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1.
J Clin Neurosci ; 110: 39-47, 2023 Apr.
Article in English | MEDLINE | ID: mdl-36791494

ABSTRACT

Access to the pineal region has always been a challenge for neurosurgeons. The parietooccipital interhemispheric transtentorial approach is a slight variation of the traditional occipital transtentorial approach that provides adequate exposure to the lesions of the pineal region without introducing additional risks. In this study, the modified parietooccipital interhemispheric transtentorial approach is discussed including step-by-step anatomical cadaveric dissections and operative images. 27 adult patients (age > 18) who were operated over a 30-year period (1992-2022) by the senior author (M.N.P.) at two clinics, Marmara University, Department of Neurosurgery, Istanbul, Turkey and Acibadem Mehmet Ali Aydinlar University, Department of Neurosurgery, Istanbul, Turkey were analyzed. Only pineal region tumors were included in the analysis. Falcotentorial meningiomas and vascular lesions including cavernomas were excluded. 5 cadaveric specimens were dissected step by step following the surgical approach. Each step was documented using a Canon EOS 5D Mark II camera with Canon 100 mm Macro Lens. Step by step images of the dissections were presented including comparison with surgical images. Additional illustrations were used to describe the surgical corridor. The surgical corridor is maintained anterior to the parietooccipital sulcus along the medial of the precuneus. No retraction to the calcarine sulcus resulted in no postoperative hemianopsia. The neurovascular structures along the surgical corridor along with the nuances of the tentorium incision and splenium resection are discussed. The parietooccipital interhemispheric transtentorial approach provides a wide and safe corridor for surgical resection of pineal tumors.


Subject(s)
Brain Neoplasms , Meningeal Neoplasms , Pineal Gland , Pinealoma , Adult , Humans , Middle Aged , Pinealoma/diagnostic imaging , Pinealoma/surgery , Pinealoma/pathology , Pineal Gland/surgery , Pineal Gland/pathology , Meningeal Neoplasms/surgery , Brain Neoplasms/surgery , Brain Neoplasms/pathology , Cadaver
2.
J Clin Neurosci ; 93: 147-154, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34656239

ABSTRACT

There are case reports and small case series in the literature reporting gas-filled pseudocysts (GFP). However, a systematic review presenting overall view of the disease and its management is still lacking. In the present study, we aimed to make a systematic review of GFP cases, and present an exemplary case of ours. Our second aim was to discuss current theories for pathogenesis of GFP. A systematic review of GFP was conducted using Preferred Reporting Items for Systematic Reviews and Meta-Analyses guideline. Two large-scaled data search engines were used. A total of 53 articles were retrieved from the literature and presented with an exemplary case of ours. Mean age of the historical cohort was 59.47 years. There were 66 male (54.1%) and 56 female (45.9%) patients. The most prevalent clinical presentation was radicular sign/symptom in lower limbs with (29.1%) or without low back pain (LBP) (67%). Gas-filled pseudocyst has most commonly been diagnosed at the lower lumbar spine (L4-L5, 45.3%; L5-S1, 37.7%). Surgery was the treatment of choice in most of the patients (80%). In the whole cohort, 79.1% of the patients had complete recovery. Gas-filled pseudocysts are rarely observed in daily practice. They present mostly in men at the age of 60s. Precise differential diagnosis determination using appropriate imaging would help clinicians treat the patients properly. Gas-filled pseudocysts should be treated similarly to other spinal pathologies causing nerve root compression.


Subject(s)
Intervertebral Disc Displacement , Low Back Pain , Radiculopathy , Female , Humans , Intervertebral Disc Displacement/diagnostic imaging , Intervertebral Disc Displacement/surgery , Low Back Pain/etiology , Lumbar Vertebrae/diagnostic imaging , Lumbar Vertebrae/surgery , Lumbosacral Region , Male , Middle Aged , Radiculopathy/diagnosis , Radiculopathy/etiology
3.
Neurol Neurochir Pol ; 50(5): 387-91, 2016.
Article in English | MEDLINE | ID: mdl-27591067

ABSTRACT

Rarely, spinal gunshot injuries result in migrating intraspinal bullets. Use of MRI is controversial and other radiographic imaging might mimic an extradural bullet, even though it is intradural and migratory. Here, we present a case of spinal missile injury resulting in an intraoperatively mobile intradural bullet. The challenges faced during diagnosis and surgical removal are described. We also show that intraoperative ultrasonography may be useful in clarifying whether the bullet is intradural. A 32-year-old male presented with weakness and paraesthesia in his right leg following an accidental gunshot injury to his spine. Facet joint destruction and an intraspinal bullet were detected. Immediate surgical removal and transpedicular instrumentation was performed. The surgical procedure was complicated by lack of an identifying dural perforation at the bullet entry point and a gliding bullet inside the spinal canal during surgery. Gliding of the bullet was caused by the pushing effect of the bone rongeur and further gliding was avoided by performing the next laminectomy with an electric drill. Where other modalities indicated for a possible extradural location, intraoperative USG clearly showed the intradural position of the bullet and provided clear images without major artifacts. Surgical treatment of a mobile intradural bullet is challenging and open to surprises. Location of the bullet may shift as result of surgical procedure itself. Laminectomy should be performed with a power drill. Where fluoroscopy was inadequate and MRI not available, intraoperative USG proved useful in ascertaining the intradural versus extradural position of the bullet and allowed for a tailored dural opening.


