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Stevens-Johnson syndrome in children.

 
, medical expert
Last reviewed: 07.07.2025
 
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Stevens-Johnson syndrome develops as a result of drug allergy after taking sulfonamides, tetracycline antibiotics, chloramphenicol, and nonsteroidal anti-inflammatory drugs.

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Symptoms of Stevens-Johnson syndrome

The onset is acute, with high fever, severe intoxication, arthraltia, myalgia, and from the first hours, progressive skin lesions are characteristic. Dark red spots with rapid formation of vesicular or, in particularly severe cases, bullous elements with serous-bloody contents appear on the skin of the face, neck, chest, and limbs (including palms and soles). Vesicles and bullae on the skin burst open, forming erosions and ulcers. Skin rashes tend to merge. In most patients, mucous membranes are also affected: conjunctivitis with keratitis, stomatitis, pharyngitis, laryngitis. Girls often have lesions of the vulva. A secondary infection often develops on the skin or in the respiratory tract and lungs. Other internal organs are usually not affected.

The sick child is urgently hospitalized; placed in a separate box. The suspected drug is canceled. Enterosorbents are prescribed (activated carbon, polyphepan, polyphen, smecta).

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Treatment of Stevens-Johnson syndrome

Prescribed prednisolone 1-2 mg/kg/day, infusion detoxification therapy - 5% glucose solution with isotonic sodium chloride solution. In the acute period of severe course, prednisolone in a dose of 3-5 mg/kg/day can be administered intravenously. Vascular drugs and antiplatelet agents (euphyllin, pentoxifylline, ticlopedin), antiproteolytic drugs - gordox, contrical, trasylol are prescribed. If a bacterial infection occurs, antibiotics are prescribed, taking into account the results of bacteriological examination.

Local treatment of erosions and ulcers is carried out similarly to the treatment of open burns using indifferent antiseptics and keratoplastics. In case of eye damage - application of ocular hydrocortisone ointment 3-4 times a day.

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