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1.
Br J Neurosurg ; 35(3): 367-369, 2021 Jun.
Article in English | MEDLINE | ID: mdl-29656658

ABSTRACT

Primary angiitis of the central nervous system (PACNS), is a rare and poorly understood disease mainly characterized by multifocal segmental inflammation of the small and medium vessels of the central nervous system. Most PACNS are multiple lesions, occurring in the supratentorial subcortical and deep white matter, and only a few cases present as a tumor-like mass lesion. Herein, we describe an extremely rare case of PACNS occurred in the cerebellum, which mimicked a cerebellar tumor. To the best of our knowledge, this is the first reported case of cerebellar tumor-like PACNS proved by histopathological examination.


Subject(s)
Cerebellar Neoplasms , Vasculitis, Central Nervous System , Central Nervous System , Cerebellar Neoplasms/diagnostic imaging , Cerebellar Neoplasms/surgery , Cerebellum/diagnostic imaging , Humans , Vasculitis, Central Nervous System/diagnostic imaging , Vasculitis, Central Nervous System/drug therapy
2.
J Craniofac Surg ; 28(2): e152-e154, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28033189

ABSTRACT

Pseudomeningocele is a collection of the cerebrospinal fluid in the extradural space due to a defect in the dura-arachnoid layer of the meninge, and manifests as a fibrous capsule in the space of subcutaneous tissues. Classically, growing skull fracture caused by the pseudomeningocele is not uncommon in the pediatric age group. However, a posttraumatic intradiploic pseudomeningoceles is extremely rare, and only a few patients have been described. Herein, the authors present a 6-year-old girl who developed an intradiploic pseudomeningocele of the occipito-cervical region after a severe head trauma.


Subject(s)
Craniocerebral Trauma/complications , Dura Mater/surgery , Meningocele/etiology , Occipital Bone/surgery , Arachnoid , Cerebrospinal Fluid , Child , Dura Mater/injuries , Female , Humans , Occipital Bone/diagnostic imaging
3.
J Craniofac Surg ; 28(1): e47-e49, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27893552

ABSTRACT

The anterior petroclinoid fold (APF) is a ligamentous structure consisting of collagen fiber and extends from the petrous apex to the anterior clinoid process. During the surgical clipping of some posterolaterally projecting posterior communicating artery aneurysms, it may pose a technical challenge due to obscuration of the aneurismal neck by the APF. Herein, the authors describe a simple and effective technique utilizing fenestration of the APF to facilitate visualization and surgical clipping of these aneurysms. To the best knowledge of us, this technique of the APF fenestration has been reported in only a few patients.


Subject(s)
Intracranial Aneurysm/surgery , Neurosurgical Procedures/methods , Sphenoid Bone/surgery , Surgical Instruments , Computed Tomography Angiography , Female , Humans , Intracranial Aneurysm/diagnosis , Middle Aged
4.
Horm Cancer ; 8(1): 49-57, 2017 02.
Article in English | MEDLINE | ID: mdl-27896672

ABSTRACT

The microRNAs (miRNAs) have been suggested as a tumor suppressor in recent years. miR-15b was reported to exert an anti-oncogenic role in the proliferation, migration, and invasion of diverse tumor cells. However, the mechanisms underlying miR-15b-mediated biology of glioblastoma are still unclear. In the present study, the expression of miR-15b was down-regulated in glioblastoma tumor tissues and U87 and U251 cells, but insulin-like growth factor receptor 1 (IGF1R) expression became up-regulated in these tumor tissues and cells (all p < 0.001). Furthermore, IGF1R expression was inversely associated with miR-15b expression. Notably, patients with lower miR-15b expression have a much shorter survival period compared with high expression (log-rank test p = 0.045). In vitro data demonstrated that miR-15b mimics inhibited the proliferation, cell cycle arrest, and invasion of U87 and U251 cells. Besides, we validated IGF1R as a direct target of miR-15b using dual luciferase assays, and IGF1R plasmids partially abrogated miR-15b mimics inhibited cell proliferation. In vivo, miR-15b mimics indeed repressed cell proliferation in mouse xenograft model. In conclusion, our study demonstrated that miR-15b inhibits the progression of glioblastoma cells through targeting IGF1R, and miR-15b can be recommended as a tumor suppressor in the progression of glioblastoma.


