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Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type

机译:Ito型(Hypomelanosis)色素镶嵌术中的总半数过度生长

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摘要

Pigmentary mosaicism of the (hypomelanosis of) Ito type is an umbrella term, which includes phenotypes characterized by mosaic hypopigmentation in the form of streaks, whorls, patchy, or more bizarre skin configurations (running along the lines of Blaschko): these cutaneous patterns can manifest as an isolated skin disorder (pigmentary mosaicism of the Ito type) or as a complex malformation syndrome in association with extracutaneous anomalies (most often of the musculoskeletal and/or nervous systems) (hypomelanosis of Ito). Affected individuals are anecdotally reported to have also partial or total body hemi-overgrowth (HOG), which often causes moderate to severe complications.We studied the occurrence and features of HOG in the 114 children and adults with mosaic pigmentary disorders of the Ito type diagnosed and followed up (from 2 to 22 years; average follow-up 16 years) at our Institutions.Eight patients (5 M, 3 F; aged 4 to 25 years; median age 16 years) out of the 114 analyzed (7%) fulfilled the criteria for unilateral HOG, with differences in diameter ranging from 0.4 to 4.0 cm (upper limbs) and 1.0 to 9.0 cm (lower limbs). Moreover, among these 8 patients, 5/8 filled in the 75th to 90th percentile for height; 6/8 had associated kyphoscoliosis; and 5/8 showed cognitive delays. No tumour complications were recorded. Overall, 6/8 HOG patients presented with additional (extracutaneous) syndromic manifestations, apart from the HOG (ie, with a clinical phenotype of hypomelanosis of Ito).The present study, which includes children and adults with the longest follow-up so far recorded, confirms the association between pigmentary mosaicism of the Ito type and HOG lowering previous estimates (7% vs 16%) for HOG in the context of mosaic hypopigmentation. A careful examination, looking at subtle to moderate asymmetries and associated complications within the spectrum of these mosaic pigmentary disorders, is recommended.
机译:Ito型(色素沉着病)的色素沉着症是一个笼统的术语,包括表现为斑纹,轮生,斑片或更怪异的皮肤形态(沿着Blaschko的线条)形式的镶嵌色素沉着不足的表型:这些皮肤形态可以表现为孤立的皮肤疾病(伊藤型色素沉着症)或伴有皮外异常(最常见的是肌肉骨骼和/或神经系统)的复杂畸形综合症(伊藤断hy症)。据报道,受影响的个体还存在部分或全身半过度生长(HOG),这通常会导致中度至严重的并发症。我们研究了114例确诊为Ito型镶嵌色素性疾病的儿童和成人中HOG的发生和特征在我们的机构中​​进行了随访(从2到22岁;平均随访16年)。在分析的114例患者中,有8例(5 M,3 F; 4至25岁;中位年龄16岁)符合单侧HOG的标准,直径差异在0.4至4.0µcm(上肢)和1.0至9.0µcm(下肢)之间。此外,在这8名患者中,有5/8位患者的身高在第75至90位之间; 6/8伴有脊柱后凸畸形; 5/8表示认知迟缓。没有记录到肿瘤并发症。总体而言,除HOG(即伊托黑素瘤的临床表型)外,有6/8名HOG患者表现出其他(皮下)症状。本研究包括随访时间最长的儿童和成人。记录表明,在马赛克色素沉着的情况下,Ito型色素镶嵌症与HOG降低了先前的HOG估计值(7%对16%)之间的关联。建议仔细检查,以检查这些镶嵌色素性疾病范围内的中度到中度不对称以及相关并发症。

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