Title : When dengue disguises itself: Uncommon presentation resembling hemophagocytic lymphohistiocytosis in a young adult
Abstract:
We describe a case of a 24-year-old male who presented with fever associated with flu-like symptoms that progressed to skin involvement with a diffuse erythematous and painful rash necessitating inpatient admission for further management. His physical examination was notable for widespread maculopapular rash of the trunk, upper and lower extremities as well as splenomegaly. Extensive investigations were remarkable for elevated liver function tests, ferritin, lactate dehydrogenase, and a peripheral smear revealing ovalocytes with reactive lymphocytes. Brucella antibodies but dengue and cytomegalovirus antibodies were still pending during his inpatient stay. Other autoimmune and infectious investigations and imaging were negative. Multidisciplinary discussions between Rheumatology, Dermatology, and Haematology resulted in primary differentials of hemophagocytic lymphohistiocytosis (HLH), drug eruption rash, and viral illness. He was started on methylprednisolone 80 mg, followed by a gradual taper in light of the differentials. A bone marrow biopsy was scheduled but patient’s family declined and he was discharged home. Upon follow-up two weeks post-discharge, the patient received a diagnosis of dengue fever based on the identification of elevated IgM and IgG levels in the initial laboratory tests conducted during the inpatient admission.