Case Reports in Otolaryngology最新文献

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Resolution of Dizziness Following Treatment for Chronic Rhinosinusitis: A Case Report From Physical Therapy Outpatient Setting. 慢性鼻窦炎治疗后头晕的解决:来自门诊物理治疗的一例报告。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-11-08 eCollection Date: 2025-01-01 DOI: 10.1155/crot/6175181
Shellie Zsoldos, Chia-Cheng Lin
{"title":"Resolution of Dizziness Following Treatment for Chronic Rhinosinusitis: A Case Report From Physical Therapy Outpatient Setting.","authors":"Shellie Zsoldos, Chia-Cheng Lin","doi":"10.1155/crot/6175181","DOIUrl":"10.1155/crot/6175181","url":null,"abstract":"<p><strong>Background and purpose: </strong>The purpose of this case report is to describe dizziness symptoms caused by sinusitis evaluated in outpatient physical therapy setting.</p><p><strong>Case description: </strong>A 59-year-old man with chronic peripheral vertigo of the right ear was referred to our outpatient physical therapy for vestibular rehabilitation. He was diagnosed with chronic peripheral vertigo of the right ear. He experienced a spinning sensation lasting for several hours, with no clear or consistent trigger for the onset of his dizziness.</p><p><strong>Intervention: </strong>Vestibular-ocular reflex (VOR) exercises were prescribed as part of a home exercise program.</p><p><strong>Outcomes: </strong>The patient was unable to perform the prescribed VOR exercises due to his travel schedule. However, he reported complete resolution of dizziness symptoms following surgical intervention and pharmacological treatment for chronic rhinosinusitis.</p><p><strong>Discussion: </strong>This case highlights the importance of a holistic approach when evaluating and treating patients with vestibular symptoms. Clinicians should consider sinus-related conditions, such as chronic rhinosinusitis, as potential contributors to dizziness.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"6175181"},"PeriodicalIF":0.4,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12619684/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145543269","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
Bilateral Choanal Atresia in a 65-Year-Old Female: A Case Report and Literature Review. 65岁女性双侧后肛门闭锁1例报告并文献复习。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-11-05 eCollection Date: 2025-01-01 DOI: 10.1155/crot/5584900
Maraam Al Qout, Abdullah Alkarni, Abdulaziz Alaraifi, Mohammad Almahdi
{"title":"Bilateral Choanal Atresia in a 65-Year-Old Female: A Case Report and Literature Review.","authors":"Maraam Al Qout, Abdullah Alkarni, Abdulaziz Alaraifi, Mohammad Almahdi","doi":"10.1155/crot/5584900","DOIUrl":"10.1155/crot/5584900","url":null,"abstract":"<p><strong>Background: </strong>Choanal atresia (CA) is a congenital condition characterized by occlusion of the nasal airway due to failure of recanalization during embryological development. It is more commonly unilateral and typically presents during infancy. In contrast, bilateral CA is a neonatal emergency that often manifests as respiratory distress at birth. The presentation of bilateral CA in late adulthood is extremely rare.</p><p><strong>Case description: </strong>This case presents an unusual case of an elderly patient diagnosed with bilateral CA at 65 years. She presented with a primary complaint of lifelong bilateral nasal obstruction and denied any symptoms suggestive of chronic rhinosinusitis. Examination revealed bilateral choanal obstruction with no visible openings in the nasal cavity. The patient underwent endoscopic transseptal repair of bilateral CA, which included perforation of the atretic plate, posterior septectomy, and flap reconstruction. Postoperative evaluation demonstrated bilaterally patent choanae, and the patient remained asymptomatic, with no further complications.</p><p><strong>Conclusion: </strong>This case highlights a rare presentation of bilateral CA diagnosed in late adulthood. Although typically detected in the neonatal period, bilateral CA can occasionally remain undiagnosed for decades. This patient represents the oldest reported case of bilateral CA in the literature, emphasizing the variability in clinical presentation and the potential for delayed diagnosis.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"5584900"},"PeriodicalIF":0.4,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12611465/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145514590","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
