检索结果-南通市图书馆

Open Journal of Modern Neurosurgery 2024年第3期14卷 218-227页

作者： Diallo Moussa Traoré youssouf Kanikomo Drissa Diarra Sounkalo Izoudine B. Koumaré sogoba youssouf sogoba Boubacar Diallo Oumar Gabriel Tour Teatching Hospital Bamako Mali Bocar Sidy Sall Teatching Hospital Kati Mali Hopital du Mali Teaching Hospital Bamako Mali

Unusual head trauma is rare with various mechanisms of occurrence. The injuries can be similar to those of road accidents but sometimes with significant complexities. The objective was to determine the frequency of this pathology in our practice, describe the different mechanisms and report the craniocerebral lesions caused by this type of trauma. Materials and Method: This was a descriptive study with retrospective collection spread over a period of 3 years. After selecting the files, the patients and/or their companions were contacted by telephone to inquire about them and then returned to the consultation for reassessment. Disease history and information were obtained from patients’ medical records. Result: The frequency of this pathology was 1.78% and his incidence was 0.4 cases per month. The average age of the patients was 13.47 years. All the victims were male. 41.17% of patients were in school. The mechanisms of trauma were the hoof blow 47.1%, the horn blow 29.4% and the stone blow 11.7% respectively. 23.5% of patients were confused and 11.7% children were in coma. One patient presented an anisocoria. The motor deficit was present in 5 cases. CT-scan made it possible to highlight a skull depressing fracture 58.8% and confirm a craniocerebral wound in 35.3%. The average time between patient admission to hospital and completion of surgery was 24.5 hours. The surgery had consisted of the trimming of cranio-cerebral wounds, exploration, duroplasty and lifting of skull depressing fracture. After 15 months of follow-up, the evolution was favorable in 53.3%, the morbidity was 33.4% and the mortality 17.6%. Conclusion: These are rare but serious conditions because they are fatal and disabling. An early and multidisciplinary management can hope to have a good favorable.

关键词： Brain Trauma Injury Insolite Unusual Skull Depressing Fracture Hoof Kick Horn Blows Stone Bows Motorcycle Gear Lever

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Unusual Brain Trauma Injury

引用

Open Journal of Modern Neurosurgery（现代神经外科学进展） 2024年第3期 218页

作者： Diallo Moussa Traoré youssouf Kanikomo Drissa Diarra Sounkalo Izoudine B. Koumaré sogoba youssouf sogoba Boubacar Diallo Oumar

来源：博看期刊评论

在线全文

博看期刊

学校读者我要写书评

暂无评论

Traumatic Spinal Cord Injuries in Gold Miners in Mali: Preliminary Study on 76 Cases

引用

World Journal of Neuroscience 2019年第3期9卷 208-215页

作者： Oumar Coulibaly Mahamadou Dama Oumar Diallo Daouda Sissoko Boubacar sogoba Singuepiré Alpha youssouf sogoba Drissa Kanikomo Hô pital du Mali Bamako Mali Hô pital Gabriel Touré University of Sciences Technics and Technologies of Bamako (USTTB) Bamako Mali

Introduction: Gold panning is the research and artisanal exploitation of gold in the auriferous areas (rivers or others). Traumatisms arising from these activities are due to severe spinal cord injury and generally affect young people in full activity. They constitute a real social handicap in Mali and even in Africa. The aim of our study is to share our expertise in the management of these vertebro-medullary traumasin these miners who currently escape to all controls in Mali. Material and Methods: From 2013 to 2016, 76 Traumatic Spine Cord Injuries (TSCI) were treated in the department of Neurosurgery of “Hôpital du Mali”. There were 73 males (96.05%) versus 03 Females (3.95%), aged between 21 - 43 years old. Results: All of our patients were admitted with deficit differing from paraparesis to tetraplegia. According to Frankel scale, we found 59 patients with complete deficits (A grade, 77.63%), and incomplete deficits in 17 cases (12 grade B, 04 grade C, 01 grade D). The X-ray standard radiographies were done in 24 cases (31.58%) from which 02 patients had been operated with these data. CT scan centered on the injured spinal segment was performed in 74 cases (97.37%). The lumbar spine was affected in 39 cases, followed by thoracolumbar junction in 19 cases and thoracic spine in 16 cases. The cervical spine was only interested in two cases. Fractures dislocations are the most frequently lesions encountered in our series. The surgical approach was performed in 74 patients and 02 patients received conservative treatment. Conclusion: Traumatic Spinal Cord Injuries (TSCI) among miners are a real disaster in Mali and continue to plague thousands of families or increase the number of disabled people in our society. It is the only work, where the person concerned is making of his own grave. And according to witnesses, several miners remained at the bottom of the wells. Their prevention must first involve users by raising the awareness of local residents and traditio

