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Acta Oto-Laryngologica Case Reports最新文献

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Potential colonization of provox voice prosthesis by Candida spp. with no sign of failure for approximately 10 years exploitation time 假丝酵母菌可能在大约10年的开发时间内定植发声假体，没有任何失败的迹象
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2021-01-01 DOI: 10.1080/23772484.2021.1927737
Jakub Spałek, P. Deptuła, B. Durnaś, G. Król, S. Kaliniak, R. Bucki, Sławomir Okła
{"title":"Potential colonization of provox voice prosthesis by Candida spp. with no sign of failure for approximately 10 years exploitation time","authors":"Jakub Spałek, P. Deptuła, B. Durnaś, G. Król, S. Kaliniak, R. Bucki, Sławomir Okła","doi":"10.1080/23772484.2021.1927737","DOIUrl":"https://doi.org/10.1080/23772484.2021.1927737","url":null,"abstract":"Abstract Vocal rehabilitation with implantation of voice prosthesis has been recognized as one of the most popular intervention for patients after total laryngectomy. The main threat to its users is leakage through the tracheo-esophageal fistula caused by prosthesis deformation and damage to the valve mechanism due to colonization with fungal or bacterial/fungal biofilms. The uniqueness of the described case represents the use of the same Provox voice prosthesis during the period of almost 10 years.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"6 1","pages":"60 - 66"},"PeriodicalIF":0.1,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2021.1927737","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41497262","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Incidental p16-positive oropharyngeal carcinoma found during tonsillectomy for palmoplantar pustulosis 掌跖脓疱病扁桃体切除术中偶然发现p16阳性口咽癌
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2021-01-01 DOI: 10.1080/23772484.2021.1935264
Mitsuo P. Sato, N. Otsuki, M. Kitano, K. Doi
{"title":"Incidental p16-positive oropharyngeal carcinoma found during tonsillectomy for palmoplantar pustulosis","authors":"Mitsuo P. Sato, N. Otsuki, M. Kitano, K. Doi","doi":"10.1080/23772484.2021.1935264","DOIUrl":"https://doi.org/10.1080/23772484.2021.1935264","url":null,"abstract":"Abstract The tonsillar crypt is thought to be a hiding site for early cancer detected after tonsillectomy for primary lesion search in cancer of unknown primary site. In rare cases, a small lesion can be detected unexpectedly during surgical treatment for chronic tonsillitis and tonsillar focal diseases. We report the case of a 47-year-old woman undergoing tonsillectomy for palmoplantar pustulosis (PPP), resulting in the diagnosis of p16-positive oropharyngeal cancer (OPC) in the left tonsil. Postoperative radiation therapy was performed due to the presence of an adhesive lesion during surgery. Radiotherapeutic adverse effects were mild and improved 3 months after the radiotherapy. The symptoms of PPP completely resolved 3 months after the tonsillectomy and no recurrence has been observed so far. With an increase in the cases of HPV-related OPCs, routine pathological examination after tonsillectomy for benign-appearing tonsils in adults is necessary to detect incidental OPC regardless of its low cost-effectiveness.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"6 1","pages":"56 - 59"},"PeriodicalIF":0.1,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2021.1935264","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41739674","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Facial nerve palsy as the presenting feature of metastatic prostatic cancer in the temporal bone 面神经麻痹是颞骨转移性前列腺癌症的表现特征
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2020-12-28 DOI: 10.1080/23772484.2020.1865165
D. Fujii, Hikari Shimoda, N. Uehara, T. Fujita, M. Teshima, H. Shinomiya, A. Kakigi, T. Terakawa, M. Fujisawa, K. Nibu
