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2.
BMC Infect Dis ; 21(1): 691, 2021 Jul 17.
Article in English | MEDLINE | ID: mdl-34273957

ABSTRACT

BACKGROUND: Female genital schistosomiasis (FGS) is a neglected tropical gynaecological disease that affects millions of women in sub-Saharan Africa (SSA). FGS is caused by Schistosoma haematobium, a parasitic carcinogen involved in the pathogenesis of squamous cell carcinoma of the bladder. Cervical cancer incidence and mortality are highest in SSA, where pre-cancerous cervical dysplasia is often detected on screening with visual inspection with acetic acid (VIA). There are no studies evaluating the association between VIA positivity and FGS diagnosed by genital PCR. METHODS: Women were recruited from the Bilharzia and HIV (BILHIV) study in Zambia a community-based study comparing genital self-sampling to provider obtained cervicovaginal-lavage for the diagnosis of FGS in women aged 18-31. FGS was defined as positive Schistosoma DNA from any genital PCR. Urogenital schistosomiasis diagnostics included urine circulating anodic antigen, urine microscopy and portable colposcopy. Participants were offered cervical cancer screening using VIA at Livingstone Central Hospital. Associations of PCR confirmed FGS and other diagnostics with VIA positivity were assessed using multivariable logistic regression. RESULTS: VIA results were available from 237 BILHIV participants. A positive Schistosoma PCR in any genital specimen was detected in 14 women (5.9%), 28.6% (4/14) of these women had positive VIA compared to 9.0% without PCR evidence of schistosome infection (20/223). Schistosoma PCR positivity in any genital specimen was strongly associated with VIA positivity (OR: 6.08, 95% CI: 1.58-23.37, P = 0.02). CONCLUSIONS: This is the first study to find an association between FGS and positive VIA, a relationship that may be causal. Further longitudinal studies are needed.


Subject(s)
Schistosomiasis haematobia/epidemiology , Uterine Cervical Dysplasia/epidemiology , Adolescent , Adult , Animals , Colposcopy/methods , Diagnostic Tests, Routine/methods , Early Detection of Cancer/methods , Female , Genitalia, Female/parasitology , Genitalia, Female/pathology , Humans , Incidence , Microscopy/methods , Polymerase Chain Reaction , Schistosoma haematobium/genetics , Schistosoma haematobium/isolation & purification , Schistosomiasis haematobia/diagnosis , Schistosomiasis haematobia/parasitology , Specimen Handling , Urinalysis/methods , Uterine Cervical Dysplasia/diagnosis , Uterine Cervical Dysplasia/parasitology , Uterine Cervical Neoplasms/diagnosis , Uterine Cervical Neoplasms/epidemiology , Uterine Cervical Neoplasms/parasitology , Young Adult , Zambia/epidemiology
3.
Mol Syndromol ; 1(2): 82-86, 2010.
Article in English | MEDLINE | ID: mdl-21045961

ABSTRACT

Persistent fetal vasculature (PFV) is most often a condition of unknown cause. It represents persisting elements of fetal ocular vessels including the hyaloid arterial network. Protein C is a vitamin K-dependent serine protease, which regulates coagulation. Deficiency of protein C leads to a prothrombotic state. We report the case of a male infant born at 34 weeks gestation to non-consanguineous parents. Ophthalmic examination found bilateral PFV, microphthalmia and vitreoretinal dysplasia. He also suffered bilateral renal vein thrombosis and purpura fulminans and was diagnosed with severe protein C deficiency. Genetic analysis of the PROC gene revealed two separate pathogenic mutations, confirming compound heterozygote status. Both parents were found to be heterozygous. While ocular manifestations (commonly haemorrhages) are often seen in protein C-deficient patients, a search of the literature reveals very few recorded cases of PFV in severe protein C deficiency. We hypothesise that protein C deficiency was the cause of PFV in this patient. Intraocular thrombotic events in utero could affect the normal development of ocular vessels and lead to persistent elements of fetal vasculature in the eye. Consideration should be given to the possibility of protein C deficiency in patients presenting with PFV, particularly if bilateral.

4.
J Ultrasound ; 13(2): 41-5, 2010 Jun.
Article in English | MEDLINE | ID: mdl-23396900

ABSTRACT

INTRODUCTION: This study is a preliminary retrospective analysis of a new imaging technique, sonographic tomography, for the determination of the exact extent of disease prior to definitive surgery for breast cancer. MATERIALS AND METHODS: Forty-one women were diagnosed with breast cancer had preoperative staging using sonographic tomography, between August 2007 and June 2008. All these women subsequently underwent bilateral contrast-enhanced MRI prior to surgery to determine if there were areas of tumor extension, multifocality, axillary adenopathy, or contralateral disease that would affect their planned surgery. Both imaging techniques were then compared retrospectively for accuracy to pathologic truth. RESULTS: Sonographic tomography accurately staged breast cancer preoperatively in 68% of cases, while MRI did so in 54% of cases. The resulting improvement in overall accuracy is 14% (2-28%). Sonographic tomography appears non-inferior to contrast enhanced, bilateral breast MRI. CONCLUSIONS: Further, prospective, study is needed to further evaluate this new imaging technique in preoperative staging prior to definitive surgery.

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