Pub Date : 2024-01-30DOI: 10.1016/j.inat.2024.101966
Hao Han, Ran Li, Dongming Fu, Zihao Zhan, Yi'ang Wu, Pengrui Jing, Bin Meng
Background
Symptomatic Tarlov cysts are extremely rare, and there is no consensus on the optimal treatment for this condition. Here, we encountered a patient with a symptomatic giant sacral Tarlov cyst and reviewed the relevant literature.
Case description
A 55-year-old male patient was diagnosed with a large sacral canal cyst based on an MRI examination four years ago. Due to mild symptoms, the patient received conservative treatment. In 2023, the patient's symptoms worsened, significantly affecting daily activities. It was suspected that the symptoms were related to the cyst. Subsequently, the patient underwent laminectomy and microsurgical excision of the cyst. Postoperatively, the patient experienced an improvement in symptoms. We conducted a review of the surgical approach used for this patient and explored alternative treatment methods proposed in the literature for similar conditions.
Conclusions
We achieved favorable outcomes by performing microsurgical excision of symptomatic giant Tarlov cysts in a 55-year-old patient. Additionally, we reviewed relevant literature regarding Tarlov cysts. The treatment approaches for this condition vary, and conservative, interventional, or surgical treatments have all shown efficacy. Therefore, it is crucial to choose an appropriate treatment plan based on the patient's specific circumstances.
{"title":"Giant symptomatic Tarlov cysts: A case report and literature review","authors":"Hao Han, Ran Li, Dongming Fu, Zihao Zhan, Yi'ang Wu, Pengrui Jing, Bin Meng","doi":"10.1016/j.inat.2024.101966","DOIUrl":"https://doi.org/10.1016/j.inat.2024.101966","url":null,"abstract":"<div><h3>Background</h3><p>Symptomatic Tarlov cysts are extremely rare, and there is no consensus on the optimal treatment for this condition. Here, we encountered a patient with a symptomatic giant sacral Tarlov cyst and reviewed the relevant literature.</p><p>Case description</p><p>A 55-year-old male patient was diagnosed with a large sacral canal cyst based on an MRI examination four years ago. Due to mild symptoms, the patient received conservative treatment. In 2023, the patient's symptoms worsened, significantly affecting daily activities. It was suspected that the symptoms were related to the cyst. Subsequently, the patient underwent laminectomy and microsurgical excision of the cyst. Postoperatively, the patient experienced an improvement in symptoms. We conducted a review of the surgical approach used for this patient and explored alternative treatment methods proposed in the literature for similar conditions.</p></div><div><h3>Conclusions</h3><p>We achieved favorable outcomes by performing microsurgical excision of symptomatic giant Tarlov cysts in a 55-year-old patient. Additionally, we reviewed relevant literature regarding Tarlov cysts. The treatment approaches for this condition vary, and conservative, interventional, or surgical treatments have all shown efficacy. Therefore, it is crucial to choose an appropriate treatment plan based on the patient's specific circumstances.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101966"},"PeriodicalIF":0.4,"publicationDate":"2024-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000124/pdfft?md5=9c3da552aba81bd406ca90bb4819a422&pid=1-s2.0-S2214751924000124-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139674314","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}
Pub Date : 2024-01-26DOI: 10.1016/j.inat.2024.101963
Rezafarhad Manteghifasaei, Mohammadali Arami, Mohammad Karimi
Introduction
Pseudotumor cerebri is one of the complex diseases in the field of neurology and neurosurgery. Although it’s classical form manifests with headache and blurred vision, and papilledema is seen in the ophthalmological examination, but its clinical manifestations can be without blurred vision and papilledema, and even without headache.
Here, we present a diagnostically challenging pseudotumor cerebri case who presented only with refractory tinnitus and had increased intracranial pressure, and the tinnitus was completely resolved with transverse sinus stenting.
Conclusion
This case showed that pseudotumor cerebri can have atypical manifestations such as resistant tinnitus without papilledema, and in these cases, intracranial pressure should be measured and its causes, especially cerebral venous sinus stenosis should be investigated and treated.