Pediatric Parapharyngeal Space Mass: Successful Outcome Following Transoral Simple Cyst Resection. 小儿咽旁间隙肿块:经口单纯囊肿切除术后的成功结果。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-10-29 eCollection Date: 2025-01-01 DOI: 10.1155/crot/9934709
Christian M Kabongo, Alexander P Marston
{"title":"Pediatric Parapharyngeal Space Mass: Successful Outcome Following Transoral Simple Cyst Resection.","authors":"Christian M Kabongo, Alexander P Marston","doi":"10.1155/crot/9934709","DOIUrl":"10.1155/crot/9934709","url":null,"abstract":"<p><strong>Background: </strong>Parapharyngeal space masses are rare lesions identified in pediatric patients. The present case describes the clinical history and surgical treatment of a parapharyngeal space in a 32-month-old female.</p><p><strong>Methods: </strong>The electronic medical record was used for this retrospective case report.</p><p><strong>Results: </strong>A 32-month-old female had a nonsignificant clinical presentation and a negative flexible laryngoscopy. Upon imaging, a mass was seen in the left parapharyngeal space. Resection of the mass was conducted. The final pathology confirmed a benign simple cyst. The patient did not have any postoperative complications.</p><p><strong>Conclusions: </strong>This case illustrates that surgical resection can be an adequate treatment method for a parapharyngeal space mass. It also adds to the literature on types of parapharyngeal space masses that may present in pediatric patients.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"9934709"},"PeriodicalIF":0.4,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12588742/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145460363","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
Diagnostic Pitfalls and Unique Radiological Insights in Thyroid Paraganglioma: A Case Report and Literature Review. 甲状腺副神经节瘤的诊断缺陷和独特的放射学见解:1例报告和文献复习。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-10-25 eCollection Date: 2025-01-01 DOI: 10.1155/crot/5395659
Ainulakbar Mughal, Fatima Syed Amanullah, Zubia Ali, Shabbir Akhtar, Sehar Suleman
{"title":"Diagnostic Pitfalls and Unique Radiological Insights in Thyroid Paraganglioma: A Case Report and Literature Review.","authors":"Ainulakbar Mughal, Fatima Syed Amanullah, Zubia Ali, Shabbir Akhtar, Sehar Suleman","doi":"10.1155/crot/5395659","DOIUrl":"10.1155/crot/5395659","url":null,"abstract":"<p><p>Paragangliomas (PGLs) are extremely rare endocrine tumors that arise from the autonomic nervous system. Their rarity contributes to their frequent misdiagnosis. Ultrasound and immunohistochemical findings are heavily relied on for correct diagnosis. We present a case of thyroid PGL in a 40-year-old female patient who presented with a 1-year history of anterior neck mass and a 4-month history of hemoptysis. Ultrasound findings showed a solitary, lobulated, hypoechoic, and vascular lesion in the right thyroid lobe. She underwent total thyroidectomy and tracheal end-to-end anastomosis. Histopathology showed cells organized in distinct nests (zellballen) pattern enclosed by a delicate fibrovascular stroma. On immunohistochemical analysis, the tumor was positive for synaptophysin, CD56, GATA-3, and S100. The patient is stable postoperatively and disease-free. The role of ultrasound is vital in forming a correct diagnosis of thyroid PGL preoperatively. We review the current literature regarding diagnostic findings and treatment of thyroid PGLs with the aim of supplementing the findings of the thyroid PGLs that have been previously reported. The creation of a robust imaging and immunohistochemical profile for this entity is needed to combat the frequent misdiagnoses that occur with thyroid PGLs.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"5395659"},"PeriodicalIF":0.4,"publicationDate":"2025-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12579563/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145432592","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
