Zerener Tamer, Sencimen Metin, Altun Ceyhan, Altug Hasan Ayberk
Departments of Oral and Maxillofacial Surgery, Center of Dental Sciences, Gulhane Medical Academy, Ankara, Turkiye.
Departments of Pediatric Dentistry, Center of Dental Sciences, Gulhane Medical Academy, Ankara, Turkiye.
Eur J Dent. 2013 Oct;7(4):497-499. doi: 10.4103/1305-7456.120651.
The congenital granular cell tumor (CGCT) is quite scarce at the infant. The patient, who has a 2-day-old female newborn, was admitted to the Department of Pediatric Dentistry. Baby had a smooth surfaced, non-fixated mass, found on the anterior part of the mandibular alveole, developing from the gingival mucosa. Clinical examination showed a 1 cm × 1 cm × 1.8 cm pedunculated, regular, pink colorful soft-tissue gob on the alveolar crest to the left side of the mandible. The gob was removed on the seventh postnatal day under general anesthesia. Then, the specimen was evaluated histopathologically. Post-operative recovery and surgical site healing was satisfactory. The CGCT is a rare, degenerative or reactive lesion of the oral cavity. The mass may surgically remove if the diagnosis is not definite clinically and this can lead therapeutic effect.
先天性颗粒细胞瘤（CGCT）在婴儿中相当罕见。该患者为一名2日龄的女婴，被收治于儿童牙科。婴儿下颌牙槽前部牙龈黏膜处有一个表面光滑、不固定的肿块。临床检查发现，在下颌骨左侧牙槽嵴处有一个1厘米×1厘米×1.8厘米的带蒂、规则、粉红色的软组织肿物。该肿物在出生后第7天在全身麻醉下被切除。随后，对标本进行了组织病理学评估。术后恢复和手术部位愈合情况良好。CGCT是一种罕见的口腔退行性或反应性病变。如果临床诊断不明确，肿物可通过手术切除，这可能带来治疗效果。
