Parotid gland

腮腺
  • 文章类型: Journal Article
    这项研究的目的是比较治疗方式,病理和临床特征,腮腺转移患者的预后。评估了二十多年来接受腮腺转移治疗的34例患者的病历。使用P/N和N1S3分期系统对头颈部皮肤鳞状细胞癌(HNcSCC)转移的患者进行回顾性重新分类。颈部转移患者的预后明显较差(P=0.025)。单因素分析还显示,腮腺切除术的程度和颈淋巴结清扫的类型并不影响无复发生存率(RFS)和总生存率(OS)。当比较P/N和S1N3分段系统的有用性时,在RFS和OS中,P期和N1S3期之间均呈正相关。腮腺切除术和伴随颈淋巴结清扫的范围仍在讨论中。全腮腺切除术和改良根治性颈清扫术并未改善RFS和OS。与P/N分期系统相比,N1S3分类不太复杂,具有更高的预测值。
    The aim of this study was to compare treatment modalities, pathological and clinical characteristics, and outcomes in patients with metastasis in a parotid gland. The medical records of 34 patients who received treatment for metastasis in the parotid gland over a twenty-year period were evaluated. Patients with head and neck cutaneous squamous cell carcinoma (HNcSCC) metastasis were retrospectively reclassified using the P/N and N1S3 staging system. Patients with neck metastasis showed a significantly poorer prognosis (P = 0.025). Univariate analysis also revealed that extent of parotidectomy and type of neck dissection did not influence recurrence free survival (RFS) and overall survival (OS). When comparing the usefulness of the P/N and S1N3 staging systems, a positive correlation was observed between the P stage and the N1S3 stage in both RFS and OS. The extent of parotidectomy and concomitant neck dissection is still under discussion. Total parotidectomy and modified radical neck dissection did not improve RFS and OS. N1S3 is a less complex classification and possesses a higher predictive value when compared to the P/N staging system.
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  • 文章类型: Case Reports
    血管肉瘤很少见,仅占头颈部肉瘤的1-2%。我们介绍了一种极为罕见的原发性非辐射诱导的腮腺血管肉瘤,其上皮样形态需要三级中心对其组织学特征的第二意见。我们讨论演示文稿,成像,诊断,特点,和这个案子的路径。由于腮腺肿块很常见,需要手术筛子以排除其他可能的情况。由于血管肉瘤的快速转移潜力,早期正确的诊断在诸如血管肉瘤等疾病中至关重要。
    Angiosarcomas are rare, accounting for only 1-2% of sarcomas in the head and neck region. We present an extremely rare case of primary non-radiation-induced angiosarcoma of the parotid with epithelioid morphology which required a tertiary center second opinion for its histological characteristics. We discuss the presentation, imaging, diagnosis, characteristics, and pathway of this case. As parotid lumps are common, a surgical sieve is required to rule out other possible conditions. Early correct diagnosis is crucial in conditions such as angiosarcomas due to their quick metastatic potential.
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  • 文章类型: Case Reports
    我们介绍一个71岁的男人,在接受上皮癌术后放疗后,发展为逐渐扩大的红斑。最初,这种情况类似于放射性皮炎或丹毒,局部使用类固醇和抗菌剂均未成功。进行了活检以进行进一步评估,显示腮腺癌的皮肤浸润。病灶继续扩大,导致吞咽困难,最终需要气管造口术。
    We present the case of a 71-year-old man who, after undergoing postoperative radiotherapy for epithelial carcinoma, developed progressively enlarging erythema. Initially, the condition resembled radiation dermatitis or erysipelas, and topical steroids and antibacterial agents were administered without success. A biopsy was performed for further evaluation, revealing a cutaneous invasion of parotid carcinoma. The lesion continued to enlarge, leading to dysphagia and ultimately necessitating a tracheostomy.
