Yu Guohua, Huang Fei, Kong Lingling, Kong Xiangmei, Zhang Luping, Xu Qing
Department of Pathology, Yuhuangding Hospital, China.
Turk J Pediatr. 2010 Sep-Oct;52(5):548-51.
Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is a rare disorder 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.
朗格汉斯细胞组织细胞增多症(LCH),以前称为组织细胞增多症X,是一种罕见的疾病,其特征是病理性朗格汉斯细胞的克隆增殖和过度积累,导致局部或全身效应。骨骼是最常受累的器官,单个颅骨病变是儿童LCH最常见的表现。然而,蝶窦受累在LCH中并不常见。在此,我们报告一例发生在蝶窦的LCH病例,该病例发生在一名7岁女孩身上,她最初表现为头痛。该女孩在去看耳鼻喉科医生的一周前已经头痛了一个月。磁共振成像(MRI)显示为炎性肉芽肿病变。进行了手术,通过苏木精-伊红(H&E)染色和免疫组织化学染色,病理诊断该疾病为单部位LCH。