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Congenital Desmoid Tumor of the Larynx: A Therapeutic Challenge. 喉先天性硬纤维瘤:治疗上的挑战。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-06-09 DOI: 10.1007/s12070-025-05488-3
Saúl Astray Gómez, Santiago Almanzo, Adrián Hernández Moya, Agustín Alamar Velázquez, Miguel Armengot Carceller

Desmoid tumors affecting vital structures can be life-threatening despite their non-malignant behavior. The lack of standardized treatment poses a therapeutic challenge, particularly regarding the sequelae in pediatric patients. A one-month-old male patient presented with respiratory distress and stridor. Endoscopic exploration and computed tomography revealed a laryngeal tumor, which was confirmed as a desmoid tumor via biopsy. Systemic chemotherapy in combination with imatinib was initiated, leading to stabilization of the tumor size. A surgical approach for desmoid tumors may be unsuitable for pediatric patients due to excessive morbidity. In such cases, targeted therapies like tyrosine kinase inhibitors can effectively control the disease.

硬纤维瘤影响重要结构,尽管其非恶性行为可危及生命。缺乏标准化的治疗提出了一个治疗挑战,特别是关于儿童患者的后遗症。1个月大的男性患者表现为呼吸窘迫和喘鸣。内窥镜检查和计算机断层扫描显示喉部肿瘤,活检证实为硬纤维瘤。系统化疗联合伊马替尼开始,导致肿瘤大小稳定。手术治疗硬纤维瘤可能不适合儿童患者,因为发病率过高。在这种情况下,像酪氨酸激酶抑制剂这样的靶向治疗可以有效地控制疾病。
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引用次数: 0
Development and Validation of a Questionnaire in Malayalam to Assess the Listening Difficulties in Mainstreamed Children with Hearing Impairment. 马拉雅拉姆语主流儿童听力障碍评估问卷的编制与验证。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-06-09 DOI: 10.1007/s12070-025-05593-3
Saumya Sundaram, Heramba Ganapathy Selvarajan, Suja K Kunnath, Prakash Boominathan

Adverse listening environments in the classroom can pose difficulties in listening for children with normal hearing (NH) and even more for children with hearing loss (HL). Listening difficulty in the classroom environment can be assessed using a culturally sensitive questionnaire in one's native language. Currently, no questionnaires are available in Malayalam, the language spoken in Kerala, India. Development and validation of Malayalam questionnaires to assess listening difficulties among children (6-12 years) with hearing loss from self, peer and teacher perceptions. Cross sectional study design was used. Items representing the construct for self, peer, and teacher perception were generated by deductive literature search. Simple, unambiguous sentences were constructed and logically sequenced; leading or biased, double-barrelled questions were avoided. Content validation was done by six experts, followed by a pilot study and cognitive interview, before administering the developed questionnaire to 60 participants. Content validation was done following Yusoff (2019) guidelines. Internal reliability and consistency were calculated using the split-half method and Cronbach's alpha. Item content validity index for self, peer, and teacher perception was 1.00, 0.97, and 1.00, respectively. Split-half method and Cronbach's alpha scores for self, peer, and teacher perception were 0.978, 0.819, 0.815, 0.791, 0.734, and 0.822, respectively. The developed questionnaire for self, peer, and teacher perception has good content validity, internal reliability, and consistency. Understanding classroom listening difficulties will facilitate devising measures for a favourable listening environment.

课堂上不利的听力环境会给听力正常的儿童(NH)造成听力困难,对听力损失的儿童(HL)造成的困难更大。课堂环境中的听力困难可以使用母语的文化敏感问卷进行评估。目前,在印度喀拉拉邦使用的语言马拉雅拉姆语中没有问卷。马拉雅拉姆问卷的开发和验证,以评估听力损失儿童(6-12岁)的听力困难,从自我,同伴和老师的看法。采用横断面研究设计。通过演绎文献检索生成了代表自我、同伴和教师感知构念的项目。简单,明确的句子被构造和逻辑顺序;避免了引导性的或有偏见的、双管齐下的问题。内容验证由六名专家完成,随后进行初步研究和认知访谈,然后向60名参与者管理开发的问卷。内容验证按照Yusoff(2019)指南进行。内部信度和一致性采用劈半法和Cronbach’s alpha进行计算。自我知觉、同伴知觉和教师知觉的项目内容效度指数分别为1.00、0.97和1.00。自我、同伴和教师知觉的分半法和Cronbach’s alpha得分分别为0.978、0.819、0.815、0.791、0.734和0.822。所编制的自我感知、同伴感知和教师感知问卷具有良好的内容效度、内部信度和一致性。了解课堂听力困难有助于制定措施,营造良好的听力环境。
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引用次数: 0
Predictive Factors of Occult Lymph Node Involvement in Advanced Laryngeal Squamous Cell Carcinoma. 晚期喉部鳞状细胞癌隐匿淋巴结累及的预测因素。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-05-27 DOI: 10.1007/s12070-025-05595-1
Jihene Houas, Monia Ghammam, Sarra Lazid, Mariem Grassa, Malika El Omri, Mouna Bellakhdher, Wassim Kermani, Mohamed Abdelkefi