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  • 文章类型: Journal Article
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  • 文章类型: Case Reports
    背景:基底细胞腺瘤是一种罕见的,唾液腺良性上皮肿瘤,仅占所有唾液腺肿瘤的1-2%。主要见于腮腺,基底细胞腺瘤也可发生在小唾液腺,常与其他良恶性唾液腺肿瘤混淆。彻底的组织病理学检查可以提供明确的诊断。
    方法:一名65岁女性患者右耳下区域出现无痛肿块。影像学显示右腮腺深叶有明显的低密度病变,最初怀疑为粘液表皮样癌。细针抽吸术尚无定论,导致决定进行全保守腮腺切除术。组织病理学证实基底细胞腺瘤,以充满粘液样物质的囊性区域和以小梁和管状模式排列的基底细胞为特征。
    结论:1991年,WHO将基底细胞腺瘤归类为一个独特的实体。细胞学上,他们模仿良性和恶性唾液以及非唾液腺肿瘤。基底细胞腺瘤的组织学标志涉及具有小圆形核的基底细胞,显示无异型。很少苍白的细胞质,和明显的外围栅栏。治疗包括手术切除,对某些变体如膜型采用更激进的方法。
    结论:这个案例突出了临床,放射学,和基底细胞腺瘤的组织病理学特征,强调准确诊断和适当手术管理的重要性。早期发现和适当的治疗对于优化基底细胞腺瘤治疗的患者预后至关重要。
    BACKGROUND: Basal cell adenoma is a rare, benign epithelial tumour of the salivary gland, comprising only 1-2 % of all salivary gland tumours. Predominantly found in the parotid gland, basal cell adenoma can also occur in minor salivary glands and are often confused with other benign and malignant salivary gland tumours. A thorough histopathological examination can provide a definitive diagnosis.
    METHODS: A 65-year-old woman presented with a painless mass in the right infra-auricular region. Imaging revealed a well-defined hypodense lesion in the deep lobe of the right parotid gland, initially suspected as mucoepidermoid carcinoma. Fine needle aspiration was inconclusive, leading to the decision to perform a total conservative parotidectomy. Histopathology confirmed basal cell adenoma, characterized by cystic areas filled with mucoid material and basaloid cells arranged in trabecular and tubular patterns.
    CONCLUSIONS: Basal cell adenoma was classified as a distinct entity by the WHO in 1991. Cytologically, they imitate both benign and malignant salivary as well as non-salivary gland tumours. The histological hallmark of basal cell adenoma involves basaloid cells with small round nuclei showing no atypia, scant pale cytoplasm, and distinct peripheral palisading. Treatment involves surgical removal, with a more radical approach for certain variants such as the membranous type.
    CONCLUSIONS: This case highlights the clinical, radiological, and histopathological features of basal cell adenoma, emphasizing the importance of accurate diagnosis and appropriate surgical management. Early detection and appropriate treatment are crucial for optimizing patient outcomes in basal cell adenoma management.
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  • 文章类型: Journal Article
    涎腺肿瘤在临床表现和组织学上高度可变。世界卫生组织(WHO)对唾液腺的22种恶性肿瘤和11种良性肿瘤进行了分类。唾液腺肿瘤的诊断基于影像学(超声,磁共振成像)和细针穿刺活检,但最终的诊断是基于切除的肿瘤组织的组织病理学检查。在这项试点研究中,我们正在测试一种新的方法来识别唾液中的肽生物标志物,该生物标志物可用于诊断唾液腺肿瘤。用于肽研究的研究材料是来自肿瘤组织和健康组织(对照样品)的洗液的提取物。同时,对患者和健康个体的唾液样本进行分析.比较组织提取物和唾液样品的肽组组成可以鉴定患者唾液中唾液腺肿瘤的潜在肽标记物。从18个肿瘤和18个健康组织样本中提取的肽组组合物,患者唾液样本(11个样本),通过LC-MS串联质谱法分析健康唾液样品(8个样品)。确定了一组109个肽,它们仅存在于肿瘤组织提取物和患者唾液样品中。一些鉴定的肽来自先前被认为是唾液腺肿瘤潜在生物标志物的蛋白质(ANXA1,BPIFA2,FGB,GAPDH,HSPB1,IGHG1,VIM)或其他组织或器官的肿瘤(SERPINA1,APOA2,CSTB,GSTP1,S100A8,S100A9,TPI1)。不幸的是,所鉴定的肽均不存在于所分析的所有样品中。这可能是由于这种类型癌症的高度异质性。令人惊讶的结果是,来自肿瘤组织的提取物不包含来自唾液腺特异性蛋白的肽(STATH,SMR3B,HTN1,HTN3)。这些结果可能表明,发展中的肿瘤抑制了唾液必需成分蛋白质的产生。
