The Turkish Journal of Pediatrics (Aug 2020)

A rare cause of secondary hemophagocytic lymphohistiocytosis: systemic loxoscelism

  • Tuğba Erat,
  • Erdal İnce,
  • Halil Özdemir,
  • Nihal Kundakçı,
  • Huban Atilla,
  • Savaş Serel,
  • Talia İleri,
  • Ceyda Karahan,
  • Aybike Korkmaz,
  • Cem Çanakçı,
  • Aysun Yahşi,
  • Ergin Çiftçi

DOI
https://doi.org/10.24953/turkjped.2020.04.014
Journal volume & issue
Vol. 62, no. 4

Abstract

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Background. Loxoscelism is caused by the bite of a specific spider type called the Loxosceles genus. In Turkey, most cases are seen after L. rufescens bites. Clinical manifestation of the bites ranges from local cutaneous reaction to severe ulcerative necrosis. Systemic loxoscelism may also occur. Case. Herein, we report a previously healthy five-year-old male patient who developed a secondary hemophagocytic lymphohistiocytosis after a presumed brown spider bite. He was treated with dexamethasone. Within the following 14 days, hemophagocytic syndrome resolved. Local hyperbaric oxygen therapy was applied to the necrotic areas. Conclusion. Secondary hemophagocytic lymphohistiocytosis may develop after systemic loxoscelism. In the presence of persistent fever, hepatosplenomegaly and laboratory findings this clinical entity should be kept in mind.

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