The Impact of Hybrid Therapy on Langerhans Cell Histiocytosis of the Mandible in an Older Male: A Case Report and Literature Review. 混合疗法对老年男性下颌骨朗格汉斯细胞组织细胞增多症的影响:1例报告及文献复习。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-10-22 eCollection Date: 2025-01-01 DOI: 10.1155/crot/2996605
Yoshifumi Matsumoto, Maki Akamatsu, Shinichi Ohba, Fumihiko Matsumoto
{"title":"The Impact of Hybrid Therapy on Langerhans Cell Histiocytosis of the Mandible in an Older Male: A Case Report and Literature Review.","authors":"Yoshifumi Matsumoto, Maki Akamatsu, Shinichi Ohba, Fumihiko Matsumoto","doi":"10.1155/crot/2996605","DOIUrl":"10.1155/crot/2996605","url":null,"abstract":"<p><strong>Background: </strong>The unusual disorder known as Langerhans cell histiocytosis (LCH), which is most frequently observed in children and young adults, is caused by the clonal proliferation of Langerhans cells. This disease is classified into several types depending on the extent of the lesion. Because it is rare diseases, there is no established standard treatment of this disease. In this report, we describe an extremely rare case of LCH that developed in the mandible of an older male. This is the first report in the world of a favorable outcome following surgical resection and local steroids administration.</p><p><strong>Case report: </strong>The patient was a 75-year-old male who complained of swelling and pain in his mandible; however, there were no abnormal findings upon intraoral examination. Panoramic radiograph, computed tomography (CT), and magnetic resonance imaging (MRI) revealed osteolytic tumors. A diagnosis of LCH was confirmed based on the pathological findings of a cluster of Langerhans cells in a biopsy specimen of a submucosal tumor. Because the patient was elderly and the primary tumor was in the mandible, radiation therapy, chemotherapy, and systemic steroid administration were difficult to tolerate due to side effects. We performed combined treatment with surgical resection and local steroids injection. He was discharged from the hospital 1 week after the operation; the intraoral wound healed after 2 months, and the pain improved.</p><p><strong>Conclusions: </strong>This report suggests that a combination of surgical resection and local steroids administration is effective in treating LCH of the mandible in elderly patients.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"2996605"},"PeriodicalIF":0.4,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12571525/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410355","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
A Case of Follicular Dendritic Cell Sarcoma of the Palatine Tonsil That Developed as a Radiation-Induced Sarcoma. 放射诱导的腭扁桃体滤泡树突状细胞肉瘤1例。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-10-19 eCollection Date: 2025-01-01 DOI: 10.1155/crot/8861715
Alyssa Yoshida, Takuya Mikoshiba, Mariko Sekimizu, Shintaro Nakamura, Ryoto Nagai, Miho Kawaida, Katsura Emoto, Hiroyuki Ozawa
{"title":"A Case of Follicular Dendritic Cell Sarcoma of the Palatine Tonsil That Developed as a Radiation-Induced Sarcoma.","authors":"Alyssa Yoshida, Takuya Mikoshiba, Mariko Sekimizu, Shintaro Nakamura, Ryoto Nagai, Miho Kawaida, Katsura Emoto, Hiroyuki Ozawa","doi":"10.1155/crot/8861715","DOIUrl":"10.1155/crot/8861715","url":null,"abstract":"<p><p>Follicular dendritic cell sarcoma is a rare malignant tumor originating from follicular dendritic cells. We present the first report of such a sarcoma of the palatine tonsils that developed as a radiation-induced sarcoma. A 78-year-old man, who had undergone chemoradiotherapy for hypopharyngeal and esophageal cancer 7 years prior, presented with discomfort during swallowing. Endoscopic pharyngeal examination revealed a tumor in the right palatine tonsil which was histopathologically diagnosed as a follicular dendritic cell sarcoma. The tumor also met the diagnostic criteria for radiation-induced sarcoma. Positron emission tomography/computed tomography revealed abnormal uptake in the right palatine tonsil and bilateral cervical lymph nodes; no distant metastases were detected. The patient underwent tumor resection using the mandibular swing approach, pharyngeal reconstruction using an anterolateral thigh flap, bilateral neck lymph node dissection, and tracheostomy. Postoperative radiotherapy was not administered because of previous irradiation; however, no apparent recurrence or metastasis was observed 4 years after surgery. Follicular dendritic cell sarcoma can develop over an extended period after previous irradiation. Extended resection with a negative margin may be pivotal in treating follicular dendritic cell sarcoma when postoperative radiotherapy cannot be administered.