Kentab Amal Y, Hassan Hamdy H, Hamad Muddathir H A, Alhumidi Ahmed
(1) Division of Paediatric Neurology, Department of Paediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
(2) Department of Radiology, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Sudan J Paediatr. 2014;14(2):61-70.
The term hypomelanosis of Ito (HI) is applied to individuals with skin hypopigmentation along the lines of Blaschko. Although it was originally described as a purely cutaneous disease, subsequent studies describing HI reported a 33% to 94% association with multiple extracutaneous manifestations, mostly of the central nervous and musculoskeletal systems. This leads to characterization of HI as a neurocutaneous disorder. We report a 10-year-old boy who presented with constellation of multiple congenital anomalies including facial dysmorphism, skin hypopigmentation, musculoskeletal, and nervous system abnormalities. The latter manifested as hypotonia, generalized seizures, and mild mental retardation. Cranial magnetic resonance imaging revealed normal finding initially, however; follow-up diffusion weighted images were suggestive of a possible iron accumulation. The facial phenotype coupled with the bilateral globus pallidi lesions were never been reported in association with HI. Thus, our patient represents a possible novel example of HI.
伊藤色素减退症(HI)这一术语用于描述沿布拉斯科线出现皮肤色素减退的个体。尽管它最初被描述为一种纯粹的皮肤病,但随后关于HI的研究报告称,它与多种皮肤外表现存在33%至94%的关联,这些表现大多涉及中枢神经和肌肉骨骼系统。这使得HI被归类为一种神经皮肤疾病。我们报告了一名10岁男孩,他出现了多种先天性异常,包括面部畸形、皮肤色素减退、肌肉骨骼和神经系统异常。后者表现为肌张力减退、全身性癫痫发作和轻度智力障碍。最初的头颅磁共振成像显示结果正常,然而,后续的弥散加权成像提示可能存在铁沉积。这种面部表型与双侧苍白球病变同时出现的情况此前从未被报道与HI相关联。因此,我们的患者可能是HI的一个新病例。