He Jian-feng, Lin Yi, Liu Jian-hua, Li Zhi-yong
From the Department of Oral and Maxillofacial Surgery, The First Affiliated Hospital, College of Medicine, Zhejiang University, Zhejiang, People's Republic of China.
Ann Plast Surg. 2014;72(6):725-8. doi: 10.1097/SAP.0b013e31826c42c2.
Congenital granular cell tumors (CGCTs), which are rare benign lesions in newborns, locate predominantly on the anterior maxillary alveolar ridge of female neonates. However, this lesion rarely occurs on the tongue, and only 9 cases have been reported in the English literature. Of the 9 cases, which have been tested for S-100 protein, 4 were immunonegative to S-100 protein. In this present case, we reported a rare case of a 4-day-old Chinese girl with a CGCT on the anterior dorsum of the tongue. The lesion was excised under general anesthesia when the newborn was 3 months old. Histologically, pseudoepitheliomatous hyperplasia of the overlying mucosa was noted in this lesion. Immunohistochemical stains showed that the granular cells were diffusely strongly positive to S-100 protein, neuron-specific enolase, and vimentin. Depending on these findings, it was diagnosed as CGCT.
先天性颗粒细胞瘤(CGCTs)是新生儿中罕见的良性病变,主要位于女性新生儿的上颌前牙槽嵴。然而,这种病变很少发生在舌部,英文文献中仅报道过9例。在这9例检测过S-100蛋白的病例中,4例对S-100蛋白免疫阴性。在本病例中,我们报告了1例罕见的4天大的中国女婴,其舌背前部患有先天性颗粒细胞瘤。该病变在新生儿3个月大时在全身麻醉下切除。组织学上,该病变可见覆盖黏膜的假上皮瘤样增生。免疫组织化学染色显示颗粒细胞对S-100蛋白、神经元特异性烯醇化酶和波形蛋白呈弥漫性强阳性。根据这些发现,诊断为先天性颗粒细胞瘤。