{"title":"Facial nerve palsy as the presenting feature of metastatic prostatic cancer in the temporal bone","authors":"D. Fujii, Hikari Shimoda, N. Uehara, T. Fujita, M. Teshima, H. Shinomiya, A. Kakigi, T. Terakawa, M. Fujisawa, K. Nibu","doi":"10.1080/23772484.2020.1865165","DOIUrl":"https://doi.org/10.1080/23772484.2020.1865165","url":null,"abstract":"Abstract Metastasis of malignant tumors to the temporal bone is relatively rare. We report a case of facial nerve palsy due to the metastatic prostatic cancer to the temporal bone with favorable and functional results. A 76-year-old man with no history of malignant tumor was referred to our hospital with a complaint of right facial nerve palsy. Based on radiological findings and a biopsy from the prostate, the patient was finally diagnosed as having metastatic prostatic cancer to the right temporal bone. More than 18 months had passed after start of the hormonal therapy, the metastatic lesion of the temporal bone had diminished, and the facial nerve palsy gradually improved. The present case suggests that favorable and functional results even in advanced metastatic prostatic cancers to temporal bone, if hormonal therapy is effective. We must keep in mind the possibility of metastatic tumor in the treatment of facial nerve palsy.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"6 1","pages":"1 - 5"},"PeriodicalIF":0.1,"publicationDate":"2020-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2020.1865165","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46408674","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pneumolabyrinth following cochlear implantation resolved after shunt adjustment 调整分流器后，人工耳蜗植入术后气腹消失
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2020-01-01 DOI: 10.1080/23772484.2020.1838906
Karin Hallin, Fredrik Stillesjö, J. Sundblom, N. Danckwardt-Lillieström
{"title":"Pneumolabyrinth following cochlear implantation resolved after shunt adjustment","authors":"Karin Hallin, Fredrik Stillesjö, J. Sundblom, N. Danckwardt-Lillieström","doi":"10.1080/23772484.2020.1838906","DOIUrl":"https://doi.org/10.1080/23772484.2020.1838906","url":null,"abstract":"Abstract We present a case of a male with a history of repeated surgeries for a cerebellar astrocytoma, leading to profound deafness and facial paresis on the left side. A ventriculoperitoneal (VP) shunt was inserted to manage hydrocephalus. At the age of 46 the hearing suddenly disappeared on the right side, where he received a cochlear implant (CI). At implant activation, impedances showed atypical high values. One month later impedance levels had further increased and the patient had no benefit from the CI. A computed tomography (CT) scan suggested air in the cochlea (pneumolabyrinth). The shunt was adjusted to elevate the cerebrospinal fluid (CSF) pressure and the pressure in the perilymph to prevent air from entering the cochlea via the round window. One year after activation the electrode impedances were normal and the hearing outcome from the implant was successful.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"5 1","pages":"81 - 85"},"PeriodicalIF":0.1,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2020.1838906","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43026569","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Laryngeal manifestations in acromegaly: A systematic review of the literature 肢端肥大症的喉部表现：文献系统综述
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2020-01-01 DOI: 10.1080/23772484.2020.1809421
H. Smaily, N. Matar
{"title":"Laryngeal manifestations in acromegaly: A systematic review of the literature","authors":"H. Smaily, N. Matar","doi":"10.1080/23772484.2020.1809421","DOIUrl":"https://doi.org/10.1080/23772484.2020.1809421","url":null,"abstract":"Abstract Laryngeal involvement in acromegaly is a rare occurrence that has been reported in several case reports. The aim of this paper is to present a clinical case followed by a systematic review of the literature. A comprehensive review of the literature was conducted in April 2020. Included articles were reviewed for, type of study, date of publication, age of patient, main symptoms, duration of symptoms, laryngoscopy findings, treatment modalities and outcomes. Twenty-six cases were reported in the literature. Dyspnea was the most reported symptom followed by stridor and dysphonia. Tracheotomy was performed in (17/26) patients and adjunct laryngeal surgeries were performed in 7 (7/26) patients. Although laryngeal manifestations are rare in acromegaly, they sometimes carry functional and vital risks. A structured and multidisciplinary approach is critical for the optimal management of the airway in slowly progressive dyspnea and in acute life-threatening situations.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"5 1","pages":"57 - 63"},"PeriodicalIF":0.1,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2020.1809421","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49479345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