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"8861715"},"PeriodicalIF":0.4,"publicationDate":"2025-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12554916/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145393916","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
Nonsurgical Management of Sinonasal Teratocarcinosarcoma With Chemoradiotherapy: A Case Report. 鼻窦畸胎瘤放化疗的非手术治疗1例报告。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-10-09 eCollection Date: 2025-01-01 DOI: 10.1155/crot/1109193
Yuki Ban, Junko Tsuda, Yosuke Okinaka, Youhei Yamamoto, Mei Sakamoto, Tomoyasu Yamagata, Yosuke Takemoto, Makoto Hashimoto, Yoshinobu Hoshii, Kazuma Sugahara
{"title":"Nonsurgical Management of Sinonasal Teratocarcinosarcoma With Chemoradiotherapy: A Case Report.","authors":"Yuki Ban, Junko Tsuda, Yosuke Okinaka, Youhei Yamamoto, Mei Sakamoto, Tomoyasu Yamagata, Yosuke Takemoto, Makoto Hashimoto, Yoshinobu Hoshii, Kazuma Sugahara","doi":"10.1155/crot/1109193","DOIUrl":"10.1155/crot/1109193","url":null,"abstract":"<p><p>Sinonasal teratocarcinosarcoma (SNTCS) is a rare, aggressive malignancy with epithelial, mesenchymal, and neuroectodermal components. We report the case of a 66-year-old man with right nasal obstruction and epistaxis. Imaging revealed a mass in the right nasal cavity and ethmoid sinus. Histopathology revealed immature squamous nests with clear cytoplasm, and immunohistochemistry confirmed multiphenotypic differentiation. Therefore, SNTCS was diagnosed. Owing to inoperability, the patient underwent chemoradiotherapy, which resulted in stable disease at 6 months. This case highlights the diagnostic complexity of SNTCS and suggests that nonsurgical management may be effective in select cases.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"1109193"},"PeriodicalIF":0.4,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12530920/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145330285","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
Case Report and Literature Review on Tracheostomal Myiasis: Clinical Presentation, Challenges, and Treatment. 气管造口蝇蛆病病例报告及文献回顾:临床表现、挑战及治疗。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-09-27 eCollection Date: 2025-01-01 DOI: 10.1155/crot/1555107
Yazieed M Albarrak, Ali M Alsudays, Mohammed A Alwabili, Khaled A Almanea, Fareed R Alghamdi, Reema A Aldawish
{"title":"Case Report and Literature Review on Tracheostomal Myiasis: Clinical Presentation, Challenges, and Treatment.","authors":"Yazieed M Albarrak, Ali M Alsudays, Mohammed A Alwabili, Khaled A Almanea, Fareed R Alghamdi, Reema A Aldawish","doi":"10.1155/crot/1555107","DOIUrl":"10.1155/crot/1555107","url":null,"abstract":"<p><p>Tracheostomal myiasis, the infestation of a tracheostomy site by fly larvae, is an uncommon and challenging condition, with limited cases reported in the medical literature. This case report aims to describe both the clinical presentation and management of tracheostomal myiasis in a patient with multiple comorbidities. The patient presented with foul-smelling discharge and visible maggots at the tracheostomy site. Management involved manual removal of larvae, surgical debridement, irrigation with iodine solution, and sealing the stoma with paraffin ointment. This case highlights the need for clinician awareness of this rare complication, particularly in patients with compromised health, and highlights the importance of preventive care and early intervention. As a single case report, it reflects the experience within a broader context of managing tracheostomy-related complications.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"1555107"},"PeriodicalIF":0.4,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12496136/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145233817","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
