Cr. Anderson et al., WELLS SYNDROME IN CHILDHOOD - CASE-REPORT AND REVIEW OF THE LITERATURE, Journal of the American Academy of Dermatology, 33(5), 1995, pp. 857-864
We report a severe case of Wells' syndrome, or eosinophilic cellulitis
, after a bee sting in a 4-year-old girl. The patient had a widespread
, painful, blistering eruption that was subsequently complicated by Ps
eudomonas aeruginosa superinfection and septicemia, hypoalbuminemia, a
nemia, and neutropenia. The skin lesions responded to systemic steroid
therapy. There was residual scarring alopecia of the scalp. There hav
e been 17 previous reports of childhood Wells' syndrome. We believe th
at this disorder is a distinct entity that should be considered in the
differential diagnosis of blistering diseases in children.