关键词： Spinal Cord Injury Gold Mali

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

A Case Report of 3C Syndrome and Literature Review

引用

Case Reports in Clinical Medicine 2022年第1期11卷 8-12页

作者： Drissa Kanikomo youssouf sogoba Moussa Diallo Mamadou Salia Diarra Oumar Coulibaly Boubacar sogoba Mahamadou Dama Mamady Coulibaly Mamadou Diallo Department of Neurosurgery Gabriel Touré Teaching Hospital Bamako Mali Department of Neurosurgery Luxembourg Hospital Bamako Mali Department of Neurosurgery H&ocirc pital du Mali Bamako Mali

Ritscher-Schinzel syndrome, or 3C (cranio-cerebello-cardiac) syndrome is a developmental disorder characterized by cranio-facial, cerebellar and cardiac anomalies. It is a rare disease with an incidence of 1/1,000,000 inhabitants, and was first described by Ritscher-Schinzel in 1987. 3C syndrome is an autosomal recessive disease caused by a mutation on the long arm of chromosome 8 to 8q24.13, the KIAA0196 locus, the strumpellin protein gene. The cardiac and cerebral anomalies are most often leading cause of death at an early age and people with 3C syndrome rarely exceed 40 years. In this paper, we report a case of Ritscher-Schinzel in 3-month-old boy who was admitted to our neurosurgical department in September 2020. Clinical examination revealed a macrocrania with head circumference at 47 cm. There was a prominence of forehead and occiput, the root of the nose which was flat, hypertelorism and micrognatism. The CT scan revealed Dandy WALKER malformation with cystic dilation of the 4th ventricle, an aplasia of the cerebellar vermis associated with a tretraventricular hydrocephalus.

关键词： Cardiac Anomalies Ritscher-Schinzel Syndrome 3C

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Primary Intramedullary Ewing’s Sarcoma: A Case Report and Review of the Literature

引用

Case Reports in Clinical Medicine 2015年第3期4卷 110-113页

作者： Oumar Coulibaly Rachid Gana youssouf sogoba Asmaa Regragui Rachid Maaqili Fouad Bellakhdar Department of Neurosurgery Hopital Ibn Sina Rabat Morocco Department of Neurosurgery Hopital du Mali Bamako Mali Center of Neuropathology Rabat Morocco

Ewing’s sarcoma, a group of primary neuroectodermal tumor (PNET), is an uncommon rare highly malignant tumor mostly affecting the bones of male patients, and accounts for approximately 10% of the primary malignant bone tumors, and occupies the second place after osteosarcoma in children’s less than 20 years. Primary intramedullary Ewing’s sarcoma is an extremely rare condition. Here, we present a case of a 16-year-old girl with progressive weakness of lower extremities, inability to walk, progressive low back pain, bilateral leg pain, paresthesia and urinary retention. Spinal MRI showed intramedullary abnormal signal focus from T11 to L3 vertebrae with moderate heterogeneous enhancement on T1 weighted sequences. After surgery, histological examination found a lot of small round-cell tumors with a high nuclear-cytoplasmic ratio, frequent mitoses and apoptotic nuclei suggesting a diagnosis of Ewing’s sarcoma and confirmed by CD99 reactivity. She had undergone adjuvant chemotherapy and irradiation and was free of symptoms since 02 years. Within this single pure case of intramedullary Ewing’s sarcoma, perhaps the 1st in the English literature, the authors described this extremely rare uncommon localization with a brief review of the literature.

