Department of Pediatric, University Hospitals Leuven, Leuven, Belgium.
Orphanet J Rare Dis. 2010 Dec 8;5:37. doi: 10.1186/1750-1172-5-37.
Rothmund-Thomson syndrome (RTS)(OMIM 268400) is a rare autosomal recessive genodermatosis characterized by poikiloderma, small stature, skeletal and dental abnormalities, cataract and an increased risk of cancer. It is caused by mutations in RECQL4 at 8q24. Immune deficiency is not described as a classical feature of the disease. Here we report the appearance of granulomatous skin lesions complicating primary Varicella Zoster Virus infection in a toddler with Rothmund Thomson syndrome and immune deficiency. Although granulomatous disorders are sometimes seen after Herpes zoster, they are even more rare after Varicella primary infection. Granulomas have hitherto not been described in Rothmund-Thomson syndrome. With this report we aim to stress the importance of screening for immune deficiency in patients with Rothmund-Thomson syndrome.
Rothmund-Thomson 综合征(RTS)(OMIM 268400)是一种罕见的常染色体隐性遗传皮肤-骨-牙综合征,其特征为斑驳色素沉着、身材矮小、骨骼和牙齿异常、白内障和癌症风险增加。它是由 8q24 上 RECQL4 基因突变引起的。免疫缺陷并不是该疾病的经典特征。在这里,我们报告了一名患有 Rothmund-Thomson 综合征和免疫缺陷的幼儿在原发性水痘带状疱疹病毒感染后出现肉芽肿性皮肤病变。尽管在带状疱疹后有时会出现肉芽肿性疾病,但在水痘原发性感染后更为罕见。肉芽肿性疾病在 Rothmund-Thomson 综合征中迄今尚未被描述。通过本报告,我们旨在强调对 Rothmund-Thomson 综合征患者进行免疫缺陷筛查的重要性。