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Survival of Toddler with Aortoesophageal Fistula after Button Battery Ingestion. 儿童误食纽扣电池后主动脉食管瘘的存活率。
IF 0.6 Pub Date : 2021-10-05 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5557054
Hannah Gibbs, Rishabh Sethia, Patrick I McConnell, Jennifer H Aldrink, Toshiharu Shinoka, Kent Williams, Kris R Jatana
Button batteries (BBs) are found in many households and are a source of esophageal foreign body in the pediatric population. Upon ingestion, significant caustic injury can occur within 2 hours leading to tissue damage and severe, potentially fatal sequelae. Aortoesophageal fistula (AEF) is a rare complication that nearly always results in mortality. We report a rare case of a toddler who developed an AEF after BB ingestion and survived following staged aortic repair. There should be a high index of suspicion for this complication with the history of BB ingestion and presence of hematemesis, hemoptysis, or melena.
纽扣电池(BBs)在许多家庭中被发现,是儿童食道异物的来源。摄入后,可在2小时内造成严重的腐蚀性损伤,导致组织损伤和严重的、可能致命的后遗症。主动脉食管瘘(AEF)是一种罕见的并发症,几乎总是导致死亡。我们报告一个罕见的情况下,一个幼儿谁发展为AEF后,摄取BB和生存后,分阶段主动脉修复。有BB摄入史和出现呕血、咯血或黑黑的患者应高度怀疑该并发症。
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引用次数: 5
A Case of Amelanotic Malignant Melanoma of the Lingual Base That Was Diagnosed Based on a Biopsy of Late Metastasis to a Lumbar Vertebra after Being Misdiagnosed as HPV-Positive Oropharyngeal Anterior Wall Squamous Cell Carcinoma. 1例口咽前壁鳞状细胞癌误诊为HPV阳性,经腰椎晚期转移活检诊断为舌根无毛恶性黑色素瘤。
IF 0.6 Pub Date : 2021-09-30 eCollection Date: 2021-01-01 DOI: 10.1155/2021/7139280
Takumi Okuda, Shinsuke Ide, Kei Kajihara, Tetsuya Tono

We report a case of amelanotic malignant melanoma (AMM) in a 66-year-old female. AMM of the lingual base was diagnosed based on a biopsy of late metastasis to the bone marrow of the L4 lumbar vertebra. The patient was initially treated with chemoradiotherapy after being misdiagnosed with poorly differentiated human papillomavirus- (HPV-) related squamous cell carcinoma of the oropharyngeal anterior wall. p16 immunostaining is used to diagnose HPV-related oropharyngeal cancer. However, while p16 expression is used as a surrogate marker of HPV infection, it is important to be aware that p16 protein overexpression can also be caused by other factors. Malignant melanoma is known to express the p16 protein. Morphologically differentiating between AMM and poorly differentiated squamous cell carcinoma based on hematoxylin-eosin staining is difficult. Therefore, in cases that are pathologically diagnosed as p16-positive poorly differentiated oropharyngeal squamous cell carcinoma, it is important to rule out AMM.