{"title":"Transvers sinus stenting for treatment of resistant tinnitus due to pseudotumor cerebri syndrome without papilloedema","authors":"Rezafarhad Manteghifasaei, Mohammadali Arami, Mohammad Karimi","doi":"10.1016/j.inat.2024.101963","DOIUrl":"10.1016/j.inat.2024.101963","url":null,"abstract":"<div><h3>Introduction</h3><p>Pseudotumor cerebri is one of the complex diseases in the field of neurology and neurosurgery. Although it’s classical form manifests with headache and blurred vision, and papilledema is seen in the ophthalmological examination, but its clinical manifestations can be without blurred vision and papilledema, and even without headache.</p><p>Here, we present a diagnostically challenging pseudotumor cerebri case who presented only with refractory tinnitus and had increased intracranial pressure, and the tinnitus was completely resolved with transverse sinus stenting.</p></div><div><h3>Conclusion</h3><p>This case showed that pseudotumor cerebri can have atypical manifestations such as resistant tinnitus without papilledema, and in these cases, intracranial pressure should be measured and its causes, especially cerebral venous sinus stenosis should be investigated and treated.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101963"},"PeriodicalIF":0.4,"publicationDate":"2024-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000094/pdfft?md5=e65f4fd969e4bfdc1280b9bbf1e4797e&pid=1-s2.0-S2214751924000094-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139637202","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}
Pub Date : 2024-01-20DOI: 10.1016/j.inat.2024.101965
IBRAHIM Al-hassana Idriss , Hounkpatin Stachys , Mehome Wilfried , Setcheou Alexis , Sieleche Christian , Tankari Aboubacar , Sawa Brice , Jermidi Cynthia , Lethongsavarn Vincent , Helias Phillipe , Assoumane Ibrahim , Kelani Aminath , Rabhi Mohammed , Sanoussi Samuila , Do Laurent
Backgroung
Primary dural lymphoma is a very rare pathology arising from the dura mater. its clinical and radiological presentation is often similar to a meningioma. Treatment typically involves surgery followed by adjuvant radiotherapy/chemotherapy. Fewer than twenty cases have been described in the literature.
Case presentation
A 73-year-old woman with a medical history of hypertension, type 2 diabetes, and dyslipidemia presented with progressive right hemiparesis. Following diagnostic evaluation, a left fronto-temporal meningioma was initially diagnosed. Complete macroscopic excision was made and the immunohistochemical showed a follicular B lymphoma according. the patient had radiotherapy and chemotherapy sessions. Follow-up at 18 months was unremarkable.
Conclusion
Primary dural lymphoma is an exceptionally rare pathology, often mimicking the radiological appearance of a meningioma. The management relies on complete tumor excision, along with a combination of radiotherapy and chemotherapy. When administered appropriately, this treatment approach offers a favorable prognosis for patients.
{"title":"Primary dural Lymphoma: A case report","authors":"IBRAHIM Al-hassana Idriss , Hounkpatin Stachys , Mehome Wilfried , Setcheou Alexis , Sieleche Christian , Tankari Aboubacar , Sawa Brice , Jermidi Cynthia , Lethongsavarn Vincent , Helias Phillipe , Assoumane Ibrahim , Kelani Aminath , Rabhi Mohammed , Sanoussi Samuila , Do Laurent","doi":"10.1016/j.inat.2024.101965","DOIUrl":"10.1016/j.inat.2024.101965","url":null,"abstract":"<div><h3>Backgroung</h3><p>Primary dural lymphoma is a very rare pathology arising from the dura mater. its clinical and radiological presentation is often similar to a meningioma. Treatment typically involves surgery followed by adjuvant radiotherapy/chemotherapy. Fewer than twenty cases have been described in the literature.</p></div><div><h3>Case presentation</h3><p>A 73-year-old woman with a medical history of hypertension, type 2 diabetes, and dyslipidemia presented with progressive right hemiparesis. Following diagnostic evaluation, a left fronto-temporal meningioma was initially diagnosed. Complete macroscopic excision was made and the immunohistochemical showed a follicular B lymphoma according. the patient had radiotherapy and chemotherapy sessions. Follow-up at 18 months was unremarkable.</p></div><div><h3>Conclusion</h3><p>Primary dural lymphoma is an exceptionally rare pathology, often mimicking the radiological appearance of a meningioma. The management relies on complete tumor excision, along with a combination of radiotherapy and chemotherapy. When administered appropriately, this treatment approach offers a favorable prognosis for patients.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101965"},"PeriodicalIF":0.4,"publicationDate":"2024-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000112/pdfft?md5=f0e22b56e4de419238736ca64f116743&pid=1-s2.0-S2214751924000112-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139538916","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}
Aneurysms arising from fenestrated proximal anterior cerebral arteries are rare. Previous studies primarily reported performing clipping. In contrast, endovascular treatment is rarely selected. In this report, we present a case of coil embolization for a ruptured aneurysm arising from a fenestrated proximal anterior cerebral artery.
