A case report of Parry–Romberg syndrome

Author:

Babaei Kiana1,Rahnama Ali2,Shurvarzi Nora3,Movahedi Ali1ORCID

Affiliation:

1. Department of Anesthesia Neyshabur University of Medical Sciences Neyshabur Iran

2. Department of Plastic Surgery Hakim Hospital, Neyshabur University of Medical Sciences Neyshabur Iran

3. Department of Operating Room Hakim Hospital, Neyshabur University of Medical Sciences Neyshabur Iran

Abstract

Key Clinical MessageParry–Romberg syndrome is characterized by progressive dystrophy in one half of the face, which usually begins in childhood. Correct and timely diagnosis of this disease, as well as a multidisciplinary approach and timely surgical treatment to minimize the psychological effects and improve the patient's appearance are of particular importance.AbstractParry–Romberg syndrome is characterized by progressive dystrophy or loss of subcutaneous tissue in one half of the face, which usually begins in childhood and continues with skin changes, and can also be associated with linear scleroderma. Although this disease has been known for more than 150 years, its exact cause and pathogenesis are not well understood. The clinical feature of Parry–Romberg syndrome that makes it possible to diagnose is unilateral idiopathic facial atrophy. The reported case is a 14‐year‐old boy who suffered from hemifacial atrophy of the frontal area since he was 7 years old was referred to a plastic and cosmetic surgery specialist and underwent surgery without systemic symptoms and in the inactive phase of the disease. Correct and timely diagnosis of this disease, as well as a multidisciplinary approach and timely and appropriate surgical treatment to minimize the psychological effects and improve the patient's appearance are of particular importance.

Funder

Neyshabur University of Medical Sciences

Publisher

Wiley

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