . Indian J Surg 1980; 42:134-7.
  9. Delbanco E. Über das gehäufte Aufreten von Talgdrusen an der Innerflähe des Präputium. Monatshefte für praktishe Dermatologie 1904; 38:536-8.
  10. Hyman AB, Brownstein MD. Tyson's "glands," sebaceous glands and papillomatosis penis. Arch Dermatol 1969;99:31-7.
  11. Piccinno R, Carrel C-F, Menni S. et al. sebacous glands mimicking molluscum contagiosum Acta Derm Venerol1990;70:344-5.
  12. Krompecher St. Die Histologie der Absonderung fur Smegma Praeputi. Anatomischer Anzeiger 1932; 75:170-176.
  13. Koning M, Streekferk JG. Kleine Kwalen in de Husiartsgeneenkunde; Smegma en Fysiologische Fimose. Ned Tijdschr Groeskd 1995; 139: 1632-4.
  14. Parkash S, Rao R, Venkatesan K. et al. Sub-preputial wetness--its nature. Ann Nat Med Sci 1982;18:109-112.
  15. Ahmed A, Jones AW. Apocrine cystodenoma: a report of two cases occurring on the prepuce. Br J Derm 1969;81:899-901.
  16. Frolich E, Shaumberg-Lever F, Kissen C. Immunelectron microscopic localization of cathepsin B in human apocrine glands. J Cutan Pathol 1993; 20: 54-60.
  17. Ahmed AA, Nerdlind K, Schulzberg M.et al. Immunoelectrochemical localization of IL-1 alpha-, IL-1 beta, IL-6 and TNF-alpha-like immunoreactivities in human prepuce apocrine glands. Arch Dermatol Res 1995; 287:764-6.
  18. Cohn BA. In search of human skin pheromones. Arch Derm 1994;130:1048-51.
  19. Neubert U, Lantze. Die Bakterielle Flora des Präeputial raumes. Hautarzt 1979; 30: 41-5.
  20. Bowen JM, Tobin N, Simpson RB, et al. Effects of washing on the bacterial flora of the stallion's penis. J Reprod Sci (Suppl) 1982;32:41-45.
  21. Birley HDL, Walker MM, Luzzie GA, et al. Clinical features and management of recurrent balanitis, association with atopy and genital washing. Genitourin Med 1993;69:400-3.
  22. Fussell EN, Kaack MB, Cherry R, et al. Adherence of bacteria to human foreskins. J Urol 1988;140:997-1001.
  23. Prabir K. Tissue distribution of constitutive and induced soluble peroxidase in rat: purification and characterization from lacrimal gland. Eur J Biochem 1992;206:59-67.
  24. Flower PJ. Ladd PW, Thomas AD, et al. An immunopathologic study of the bovine prepuce. Vet Pathol 1983; 30:199-202.
  25. Coppa GV, Gabriella O, Giorgi P, et al. Preliminary study of breastfeeding and bacterial adhesion to uroepithelial cells. Lancet 1990; 358:568-571.
  26. Mueller ER, Steinhardt G, Naseer S. The incidence of genitourinary tract abnormalities in circumcised and uncircumcised boys presenting with an initial urinary tract infection by 6 months of age. Pediatrics (Suppl) 1997;100:580.
  27. Van Howe RS. Variability in penile appearance and penile findings: a prospective study. Br J Urol 1997; 80: 776-782.
  28. Fergusson DM, Lawton JM, Shannon FT. Neonatal circumcision and penile problems: an 8 year longitudinal study. Pediatrics 1988; 81:537-541.[Link to www.pediatrics.org]
  29. Enzenauer RW, Dotson CR, Leonard T. et al. Increased incidence of neonatal staphylococcal pyoderma in males. Mil Med 1984;149:408-410.
  30. Enzenauer RW, Dotson CR, Leonard T. et al.. Male predominance in persistent staphylococcal colonization and infection of the newborn. Hawaii Med J 1985;44:389-90, 392, 394-6.
  31. Winkelmann RK. The erogenous zones: their nerve supply and its significance. Proc Staff Meet Mayo Clin 1959;34:39-47.