A sixty-five-year-old woman was transferred to the emergency department of our hospital owing to sudden onset of severe headache and vomiting. A head computed tomography scan showed a diffuse subarachnoid hemorrhage. A cerebral angiogram revealed an aneurysm at the fenestration of the A1 segment. Coil embolization of the aneurysm was performed, and the aneurysm was completely occluded. Both fenestration channels were preserved.
The patient’s clinical course was good, and she was discharged from the hospital twenty-six days after admission. Coil embolization of a ruptured aneurysm in the fenestration of the A1 segment was possible without sacrificing the parent arteries forming the fenestration. However, securing a working projection proved difficult due to the aneurysm being surrounded by two parent arteries forming the fenestration.
{"title":"Successful endovascular treatment of a ruptured saccular aneurysm arising from a fenestrated proximal anterior cerebral artery","authors":"Kazumasa Senju , Yoshinobu Horio , Takashi Morishita , Dai Kawano , Takayuki Koga , Kazunori Oda , Hironori Fukumoto , Takaaki Amamoto , Hiromasa Kobayashi , Koichiro Takemoto , Mitsutoshi Iwaasa , Hiroshi Abe","doi":"10.1016/j.inat.2024.101964","DOIUrl":"https://doi.org/10.1016/j.inat.2024.101964","url":null,"abstract":"<div><p>Aneurysms arising from fenestrated proximal anterior cerebral arteries are rare. Previous studies primarily reported performing clipping. In contrast, endovascular treatment is rarely<!--> <!-->selected. In this report, we present a case of coil embolization for a ruptured aneurysm arising from a fenestrated proximal anterior cerebral artery.</p><p>A sixty-five-year-old woman was transferred to the emergency department of our hospital owing to sudden onset of severe headache and vomiting. A head<!--> <!-->computed tomography scan<!--> <!-->showed a diffuse subarachnoid hemorrhage. A cerebral angiogram revealed an aneurysm at the fenestration of the A1 segment. Coil embolization of the aneurysm was performed, and the aneurysm was completely occluded. Both fenestration channels were preserved.</p><p>The patient’s clinical course was good, and she was discharged from the hospital twenty-six days after admission. Coil embolization of a ruptured aneurysm in the fenestration of the A1 segment was possible without sacrificing the parent arteries forming the fenestration. However, securing a working projection proved difficult due to the aneurysm being surrounded by two parent arteries forming the fenestration.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101964"},"PeriodicalIF":0.4,"publicationDate":"2024-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000100/pdfft?md5=073ef759960d375b7572a967d9160d8c&pid=1-s2.0-S2214751924000100-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139505447","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}
Adult-onset tethered cord syndrome (ATCS) is occasionally reported, but older adult onset is very rare. We treated a patient who was asymptomatic until older adulthood and then developed subacute exacerbation of neurological symptoms.
Case description
A 76-year-old woman presented with bilateral leg pain, numbness, and weakness plus low back pain and dysuria for 1 month. Imaging showed a retained medullary cord with a syrinx and an enhanced mass lesion. She was diagnosed with symptomatic ATCS and underwent surgery. Intraoperative findings were an intramedullary syrinx and inflammatory granulation due to adhesive arachnoiditis.
Conclusion
We experienced a very rare case in which an older adult developed ATCS. Caution is required because idiopathic adhesive arachnoiditis can exacerbate the neurological symptoms.
