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1.
World Neurosurg ; 181: 93-95, 2022 Oct 08.
Article in English | MEDLINE | ID: mdl-36220491

ABSTRACT

BACKGROUND: External ventricular drain (EVD) is a basic operation in neurosurgery. Due to the limitation of its safe duration, some patients need to receive multiple drainage operations. We describe the long tunneled EVD (LTEVD) with shunt valves that effectively avoid multiple operations as a technical note. METHODS: The difference is that the middle part of the drainage tube is connected by an externalized shunt valve. The drainage tube is buried under the skin and the outlet is in the abdomen. The technique and more details are described. RESULTS: The connection between the LTEVD and the shunt valve is simple and the required materials are easily accessible. Externalized valves allow the cerebrospinal fluid to be visualized and more controllable, making it easier for physicians to manage the cerebrospinal fluid. No drainage tube failure or secondary infection was observed. The indwelling time of the drainage tube was greatly extended. CONCLUSIONS: LTEVD is effective and simple. It allows visual control of drainage flow, prolonging catheter indwelling time and eliminating the need for multiple surgeries.

2.
Transl Neurosci ; 12(1): 309-319, 2021 Jan 01.
Article in English | MEDLINE | ID: mdl-34434564

ABSTRACT

Vasculogenic mimicry (VM) is different from classical tumor angiogenesis and does not depend on endothelial cells. VM is closely related to the prognosis of various cancers. Canstatin was first identified as an endogenous angiogenesis inhibitor. In the present study, the inhibitory effect of canstatin on VM formation was evaluated. Human glioblastoma cell lines U87 and U251 were letivirally transduced to overexpress canstatin gene or GFP as control. In vitro assays showed that canstatin overexpression reduced the tube formation of U87 and U251 cells in Matrigel. A xenograft glioma model was created by subcutaneous injection of lentivirally modified U87 cells into nude mice. The results of in vivo experiments showed that canstatin gene introduction inhibited the growth of glioma xenografts. In tumor xenografts overexpressing canstatin, U87-mediated formation of VM-like structures and VM-related VEGF (vascular endothelial growth factor) expression were remarkably reduced. Canstatin overexpression also decreased the phosphorylation of Akt and reduced the expression of Survivin in vitro. In addition, HIF-1α production and MMP-2 secretion were decreased by canstatin overexpression. Therefore, these results suggested a protective role of canstatin during VM-like structure formation of glioma probably via inhibiting signaling pathways inducing vasculogenic mimicry.

3.
J Craniofac Surg ; 32(3): 1132-1135, 2021 May 01.
Article in English | MEDLINE | ID: mdl-33003160

ABSTRACT

OBJECTIVE: This study aimed to improve the accuracy and efficacy of the keyhole transsylvian approach to remove hypertensive basal ganglia hemorrhage. The authors presented a stable keyhole craniotomy based on anterior squamous suture to expose insular cortex and basal ganglia. METHODS: Twenty-nine patients with hypertensive basal ganglia hemorrhage were treated with keyhole surgery and studied in Guangdong sanjiu brain hospital. RESULTS: By using a bone suture marked keyhole transsylvian approach, near-complete (90%) hematoma evacuation was achieved in 21 cases (72.4), 70% to 90% in 8 cases (24.1), and less than 70% in 1 case (3.4%). In our cohort, 55.1% (16/29) with good function (GOS score 4-5), 41.3% (12/29) with disability (GOS score 3), and 3.4% (1/29) in a vegetative state (GOS score 2). No patients died within 6 months of operation. CONCLUSIONS: Our method can greatly minimize the bone exposure and precisely located the distal Sylvian fissure. A stable keyhole craniotomy based on bone suture can be identically safe and effective in comparison with classic surgery, and it consumes less time and less intra-operative bleeding.


Subject(s)
Basal Ganglia Hemorrhage , Carcinoma, Squamous Cell , Basal Ganglia Hemorrhage/surgery , Craniotomy , Humans , Retrospective Studies , Sutures , Treatment Outcome
4.
World Neurosurg ; 143: 168-170, 2020 11.
Article in English | MEDLINE | ID: mdl-32750517

ABSTRACT

BACKGROUND: Intracranial solitary fibrous tumor (SFT)/hemangiopericytoma (HPC) is rare. In this report, a case of epidural hematoma (EDH) that eventually evolved into SFT/HPC is presented. We describe the possible association between the 2 diseases, which has not been previously reported. CASE DESCRIPTION: A 40-year-old man suffered from an EDH in the right parietal area 12 years ago and accepted conservative treatment. Follow-up computed tomography (CT) scan shows that the density of the right EDH gradually changed from uniform slightly lower density to mixed density. A new CT scan revealed an epidural mass extending to the subcutaneous with local bone destruction. An operation was performed via a large right parietal craniotomy, and the final diagnosis was World Health Organization grade III SFT/HPC after histopathologic examination and immunohistochemical verification. The patient died of deterioration of brain disease 3 months after the final diagnosis. CONCLUSIONS: To our knowledge, this is the first report that HPC occurred in the epidural cavity. We are the first time to describe the possible association between EDH and HPC.


Subject(s)
Epidural Neoplasms/complications , Epidural Neoplasms/diagnostic imaging , Hemangiopericytoma/complications , Hemangiopericytoma/diagnostic imaging , Hematoma, Epidural, Cranial/diagnostic imaging , Hematoma, Epidural, Cranial/etiology , Skull Neoplasms/complications , Skull Neoplasms/diagnostic imaging , Solitary Fibrous Tumors/complications , Solitary Fibrous Tumors/diagnostic imaging , Adult , Conservative Treatment , Craniotomy , Epidural Neoplasms/surgery , Epidural Space/diagnostic imaging , Fatal Outcome , Hemangiopericytoma/surgery , Hematoma, Epidural, Cranial/surgery , Humans , Male , Neurosurgical Procedures , Parietal Bone/diagnostic imaging , Skull Neoplasms/surgery , Solitary Fibrous Tumors/surgery , Tomography, X-Ray Computed
5.
World Neurosurg ; 139: 182-185, 2020 07.
Article in English | MEDLINE | ID: mdl-32305607

ABSTRACT

BACKGROUND: Intracranial bronchogenic cysts (BCs) are extremely rare. To our knowledge, this is the first report of a BC in which lesions involve the middle and posterior cranial fossa, as well as the infratemporal fossa. CASE DESCRIPTION: We present the case of a 38-year-old woman who suffered from a cranial nerve dysfunction for 2 years. Magnetic resonance imaging showed that there were skull base communication lesions across the middle and posterior fossa. The patient was operated on through an infratemporal fossa approach. The final diagnosis was BC after histopathologic examination and immunohistochemical verification. The patient's neurologic dysfunction was partially ameliorated at the half-year follow-up. CONCLUSIONS: Intracranial BCs are rare. However, they should be considered in the differential diagnosis for cystic lesions with edge enhancement or extracranial extension.


Subject(s)
Bronchogenic Cyst/surgery , Skull Base/surgery , Adult , Bronchogenic Cyst/complications , Bronchogenic Cyst/diagnostic imaging , Bronchogenic Cyst/pathology , Cranial Fossa, Middle , Cranial Fossa, Posterior , Craniotomy , Facial Paralysis/etiology , Female , Hearing Loss/etiology , Humans , Hypesthesia/etiology , Magnetic Resonance Imaging , Neurosurgical Procedures , Skull Base/diagnostic imaging , Skull Base/pathology , Tomography, X-Ray Computed
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