Parapharyngeal Space

咽旁空间
  • 文章类型: Journal Article
    背景:甲状腺乳头状癌(PTC)是最常见的甲状腺癌类型。在极少数情况下,PTC已转移到咽后和咽旁淋巴结。据推测,这是由于淋巴通道异常或先前颈部解剖后的逆行淋巴流而发生的。
    方法:以关键词“咽旁,“咽后”,“和”甲状腺乳头状癌。\"
    结果:共135例,共确定了46篇文章。最常见的症状是淋巴结肿大,其次是咽部肿块和呼吸困难。38.03%的患者无症状。包括初始治疗史在内的病例,94.44%有颈清扫史。经宫颈入路是切除肿瘤最常用的方法,尽管近年来也使用了经口机器人手术(TORS)。
    结论:PTC转移到咽后和咽旁淋巴结是一种罕见的情况,由于其惰性性质,可能难以诊断。
    BACKGROUND: Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer. In rare instances, PTC has metastasized to the retropharyngeal and parapharyngeal nodes. This is hypothesized to occur due to an aberrant lymphatic channel or via retrograde lymphatic flow following previous neck dissection.
    METHODS: A literature search was conducted with keywords \"parapharyngeal,\" \"retropharyngeal,\" and \"papillary thyroid carcinoma.\"
    RESULTS: 46 articles were identified for a total of 135 cases. The most common presenting symptom was lymphadenopathy followed by pharyngeal mass and dyspnea. 38.03 % of patients were asymptomatic. Of cases including initial treatment history, 94.44 % had a history of neck dissection. The transcervical approach was the most utilized to resect the tumors, although in recent years trans-oral robotic surgery (TORS) has also been used.
    CONCLUSIONS: PTC metastatic to the retropharyngeal and parapharyngeal nodes is a rare occurrence that can be difficult to diagnose due its indolent nature.
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  • 文章类型: Journal Article
    咽旁间隙已被描述为倒金字塔形状,头骨的底部和舌骨的大角在顶部。咽旁间隙肿瘤占头颈部肿瘤的0.5%,该区域可发生多种肿瘤类型,其中80%是良性的,最常见的是唾液腺多形性腺瘤和神经源性肿瘤。我们介绍了一名39岁的妇女,她因左侧颈部疼痛而住院,左耳有阻塞感,听力下降10个月。影像学显示肿块与颅骨无关,患者通过经口入路进行了手术切除,发现肿块的内容物是脑脊液,咽旁间隙的脑膜膨出是罕见的。患者主要表现为疼痛症状,最终通过神经阻滞治疗得到缓解。
    The parapharyngeal space has been described as an inverted pyramid shape with the base of the skull and the great cornu of the hyoid bone at the top. Tumors of the parapharyngeal space account for 0.5% of head and neck tumors and a wide range of tumor types can occur in this area, 80% of which are benign, the most common being pleomorphic adenomas of the salivary glands and neurogenic tumors. We present a 39-year-old woman who was hospitalized due to left-sided neck pain with a feeling of blockage in the left ear and hearing loss for 10 months. Imaging showed that the mass was not connected to the cranium and the patient underwent surgical resection via a transoral approach, where the contents of the mass were found to be cerebrospinal fluid, and meningocele in the parapharyngeal space is a rare occurrence. The patient presented mainly with painful symptoms, which were eventually relieved by nerve block therapy.
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  • 文章类型: Journal Article
    孤立性纤维瘤(SFT)通常被描述为由胸膜引起的病变。很少,已在咽旁间隙(PS)中进行了描述。本研究旨在报告PS中的2例SFT,并就此主题进行文献综述。两名患者在PS中接受SFT手术切除,被报道。关于PS的SFT的文献综述,也进行了。对2例患者进行分析。两名患者都接受了手术切除,其次是辅助放疗,对于由PS产生的SFT。术后病程顺利,两名患者术后均恢复良好。随访期间未确诊复发。PS的SFT是不常见的实体。手术切除是最常用的治疗方法,对于有复发危险因素或远处转移的患者,应考虑辅助放疗。
    The solitary fibrous tumor (SFT) is usually described as a lesion arising from the pleura. Rarely, it has been described in the parapharyngeal space (PS). This study aims to report two cases of SFT in the PS and to perform a literature review on this topic. Two patients undergoing surgical resection of a SFT in the PS, were reported. A literature review on SFT of the PS, was also performed. Two patients were analyzed. Both patients underwent surgical resection, followed by adjuvant radiotherapy, for SFT arising from the PS. The postoperative course was uneventful and both patients recovered well after the procedure. No recurrences were diagnosed during the followup. SFT of the PS is an infrequent entity. Surgical resection is the most used treatment, and adjuvant radiation should be considered in patients with recurrence risk factors or distant metastases.