{"title":"Adult-onset tethered cord syndrome with a retained medullary cord due to adhesive arachnoiditis","authors":"Akitaka Yoshimura , Hisaaki Uchikado , Youhei Iguchi , Shota Fujimura , Hideki Ohta","doi":"10.1016/j.inat.2024.101960","DOIUrl":"10.1016/j.inat.2024.101960","url":null,"abstract":"<div><h3>Background</h3><p>Adult-onset tethered cord syndrome (ATCS) is occasionally reported, but older adult onset is very rare. We treated a patient who was asymptomatic until older adulthood and then developed subacute exacerbation of neurological symptoms.</p></div><div><h3>Case description</h3><p>A 76-year-old woman presented with bilateral leg pain, numbness, and weakness plus low back pain and dysuria for 1 month. Imaging showed a retained medullary cord with a syrinx and an enhanced mass lesion. She was diagnosed with symptomatic ATCS and underwent surgery. Intraoperative findings were an intramedullary syrinx and inflammatory granulation due to adhesive arachnoiditis.</p></div><div><h3>Conclusion</h3><p>We experienced a very rare case in which an older adult developed ATCS. Caution is required because idiopathic adhesive arachnoiditis can exacerbate the neurological symptoms.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101960"},"PeriodicalIF":0.4,"publicationDate":"2024-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000069/pdfft?md5=8121443afc09311052bb2dfaae04074c&pid=1-s2.0-S2214751924000069-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139636233","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}
Pub Date : 2024-01-19DOI: 10.1016/j.inat.2024.101961
Ali Mokhtari , Mehran Haddadi , Amin Mokhtari , Donya Sheibani Tehrani
Introduction
Choosing a promising specialty for medical students is not an easy decision, particularly in a field like neurosurgery known for its high levels of stress. However, in recent years, there has been a decrease in interest, especially among female students, in choosing surgical specialties. Therefore, the present study aimed to identify influential factors in the selection of neurosurgery as a specialty from the perspective of medical students.
Methods
This descriptive-analytical study was conducted in 2023 at the Shahr-e Kord University of Medical Sciences. we estimated a sample size of 425 individuals from the study population. We collected the data using a questionnaire, which was administered through an online questionnaire system.
Results
Male and female perceptions of neurosurgery was similar across many of the surveyed factors, except for: “Male dominated”,“ Tolerant of criticism”, “Duration of residency” and “Must be an athlete”. The factor analysis reduced the 28-variable dimensionality to six latent factors that accounted for 60.72% of the variance found. The factor analysis recognized that, although male and female medical students do have some similar Survey Variable, the influence or weighing of those preferences is different for male and female students. The first latent factor for females consisted of: “Diverse patient population,” and “Procedural based.” The first latent factor for males consisted of: “Male dominated,” and “Prestige.”
Conclusion
The factor analysis indicated that male and female students weight differently when selecting a specialty; this difference may account for the large differences in proportion between males and females in Neurosurgery residency.
{"title":"Factors affecting the choice of neurosurgery: Medical student’s perspective","authors":"Ali Mokhtari , Mehran Haddadi , Amin Mokhtari , Donya Sheibani Tehrani","doi":"10.1016/j.inat.2024.101961","DOIUrl":"https://doi.org/10.1016/j.inat.2024.101961","url":null,"abstract":"<div><h3>Introduction</h3><p>Choosing a promising specialty for medical students is not an easy decision, particularly in a field like neurosurgery known for its high levels of stress. However, in recent years, there has been a decrease in interest, especially among female students, in choosing surgical specialties. Therefore, the present study aimed to identify influential factors in the selection of neurosurgery as a specialty from the perspective of medical students.</p></div><div><h3>Methods</h3><p>This descriptive-analytical study was conducted in 2023 at the Shahr-e Kord University of Medical Sciences. we estimated a sample size of 425 individuals from the study population. We collected the data using a questionnaire, which was administered through an online questionnaire system.</p></div><div><h3>Results</h3><p>Male and female perceptions of neurosurgery was similar across many of the surveyed factors, except for: “Male dominated”,“ Tolerant of criticism”, “Duration of residency” and “Must be an athlete”. The factor analysis reduced the 28-variable dimensionality to six latent factors that accounted for 60.72% of the variance found. The factor analysis recognized that, although male and female medical students do have some similar Survey Variable, the influence or weighing of those preferences is different for male and female students. The first latent factor for females consisted of: “Diverse patient population,” and “Procedural based.” The first latent factor for males consisted of: “Male dominated,” and “Prestige.”</p></div><div><h3>Conclusion</h3><p>The factor analysis indicated that male and female students weight differently when selecting a specialty; this difference may account for the large differences in proportion between males and females in Neurosurgery residency.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101961"},"PeriodicalIF":0.4,"publicationDate":"2024-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000070/pdfft?md5=7c180990bc0363188f4b4d77dbb812e7&pid=1-s2.0-S2214751924000070-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139548811","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}
Due to less than favorable conditions in low and low-middle-income countries, surgeons have had to carefully craft improvised devices to try and mimic the functionality and level of innovation in the developed countries. In this review, we sought to examine the existing literature to review the alternative ways by which intracranial pressure is measured when standard devices are inaccessible. Furthermore, we aimed to see how these devices are made and how much they cost.
