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Langerhans cell histiocytosis of the sphenoid sinus: a case report

机译:蝶窦朗格汉斯细胞组织细胞增生症1例

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摘要

Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is a rare disordeE characterized by clonal proliferation and excess accumulation of pathologic langerhans cells causing local or systemic effects. Bone is the most common organ involved and a single skull lesion is the most frequent presentation of childhood LCH. However, sphenoid sinus is an uncommon condition of involvement in LCH. Here we report a case of LCH in the sphenoid sinus, which occurred in a seven-year-old girl who presented initially with headache. The girl had suffered from headache for one month before she went to an otorhinolaryngologist one week before. Magnetic resonance imaging (MRI) showed a lesion of inflammatory granuloma. Surgery was performed and the disease was diagnosed pathologically as single-site LCH via hematoxylin-eosin (H&E) and immunohistochemical staining.
机译:朗格汉斯细胞组织细胞增生症(LCH),以前称为组织细胞增生症X,是一种罕见的disordeE,其特征是克隆性增殖和病理性朗格汉斯细胞的过量积累引起局部或全身性作用。骨骼是最常见的脏器,而单个颅骨病变是儿童LCH最常见的表现。但是,蝶窦是LCH的罕见情况。在这里,我们报告了蝶窦中的LCH病例,该病例发生在最初出现头痛的7岁女孩中。这个女孩头痛了一个月,一个星期前去了耳鼻喉科医生。磁共振成像(MRI)显示炎性肉芽肿病灶。进行手术,并通过苏木精-伊红(H&E)和免疫组化染色在病理上诊断为单部位LCH。

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