我们报告一例无黑色素瘤恶性黑色素瘤(AMM)在一个66岁的女性。舌底AMM的诊断是基于对L4腰椎骨髓晚期转移的活检。在被误诊为低分化人乳头瘤病毒(HPV)相关口咽前壁鳞状细胞癌后,患者最初接受放化疗。p16免疫染色用于hpv相关口咽癌的诊断。然而,虽然p16表达被用作HPV感染的替代标志物,但重要的是要意识到p16蛋白过表达也可能由其他因素引起。恶性黑色素瘤已知表达p16蛋白。基于苏木精-伊红染色在形态学上区分AMM和低分化鳞状细胞癌是困难的。因此,在病理诊断为p16阳性低分化口咽鳞状细胞癌的病例中,排除AMM很重要。
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引用次数: 1
Presence of Two Separate Hairy Polyps with Meningothelial Elements in a 15-Month-Old Child. 一个15个月大的婴儿出现两个独立的毛状息肉并伴有脑膜上皮成分。
IF 0.6 Pub Date : 2021-09-21 eCollection Date: 2021-01-01 DOI: 10.1155/2021/1844244
Ahmad Saeed A Alghamdi, Nasser Almutairi, Ghassan Alokby
Hairy polyps are benign embryological tumors of the head and neck region that are derived from two germinal layers, the ectoderm and mesoderm. At an incidence of 1 : 40000, hairy polyps are considered rare growths. Presenting symptoms of hairy polyps can vary greatly depending on the size and location of the tumor. To the best of our knowledge, our reported case is the first in the literature to highlight an extremely rare occurrence of two separate hairy polyps being simultaneously present in one patient, in the clivus and the nasion, with the presence of meningothelial cells within both tumors, histopathologically. With surgical resection as the management of choice, the approach of surgery differs greatly depending on many factors. Since the patient in our reported case had a cleft palate, we used a combined transnasal and transoral approach to fully release the clival mass and a direct skin incision for the nasion mass. Recurrence after complete surgical resection is rare, and if happens, it should rise suspicion of histopathologically misdiagnosed tumor. We amplified the importance of advanced radiological investigations along with proper multidisciplinary teamwork to exclude CNS connections and other histologically malignant tumors and to early pick up a possible simultaneous lesion.
毛状息肉是头颈部的良性胚胎肿瘤,起源于两个生发层,外胚层和中胚层。毛状息肉的发病率为1:40 000,被认为是罕见的生长。根据肿瘤的大小和位置不同,毛状息肉的症状也会有很大的不同。据我们所知,我们报告的病例是文献中第一个强调在一个患者中同时出现两个独立的毛状息肉的极其罕见的病例,在斜坡和鼻腔,在两个肿瘤中都存在脑膜上皮细胞,组织病理学。手术切除作为治疗的选择,手术的方法因许多因素而有很大的不同。由于我们报告的病例患者有腭裂,我们采用经鼻和经口联合入路来完全释放斜坡肿块,并直接皮肤切口切除鼻腔肿块。完全手术切除后复发是罕见的,如果发生,应引起组织病理学误诊肿瘤的怀疑。我们强调了先进的放射学检查以及适当的多学科合作的重要性,以排除中枢神经系统连接和其他组织学上的恶性肿瘤,并早期发现可能同时发生的病变。
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引用次数: 0
Nasopharyngeal Coil Dislocation of an Embolized Internal Carotid Artery Pseudoaneurysm. 栓塞性颈内动脉假性动脉瘤鼻咽线圈脱位。
IF 0.6 Pub Date : 2021-09-11 eCollection Date: 2021-01-01 DOI: 10.1155/2021/4270441
Nazli Ay, Ingo Todt, Holger Sudhoff

Objective: Severe epistaxis caused by ruptured intracranial pseudoaneurysms can be effectively treated by coil embolization. This is generally an efficient and safe procedure and provides sufficient protection recurrent epistaxis. However, complications such as aneurysm rupture, arterial dissection, bleeding, and emboli can occur. A dislocation of a nasopharyngeal coil is an extremely rare event. Patient. We present a case of a 61-year-old patient with a recurrent undifferentiated nasopharyngeal carcinoma (NPC) treated with severe epistaxis. Initially, epistaxis was successfully controlled by a nasal packing. Recurrent bleeding despite packing required a neuroradiological intervention. An intracranially ruptured pseudoaneurysm was detected by magnetic resonance imaging (MRI) and computed tomography (CT), originating from the internal carotid artery at the junction of the petrous part to the cavernous part. Coiling and endovascular plug embolization was performed for the treatment of aneurysm. Ten months later, the patient removed a foreign body out of his left nose. It was dislocated coil material due to radionecrosis. MRI confirmed sufficient embolization of the internal carotid artery.

Conclusions: This case report highlights the possibility of a nasopharyngeal coil dislocation of an embolized internal carotid artery aneurysm emerging as a nasal foreign body.

