Martínez-Lage Juan F, Almagro María José, Ferri-Ñiguez Belén, Izura Azanza Virginia, Serrano Cristina, Domenech Ernesto
Regional Service of Neurosurgery, Virgen de la Arrixaca University Hospital, El Palmar, 30120, Murcia, Spain.
Childs Nerv Syst. 2011 Apr;27(4):609-16. doi: 10.1007/s00381-010-1308-6. Epub 2010 Oct 27.
Occult spinal dysraphism (OSD) encompasses various conditions. A dermal sinus tract (DST) consists of a duct communicating to the skin with deep structures that carries an important risk of infection. A different lesion consisting of a translucent skin opening and a fibrous tract that lacks a lumen can also be found in OSD. We termed this lesion pseudo-dermal sinus tract.
We reviewed clinical features of 20 patients with spinal skin orifices. The patients were classified into two categories: group 1 comprised children with true DST and group 2 included patients with skin dimples resembling a DST.
The aim of this study was to analyze differential features of patients in these two groups as they behaved dissimilarly in regard to clinical significance and outcomes, especially those concerning infectious risk.
Children of group 1 (n = 8) presented with tiny skin orifices and with superficial or deep infection. In contrast, group 2 (n = 12) mostly manifested with neurological symptoms. No patient in group 2 developed an infection preoperatively. In both groups, magnetic resonance showed tracts that ended in different structures. Histopathology of the lesions were dissimilar, those of group 1 being hollow tubular structures lined by epithelium while those of group 2 being solid tracts of fibrous connective tissue.
DST constitutes a clinicopathological diagnosis. Although sharing some common cutaneous and neuroimaging findings, both groups behaved differently. Patients of group 1 tended to show up with infection requiring urgent surgery. Patients of group 2 often presented with neurological manifestations and skin lesions, but needed no immediate operation.
隐匿性脊柱裂(OSD)包含多种病症。皮样窦道(DST)是一种与皮肤和深部结构相通的管道,具有重要的感染风险。在OSD中还可发现另一种由半透明皮肤开口和无管腔的纤维束组成的病变。我们将这种病变称为假性皮样窦道。
我们回顾了20例脊柱皮肤开口患者的临床特征。患者分为两类:第1组为患有真性DST的儿童,第2组包括皮肤酒窝样病变类似DST的患者。
本研究的目的是分析这两组患者的差异特征,因为它们在临床意义和预后方面表现不同,尤其是在感染风险方面。
第1组(n = 8)的儿童表现为微小的皮肤开口以及浅表或深部感染。相比之下,第2组(n = 12)大多表现为神经症状。第2组术前无患者发生感染。两组磁共振成像均显示纤维束终止于不同结构。病变的组织病理学不同,第1组为内衬上皮的中空管状结构,而第2组为纤维结缔组织的实性纤维束。
DST构成一种临床病理诊断。尽管两组有一些共同的皮肤和神经影像学表现,但表现不同。第1组患者倾向于出现需要紧急手术的感染。第2组患者常表现为神经症状和皮肤病变,但无需立即手术。