颞骨郎格汉斯细胞组织细胞增多症1例报告

Ahmed Abdelrahman Abdelziz, N. Osman, M. Gayyed
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引用次数: 0

摘要

郎格罕细胞组织细胞增多症(LCH)是一种罕见的疾病,其特征是郎格罕氏细胞增殖失控。我们报告一例5岁女孩,左耳后肿胀、耳垂和耳漏持续2个月。颞骨的高分辨率计算机断层扫描显示破坏性的扩张组织密度块。在扩散重量磁共振成像中,表观扩散系数为1.08×10³mm²/s。耳后切口显示粉红色,坚固的肉芽肿性肿块占据中耳和乳突。组织病理学检查显示郎格汉斯组织细胞和嗜酸性粒细胞混合。CD1和S100免疫组化阳性。
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Langerhans Cell Histiocytosis in Temporal Bone: Case Report
Langerhans cell histiocytosis (LCH) is a rare disorder characterized by uncontrolled proliferation of Langerhans cells. We report a case of a 5-years old girl with left post auricular swelling, otalagia and otorrhea of 2 month duration, High resolution computed tomography of temporal bone show destructive expanding tissue density mass. Apparent diffusion coefficient is 1.08×10³ mm²/s in diffusion weight magnetic resonance imaging .Post auricular incision revealed a pinkish, firm granulomatous mass occupied middle ear and mastoid Histopathological examination revealed a mixture of Langerhans histocytes and eosinophils. CD1 and S100 are positive in mmunohistochemistry.
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