Subject(s)
Cell Proliferation/genetics , Glioblastoma/genetics , Glioblastoma/metabolism , MicroRNAs/metabolism , Receptors, Somatomedin/metabolism , Animals , Cell Line, Tumor , Down-Regulation , Gene Expression Regulation, Neoplastic , Genes, Tumor Suppressor , Glioblastoma/mortality , Humans , Male , Mice , Mice, Inbred BALB C , Mice, Nude , Receptor, IGF Type 1 , Up-Regulation , Xenograft Model Antitumor Assays
5.
J Craniofac Surg ; 27(8): e773-e775, 2016 Nov.
Article in English | MEDLINE | ID: mdl-28005820

ABSTRACT

Brain abscess is a rare but potentially lethal infection of brain parenchyma, requiring prompt surgical intervention and high-dose antibiotic therapy. Brain abscess is a known complication of surgically treated intracerebral hemorrhage (ICH), but it is exceptionally rare that it occurs at the same site of a nonoperated ICH. Such cases may result from hematogenous spread from distant foci (pneumonia, infectious endocarditis) or contiguous sites. Herein, the authors report a case of 75-year-old woman presenting with a brain abscess 6 weeks after a nonoperated ICH. As the patient suffered from pneumonia during the course of ICH, the authors suspected that the brain abscess might originate from the pneumonia via hematogenous spread. The awareness of brain abscess formation at the site of ICH is of great importance for early diagnosis and prompt treatment.


Subject(s)
Brain Abscess/etiology , Cerebral Hemorrhage/complications , Occipital Lobe , Parietal Lobe , Pneumonia/complications , Aged , Brain Abscess/diagnostic imaging , Cerebral Hemorrhage/diagnostic imaging , Female , Humans , Magnetic Resonance Imaging , Occipital Lobe/diagnostic imaging , Parietal Lobe/diagnostic imaging , Tomography, X-Ray Computed
6.
J Craniofac Surg ; 27(7): e619-e620, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27483108

ABSTRACT

Dumbbell-shaped epidural cavernous hemangiomas (CHs) are extremely rare, and they are easily misdiagnosed as spinal schwannomas. Herein, the authors report 1 rare case of dumbbell-shaped epidural CH in the thoracic spine. To the best of our knowledge, only a few cases of dumbbell-shaped epidural CHs in thoracic spine have been reported. Furthermore, the clinical characteristics and treatments for spinal epidural CHs were investigated and reviewed.


Subject(s)
Epidural Neoplasms/diagnosis , Hemangioma, Cavernous/diagnosis , Neurilemmoma/diagnosis , Diagnosis, Differential , Female , Humans , Thoracic Vertebrae , Young Adult
7.
J Craniofac Surg ; 27(7): e623-e626, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27513787

ABSTRACT

Cerebellar glioblastoma multiforme (cGBM) is rare in adults, accounting for <1% of all patients with glioblastoma multiforme (GBM). The accurate diagnosis of cGBM is important for establishing a suitable therapeutic schedule. However, the diagnosis of cerebellar GBM is not usually suspected preoperatively because of its rarity. Generally, patients with cGBMs typically presented with symptoms of raised intracranial pressure, and infrequently cerebellar symptoms such as gait ataxia and disequilibrium. Nevertheless, the authors reported a cGMB patient, with his clinical presentations and imaging characteristics mimicking a vestibular schwannoma. To the best of our knowledge, this is the first reported patient with cGBM mimicking a vestibular schwannoma. Furthermore, the diagnosis, treatment, and prognosis for cGBM were broadly investigated.


Subject(s)
Cerebellar Neoplasms/diagnosis , Glioblastoma/diagnosis , Neuroma, Acoustic/diagnosis , Diagnosis, Differential , Humans , Male , Middle Aged
8.
J Craniofac Surg ; 27(3): e311-3, 2016 May.
Article in English | MEDLINE | ID: mdl-27092919

ABSTRACT

Astrocytomas are the most common intramedullary spinal cord tumors in pediatric and adolescent patients and the incidence decreases with age. Spinal oligoastrocytoma, which is a mixed glioma with distinct astrocytic and oligodendroglial components, is an extremely rare pathology of the spinal cord. To authors' best of knowledge, there are only 7 spinal oligoastrocytomas reported in the English literature. Here, the authors report a patient of a pathologically confirmed spinal oligoastrocytoma, who presented with severe left leg pain and numbness. This patient reminds us of the rarity of spinal oligoastrocytoma, and the treatment and prognosis were also investigated and reviewed.


