S. haematobium as a common cause of genital morbidity in girls: a cross-sectional study of children in South Africa

Ingrid Elise Amlie Hegertun, Kristin Marie Sulheim Gundersen, Elisabeth Kleppa, Siphosenkosi Gift Zulu, Svein Gunnar Gundersen, Myra Taylor, Jane D Kvalsvig, Eyrun Floerecke Kjetland, Ingrid Elise Amlie Hegertun, Kristin Marie Sulheim Gundersen, Elisabeth Kleppa, Siphosenkosi Gift Zulu, Svein Gunnar Gundersen, Myra Taylor, Jane D Kvalsvig, Eyrun Floerecke Kjetland

Abstract

Background: Schistosoma (S.) haematobium infection is a common cause of genital morbidity in adult women. Ova in the genital mucosal lining may cause lesions, bleeding, pain, discharge, and the damaged surfaces may pose a risk for HIV. In a heterogeneous schistosomiasis endemic area in South Africa, we sought to investigate if young girls had genital symptoms and if this was associated with urinary S. haematobium.

Methodology: In a cross-sectional study of 18 randomly chosen primary schools, we included 1057 schoolgirls between the age of 10 and 12 years. We interviewed assenting girls, whose parents had consented to their participation and examined three urines from each of them for schistosome ova.

Principal findings: One third of the girls reported to have a history of genital symptoms. Prior schistosomal infection was reported by 22% (226/1020), this was associated with current genital symptoms (p<0.001). In regression analysis the genital symptoms were significantly associated both with urinary schistosomiasis (p<0.001) and water contact (p<0.001).

Conclusions: Even before sexually active age, a relatively large proportion of the participating girls had similar genital symptoms to those reported for adult genital schistosomiasis previously. Anti-schistosomal treatment should be considered at a young age in order to prevent chronic genital damage and secondary infections such as HIV, sexually transmitted diseases and other super-infections.

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1. Map of Ugu district in…
Figure 1. Map of Ugu district in South Africa.
The coastal areas are inhabited by the more affluent and the schools here were excluded.
Figure 2. Genital and urinary symptoms in…
Figure 2. Genital and urinary symptoms in girls of two S. haematobium positive groups and three negative risk groups.
aLikelihood ratio. bThree urines investigated for S. haematobium ova, all were negative. cMore than 50 S. haematobium ova per 10 ml urine. d1–49 ova per 10 ml urine. eThese girls have water body contact (e.g. river, dam or lake). fThese girls deny water body contact.

