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儿童皮肤局限性朗格汉斯细胞组织细胞增多症

Skin-limited Langerhans' cell histiocytosis in children.

作者信息

Hussein Mahmoud Rezk A

机构信息

Departments of Pathology, Assir Central (Abha, KSA) and Assuit University Hospitals, Assuit University, Assuit Eqypt.

出版信息

Cancer Invest. 2009 Jun;27(5):504-11. doi: 10.1080/07357900802216452.

Abstract

Langerhans' cells are dendritic cells derived from precursors in the bone marrow. They constitute 2-4% of the resident epidermal cells and are found within the epidermis above the basal layer. They function as immunologic cells by recognizing antigens and presenting them to T cell lymphocytes. Langerhans' cell histiocytosis is a rare pathology characterized by an abnormal clonal proliferation of Langerhans' cells that infiltrates different organs of the human body. The proliferating Langerhans' cells appears to be primarily responsible for the clinical manifestations. The stimulus for their proliferation is unknown. Among different organs, cutaneous involvement is encountered in 40% of cases. The aim of this investigation is to review the clinicopathologic, immunologic and ultrastructural features of skin-confined Langerhans' cell histiocytosis in children through seven case series. Four boys and two girls with age range of 1 year to 8 years presented with scaling, crusted papules, nodules and papulonodular lesions (two cases each). The locations included the face (three cases), scalp, trunk and vulva (one case each). The histological features included histiocytic reaction (one case), granulomatous reactions (three cases) and both granulomatous and histiocytic reactions (two cases). The diagnosis was confirmed by histochemical (S-100 + CD1a +) and ultrastructural studies (Birbeck granules). Langerhans' cell histiocytosis is a rare disease with pleomorphic cutaneous clinical expressions. Three types of skin lesions usually occur: nodules (common), scaling, or crusted papules (next in frequency) and finally soft, yellow papular xanthomas (rare). Three types of histological pictures are seen: histiocytic, granulomatous (common) and xanthomatous (rare).

摘要

朗格汉斯细胞是源自骨髓前体细胞的树突状细胞。它们占常驻表皮细胞的2 - 4%,位于基底层上方的表皮内。它们通过识别抗原并将其呈递给T淋巴细胞发挥免疫细胞的功能。朗格汉斯细胞组织细胞增多症是一种罕见的病理学疾病,其特征是朗格汉斯细胞异常克隆增殖并浸润人体的不同器官。增殖的朗格汉斯细胞似乎是临床表现的主要原因。其增殖的刺激因素尚不清楚。在不同器官中,40%的病例会出现皮肤受累。本研究的目的是通过七个病例系列回顾儿童皮肤局限性朗格汉斯细胞组织细胞增多症的临床病理、免疫和超微结构特征。四名男孩和两名女孩,年龄在1岁至8岁之间,表现为鳞屑性、结痂丘疹、结节和丘疹结节性病变(各两例)。病变部位包括面部(三例)、头皮、躯干和外阴(各一例)。组织学特征包括组织细胞反应(一例)、肉芽肿反应(三例)以及肉芽肿和组织细胞反应(两例)。通过组织化学(S - 100 + CD1a +)和超微结构研究(Birbeck颗粒)确诊。朗格汉斯细胞组织细胞增多症是一种罕见疾病,具有多形性皮肤临床表现。通常会出现三种类型的皮肤病变:结节(常见)、鳞屑性或结痂丘疹(其次常见),最后是柔软的黄色丘疹性黄瘤(罕见)。可见三种类型的组织学表现:组织细胞型、肉芽肿型(常见)和黄瘤型(罕见)。

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