Subject(s)
Foreign Bodies/surgery , Foreign-Body Migration/surgery , Spinal Injuries/surgery , Wounds, Gunshot/surgery , Adult , Dura Mater/diagnostic imaging , Dura Mater/surgery , Humans , Magnetic Resonance Imaging , Male , Tomography, X-Ray Computed , Treatment Outcome , Ultrasonography , Wounds, Gunshot/diagnostic imaging , Zygapophyseal Joint/injuries , Zygapophyseal Joint/surgery
4.
J Clin Neurosci ; 17(2): 232-6, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20036554

ABSTRACT

This study aimed to compare cerebral arteriovenous malformations (cAVM) and cerebral cavernous malformations (CCM) with regard to the immunohistochemical expressions of matrix metalloproteinases (MMP) and selected extracellular matrix (ECM) proteins, which have a role in the regulation of angiogenesis. Fresh-frozen surgical specimens from patients with cAVM (n=14) and CCM (n=15) were immunohistochemically stained with antibodies for MMP-2, MMP-9, laminin, fibronectin and tenascin. To compare cAVM and CCM, expression of each protein was graded using a four-point scoring system for each histological layer of the lesion. MMP-2 and MMP-9 were more strongly expressed in the vascular walls of CCMs compared to cAVMs for all comparable layers: endothelium, subendothelium and the perivascular space. The stronger expression of MMP and other EMP associated with early angiogenesis in CCMs compared to AVMs may support the hypothesis that CCMs occur at earlier embryogenic stages than AVMs.


Subject(s)
Extracellular Matrix Proteins/metabolism , Intracranial Arteriovenous Malformations/metabolism , Matrix Metalloproteinases/metabolism , Neovascularization, Pathologic/metabolism , Biomarkers/analysis , Biomarkers/metabolism , Cerebral Arteries/abnormalities , Cerebral Arteries/metabolism , Cerebral Arteries/physiopathology , Cerebral Veins/abnormalities , Cerebral Veins/metabolism , Cerebral Veins/physiopathology , Endothelial Cells/metabolism , Endothelial Cells/pathology , Extracellular Matrix Proteins/analysis , Fibronectins/analysis , Fibronectins/metabolism , Gene Expression Regulation, Developmental/physiology , Humans , Immunohistochemistry , Intracranial Arteriovenous Malformations/pathology , Intracranial Arteriovenous Malformations/physiopathology , Laminin/analysis , Laminin/metabolism , Matrix Metalloproteinase 2/analysis , Matrix Metalloproteinase 2/metabolism , Matrix Metalloproteinase 9/analysis , Matrix Metalloproteinase 9/metabolism , Matrix Metalloproteinases/analysis , Neovascularization, Pathologic/pathology , Neovascularization, Pathologic/physiopathology , Tenascin/analysis , Tenascin/metabolism
5.
Acta Neurochir (Wien) ; 151(9): 1081-8, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19415176

ABSTRACT

BACKGROUND: The aim of this study was to assess whether individuals without symptoms of trigeminal neuralgia exhibit vascular compression of the trigeminal nerve. This was investigated using ultra-high-field MR imaging. METHODS: One hundred subjects were imaged using a 3-T magnet and high-spatial-resolution three-dimensional (3D) MR imaging with 3D constructive interference in steady-state sequences. FINDINGS: Neurovascular compression (NVC) was detected in 92 of the individuals, with 83 cases bilateral and 9 unilateral. In total, 175 (87.5%) of the 200 nerves examined showed NVC. In 58% of the affected individuals, the vessel was compressing a site in the proximal third of the trigeminal nerve. Eighty-six percent of the compressing vessels were arteries, and 14% were veins. CONCLUSIONS: Ours is the first study to have evaluated NVC of the trigeminal nerve in asymptomatic individuals using 3-T MR imaging. The high prevalence of compression we observed is close to rates of NVC that have been documented in large series of microvascular decompression for trigeminal neuralgia. Our findings strongly suggest that vascular compression of the trigeminal nerve is not necessarily pathological.