Methodology
The PRISMA extension for scoping reviews was utilized. Databases and Grey Literature (PubMed, Google Scholar, and AJOL) were searched extensively, and papers reporting on the use of improvised intracranial pressure monitoring were included. The devices were grouped into two setups and described extensively. The cost of the devices was also estimated. We extracted the relevant information after identifying the papers that would be used in our review study.
Results
3 papers satisfied our eligibility criteria and were used in the review. Two setups were discussed. The first setup involved the use of a makeshift device made up of a size 6 feeding tube/soft silicon catheter, a central venous pressure manometer and sterile 0.9% saline as the coupling agent, while the second setup involved the use of a size 8 feeding tube, a pressure line extension, dome, transducer, and monitor. Both devices cost less than USD 20, a price far cheaper than the standard ICP devices quoted at about USD 800.
Conclusion
Our review posits that these makeshift devices have certain advantages and may be useful in the rural and less developed parts of the world. It also serves as an area for intervention, especially in the context of global neurosurgery.
{"title":"Improvised intracranial pressure monitors in the developing World: A scoping review","authors":"Damilola Jesuyajolu, Abdulahi Zubair, Temidayo Osunronbi, Gamaliel Aremu","doi":"10.1016/j.inat.2024.101959","DOIUrl":"https://doi.org/10.1016/j.inat.2024.101959","url":null,"abstract":"<div><h3>Introduction</h3><p>Due to less than favorable conditions in low and low-middle-income countries, surgeons have had to carefully craft improvised devices to try and mimic the functionality and level of innovation in the developed countries. In this review, we sought to examine the existing literature to review the alternative ways by which intracranial pressure is measured when standard devices are inaccessible. Furthermore, we aimed to see how these devices are made and how much they cost.</p></div><div><h3>Methodology</h3><p>The PRISMA extension for scoping reviews was utilized. Databases and Grey Literature (PubMed, Google Scholar, and AJOL) were searched extensively, and papers reporting on the use of improvised intracranial pressure monitoring were included. The devices were grouped into two setups and described extensively. The cost of the devices was also estimated. We extracted the relevant information after identifying the papers that would be used in our review study.</p></div><div><h3>Results</h3><p>3 papers satisfied our eligibility criteria and were used in the review. Two setups were discussed. The first setup involved the use of a makeshift device made up of a size 6 feeding tube/soft silicon catheter, a central venous pressure manometer and sterile 0.9% saline as the coupling agent, while the second setup involved the use of a size 8 feeding tube, a pressure line extension, dome, transducer, and monitor. Both devices cost less than USD 20, a price far cheaper than the standard ICP devices quoted at about USD 800.</p></div><div><h3>Conclusion</h3><p>Our review posits that these makeshift devices have certain advantages and may be useful in the rural and less developed parts of the world. It also serves as an area for intervention, especially in the context of global neurosurgery.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101959"},"PeriodicalIF":0.4,"publicationDate":"2024-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000057/pdfft?md5=44e4fe4a770bad464aac215230ab18e4&pid=1-s2.0-S2214751924000057-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139434629","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}
Pub Date : 2024-01-11DOI: 10.1016/j.inat.2024.101957
Divya Madhala , Archana Balasubramanian , Lawrence D Cruze , D. Balasubramanian
Prolactinomas are the most common pituitary tumors and are treated with surgery with or without dopamine agonists. Amyloid in prolactinoma is known to occur, but spherical type of amyloid deposition is extremely rare and can pose a diagnostic challenge during intraoperative consultation. They do not respond to medical treatment with dopamine agonists and enlarge in size or undergo fibrosis, causing a failure of medical therapy. Hence, it needs to be identified preoperatively by imaging to institute appropriate management. Here we report a case of a 50 year male with symptoms of burning sensations in the left upper limb and temporal seizures for 4 months. Magnetic resonance imaging showed a well-defined lobulated lesion measuring 4x3.5x3cm eroding the floor of sella. Histology showed spherical, eosinophilic amyloid material with focal cellular areas. Immunohistochemistry and serum levels were high for prolactin. 11 months later, the patient was readmitted with CSF rhinorrhea. The biopsy revealed abundant spherical amyloid with scant cellularity suggesting a recurrence.
