scholarly journals Sinking skin flap syndrome after unilateral cranioplasty and ventriculoperitoneal shunt in a patient with bilateral decompressive craniectomy

2016 ◽  
Vol 5 ◽  
pp. 6-8 ◽  
Author(s):  
Jun Watanabe ◽  
Jun Maruya ◽  
Keiichi Nishimaki
2015 ◽  
Vol 123 (5) ◽  
pp. 1170-1175 ◽  
Author(s):  
Claire J. Creutzfeldt ◽  
Marcelo D. Vilela ◽  
William T. Longstreth

OBJECT Two patients who underwent decompressive craniectomy after head trauma deteriorated secondary to paradoxical herniation, one after lumbar puncture and the other after ventriculoperitoneal shunting. They motivated the authors to investigate further provoked paradoxical herniation. METHODS The authors reviewed the records of 205 patients who were treated at a single hospital with decompressive craniectomy for head trauma to identify those who had had lumbar puncture performed or a ventriculoperitoneal shunt placed after craniectomy but before cranioplasty. Among the patients who met these criteria, those with provoked paradoxical herniation were identified. The authors also sought to identify similar cases from the literature. Exact binomials were used to calculate 95% CIs. RESULTS None of 26 patients who underwent a lumbar puncture within 1 month of craniectomy deteriorated, whereas 2 of 10 who underwent a lumbar puncture 1 month afterward did so (20% [95% CI 2.4%–55.6%]). Similarly, after ventriculoperitoneal shunting, 3 of 10 patients deteriorated (30% [95% CI 6.7%–65.2%]). Timing of the procedure and the appearance of the skin flap were important factors in deterioration after lumbar puncture but not after ventriculoperitoneal shunting. A review of the literature identified 15 additional patients with paradoxical herniation provoked by lumbar puncture and 7 by ventriculoperitoneal shunting. CONCLUSIONS Lumbar puncture and ventriculoperitoneal shunting carry substantial risk when performed in a patient after decompressive craniectomy and before cranioplasty. When the condition that prompts decompression (such as brain swelling associated with stroke or trauma) requires time to resolve, risk is associated with lumbar puncture performed ≥ 1 month after decompressive craniectomy.


2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
Noman Ahmed Jang Khan ◽  
Saad Ullah ◽  
Waseem Alkilani ◽  
Hassan Zeb ◽  
Hassan Tahir ◽  
...  

Sinking skin flap syndrome is rare phenomenon that occurs in patients with large craniectomies. Alteration in normal anatomy and pathophysiology can result in wide variety of symptoms including altered mental status, hemodynamic instability, and dysautonomias. Management is largely conservative. We here present a case of a patient with large craniectomy who was admitted to our hospital with pneumonia. Later on, he developed worsening mental status and CT head revealed sinking skin flap with significant midline shift. This is a very rare case of neurological deterioration after craniectomies, commonly known as sinking skin flap syndrome. To our knowledge, only few cases have been reported so far.


2018 ◽  
Vol 09 (02) ◽  
pp. 232-239 ◽  
Author(s):  
Raja K. Kutty ◽  
Sunilkumar Balakrishnan Sreemathyamma ◽  
Jyothish Sivanandapanicker ◽  
Prasanth Asher ◽  
Rajmohan Bhanu Prabhakar ◽  
...  

ABSTRACTIntroduction:Ventriculomegaly and hydrocephalus (HCP) are sometimes a bewildering sequela of decompressive craniectomy (DC). The distinguishing criteria between both are less well defined. Majority of the studies quoted in the literature have defined HCP radiologically, rather than considering the clinical status of the patient. Accordingly, these patients have been treated with permanent cerebrospinal fluid (CSF) diversion procedures. We hypothesize that asymptomatic ventriculomegaly following DC should undergo aspiration with cranioplasty and be followed up regularly. Materials and Methods: All patients with post-DC who were scheduled for cranioplasty and satisfied the radiological criteria for HCP were included. These patients were categorized into two groups. Group 1 included ventriculomegaly with clinical signs attributable to HCP and Group 2 constituted ventriculomegaly but no clinical signs attributable to HCP. All patients in Group 1 underwent ventriculoperitoneal shunt followed by cranioplasty, whereas all patients in Group 2 underwent cranioplasty along with simultaneous ventriculostomy and temporary aspiration of the lateral ventricle. All patients were regularly followed as the outpatient basis. Results: There were 21 patients who developed ventriculomegaly following DC. There were 10 patients in Group 1 and 11 patients in Group 2. The average duration of follow-up was from 6 months to 2 years. Two patients in the shunt group - (group 1) had over drainage and required revision. One patient in aspiration group - (group 2) required permanent CSF diversion. Conclusion: Cranioplasty with aspiration is a viable option in selected group of patients in whom there is ventriculomegaly but no signs or symptoms attributable to HCP.


2017 ◽  
Vol 31 (2) ◽  
pp. 186-190
Author(s):  
Ona Lapteva ◽  
Ugnius Ksanas ◽  
Jelena Scerbak

Abstract Sinking skin flap syndrome is a rare complication following decompressive craniectomy. The pathogenesis is based on disturbed cerebral autoregulation and as a consequence dicreased CBF and cerebral metabolism. This results in neurologic disturbances, i. e. mental changes and focal deficits. The authors present the patient who developed the motor trephine syndrome after decompressive craniectomy following complicated giant posterior cerebral artery aneurysm clipping.


2018 ◽  
Vol 11 (9) ◽  
pp. 241-243 ◽  
Author(s):  
Nicholas Fawley ◽  
Chiedozie Udeh

2008 ◽  
Vol 43 (1) ◽  
pp. 51 ◽  
Author(s):  
Pan Yeal Han ◽  
Jae Hoon Kim ◽  
Hee In Kang ◽  
Joo Seung Kim

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