parotid gland swelling

腮腺肿胀
  • 文章类型: Case Reports
    中心静脉导管(CVC)放置是ICU中的常规程序,但可能与各种并发症有关。包括错位和血栓形成。我们介绍了一名84岁女性在超声引导下通过锁骨下静脉放置后,由于导管相关的颈外静脉血栓形成而导致腮腺肿大的罕见病例。该病例采用全身抗凝和导管拔除治疗。它强调了确认正确的CVC尖端定位的重要性,并强调了对术后胸部X射线的需求。
    Central venous catheter (CVC) placement is a routine procedure in ICUs but can be associated with various complications, including misplacement and thrombosis. We present a rare case of parotid gland enlargement due to catheter-related thrombosis of the external jugular vein following ultrasound-guided placement through the subclavian vein in an 84-year-old woman. This case was managed with systemic anticoagulation and catheter removal. It emphasizes the importance of confirming correct CVC tip positioning and highlights the need for a post-procedure chest X-ray.
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  • 文章类型: Case Reports
    Primary Sjögren\'s syndrome (pSS) is an autoimmune systemic disease characterized by the destruction of exocrine glands, mainly salivary and lacrimal glands. The diagnosis is generally made upon objective tests aimed at assessing salivary and lacrimal glandular function, autoantibody assays, and the results of labial salivary gland biopsies. A major salivary gland biopsy is usually reserved to assess lymphoproliferative complications. Recently, the sonographic evaluation of the major salivary glands has gained a crucial role in assessing the glandular parenchyma and early detecting abnormalities, while the role of ultrasonography in the assessment of lacrimal glands is still secondary. Our case report is about a male patient who presented parotid gland swelling and purpuric lesions, with preserved salivary and lacrimal glandular function. Considering the presence of risk factors associated with lymphoproliferative development and the peculiar characteristics detected by salivary and lacrimal gland ultrasonography, we performed a parotid gland biopsy, confirming Sjögren\'s syndrome. Our case demonstrates that lacrimal gland ultrasonography could be implemented, along with major salivary gland ultrasonography, as a routine procedure in evaluating patients with suspected or definite diagnoses of pSS.
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  • 文章类型: Case Reports
    急性术后短暂性唾液腺炎,也被称为麻醉腮腺炎,是一种短暂的罕见情况,通常是良性的,和自限性性质涉及单侧或双侧腮腺。确切的机制和病因尚未完全说明,但是致病因素可能包括,肺小耳炎,静脉充血,唾液分泌过多,手术位置,围手术期脱水,围手术期使用阿托品等药物,琥珀酰胆碱,吗啡,麻黄碱,还有异丙酚.我们报告了一例31岁的孕妇,她在脊髓麻醉下接受了选择性剖宫产。术后5小时,她出现了累及腮腺两侧的面部肿胀。地塞米松与静脉内(IV)液体和对乙酰氨基酚静脉内给予。肿胀逐渐改善并在48小时后完全消退。这是一个麻醉腮腺炎的病例,麻醉后可能出现的罕见病例之一。意识,早期识别和通过补液和皮质类固醇的支持性管理对于患者的放心至关重要,平滑回归,和恢复,并避免极其罕见的情况,因为这种情况会进展为气道阻塞。
    Acute postoperative transient sialadenitis, also known as anesthesia mumps, is a rare condition that is transient, usually benign, and self-limiting in nature involving unilateral or bilateral parotid glands. The exact mechanism and etiology have not been fully explained, but the causative factors may include, pneumoparotitis, venous congestion, excess saliva secretion, surgical position, perioperative dehydration, and perioperative use of drugs such as atropine, succinylcholine, morphine, ephedrine, and propofol. We report a case of a 31-year-old pregnant lady who was admitted for elective cesarean section under spinal anesthesia. She developed facial swelling involving the parotid area bilaterally five hours postoperatively. Dexamethasone was given intravenously with intravenous (IV) fluids and paracetamol. The swelling improved gradually and resolved completely after 48 hours. This is a case of anesthesia mumps, one of the rare cases that may develop after anesthesia. Awareness, early recognition and supportive management by rehydration and corticosteroids are essential for the patient\'s reassurance, smooth regression, and recovery, and to avoid extremely rare situations as this condition can progress into airway obstruction.
