Displaying all 8 publications

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  1. Lee HK, Ghani AR, Sayuthi S, Abdullah J, Mustaffa F, Othman N, et al.
    Med J Malaysia, 2007 Oct;62(4):339-40.
    PMID: 18551942 MyJurnal
    We report a case of 50-year-old man who was presented with recurrent episodes of left sided hemiparesis. CT scan and MRI brain revealed a large intraventricular fatty lesion. Histopathological examination showed a picture of angiolipoma.
    Matched MeSH terms: Cerebral Ventricle Neoplasms/diagnosis*; Cerebral Ventricle Neoplasms/radiography; Cerebral Ventricle Neoplasms/surgery
  2. Idris Z, Ghani AR, Idris B, Muzaimi M, Awang S, Pal HK, et al.
    Minim Invasive Neurosurg, 2011 Jun;54(3):125-7.
    PMID: 21863520 DOI: 10.1055/s-0031-1277198
    Shunt surgery is frequently chosen to manage periventricular metastasis of pineal region tumours which obscured the floor of the third ventricle. However, this procedure falls short due to distant metastasis. Neuronavigation-guided endoscopic surgery offers a viable alternative.
    Matched MeSH terms: Cerebral Ventricle Neoplasms/radiography; Cerebral Ventricle Neoplasms/secondary; Cerebral Ventricle Neoplasms/surgery*
  3. Harrower G
    Matched MeSH terms: Cerebral Ventricle Neoplasms
  4. Tan SP, Abdullah BJ, Waran V, Liew WF
    Neuroradiology, 2003 Jan;45(1):53-5.
    PMID: 12525956
    We present a rare indirect nontraumatic cerebrospinal fluid (CSF) fistula secondary to a fourth ventricle ependymoma. The fistula resulted from rupture of the left temporal horn, distant from the tumour. The fistula was well demonstrated by MRI. High-resolution CT demonstrated a defect in the roof of the sphenoid sinus, but no leakage of CSF was seen on CT cisternography.
    Matched MeSH terms: Cerebral Ventricle Neoplasms/complications*; Cerebral Ventricle Neoplasms/diagnosis
  5. Pyn CC, Arumugasamy N
    Med J Malaysia, 1976 Sep;31(1):65-8.
    PMID: 1023016
    Matched MeSH terms: Cerebral Ventricle Neoplasms/etiology*; Cerebral Ventricle Neoplasms/radiography
  6. Anderson I, Kumar R, Patankar T, Tyagi A
    BMJ Case Rep, 2014;2014.
    PMID: 25257888 DOI: 10.1136/bcr-2014-205736
    We present the case of a 24-year-old man who presented with vertigo and right-sided weakness. Subsequent imaging demonstrated a lateral ventricle haemangioblastoma. This is the first case ever to be treated with surgical excision augmented by preoperative endovascular embolisation, as illustrated with perfusion CT scanning performed pre-embolisation and postembolisation. We present the case followed by a summary of the previously published cases and a discussion of the advantages of perfusion scanning and endovascular embolisation in these highly vascular (and therefore potentially dangerous) lesions.
    Matched MeSH terms: Cerebral Ventricle Neoplasms/radiography; Cerebral Ventricle Neoplasms/therapy*
  7. Jayapalan RR, Mun KS, Wong KT, Sia SF
    World Neurosurg X, 2019 Apr;2:100006.
    PMID: 31218281 DOI: 10.1016/j.wnsx.2018.100006
    Background: Rosette-forming glioneuronal tumor (World Health Organization grade I) is considered as a benign tumor with very low potential for progression. The potential for malignant transformation of this tumor is not known and has never been reported before in literature.

    Case Description: We report a 42-year-old man, diagnosed with rosette-forming glioneuronal tumor of the fourth ventricle with a positive isocitrate dehydrogenase 1 mutation, progressed to glioblastoma after 6 years from diagnosis. We discuss the clinical history, radiological findings, and histopathological characteristic with immunohistochemistry findings observed in this unique case.

    Conclusions: Despite being acceptable as benign, based on our observations in this case, there is a potential for malignant transformation of rosette-forming glioneuronal tumor. The role of isocitrate dehydrogenase 1 mutation leading to malignant transformation could not be established as our finding is novel and further prospective studies are required to prove this association.

    Matched MeSH terms: Cerebral Ventricle Neoplasms
  8. Idris Z, Johnson JR, Abdullah JM
    J. Neurosurg., 2015 Mar;122(3):504-10.
    PMID: 25343181 DOI: 10.3171/2014.9.JNS132683
    The splenial-habenular junctional area is an alternative site for neuroendoscopic fenestration to divert CSF flow into the quadrigeminal cistern in cases in which endoscopic third ventriculostomy is not amenable. In some patients with obstructive hydrocephalus, the splenium of the corpus callosum can be elevated from the habenular complex. This exposes the membranous connection between the splenium and habenula, which can be fenestrated to divert the CSF flow into the quadrigeminal cistern. This technique can be performed in patients in whom the foramen of Monro or the third ventricle is blocked by a lesion. Here, the authors present 3 complex cases that were managed by neuronavigation-guided transventricular transcavum endoscopic fenestration of the splenial-habenular junctional area. These cases may increase the knowledge and understanding of the anatomy of this region.
    Matched MeSH terms: Cerebral Ventricle Neoplasms/surgery*
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