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1.
Turk Neurosurg ; 28(1): 105-110, 2018.
Article in English | MEDLINE | ID: mdl-27476924

ABSTRACT

AIM: It is well known that treatment modalities against secondary damage due to spinal cord injury (SCI) are very important. This phase has been researched in many experimental studies. Apoptosis is one of the major mechanisms of secondary damage on spinal cord. The present study was undertaken to determine if quetiapine, a 5-HT2 receptor blocker atypical antipsychotic agent can rescue neuronal cells from apoptosis in a SCI model. MATERIAL AND METHODS: Thirty-two female Wistar rats were separated to 4 equal groups. Total laminectomy was performed at T5-7 level and spinal cord injury was produced by using the clip compression technique. Each rat from groups "1 day" (D-I) and "7 days" (D-II) was daily injected intraperitoneally with Quetiapine (10 mg/kg/day). No treatment was administered to the control groups "1 day" (K-I) and "7 days" (K-II). At the end of follow-up periods, all animals were sacrificed and spinal cords were removed. Apoptotic cells were evaluated by using immunohistochemical technique (TUNEL) in injured spinal cord specimens. RESULTS: There was a statistically significant difference while counting ApopTag positive cells, both at 1 day groups of K-I and D-I (p=0.00000008) and at 7 day groups of K-II and D-II (p=0.000005). Unlike the 1-day period, a statistically significant difference was found between grey and white matter ApopTag positive cells at the 7 < sup > th < /sup > day (p=0.0001). CONCLUSION: Quetiapine has a protective effect on secondary damage caused by SCI, while also can be used in post-traumatic stress disorder, depression and agitation as a versatile agent.


Subject(s)
Quetiapine Fumarate/administration & dosage , Spinal Cord Injuries/drug therapy , Spinal Cord Injuries/surgery , Acute Disease , Animals , Female , Laminectomy/methods , Laminectomy/trends , Male , Random Allocation , Rats , Rats, Wistar , Spinal Cord Injuries/pathology , Treatment Outcome
2.
Turk Neurosurg ; 21(4): 471-6, 2011.
Article in English | MEDLINE | ID: mdl-22194102

ABSTRACT

AIM: Cerebro-spinal fluid (CSF) leakage caused by defects on the dura mater after trauma or some neurosurgical interventions is an important issue. In this study, we investigated the effects of local and systemic use of phenytoin sodium on dural healing. MATERIAL AND METHODS: Thirty-six male Wistar rats were divided into control, local phenytoin and systemic phenytoin groups with 12 rats in each. For each group, a dura defect was created at thoracic segment. Subjects were sacrificed at following 1st and 6th weeks and damaged segments were isolated. The results were compared histopathologically by Hematoxylin-Eosin and Masson-Trichrome staining. Criteria for the rate of collagen, neovascularization, and granulation formation were assessed semi quantitatively according to the histological assessment scale modified by Ozisik et al. RESULTS: Better healing was achieved in the systemic and local phenytoin groups than in the control group. The level of healing was significantly higher in the systemic group in both early and late periods than in other groups (p < 0.01). The level of healing in the late-local group was also statistically significantly higher than that in the control group. CONCLUSION: We observed that both systemic and local uses of phenytoin sodium (especially systemic) have positive effects on dura healing.


Subject(s)
Anticonvulsants/pharmacology , Cerebrospinal Fluid Rhinorrhea/drug therapy , Dura Mater/injuries , Phenytoin/pharmacology , Wound Healing/drug effects , Animals , Cerebrospinal Fluid Leak , Cerebrospinal Fluid Rhinorrhea/metabolism , Disease Models, Animal , Dura Mater/metabolism , Dura Mater/surgery , Granulation Tissue/drug effects , Male , Neurosurgical Procedures , Rats , Rats, Wistar
3.
Turk Neurosurg ; 20(1): 66-8, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20066625

ABSTRACT

INTRODUCTION: Aplasia cutis congenita (ACC), is a rare anomaly presenting with a solitary scalp lesion of skin abrasion. Lesions can be multiple and on different surfaces of the body but are mostly seen on the scalp (%70) as a solitary lesion. As it is a rare disease, we aimed to describe our case with ACC. CASE REPORT: Our case was a newborn infant with a large full thickness skin and skull defect on the scalp at birth. He also had hypoplasia on the fingers, omphalocele, ectopic anus, cleft lip and palate anomalies and multiple cardiac anomalies. We planned further evaluation but he died 23 hours after birth because of cardiac problems. DISCUSSION: Multiple factors have been described as etiological factors for ACC but the etiology is not clear yet. ACC may also be associated with some syndromes. Management strategies are based on the size, presence of an underlying skull defect and the child's physical condition.


