A 12-year-old non-Indigenous girl from a regional community in Central Australia presented with several months of increased tiredness, pharyngitis, poor appetite and abdominal discomfort. She had a history of Crohn’s disease diagnosed 4 years earlier and managed with bimonthly infliximab infusions. She also had a history of iron deficiency, eczema managed with topical steroids and nut allergy. She had received several courses of oral antibiotics for pharyngitis from her general practitioner, without improvement. She had no history of vomiting, altered bowel habit, fever, camping or overseas travel, and her immediate family and pet dogs were well. On examination, she had mild abdominal tenderness and angular chelitis. She was noted to have a linear, pruritic maculopapular rash that extended from the left lateral malleolus to the posterior aspect of her calf and along her posteromedial thigh (Figs 1-3). The rash had first appeared several weeks before on her ankle and calf and had advanced proximally over the next week. The patient had not had any rashes elsewhere and had no history of generalised pruritus or urticaria. Investigations demonstrated a normal full blood examination, including a normal eosinophil count of 0.3 × 10/L and normal erythrocyte sedimentation rate and C-reactive protein. Her ferritin decreased to 16 μg/L. No acute stool sample was collected, but six previous samples cultured and examined for ova, cysts and parasites were normal. Strongyloides stercoralis serology was performed using an IgG enzyme-linked immunosorbent assay (ELISA) using the soluble fraction of filariform S. stercoralis larvae. The patient’s ELISA result was elevated, with an optical density of 0.44 units (normal range ≤0.2 units). In light of her immune compromise, the patient was treated with weekly oral ivermectin until her symptoms resolved. Repeat serology 3 months after treatment was initiated was <0.2. Her younger sibling was also receiving infliximab infusions for Crohn’s disease and was treated for positive S. stercoralis serology. Household contacts and pet dogs were treated with a standard course of oral ivermectin, receiving two doses 1 week apart.
[1]
Angela Wilson,et al.
Paediatric Strongyloidiasis in Central Australia
,
2018,
Tropical medicine and infectious disease.
[2]
Sinuon Muth,et al.
Different but overlapping populations of Strongyloides stercoralis in dogs and humans—Dogs as a possible source for zoonotic strongyloidiasis
,
2017,
PLoS neglected tropical diseases.
[3]
A. Esterman,et al.
Control of chronic Strongyloides stercoralis infection in an endemic community may be possible by pharmacological means alone: Results of a three-year cohort study
,
2017,
PLoS neglected tropical diseases.
[4]
J. McCarthy,et al.
Strongyloides seroprevalence before and after an ivermectin mass drug administration in a remote Australian Aboriginal community
,
2017,
PLoS neglected tropical diseases.
[5]
A. Apolo,et al.
Rapid development of migratory, linear, and serpiginous lesions in association with immunosuppression.
,
2014,
Journal of the American Academy of Dermatology.
[6]
T. Nutman,et al.
Diagnostic Accuracy of Five Serologic Tests for Strongyloides stercoralis Infection
,
2014,
PLoS neglected tropical diseases.
[7]
P. Vounatsou,et al.
Strongyloides stercoralis: Global Distribution and Risk Factors
,
2013,
PLoS neglected tropical diseases.
[8]
P. Chiodini,et al.
The Laboratory Diagnosis and Follow Up of Strongyloidiasis: A Systematic Review
,
2013,
PLoS neglected tropical diseases.
[9]
C. Hennequin,et al.
Evaluation of a Rapid Enzyme-Linked Immunosorbent Assay for Diagnosis of Strongyloidiasis
,
2010,
Journal of Clinical Microbiology.
[10]
P. Steinmann,et al.
Strongyloidiasis--the most neglected of the neglected tropical diseases?
,
2009,
Transactions of the Royal Society of Tropical Medicine and Hygiene.