Management of hydrocephalus and subdural hygromas in pediatric patients after decompression of Chiari malformation type I: case series and review of the literature

被引:8
|
作者
Vivas, Andrew C. [2 ]
Shimony, Nir [1 ]
Jackson, Eric M. [3 ]
Xu, Risheng [3 ]
Jallo, George I. [1 ,3 ]
Rodriguez, Luis [1 ]
Tuite, Gerald F. [1 ]
Carey, Carolyn M. [1 ]
机构
[1] Johns Hopkins All Childrens Inst Brain Protect Sc, Dept Neurosurg, St Petersburg, FL USA
[2] Univ S Florida, Dept Neurosurg, Tampa, FL USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21205 USA
关键词
Chiari I malformation; complication; hydrocephalus; posterior fossa decompression; subdural hygromas; FORAMEN MAGNUM DECOMPRESSION; CRANIOCERVICAL DECOMPRESSION; SYRINGOMYELIA; COMPLICATION; POPULATION; DURAPLASTY; FOSSA;
D O I
10.3171/2018.4.PEDS17622
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE Hydrocephalus associated with subdural hygromas is a rare complication after decompression of Chiari malformation type I (CM-I). There is no consensus for management of this complication. The authors present a series of 5 pediatric patients who underwent CM-I decompression with placement of a dural graft complicated by posterior fossa hygromas and hydrocephalus that were successfully managed nonoperatively. METHODS A retrospective review over the last 5 years of patients who presented with hydrocephalus and subdural hygromas following foramen magnum decompression with placement of a dural graft for CM-I was conducted at 2 pediatric institutions. Their preoperative presentation, perioperative hospital course, and postoperative re-presentation are discussed with attention to their treatment regimen and ultimate outcome. In addition to reporting these cases, the authors discuss all similar cases found in their literature review. RESULTS Over the last 5 years, the authors have encountered 194 pediatric cases of CM-I decompression with duraplasty equally distributed at the 2 institutions. Of those cases, 5 pediatric patients with a delayed postoperative complication involving hydrocephalus and subdural hygromas were identified. The 5 patients were managed nonoperatively with acetazolamide and high-dose dexamethasone; dosages of both drugs were adjusted to the age and weight of each patient. All patients were symptom free at follow-up and exhibited resolution of their pathology on imaging. Thirteen similar pediatric cases and 17 adult cases were identified in the literature review. Most reported cases were treated with CSF diversion or reoperation. There were a total of 4 cases previously reported with successful nonoperative management. Of these cases, only 1 case was reported in the pediatric population. CONCLUSIONS De novo hydrocephalus, in association with subdural hygromas following CM-I decompression, is rare. This presentation suggests that these complications after posterior fossa decompression with duraplasty can be treated with nonoperative medical management, therefore obviating the need for CSF diversion or reoperation.
引用
收藏
页码:426 / 438
页数:13
相关论文
共 50 条
  • [21] CHIARI MALFORMATION TYPE I: A REVIEW OF LITERATURE TO COMPARE BONY POSTERIOR FOSSA DECOMPRESSION WITH AND WITHOUT DURAPLASTY
    Tam, K. P.
    Foroughi, M.
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2019, 90 (03): : E49 - E49
  • [22] Endoscopic third ventriculostomy for hydrocephalus after craniovertebral decompression for Chiari malformation type I: technical nuances and surgical pitfalls
    Pepper, Joshua
    Rodrigues, Desiderio
    Gallo, Pasquale
    CHILDS NERVOUS SYSTEM, 2023, 39 (12) : 3501 - 3507
  • [23] Endoscopic third ventriculostomy for hydrocephalus after craniovertebral decompression for Chiari malformation type I: technical nuances and surgical pitfalls
    Joshua Pepper
    Desiderio Rodrigues
    Pasquale Gallo
    Child's Nervous System, 2023, 39 : 3501 - 3507
  • [24] Contemporary occurrence of hydrocephalus and Chiari I malformation in sagittal craniosynostosis. Case report and review of the literature
    Sgulo, Francesco Giovanni
    Spennato, Pietro
    Aliberti, Ferdinando
    Di Martino, Giuliana
    Cascone, Daniele
    Cinalli, Giuseppe
    CHILDS NERVOUS SYSTEM, 2017, 33 (01) : 187 - 192
  • [25] Contemporary occurrence of hydrocephalus and Chiari I malformation in sagittal craniosynostosis. Case report and review of the literature
    Francesco Giovanni Sgulò
    Pietro Spennato
    Ferdinando Aliberti
    Giuliana Di Martino
    Daniele Cascone
    Giuseppe Cinalli
    Child's Nervous System, 2017, 33 : 187 - 192
  • [26] Hemifacial spasm and trigeminal neuralgia in Chiari's I malformation with hydrocephalus: Case report and literature review
    Liu, Jiang
    Yuan, Yue
    Zang, Li
    Fang, Ying
    Liu, Hongjun
    Yu, Yanbing
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2014, 122 : 64 - 67
  • [27] Posterior fossa decompression with or without duraplasty in patients with Chiari type I malformation: A systematic review
    Xin, Yexin
    Xu, Zhentao
    Dong, Zhaogang
    Xiao, Yilei
    ASIAN JOURNAL OF SURGERY, 2024, 47 (04) : 1961 - 1962
  • [28] Interdisciplinary management of patients with Chiari Malformation Type I
    Kinjo, Beatriz L.
    Mezzadri, Juan Jose M.
    Molina, Lourdes V.
    Gestro, Daniel H.
    Figuerola, Maria D. L.
    CEPHALALGIA, 2017, 37 : 41 - 42
  • [29] Acquired Chiari malformation Type I associated with a supratentorial arteriovenous malformation - Case report and review of the literature
    O'Shaughnessy, BA
    Bendok, BR
    Parkinson, RJ
    Shaibani, A
    Walker, MT
    Shakir, E
    Batjer, HH
    JOURNAL OF NEUROSURGERY, 2006, 104 (01) : 28 - 32
  • [30] Incidence and management of postoperative pseudomeningocele and cerebrospinal fluid leak after Chiari malformation type I decompression
    Atchley, Travis J.
    Alam, Yasaman
    Gross, Evan
    Laskay, Nicholas M. B.
    Estevez-Ordonez, Dagoberto
    Schmalz, Philip G. R.
    Fisher, Winfield S., III
    NEUROSURGICAL FOCUS, 2023, 54 (03)