    Salivary gland tumors are highly variable in clinical presentation and histology. The World Health Organization (WHO) classifies 22 types of malignant and 11 types of benign tumors of the salivary glands. Diagnosis of salivary gland tumors is based on imaging (ultrasound, magnetic resonance imaging) and fine-needle aspiration biopsy, but the final diagnosis is based on histopathological examination of the removed tumor tissue. In this pilot study, we are testing a new approach to identifying peptide biomarkers in saliva that can be used to diagnose salivary gland tumors. The research material for the peptidomic studies was extracts from washings of neoplastic tissues and healthy tissues (control samples). At the same time, saliva samples from patients and healthy individuals were analyzed. The comparison of the peptidome composition of tissue extracts and saliva samples may allow the identification of potential peptide markers of salivary gland tumors in patients\' saliva. The peptidome compositions extracted from 18 tumor and 18 healthy tissue samples, patients\' saliva samples (11 samples), and healthy saliva samples (8 samples) were analyzed by LC-MS tandem mass spectrometry. A group of 109 peptides was identified that were present only in the tumor tissue extracts and in the patients\' saliva samples. Some of the identified peptides were derived from proteins previously suggested as potential biomarkers of salivary gland tumors (ANXA1, BPIFA2, FGB, GAPDH, HSPB1, IGHG1, VIM) or tumors of other tissues or organs (SERPINA1, APOA2, CSTB, GSTP1, S100A8, S100A9, TPI1). Unfortunately, none of the identified peptides were present in all samples analyzed. This may be due to the high heterogeneity of this type of cancer. The surprising result was that extracts from tumor tissue did not contain peptides derived from salivary gland-specific proteins (STATH, SMR3B, HTN1, HTN3). These results could suggest that the developing tumor suppresses the production of proteins that are essential components of saliva.
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  • 文章类型: Journal Article
    Objective:To explore the safety and aesthetic effect of modified Z-shaped cosmetic incision in parotid benign tumor resection. Methods:A prospective study was conducted. A total of 44 patients with benign parotid tumor resection were randomly divided into experimental group(n=22) and control group(n=22). The experimental group underwent modified Z-shaped cosmetic incision, while the control group underwent the traditional S-shaped incision. The surgical duration, hospital stay, complications and maxillofacial aesthetics were compared between the two groups. Results:There was no significant difference in gender, age, surgical method, pathological type between the experimental group and the control group(P>0.05). The maxillofacial aesthetics and surgical duration of the two groups was statistically significant(P<0.05), while there was no statistically significant difference in terms of hospitalization days, surgical complications and Vancouver scar scale score (P>0.05). Conclusion:The modified Z-shaped cosmetic incision has a better effect on improving the maxillofacial aesthetics after benign parotid tumor resection, and compared with the traditional S-shaped incision, the safety is consistent, so it is worthy of clinical promotion and application.
    目的:探讨改良Z形美容切口在腮腺良性肿瘤切除术中的安全性和美学效果。 方法:采用前瞻性研究,将44例行腮腺良性肿瘤切除术的患者随机分为试验组(22例)和对照组(22例)。试验组采用改良Z形美容切口,对照组采用传统S形切口,比较2组在手术时长、住院天数、并发症以及颌面部美观方面的统计学差异。 结果:试验组和对照组在性别、年龄、手术方式、病理类型比较,差异无统计学意义(P>0.05);2组对手术持续时间、视觉模拟评分进行比较,差异有统计学意义(P<0.05),但住院天数、手术并发症及温哥华瘢痕量表评分比较,差异无统计学意义(P>0.05)。 结论:改良Z形美容切口在改善腮腺良性肿瘤切除术后颌面部美观方面的效果更好,且与传统S形切口相比较,安全性一致,因此值得临床推广和应用。.
