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- Case Report
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A Belgian traveler returning from Laos developed acute schistosomiasis. Feces microscopy and polymerase chain reaction (PCR) followed by sequence analysis revealed Schistosoma mekongi. Schistosome antibody test results and real-time PCR in serum were initially negative or not interpretable. A HRP-2 antigen test for Plasmodium falciparum and an enzyme-linked immunosorbent assay (ELISA) antibody test for Trichinella yielded false-positive results.
- Top of page
- Case Report
- Declaration of Interests
A 27-year-old male Belgian traveler developed low grade fever, night sweats, and cough soon after returning from a 4 months' adventurous travel to Laos, Cambodia, and Yunnan province in south China. He had lost some weight but had neither diarrhea nor anorexia. He was a practicing vegetarian.
He had, together with his girlfriend, visited the “Four Thousand Islands” (Si Pan Don) region, a conglomerate of islets situated in the Mekong River straddling the Laos–Cambodian border, 5 weeks prior. He reportedly took a daily swim in the Mekong River for 1 week (D0 = first day of exposure), as well as in a sandy old river bend with stagnant water at the southernmost part of Khong Island, called Don Det, on one occasion. He did not report swimming in rivers or ponds elsewhere during his travel.
Symptoms started about 6 weeks after exposure (D45). The patient consulted his family physician 10 days later (D55) and was referred at the outpatient clinic of the Institute of Tropical Medicine, Antwerp, Belgium (ITMA) 5 days thereafter (D60), when symptoms had already subsided. Clinical signs were unremarkable. Ultrasound revealed a modest spleen enlargement, and the routine laboratory workup showed a marked hypereosinophilia (Table 1). Chest X-ray was normal.
Table 1. Acute schistosomiasis with Schistosoma mekongi: clinical and laboratory data
|Treatmenta|| || || ||PZQ||Steroids||PZQ|| |
|Abdominal pain||−|| ||−||−||+||−||−|
|Eosinophil count (n/μL)|| ||1,929||8,290|| ||15,530||1,160||500|
|IgE (IU/μL)|| ||n/a||593|| ||472||395||n/a|
|Schistosoma ab IHA|| ||n/a||n/exe|| ||n/exe||n/exe||1/320|
|Schistosoma ab ELISA|| ||n/a||−|| ||+||+||+|
|S mekongi PCR; feces|| ||n/a||+|| ||n/a||n/a||−|
|Schistosoma sp. PCR; serum|| ||n/a||−c|| ||−c||+||−|
|Eggs in feces (epg)|| ||−||50|| ||n/a||−||−|
|Trichinella ab ELISA|| ||n/a||+b|| ||+b||−||−|
|Pf HRP-2 Ag test|| ||n/a||+b|| ||+b||+†||−|
Two serum antischistosome antibody tests were performed at the initial and the subsequent visits: an in-house enzyme-linked immunosorbent assay (ELISA) using a Schistosoma mansoni antigen (mixture of egg and adult worm extract), and an indirect hemagglutination inhibition assay (IHA), using a S mansoni adult worm extract (ELI.H.A Schistosoma, ELITech Group, Puteaux, France), with titration and cut-off at 1/80 (positive at ≥1/160). Up to 15 weeks after exposure (D105), the IHA could not be interpreted because of the presence of antibodies reacting with sheep RBC in the patient's serum. The result of schistosome ELISA antibody test was negative at the first visit (D60), while that of the Trichinella antibody test and the malaria HRP-2 antigen test were positive. Blood smear and polymerase chain reaction (PCR) for malaria, as well as the Plasmodium falciparum antibody test, were all negative. At D60, microscopy after enrichment for ova and parasites revealed 50 ova of S mekongi per gram of feces (Figure 1).
To confirm species identification, real-time PCR and conventional PCR followed by sequence analysis were performed on a fecal sample on D60 and D225. DNA was extracted using a QIAamp DNA stool mini kit (Qiagen). Sequencing of the real-time PCR product and of the complete Internal Transcribed Spacer (ITS) rRNA region amplified by the conventional PCR demonstrated the presence of S mekongi DNA. The 733 bp sequence amplified using the ITS4 and ITS5 primers was identical to S mekongi from GenBank (accession number U82284 and SMU22169) with the exception of a single base pair transition.
A real-time PCR using the Sm1-7 PCR test targeting the 121-bp tandem repeat sequence common to human schistosomes[4, 5] revealed cell-free schistosome DNA in serum at D105 but not at D60, D72, and D225 (Table 1). Instead of using 10 mL of plasma as in the original setup, DNA extraction was performed on 1.5 mL of serum on D60 and D72 and on 2 mL of serum on D105 and D225, quantities that proved to be sufficient in S mansoni infections.[4, 6]
The patient was given a single dose of praziquantel at D69, when symptoms had already subsided for 2 weeks. He declined concomitant corticosteroid treatment but was warned of a possible exacerbation of symptoms. He consulted 3 days later (D72) because of high-grade fever, severe and blood-stained diarrhea, abdominal colics, and some cough, starting a few hours after praziquantel ingestion. By that time the eosinophil count increased to 15.350/µL and the schistosome ELISA antibody test had turned positive. The patient was treated with oral corticosteroids (methylprednisolone 32 mg o.d. gradually tapering to nil in 14 days). Symptoms disappeared promptly after the first dose and never reappeared. At a control visit at D105, the patient was asymptomatic, eosinophil count had lowered dramatically, and a stool sample was negative for S mekongi eggs. A second treatment with praziquantel was given. No symptoms appeared thereafter. At a control visit 6 months later (D225), the eosinophil count had returned to normal, and PCR was negative both in feces and serum.
His companion had bathed at the same spot in the Mekong River, but never developed symptoms. A schistosome antibody test taken elsewhere 3 months after exposure showed a positive result, and she was reportedly treated without developing symptoms.