{"title":"Spherical type of amyloidogenic pituitary prolactinoma in a 50 year old male","authors":"Divya Madhala , Archana Balasubramanian , Lawrence D Cruze , D. Balasubramanian","doi":"10.1016/j.inat.2024.101957","DOIUrl":"https://doi.org/10.1016/j.inat.2024.101957","url":null,"abstract":"<div><p>Prolactinomas are the most common pituitary tumors and are treated with surgery with or without dopamine agonists. Amyloid in prolactinoma is known to occur, but spherical type of amyloid deposition is extremely rare and can pose a diagnostic challenge during intraoperative consultation. They do not respond to medical treatment with dopamine agonists and enlarge in size or undergo fibrosis, causing a failure of medical therapy. Hence, it needs to be identified preoperatively by imaging to institute appropriate management. Here we report a case of a 50 year male with symptoms of burning sensations in the left upper limb and temporal seizures for 4 months. Magnetic resonance imaging showed a well-defined lobulated lesion measuring 4x3.5x3cm eroding the floor of sella. Histology showed spherical, eosinophilic amyloid material with focal cellular areas. Immunohistochemistry and serum levels were high for prolactin. 11 months later, the patient was readmitted with CSF rhinorrhea. The biopsy revealed abundant spherical amyloid with scant cellularity suggesting a recurrence.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101957"},"PeriodicalIF":0.4,"publicationDate":"2024-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751924000033/pdfft?md5=3a7948359c043d6fd3e44a8e7eac63ab&pid=1-s2.0-S2214751924000033-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139435926","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}
Pub Date : 2024-01-09DOI: 10.1016/j.inat.2023.101954
Mekdes Musie Awano, Eyob Zenebe Wendimagegnehu
Background
Dermal sinus tract is a rare type of spinal dysraphism. It is usually associated with other types of spinal congenital anomalies. This work shows the rare co-occurrence of primary and secondary neurulation defect in a single patient.
Case presentation
We introduce a 2 year old boy who presented with a sacral dimple. He had a complex underlying spinal neural tube defect, dermal sinus tract, dermoid cyst, filum terminale lipoma, tethered spinal cord and syringomyelia. He was managed with excision of the dermal sinus tract, dermoid cyst and filum terminale lipoma with untethering of the spinal cord. He had a good post operative outcome without any neurologic deficit.
Conclusion
This case shows how a simple skin dimple can be an indicator of underlying complex spinal dysraphism. It also shows the co-occurrence of primary and secondary neurulation defect which suggests the complex nature of the neurulation process.
{"title":"A rare complex association of dermal sinus tract, dermoid cyst, filum terminale lipoma, tethered spinal cord and syringomyelia: A case report and literature review","authors":"Mekdes Musie Awano, Eyob Zenebe Wendimagegnehu","doi":"10.1016/j.inat.2023.101954","DOIUrl":"https://doi.org/10.1016/j.inat.2023.101954","url":null,"abstract":"<div><h3>Background</h3><p>Dermal sinus tract is a rare type of spinal dysraphism. It is usually associated with other types of spinal congenital anomalies. This work shows the rare co-occurrence of primary and secondary neurulation defect in a single patient.</p></div><div><h3>Case presentation</h3><p>We introduce a 2 year old boy who presented with a sacral dimple. He had a complex underlying spinal neural tube defect, dermal sinus tract, dermoid cyst, filum terminale lipoma, tethered spinal cord and syringomyelia. He was managed with excision of the dermal sinus tract, dermoid cyst and filum terminale lipoma with untethering of the spinal cord. He had a good post operative outcome without any neurologic deficit.</p></div><div><h3>Conclusion</h3><p>This case shows how a simple skin dimple can be an indicator of underlying complex spinal dysraphism. It also shows the co-occurrence of primary and secondary neurulation defect which suggests the complex nature of the neurulation process.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101954"},"PeriodicalIF":0.4,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214751923002372/pdfft?md5=5721bbd345936b5a221a8fa266c00bd4&pid=1-s2.0-S2214751923002372-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139433883","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}
Amidst progressive improvement of microsurgical techniques, facial nerve (FN) dysfunction is one of the most common complications after vestibular schwannoma (VS) resection. The current study discusses the risk factors associated with FN dysfunction, preservation of FN, and the patient’s quality of life (QoL). In addition, the use of exoscope and FN outcomes was discussed.