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  • 文章类型: Journal Article
    癌细胞性病变代表一组良性和潜在的癌前肿瘤,其特征是癌细胞的积累。它们很大,颗粒状,和嗜酸性细胞。诊断腮腺嗜酸细胞性病变通常涉及成像技术的组合,比如超声波,计算机断层扫描(CT)扫描,磁共振成像(MRI)。细针抽吸(FNA)活检和组织病理学检查仍然是这些病变的主要诊断工具。准确的诊断对于适当的管理决策至关重要。腮腺嗜酸细胞病变的治疗选择包括手术,保守管理,和放射治疗(RT)。然而,在头部和颈部,辐射剂量可能是一把双刃剑。虽然RT是一种治疗方式,低辐射剂量可以促进腮腺嗜酸细胞病变的发展。嗜酸细胞性病变患者的预后通常良好,特别是当病变是良性的并且管理得当时。当前的研究集中在低剂量辐射暴露对嗜酸细胞性病变的潜在分子机制上。低辐射剂量后这些病变的发展代表了重要的临床关注。本手稿提供了有关腮腺嗜酸细胞病变的当前知识的全面概述,包括风险因素,诊断,治疗方案,和正在进行的研究,为临床医生和研究人员提供有价值的见解。
    Oncocytic lesions represent a group of benign and potentially precancerous tumors characterized by the accumulation of oncocytes, which are large, granular, and eosinophilic cells. Diagnosing oncocytic lesions in the parotid gland typically involves a combination of imaging techniques, such as ultrasound, Computed Tomography (CT) scans, and Magnetic Resonance Imaging (MRI). Fine-needle aspiration (FNA) biopsy with histopathological examination remains the primary diagnostic tool for these lesions. Accurate diagnosis is crucial for appropriate management decisions. Treatment options for oncocytic lesions in the parotid gland include surgery, conservative management, and radiation therapy (RT). However, in the head and neck region, radiation doses can be a double-edged sword. While RT is a treatment modality, low radiation doses can promote the development of oncocytic lesions in the parotid gland. The prognosis for patients with oncocytic lesions is generally favorable, especially when the lesions are benign and appropriately managed. Current research focuses on the molecular mechanisms underlying oncocytic lesions in response to low-dose radiation exposure. The development of these lesions following low radiation doses represents a significant clinical concern. This manuscript provides a comprehensive overview of the current knowledge regarding oncocytic lesions in the parotid gland, including risk factors, diagnosis, treatment options, and ongoing research, offering valuable insights for clinicians and researchers.
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  • 文章类型: Case Reports
    背景:Warthin肿瘤(WT)是唾液腺中第二常见的良性肿瘤。它的生长速度缓慢,最常见于腮腺。大多数患者出现耳下/耳前无痛性肿块的偶然发现。除了肿瘤的上皮成分,WT在特征上与被认为是良性的淋巴间质相关。虽然有一些关于WT中淋巴成分恶性转化的报道,WT合并套细胞淋巴瘤(MCL)的病例极为罕见。据我们所知,英语文献中描述了两种情况。在这里,我们报告了一例WT合并MCL的70岁女性患者,并强调仔细检查WT中淋巴间质的重要性,以免错过并发淋巴瘤。
    方法:一名70岁的中国女性,有40年的吸烟史,有1年的右颌下肿块史,近期肿大。
    方法:颈部超声(US)和计算机断层扫描(CT)扫描显示右腮腺中有一个界限明确的肿块,最大直径为3.1cm。对肿块进行手术切除。组织病理学检查显示肿瘤上皮的特征性双层,具有突出的淋巴间质,建议WT。此外,形态学和免疫组织化学研究证实了MCL的共存。此后,该病例的最终诊断为WT合并MCL.
    方法:患者在临床评估后分期为I期。由于腮腺病变生长缓慢,密切观察是通过定期临床和放射学监测决定的。
    结果:目前,通过临床评估,患者显示病情稳定。
    结论:据我们所知,报告的WT合并MCL的病例非常罕见。该病例强调了对WT的淋巴间质进行全面评估的重要性,以避免在碰撞肿瘤中漏诊淋巴瘤成分。
    BACKGROUND: Warthin tumor (WT) is the second most common benign tumor in salivary gland. It has a slow growth rate and most frequently occurs in the parotid gland. Most patients present with an incidental finding of a painless mass inferior/anterior to the ear. Besides the epithelial component of the tumor, WT is characteristically associated with lymphoid stroma that is considered benign. While there have been a few reports of malignant transformation of the lymphoid components in WT, cases of WT concomitant with mantle cell lymphoma (MCL) are extremely rare. To the best of our knowledge, two cases have been described in the English literature. Herein, we report a case of WT concomitant with MCL in a 70-year-old female patient, and emphasize the importance of careful examination of lymphoid stroma in WT so that concurrent lymphoma is not missed.
