Department of Dermatology, The Second Xiangya Hospital of Central South University, Changsha, China.
Am J Dermatopathol. 2022 Apr 1;44(4):287-290. doi: 10.1097/DAD.0000000000002117.
Xanthoma disseminatum (XD) is a rare non-Langerhans cell histiocytosis characterized by xanthomatous lesions in the absence of hyperlipidemia. XD usually develops in young adults, and there are rare cases among children. BRAF mutations are frequent in Langerhans cell histiocytosis and Erdheim-Chester disease but absent or only rarely detected in other histiocytosis. Herein, we described a 6-year-old Chinese girl presented with generalized skin lesions and diabetes insipidus for 5 months. There were multiple periorbital xanthelasma with histopathological features of foamy histiocytes infiltration with Touton cells. Pituitary magnetic resonance imaging showed pituitary enlargement and pituitary stalk thickening. The presence of BRAF p.V600E mutation makes this case distinctive and also offers a potential therapeutic target. According to our review of the literature, this is the first pediatric XD with diabetes insipidus and BRAF mutation.
播散性黄色瘤(XD)是一种罕见的非朗格汉斯细胞组织细胞增生症,其特征为黄色瘤病变,无高脂血症。XD 通常发生在年轻成年人中,儿童中罕见。BRAF 突变在朗格汉斯细胞组织细胞增生症和 Erdheim-Chester 病中很常见,但在其他组织细胞增生症中缺失或很少检测到。在此,我们描述了一名 6 岁中国女孩,因全身皮肤病变和 5 个月的尿崩症就诊。有多发性眶周黄色瘤,组织病理学特征为泡沫状组织细胞浸润伴 Touton 细胞。垂体磁共振成像显示垂体增大和垂体柄增粗。BRAF p.V600E 突变的存在使该病例具有特征性,也提供了一个潜在的治疗靶点。根据我们对文献的回顾,这是首例伴有尿崩症和 BRAF 突变的儿童 XD。