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  • 文章类型: Case Reports
    口腔颌面外科医生经常面临异物移位到口腔周围组织和头颈部软组织的临床挑战。这主要是由于外伤或在牙科治疗期间无意中发生的。除了上颌窦,牙科治疗期间医源性异物移位可能发生在头颈部16个不同的筋膜间隙之一。与牙科治疗有关的常见移位的异物包括牙根或碎片,局部麻醉针,植入物和修复。移位的异物的临床后遗症取决于其大小,形状,解剖位置和靠近重要结构。尽管患者可能在相当长的时间内保持无症状,残留的异物会导致持续的疼痛,由于炎症引起的软组织反复感染和疤痕,所有这些都可能使延迟检索复杂化。除了历史,诸如平片和计算机断层扫描(CT)之类的成像方式有助于定位移位的异物及其随后的检索。可以通过口内尝试手术取回,经宫颈和内镜入路。此外,手术可以通过实时成像,如透视辅助。本报告旨在详细介绍正畸微型螺钉意外移位的情况,通常用作临时锚固装置(TAD),进入咽部外侧空间,同时尝试放置在下颌磨牙后区域。病例报告还描述了使用口内方法并使用C臂射线照相成像进行荧光透视检查的TAD螺钉的手术取出程序。该病例在相关文献综述的同时进行了报道,因为它不仅解释了正畸微型螺钉放置的罕见并发症,而且还详细说明了从头颈部筋膜间隙中去除移位异物的方式,否则直接无法访问。
    Oral and maxillofacial surgeons are often faced with the clinical challenge of foreign body displacement into the perioral tissues and soft tissues of the head and neck. This mainly occurs either because of trauma or inadvertently during dental treatment. In addition to the maxillary sinus, iatrogenic foreign body displacement during dental treatment could happen into one of the 16 distinct fascial spaces of the head and neck region. Commonly displaced foreign bodies related to dental treatment include tooth roots or fragments, local anesthetic needles, implants and restorations. The clinical sequelae of a displaced foreign body depend on its size, shape, anatomic location and proximity to vital structures. Although patients may remain asymptomatic for a considerable amount of time, retained foreign bodies result in persistent pain, recurrent infection and scarring of soft tissue due to inflammation, all of which may complicate delayed retrieval. In addition to the history, imaging modalities such as plain radiographs and computed tomography (CT) help in locating the displaced foreign body and its subsequent retrieval. Surgical retrieval may be attempted through intraoral, transcervical and endoscopic approaches. Additionally, surgery may be aided by real-time imaging such as fluoroscopy. The present report aims to detail a case of inadvertent displacement of an orthodontic mini-screw, commonly used as a temporary anchorage device (TAD), into the lateral pharyngeal space, while attempting placement in the mandibular retromolar area. The case report also describes the surgical retrieval procedure of the TAD screw using an intraoral approach and with fluoroscopy guidance using C-Arm radiographic imaging. This case is reported along with the pertinent review of literature, as it not only explains a rare complication of orthodontic mini-screw placement but also details a modality to remove displaced foreign bodies from fascial spaces of the head and neck, which are otherwise directly inaccessible.