  32. Dogiel AS. Die Nervenendigungen in der Haut der Genitalorganen in der Äusseren Menschen. Archiv für Microskopische der Anatomia 1893;41:585-612.
  33. Winkelmann RK. The cutaneous innervation of the newborn prepuce. J Invest Dermat 1956;26:53-67.
  34. De Girolamo A, Cecio A. Contributo alla conoscensza dell'innervazione sensitiva del prepuzio nell'uomo. Boll Ital Biol Sperimentale1968;44:1521-2.
  35. Ohmori D. Über die Entwicklung der Innervation der Genitalapparate als peripheren Aufnameapparat der Genitalen Reflex. Zeitschift für Anatomie und Entwicklungeschichte 1924; 70:347-50.
  36. Bazett HC, Mcglane B, Williams RG, et al. Depth, distribution and probable identification in the prepuce of sensory end-organs concerned in sensations of temperature and touch; thermometric conductivity. Arch Neurol Psychiat 1932;27:489-507.
  37. Taylor JR, Lockwood AP, Taylor AJ. The prepuce: specialized mucosa of the penis and its loss to circumcision. Br J Urol 1996;77:591-595.
  38. Bourlond A, Winkelmann RK. L'innervation du prÉpuce chez le nouveau-nÉ. Arch Belg Derm Syph 1965;21:139-56.
  39. Halata Z, Munger BL. The neuroanatomical basis for the protopathic sensibility of the human glans penis. Brain Research 1986;371-205-230.
  40. Lander MM. The human prepuce. In: Denniston GC, Milos MF, eds. Sexual mutilation: a human tragedy: Plenum 1997:79-81.
  41. Justkiewenski S, Vaysse Ph, Moscovici J. et al. A study of the arterial blood supply to the penis. Anat Clin 1982;4:101.
  42. Hinman F. Jr. The blood supply to preputial island flaps. Urol 1991;145:232-5.
  43. Van Howe RS, Cold CJ. Advantages and disadvantages of neonatal circumcision. JAMA 1997;278:203.
  44. Weiss GN, Sanders SM, Westbrook KC. The distribution and density of Langerhans cells in the human prepuce. cause of a diminished immune response? Israel J. Med Sci 1993;29-42-3.
  45. Kayaba H, Tamura H, Kitajima S, et al. Analysis and retractability of the prepuce in 603 Japanese boys. Urol 1996;156:813-5.
  46. Gairdner D. The fate of the foreskin: a study of circumcision. BMJ 1949; 2:1433-7.
  47. Berman B, Chen VL, France DS, et al. Anatomical mapping of epidermal Langerhans cell densities in adults. Br J Derm 1983; 109:553-8.
  48. Spira IA, Marx PA, Patterson BK. et al.Cellular targets of infection and route of viral disssemination after introvaginal inoculation of simian immunodeficiency virus into rhesus macaques. J Exp Med 1996;183:215-25.
  49. Fink AJ. A possible explanation for heterosexual male infections with AIDS. N Engl J Med 1986;315:1167.
  50. Bwaya JJ, Omari AM. utere AN. et al. Long distance truck-drivers: I. Prevalence of sexually transmitted diseases (STDs). East Africa Med J 1991;68:425-9.
  51. Bwayo J, Plummer F, Omari M. et al. Human immunodeficiency virus infection in long distance truck drivers in East Africa. Arch Intern Med 1994;154:1291-6.
  52. Kreiss JK, Hopkins SG. The association between circumcision status and human immunodeficiency virus infection among homosexual men. J Infect Dis 1993; 168:1404-8.
  53. Cameron DW, Simonsen, JN, D'Costa LJ, et al.Female to male transmission of human immunodeficiency virus type 1 risk factors for seroconversion in men. Lancet 1989; 2: 403-7.
  54. Greenblatt RM, Lukeha SA, Plummer FA, et al. Genital ulceration as a risk factor for human immunodeficiency virus infection. AIDS 1988;2:47-50.
