{"title":"A Late Complication Related to Percutaneous Implantable Leads for Spinal Cord Stimulation: Myelopathy due to Fibrous Scar Tissue.","authors":"Takuma Maeda, Takashi Agari, Takashi Komori, Keisuke Takai","doi":"10.2176/jns-nmc.2024-0106","DOIUrl":"10.2176/jns-nmc.2024-0106","url":null,"abstract":"<p><p>A 59-year-old woman, after surgery for cubital tunnel syndrome, developed complex regional pain syndrome in her right upper limb. Spinal cord stimulation (SCS) electrodes were placed at the C2-C5 level. A conventional low-frequency tonic stimulation was carried out, which attenuated pain. However, 4 years later, left-sided motor weakness and tolerance to SCS therapy occurred. Magnetic resonance imaging revealed epidural granulation tissue around the electrodes that severely compressed the cervical cord. We surgically removed the granuloma, which attenuated motor weakness. A histological examination showed that an allergic reaction to platinum or the insulator appeared responsible for fibrosis.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"273-278"},"PeriodicalIF":0.0,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11524615/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142549996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Nail Penetration in the Superior Sagittal Sinus: A Case Report of a Nail Gun Injury.","authors":"Yuichi Fujiyama, Sadahiro Nomura, Kouhei Haji, Hiroko Kanaya, Natsumi Fujii, Fumiaki Oka, Hideyuki Ishihara","doi":"10.2176/jns-nmc.2024-0026","DOIUrl":"10.2176/jns-nmc.2024-0026","url":null,"abstract":"<p><p>The number of penetrating brain injuries (PBI) is low, and the materials of PBI, including bullets, nails, chopsticks, wood, and missiles, vary widely. We report a case in which a nail penetrated the superior sagittal sinus (SSS) and advanced between the cerebral falx but was managed favorably. A 25-year-old male was bruised by a nail gun falling on his head, triggering the ejection of a 3-inch nail into his head. He presented with no symptoms other than mild bleeding and head pain. The patient did not notice the nail injection. Computed tomography (CT) and angiogram revealed that the nail entered parallel to the midline in the interhemispheric fissure through SSS, and there was no intracranial hemorrhage. A bilateral frontoparietal craniotomy was performed with the nail left fixed to the skull. After confirming that the cerebral falx enveloped the entire length of the nail, we extirpated it and sealed the entrance to the SSS. The patient recovered with no neurological deficits, and postoperative images confirmed preservation of the antegrade venous return of the SSS. We observed a case of nail penetration in the SSS. It was essential to perform a thorough imaging examination and the extraction under direct observation using a microscope.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"279-283"},"PeriodicalIF":0.0,"publicationDate":"2024-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11524613/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142550012","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Coil Embolization of a Ruptured Traumatic Pseudoaneurysm of the Middle Meningeal Artery: A Case Report.","authors":"Naoki Nishizawa, Tomoki Kidani, Shin Nakajima, Yonehiro Kanemura, Katsunori Asai, Nobuyuki Izutsu, Saki Kawamoto, Koji Kobayashi, Mikako Nomoto, Yosuke Fujimi, Masayoshi Kida, Toshiyuki Fujinaka","doi":"10.2176/jns-nmc.2024-0073","DOIUrl":"10.2176/jns-nmc.2024-0073","url":null,"abstract":"<p><p>Traumatic pseudoaneurysms of the middle meningeal artery (MMA) are rare and have a poor prognosis due to their high risk of rupture. This study presents a case of a 53-year-old man who experienced rupture of an MMA pseudoaneurysm 10 days after craniotomy for an acute subdural hematoma caused by a blunt head injury. He also had an accompanying temporal bone fracture extending to the skull base. Initial imaging showed no evidence of cerebrovascular injury. The rupture resulted in a temporal hemorrhage with intraventricular extension that caused acute hydrocephalus. Digital subtraction angiography showed that the pseudoaneurysm was located just below the right temporal bone fracture. Coil embolization of the aneurysm was performed and complete occlusion was achieved. His hydrocephalus was addressed with placement of an external ventricular drain, which was later converted to a ventriculoperitoneal shunt. There was no rebleeding and he was transferred to a convalescent hospital. Traumatic MMA pseudoaneurysms usually develop several days after injury and are thus not present on imaging immediately after injury. Aggressive treatment is warranted due to their poor prognosis.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"257-262"},"PeriodicalIF":0.0,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11563658/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142635575","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
NMC case report journalPub Date : 2024-09-21eCollection Date: 2024-01-01DOI: 10.2176/jns-nmc.2024-0146
Kotaro Kohara, Shiro Horisawa, Takakazu Kawamata
