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The diagnostic value of skin lesions in split cord malformations.

机译:皮损对裂脐畸形的诊断价值。

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摘要

Split cord malformations (SCMs) are rare congenital anomalies of the spine which are usually diagnosed and treated in early childhood. Asymptomatic patient can appear in adult life without diagnosis. Cutaneous signs are often the initial marker of congenital spine abnormalities, especially SCMs. Although numerous cutaneous lesions have been described that may occur with SCMs including abnormal hair growth, hemangiomas, telengiectasias, pigmentation anomalies, subcutaneous mass lesions, and dermal sinus tracts, there is no study demonstrating a correlation between skin lesions and the type of SCM. We reported the cutaneous findings of 14 adult patients who were investigated clinically and radiologically with a diagnosis of SCM. Hypertrichosis was the most common cutaneous lesion (79%) and faun tail was observed among six (55%) of the 11 patients who had hypertrichosis. The SCM was type I in all of the patients with faun tail. Silky down was observed among 5 (45%) patients as a solitary skin lesion or associated with dysplastic skin or capillary hemangioma. A statistically significant correlation between the skin markers and the type of SCM was found, and this correlation can help physicians weigh their diagnostic considerations in SCM.
机译:脊髓分裂畸形(SCM)是脊柱罕见的先天性畸形,通常在儿童早期就得到诊断和治疗。无症状患者可在成人生活中出现而无需诊断。皮肤症状通常是先天性脊柱异常的初始标志,特别是SCM。尽管已经描述了SCM可能发生的许多皮肤损伤,包括异常的毛发生长,血管瘤,玻璃体细支气管扩张,色素沉着异常,皮下块状损伤和皮肤窦道,但尚无研究表明皮肤损伤与SCM类型之间存在相关性。我们报告了14位成年患者的皮肤发现,这些患者经临床和放射学检查诊断为SCM。高毛发症是最常见的皮肤病变(79%),在11名高毛发症患者中有6名(55%)观察到了法恩尾巴。在所有患有Faun尾巴的患者中,SCM均为I型。在5名(45%)患者中观察到柔滑下来是孤立的皮肤病变或与增生性皮肤或毛细血管血管瘤相关。发现皮肤标志物和SCM类型之间具有统计上的显着相关性,这种相关性可以帮助医生权衡他们在SCM中的诊断考虑因素。

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