Subject(s)
Ectodermal Dysplasia/complications , Nervous System Malformations/complications , Skull/abnormalities , Anal Canal/abnormalities , Fatal Outcome , Humans , Infant, Newborn , Male , Urinary Bladder/abnormalities
4.
Surg Neurol ; 71(3): 332-6, discussion 336, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18440605

ABSTRACT

BACKGROUND: The aim of the study is to assess the effects of infliximab, a TNF-alpha receptor blocker, in a spinal cord clip compression injury model. METHODS: Clip compression injury model was used for producing spinal cord injury on 32 adult, male Wistar rats (Gazi University Animal Research Laboratory, Ankara, Turkey). After exposing the vertebral column between T7 and T10, total laminectomy was performed with the assistance of a high-speed drill and a surgical microscope. The dura was left intact. Spinal cord injury was performed on all rats with application of a 70-g closing force aneurysm clip for 1 minute. The rats were randomly allocated into 4 groups. Control group received no further therapy, whereas the other 3 groups received methylprednisolone (30 mg/kg intraperitoneal), infliximab (5 mg/kg subcutaneous), and a mixture of these 2 agents. All rats were killed 72 hours later, and the level of lipid peroxides in traumatized spinal cord tissue were measured as thiobarbituric acid-reactive material and determined using the method of Mihara and Uchiyama (Determination of malonaldehyde precursor in tissue by thiobarbituric acid test. Anal Biochem 1978;86(1):271-8). RESULTS: Treatment with infliximab and methylprednisolone decreased MDA levels in rats with spinal cord injury with a statistically significant difference. In addition, combined therapy achieved a more profound decrease in tissue MDA levels, which was also statistically significant. CONCLUSIONS: Infliximab is found as effective as methylprednisolone on spinal cord clip compression injury. Moreover, the combination of these 2 agents demonstrated higher efficacy suggesting a synergistic effect between these 2 agents. However, further studies regarding functional and behavioral analyses as well as biochemical markers are required.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Antibodies, Monoclonal/pharmacology , Neuroprotective Agents/pharmacology , Spinal Cord Compression/drug therapy , Animals , Biomarkers/metabolism , Disease Models, Animal , Infliximab , Injections, Intraperitoneal , Lipid Peroxidation/drug effects , Male , Malondialdehyde/metabolism , Methylprednisolone/pharmacology , Rats , Rats, Wistar , Recovery of Function/drug effects , Spinal Cord Compression/metabolism , Thiobarbituric Acid Reactive Substances/metabolism , Tumor Necrosis Factor-alpha/antagonists & inhibitors
5.
Turk Neurosurg ; 18(1): 52-5, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18382979

ABSTRACT

Spinal canal extradural arachnoid cyst is an uncommon, expanding lesion which may communicate with the subarachnoid space. They may be either intra or extradural with intradural cysts being less common. Spinal arachnoid cysts are usually in the thoracic spine, and they may cause symptoms due to spinal cord compression. Although surgery is the preferred way of management, there are reported cases with long term follow-up in the literature. Here we present a 14-year-old female who presented with intermittent low back pain for 1 year and a spinal arachnoid cyst that was followed for two years without any neurological deterioration.


