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Melkersson–Rosenthal syndrome is a rare neuromucocutaneous granulomatous syndrome of unknown etiology characterized by a classical triad of relapsing orofacial edema, recurrent peripheral facial palsy, and lingua plicata. However, the classical triad is seen in only a minority of the cases. The majority of patients present with mono- or oligosymptomatic forms of the disease. Childhood onset of Melkersson–Rosenthal syndrome is extremely rare, and only a few cases have been described in the literature. This paper reports the case of an 8-year-old girl with cheilitis granulomatosa. Two years after the initial presentation, she presented with a unilateral peripheral facial palsy and a diagnosis of Melkersson– Rosenthal syndrome was established. The aim of this paper is to raise awareness among otolaryngologists of this condition in children presenting with orofacial swelling and/or peripheral facial palsy. Since symptoms do not always occur simultaneously, diagnosis often requires repeated follow-ups. Early recognition and a multidisciplinary approach to this condition are crucial to minimize recurrences and prevent orofacial dysfunction and its associated implications for the child’s psychosocial well-being.
Cite this article as: Surmont C, Boudewyns A, Mariën S, et al. Facial palsy in a child with a history of cheilitis granulomatosa: Melkersson– Rosenthal syndrome. B-ENT. 2023;19(4):242-244.