scholarly journals Upward transtentorial herniation following frontoorbital advancement for syndromic craniosynostosis: case report

2015 ◽  
Vol 38 (5) ◽  
pp. E8
Author(s):  
Vivek Mehta ◽  
Joshua Bakhsheshian ◽  
Amir H. Dorafshar ◽  
Edward S. Ahn

The authors describe the case of a boy with Muenke syndrome, an autosomal dominant disorder associated with craniosynostosis. The family history was significant for syndromic craniosynostosis in the patient’s maternal grandmother, who died in adulthood after a craniofacial reconstruction. The patient, her grandson, underwent craniofacial reconstruction surgery at the age of 9 months and developed upward transtentorial herniation. Imaging findings revealed remote cerebellar hemorrhage after a large quantity of supratentorial CSF was drained during postoperative Day 1. The clinical course was further complicated by cerebral sinus thrombosis, which was diagnosed after a fourth surgical procedure. Upward transtentorial herniation can occur when a significant increase in intracranial pressure in the posterior fossa causes displacement of the central lobule and superior surfaces of the cerebellum upward through the incisura tentorii. This is a rare but well-documented phenomenon that commonly occurs in the setting of an expansive posterior fossa lesion or excessive supratentorial CSF loss. To help clinicians recognize and prevent this rare but potentially fatal complication, the authors review the postulated mechanisms by which this process may occur.

Author(s):  
Mayank Tyagi ◽  
Surya K. Dube ◽  
Vanitha Rajagopalan ◽  
Gyaninder P. Singh

Abstractβ-thalassemia are a group of inherited blood disorders with reduced hemoglobin levels. β-thalassemia major is the severe form of disease, and the patients often display an array of associated organ dysfunction which thus increase the risk associated with surgery and anesthesia. Patients with β-thalassemia major can have multiple pathological defects that may lead to thromboembolic events. Here, we report such a case who was complicated by occurrence of cerebral sinus thrombosis and presented for decompressive hemicraniectomy under general anesthesia. The anesthetic challenges during in such scenario have been discussed.


2012 ◽  
Vol 9 (2) ◽  
pp. 116-118 ◽  
Author(s):  
Leonardo Rangel-Castilla ◽  
Steven W. Hwang ◽  
Andrew Jea ◽  
William E. Whitehead ◽  
Daniel J. Curry ◽  
...  

Multiple-suture synostosis is typically associated with syndromic craniosynostosis but has been occasionally reported in large series of nonsyndromic children. The diagnosis of multiple fused sutures usually occurs at the same time, but rarely has the chronological development of a secondary suture synostosis been noted. The development of secondary bicoronal suture synostosis requiring surgical intervention has only been reported, to date, after surgical intervention and is hypothesized to arise from a disruption of inhibitory factors from the dura. The disinhibition of these factors permits the sutures to then fuse at an early stage. The authors report on a patient who developed secondary unilateral coronal synostosis after the diagnosis of an isolated sagittal synostosis. The secondary synostosis was identified at the time of the initial surgical intervention and ultimately required a second procedure of a frontoorbital advancement. The clinical appearance of this phenomenon may be subtle, and surgeons should monitor for the presence of secondary synostosis during surgery as it may require intervention. Failure to identify the secondary synostosis may necessitate another surgery or result in a poor cosmetic outcome. The authors recommend close clinical follow-up for the short term in patients with isolated sagittal synostosis.


Stroke ◽  
2004 ◽  
Vol 35 (12) ◽  
pp. 2820-2825 ◽  
Author(s):  
Christoph M. Kosinski ◽  
Michael Mull ◽  
Michael Schwarz ◽  
Benno Koch ◽  
Rolf Biniek ◽  
...  

Neurology ◽  
2000 ◽  
Vol 55 (6) ◽  
pp. 903-903
Author(s):  
R. A. Rodas ◽  
J. J. Raizer ◽  
L. M. DeAngelis

Author(s):  
K. Spitzer ◽  
J. Freitag ◽  
A. Thie ◽  
L. Lachenmayer ◽  
G. Siepmann

Stroke ◽  
1997 ◽  
Vol 28 (8) ◽  
pp. 1607-1609 ◽  
Author(s):  
José Manuel Valdueza ◽  
Lutz Harms ◽  
Florian Doepp ◽  
Jürgen Koscielny ◽  
Karl Max Einhäupl

2019 ◽  
Vol 12 (1) ◽  
pp. e227302 ◽  
Author(s):  
Christodoulos Dolapsakis ◽  
Eleftheria Kranidioti ◽  
Sofia Katsila ◽  
Michael Samarkos

We report a case of septic thrombosis of the right cavernous sinus in a diabetic woman in her late 70’s due to ipsilateral sphenoid sinusitis. The diagnosis was delayed and made only after the abrupt and dramatic appearance of the manifestations of sinus thrombosis. The patient developed, among the other symptoms, right peripheral facial palsy, which is a very rare manifestation in cavernous sinus thrombosis (CST). She was treated with broad-spectrum antibiotics and enoxaparin. The day of the scheduled drainage of sphenoid sinus—24 hours after the initiation of anticoagulation—she developed fatal subarachnoid haemorrhage. Our case demonstrates the difficulty of timely diagnosis of acute sphenoid sinusitis which has emerged as the most common primary infectious source potentially leading in CST. It also underscores the uncertainty concerning the use of anticoagulation in cerebral sinus thrombosis of infectious origin.


Angiology ◽  
2008 ◽  
Vol 59 (6) ◽  
pp. 765-768 ◽  
Author(s):  
Shingo Sakamoto ◽  
Koichi Akutsu ◽  
Kayoko Kawase ◽  
Tatsuro Takada ◽  
Hidenori Seyama ◽  
...  

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