  55. Diallo MO, Ackash AN, LaFontaine M-F, et al. HIV-1 and HIV-2 infections in men attending sexually transmitted disease clinics in Abidijan, Cote d'Ivoire. AIDS 1992;6:581-5.
  56. Simonsen JN, Cameron DW, Gakinya MN, et al. Human immunodeficiency virus infection among men with sexually transmitted diseases. N Engl J Med 1988; 319:274-8.
  57. Tyndall MW, Ronald AR, Agoki E, et al. Increased risk of infection with genital ulcer disease in Kenya. Clin Infect Dis 1996;23:449-453.
  58. Nasio JM, Nagelkerke NO, Mwatha A, et al. Genital ulcer disease amongst STD clinic attenders in Nairobi; association with HIV-1 and circumcision status. Int J STD AIDS 1996;7:410-414.
  59. Mehendale SM, Shepherd ME, Divekar AD,et al. Evidence for high prevelance and rapid transmission of HIV among individuals attending STD clinics in Pune, India. Indian J Med Res 1996; 104: 327-35.
  60. Sassan-Morokro M, Greenberg AE, Coulibaly IM. et al. High rates of sexual contact with female sex workers, sexually transmitted disease and condom neglect among HIV infected and uninfected men with tuberculosis in Abijan, Cote d'Ivoire. J Acquired Immune Defic Syndr Hum Retrovirol 1996;11:183-7.
  61. Hunter DJ, Maggwa BN, Mati JKG, et al. Sexual behavior, sexually transmitted diseases, male circumcision and risk of HIV infection among women in Nairobi, Kenya. AIDS 1994;8:93-9.
  62. Seed J, Allen S, Theiry M, et al. Male circumcision, sexually transmitted disease and risk of HIV. J Acquired Immune Defic Syndr Hum Retrovirol 1995;8:83-90.
  63. Malamba SS, Wagner HJ, Maude G, et al. Risk factors for HIV-1 Infection in adults in a rural Ugandan community: a case control study. AIDS 1994; 8: 253-257.
  64. Urassa M, Todd J, Boerra JT, et al. Male circumcsion and susceptibility to HIV infection among men in Tanzania. AIDS 1997;11,73-80. [study 4]
  65. Barongo LR, Borgdorff W, Mosha FF, et al. The epidemiology of HIV-1 infection in rural areas, roadside settlements and rural villages in Mwanza Region, Tanzania. AIDS 1992;6:1521-8.
  66. Grosskurth H, Mosha F, Todd J, et al. A community trial of the impact of improved sexually transmitted disease treatment on the HIV epidemic in rural Tanzania: 2. Baseline survey results. AIDS 1995;9:927-34.
  67. Chao A, Bulterys M, Musanganire F, et al. Risk factors associated with prevalent HIV-1 infection among pregnant women in Rwanda. National University of Rwanda-Johns Hopkins University AIDS Research Team. Int J Epidemiol 1994;23:371-380.
  68. Urassa M, Todd J, Boerra JT, et al. Male circumcision and susceptibility to HIV infection among men in Tanzania. AIDS 1997;11:73-80. [study 1]
  69. Hira SK, Kamanga J, Mcuacua R, et al. Genital ulcers and male circumcision as risk factors for acquiring HIV-1 in Zambia. J Infect Dis 1990;161:584-5.
  70. Pépin J, Quigley M, Todd J, et al. Association between HIV-2 Infection and genital ulcer diseases among male sexually transmitted disease patients in The Gambia. AIDS 1992;6:489-93.
  71. Bollinger RC, Brookmeyer RS, Mehendale SM,l et al. Risk factors and clinical presentation of acute primary HIV infection in India. JAMA 1997; 278:2085-9.
  72. Chiasson M, Stoneburner RL, Hildebrandt DS, et al. Heterosexual transmission of HIV-1 associated with use of smokable freebase cocaine (crack). AIDS 1991;5:1121.
  73. Carael M, Van De Perre, PH, Lepage PH, et al. Human immunodeficiency virus transmission among heterosexual couples in Africa. AIDS 1988;2:201-5.