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  • 文章类型: Case Reports
    精氨酸酶缺乏症是一种进行性神经系统疾病,其特征是间歇性高氨血症危象。我们的患者在童年时期被诊断出患有脑瘫(痉挛性截瘫)并接受了康复治疗。她从5岁起就患有腮腺肿胀,在肝功能障碍变得明显之前,8岁时出现高淀粉酶血症.25岁时,她出现高氨血症和天冬氨酸转氨酶和丙氨酸转氨酶升高。在27岁时,由于高精氨酸血症和红细胞中缺乏精氨酸酶活性,她被诊断为精氨酸酶缺乏症。肝硬化也存在。由于反复的病毒感染,她因发作性高氨血症而多次住院,不均衡的饮食,对药物的依从性差。
    Arginase deficiency is a progressive neurological disorder characterized by episodic hyperammonemia crises. Our patient had been diagnosed with cerebral palsy (spastic paraplegia) in childhood and received rehabilitation. She had suffered parotid swelling since the age of 5 years, prior to liver dysfunction becoming apparent, and then developed hyperamylasemia at 8 years of age. At age 25 years, she presented with hyperammonemia and elevations of aspartate aminotransferase and alanine aminotransferase. At age 27 years, she was diagnosed with arginase deficiency due to hyperargininemia and absent arginase activity in erythrocytes. Liver cirrhosis was also present. She was hospitalized several times for management of episodic hyperammonemia due to recurrent viral infections, an unbalanced diet, and poor compliance with medications.
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  • 文章类型: Case Reports
    免疫球蛋白G4相关疾病(IgG4RD)预后良好,但由于其临床表现广泛,诊断困难,普通从业者的意识有限,和各种差异。这里,我们介绍了一个老年男性的病例,他出现了复发性龋齿,复发性鼻窦炎,持续的口干,干眼伴双侧腮腺肿大,无淋巴结肿大。进一步评估患者,发现IgG4水平升高,腮腺组织病理学检查显示淋巴细胞浸润,生发中心无任何肉芽肿性病变,免疫组织化学(IHC)显示IgG4阳性浆细胞。患者被诊断为IgG4RD,并开始使用皮质类固醇,之后症状有所改善。
    Immunoglobulin G4-related disease (IgG4 RD) has a fair prognosis but its diagnosis has been difficult due to the condition\'s wide range of clinical manifestations, limited awareness among common practitioners, and various differentials. Here, we present a case of an elderly male who presented with recurrent dental caries, recurrent sinusitis, persistent dry mouth, and dry eyes along with bilateral parotid gland enlargement without any lymphadenopathy. The patient was evaluated further and found to have elevated levels of IgG4 and on histopathological examination of the parotid gland showed lymphocytic infiltrate with germinal centers without any granulomatous lesions and IgG4-positive plasma cells on immunohistochemistry (IHC). The patient was diagnosed with IgG4 RD and was started on corticosteroids, after which there was a symptomatic improvement.
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  • 文章类型: Case Reports
    据报道,一名64岁妇女的病例,在右下颌饱满度的先前区域出现了新发作的疼痛。临床检查,MRI,细针穿刺细胞学检查证实诊断为良性腮腺肿瘤-多形性腺瘤,通过全腮腺切除术完全切除肿瘤进行治疗。在评估口面疼痛患者时,口腔保健提供者应该认识到所有潜在的鉴别诊断,特别是在设置危险信号,如持续或扩大面部肿胀/丰满。
    A case of a 64-year-old woman is reported, who developed new-onset pain over a preexisting area of right mandibular fullness. Clinical examination, MRI, and fine-needle aspiration cytology confirmed the diagnosis of a benign parotid gland tumor-pleomorphic adenoma, which was treated by total parotidectomy with complete removal of the tumor. When evaluating a patient with orofacial pain, oral health care providers should be cognizant of all potential differential diagnoses, especially in the setting of red flags such as persistent or enlarging facial swelling/fullness.