Objective: Determine the rate of occult lymph node metastasis in advanced laryngeal squamous cell carcinoma and identify its predictive factors.

Methods: A retrospective study including 98 patients with laryngeal cancer classified as T3-T4 N0, who underwent bilateral lymph node dissection in sectors II, III and IV.

Result: The median age of our patients was 61. The main symptom was dysphonia (96%). On CT scan, the thyroid cartilage was invaded in 53.5% of cases, and the HTE space in 50% of cases. It was essentially laryngeal squamous cell carcinoma of high grade in 6.1% of cases and of low grade in 93.9% of cases. We found lymph node involvement in 33 lymph node dissections (33.6%) in 24 patients (24.4%) with extranodal extension in 4 cases. Level IIA and III were the most commonly affected, with 28.6% and 21.4% of cases respectively. We noted a vascular emboli and perineural invasion in 5 patients. The predictive factors for MGO in our present study were age over 65, invasion of the subglottic stage, involvement of the thyroid cartilage, the hyo-thyro-epiglottic space, peri-neural invasion and limits of resection.

Conclusion: The criteria for performing lymph node dissection in cases of laryngeal cancer are becoming more restricted for patients with clinically negative lymph nodes (cN0). Nevertheless, for cases of locally advanced tumors, proactive lymph node dissection is advocated, particularly when certain predictive factors for hidden lymph node metastases are present.

目的:探讨晚期喉部鳞状细胞癌隐匿淋巴结转移率及其预测因素。方法:回顾性分析98例T3-T4 N0型喉癌患者行双侧II、III、iv区淋巴结清扫术。结果:患者中位年龄61岁。主要症状为语音障碍(96%)。CT扫描显示53.5%的甲状软骨受累,50%的甲状软骨受累。它本质上是喉部鳞状细胞癌,高级别的病例占6.1%,低级别的病例占93.9%。我们发现24例(24.4%)患者中33例(33.6%)淋巴结受累,4例结外延伸。IIA级和III级最常见,分别占28.6%和21.4%。我们注意到5例患者有血管栓塞和神经周围浸润。在我们的研究中,MGO的预测因素是年龄超过65岁,声门下期的侵犯,甲状腺软骨的累及,甲状腺-会厌间隙,周围神经的侵犯和切除的限制。结论:临床上淋巴结阴性(cN0)的喉癌患者行淋巴结清扫的标准越来越严格。然而,对于局部晚期肿瘤的病例,提倡主动淋巴结清扫,特别是当存在隐藏淋巴结转移的某些预测因素时。
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引用次数: 0
Bone wax-induced nasal polyposis: a rare complication following frontal reconstructive surgery. 骨蜡引起的鼻息肉病:额部重建手术后的罕见并发症。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-05-23 DOI: 10.1007/s12070-025-05579-1
Madhuri Mruthyunjaya Gudikote, Prashanth Alle, Anitha N Nagadi, Murali Mohan, Ravi Sachidananda

Bone wax is a waxy substance used for mechanical control of bleeding from bone surfaces during surgical procedures. Bone wax can cause local inflammatory reactions like granuloma formation, infection, impaired bone healing, osteo-hypertrophy and rarely rhinosinusitis. Bone wax is widely used in neurosurgical and ENT procedures. Complications secondary to bone wax are difficult to ascertain on clinical grounds as it is largely thought to be inert. It can be challenging to diagnose this in imaging studies as bone wax can be mistaken for air or soft tissue. We report a case of unilateral nasal polyp secondary to the herniation of bone wax through the frontal recess into the nasal cavity.