Subject(s)
Basilar Artery/pathology , Image Processing, Computer-Assisted/methods , Magnetic Resonance Imaging/methods , Trigeminal Nerve/pathology , Trigeminal Neuralgia/pathology , Adolescent , Adult , Aged , Basilar Artery/physiopathology , Causality , Cranial Fossa, Middle/blood supply , Cranial Fossa, Middle/pathology , Cranial Fossa, Middle/physiopathology , Decompression, Surgical/methods , Female , Humans , Male , Middle Aged , Neurosurgical Procedures/methods , Predictive Value of Tests , Reproducibility of Results , Trigeminal Nerve/blood supply , Trigeminal Nerve/physiopathology , Trigeminal Neuralgia/physiopathology , Trigeminal Neuralgia/surgery , Vascular Surgical Procedures/methods
6.
J Clin Neurosci ; 16(2): 338-40, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19056276

ABSTRACT

The trigemino-cardiac reflex (TCR) is a well-known reflexive response in which bradycardia, hypotension, and gastric hypermotility are induced by stimulation of a peripheral or central portion of the trigeminal nerve. This reflex occurs during craniofacial surgery and other operations on or near the cerebellopontine angle, petrosal sinus, orbit and trigeminal ganglion. TCR is a well-known, although not well documented, phenomenon commonly observed during trans-sphenoidal surgery for resection of pituitary adenomas. We report a case in which asystole occurred during trans-sphenoidal surgery on a pituitary adenoma that was infiltrating the right cavernous sinus. When the anesthesiologist reported asystole, the team stopped manipulation and administered intravenous atropine. Intra-operative MRI showed a small tumour remnant in the right cavernous sinus. The operation was terminated but subsequent radiosurgery was planned for the residual tumor. Although TCR is rare and usually self-limiting, this case led us to change our treatment strategy. Surgeons who perform trans-sphenoidal surgery should be aware of this potential problem. Invasive pituitary adenomas should be removed gently and the risk of triggering TCR should be kept in mind.


Subject(s)
Heart Arrest/etiology , Neurosurgical Procedures/adverse effects , Pituitary Neoplasms/surgery , Reflex/physiology , Sphenoid Sinus/surgery , Trigeminal Nerve/physiology , Female , Humans , Intraoperative Complications , Magnetic Field Therapy/methods , Middle Aged
7.
J Clin Neurosci ; 13(9): 950-2, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17049863

ABSTRACT

Superficial siderosis of the central nervous system is a rare, progressive, irreversible and debilitating neurological disease characterized by the deposition of haemosiderin in the leptomeninges and the subpial layers of the brain and spinal cord. The main clinical findings are progressive bilateral sensorineural hearing loss, cerebellar ataxia and pyramidal tract signs. The present report describes a 49-year-old woman who presented with intermittent headache of 5 years duration. The pain had become more severe in the previous 6 months. Neurological examination revealed nothing abnormal. Computed tomography showed a cystic mass with apparent internal haemorrhage in the right frontal lobe and T(2)-weighted magnetic resonance imaging showed material of low signal intensity coating the entire surface of the brain. The mass was completely excised via craniotomy. A histopathological study identified the mass as a papillary glioneuronal tumour. The patient recovered well and is still neurologically normal 1 year later. This is the first documented case of superficial siderosis caused by this type of tumour.


Subject(s)
Brain Neoplasms/complications , Cerebral Hemorrhage/etiology , Frontal Lobe/pathology , Ganglioglioma/complications , Meninges/pathology , Siderosis/etiology , Brain Neoplasms/diagnostic imaging , Brain Neoplasms/pathology , Cerebral Hemorrhage/physiopathology , Craniotomy , Female , Frontal Lobe/physiopathology , Ganglioglioma/diagnostic imaging , Ganglioglioma/pathology , Headache/etiology , Headache/physiopathology , Humans , Magnetic Resonance Imaging , Meninges/diagnostic imaging , Meninges/physiopathology , Middle Aged , Siderosis/diagnostic imaging , Siderosis/pathology , Tomography, X-Ray Computed , Treatment Outcome
8.
J Clin Neurosci ; 12(2): 172-4, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15749422

ABSTRACT

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an autosomal-recessive disease associated with multiple deletions of mitochondrial DNA in skeletal muscle. MNGIE is a multisystem syndrome affecting muscle, peripheral, and central nervous systems and the gastrointestinal tract. A 25-year-old man is presented with 3 years history of right sided trigeminal neuralgia. He has been diagnosed as MNGIE based on clinical, neurophysiological and pathological findings. He had also received medical therapy and two radiofrequency thermocoagulations for the treatment of trigeminal neuralgia. Gamma Knife radiosurgery was performed and resulted in partial relief. To our knowledge, this is the first case in the literature of MNGIE with trigeminal neuralgia. An analogy is suggested between multiple sclerosis and MNGIE as a cause for trigeminal neuralgia in this patient.


