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1.
Surg Neurol Int ; 13: 146, 2022.
Article in English | MEDLINE | ID: mdl-35509579

ABSTRACT

Background: Tumefactive demyelinating lesions (TDL) share similar clinical features and magnetic resonance imaging (MRI) characteristics with high grade glioma (HGG). This study develops an approach to navigating this diagnostic dilemma, with significant treatment implications as the management of both entities is drastically different. Methods: A retrospective analysis of 41 TDLs and 91 HGG with respect to demographics, presentation and classical MRI characteristics was performed. A diagnostic pathway was then developed to help diagnose TDLs based on whole neuraxis MRI and cerebrospinal fluid (CSF) examination. Results: The diagnosis of TDL is more likely than HGG in younger females who present with subacute or chronic symptoms. MRI characteristics favoring TDL over HGG include smaller size, open rim enhancement, little or no associated edema or mass effect and the presence of a T2 hypointense rim. MRI of the whole neuraxis for detection of other lesions typical of multiple sclerosis (MS), in combination with a lumbar puncture (LP) showing positive CSF-specific oligoclonal bands (OCB), was positive in 90% of the TDL cohort. Conclusion: The diagnostic pathway, proposed on the basis of specific clinicoradiological features, should be followed in patients with suspected TDL. If MRI demonstrates other lesions typical of MS and LP demonstrates positive CSF-specific OCBs, then patients should undergo a short course of IV steroids to look for clinical improvement. Patients, who continue to deteriorate, do not demonstrate other lesions on MRI or where the LP is negative for CSF-specific OCB, should be considered for biopsy if safe to do so. This pathway will give the patients the best chance at neurological preservation.

2.
J Clin Neurosci ; 79: 95-99, 2020 Sep.
Article in English | MEDLINE | ID: mdl-33070927

ABSTRACT

Instrumented fixation of the C1-C2 motion segment is a standard surgical technique to stabilise that spinal segment. Instability at C1-C2 can arise from a number of conditions. Fixation of the C1 lateral mass usually involves dissection and exposure of the C2 nerve root and the posterior wall of the C2 lateral mass which can result in significant bleeding from the venous plexus. Whilst image guidance is increasing in accessibility, there are few public hospitals in Australia that have access to this technology. The authors describe their technique for insertion of a C1 lateral mass screw over a threaded K-wire to avoid extensive dissection of the C2 nerve root, reducing the risk of significant haemorrhage from the epidural venous plexus during the procedure. A retrospective analysis was undertaken on 18 consecutive patients who underwent C1-C2 instrumented fixation using this technique. Indications for C1-C2 instrumented fixation included traumatic injury (10 patients), failure of non-operative management of odontoid fractures (5 patients), pathological fractures of C2 (2 patients) and inflammatory conditions (1 patient). All patients underwent successful C1-C2 stabilisation using this technique. Blood loss did not exceed 400mls in any patient. There were no vertebral artery injuries and no patient experienced a neurological deterioration. The authors propose that their technique for insertion of a C1 lateral mass screw over a threaded K-wire is safe and effective with a low risk of neurological or vertebral artery injury. The technique may be considered as a slight modification of the Harm's procedure to reduce disturbance of the adjacent venous plexus and thereby reduction in intraoperative bleeding and operative time.


Subject(s)
Atlanto-Axial Joint/surgery , Spinal Fusion/instrumentation , Spinal Fusion/methods , Adult , Aged , Aged, 80 and over , Australia , Bone Screws , Female , Humans , Middle Aged , Postoperative Complications/prevention & control , Retrospective Studies , Spinal Fusion/adverse effects , Surgery, Computer-Assisted/instrumentation , Surgery, Computer-Assisted/methods
3.
J Clin Neurosci ; 51: 65-66, 2018 May.
Article in English | MEDLINE | ID: mdl-29483007

ABSTRACT

Migration of the distal catheter of a ventriculoperitoneal shunt to the scrotum is a documented but rare event. We present a case in which a 13 month old infant with hydrocephalus had recurrent migration of the peritoneal catheter to the right scrotum associated with a developing hydrocele. The patient underwent two revision operations and the distal catheter was ultimately shortened. He later underwent bilateral inguinal hernia repairs.


Subject(s)
Foreign-Body Migration/diagnostic imaging , Foreign-Body Migration/surgery , Scrotum/diagnostic imaging , Scrotum/surgery , Ventriculoperitoneal Shunt/adverse effects , Catheters, Indwelling/adverse effects , Foreign-Body Migration/etiology , Hernia, Inguinal/diagnostic imaging , Hernia, Inguinal/etiology , Hernia, Inguinal/surgery , Humans , Hydrocephalus/diagnostic imaging , Hydrocephalus/surgery , Infant , Male , Recurrence , Reoperation/methods , Testicular Hydrocele/diagnostic imaging , Testicular Hydrocele/etiology , Testicular Hydrocele/surgery
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