骨蜡是一种蜡状物质,用于外科手术中骨表面出血的机械控制。骨蜡可引起局部炎症反应,如肉芽肿形成、感染、骨愈合受损、骨肥大,很少会引起鼻窦炎。骨蜡广泛用于神经外科和耳鼻喉科手术。继发于骨蜡的并发症在临床上很难确定,因为它在很大程度上被认为是惰性的。由于骨蜡可能被误认为是空气或软组织,因此在影像学研究中诊断这种情况可能具有挑战性。我们报告一例单侧鼻息肉继发于骨蜡突出通过额窝进入鼻腔。
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引用次数: 0
Castleman's Disease-Unicentric Neck Lymphadenoapthy: Case Report and Review of Literature. Castleman病-单中心性颈部淋巴结肿大:病例报告及文献复习。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-06-08 DOI: 10.1007/s12070-025-05641-y
Arsheed Hussain Hakeem, Novfa Iftikhar, Michelle D Padua

Castleman's disease is rare lymphoproliferative disorder mostly seen in the mediastinum. We report a case of Castleman's disease involving a single lymph node at the left level II A in a 27-year-old female whose definitive diagnosis was made only on histological examination. Isolated Castleman's disease of the level II A lymph node is rare and a thorough clinical and histological examination is necessary to rule out the systemic form of the disease. Clinically two types of the Castleman's disease are seen, a unicentric variety where either a single lymph node or region is involved microscopically and multicentric variety where various lymph node regions are involved. Surgical excision is the standard of management for the unicentric Castleman's disease and has good prognosis, whereas the multicentric type is associated with systemic symptoms and has a poor prognosis. Although, microscopically, they can be classified as-hyaline vascular, plasma cell, transitional and stromal rich type, but their clinical significance is not clear.

Castleman氏病是一种罕见的淋巴细胞增生性疾病,多见于纵隔。我们报告一个27岁女性的Castleman病的病例,其左侧II级a的单一淋巴结仅在组织学检查中做出明确诊断。孤立的A级淋巴结Castleman病是罕见的,彻底的临床和组织学检查是必要的,以排除全身性形式的疾病。临床上可以看到两种类型的Castleman病,单中心型显微镜下可见单个淋巴结或区域受累,多中心型显微镜下可见多个淋巴结区域受累。手术切除是治疗单中心型Castleman病的标准方法,预后良好,而多中心型Castleman病伴有全身症状,预后较差。显微镜下可分为透明血管型、浆细胞型、移行型和富间质型,但临床意义尚不明确。
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引用次数: 0
Comment on: Impact of Cochlear Radiotherapy Dose on Hearing Loss in Carcinoma Oropharynx Treated by Concurrent Chemoradiotherapy Using Simultaneous Integrated Boost Volumetric Modulated Arc Therapy (SIB -VMAT). 评论:使用同步综合增强体积调制电弧治疗(SIB -VMAT)的同步放化疗治疗口咽癌患者耳蜗放疗剂量对听力损失的影响。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-06-12 DOI: 10.1007/s12070-025-05705-z
Erkan Topkan, Duriye Ozturk, Ugur Selek
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引用次数: 0
Management of Parotid Fistula with Sodium Tetradecyl Sulphate and Intraparenchymal Botulinum Toxin Injection. 硫酸十四烷基钠联合肝实质内肉毒毒素注射治疗腮腺瘘。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-05-29 DOI: 10.1007/s12070-025-05544-y
Song Yeu Wong, Nasibah Mohamad, Norsyamira Aida Mohamad Umbaik, Norhafiza Mat Lazim

A salivary gland fistula occurs when there is abnormal communication between the skin and the salivary gland or duct. Most of the cases are due to complications of head and neck surgery such as parotidectomy or trauma. At the moment, there are no consensus treatment guidelines for managing salivary gland fistulas. Most cases are treated conservatively; however, the management of ductal fistula can be challenging and typically requires more aggressive measures than conservative ones. We report a case of an elderly with a neck abscess complicated with a parotid fistula after incision and drainage. He presented with wound breakdown and persistent saliva leakage from the wound. The fistulogram showed communication between the Stensen's duct and the external fistula opening. We performed sclerotherapy by injecting Sodium Tetradecyl Sulphate into the fistula tract and ultrasound-guided intraparenchymal Botulinum Toxin type A injection over the affected parotid gland. The management of salivary gland fistula is discussed, focusing on the role of Botulinum Toxin type A injection and Sodium Tetradecyl Sulphate for the management of the fistula.