References

    1. Leutscher PD, Ravaoalimalala VE, Raharisolo C, Ramarokoto CE, Rasendramino M, et al. (1998) Clinical findings in female genital schistosomiasis in Madagascar. Trop Med Int Health 3: 327–332.
    1. Kjetland EF, Kurewa EN, Ndhlovu PD, Gwanzura L, Mduluza T, et al. (2008) Female genital schistosomiasis - a differential diagnosis to sexually transmitted disease: Genital itch and vaginal discharge as indicators of genital S. haematobium morbidity in a cross-sectional study in endemic rural Zimbabwe. Tropical medicine and international health 13: 1509–1517.
    1. Kjetland EF, Ndhlovu PD, Mduluza T, Gomo E, Gwanzura L, et al. (2005) Simple clinical manifestations of genital Schistosoma haematobium infection in rural Zimbabwean women. American Journal of Tropical Medicine and Hygiene 72: 311–319.
    1. Hotez PJ, Fenwick A, Kjetland EF (2009) Africa's 32 Cents Solution for HIV/AIDS. PLoS Negl Trop Dis 3: e430.
    1. Steinmann P, Keiser J, Bos R, Tanner M, Utzinger J (2006) Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infectious Diseases 6: 411–425.
    1. Kjetland EF, Leutscher PD, Ndhlovu PD (2012) A review of female genital schistosomiasis. Trends in Parasitology 28: 58–65.
    1. Berry A (1966) A cytopathological and histopathological study of bilharziasis of the female genital tract. Path Bact 91: 325–337.
    1. Badawy AH (1962) Schistosomiasis of the cervix. Br Med J 1: 369–372.
    1. Charlewood GP, Shippel S, Renton H (1949) Schistosomiasis in gynaecology. J Obstet Gynaecol Br Emp 56: 367–385.
    1. Jourdan PM, Holmen SD, Gundersen SG, Roald B, Kjetland EF (2011) HIV target cells in Schistosoma haematobium-infected female genital mucosa. American journal of tropical medicine and hygiene 85: 1060–1064.
    1. Jourdan PM, Roald B, Poggensee G, Gundersen SG, Kjetland EF (2011) Increased vascularity in cervicovaginal mucosa with Schistosoma haematobium infection. PLoS Negl Trop Dis 5: e1170.
    1. Poggensee G, Kiwelu I, Saria M, Richter J, Krantz I, et al. (1998) Schistosomiasis of the lower reproductive tract without egg excretion in urine. American Journal of Tropical Medicine and Hygiene 59: 782–783.
    1. Feldmeier H, Poggensee G, Krantz I (1998) Puberty and age intensity profiles in schistosome infections: another hypothesis. Parasitology Today 14: 435.
    1. Savioli L, Gabrieli A, Neve H (1990) Vulvar Schistosomiasis haematobium lesion treated with Praziquantel. Trop Doc 20: 45–46.
    1. Laven JS, Vleugels MP, Dofferhoff AS, Bloembergen P (1998) Schistosomiasis haematobium as a cause of vulvar hypertrophy. Eur J Obstet Gynecol Reprod Biol 79: 213–216.
    1. Downs JA, Mguta C, Kaatano GM, Mitchell KB, Bang H, et al. (2011) Urogenital schistosomiasis in women of reproductive age in Tanzania's Lake Victoria region. American Journal of Tropical Medicine and Hygiene 84: 364–369.
    1. Kjetland EF, Ndhlovu PD, Gomo E, Mduluza T, Midzi N, et al. (2006) Association between genital schistosomiasis and HIV in rural Zimbabwean women. AIDS 20: 593–600.
    1. Mosunjac MB, Tadros T, Beach R, Majmudar B (2003) Cervical schistosomiasis, human papilloma virus (HPV), and human immunodeficiency virus (HIV): a dangerous coexistence or coincidence? Gynecol Oncol 90: 211–214.
    1. Siddappa NP, Hemashettar G, Shanmuganathan V, Semenya AA, Sweeney ED, et al. (2011) Schistosoma mansoni enhances host susceptibility to mucosal but not intravenous challenge by R5 Clade C SHIV. PLoS Negl Trop Dis 5: e1270.
    1. Fenwick A, Webster JP, Bosque-Oliva E, Blair L, Fleming FM, et al. (2009) The Schistosomiasis Control Initiative (SCI): rationale, development and implementation from 2002–2008. Parasitology 1–12.
    1. Statistics South Africa (2001) Census: Primary tables KwaZulu-Natal. Report No: 03-02-08.
    1. Kvalsvig JD (1986) The effects of Schistosomiasis haematobium on the activity of school children. J Trop Med Hyg 89: 85–90.
    1. Thomassen Morgas DE, Kvalsvig JD, Gundersen SG, Taylor M, Kjetland EF (2010) Schistosomiasis and water-related practices in school girls in rural KwaZulu-Natal, South Africa. Southern Afr J Epidemiol Infect 25: 30–33.
    1. WHO editor (2011) Helminth control in school-age children. A guide for managers of control programmes. Second edition ed: Preventive Chemotherapy and Transmission Control (PCT), Department of Control of Neglected Tropical Diseases (NTD), World Health Organization, 20, Avenue Appia, 1211 Geneva 27, Switzerland.
    1. Kjetland EF, Ndhlovu PD, Kurewa EN, Midzi N, Gomo E, et al. (2008) Prevention of gynecologic contact bleeding and genital sandy patches by childhood anti-schistosomal treatment. American Journal of Tropical Medicine and Hygiene 79: 79–83.
    1. Fischer GO (2001) Vulval disease in pre-pubertal girls. Australas J Dermatol 42: 225–234; quiz, 235–226.
    1. Jaquiery A, Stylianopoulos A, Hogg G, Grover S (1999) Vulvovaginitis: clinical features, aetiology, and microbiology of the genital tract. Arch Dis Child 81: 64–67.
    1. Hull T, Hilber AM, Chersich MF, Bagnol B, Prohmmo A, et al. (2011) Prevalence, motivations, and adverse effects of vaginal practices in Africa and Asia: findings from a multicountry household survey. J Womens Health (Larchmt) 20: 1097–1109.
    1. Stothard JR, Sousa-Figueiredo JC, Standley C, Van Dam GJ, Knopp S, et al. (2009) An evaluation of urine-CCA strip test and fingerprick blood SEA-ELISA for detection of urinary schistosomiasis in schoolchildren in Zanzibar. Acta Tropica 111: 64–70.
    1. Utzinger J, N'Goran EK, Tanner M, Lengeler C (2000) Simple anamnestic questions and recalled water-contact patterns for self-diagnosis of Schistosoma mansoni infection among schoolchildren in western Cote d'Ivoire. American Journal of Tropical Medicine and Hygiene 62: 649–655.
    1. Lengeler C, Utzinger J, Tanner M (2002) Screening for schistosomiasis with questionnaires. Trends Parasitol 18: 375–377.
    1. Bland KG, Gelfand M (1970) The effects of schistosomiasis on the cervix uteri in the African female. The Journal of obstetrics and gynaecology of the British Commonwealth 77: 1127–1131.
    1. Jourdan PM, Poggensee G, Gundersen SG, Roald B, Kjetland EF (2011) Increased cervicovaginal vascularity in association with Schistosoma haematobium ova. PLoS Negl Trop Dis 5: e1170.
    1. Poggensee G, Kiwelu I, Weger V, Goppner D, Diedrich T, et al. (2000) Female genital schistosomiasis of the lower genital tract: prevalence and disease-associated morbidity in Northern Tanzania. J Infect Dis 181: 1210–1213.
    1. Stothard JR (2012) Female genital schistosomiasis - icebergs of morbidity ahead? Trends in Parasitology 28: 174–175.
    1. Stothard JR, Gabrielli AF (2007) Schistosomiasis in African infants and preschool children: to treat or not to treat? Trends Parasitol 23: 83–86.
    1. WHO (1998) Report of the WHO informal consultation on schistosomiasis control. 1–45.

Source: PubMed

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