Crouzon’s Syndrome with a Dominant Sinus Pericranii Draining Transverse Sinus: Report of a Rare Association and Review of Literature

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY Pediatric Neurosurgery Pub Date : 2022-03-18 DOI:10.1159/000524134
S. Kumari, S. Verma, P. Singh
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引用次数: 0

Abstract

Introduction: Crouzon’s syndrome and sinus pericranii (SP) are rare entities. Only few cases having both the features are reported. SP most commonly drains in relation to superior sagittal sinus and their communication to major posterior dural sinuses is rare. Case Report: We report a rare case of Crouzon’s syndrome with SP at a suboccipital location with termination of left transverse sinus into the SP draining further through the extracranial suboccipital and extravertebral cervical venous plexi into external jugular veins. Distal transverse sinus and sigmoid sinus on the left side were absent. Conclusion: Crouzon’s syndrome with SP is an extremely rare entity. SP with communication to major posterior dural venous sinuses is also rare and mostly associated with multi-suture craniosynostosis. Management depends on the volume of venous blood they are draining. Most of them are dominant type and their occlusion is not feasible. Preoperative diagnosis of a dominant SP is essential for proper surgical planning as it needs to be preserved mandatorily to prevent cerebral venous infarction.
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克鲁松综合征伴优势鼻窦围壁引流横鼻窦:罕见关联报告及文献回顾
简介:Crouzon综合征和颅周窦(SP)是罕见的实体。只有少数病例同时具有这两种特征。SP最常与上矢状窦相连,与硬脑膜后窦相通的情况很少。病例报告:我们报告一例罕见的Crouzon综合征伴枕下位置的SP,左侧横窦终止进入SP,通过颅外枕下和椎外颈静脉丛进入颈外静脉。左侧远端横窦和乙状窦未见。结论:伴有SP的Crouzon综合征是一种极为罕见的疾病。与硬脊膜后静脉窦相通的SP也很少见,且多与多缝合线颅缝闭塞有关。治疗取决于他们抽走的静脉血量。多数为优势型,闭塞不可行。术前诊断优势性脑脊液对于正确的手术计划至关重要,因为它需要被强制保留以防止脑静脉梗死。
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来源期刊
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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