目的:对颅内假性动脉瘤破裂引起的严重鼻出血进行线圈栓塞治疗是有效的。这通常是一个有效和安全的程序,并提供足够的保护复发性鼻出血。然而,并发症如动脉瘤破裂、动脉剥离、出血和栓塞可能发生。鼻咽线圈脱位是一种极为罕见的事件。病人。我们报告一个61岁的复发性未分化鼻咽癌(NPC)伴严重鼻出血的病例。最初,鼻出血通过鼻腔填充物成功控制。再出血,尽管包装需要神经放射干预。通过磁共振成像(MRI)和计算机断层扫描(CT)发现颅内破裂的假性动脉瘤,起源于内颈动脉在岩部和海绵体部分的交界处。动脉瘤的治疗采用卷取和血管内栓塞术。十个月后,病人从左鼻子取出了一个异物。由于放射性腐蚀导致线圈材料错位。MRI证实颈内动脉充分栓塞。结论:本病例报告强调了栓塞的颈内动脉瘤出现鼻咽线圈脱位的可能性。
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引用次数: 2
A Rare Case of Posttraumatic Bilateral BPPV Presentation. 一例罕见的创伤后双侧BPPV表现。
IF 0.6 Pub Date : 2021-09-06 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8636676
Sinisa Maslovara, Andro Kosec, Ivana Pajic Matic, Anamarija Sestak

A rare case of a 38-year-old female patient who developed benign paroxysmal positional vertigo (BPPV) three weeks after head trauma is presented. The disease manifested bilaterally, which is not uncommon posttraumatically, but in this case, it manifested itself as canalithiasis of the posterior canal on both sides and cupulolithiasis of the right lateral canal, which to our knowledge is a unique and, until now, unpublished case. The aim of this review is to point out the fact that, in such a complex multicanal and bilateral clinical presentation of BPPV, it is not sufficient to perform only positioning but also additional laboratory tests. With a good knowledge of the etiopathogenesis, pathophysiology and clinical forms of BPPV, we can, in most cases, make an accurate and precise diagnosis of the disease and carry out appropriate treatment.

一个罕见的情况下,38岁的女性患者谁发展良性阵发性位置性眩晕(BPPV)三周后,头部创伤提出。该疾病表现为双侧,这在创伤后并不罕见,但在本病例中,它表现为两侧后椎管管结石和右侧外侧椎管结石,据我们所知,这是一个独特的,直到现在,未发表的病例。这篇综述的目的是指出这样一个事实,即在BPPV如此复杂的多肛管和双侧临床表现中,仅仅进行定位是不够的,还要进行额外的实验室检查。了解了BPPV的发病机制、病理生理和临床表现,在大多数情况下,我们可以准确、准确地诊断疾病并进行适当的治疗。
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引用次数: 1
The Rare Cases of Parotid Gland Arteriovenous Malformations. 腮腺动静脉畸形的罕见病例分析。
IF 0.6 Pub Date : 2021-09-02 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6072155
Manish Gupta, Vijay Shrawan Nijhawan, Cynthia Kaur, Sukhpreet Kaur, Akanksha Gupta

Arteriovenous malformation (AVM) results from errors in vascular development during embryogenesis; absent capillary beds lead to shunting directly from the arterial to venous circulation. Although it is common in the head and neck region, AVMs located in the parotid gland are quite rare. Here, we report two cases of arteriovenous malformation of the parotid gland that presented to our out-patient setup with swelling in the parotid region and were diagnosed as arteriovenous malformation on histopathological study after surgical resection.

动静脉畸形(AVM)是胚胎发育过程中血管发育错误的结果;没有毛细血管床导致动脉循环直接分流到静脉循环。虽然它常见于头颈部,但位于腮腺的avm是相当罕见的。在此,我们报告两例腮腺动静脉畸形的病例,他们出现在我们的门诊,在腮腺区域肿胀,并在手术切除后的组织病理学检查中被诊断为动静脉畸形。
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引用次数: 2
Osteochondroma Arising from the Thyroid Cartilage: A Case Report and Literature Review. 甲状腺软骨骨软骨瘤1例报告及文献复习。
IF 0.6 Pub Date : 2021-09-02 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8286012
Jessa E Miller, Shaghauyegh S Azar, Dinesh K Chhetri

Introduction: Osteochondromas are relatively common benign bone tumors often located at the metaphyseal ends of long bones; however, they are rare in the head and neck region. The objective of this study is to present a case of an osteochondroma arising from the thyroid cartilage causing insidious dysphonia and to present a literature review.

Methods: The medical record of a patient treated for osteochondroma of the thyroid cartilage was reviewed. A literature search on osteochondromas was conducted using PubMed and Google Scholar. The epidemiology, presentation, diagnosis, treatment, and outcomes of osteochondromas were reviewed.