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  • 文章类型: Journal Article
    OBJECTIVE: To assess the prevalence of parotid gland swelling (PGS), and its association with features of Sjögren\'s syndrome (SS) and other causes of sialadenosis in a Latin-American cohort of primary SS.
    METHODS: We included 668 patients from Argentina, Brazil, Mexico, and Paraguay. We retrospectively registered demographics, disease duration, oral/ocular symptoms, serology and scored the basal ESSDAI. We defined PGS as a recurrent or persistent increase of volume of any parotid glands during adulthood (self-reported and/or physical examination). We registered the presence of diabetes mellitus, dyslipidaemia, body mass index, and alcohol consumption. We used logistic regression analysis reporting OR and 95% CI.
    RESULTS: PGS was present in 242 patients (36.2%): 78 previous to SS diagnosis, 86 concomitantly, 73 during follow-up, and five unknown. At the multivariate analysis, PGS was associated with RF (OR 2.47, 95% CI 1.1-6.5, p= 0.0001), basal articular ESSDAI domain (OR 1.63, 95% CI 1.01-2.6, p= 0.04), and alcohol consumption (OR 2.42, 95% CI 1.41-4-15). Patients with PGS during the follow-up had a higher prevalence of alcohol consumption (45.3%) compared with the remaining PGS cases (26.8%; OR 2.41 95% CI 1.2-4.7), or patients without parotid gland swelling (15.6%; OR 3.8 95% CI 1.7-8.2) in all the adjusted models.
    CONCLUSIONS: PGS generally precedes or presents concomitantly with SS diagnosis, and is related to RF and articular activity. Alcohol consumption is an additional factor in PGS, especially during follow-up. The meaning of this last finding as well as its prognostic implications remains to be elucidated and deserves further evaluation in prospective studies.
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  • 文章类型: Journal Article
    唾液腺病(唾液腺病)是一种慢性,非炎性,非肿瘤性,双边,唾液腺通常无痛增大,最常影响腮腺。大约50%的病例与潜在的疾病过程有关。唾液腺病的发病机制尚不清楚,但可能是自主神经病变的结果。管理的关键是诊断和管理任何控制不佳的基础医疗过程。
    Sialadenosis (sialosis) is a chronic, noninflammatory, nonneoplastic, bilateral, often painless enlargement of the salivary glands, most frequently affecting the parotid glands. Approximately 50% of cases are associated with an underlying disease process. The pathogenesis of sialadenosis is unknown but likely results from an autonomic neuropathy. The key to management is diagnosis and management of any poorly controlled underlying medical process.
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  • 文章类型: Journal Article
    We encountered a 59-year-old man who first underwent left internal carotid endarterectomy for left internal carotid artery stenosis and then presented with postoperative swelling of the bilateral salivary glands. He then developed upper airway obstruction that required emergency tracheal intubation. The most likely cause was thought to be anesthesia mumps, which involves a complex interaction of multiple factors including pneumoparotitis, venous congestion, and excess saliva secretion. Many cases of salivary gland swelling recover after follow-up observation alone if there are no inflammatory findings; however, severe complications may sometimes occur. If upper airway obstruction develops as in the present case, then emergency airway management must also be considered and conscientious observation is necessary.
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  • 文章类型: Case Reports
    A diffuse, chronic, usually bilateral, noninflammatory, nonneoplastic enlargement of major salivary glands is termed as Sialosis or Sialadenosis. It is an extremely uncommon cause for enlargement of the parotid gland. We hereby present a case of a 45-year-old female patient having a swelling at the left preauricular region. The swelling was gradually increasing in size since 6 months. On clinical examination, the swelling was 3 cm × 3 cm, mobile, and nontender. On ultrasonography, it was suggestive of benign parotid lesion or parotitis with cervical lymphadenopathy. On fine needle aspiration cytology, it was suggestive of sialadenosis. This is an extremely rare salivary gland lesion with specific cellular features. It is very important to distinguish sialadenosis from other causes of enlargement of the parotid gland as treatment modality differs.
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