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Turkish Journal of Pediatrics 2020

A rare cause of secondary hemophagocytic lymphohistiocytosis: systemic loxoscelism

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
Tuğba Erat
Aysun Yahşi
Cem Çanakçı
Aybike Korkmaz
Ceyda Karahan
Talia İleri
Savaş Serel
Huban Atilla
Nihal Kundakçı
Halil Özdemir

Maneno muhimu

Kikemikali

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.

Keywords: hemophagocytic lymphohistiocytosis; necrotic arachnidism; systemic loxoscelism; violin spiders.

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