Kershenovich Amir, Price Angela V, Koral Korgun, Goldman Stan, Swift Dale M
Department of Pediatric Neurosurgery, Children's Medical Center Dallas, University of Texas Southwestern, Dallas, Texas 75235, USA.
J Neurosurg Pediatr. 2008 Nov;2(5):304-9. doi: 10.3171/PED.2008.2.11.304.
The second most frequent central nervous system involvement pattern in Langerhans cell histiocytosis (LCH) is a rare condition documented in a number of reports called "neurodegenerative LCH" (ND-LCH). Magnetic resonance images confirming the presence of the disease usually demonstrate striking symmetric bilateral hyperintensities predominantly in the cerebellum, basal ganglia, pons, and/or cerebral white matter. The authors here describe for the first time in the literature a patient with ND-LCH and concomitant hydrocephalus initially treated using endoscopic third ventriculostomy (ETV). This 9-year-old boy, who had undergone chemotherapy for skin and lung LCH without central nervous system involvement at the age of 10 months, presented with acute ataxia, headaches, and paraparesis and a 1-year history of gradually increasing clumsiness. Magnetic resonance images showed obstructive hydrocephalus at the level of the aqueduct of Sylvius and signs of ND-LCH. After registering high intracranial pressure (ICP) spikes with an intraparenchymal pressure monitor, an ETV was performed. A second ETV was required months later because of ostomy occlusion, and finally a ventriculoperitoneal shunt was placed because of ostomy reocclusion. Endoscopic third ventriculostomy was initially considered the treatment of choice to divert cerebrospinal fluid without leaving a ventriculoperitoneal shunt and to obtain biopsy specimens from the periinfundibular recess area. The third ventriculostomy occluded twice, and an endoscopic aqueduct fenestration was unsuccessful. The authors hypothesized that an inflammatory process related to late ND disease was responsible for the occlusions. Biopsy specimens from the infundibular recess and fornix column did not show histopathogical abnormalities. Increased ICP symptoms resolved with cerebrospinal fluid diversion. This case is the first instance of ND-LCH with hydrocephalus reported in the literature to date. Shunt placement rather than ETV seems to be the favorable choice in relieving elevated ICP.
朗格汉斯细胞组织细胞增多症(LCH)中第二常见的中枢神经系统受累模式是一种在多篇报告中记载的罕见病症,称为“神经退行性LCH”(ND-LCH)。确认该疾病存在的磁共振成像通常显示出明显的对称性双侧高信号,主要位于小脑、基底神经节、脑桥和/或脑白质。本文作者首次在文献中描述了一名患有ND-LCH并伴有脑积水的患者,最初采用内镜下第三脑室造瘘术(ETV)进行治疗。这名9岁男孩在10个月大时因皮肤和肺部LCH接受了化疗,当时尚无中枢神经系统受累,此次出现急性共济失调、头痛和轻截瘫,并有1年逐渐加重的笨拙病史。磁共振成像显示在中脑导水管水平存在梗阻性脑积水以及ND-LCH的征象。在通过脑实质内压力监测仪记录到颅内压(ICP)急剧升高后,实施了ETV。数月后因造瘘口闭塞需要再次进行ETV,最终因造瘘口再次闭塞而置入了脑室腹腔分流管。内镜下第三脑室造瘘术最初被认为是引流脑脊液的首选治疗方法,无需留置脑室腹腔分流管,并可从漏斗周隐窝区域获取活检标本。第三脑室造瘘口两次闭塞,内镜下中脑导水管开窗术未成功。作者推测与晚期ND疾病相关的炎症过程是闭塞的原因。来自漏斗隐窝和穹窿柱的活检标本未显示组织病理学异常。脑脊液分流后ICP升高的症状得到缓解。该病例是迄今为止文献中报道的首例伴有脑积水的ND-LCH。在缓解升高的ICP方面,置入分流管而非ETV似乎是更有利的选择。