Parry–Romberg Syndrome in Two Young Afghan Patients: First Case Report

سال انتشار: 1405
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 101

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JR_AJBMS-3-1_011

تاریخ نمایه سازی: 1 تیر 1405

چکیده مقاله:

Parry–Romberg syndrome (PRS), or progressive hemifacial atrophy, is a rare neurocutaneous disorder characterized by unilateral, slowly progressive atrophy of facial soft tissues and, in some cases, underlying bone. Reports from South-Central Asia are scarce, and no confirmed cases have previously been documented from Afghanistan. We report two young Afghan patients—an ۱۸-year-old male and a ۲۲-year-old female—who presented with insidious, progressive left-sided facial atrophy without prior trauma, infection, or autoimmune disease. Clinical examination revealed unilateral soft-tissue wasting, skin thinning, and facial asymmetry, with normal neurological findings. Computed tomography demonstrated atrophy of subcutaneous fat and facial musculature with subtle osseous thinning. Follow-up over ۶ and ۴ months showed no further progression. Quantitative imaging revealed an ۱۸–۲۲% reduction in soft-tissue thickness in one patient and ۱۵–۱۷% in the other. The left-sided predominance observed is consistent with international reports. Although the etiology of PRS remains unclear, early recognition is essential due to its functional, aesthetic, and psychosocial impact. These cases highlight potential underdiagnosis in low-resource settings and emphasize the importance of reporting PRS from underrepresented regions.Parry–Romberg syndrome (PRS), or progressive hemifacial atrophy, is a rare neurocutaneous disorder characterized by unilateral, slowly progressive atrophy of facial soft tissues and, in some cases, underlying bone. Reports from South-Central Asia are scarce, and no confirmed cases have previously been documented from Afghanistan. We report two young Afghan patients—an ۱۸-year-old male and a ۲۲-year-old female—who presented with insidious, progressive left-sided facial atrophy without prior trauma, infection, or autoimmune disease. Clinical examination revealed unilateral soft-tissue wasting, skin thinning, and facial asymmetry, with normal neurological findings. Computed tomography demonstrated atrophy of subcutaneous fat and facial musculature with subtle osseous thinning. Follow-up over ۶ and ۴ months showed no further progression. Quantitative imaging revealed an ۱۸–۲۲% reduction in soft-tissue thickness in one patient and ۱۵–۱۷% in the other. The left-sided predominance observed is consistent with international reports. Although the etiology of PRS remains unclear, early recognition is essential due to its functional, aesthetic, and psychosocial impact. These cases highlight potential underdiagnosis in low-resource settings and emphasize the importance of reporting PRS from underrepresented regions.

نویسندگان

Abdul Ghafar Ghayur

Esteqlal Hospital, Plastic and Burn Surgery Department, Kabul, Afghanistan

Ahmadshah Wazir

Esteqlal Hospital, Plastic and Burn Surgery Department, Kabul, Afghanistan

Habibullah Azimi

Plastic and Burn surgery Department, Esteqlal Hospital, Kabul Afghanistan

Sherin Alem Ibrahimkhail

Esteqlal Hospital, Plastic and Burn Surgery Department, Kabul, Afghanistan

Mohammad Sharif Yusufi

Esteqlal Hospital, Plastic and Burn Surgery Department, Kabul, Afghanistan

Taqi Baran

Esteqlal Hospital, Plastic and Burn Surgery Department, Kabul, Afghanistan

Jawid Sazish

Esteqlal Hospital, Plastic and Burn Surgery Department, Kabul, Afghanistan