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新生儿出生时即有一个大型先天性黑素细胞痣,其上出现结节性损害,伴发播散性 Spitz 痣疹样发疹。

Nodular lesions arising in a large congenital melanocytic naevus in a newborn with eruptive disseminated Spitz naevi.

机构信息

Department of Dermatology, Hospital Universitario La Paz, Universidad Autónoma de Madrid, 28046 Madrid, Spain.

出版信息

Br J Dermatol. 2011 Nov;165(5):1138-42. doi: 10.1111/j.1365-2133.2011.10502.x.

Abstract

Congenital malignant melanoma within a pre-existing large congenital melanocytic naevus (CMN) is exceedingly rare. Its incidence is difficult to determine due to the small number of reported cases and because of problems associated with diagnosis. Some benign nodular proliferations (called proliferative nodules) arising in CMN, while rare, are significantly more common and can mimic malignant melanoma clinically or histologically. There are no reported cases of congenital melanoma or benign proliferative nodules in CMN in patients who also had eruptive disseminated Spitz naevi. We describe a girl who was noted to have a dark-brown plaque with several large erythematous nodules affecting the scalp at delivery, in addition to multiple erythematous dome-shaped papules that developed in a disseminated manner over several months, beginning at 10 days of age. It was difficult, not only clinically but also histologically, to determine the benign or malignant nature of all of these lesions. As primary cutaneous melanoma, atypical proliferative nodules in CMN, bland CMN or CMN with foci of increased cellularity and Spitz naevi show clear differences in the genetic aberration patterns, comparative genomic hybridization (CGH) could be a diagnostic help in ambiguous cases such as this. CGH performed on this patient showed multiple DNA copy number changes in the most atypical nodule, but such alterations could not be found in the remainder of the lesions. CGH showed differences between the nodular lesions that occurred in the CMN and helped us in supporting the diagnosis of this unique case of benign proliferative nodules and a possible congenital melanoma arising in a large CMN, associated with multiple widespread eruptive Spitz naevi.

摘要

先天性恶性黑色素瘤合并原有大型先天性黑色素细胞痣(CMN)极为罕见。由于报告病例数量较少,且诊断相关问题,其发病率难以确定。一些在 CMN 中发生的良性结节性增生(称为增生性结节)虽然罕见,但更为常见,在临床上或组织学上可模拟恶性黑色素瘤。在同时患有播散性 Spitz 痣的患者中,尚未有先天性黑色素瘤或 CMN 中的良性增生性结节的报告病例。我们描述了一名女孩,她在分娩时被发现头皮上有一个暗褐色斑块,伴有几个大的红斑结节,此外,在出生后 10 天开始,还出现了多个以播散方式分布的红斑状圆顶丘疹。这些病变不仅在临床上,而且在组织学上,其良性或恶性性质都很难确定。由于原发性皮肤黑色素瘤、CMN 中的非典型增生性结节、良性 CMN 或 CMN 中伴有细胞增多灶和 Spitz 痣,在遗传异常模式上存在明显差异,因此比较基因组杂交(CGH)可能有助于诊断这种模棱两可的病例。对该患者进行的 CGH 显示在最不典型的结节中有多个 DNA 拷贝数改变,但在其余病变中未发现这些改变。CGH 显示了 CMN 中发生的结节性病变之间的差异,并帮助我们支持了该独特病例的良性增生性结节和可能起源于大型 CMN 的先天性黑色素瘤的诊断,该病例与多发性广泛播散性 Spitz 痣有关。

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