    METHODS: A 70-year-old Chinese woman with a 40-year history of cigarette smoking presented with a one year history of a right submaxillary mass with recent enlargement.
    METHODS: Cervical ultrasound (US) and computed tomography (CT) scans of the neck revealed a well-circumscribed mass in the right parotid with a maximum diameter of 3.1 cm. Surgical resection of the mass was performed. Histopathological examination revealed a characteristic double-layer of neoplastic epithelium with prominent lymphoid stroma, suggesting WT. In addition, morphology and immunohistochemistry studies confirmed the coexistence of MCL. Thereafter, the final diagnosis of this case was WT concomitant with MCL.
    METHODS: The patient was staged as stage I after clinical assessment. Due to the slow growth of parotid lesions, close observation was decided with periodic clinical and radiological monitoring.
    RESULTS: Currently, the patient demonstrates a stable disease by clinical evaluation.
    CONCLUSIONS: To the best of our knowledge, reported cases of WT concomitant with MCL are very rare. This case highlights the importance of a comprehensive assessment of the lymphoid stroma of WT to avoid missed diagnosis of a lymphoma component in a collision tumor.
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  • 文章类型: Journal Article
    目的:建立基于MRI影像组学特征并结合临床特征的影像组学列线图,以区分多形性腺瘤(PA)和Warthin瘤(WT)。
    方法:在2017年7月至2023年6月期间,本研究纳入了经组织病理学证实的294例PA(n=159)和WT(n=135)患者。分析临床资料及MRI表现等临床因素,建立临床模型。从T1WI和FS-T2WI中提取并选择10个MRI影像组学特征,用于建立影像组学模型并计算影像组学评分(Rad-scores)。将临床因素和Rad评分组合起来作为组合模型的关键参数。通过接收机操作特征(ROC)曲线和决策曲线分析(DCA),对三个模型的判别值进行了验证和比较,表现最好的组合模型以放射组学列线图的形式可视化.
    结果:组合模型在训练集(AUC=0.998)和测试集(AUC=0.993)中对PA和WT表现出出色的判别性能,并且与临床模型和影像组学模型相比在训练集(AUC=0.996,0.952)和测试模型(AUC=0.954,0.849)中表现更好。DCA显示,与另外两种模型相比,组合模型在区分腮腺PA和WT方面提供了更多的总体临床有用性。
    结论:基于MRI影像组学特征的分析影像组学列线图,结合临床因素,能有效区分PA和WT。
    OBJECTIVE: To establish a radiomics nomogram based on MRI radiomics features combined with clinical characteristics for distinguishing pleomorphic adenoma (PA) from warthin tumor (WT).
    METHODS: 294 patients with PA (n = 159) and WT (n = 135) confirmed by histopathology were included in this study between July 2017 and June 2023. Clinical factors including clinical data and MRI features were analyzed to establish clinical model. 10 MRI radiomics features were extracted and selected from T1WI and FS-T2WI, used to establish radiomics model and calculate radiomics scores (Rad-scores). Clinical factors and Rad-scores were combined to serve as crucial parameters for combined model. Through Receiver operator characteristics (ROC) curve and decision curve analysis (DCA), the discriminative values of the three models were qualified and compared, the best-performing combined model was visualized in the form of a radiomics nomogram.
    RESULTS: The combined model demonstrated excellent discriminative performance for PA and WT in the training set (AUC=0.998) and testing set (AUC=0.993) and performed better compared with the clinical model and radiomics model in the training set (AUC=0.996, 0.952) and testing model (AUC=0.954, 0.849). The DCA showed that the combined model provided more overall clinical usefulness in distinguishing parotid PA from WT than another two models.
    CONCLUSIONS: An analytical radiomics nomogram based on MRI radiomics features, incorporating clinical factors, can effectively distinguish between PA and WT.
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