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An Organotypic High Throughput System for Characterization of Drug Sensitivity of Primary Multiple Myeloma Cells
Published on: July 15, 2015
Wells' Syndrome Mimicking Angioedema and Revealing a Multiple Myeloma: A Case Report
Lamia Mansour Billah1, Soumiya Chiheb2, Madiha Eljazouly2
1Dermatology and Venerology, Cheikh Khalifa International University Hospital, Mohammed VI University of Health Sciences, Casablanca, MAR.
Abstract:
Wells' syndrome (WS), or eosinophilic cellulitis, is a rare inflammatory dermatosis with a variety of clinical presentations. It typically manifests with recurrent pruritic erythematous plaques and edematous swellings, which can be mistaken for other conditions, such as erysipelas or angioedema. We report an unusual presentation of WS localized on the face of a 60-year-old male with a history of recurrent facial plaques, mistakenly treated as angioedema. After an extensive evaluation, a diagnosis of smoldering multiple myeloma was revealed as an underlying neoplastic condition. This case highlights the importance of considering Wells' syndrome in differential diagnoses of recurrent cellulitis-like presentations, even in the absence of peripheral eosinophilia, and underscores the need for histopathological confirmation for an accurate diagnosis.