Primary Posterior Neck Hydatid Cyst: A Case Report and Review of the Literature. 原发性后颈部包虫病1例报告及文献复习。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2025-09-26 eCollection Date: 2025-01-01 DOI: 10.1155/crot/6909432
Gibran Atwi, Charbel Saad, Samer Serhal, Rami Saade
{"title":"Primary Posterior Neck Hydatid Cyst: A Case Report and Review of the Literature.","authors":"Gibran Atwi, Charbel Saad, Samer Serhal, Rami Saade","doi":"10.1155/crot/6909432","DOIUrl":"10.1155/crot/6909432","url":null,"abstract":"<p><p><b>Introduction:</b> Hydatid cyst disease is an endemic parasitic infection caused by <i>Echinococcus granulosus</i>. Hydatid cysts occur mainly in the liver and lungs and are rare in the head and neck region, even in endemic areas. Due to their nonspecific clinical manifestations, diagnostic challenges are encountered in such atypical presentations. <b>Case Presentation:</b> We report the case of a 6-year-old girl who presented with a progressively enlarging, painless left postauricular mass. Radiological assessment revealed a well-circumscribed, unilocular cystic lesion at level V of the neck. Surgical resection was performed, and histopathology confirmed a hydatid cyst. Postoperatively, the patient was treated with albendazole. No recurrence was observed at follow-up. <b>Clinical Discussion:</b> Hydatid cysts in the cervical region are exceptionally rare, with only a few cases documented in the literature. The disease can remain asymptomatic for years, often presenting as a slow-growing mass. Imaging with ultrasound and CT is critical in preoperative diagnosis. The gold standard of treatment remains complete surgical excision, reinforced by anthelmintic therapy to prevent recurrence. <b>Conclusion:</b> Although rare, hydatid cyst disease should remain among the differential diagnoses of cystic neck masses, especially in endemic areas. Early diagnosis and intervention are essential in evading complications of the disease such as anaphylaxis or recurrence. Ultimately, prevention remains the most effective strategy, emphasizing the need for community awareness, hygienic practices, and coordinated control efforts to break the parasite's life cycle.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"6909432"},"PeriodicalIF":0.6,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12494480/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145233735","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
A Sinonasal Myxoma Arising From the Inferior Nasal Concha: Report of a Rare Case and Review of the Literature. 下鼻甲发生鼻窦黏液瘤1例报告及文献复习。
IF 0.4
Case Reports in Otolaryngology Pub Date : 2025-09-23 eCollection Date: 2025-01-01 DOI: 10.1155/crot/5590381
Hesam Jahandideh, Maryam Arab, Maryam Roomiani
{"title":"A Sinonasal Myxoma Arising From the Inferior Nasal Concha: Report of a Rare Case and Review of the Literature.","authors":"Hesam Jahandideh, Maryam Arab, Maryam Roomiani","doi":"10.1155/crot/5590381","DOIUrl":"10.1155/crot/5590381","url":null,"abstract":"<p><p>Head and neck myxomas are extremely rare neoplasms, and only a few reports have been in the literature. Specifically, reports of myxomas of the nose and paranasal sinuses are sporadic. Here, we present a rare case of a 47-year-old female with progressive nasal obstruction who was found to have a myxoma arising within the inferior nasal concha-the first reported case of its kind. The diagnosis was confirmed by biopsy, and endoscopic transnasal resection (ETNR) was conducted. ETNR proved effective in resolving symptoms of nasal myxoma, with complete removal of the tumor and no recurrence on follow-up. The operation is described, and the literature on the subject is reviewed.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2025 ","pages":"5590381"},"PeriodicalIF":0.4,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12483728/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145207996","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
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