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SOUTHEASTASIANJ TROPMEDPUBLICHEALTH
1322 Vol 41 No. 6 November 2010
Correspondence: Dr Keng-Yin Loh, Interna-tional Medical University Malaysia, JalanRasah, Seremban 70300, Malaysia.Tel: (06) 012 237 3328E-mail: [email protected]
CASE REPORT
HYPEREOSINOPHILIA RESPONDING TO EMPIRICAL
ANTIHELMINTHIC TREATMENT
Keng-Yin Loh and Xin-Er Lee
International Medical University Malaysia, Seremban, Malaysia
Abstract. We report a 20-year-old college student presents with bilateral ankleedema associated with hypereosinophilia following a history of traveling in a ru-ral area. Physical examinations and investigations failed to diagnose any underly-ing cause. She was treated with antihelminth medication and the edema subsided
within a week and the eosinophil counts normalized within two weeks.
Key works: hypereosinophilia, edema, antihelminthic treatment
INTRODUCTION
An eosinophil count of 1-3% is nor-mal for adult (Rothenberg, 1998).Eosino-phil can be caused by parasitic infectionssuch as ascariasis, filariasis, and allergics,such as asthma and eczema (Weller and
Bubley, 1994; Ackerman and Butterfield,2000). Eosinophilia has also been associ-ated with malignancies, such as lym-phoma and myloproliferative disordersand autoimmune connective tissue disor-ders (Clauw and Crofford, 1994).
The major step in managing a patientwith eosinophilia is to ascertain the under-lying cause and to treat accordingly. How-ever if underlying causes failed to be diag-
nosed, empirical therapy with antihelminthfor patients presenting with eosinophiliamay be helpful especially if they are froman endemic area for parasitic helminth in-festation. This clinical case illustrated a pa-
tient with hypereosinophilia respondedwell to antihelminth treatment empirically.
CASE REPORT
A 25- year-old college student fromMalaysia, presented with a 2 week history
of lethargy and pedal edema (Fig1). Shedenied any significant past medical his-tory. The only significant history was 6weeks prior to presentation she went on atrip to Cambodia, but denied any fever,injury or known infection. The physicalexamination revealed only pedal edema.The complete blood count (Fig 2) showeda hemoglobin of 13.7g%, a total white
blood cell count of 14.2 x 106/l, with 25%
neutrophils, 19% lymphocytes, 4%mono-cytes, 1% basophils and 51% eosinophils.He platelet count was 236x106/l. Her urineanalysis, renal function and liver functiontests were normal. Stool microscopy wasnegative for ova and parasites. A magneticresonance image (MRI) of her chest, ab-domen and pelvis was negative. A connec-tive tissue disease screen was also nega-tive. Bone marrow aspiration was not per-
formed due to patient refusal.
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HYPEREOSINOPHILIARESPONDINGTOEMPIRICALTREATMENT
Vol 41 No. 6 November 2010 1323
to rule out leukemia.
Since the investigations in this patientwere normal and no specific cause wasidentified, she was started antihelminthicempirical treatment. This approach was ap-
propriate in view of a recent travel historyand the fact that parasitic infections remaina major cause of hypereosinophilia world-wide (Weller and Bubley, 1994; Rothenberg,1998; Ackerman and Butterfield, 2000).
REFERENCES
Ackerman SJ, Butterfield JH. Eosinophilia,eosinophil-associated diseases, and the
hypereosinophilic syndrome. In: Hoffman
R, Benz EJ Jr, Shattil SJ, eds. Hematology:basic principles and practice. 3rded. New
York: Churchill Livingstone, 2000: 702-20.
Clauw DJ, Crofford LJ. Eosinophilic rheumaticdisorders. Rheum Dis Clin North Am 1995;21: 231-46.
Rothenberg ME. Eosinophilia. N Engl J Med
1998; 338: 1592-600.
Weller PF, Bubley GJ. The idiopathichypereosinophilic syndrome. Blood1994;
83: 2759-79.
Fig 2Peripheral blood film of patient show-
ing the typical bilobed nucleus of eosi-nophils and cytoplasmic granules
stained pink with Wright-Giemsa stain(x1,000).
Fig 1Pedal edema of patient.
In view of the hypereosinophilia withno clinical or laboratory evidence of he-matological malignancy, she was treatedempirically with albendazole 400 mg dailyfor 3 consecutive days. Her limb edemasubsided on Day 3 of treatment and a re-peat differential counts showed a markedreduction in eosinophil count to 35%. Oneweek later it was 10% and two weeks laterit was 3%. She is currently asymptomatic.
DISCUSSION
The management of eosinophilia in-cludes determining the cause and treatingit accordingly. Necessary investigationsinclude stool examinations to detect intes-tinal helminthes, connective tissue screen-ing and to screening for cardiac, hepaticand renal involvement. Bone marrow as-
piration and biopsy should be considered