Subject(s)
Mitochondrial Encephalomyopathies/complications , Trigeminal Neuralgia/etiology , Adult , Central Nervous System Diseases/complications , Central Nervous System Diseases/pathology , Gastrointestinal Tract/pathology , Humans , Magnetic Resonance Imaging , Male , Mitochondrial Encephalomyopathies/pathology , Mitochondrial Encephalomyopathies/physiopathology , Multiple Sclerosis/etiology , Peripheral Nervous System Diseases/complications , Radiosurgery , Syndrome , Trigeminal Neuralgia/surgery
9.
Neuroradiology ; 45(12): 900-4, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14551761

ABSTRACT

In this study, we examined the anatomical variations of the subependymal veins in the region of the foramen of Monro and the third ventricle by MR time of flight (TOF) venography. Fifty healthy subjects, ten patients with third-ventricle tumors, and four patients with lateral-ventricle tumors were included in the study. The courses of the anterior septal vein (ASV), thalamostriate vein (TSV), and internal cerebral vein (ICV) were studied. The proximity of the venous angle, the false venous angle, and the ASV-ICV junction to the posterior margin of the foramen of Monro was measured. In 69 (53.9%) sides, the ASV-ICV junction was located at the venous angle and at the posterior margin of the foramen of Monro. In 59 (46.1%) sides, the ASV-ICV junction was located beyond the foramen of Monro. Our study shows the high incidence of posteriorly located ASV-ICV junctions, which can be crucial in the planning of a better surgical approach. We strongly recommend that MR venography, which is a short radiological examination, be used before one operates on third-ventricle and lateral-ventricle tumors.


Subject(s)
Cerebral Veins/diagnostic imaging , Cerebral Ventricle Neoplasms/diagnostic imaging , Ependyma/blood supply , Magnetic Resonance Angiography , Phlebography , Third Ventricle/blood supply , Cerebral Ventriculography , Ependyma/diagnostic imaging , Humans , Reproducibility of Results , Third Ventricle/diagnostic imaging
10.
J Clin Neurosci ; 9(5): 549-52, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12383413

ABSTRACT

The aim of this study is to determine the impact of surgery on tumor progression and malignant degeneration in hemispheric diffuse astrocytoma WHO grade II. Twenty-eight patients who were operated or underwent stereotactic biopsy for hemispheric diffuse astrocytoma WHO grade II at Marmara University between January 1987 and January 1996, were prospectively reviewed for the presence of recurrence and histopathological dedifferentiation at their fourth years after the initial treatment. Twenty-two patients underwent surgical resection. Of this group, 7 patients had a total, 11 had a subtotal and 4 patients had a partial resection. Six patients underwent stereotactic biopsy. All patients, except for the ones in whom a radiological total surgical removal could be achieved, received postoperative radiotherapy. In the total surgical-removal group only one patient had recurrence, while no upgrade was noted. All of the patients in the partial resection and stereotactic biopsy groups recurred at a higher grade. Our results indicate that both tumor progression and histopathological dedifferentiation were less commonly seen when a total or subtotal resection could be achieved. So, surgery, as radical as possible, should be the choice of treatment in low-grade hemispheric astrocytomas.


Subject(s)
Astrocytoma/pathology , Astrocytoma/surgery , Brain Neoplasms/pathology , Brain Neoplasms/surgery , Neurosurgical Procedures , Adolescent , Adult , Aged , Astrocytoma/radiotherapy , Brain Neoplasms/radiotherapy , Case-Control Studies , Child , Child, Preschool , Combined Modality Therapy , Disease Progression , Female , Follow-Up Studies , Humans , Image Processing, Computer-Assisted , Infant , Magnetic Resonance Imaging , Male , Middle Aged , Neoplasm Recurrence, Local , Prospective Studies , Treatment Outcome
11.
J Neurosurg Sci ; 44(4): 226-9, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11327292

ABSTRACT

A rare cause of acute visual loss due to a chiasmal cavernous malformation is presented. Acute visual loss was due to local hemorrhage and volume expansion of the cavernous malformation inside and outside of the optic chiasma. This unique location of cavernous malformation is associated with a risk of permanent loss of the vision. Cavernous malformations of optic chiasma should be carefully evaluated and considered for possible preventative surgical resection before it becomes symptomatic.


Subject(s)
Cerebral Arteries/abnormalities , Hemangioma, Cavernous/surgery , Optic Chiasm/abnormalities , Optic Chiasm/blood supply , Vision Disorders/etiology , Acute Disease , Adult , Female , Hemangioma, Cavernous/diagnosis , Hemangioma, Cavernous/etiology , Humans , Magnetic Resonance Imaging , Optic Chiasm/surgery , Tomography, X-Ray Computed , Treatment Outcome
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