االورام الليفية العصبية (NFs (في تجويف الفم أورام عصبية نادرة يمكن أن تظهر بشكل فردي أو متعدد عندما ترتبط بالورم الليفي من النوع االول (1 NF.(الأورام الليفية العصبية المنفردة داخل الفم غير المرتبطة بـ 1 NF متفرقة وتشبه أي من اورام الأنسجة الرخوة الأخرى في تجويف الفم. يصف المؤلفون حالة سيدة صماء بكماء تبلغ من العمر 94 عاما اتت الى العيادة الخارجية وفي المنطقة الأمامية الجانبية
من لسانها كتلة انفرادية تنمو ببطء تم عالجها بنجاح في العيادة مع الاستئصال الكامل تحت التخدير الموضعي دون مضاعفات.
Neurofibromas (NFs) are rare neurogenic tumors of the oral cavity. They can present as solitary or multiple when associated with neurofibromatosis-1 (NF-1)/von Recklinghausen's disease. Solitary intraoral NFs unassociated with NF-1 are sporadic and mimic any other soft tissue tumor of the oral cavity. The authors report a case of a 49-year-old deaf-mute lady who presented with slowly growing solitary mass in the anterolateral aspect of the tongue, which was successfully managed in the outpatient clinic with complete excision and base cauterization under local anesthesia without complicationsز
References used
Kim DH, Murovic JA, Tiel RL, Kline DG. Operative outcomes of 546 Louisiana State University Health Sciences Center peripheral nerve tumors. Neurosurg Clin N AM 2004; 15:177.
Brooks DG. The neurofibromatosis: hereditary predisposition to multiple peripheral nerve tumors. Neurosurg Clin N Am 2004; 15:145.
Bruce R Korf, Mina Lobbous& Laura K Metrock. (2020). Neurofibromatosis type 1 (NF1): Pathogenesis, clinical features, and diagnosis. In Elizabeth TePas (Ed.), UpToDate. Retrieved May 9, 2020, from https://www.uptodate.com/contents/neurofibr omatosis-type-1-nf1-pathogenesis-clinicalfeatures-and-diagnosis
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