Langerhans cell hystiocytosis mimicking necrotizing ulcerative periodontitis - A case report

Antu Kizhakethodikayil, Manisha Tanaji Sherkhane, Bindu Pekkodath, D. Devraj, L. Thomas, N. Kumar
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Abstract

Langerhans cell histiocytosis (LCH) is a rare disease characterized by abnormal proliferation of bone marrow derived histiocytes followed by their deposition in tissues elsewhere in the body causing damage. Oral manifestations of LCH can sometimes be the only presenting symptoms or the first sign of a disseminated disease. Ulcerated lesions of oral mucosa are one of the common clinical manifestations and can help in early diagnosis of the disease when presented. Since the clinical features mimics several other diseases of oral and maxillofacial region it can be misdiagnosed easily as other pathologies. This article highlights the clinicopathological features of a case of LCH in an elderly patient who has reported to our outpatient department.
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朗格汉斯细胞增生模拟坏死性溃疡性牙周炎1例报告
朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的疾病,其特征是骨髓来源的组织细胞异常增殖,然后沉积在身体其他组织中造成损伤。LCH的口腔表现有时可能是唯一的表现症状或播散性疾病的第一个征兆。口腔黏膜溃疡性病变是常见的临床表现之一,当出现溃疡性病变时有助于早期诊断。由于临床特征与口腔颌面部其他几种疾病相似,极易误诊为其他病变。这篇文章强调了一例LCH的老年患者的临床病理特点,谁已经报告到我们的门诊部。
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