Results: A 50-year-old female presented with nine months of dysphonia and aphonic voice breaks. Laryngovideostroboscopy revealed a left false vocal fold fullness, glottal gap, and vibratory phase asymmetry. A CT neck demonstrated a well-circumscribed 5 × 8 × 9 mm mass arising from the left thyroid cartilage lamina with a thin calcified rim and a heterogeneous decreased attenuation center. The tumor was excised surgically. Histopathologic analysis demonstrated hyaline cartilage overlying lamellar bone with fatty bone marrow, consistent with osteochondroma. English language literature review revealed no cases of osteochondroma of the thyroid cartilage. The presenting features of osteochondroma may depend on the size and location of the lesion. It is critical to differentiate between benign and malignant bone tumors, and physicians must rely on their clinical examination, radiographic findings, and histopathologic analysis to make the correct diagnosis.

Conclusions: Osteochondromas of the laryngeal framework are extremely rare, and to our knowledge, there have been no reports in the literature of this tumor arising from the thyroid cartilage. Dysphonia may be the presenting symptom in a patient with a thyroid cartilage mass causing restricted mobility of the true vocal folds.

骨软骨瘤是一种较为常见的良性骨肿瘤,常位于长骨干骺端;然而,他们是罕见的头颈部区域。本研究的目的是提出一个由甲状腺软骨引起的骨软骨瘤的病例,并进行文献回顾。方法:回顾性分析1例甲状软骨骨软骨瘤的临床资料。使用PubMed和Google Scholar对骨软骨瘤进行文献检索。本文综述了骨软骨瘤的流行病学、表现、诊断、治疗和预后。结果:一名50岁的女性表现为九个月的发音障碍和语音中断。喉部频闪镜检查显示左假声带丰满、声门间隙及振动相位不对称。颈部CT显示左侧甲状腺软骨层有一个边界清晰的5 × 8 × 9 mm肿块,边缘呈薄钙化,中心呈非均匀性衰减。手术切除了肿瘤。组织病理学分析显示透明软骨覆盖板层骨并伴有脂肪性骨髓,符合骨软骨瘤。英文文献复习未发现甲状软骨骨软骨瘤病例。骨软骨瘤的表现可能取决于病变的大小和位置。鉴别骨肿瘤的良恶性是至关重要的,医生必须依靠临床检查、影像学表现和组织病理学分析来做出正确的诊断。结论:喉架骨软骨瘤极为罕见,据我们所知,尚无文献报道这种肿瘤起源于甲状腺软骨。发音障碍可能是甲状腺软骨肿块患者的主要症状,引起真声带活动受限。
{"title":"Osteochondroma Arising from the Thyroid Cartilage: A Case Report and Literature Review.","authors":"Jessa E Miller,&nbsp;Shaghauyegh S Azar,&nbsp;Dinesh K Chhetri","doi":"10.1155/2021/8286012","DOIUrl":"https://doi.org/10.1155/2021/8286012","url":null,"abstract":"<p><strong>Introduction: </strong>Osteochondromas are relatively common benign bone tumors often located at the metaphyseal ends of long bones; however, they are rare in the head and neck region. The objective of this study is to present a case of an osteochondroma arising from the thyroid cartilage causing insidious dysphonia and to present a literature review.</p><p><strong>Methods: </strong>The medical record of a patient treated for osteochondroma of the thyroid cartilage was reviewed. A literature search on osteochondromas was conducted using PubMed and Google Scholar. The epidemiology, presentation, diagnosis, treatment, and outcomes of osteochondromas were reviewed.</p><p><strong>Results: </strong>A 50-year-old female presented with nine months of dysphonia and aphonic voice breaks. Laryngovideostroboscopy revealed a left false vocal fold fullness, glottal gap, and vibratory phase asymmetry. A CT neck demonstrated a well-circumscribed 5 × 8 × 9 mm mass arising from the left thyroid cartilage lamina with a thin calcified rim and a heterogeneous decreased attenuation center. The tumor was excised surgically. Histopathologic analysis demonstrated hyaline cartilage overlying lamellar bone with fatty bone marrow, consistent with osteochondroma. English language literature review revealed no cases of osteochondroma of the thyroid cartilage. The presenting features of osteochondroma may depend on the size and location of the lesion. It is critical to differentiate between benign and malignant bone tumors, and physicians must rely on their clinical examination, radiographic findings, and histopathologic analysis to make the correct diagnosis.</p><p><strong>Conclusions: </strong>Osteochondromas of the laryngeal framework are extremely rare, and to our knowledge, there have been no reports in the literature of this tumor arising from the thyroid cartilage. Dysphonia may be the presenting symptom in a patient with a thyroid cartilage mass causing restricted mobility of the true vocal folds.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2021-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433032/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39411599","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}
引用次数: 0
Unilateral Cysticercosis of the Parotid Gland: Case Report, Diagnosis, and Clinical Management. 单侧腮腺囊虫病:病例报告、诊断和临床处理。
IF 0.6 Pub Date : 2021-07-31 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9999441
Zachary Elwell, Shethal Bearelly, Khalid Aboul-Nasr, Jonathan Lara

