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Cutaneous Langerhans cell histiocytosis presenting with hypopigmented lesions: Report of two cases and review of literature

机译:皮肤朗格汉斯细胞组织菌呈呈现出低分气病变:两种病例报告和文学审查

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Abstract Langerhans cell histiocytosis is a rare group of disorders that results from the abnormal proliferation and accumulation of dendritic‐derived cells in various organs of the body, such as the skin and bones. Hypopigmented macules are a rare cutaneous presentation of Langerhans cell histiocytosis that may pose a diagnostic dilemma when no other findings of Langerhans cell histiocytosis are present at the time of examination. We present 2 cases of the hypopigmented variant of Langerhans cell histiocytosis, including a case with histopathologic features of regression, and a review of the literature. These cases highlight the importance of including Langerhans cell histiocytosis in the differential diagnosis of an infant with hypopigmented macules and papules.
机译:摘要朗格汉斯细胞组织细胞症是一种稀有的一组疾病,其来自身体各种器官中树枝状衍生细胞的异常增殖和积累,例如皮肤和骨骼。 低次蛋白杀菌是一种罕见的朗格汉斯细胞组织细胞症的皮肤呈现,当时在检查时没有其他发现朗格汉斯细胞组织菌作用时诊断困境。 我们介绍了朗格汉斯细胞组织细胞症的次次次次次次次患者,包括患有回归的组织病理学特征,以及对文献的综述。 这些案例突出了在婴儿患有低分造的斑疹和丘疹的婴儿的鉴别诊断中含有朗格汉斯细胞组织细胞症的重要性。

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