{"title":"Sustainable Improvement of Anterocollis-type Cervical Dystonia with a Hanger Reflex Device: A Case Report.","authors":"Kotaro Kohara, Shiro Horisawa, Takakazu Kawamata","doi":"10.2176/jns-nmc.2024-0146","DOIUrl":"10.2176/jns-nmc.2024-0146","url":null,"abstract":"<p><p>The hanger reflex is an automatic head rotation movement. When individuals wear a wire clothes hanger on the head to compress the frontotemporal region, the head spontaneously rotates toward the compressed side. The device to induce the hanger reflex was first developed for treating rotation-type cervical dystonia, followed by the development of a device for anterocollis-type cervical dystonia. However, there is a lack of comprehensive clinical reports on hanger reflex treatments, especially for anterocollis-type dystonia. We present the case of anterocollis that completely resolved after hanger reflex treatment without any other invasive treatment. In the treatment, patients wear the device on their heads for 30 min once per day. Hanger reflex treatment is an easy, simple, noninvasive, and inexpensiveness approach that may be considered the first choice for cervical dystonia.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"263-266"},"PeriodicalIF":0.0,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11563657/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142635577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"An Adult Case of Genetically Confirmed Hyperekplexia Presenting with Head Trauma.","authors":"Natsumi Baba, Tomoyuki Kawataki, Takeshi Taketani, Hiroyuki Kinouchi","doi":"10.2176/jns-nmc.2024-0088","DOIUrl":"https://doi.org/10.2176/jns-nmc.2024-0088","url":null,"abstract":"<p><p>Hyperekplexia is a rare neurological disorder that is characterized by an excessive startle response to unexpected stimuli. Recently, heterogeneous causative genes have been identified. Most cases are diagnosed during the neonatal period from hypertonia or stiffness. Adult cases are relatively rare and can cause severe head injury, but they are often misdiagnosed, typically as epilepsy or psychiatric disorders, due to the rarity of the pathology. This report describes a genetically confirmed case of hyperekplexia in an adult with head trauma, highlighting the features of head trauma and discussing potential pitfalls in the diagnosis of adult patients with hyperekplexia.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"237-241"},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11407916/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142305517","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A Case of Hanging with Limited Specific Postmortem Brain Imaging.","authors":"Arata Nagai, Tomoya Kobayashi, Kyuzo Kurosawa, Kuniyasu Niizuma, Hidenori Endo","doi":"10.2176/jns-nmc.2024-0113","DOIUrl":"https://doi.org/10.2176/jns-nmc.2024-0113","url":null,"abstract":"<p><p>In Japan, the number of autopsies has steadily decreased. Therefore, postmortem imaging methods have positioned as valuable supplemental or complementary tools in autopsy procedures. We clinicians are increasingly faced with the need to infer cause of death from postmortem imaging findings. We report computed tomography (CT) and magnetic resonance imaging (MRI) findings of a 41-year-old man who committed suicide by hanging. CT revealed fractures of the left superior horn of the thyroid cartilage. Head MRI showed high signal intensity in the basal ganglia on the T<sub>1</sub>-weighted image and high-intensity rims along the cerebral cortex on the diffusion-weighted image; however, these were considered normal postmortem changes. There were no significant findings in the heart, major blood vessels, or abdominal organs. The contents of the stomach were minimal, and no tablets or other evidence suggestive of drug overdose were identified. Traumatic changes were not observed. Based on the scene and his circumstances, it was speculated that he died by hanging and an autopsy was not performed. This case highlights the importance of understanding normal postmortem brain imaging changes to estimate the true cause of death.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"249-255"},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11407918/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142305516","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Neurosarcoidosis Complicated by Noncommunicating Hydrocephalus with Atypical Presentation, Diagnosed and Treated with Endoscopic Surgery: A Case Report.","authors":"Sho Matsunaga, Yusuke Kimura, Naoya Watanabe, Yukinori Akiyama, Nobuhiro Mikuni","doi":"10.2176/jns-nmc.2023-0298","DOIUrl":"https://doi.org/10.2176/jns-nmc.2023-0298","url":null,"abstract":"<p><p>Neurosarcoidosis is a condition that is characterized by the occurrence of noncaseating epithelioid granulomas in various organs throughout the body, including the lungs, heart, and central nervous system. It is particularly prevalent in cases of noncommunicating hydrocephalus. While its clinical presentations may vary, neurological deficits such as hemiparesis are extremely uncommon. We herein present a case of unilateral hydrocephalus resulting from neurosarcoidosis presenting with hemiparesis. A 58-year-old woman exhibited right hemiparesis, altered mental status, and aphasia persisting for 1 month. Magnetic resonance imaging showed unilateral hydrocephalus of uncertain etiology. The patient underwent external ventricular drainage, endoscopic fenestration of the septum pellucidum (septostomy), and lesion biopsy, which led to a histopathological diagnosis. Hemiparesis can accompany unilateral hydrocephalus caused by neurosarcoidosis. Endoscopic procedures provide an effective option for the diagnosis and treatment of noncommunicating hydrocephalus caused by neurosarcoidosis.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"243-247"},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11407917/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142305518","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