Cysticercosis is a systemic parasitic infection caused by the establishment of the larval form of the parasitic cestode, Taenia solium. Cysticercosis is acquired via the fecal-oral route and is prevalent in low- and middle-income countries (LMICs). Patients typically manifest with skeletal muscle, subcutaneous, or central nervous system involvement. Though there are reports of oral mucosa involvement, solitary involvement of the parotid gland is rare. This is a rare case of a 57-year-old man diagnosed with parotid cysticercosis by imaging and FNA. He was successfully treated by anthelminthic therapy and needle aspiration. The patient has been seen back several times. The cyst is not palpable, and he is satisfied. Parotid cysticercosis should be considered in the differential of a parotid mass in patients who have traveled to endemic regions. Though prior reports have indicated the importance of surgical excision, this patient was treated medically.

囊虫病是一种全身性寄生虫感染,由寄生绦虫(带绦虫)的幼虫形成引起。囊虫病是通过粪-口途径获得的,在低收入和中等收入国家普遍存在。患者典型表现为骨骼肌、皮下或中枢神经系统受累。虽然有口腔粘膜受累的报告,单独受累腮腺是罕见的。这是一个罕见的病例,57岁的男性诊断为腮腺囊虫病影像学和FNA。通过驱虫药和针吸治疗成功。这个病人已经复诊好几次了。囊肿摸不到,他很满意。曾到流行地区旅行的患者在鉴别腮腺肿块时应考虑腮腺囊虫病。虽然先前的报告指出手术切除的重要性,但该患者接受了药物治疗。
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引用次数: 2
Traumatic Cochlear Implant Electrode Extrusion: Considerations, Management, and Outcome. 外伤性人工耳蜗电极挤压:考虑、处理和结果。
IF 0.6 Pub Date : 2021-07-30 eCollection Date: 2021-01-01 DOI: 10.1155/2021/2918859
Ching Yee Chan, Feifan Wang, Haryani Omar, Henry Kun Kiaang Tan

Cochlear implantation is the mainstay for patients with severe to profound hearing loss that do not benefit from hearing aids. Falls and head trauma can cause direct damage to the implant, of which hard failure is the most common complication. Traumatic electrode migration is an uncommon occurrence. Our patient underwent successful electrode advancement of a partially migrated, normal functioning electrode two months after head injury. We discuss the factors influencing the decision-making process, progress, and outcomes.

对于不能从助听器中获益的严重到深度听力损失患者,人工耳蜗植入术是主要的治疗手段。跌倒和头部外伤可对假体造成直接损伤,其中硬衰竭是最常见的并发症。外伤性电极迁移并不常见。我们的病人在头部受伤两个月后成功地进行了部分迁移、功能正常的电极推进。我们讨论了影响决策过程、进展和结果的因素。
{"title":"Traumatic Cochlear Implant Electrode Extrusion: Considerations, Management, and Outcome.","authors":"Ching Yee Chan,&nbsp;Feifan Wang,&nbsp;Haryani Omar,&nbsp;Henry Kun Kiaang Tan","doi":"10.1155/2021/2918859","DOIUrl":"https://doi.org/10.1155/2021/2918859","url":null,"abstract":"<p><p>Cochlear implantation is the mainstay for patients with severe to profound hearing loss that do not benefit from hearing aids. Falls and head trauma can cause direct damage to the implant, of which hard failure is the most common complication. Traumatic electrode migration is an uncommon occurrence. Our patient underwent successful electrode advancement of a partially migrated, normal functioning electrode two months after head injury. We discuss the factors influencing the decision-making process, progress, and outcomes.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2021-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8349271/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39296363","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}
引用次数: 3
Frontal Sinus "Hump": An Anatomical Risk Factor for Anterior Skull Base Injury in the Endoscopic Modified Lothrop Approach (Outside-In Frontal Drill-Out). 额窦“驼峰”:内镜下改良Lothrop入路(由外向内额部钻出)前颅底损伤的解剖学危险因素。
IF 0.6 Pub Date : 2021-07-22 eCollection Date: 2021-01-01 DOI: 10.1155/2021/3402496
Teppei Takeda, Kazuhiro Omura, Haw Torng, Teru Ebihara, Satoshi Aoki, Kosuke Tochigi, Hiromi Kojima, Nobuyoshi Otori