  74. Moss GB, Clemerson D, D'Costa L, et al. Association of cervical ectopy with heterosexual transmission of human immunodeficency virus: results of a study of couples in Nairobi, Kenya. J Infect Dis 1991;164:588-91.
  75. Allen S, Lindan C, Serufilira A, et al. Human immunodeficiency virus infection in urban Rwanda: demographic and behavioral correlate in a representative sample of childbearing women. JAMA 1991; 266:1657-63.
  76. Seidlin M, Vogler M, Lee E, et al. Heterosexual transmission of HIV in a cohort of couples in New York City. AIDS 1993;7:1247-54.
  77. Konde-Lule JK. Bergley SF, Downing R. Knowledge attitudes and practices concerning AIDS in Ugandans. AIDS 1989;3:513-18.
  78. Van de Perre P, Clumeck N, Steens M, et al. Seroepidemiological study on sexully transmitted diseases and hepatitis B in African promiscuous heterosexuals in relation to HTLV-III infection. Eur J Epidemiol 1987;3:14-8.
  79. Quigley M, Munguti K, Grosskurth H, et al. Sexual behavior patterns and other risk factors for HIV infection in rural Tanzania: a case control study. AIDS 1997;11:237-48.
  80. Urassa M, Todd J, Boerma JT, et al. Male circumcision and susceptibility to HIV infection among men in Tanzania. AIDS 1997;11:73-80.[study 2]
  81. Urassa M, Todd J, Boerma JT, et al. Male circumcision and susceptibility to HIV infection among men in Tanzania. AIDS 1997;11:73-80.[study 3]
  82. Urassa M, Todd J, Boerma JT, et al. Male circumcision and susceptibility to HIV infection among men in Tanzania. AIDS 1997;11:73-80. [study 5]
  83. Hudson CP, Hennis AJM, Kataaha P, et al. Risk factors for the spead of AIDS in rural Africa, hepatitis B and syphilis in southwestern Uganda AIDS 1988; 2: 255-60.
  84. Schoen EJ. Benefits of newborn circumcision: is Europe ignoring medical evidence? Arch Dis Child 1997; 77: 258-60.
  85. Weiss GN, Prophylactic neonatal surgery and infectious diseases. Pediatr Infect Dis J 1997;16:727-34.
  86. Storms, MR. AAFP fact sheet on neonatal circumcision: a need for updating. Am Fam Physician 1996;54:1216,1218.
  87. Marck J. Aspects of male circumcision in sub-equatorial African cultural history. Health Transition Review 1997; 7:357-59.
  88. Moses S, Bradley JE, Nagelkerke NJD, et al. Geographical patterns of male circumcision practice in Africa: association with HIV seroprevalence. Int J Epidemiol 1990;19:693-7.
  89. Sow PS, Diop BM, Barry HL, et al. TÉtanus et practique traditionnelle à Dakar (à propos de 141 cas). Dakar Med 1993; 38:55-9.
  90. Hardy DB. Cultural practices contributing to the transmission of human immunodeficiency virus in Africa. Rev Infect Dis 1987;9:1109-19.
  91. Annobil SH, Al-Hilf A, Kazie T. Primary tuberulosis of the penis in an infant. Tubercle 1990; 71:229-30.
  92. Crowley IP, Kesner KM. Ritual circumcision (umkhwetha) among the Xhosa of the Ciskei. Br J Urol 1990;66:318-321.
  93. Phillips K, Ruttman T, Viljoen J. Flying doctors, saving costs. S Afr Med J 1996; 86:1557-8.
  94. Blass DP, Jr., Healey JJ, Waldhausen JHT. Necrotizing fasciitis after Plastibell circumcision. J Pediatr 1997;131;459-62.
  95. Williams N, Kapila L. Complications of circumcision. Br J Surg 1993;80:1231-6.
  96. Hitchcock R. Commentary on: Benefits of newborn circumcision: is Europe ignoring medical evidence? Arch Dis Child 1997:77:250.
  97. Wise J. HIV epidemic is far worse than thought. BMJ 1997;3:5:1486.[Link to www.bmj.com]

Citation:

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