Subject(s)
Arachnoid Cysts/pathology , Arachnoid Cysts/surgery , Magnetic Resonance Imaging , Spinal Cord Compression/pathology , Spinal Cord Compression/surgery , Adolescent , Arachnoid Cysts/complications , Disease Progression , Female , Humans , Low Back Pain/etiology , Low Back Pain/pathology , Low Back Pain/surgery , Spinal Cord Compression/etiology , Thoracic Vertebrae , Treatment Refusal
6.
Childs Nerv Syst ; 23(6): 719-21, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17364209

ABSTRACT

INTRODUCTION: Iniencephaly, a neural tube defect involving occiput and inion and combined with rachischisis of the cervical, thoracic spine, and retroflexion position of the head is a very rare congenital abnormality of the fetus-newborn with a 0.1-10 of 10,000 prevalence. This abnormality's prognosis is thought to be dismal. This abnormality can be associated with other abnormalities such as anencephaly, encephalocele, hydrocephalus, cyclopia, absence of the mandible, cleft lip and palate, cardiovascular disorders, diaphragmatic hernia, renal abnormalities, overgrowth of the arms compared to the legs, and club food and gastrointestinal atresia. DISCUSSION: Most of the patients are dead born, and the others die in a few hours. There are only six previously documented long-term survivors. In our case, our patient with iniencephalic signs and findings is still living. She is 2 years old now. We think that this patient presents a mild form of iniencephaly.


Subject(s)
Abnormalities, Multiple , Child Development , Encephalocele/diagnosis , Neural Tube Defects/diagnosis , Skull/abnormalities , Survivors , Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/mortality , Child, Preschool , Encephalocele/complications , Encephalocele/mortality , Female , Humans , Infant , Infant, Newborn , Neural Tube Defects/complications , Neural Tube Defects/mortality , Prenatal Diagnosis , Ultrasonography
7.
Childs Nerv Syst ; 23(5): 573-6, 2007 May.
Article in English | MEDLINE | ID: mdl-17053937

ABSTRACT

OBJECTIVE: Teratoma is the most frequently encountered intracranial tumor at birth and constitutes 18-20% of all germ cell tumors. They are usually located in pineal and suprasellar regions. The authors aim to report an extremely unusual presentation, location, and appearance of a teratoma in a newborn. CASE REPORT: A soft tissue swelling in the vertex was detected in a 1-month-old girl. Neurological examination was normal. A big, cystic-solid lesion beginning from pineal region and extending to the scalp was detected in magnetic resonance imaging. It is interesting to note that cerebral venous angiography showed that the superior sagittal sinus (SSS) was divided into three branches at the level of the lesion and they joined together distally. The tumor was excised totally. Histopathological examination revealed the diagnosis of a mature cystic teratoma. CONCLUSION: A mature cystic teratoma mimicking parietal encephalocele is extremely rare. Germ cell tumors should be kept in mind in the differential diagnosis of all midline lesions with unusual radiographic appearance. Cerebral venous angiography or MR angiography must be performed for the diagnosis and the surgical planning in lesions located near SSS.


Subject(s)
Encephalocele/pathology , Parietal Lobe/pathology , Pinealoma/pathology , Teratoma/pathology , Cerebral Angiography , Diagnosis, Differential , Female , Humans , Infant , Magnetic Resonance Angiography , Magnetic Resonance Imaging , Neurosurgical Procedures , Pinealoma/congenital , Pinealoma/surgery , Teratoma/congenital , Teratoma/surgery
8.
J Neurosurg ; 103(1 Suppl): 79-82, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16122010

ABSTRACT

Myelomeningocele presenting as a retromediastinal mass originating from the midline defect through the fused T-4, T-5, and T-6 VBs is described. An 11-year-old boy with a completely normal systemic and neurological examination suffering pulmonary problems such as effort dyspnea and severe kyphosis was evaluated and an anterior thoracic myelomeningocele was diagnosed. The boy underwent surgery for excision of the meningomyelocele sac and correction of kyphoscoliosis. His year-long follow-up period as an outpatient was uneventful. A comprehensive PubMed search of the literature returned no results for an "anterior thoracic myelomeningocele" query. To the best of the authors' knowledge, this is the only case described in the literature.


Subject(s)
Mediastinal Diseases/surgery , Meningomyelocele/surgery , Child , Humans , Kyphosis/etiology , Kyphosis/surgery , Male , Mediastinal Diseases/complications , Meningomyelocele/complications , Scoliosis/etiology , Scoliosis/surgery , Treatment Outcome
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