Skull base injuries caused by the outside-in frontal drill-out technique have not been reported. In this report, we chose an outside-in approach to open the frontal sinus for olfactory neuroblastoma resection. Although we identified the first olfactory fibre, the anterior skull base was damaged while drilling into the frontal sinus on the tumour side. We reconstructed the skull base in multiple layers using fascia and cartilage. Postoperative cerebrospinal fluid leakage or intracranial haemorrhage was not observed. In this case, a morphological difference existed in the posterior wall of the frontal sinus between the right and left sides, like a "hump" in the posterior wall of the frontal sinus. This case of damage to the anterior skull base that could not be avoided by identifying the first olfactory fibre alone is the first published case of skull base injury caused by the outside-in approach due to morphological variations of the frontal sinus and skull base. In this approach, the posterior wall of the frontal sinus cannot be observed because the intraoperative landmark is limited to the first olfactory fibre. Therefore, morphological variations of the posterior wall of the frontal sinus should be analysed in advance to prevent cranial base injury.

由外向内额部钻孔技术造成颅底损伤尚未见报道。在本报告中,我们选择了一种由外而内的方法来打开额窦进行嗅神经母细胞瘤切除术。虽然我们发现了第一嗅纤维,但在肿瘤一侧的额窦钻孔时,前颅底受损。我们利用筋膜和软骨重建了多层颅底。术后未见脑脊液漏或颅内出血。在本例中,左右两侧额窦后壁存在形态差异,如额窦后壁出现“驼峰”。本例前颅底损伤不能通过单独识别第一嗅纤维来避免,这是第一例因额窦和颅底形态变化而由外向内入路引起颅底损伤的病例。在这种入路中,由于术中标记仅限于第一嗅纤维,因此无法观察到额窦后壁。因此,应提前分析额窦后壁的形态学变化,防止颅底损伤。
{"title":"Frontal Sinus \"Hump\": An Anatomical Risk Factor for Anterior Skull Base Injury in the Endoscopic Modified Lothrop Approach (Outside-In Frontal Drill-Out).","authors":"Teppei Takeda,&nbsp;Kazuhiro Omura,&nbsp;Haw Torng,&nbsp;Teru Ebihara,&nbsp;Satoshi Aoki,&nbsp;Kosuke Tochigi,&nbsp;Hiromi Kojima,&nbsp;Nobuyoshi Otori","doi":"10.1155/2021/3402496","DOIUrl":"https://doi.org/10.1155/2021/3402496","url":null,"abstract":"<p><p>Skull base injuries caused by the outside-in frontal drill-out technique have not been reported. In this report, we chose an outside-in approach to open the frontal sinus for olfactory neuroblastoma resection. Although we identified the first olfactory fibre, the anterior skull base was damaged while drilling into the frontal sinus on the tumour side. We reconstructed the skull base in multiple layers using fascia and cartilage. Postoperative cerebrospinal fluid leakage or intracranial haemorrhage was not observed. In this case, a morphological difference existed in the posterior wall of the frontal sinus between the right and left sides, like a \"hump\" in the posterior wall of the frontal sinus. This case of damage to the anterior skull base that could not be avoided by identifying the first olfactory fibre alone is the first published case of skull base injury caused by the outside-in approach due to morphological variations of the frontal sinus and skull base. In this approach, the posterior wall of the frontal sinus cannot be observed because the intraoperative landmark is limited to the first olfactory fibre. Therefore, morphological variations of the posterior wall of the frontal sinus should be analysed in advance to prevent cranial base injury.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":null,"pages":null},"PeriodicalIF":0.6,"publicationDate":"2021-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321740/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39267175","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}
引用次数: 0
期刊
Case Reports in Otolaryngology
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