Department of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, Salerno, Italy.
Am J Case Rep. 2022 Jun 24;23:e936142. doi: 10.12659/AJCR.936142.
BACKGROUND Long arm (q) deletion syndrome of chromosome 18 is a congenital chromosomal disorder. The specialist dental management of patients with 18q deletion is a challenge, as these individuals fall into the category of patients with special needs. The aim of this work was to describe the surgical and dental management in hospital of a patient with long arm deletion syndrome of chromosome 18 (18q). CASE REPORT An 8-year-old patient with deletion syndrome of chromosome 18 (18q) was referred to the Department of Dentistry and Oral Surgery. The patient presented dental pain and difficult feeding. The examination of the oral cavity revealed a destructive carious lesion of the lower right second deciduous molar and the need to perform a frenectomy due to the short lingual frenulum, which limited the movements of the tongue. Given the complex management of the patient, it was necessary to carry out surgical procedures in the operating room. Frenectomies of the lower labial and lingual frenulum were carried out with the aid of an electric scalpel with an ultra-sharp microdissection needle. At 2-month follow-up, the patient presented with good extraction site healing and satisfactory lingual mobility, along with improvements of speech and feeding. CONCLUSIONS Dental involvement in patients with deletion syndrome of the long arm of chromosome 18 is poorly documented in the literature. The hospital regimen appears to be the criterion standard for the management of the patient with long arm deletion syndrome of chromosome 18.
18 号染色体长臂缺失综合征是一种先天性染色体疾病。患有 18q 缺失的患者的专业牙科管理是一个挑战,因为这些患者属于特殊需要患者类别。本工作的目的是描述 18 号染色体长臂缺失综合征(18q)患者的医院手术和牙科管理。
一名 8 岁的 18q 染色体缺失综合征患者被转介到牙科和口腔外科。该患者出现牙痛和进食困难。口腔检查显示右下第二乳磨牙有破坏性龋齿病变,需要进行舌系带切除术,因为舌系带短限制了舌头的运动。鉴于患者的复杂管理,需要在手术室进行手术。在电动手术刀的辅助下,使用超锋利的微型解剖针进行下唇和舌系带的切除术。2 个月随访时,患者的拔牙部位愈合良好,舌部活动度满意,言语和进食功能均得到改善。
18 号染色体长臂缺失综合征患者的牙科参与在文献中记录较少。医院方案似乎是 18 号染色体长臂缺失综合征患者管理的标准。