Inserra Maria Cristina, Di Mari Alessia, Passaniti Giulia, Cannizzaro Maria Teresa, La Rosa Giuliana, Poli Daniela, Gitto Placido, Patanè Laura, Romeo Placido
CAST Radiology Department, A.U.O. Policlinico "G.Rodolico-San Marco," Catania, Italy.
Department of Medical Surgical Sciences and Advanced Technologies "GF Ingrassia," University Hospital Policlinico "G. Rodolico-San Marco," Catania, Italy.
Glob Med Genet. 2023 Oct 10;10(4):271-277. doi: 10.1055/s-0043-1775980. eCollection 2023 Dec.
Arterial tortuosity syndrome (ATS) is a very rare autosomal recessive disorder that affects the connective tissue. The incidence of ATS is not well known and to date only 106 patients have been described in the literature. ATS affects medium and large size arteries, leading to widespread elongation and intensification of the average vessel tortuousness, responsible of several loops and kinks. Like other connective tissue disorders, ATS can present with joint laxity, hernias, pectus excavatum, scoliosis or other musculoskeletal abnormalities, and ocular defects. Due to the extreme variability of clinical symptoms and the fact that ATS has no curative management, prompt diagnosis is of tremendous importance to prevent disease-associated complications. In this situation, imaging techniques have a central role. In this study, we describe a rare case of a male newborn with tortuosity and lengthening of the main arterial and venous medium and large caliber branches with associated aortic coarctation who passed away prematurely. The finding of aortic coarctation in a newborn with ATS has rarely been described in the literature.
动脉迂曲综合征(ATS)是一种非常罕见的常染色体隐性遗传病,会影响结缔组织。ATS的发病率尚不清楚,迄今为止,文献中仅描述了106例患者。ATS会影响中大型动脉,导致平均血管迂曲广泛延长和加剧,形成多个袢和扭结。与其他结缔组织疾病一样,ATS可表现为关节松弛、疝气、漏斗胸、脊柱侧弯或其他肌肉骨骼异常以及眼部缺陷。由于临床症状的极端变异性以及ATS尚无治愈性治疗方法,因此及时诊断对于预防疾病相关并发症极为重要。在这种情况下,成像技术起着核心作用。在本研究中,我们描述了一例罕见的男性新生儿病例,其主要中大型动静脉分支迂曲并延长,伴有主动脉缩窄,该患儿过早夭折。文献中很少描述患有ATS的新生儿出现主动脉缩窄的情况。