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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شناسه ملی سند علمی:
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.
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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