Evidence map›Paper›PMID 42599851›Full record

ArticleThe American journal of case reports2026

Systemic Reaction After Centipede Bite in a Child: Diagnostic Challenges Between Toxic and Hypersensitivity Mechanisms.

Takatoshi Murakami, Yusuke Miyashita, Toshihiko Nonaka, Mika Ogata, Kimitoshi Nakamura

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In one paragraph

Article in The American journal of case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Takatoshi MurakamiDepartment of Pediatrics, Amakusa Medical Center, Amakusa, Kumamoto, Japan.
Yusuke MiyashitaDepartment of Pediatrics, Amakusa Medical Center, Amakusa, Kumamoto, Japan.
Toshihiko NonakaDepartment of Pediatrics, Amakusa Medical Center, Amakusa, Kumamoto, Japan.
Mika OgataDepartment of Pediatrics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Kimitoshi NakamuraDepartment of Pediatrics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Centipede (Scolopendra subspinipes) envenomation typically causes localized pain and swelling and is generally considered a self-limited condition. However, systemic reactions resembling hypersensitivity responses, such as generalized urticaria and respiratory discomfort, have occasionally been reported. Differentiation of toxic venom effects from immunologically mediated reactions remains challenging, particularly in pediatric patients, because standardized diagnostic testing for centipede venom allergy is unavailable. CASE REPORT A previously healthy 4-year-old girl developed generalized urticaria, facial swelling, pallor, and transient respiratory discomfort approximately 10 minutes after sustaining multiple nocturnal centipede bites indoors. Cutaneous manifestations appeared at sites distant from the bite locations, a finding potentially compatible with a systemic reaction rather than a purely localized toxic effect. Vital signs remained stable, and symptoms improved spontaneously without pharmacologic intervention. Hymenoptera-venom-specific IgE testing performed several weeks later showed weak positivity (class 1), although the patient had no prior history of bee or wasp stings. Considering the possibility of recurrent systemic reactions in environments where repeated exposure may occur, an epinephrine auto-injector was prescribed for emergency preparedness. CONCLUSIONS This case highlights diagnostic challenges in distinguishing toxic and allergic mechanisms after arthropod envenomation in children. The persistence of venom-specific IgE beyond the acute phase may suggest susceptibility to venom-related hypersensitivity, rather than a transient response to envenomation. Even when symptoms resolve spontaneously and definitive diagnostic confirmation is unavailable, careful clinical assessment and risk stratification remain essential. Preparedness for possible future anaphylaxis should be considered when systemic symptoms occur after arthropod exposure.

Indexed as

ArthropodsArthropod VenomsBites and StingsVenom HypersensitivityAnimalsChild, PreschoolDiagnosis, DifferentialFemaleHumansImmunoglobulin EPallorUrticariaArthropod VenomsImmunoglobulin E

Identifiers

PMID42599851
PMCPMC13483510

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