Subject(s)
Spinal Cord Neoplasms/surgery , Chemoradiotherapy, Adjuvant , Combined Modality Therapy , Humans , Laminectomy , Lumbar Vertebrae/diagnostic imaging , Lumbar Vertebrae/surgery , Male , Middle Aged , Neoplasm Grading , Prognosis , Spinal Cord Neoplasms/diagnostic imaging , Spinal Cord Neoplasms/pathology , Thoracic Vertebrae/diagnostic imaging , Thoracic Vertebrae/pathology , Thoracic Vertebrae/surgery
10.
J Craniofac Surg ; 27(2): e128-30, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26845092

ABSTRACT

Both of Pituitary adenoma (PA) and Rathke cleft cyst (RCC) are the most common and benign sellar lesions. Generally, the origin of RCC is considered to be derived from remnants of Rathke punch, while PA is formed by proliferation of the anterior wall of Rathke pouch. Although they have a possibility to share a common embryological origin, the coexistence of PA and RCC is extremely rare. Here, the authors report a 50-year-old male patient who was found to have a large cystic sellar lesion, and surgical resection revealed components of a RCC coexisting with a PA. This collision reminded us of the possibility of RCC coexisting with PA. Furthermore, a clinicopathologic relation of them were reviewed and investigated.


Subject(s)
Adenoma/complications , Adenoma/surgery , Central Nervous System Cysts/surgery , Neoplasms, Multiple Primary/surgery , Pituitary Neoplasms/surgery , Adenoma/diagnosis , Adenoma/pathology , Central Nervous System Cysts/diagnosis , Central Nervous System Cysts/pathology , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neoplasms, Multiple Primary/diagnosis , Neoplasms, Multiple Primary/pathology , Pituitary Gland/pathology , Pituitary Neoplasms/diagnosis , Pituitary Neoplasms/pathology
12.
Tumour Biol ; 37(6): 7921-8, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26700671

ABSTRACT

Glioblastoma (GBM) represents one of most common tumors in humans. However, the biological processes and molecular mechanisms of GBM are still unclear. It is known that microRNA-520b (miR-520b) participates in the development of various tumor progressions. The present study was to evaluate the level of miR-520b in GBM tissues and cells. We further investigated the molecular mechanisms of miR-520b in U87 and U251 cell lines. Here, our data showed that the expression levels of miR-520b were significantly reduced in clinical GBM tissues and cell lines. Accordingly, the expression levels of cyclin D1 were significantly increased in clinical GBM tissues and cell lines. Ectopic expression of miR-520b in U87 and U251 cells resulted in decreased cell proliferation and enhanced cell apoptosis. Further study characterized the 3' untranslated region (3'-UTR) of cyclin D1 gene as a direct target of miR-520b in U87 and U251 cells as determined by luciferase reporter assays. In addition, ectopic expression of miR-520b led to the down-regulation of phosphorylated retinoblastoma (p-Rb, a downstream effector of cyclin D1), while the overexpression of cyclin D1 reversed the miR-520b-induced inhibition of p-Rb expression. In conclusion, this study highlights the importance of miR-520b in regulating the proliferation and apoptosis of GBM by directly targeting cyclin D1, and miR-520b may represent a potential therapeutic strategy for GBM.


Subject(s)
Cyclin D1/metabolism , Glioblastoma/pathology , MicroRNAs/metabolism , Apoptosis/genetics , Blotting, Western , Cell Line, Tumor , Cell Proliferation , Cyclin D1/genetics , Gene Expression Regulation, Neoplastic , Glioblastoma/metabolism , Humans , Reverse Transcriptase Polymerase Chain Reaction
14.
J Craniofac Surg ; 25(4): 1551-2, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24926722

ABSTRACT

Lumbar drainage (LD) is considered as a simple and effective procedure for the treatment of intracerebral hemorrhage with ventricular involvement. However, cerebrospinal fluid overdrainage and hypovolemia due to LD could induce severe fatal complications, which include transtentorial herniation and infratentorial hemorrhage. Here, we describe a 63-year-old man with transtentorial herniations and Duret hemorrhage attributable to LD after the operation of thalamic hematoma removal. This is probably the first reported case of severe complications of LD. Thus, complications related to transtentorial herniations and Duret hemorrhage should be kept in mind while performing LD.


Subject(s)
Cerebrospinal Fluid Leak/etiology , Drainage/adverse effects , Dura Mater , Hernia/etiology , Hypovolemia/cerebrospinal fluid , Cerebral Hemorrhage/surgery , Coma/etiology , Humans , Male , Middle Aged
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