关键词： Ewing Sarcoma Primary Intramedullary PNET Spinal MRI

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Surgical Repair of Growing Skull Fracture: A Case Report

引用

Case Reports in Clinical Medicine 2022年第3期11卷 79-83页

作者： youssouf sogoba Seybou Hassane Diallo Moussa Diallo Drissa Kanikomo Boubacar sogoba Oumar Coulibaly Mahamadou Dama Mamadou Salia Diarra Oumar Diallo youssoufa Maiga Department of Neurosurgery Gabriel Touré Teaching Hospital Bamako Mali Department of Neurology Gabriel Touré Teaching Hospital Bamako Mali Department of Neurosurgery H&ocirc pital du Mali Bamako Mali Department of Neurosurgery H&ocirc pital Luxambourg Bamako Mali

Background: Growing skull fractures (GSF) are a rare complication of pediatric head trauma that comprises post-traumatic skull defect associated with an underlying dural tear and an intact arachnoid membrane. They are often misdiagnosed, and delay in management can lead to progression of the disease with neurological sequelae. GSF are rare and their incidence has been estimated as 0.05% - 1% of all pediatric skull fractures. This low incidence and the subtlety of its presentation often make diagnosis challenging with consequent delay in management. Surgery is recommended to treat GSF and involved dural repair with or without cranioplasty. In this paper, we report a case of a patient with GSF in whom the surgical repair was successful with good cosmetic and functional outcome. Case Report: A 12 months old girl was admitted to our neurosurgical department with right parietal swelling that had been gradually enlarging over 3 months. The history of the disease began when the girl was 1 month old with a fall with cranial impact resulting in head trauma with initial loss of consciousness. At presentation the girl was alert with normal consciousness. Clinical examination revealed the deformed skull with large pulsatile and painless swelling lesion in the right parietal region and hemiparesis on the left side. The CT scan revealed type 3 GSF including parietal bone diastasis with hypodense fluid collection that mimicked the leptomeningeal and porencephalic cyst. Surgical repair was performed. The post-operative course was uneventful and the child was discharged home five days after surgical intervention. Conclusion: GSF can lead to serious neurologic complications. Therefore educating parents on this potential outcome and close follow-up with clinical and imaging screening is recommended to screen children at risk for the development of the disease.

关键词： Growing Skull Fracture Head Trauma Dural Tear

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Bilateral Chronic Subdural Hematoma after Endoscopic Third Ventriculostomy in a Child: A Case Report and Review of the Literature

引用

World Journal of Neuroscience 2018年第1期8卷 44-49页

作者： Oumar Coulibaly Oumar Diallo Mahamadou Dama Bourama Kané Feng Zhou youssouf sogoba Drissa Kanikomo Department of Neurosurgery Hopital du Mali U.S.T.T.B Bamako Mali Department of Pediatrics Hopital du Mali U.S.T.T.B Bamako Mali The First Affiliated Hospital of Medical School of Zhejiang University Zhejiang China Department of Neurosurgery Hopital Gabriel Touré U.S.T.T.B Bamako Mali

Hydrocephalus had been managed by ventriculoperitoneal shunt (VPS) or endoscopic third ventriculostomy (ETV) since several years. But these two different technics had some complications that must be managed promptly to avoid eventual fatal evolution. Chronic subdural hematomas after ETV is among these complications and is a very rarely situation observed in our department. This rare event associated with malaria in a child is considered to have a high mortality. Here we report a rare case of bilateral chronic subdural hematoma occurring in a 4-month-old boy after ETV and we discuss the likely pathogenesis and the difficulties of management.

关键词： Hydrocephalus ETV Chronic Subdural Hematoma Malaria

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

A Case Report of an Invasive Scalp Actinomycosis

引用

Case Reports in Clinical Medicine 2021年第2期10卷 34-38页

作者： youssouf sogoba Jean Paul Dembele Boubacar sogoba Moussa Diallo Seybou Hassane Diallo Oumar Coulibaly Quenum Kisito Oumar Diallo Drissa Kanikomo youssoufa Maiga Department of Neurosurgery H&ocirc pital Gabriel Touré Bamako Mali Department of Infectious Diseases H&ocirc pital du Point G Bamako Mali Department of Neurologie H&ocirc pital Gabriel Touré Bamako Mali Department of Neurosurgery H&ocirc pital du Mali Bamako Mali Department of Neurosurgery University Hospital of Parakou Parakou Benin

