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新生儿巨大先天性黑素细胞痣:两例报告。

Giant congenital melanocytic nevi in neonates: report of two cases.

机构信息

Department of Pediatrics, Lo-Tung Pohai Hospital, Ilan, Taiwan.

出版信息

Pediatr Neonatol. 2010 Feb;51(1):61-4. doi: 10.1016/S1875-9572(10)60012-5.

Abstract

Giant congenital melanocytic nevi are rare, with an estimated incidence of approximately 1 in 20,000 live births. They increase the lifetime risk for malignant melanoma and neurological deficits, including leptomeningeal melanocytosis and epilepsy. Recently, we encountered two patients in whom giant congenital melanocytic nevi were noted at birth. Case 1 presented with the largest nevus spreading across the posterior scalp, neck, chest wall, shoulder and upper back. At the age of 2 months, magnetic resonance imaging (MRI) was performed and no leptomeningeal melanocytosis was found. Case 2 presented with a huge nevus covering most parts of the lower abdomen, lower back, buttocks and bilateral upper thighs. She also had normal MRI findings in the newborn period. At the age of 7 years, leptomeningeal thickening on the surface of the junction between the pons and midbrain was found on brain MRI although she was neurologically asymptomatic. Here, we describe these two cases with congenital melanocytic nevi and review the literature about its clinical manifestations, outcomes, risks for malignant melanoma and neurocutaneous melanosis, and possible surgical interventions.

摘要

先天性巨大黑素细胞痣罕见,估计每 20000 例活产儿中约有 1 例。它们会增加恶性黑色素瘤和神经缺陷的终身风险,包括软脑膜黑素细胞增多症和癫痫。最近,我们遇到了两名出生时就患有先天性巨大黑素细胞痣的患者。病例 1 的痣最大,分布在后头部、颈部、胸壁、肩部和上背部。2 个月大时进行了磁共振成像(MRI)检查,未发现软脑膜黑素细胞增多症。病例 2 出生时就有一个巨大的痣,覆盖了下腹、下背部、臀部和双侧大腿上部的大部分区域。新生儿期 MRI 检查结果正常。7 岁时,脑 MRI 发现脑桥和中脑交界处表面脑膜增厚,尽管她没有神经系统症状。在此,我们描述了这两例先天性黑素细胞痣患者,并回顾了其临床表现、结局、恶性黑色素瘤和神经皮肤黑变病的风险以及可能的手术干预的相关文献。

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