Auvin Stéphane, Cuvellier Jean-Christophe, Vinchon Mathieu, Defoort-Dhellemes Sabine, Soto-Ares Gustavo, Nelken Brigitte, Vallée Louis
Department of Pediatric Neurology, University Hospital, Lille, France.
Brain Dev. 2008 Feb;30(2):164-8. doi: 10.1016/j.braindev.2007.07.004. Epub 2007 Aug 27.
Juvenile xanthogranuloma (JXG) is one of the most common non-Langerhans cell histiocytosis in children. Usually cutaneous, there are disseminated forms. However, neurological localization remains exceptional. A 7-month-old boy had been admitted for subdural effusion due to non-accidental head injury and skin nodular lesions. A biopsy of a skin lesion was considered suggestive of JXG. Skin, eyes, brain, lungs, liver, and testicles were involved. Systemic treatment of JXG was begun with vinblastine. It allowed the regression of skin, lung, and CNS lesions. At age of 11 years, he had not reappearance of the xanthogranuloma. This report emphasizes the possible presentation of xanthogranuloma with subdural effusions, the organs which should be examined in case of disseminated forms and the efficiency of vinblastin.
幼年性黄色肉芽肿(JXG)是儿童中最常见的非朗格汉斯细胞组织细胞增生症之一。通常累及皮肤,也有播散型。然而,神经定位仍较为罕见。一名7个月大的男孩因非意外性头部损伤导致硬膜下积液和皮肤结节性病变入院。皮肤病变活检提示为JXG。病变累及皮肤、眼睛、脑、肺、肝和睾丸。开始用长春新碱对JXG进行全身治疗。这使得皮肤、肺和中枢神经系统病变消退。11岁时,他的黄色肉芽肿未再复发。本报告强调了黄色肉芽肿可能伴有硬膜下积液的表现、播散型病例应检查的器官以及长春新碱的疗效。