Senanayake Manouri P, Karunaratne Irantha
Department of Pediatrics, Faculty of Medicine, University of Colombo, Kynsey Road, Colombo 008, Sri Lanka.
J Med Case Rep. 2014 Aug 22;8:283. doi: 10.1186/1752-1947-8-283.
Riga-Fede disease is a rare pediatric condition in which chronic lingual ulceration results from repetitive trauma. Neonatal teeth or underlying neuro-developmental disorders which include Down syndrome are described as causative factors, but to the best of our knowledge, this is the first case report of both Down syndrome and natal teeth coexisting. The need for early extraction in the presence of two risk factors is highlighted in this case report.
An 18-month-old Sinhalese male presented with an ulcerating lingual mass on the ventral surface of the tongue. The lesion had progressed over the past six months. He also had clinically diagnosed Down syndrome.The ulcer was non-tender, indurated, and had elevated margins. It was not bleeding and two natal teeth in lower central dentition were seen in apposition with the lesion. There was no regional lymphadenopathy but the ulcer was causing concerns as it mimicked a malignant lesion. A clinical diagnosis of Riga-Fede disease caused by raking movements of the tongue against anterior natal teeth by a child who was developmentally delayed and prone to suck on his tongue was made. The mother was reassured and the natal teeth were extracted.
Early extraction of natal teeth is recommended only if there is a risk of aspiration or interference with breast feeding. Although Down syndrome is among the neuro-developmental conditions that lead to this lesion, its occurrence is usually at an older age. The presence of natal teeth together with Down syndrome caused the lesion to occur in infancy. Awareness of the benign nature of this rare condition by pediatricians and dental practitioners is important as it will allay anxiety and avoid unnecessary biopsy. This case also highlights the impact of two risk factors and needs consideration as an added indication for the early extraction of natal teeth.
里加 - 费德氏病是一种罕见的儿科疾病,慢性舌部溃疡由反复创伤引起。新生儿牙齿或包括唐氏综合征在内的潜在神经发育障碍被描述为致病因素,但据我们所知,这是首例唐氏综合征和诞生牙并存的病例报告。本病例报告强调了在存在两种风险因素时早期拔牙的必要性。
一名18个月大的僧伽罗族男性因舌腹面出现溃疡性舌肿物前来就诊。该病变在过去六个月中有所进展。他还被临床诊断为唐氏综合征。溃疡无压痛、质地坚硬,边缘隆起。溃疡不出血,在下颌中切牙部位可见两颗诞生牙与病变相邻。无区域淋巴结肿大,但该溃疡因其类似恶性病变而令人担忧。临床诊断为里加 - 费德氏病,病因是一名发育迟缓且有吮舌倾向的儿童舌头反复摩擦前位诞生牙。安抚了患儿母亲后,拔除了诞生牙。
仅在存在误吸风险或妨碍母乳喂养的情况下,才建议早期拔除诞生牙。虽然唐氏综合征是导致该病变的神经发育疾病之一,但其通常在较大年龄出现。诞生牙与唐氏综合征并存导致病变在婴儿期发生。儿科医生和牙科医生了解这种罕见疾病的良性性质很重要,因为这将减轻焦虑并避免不必要的活检。本病例还强调了两种风险因素的影响,需要将其作为早期拔除诞生牙的额外指征加以考虑。