Kadivar Maliheh, Sangsari Razieh, Alavi Azin
Department of Neonatal Care Unit, Children's Hospital Medical Center, Tehran University of Medical Sciences, Tehran, Iran;
Department of Obstetrics and Gynecology, Shariati Hospital, Hormozgan University of Medical Sciences, Hormozgan, Iran.
Iran J Med Sci. 2014 Mar;39(2):144-7.
Congenital granular cell tumor (GCT) is a relatively rare intraoral benign tumor, approximately 200 cases of which have been reported in the neonatal period worldwide. The newborn infant may have feeding problems and respiratory difficulties due to airway obstruction. This lesion may be diagnosed by prenatal ultrasonography and simple resection is mostly required. We report a case of an adult type of GCT in a newly born infant, who presented with an intraoral protruding mass with a prenatal diagnosis. This article describes the prenatal course, clinical, and pathological characteristics, and management of the GCT.
先天性颗粒细胞瘤(GCT)是一种相对罕见的口腔内良性肿瘤,全球范围内新生儿期报告的此类病例约有200例。由于气道阻塞,新生儿可能会出现喂养问题和呼吸困难。这种病变可通过产前超声诊断,大多需要进行简单切除。我们报告一例新生儿期的成人型GCT病例,该患儿产前诊断为口腔内突出肿物。本文描述了该GCT的产前病程、临床和病理特征以及治疗方法。