Unrecognized oral manifestations of Langerhans cell histiocytosis which progressed to systemic disease

I. Alajbeg , V. Vucicevic Boras , R. Femenic , A. Cekic-Arambasin , M. Anicic , J. Kelecic , I.Z. Alajbeg
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引用次数: 13

Abstract

A 2.5 years old boy was referred to the Department of oral medicine because of substantial erythema and ulcerations on palatal, buccal and alveolar regions. Unfortunately, it took two subsequent visits to our Department in six-months intervals, and re-evaluation at Pediatric oncology clinic where diagnosis of Langerhans cell histiocytosis (LCH) was finally established. At that stage, disease already progressed to multisystem life-threatening presentation, requiring aggressive treatment. Therefore, this case is a reminder of the possibility of occurrence of this rare disease in the oral cavity which might manifest itself in multiple presentations thus easily leading to the misdiagnosis and therefore it could be easily overlooked by dentists.

朗格汉斯细胞组织细胞增多症发展为全身性疾病的未被识别的口腔表现
一名2岁半男童因腭部、颊部及牙槽区出现红斑及溃疡而转介口腔内科。不幸的是,此后每隔6个月到我科就诊两次,并在儿科肿瘤诊所重新评估,最终确诊为朗格汉斯细胞组织细胞增生症(LCH)。在这个阶段,疾病已经发展到危及多系统,需要积极的治疗。因此,这个病例提醒我们这种罕见的疾病在口腔中发生的可能性,它可能表现为多种表现,容易导致误诊,因此很容易被牙医忽视。
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