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1型神经纤维瘤病患者人字缝区域的颅骨缺损。

Calvarial defects in the region of the lambdoid suture in neurofibromatosis type-1 patients.

作者信息

Solanki Chirag, Ramachandran Sudheesh, Devi Bhagvatula Indira, Sharma Rajeev

机构信息

Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India.

Department of Neurosurgery, PGIMER and Dr. RML Hospital, New Delhi, India.

出版信息

J Pediatr Neurosci. 2015 Jan-Mar;10(1):22-4. doi: 10.4103/1817-1745.154322.

Abstract

Rare type of calvarial defects seen in patients with neurofibromatosis type-1 (NF1) is presented. The issues of pathogenesis and management are discussed. Two cases of NF1 with skull defects in the region of the lambdoid suture are reported. The possible etiological basis and nature of these type of defects and management issues are discussed. The calvarial skull defects in the lambdoid suture region are rare defects in NF1 patients. The possible reason of the progressive nature of these type of lesions can be the cerebrospinal fluid pulsations behaving like "growing skull fractures," especially when not associated with structural lesions. It leads to progressive enlargement of the small congenital defects in the region of the lambdoid suture and abnormal susceptibility of bones for resorption. For these defects, conservative management is suggested due to its progressive nature and high chances of operative treatment failure.

摘要

本文介绍了1型神经纤维瘤病(NF1)患者中罕见的颅骨缺损类型。讨论了其发病机制和治疗问题。报告了2例NF1患者在人字缝区域出现颅骨缺损的病例。讨论了这些类型缺损的可能病因基础、性质及治疗问题。人字缝区域的颅骨缺损在NF1患者中较为罕见。这些类型病变呈进行性发展的可能原因可能是脑脊液搏动类似“生长性颅骨骨折”,尤其是在不伴有结构性病变时。这会导致人字缝区域小的先天性缺损进行性扩大,且骨骼对吸收异常敏感。鉴于这些缺损的进行性本质以及手术治疗失败的高概率,建议采取保守治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af1e/4395938/f390fcc32217/JPN-10-22-g001.jpg

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