Please use this identifier to cite or link to this item: https://hdl.handle.net/10321/2979
Title: Cervical cytology as a diagnostic tool for female genital schistosomiasis : correlation to cervical atypia and Schistosoma polymerase chain reaction
Authors: Pillay, Pavitra 
van Lieshout, Lisette 
Taylor, Myra 
Sebitloane, Motshedisi 
Zulu, Siphosenkosi Gift 
Kleppa, Elisabeth 
Roald, Borghild 
Kjetland, Eyrun Floerecke 
Keywords: Cervical atypia;Cytology;Female genital schistosomiasis;Gynecology;Laboratory diagnostics;Real-time polymerase chain reaction
Issue Date: 20-Apr-2016
Publisher: Cytopathology Foundation Inc with Wolters Kluwer
Source: Pillay, P. et al. 2016. Cervical cytology as a diagnostic tool for female genital schistosomiasis : correlation to cervical atypia and Schistosoma polymerase chain reaction. Cytojournal. 13: 10.
Journal: CytoJournal 
Abstract: 
Background:

Female genital schistosomiasis (FGS) is a tissue reaction to lodged ova of Schistosoma haematobium in the genital mucosa. Lesions can make the mucosa friable and prone to bleeding and discharge. Women with FGS may have an increased risk of HIV acquisition, and FGS may act as a cofactor in the development of cervical cancer.
Objectives:

To explore cytology as a method for diagnosing FGS and to discuss the diagnostic challenges in low-resource rural areas. The correlation between FGS and squamous cell atypia (SCA) is also explored and discussed. Cytology results are compared to Schistosoma polymerase chain reaction (PCR) in vaginal lavage and urine and in urine microscopy.
Materials and Methods:

In a clinical study, 394 women aged between 16 and 23 years from rural high schools in KwaZulu-Natal, South Africa, underwent structured interviews and the following laboratory tests: Cytology Papanicolaou (Pap) smears for S. haematobium ova and cervical SCA, real-time PCR for Schistosoma-specific DNA in vaginal lavage and urine samples, and urine microscopy for the presence of S. haematobium ova.
Results:

In Pap smears, S. haematobium ova were detected in 8/394 (2.0%). SCA was found in 107/394 (27.1%), seven of these had high-grade squamous intraepithelial lesion (HSIL). Schistosoma specific DNA was detected in 38/394 (9.6%) of vaginal lavages and in 91/394 (23.0%) of urines. Ova were found microscopically in 78/394 (19.7%) of urines.
Conclusion:

Schistosoma PCR on lavage was a better way to diagnose FGS compared to cytology. There was a significant association between S. haematobium ova in Pap smears and the other diagnostic methods. In low-resource Schistosoma-endemic areas, it is important that cytology screeners are aware of diagnostic challenges in the identification of schistosomiasis in addition to the cytological diagnosis of SCA. Importantly, in this study, three of eight urines were negative but showed Schistosoma ova in their Pap smear, and one of them was also negative for Schistosoma DNA in urine. In this study, SCA was not significantly associated with schistosomiasis. HSIL detected in this young population might need future consideration.
URI: http://hdl.handle.net/10321/2979
ISSN: 0974-5963 (print)
1742-6413 (online)
DOI: 10.4103/1742-6413.180784
Appears in Collections:Research Publications (Applied Sciences)

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