A spontaneous partially thrombosed ductal aneurysm presenting with left recurrent laryngeal nerve palsy 一例自发性部分血栓性导管瘤伴左喉返神经麻痹
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2020-01-01 DOI: 10.1080/23772484.2020.1725388
Abhilasha Goswami, Anand Das
{"title":"A spontaneous partially thrombosed ductal aneurysm presenting with left recurrent laryngeal nerve palsy","authors":"Abhilasha Goswami, Anand Das","doi":"10.1080/23772484.2020.1725388","DOIUrl":"https://doi.org/10.1080/23772484.2020.1725388","url":null,"abstract":"Abstract Ductus arteriosus aneurysm is a rare clinical entity, with most cases found in the paediatric population. Patients with ductus arteriosus aneurysms become symptomatic due to the pressure exerted by the aneurysm on the surrounding structures. In adults, hoarseness due to ductus arteriosus aneurysm impinging on the left recurrent laryngeal nerve is a rare condition. Here, we present a case of a 60-year old Indian woman, who presented with hoarseness secondary to a ductus arteriosus aneurysm – a diagnosis consistent with Ortner’s syndrome. Key points Aneurysms of a patent ductus arteriosus (PDA) is a rare condition, especially in adults. Hoarseness due to a PDA aneurysm impinging on the left recurrent laryngeal nerve is a rare cause of Ortner’s syndrome. Emergency surgery is needed if a PDA aneurysm breaks off. It is essential to perform a detailed cardiovascular examination, besides a thorough laryngological examination in all cases coming with hoarseness. Prompt treatment of the underlying cause of hoarseness is vital for the complete recovery of voice.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"5 1","pages":"23 - 27"},"PeriodicalIF":0.1,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2020.1725388","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44612396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chondroid chordoma of the parapharyngeal space: A case report and review of literature 咽旁间隙软骨样脊索瘤1例报告及文献复习
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2020-01-01 DOI: 10.1080/23772484.2020.1827952
N. Alobida, Aseel Doubi, Mohammed Alswayyed, Dima Z. Jamjoom, K. Al-Qahtani
{"title":"Chondroid chordoma of the parapharyngeal space: A case report and review of literature","authors":"N. Alobida, Aseel Doubi, Mohammed Alswayyed, Dima Z. Jamjoom, K. Al-Qahtani","doi":"10.1080/23772484.2020.1827952","DOIUrl":"https://doi.org/10.1080/23772484.2020.1827952","url":null,"abstract":"Abstract Parapharyngeal space (PPS) tumors are a rare entity and account for less than 1% of all head and neck tumors. Although they exhibit a benign behavior, malignant neoplasms may arise from any of the structure contained in the space. Differential diagnosis of a PPS mass can be determined based on its origin from the prestyloid or poststyloid space. Furthermore, the choice of surgical approach is dictated by the size of the tumor, its location, its relationship to the great vessels, and suspicion of malignancy. Chordomas are rare, slow-growing tumors arising from remnants of the notochord. They are locally aggressive malignant neoplasms. The majority of head and neck chordomas arise in the skull base with a small minority arising along the cervical spine. In this report, we describe the first case of a patient with a chondroid chordoma of the PPS with no direct involvement of the axial skeleton.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"5 1","pages":"69 - 73"},"PeriodicalIF":0.1,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2020.1827952","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47433946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Pleomorphic adenoma of the external auditory canal: A common tumour in an uncommon site 外耳道多形性腺瘤:一种少见部位的常见肿瘤
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2020-01-01 DOI: 10.1080/23772484.2020.1803075
S. Ayodele, O. A. Afolabi, O. Folaranmi, F. Ologe
