Rai Santosh, Kalakoti Piyush, Syed Mm Aarif, Thacker Purujit J, Jain Rishi, Kalra Gaurav
Pravara Rural Hospital and Rural Medical College, Loni, Maharashtra, 413736, India.
J Med Case Rep. 2011 Jul 1;5:267. doi: 10.1186/1752-1947-5-267.
Congenital melanocytic nevi are among the several known risk factors for the development of melanoma. Neurocutaneous melanosis is a rare, congenital, non-hereditary disorder characterized by the presence of multiple and/or giant congenital melanocytic nevi. It is a rare condition, with fewer than 200 cases reported in the literature. Its association with tuberous sclerosis complex, a form of the neurocutaneous syndrome, is an unusual finding which, to the best of our knowledge, has not been documented in the English literature so far. Herein we present the first case documenting such an association in a 16-year-old post-pubertal Indian girl.
In this report, we describe the case of a 16-year-old Indian girl who presented to our hospital with swelling on the scalp which had progressed from the hairline to just above the left brow, causing mechanical ptosis. She was born with a black-pigmented triangular patch covered with hair over the scalp which had increased in size over a period of eight years after birth. An X-ray of her skull and ultrasonography revealed soft tissue swelling in the left temporofrontoparietal region. Magnetic resonance imaging of her brain showed the presence of 8.99 cm × 2.26 cm abnormal signal intensity involving the scalp, a few small tubers with cortical dysplasia in the left frontoparietal region with asymmetric dilatation, and the presence of calcified subependymal nodules within the left lateral ventricle. These findings were suggestive of tuberous sclerosis. A histopathological examination of the swelling was suggestive of congenital melanocytic nevi. The patient underwent surgery. Excision of the tumor with primary skin grafting was done, with the graft being taken from the medial aspect of the right thigh.
This case warrants further research to provide concrete evidence of an association of neurocutaneous melanoma with tuberous sclerosis complex. Research should be conducted to prove whether this is an unusual association or a new syndrome. Also, similar cases in other parts of the globe should be documented, as they would provide substantial support for such an association.
先天性黑素细胞痣是已知的黑色素瘤发生的几种危险因素之一。神经皮肤黑素沉着症是一种罕见的先天性非遗传性疾病,其特征是存在多个和/或巨大的先天性黑素细胞痣。这是一种罕见病症,文献报道的病例少于200例。其与结节性硬化症(一种神经皮肤综合征)的关联是一个不寻常的发现,据我们所知,迄今为止英文文献中尚未有记载。在此,我们报告首例记录一名16岁青春期后印度女孩存在这种关联的病例。
在本报告中,我们描述了一名16岁印度女孩的病例,她因头皮肿胀前来我院就诊,肿胀从发际线延伸至左眉上方,导致机械性上睑下垂。她出生时头皮上有一块黑色色素沉着的三角形毛发覆盖斑块,出生后八年间面积不断增大。她的颅骨X线检查和超声检查显示左颞额顶部软组织肿胀。脑部磁共振成像显示头皮存在8.99 cm×2.26 cm异常信号强度,左额顶叶区域有一些伴有皮质发育异常的小结节且不对称扩张,左侧脑室内有钙化的室管膜下结节。这些发现提示结节性硬化症。肿胀部位的组织病理学检查提示先天性黑素细胞痣。患者接受了手术。进行了肿瘤切除及一期皮肤移植,移植皮片取自右大腿内侧。
该病例值得进一步研究,以提供神经皮肤黑素沉着症与结节性硬化症关联的确切证据。应开展研究以证明这是一种异常关联还是一种新综合征。此外,全球其他地区的类似病例也应记录在案,因为这将为这种关联提供有力支持。