The term virus associated hemophagocytic syndrome describes a disorder
characterised by a benign generalized histiocytic proliferation with
marked hemophagocytosis associated with a systemic virus infection. The
mortality for patients with infection associated hemophagocytic syndrome
is very high(1). We describe a 12-year-old girl who had fatal
hemophagocytic syndrome associated with dengue hemorrhagic fever. A
literature search shows fewer than 20 case reports of dengue related
hemophagocytosis(2).
A 12-year-old, previously healthy girl presented with
fever for 5 days. On examination she was febrile, sick looking with normal
vital signs. Her liver was palpable 3 cm below the right costal margin,
and spleen was not palpable. She had malena on the second hospital day.
She was started on intravenous fluids, and ceftriaxone. She developed
tachypnea, epigastric tenderness and hypotension on fourth hospital day.
She was resuscitated with IV fluids, fresh frozen plasma and dopamine
support. She had high grade spiky fever throughout hospital stay ranging
between 101oF-105oF. On 11th
hospital day she developed dyspnea and her chest X-ray showed
bilateral consolidation. She was started on intravenous ceftazidime and
within few hours her respiratory distress rapidly progressed and she died
inspite of ventilatory support.
Her complete blood count showed a total WBC count of
2.9 x 103/µL, Hb of 9.4 g/dL and platelet count of
90,000/µL. Repeat blood counts done six times during hospital stay showed
persistent leucopenia, thrombocytopenia and anemia. Blood and urine
culture were sterile. Anti dengue IgG was positive (40.20 pu) and IgM was
also positive (11.4 pu) suggestive of secondary dengue infection. Bone
marrow biopsy study showed features of erythrophagocytosis.
A study by Chih-Jungchen, et al.(3) has
shown that 61.1% of children with hemophagocytosis had infection
associated hemophagocytosis. Normally fever does not persist for more than
7 days in dengue hemorrhagic fever and thrombocytopenia resolves in a few
days. But children with dengue fever associated hemophagocytosis have an
atypical evolution of dengue hemorrhagic fever with prolonged fever and
persistent abdominal pain(4). Our child had prolonged high spiky fevers
for 16 days and persistent cytopenias and sucummbed to sepsis inspite of
antibiotic therapy. Clinicians should consider the possibility of
hemophagocytosis in children having dengue hemorrhagic fever complicated
with prolonged spiky fever and persistent pancytopenia.
References
1. Sullivan JL, Woda BA. Lymphohistiocytic Disorders.
In: David GN,Ginsburg D, OrKin SH, Look AT, editors. Nathan and
Oski’s Hematology of Infancy and Childhood. 6th edn. Philadelphia:
Saunders; 2003. p. 1380-1381.
2. Jain D, Singh T. Dengue virus related
hemophagocytosis: a rare case report. Hematology 2008; 13: 286-288.
3. Chen CJ, Huang YC, Jaing TH, Hung IJ, Yang CP, Chang
LY, et al. Hemophagocytic syndrome: a review of 18 pediatric cases.
J Microbiol Immunol Infect 2004; 37: 157-163.
4. Rueda E, Mendez A, Gonzalez G. Hemophagocytic
syndrome associated with dengue hemorrhagic fever. Biomedica 2002; 22:
160-166.