Krishnamurthy Arvind, Ramshankar Vijayalakshmi, Majhi Urmila, George Rinku
Department of Surgical Oncology, Cancer Institute (Women's India Association), Adyar, Chennai, Tamil Nadu, India.
Ann Maxillofac Surg. 2013 Jul;3(2):192-4. doi: 10.4103/2231-0746.119219.
Primitive neuroectodermal tumor (PNET) is a broad term that includes a wide array of lesions with varying differentiating potential affecting both the central and peripheral nervous system. Peripheral PNET (pPNET), a variant of PNET, is known to arise in many places throughout the body; involvement of the mandible is however rare. A review of the scientific literature describes only seven reports of pPNET to be arising from the mandible. Given their insidious clinical symptoms, variable locations and rarity, the accurate diagnosis of peripheral PNETs poses a challenge for clinicians. PNETs exhibits characteristic immunophenotypical and genetic features that distinguish them from other small round cell tumors. A multidisciplinary approach is necessary to manage patients affected by PNET. There is however no consensus about the best therapeutic strategy. We recently got to treat a young patient with mandibular PNET; the clinical course as well as the histopathology with immunohistochemistry correlation of this rare entity is discussed.
原始神经外胚层肿瘤(PNET)是一个广义术语,涵盖了一系列具有不同分化潜能、影响中枢和周围神经系统的病变。外周原始神经外胚层肿瘤(pPNET)是PNET的一种变体,已知可发生于全身多个部位;然而,下颌骨受累情况罕见。对科学文献的回顾仅描述了7例起源于下颌骨的pPNET报告。鉴于其隐匿的临床症状、多变的位置和罕见性,外周PNET的准确诊断对临床医生构成了挑战。PNET具有特征性的免疫表型和基因特征,使其有别于其他小圆细胞肿瘤。对于受PNET影响的患者,多学科方法是必要的。然而,关于最佳治疗策略尚无共识。我们最近治疗了一名患有下颌骨PNET的年轻患者;本文讨论了这个罕见病例的临床过程以及组织病理学与免疫组织化学的相关性。