当皮肤与唾液腺或导管之间存在异常通信时,就会发生唾液腺瘘。大多数病例是由于头颈部手术的并发症,如腮腺切除术或外伤。目前,对于唾液腺瘘管的治疗尚无一致的指导方针。大多数病例采用保守治疗;然而,导管瘘的管理是具有挑战性的,通常需要比保守的更积极的措施。我们报告一例老年人颈部脓肿合并腮腺瘘后,切开和引流。他表现为伤口破裂和持续的唾液渗出。瘘管造影显示斯坦森导管与外瘘口相通。我们通过在瘘管道内注射硫酸十四烷基钠和超声引导下在腮腺上注射A型肉毒杆菌毒素进行硬化治疗。本文讨论了唾液腺瘘的治疗,重点讨论了A型肉毒毒素注射液和硫酸十四烷基钠对唾液腺瘘的治疗作用。
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引用次数: 0
Extranodal Peripheral T-Cell Lymphoma with Oro-Nasal Erosion - A Diagnostic Dilemma: A Case Report with Literature Review. 结外周围t细胞淋巴瘤合并口鼻糜烂-诊断困境:一例报告并文献复习。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-05-29 DOI: 10.1007/s12070-025-05622-1
Gunjan Vyas, Aradhana Singh, C L Nawal, Hardik Solanki, Avinash Jain, Daneshwar C Junjappanavar

Extranodal peripheral T-cell lymphomas (PTCLs) are rare and commonly affect patients with immunosuppression or systemic autoimmune disorders. The involvement of oral cavity is extremely rare, and the chances of missing the initial diagnosis are high. A case of 38-year-old, previously healthy male presented with whitish ulcerative lesion (3 × 1.5 cm) over the soft palate crossing the midline with uvula involvement and nasal stuffiness for the last 4- and 8-months, respectively. Initial investigations were unremarkable, and the case was discharged following conservative management. However, 1-month later, the case returned with difficulty in swallowing and a destructive ulcer over the soft palate causing palatal perforation (1 × 3 cm), resulting in the formation of an oro-nasal fistula and destruction of uvula. Various investigations, including CECT brain and thorax, serology, and inflammatory markers, as well as those for autoimmune disorder were unremarkable. CECT face revealed soft palate erosion with complex deviated nasal septum. Nasal mucosal biopsy revealed atypical lymphoid cells with high anaplasia, and angiocentric spread in certain tumor cells suggesting lymphoproliferative disorder. Immunohistochemistry was positive for CD3, CD5, and CD7. Thus, diagnosis of extranodal aggressive PTCL was reached, and chemotherapy with CHOP regimen was initiated. However, following second cycle, the patient succumbed.

结外周围t细胞淋巴瘤(PTCLs)是罕见的,通常影响免疫抑制或全身自身免疫性疾病的患者。累及口腔是极为罕见的,错过初步诊断的机会很高。1例38岁男性,既往健康,在过去4个月和8个月分别表现为软腭上的白色溃疡性病变(3 × 1.5 cm),穿过中线并累及小舌和鼻塞。初步调查结果不显著,病例在保守治疗后出院。然而,1个月后,患者因吞咽困难和软腭破坏性溃疡返回,导致腭穿孔(1 × 3 cm),导致口鼻瘘形成和小舌破坏。各种检查,包括脑部和胸部的CECT,血清学和炎症标志物,以及自身免疫性疾病的检查均无显著差异。CECT面部显示软腭糜烂伴鼻中隔复杂偏曲。鼻黏膜活检显示非典型淋巴样细胞高度增生,某些肿瘤细胞呈血管中心性扩散,提示淋巴增生性疾病。免疫组化CD3、CD5、CD7阳性。因此,诊断为结外侵袭性PTCL,并开始CHOP方案化疗。然而,在第二个周期后,患者死亡。
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引用次数: 0
A Rare Case of Microtia with Joint Formation Between Zygomatic Part of Temporal Bone and Mandibular Condyle. 颞骨颧部与下颌髁间关节形成的罕见小畸形1例。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-06-05 DOI: 10.1007/s12070-025-05650-x
H L Ashwini, Pritam Yadav

A case of a 10-year-old girl with rare association of temporomandibular joint anomaly with external and middle ear anomalies. It emphasizes on the importance of evaluating temporomandibular joint, mandibular condyle, temporal & petrous bone on HRCT in cases of external or middle ear anomalies for categorization, effective management, and reducing the overall childhood disability burden.

