McClelland Shearwood, Charnas Lawrence R, SantaCruz Karen S, Garner Hart P, Lam Cornelius H
Department of Neurosurgery, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
J Neurosurg. 2007 Dec;107(6 Suppl):500-3. doi: 10.3171/PED-07/12/500.
Neurocutaneous melanosis (NM) coexisting with the Dandy-Walker complex (DWC) is a rare condition, with fewer than 15 cases reported in the literature. The authors present a case of an infant with NM and DWC suffering from progressive brainstem compression following ventriculoperitoneal (VP) shunt placement for hydrocephalus. This 1-year-old boy with congenital melanocytic nevi had met normal developmental milestones until the age of 11 months, when he began regressing in ambulation and language function. Intractable vomiting had developed 1 week later. Magnetic resonance (MR) imaging of the brain revealed DWC with hydrocephalus, and spinal MR images demonstrated a proliferative process within the meninges, consistent with NM. The patient underwent right frontal VP shunt placement resulting in immediate symptom relief, but 3 weeks later became irritable, increasingly lethargic, unable to pull to stand, and unable to tolerate solid food without choking. Due to these symptoms and intractable vomiting, the patient presented to the authors' institution. Brain MR imaging revealed a new-onset diffuse cystic process with anterior and posterior brainstem compression, marked kinking of the cervicomedullary junction, melanocyte pigmentation of the left temporal lobe, diffuse leptomeningeal enhancement, and no evidence of hydrocephalus. Consistent with these imaging findings, the degree of brainstem involvement upon gross visualization predictably deterred resection attempts beyond those necessary for biopsy. Pathological examination revealed diffuse melanocytosis, and the family decided not to pursue aggressive measures postoperatively. This report indicates the potential for rapid intracranial manifestation of diffuse melanocytosis in NM patients. Although the prognosis is poor, early neurosurgical involvement in these patients may provide tissue diagnosis and the potential for decompression if the process is caught early in its course.
神经皮肤黑素沉着症(NM)与丹迪-沃克复合体(DWC)并存是一种罕见病症,文献报道的病例不足15例。作者报告了1例患有NM和DWC的婴儿病例,该婴儿因脑积水行脑室腹腔(VP)分流术后出现进行性脑干受压。这个1岁先天性黑素细胞痣男孩在11个月大之前发育正常,之后其行走和语言功能开始退化。1周后出现顽固性呕吐。脑部磁共振(MR)成像显示DWC伴脑积水,脊柱MR图像显示脑膜内有增生性病变,符合NM表现。患者接受了右侧额叶VP分流术,术后症状立即缓解,但3周后变得烦躁、愈发嗜睡,无法扶站,无法耐受固体食物且进食时易呛噎。由于这些症状和顽固性呕吐,患者转诊至作者所在机构。脑部MR成像显示出现新的弥漫性囊性病变,伴有脑干前后受压、颈髓交界处明显扭结、左侧颞叶黑素细胞色素沉着、软脑膜弥漫性强化,且无脑积水迹象。与这些影像学表现一致,肉眼观察到的脑干受累程度可预见地阻碍了活检以外的切除尝试。病理检查显示弥漫性黑素细胞增多,家属决定术后不采取积极治疗措施。本报告提示NM患者弥漫性黑素细胞增多症有迅速出现颅内表现的可能。尽管预后较差,但对于这些患者,早期神经外科干预可能有助于进行组织诊断,并在病程早期发现病变时提供减压的可能性。