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首页> 外文期刊>Pediatric dermatology >Analysis of 36 cases of blaschkoid dyspigmentation: Reading between the lines of Blaschko
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Analysis of 36 cases of blaschkoid dyspigmentation: Reading between the lines of Blaschko

机译:blaschkoid色素沉着症36例分析:Blaschko的血缘阅读

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Genetic mosaicism indicated by lines of Blaschko pigmentary changes has been described under a number of different and confusing terms, including hypomelanosis of Ito, linear and whorled nevoid hypermelanosis, nevus depigmentosus, and cutis tricolor. Moreover, extracutaneous findings, particularly serious neurologic defects, have been reported in a large number of these cases. We reviewed the cutaneous and extracutaneous findings in 36 patients referred to the Harriet Lane Pediatric Dermatology Clinic, Johns Hopkins University, from June 12, 2008, to May 24, 2009, for evaluation of macular lesions along the lines of Blaschko. Patients with dyspigmentation along the lines of Blaschko and no history of preceding inflammatory skin lesions were identified for inclusion in a database at their initial visit. Information on age at presentation; sex; age when first diagnosed; type, pattern, and location of the pigmentary anomaly; and extracutaneous abnormalities noted on a review-of-systems questionnaire and physical examination was recorded for each child. Patients were asked to follow up within 6 to 12 months of the initial visit. Patients included 13 boys and 23 girls ages 3 months to 15 years with lesions noted from birth to 12 years. Lesions were hypopigmented in 21 patients and hyperpigmented in 15. No patients presented with hypopigmented and hyperpigmented lesions. Extracutaneous findings were noted in five children (13.9%). Historically, cases of Blaschkoid hypopigmentation and hyperpigmentation have been associated with a high percentage of extracutaneous manifestations, particularly neurologic and neurodevelopmental defects. In our study, only five patients (13.9%) were noted to have extracutaneous abnormalities, and these findings may have been coincidental. We propose the term 'Blaschkoid dyspigmentation' to describe the cutaneous findings. Although serious extracutaneous findings may occur in children with Blaschkoid dyspigmentation and results of careful physical examination and review of systems should direct an evaluation, serious extracutaneous findings occur in a minority of patients.
机译:Blaschko色素变化系所指示的遗传镶嵌性已在许多不同且令人困惑的术语下进行了描述,包括伊托黑素病,线状和轮状无间隙黑素病,痣脱皮和三色角质。此外,在许多这类病例中已报道了皮外发现,特别是严重的神经系统缺陷。我们回顾了2008年6月12日至2009年5月24日期间转诊至约翰霍普金斯大学哈里特·莱恩小儿皮肤病诊所的36例患者的皮肤和皮外发现,以评估Blaschko的黄斑病变。在初次就诊时,已将患有Blaschko路线上色素沉着的患者和先前无炎症性皮肤病史的患者确定为数据库中的患者。演讲时的年龄信息;性别;首次诊断的年龄;色素异常的类型,样式和位置;系统回顾问卷中记录了皮下异常情况,并对每个孩子进行了身体检查。要求患者在初次就诊后6到12个月内进行随访。患者包括年龄在3个月至15岁之间的13名男孩和23名女孩,从出生到12岁均发现病灶。皮损为色素沉着的有21例,色素沉着为15的患者。没有患者出现色素沉着和色素沉着的病变。注意到有五个儿童(13.9%)的皮外发现。从历史上看,Blaschkoid色素沉着和色素沉着过多的病例与高比例的皮外表现有关,尤其是神经系统和神经发育缺陷。在我们的研究中,仅五名患者(13.9%)被发现有皮外异常,这些发现可能是偶然的。我们提出术语“ Blaschkoid色素沉着”来描述皮肤发现。尽管患有Blaschkoid色素沉着的儿童可能会出现严重的皮下发现,并且应仔细评估体检和系统检查的结果来指导评估,但少数患者会出现严重的皮下发现。

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