Congenital wells syndrome

Ben Zion Garty*, Meora Feinmesser, Michael David, Shraga Gayer, Yehuda L. Danon

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


We describe a girl with eosinophilic cellulitis (Wells syndrome) in whom the disease appeared immediately after birth with subcutaneous nodules on the scalp and trunk, followed by the characteristic skin swelling and erythema at the age of 6 months. The lesions disappeared after a few weeks, but recurred several times. The mother had consumed large quantities of medications during the pregnancy, including iron, vitamins, and 'natural remedies'. Based on time of onset, this may be regarded as a unique case of congenital Wells syndrome, its relation to the medications taken by the mother remains speculative. Subcutaneous nodules may be the presenting sign of Wells syndrome in children.

Original languageEnglish
Pages (from-to)312-315
Number of pages4
JournalPediatric Dermatology
Issue number4
StatePublished - 1997


Dive into the research topics of 'Congenital wells syndrome'. Together they form a unique fingerprint.

Cite this