{"title":"Pleomorphic adenoma of the external auditory canal: A common tumour in an uncommon site","authors":"S. Ayodele, O. A. Afolabi, O. Folaranmi, F. Ologe","doi":"10.1080/23772484.2020.1803075","DOIUrl":"https://doi.org/10.1080/23772484.2020.1803075","url":null,"abstract":"Abstract Background/aim Pleomorphic adenoma is a common slow growing benign tumour that is known to occur mainly in the salivary glands. Case reports of pleomorphic adenomas originating from the external auditory canal have been extremely rare. Case presentation We report the case of a 64-year-old patient who presented with 2-year history of a slow growing mass of the left external auditory canal. Excision of the mass was performed and pathology was consistent with pleomorphic adenoma. Conclusion Pleomorphic adenomas of the external auditory canal are uncommon and can be easily misdiagnosed as aural polyps or granulation tissue. Biopsies are often necessary for an accurate diagnosis.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"5 1","pages":"64 - 68"},"PeriodicalIF":0.1,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2020.1803075","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41593129","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Infectious mononucleosis-related tonsillar hyperplasia mimicking T-cell lymphoma on histopathology: A rare case and review 传染性单核细胞增多症相关扁桃体增生模拟t细胞淋巴瘤的组织病理学研究:一例罕见病例及复习
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2020-01-01 DOI: 10.1080/23772484.2020.1735251
Usman Asad, Irfan Warraich, Winslo K. Idicula
{"title":"Infectious mononucleosis-related tonsillar hyperplasia mimicking T-cell lymphoma on histopathology: A rare case and review","authors":"Usman Asad, Irfan Warraich, Winslo K. Idicula","doi":"10.1080/23772484.2020.1735251","DOIUrl":"https://doi.org/10.1080/23772484.2020.1735251","url":null,"abstract":"Abstract Infectious mononucleosis (IM) with histopathologic characteristics of T-cell lymphoma is uncommon. IM, caused by Epstein-Barr virus, is a self-limiting, benign lymphoproliferative disorder. Transferred through saliva, blood, and semen, it presents clinically in adolescents with fever, pharyngitis, and lymphadenopathy. While literature has reported cases of IM mimicking Hodgkin’s lymphoma, the histopathologic resemblance of IM to T-cell lymphomas is uncommon. In this report, we present a patient who clinically presented with symptoms of IM, which was confirmed through the monospot test. The novelty of this case was that tonsillar hyperplasia initially was interpreted as T-cell lymphoma in a patient with IM.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"5 1","pages":"33 - 37"},"PeriodicalIF":0.1,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2020.1735251","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47384879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Ancient neurilemmoma of the facial nerve in the parotid gland 腮腺面神经的古老神经鞘瘤
IF 0.1
Acta Oto-Laryngologica Case Reports Pub Date : 2020-01-01 DOI: 10.1080/23772484.2020.1806718
Abhilasha Goswami, Mukul Patar
{"title":"Ancient neurilemmoma of the facial nerve in the parotid gland","authors":"Abhilasha Goswami, Mukul Patar","doi":"10.1080/23772484.2020.1806718","DOIUrl":"https://doi.org/10.1080/23772484.2020.1806718","url":null,"abstract":"Abstract Facial nerve neurilemmomas or schwannomas are encapsulated benign tumors arising from the Schwann cells of the seventh cranial nerve. Most of the facial nerve neurilemmomas occur in the intratemporal region, with only 9% of cases involving a portion of the extratemporal segment, such as the intraparotid portion. Facial nerve neurilemmomas occurring within the parotid gland are rare. Here, we report a case of intraparotid facial nerve neurilemmoma in an 11-year-old female that had undergone degenerative changes, i.e. ancient schwannoma. Clinical features, pre-operative, intraoperative and histopathological features are discussed in detail. This case is important as it is rare in younger age groups, and is often an ignored entity, especially in the parotid region.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"5 1","pages":"52 - 56"},"PeriodicalIF":0.1,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2020.1806718","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49263326","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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