Background: Actinomycosis is a bacterial infection characterized by a chronic, suppurative and granulomatous process. The causative organism was identified in 1891 as Actinomycosis israelii. The disease is usually caused by the introduction of the bacteria through minor wound. Actinomycosis was classified by Cope into 3 different forms: cervicofacial (50%), pulmonothoracic (30%) and abdominopelvic (20%). Actinomycosis is an insidious disease but occasionally the clinical course can be more aggressive, involving underline tissue and organs. Involvement of scalp by actinomycosis is rare causing diagnostic dilemma and could be mistaken for different pathologies, such as tuberculosis or carcinoma. The most common clinical findings are local tumefaction with abscesses and sinuses draining pus that contains the granule of the causative organism. CT scan and MRI are aspecific for diagnosis, but they can help in defining the localization and the extension of the lesion. The certain diagnostic is based on cytology and/or biopsy. Case: A 24 year-old-man was admitted to our neurosurgical department with a 16-month history of multiple scalp ulcerated lesions and swelling of the head. He was complaining of headache. Physical examination revealed multiple scalp subcutaneous nodules and ulcerated lesions with swelling of the head. Our examination of the oral cavity revealed a poor oral hygiene condition with multiple caries. The CT scan revealed multiple scalp subcutaneous masses with chronic inflammatory changes of the skull. Routine laboratory test was normal. Surgical biopsy was performed and the histological result was compatible with actinomycosis. After histological confirmation, parenteral Penicillin 20 million units daily were given for 4 weeks. Clinical improvement was observed after completing a 4-week regimen of intravenous antibiotics. Conclusion: Involvement of scalp by actinomycosis could be mistaken for dif

关键词： Actinomycosis Bacterial Infection Computed Tomography

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Infracallosal Aneurysm Rupture Revealed by Chronic Subdural Hematoma: A Case Report

引用

World Journal of Neuroscience 2022年第3期12卷 112-117页

作者： Mahamadou Dama Oumar Diallo Oumar Coulibaly Daouda Sissoko Theodore H. M. Coulibaly Aliou Maiga youssouf sogoba Neurosurgery Department University Hospital of Mali Bamako Mali Anesthesiology Department University Hospital of Mali Bamako Mali Siramana Medical-Surgical Clinic Bamako Mali Neurosurgery Department University Hospital Gabriel Touré Bamako Mali

Chronic subdural hematoma (CSDH) is one of the most common entities seen in neurosurgery. We report a case of infracallosal aneurysm revealed by CSDH in a 52 years old woman. She presented 3 days alteration of consciousness in 2019 and repeated in September 2020 a severe headache and dizziness. There was no history of others symptoms, nor head trauma. Routine blood examination and coagulation profile were normal. Emergency computed tomography (TC) showed a left temporoparietal-occipital CSDH. Cerebral Angio CT found a bilobated of A2 aneurysm. The precallosal interhemispheric approach was made and clipping the aneurysm after evacuation of CSDH without complication. CSDH is one of the revealed features of intracerebral aneurysm rupture.

关键词： CSDH Cerebral Hemorrhage Infracallosal Aneurysm SAH

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Conservative Treatment in Grisel’s Syndrome Following Tonsillectomy

引用

World Journal of Neuroscience 2018年第1期8卷 38-43页

作者： youssouf sogoba Abdoulaye Barry Issa Amadou Boubacar sogoba Drissa Kanikomo Seybou Hassane Diallo Oumar Coulibaly youssoufa Maiga Siaka Soumaoro Dianguina dit Noumou Soumaré Kadidiatou Singaré Mohamed Keita Department of Neurosurgery Hopital Gabriel Touré Bamako Mali Department of Pediatrics Hopital de Kati Bamako Mali Department of Pediatric Surgery Hopital Gabriel Touré Bamako Mali Department of Neurology Hopital Gabriel Touré Bamako Mali Department of ENT Hopital Gabriel Touré Bamako Mali Department of Pneumonology Hopital du Point G Bamako Mali

Grisel’s syndrome is a rare complication that is characterized by non-traumatic atlantoaxial subluxation. It is most commonly seen in children after an upper respiratory tract infection or neck surgery, such as an adenoidectomy, tonsillectomy and mastoidectomy. Grisel’s Syndrome is characterized by torticollis and a limited range of motion of the neck with pain. Here the authors report a case of a Malian 5-year-old girl with Grisel’s syndrome following tonsillectomy. The patient’s complaints were fully resolved after 2 weeks of conservative treatment.

关键词： Atlantoaxial Subluxation Grisel’s Syndrome Torticollis

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：