一个10岁的女孩,罕见的颞下颌关节异常伴有外耳和中耳异常。它强调了在外耳或中耳异常的情况下,在HRCT上评估颞下颌关节、下颌髁、颞骨和岩石骨的重要性,以进行分类,有效管理,并减少整体儿童残疾负担。
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引用次数: 0
A Rare Concurrence of Anaplastic and Papillary Thyroid Carcinomas: A Case Report and Literature Review. 罕见的间变性甲状腺乳头状癌合并1例报告及文献复习。
IF 0.4 Q4 SURGERY Pub Date : 2025-08-01 Epub Date: 2025-06-23 DOI: 10.1007/s12070-025-05797-7
Monika Maharjan, Zahed Ali Qamer, Bheru Dan Charan, Manu Malhotra, Ravi Hari Phulware

Background: Anaplastic thyroid carcinoma (ATC) is a rare, undifferentiated thyroid malignancy with a poor prognosis and rapid clinical progression. It accounts for less than 10% of thyroid cancers but contributes disproportionately to thyroid cancer-related mortality. Histologically, ATC exhibits significant pleomorphism and can present with diverse morphological patterns, often coexisting with differentiated thyroid carcinoma.

Case presentation: We report a case of a 39-year-old female with a 20-year history of anterior neck swelling, which rapidly progressed over six months. Imaging revealed a heterogeneously enhancing lesion in the right thyroid lobe with extrathyroidal extension and cervical lymphadenopathy. The patient underwent total thyroidectomy with central and lateral neck dissection. Histopathological examination demonstrated a high-grade malignant tumor composed of spindle-shaped, pleomorphic, and multinucleated giant cells with focal osteoid formation, consistent with ATC. A coexistent focus of papillary thyroid carcinoma was also identified. Immunohistochemistry revealed PAX8 negativity and SATB2 positivity, supporting its emerging role as a diagnostic marker for ATC.

Conclusion: This case highlights an unusual presentation of ATC in a relatively young patient. The presence of osteoclast-like giant cells and osteoid formation adds to the histological complexity. Accurate diagnosis requires a multidisciplinary approach integrating clinical, radiological, histopathological and immunohistochemical findings. Early recognition and surgical intervention are crucial given the aggressive nature and rapid progression of ATC. Emerging biomarkers like SATB2 may enhance diagnostic sensitivity, especially in challenging morphological variants.

背景:间变性甲状腺癌(ATC)是一种罕见的未分化甲状腺恶性肿瘤,预后差,临床进展迅速。它占甲状腺癌的不到10%,但对甲状腺癌相关死亡率的贡献却不成比例。组织学上,ATC表现出明显的多形性,可呈现多种形态,常与分化型甲状腺癌共存。病例介绍:我们报告了一个39岁的女性,有20年的前颈部肿胀史,其快速进展超过6个月。影像显示右甲状腺叶呈非均匀强化病变,伴甲状腺外展及颈淋巴肿大。患者行甲状腺全切除术并中央及外侧颈部清扫术。组织病理学检查显示为高级别恶性肿瘤,由梭形、多形性和多核巨细胞组成,伴局灶性类骨形成,符合ATC。同时还发现了甲状腺乳头状癌的共存病灶。免疫组织化学显示PAX8阴性和SATB2阳性,支持其作为ATC诊断标志物的新兴作用。结论:本病例在一个相对年轻的患者中突出了一个不寻常的ATC表现。破骨细胞样巨细胞和类骨形成的存在增加了组织学的复杂性。准确的诊断需要综合临床、放射学、组织病理学和免疫组织化学结果的多学科方法。鉴于ATC的侵袭性和快速进展,早期识别和手术干预至关重要。新兴的生物标志物如SATB2可能会提高诊断的敏感性,特别是在具有挑战性的形态变异中。
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引用次数: 0
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Indian Journal of Otolaryngology and Head and Neck Surgery
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