Method
We searched PubMed and Scopus using the search terms vestibular schwannoma, acoustic neuroma, risk factors, facial nerve dysfunction, and microsurgery. Linkage or association studies available in full text were analyzed regarding risk factors of FN dysfunction after sporadic VS resection.
Results
We categorized risk factors for FN dysfunction into three groups: non-tumoral, tumoral, and surgical. Tumoral factors were identified as the most significant predictors of FN dysfunction, including large tumor size, tumor extension, FN adhesion, the presence of cystic lesions, and advanced tumor stage. Data regarding non-tumoral factors, such as age and sex, showed heterogeneity and inconsistency. While the middle cranial fossa (MCF) approach may lead to increased FN injury, it was not deemed a significant predictor of FN dysfunction. Furthermore, employing intraoperative monitoring of the FN was linked with improved FN outcomes.
Conclusions
Our review indicates that mounting evidence supports the association of cystic lesions, large tumors, and tumor adhesion to the FN as critical predictors of adverse FN outcomes. When these risk factors necessitate partial resection, radiological follow-up is imperative to monitor for tumor recurrence and to determine the necessity of further surgical intervention.
{"title":"Risk factors of facial nerve dysfunction after sporadic vestibular schwannoma resection - A narrative review with illustrative cases","authors":"Samuel Berchi Kankam , Aidin Shakeri , Mahsa Mohamadi , Abdulrazaq Olamilekan Ahmed , Mohammad Mirahmadi Eraghi , Negar Ghaffari , Adrina Habibzadeh , Lindelwa Mmema , Alireza Khoshnevisan , Hiva Saffar","doi":"10.1016/j.inat.2024.101955","DOIUrl":"https://doi.org/10.1016/j.inat.2024.101955","url":null,"abstract":"<div><h3>Background</h3><p>Amidst progressive improvement of microsurgical techniques, facial nerve (FN) dysfunction is one of the most common complications after vestibular schwannoma (VS) resection. The current study discusses the risk factors associated with FN dysfunction, preservation of FN, and the patient’s quality of life (QoL). In addition, the use of exoscope and FN outcomes was discussed.</p></div><div><h3>Method</h3><p>We searched PubMed and Scopus using the search terms vestibular schwannoma, acoustic neuroma, risk factors, facial nerve dysfunction, and microsurgery. Linkage or association studies available in full text were analyzed regarding risk factors of FN dysfunction after sporadic VS resection.</p></div><div><h3>Results</h3><p>We categorized risk factors for FN dysfunction into three groups: non-tumoral, tumoral, and surgical. Tumoral factors were identified as the most significant predictors of FN dysfunction, including large tumor size, tumor extension, FN adhesion, the presence of cystic lesions, and advanced tumor stage. Data regarding non-tumoral factors, such as age and sex, showed heterogeneity and inconsistency. While the middle cranial fossa (MCF) approach may lead to increased FN injury, it was not deemed a significant predictor of FN dysfunction. Furthermore, employing intraoperative monitoring of the FN was linked with improved FN outcomes.</p></div><div><h3>Conclusions</h3><p>Our review indicates that mounting evidence supports the association of cystic lesions, large tumors, and tumor adhesion to the FN as critical predictors of adverse FN outcomes. When these risk factors necessitate partial resection, radiological follow-up is imperative to monitor for tumor recurrence and to determine the necessity of further surgical intervention.</p></div>","PeriodicalId":38138,"journal":{"name":"Interdisciplinary Neurosurgery: Advanced Techniques and Case Management","volume":"36 ","pages":"Article 101955"},"PeriodicalIF":0.4,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S221475192400001X/pdfft?md5=588e11dd46f6df2b5173dc80abf7bbf0&pid=1-s2.0-S221475192400001X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139436032","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}