NMC case report journalPub Date : 2024-08-10eCollection Date: 2024-01-01DOI: 10.2176/jns-nmc.2024-0095
Ako Matsuhashi, Shogo Dofuku, Satoshi Koizumi, Rika Nakamura, Hiroshi Narasaki, Ken Kazama, Ichiro Yonekura, Hideaki Imai
{"title":"A Rare Case of Ruptured Distal Posterior Cerebral Artery Aneurysm Followed by Middle Cerebral Artery Occlusion due to Delayed Diagnosis of Infective Endocarditis.","authors":"Ako Matsuhashi, Shogo Dofuku, Satoshi Koizumi, Rika Nakamura, Hiroshi Narasaki, Ken Kazama, Ichiro Yonekura, Hideaki Imai","doi":"10.2176/jns-nmc.2024-0095","DOIUrl":"10.2176/jns-nmc.2024-0095","url":null,"abstract":"<p><p>A 31-year-old female presented to our hospital with sudden headache and altered consciousness. Computed tomography showed left acute subdural hematoma, and digital subtraction angiography revealed a small aneurysm on the left distal posterior cerebral artery. Coil embolization was conducted, and the patient was discharged with no neurological deficits. However, two weeks later, she presented with complete left hemiplegia and with the National Institutes of Health Stroke Scale of 20. Magnetic resonance angiography showed the occlusion of right middle cerebral artery, and the Diffusion-Weighted Imaging-Alberta Stroke Program Early Computed Tomography Score was four. Mechanical thrombectomy was conducted. Complete recanalization was achieved, and the patient recovered favorably. Although she showed no symptoms of infection such as fever throughout the treatment of aneurysm and thrombectomy, her blood culture was positive for <i>streptococcus mitis</i>. Furthermore, the thrombus retrieved by thrombectomy showed bacterial mass, and transesophageal echocardiography (TEE) showed vegetation on the mitral valve that could not be detected by transthoracic echocardiography. Therefore, the patient was diagnosed with infective endocarditis (IE). She was administered penicillin for 6 weeks and was discharged with no neurological deficits. When treating young patients with small aneurysms in rare locations, IE should be suspected, and blood culture and TEE should be conducted, even when there are no obvious symptoms of systemic infection.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"221-225"},"PeriodicalIF":0.0,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11368417/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142121542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Combined Mechanical Thrombectomy for Multiple Cerebral Venous Sinus Thrombosis Involving the Straight Sinus: A Case Report.","authors":"Tomohiro Matsuda, Mami Hanaoka, Noriya Enomoto, Tadashi Yamaguchi, Takeshi Miyamoto, Hitoshi Niki, Kazuhito Matsuzaki","doi":"10.2176/jns-nmc.2024-0077","DOIUrl":"10.2176/jns-nmc.2024-0077","url":null,"abstract":"<p><p>The proportion of cerebral venous sinus thrombosis involving the straight sinus (StS) is low, and the prognosis is poor. We report a case of multiple sinus thrombosis involving StS in which the patient underwent mechanical thrombectomy (MT) using a stent retriever and an aspiration catheter (combined MT) with a good postoperative course. A 15-year-old girl was admitted to our hospital with rapid loss of consciousness. Magnetic resonance imaging (MRI) revealed thrombosis of the bilateral internal cerebral veins, vein of Galen, StS, torcular herophili (TH), and right transverse sinus (TS), as well as edema mainly in the left thalamus, basal ganglia, and corpus callosum. Systemic heparinization was initiated, and combined MT was performed. Although complete recanalization of the TH and right TS via the left internal jugular vein was achieved, the microwire could not be advanced to the StS. Hence, the approach route was changed to remove the thrombus from the superior sagittal sinus and successfully reach the StS via the right TS. Partial recanalization of the StS was achieved, and venous congestion was improved. Two months after MT, the patient returned to school without neurological deficits. MRI performed 3 months after MT revealed disappearance of the edema and complete recanalization of the StS. In this case, StS catheterization via the left TS was not possible. However, we could reach the right TS, which were recanalized first. Partial recanalization of the StS can be expected a good prognosis under the patency of the TH and TS.</p>","PeriodicalId":101331,"journal":{"name":"NMC case report journal","volume":"11 ","pages":"227-231"},"PeriodicalIF":0.0,"publicationDate":"2024-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11368415/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142121543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}