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  • 文章类型: Case Reports
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  • 文章类型: Journal Article
    海绵状血管瘤是一种非癌性血管生长,起源于头颈部区域的不同部位。然而,咽旁间隙对其发生的贡献很小。我们介绍了一个右咽旁海绵状血管瘤的病例,非常罕见的临床表现。这是一名57岁的女性,出现3个月的喉咙不适。考试发现显示出柔和的,弥漫,和右颈上腹部区域的非脉动性肿块。对比的计算机地形扫描显示右咽旁间隙有多个钙化。T2加权磁共振成像显示右咽旁间隙肿块,高信号和多个静脉,动态血管造影无明显变化。经颈入路手术切除,组织病理学报告显示海绵状血管瘤伴钙化血栓。总之,手术介入是治疗的主要手段,经宫颈入路是海绵状血管瘤手术切除最常用的方法。
    Cavernous hemangioma is a noncancerous vascular growth that arises from different parts of the head and neck region. However, parapharyngeal space contributes a very small percentage for its occurrence. We present a case of right parapharyngeal cavernous hemangioma, a very rare clinical presentation. This is a 57-year-old female presented with throat discomfort for 3 months. Examination finding showed a soft, diffuse, and non-pulsating mass over the right upper jugulodigastric region. A contrasted computed topographic scan revealed multiple calcifications in right parapharyngeal space. T2-weighted magnetic resonance imaging showed right parapharyngeal space mass with high signal and multiple phleboliths and dynamic angiogram unremarkable. Surgical resection done via transcervical approach and histopathological report revealed cavernous hemangioma with calcified thrombi. In conclusion, surgical intervention is the mainstay treatment and transcervical approach which is adopted in this case is the commonest approach used in surgical resection of cavernous hemangioma.
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  • 文章类型: Case Reports
    背景:脂肪母细胞瘤是一种由胚胎脂肪细胞引起的罕见良性肿瘤。它主要在婴儿期和儿童早期发展。我们提供了一个10个月大的儿童的案例研究,该儿童治疗了颞下窝和咽旁间隙的广泛肿瘤。还报告了对80例头颈部脂肪母细胞瘤儿童的60例报告的系统评价。
    方法:对1964年至2022年在PubMed数据库中发表的包括儿童头颈部脂肪母细胞瘤在内的所有文章进行了系统评价。儿童头颈部广泛脂肪母细胞瘤的临床表现。
    结果:在所有纳入标准的基础上,共确定了83篇关于小儿脂肪母细胞瘤的文章。有36F(45%)和39M(48%),在6名患者中,(7%)性别未作具体说明。年龄范围从0mth(6h)到15yo(180mth)。22例(27%)肿瘤位于头部,而颈部面积占53例(65%)。在6例(7%)中显示了没有精确位置的一般描述。所有患者均接受完整的手术切除。在分析的文章中,有6%的临床病例注意到手术后复发。
    结论:脂肪母细胞瘤的特征是迅速增长的脂肪团。选择的治疗方法是完全手术切除。在病理难以触及的选定病例中,由于质量的广泛渗透,我们建议与跨学科团队一起执行该程序。在描述的晚期脂肪母细胞瘤病例中,内窥镜检查辅助和微清创器大大促进了病理学的去除。这是儿科文献中报道的头颈部脂肪母细胞瘤的唯一病例,由于广泛受累和疾病的位置,颅神经V2和V3的下牙槽支无法幸免。需要长期随访甚至10年,因为据报道这些肿瘤有复发的趋势。
    BACKGROUND: Lipoblastoma is a rare and benign tumor arising from embryonal fat cells. It develops primarily in infancy and early childhood. We present a case study of a 10-month-old child treated for an extensive tumor of the infratemporal fossa and parapharyngeal space. The systematic review of 60 reports in 80 children with lipoblastoma of the head and neck is also reported.
    METHODS: Systematic review of all articles included lipoblastomas of the head and neck area in children published from 1964 to 2022 in the PubMed database was conducted. Clinical presentation of extensive lipoblastoma of the head and neck in a child.
    RESULTS: On the basis of all inclusion criteria 83 articles were identified concerning pediatric lipoblastoma. There were 36 F (45%) and 39 M (48%), in 6 patients, (7%) gender was not specified. Ages ranged from 0mth (6h) to 15 yo (180mth). The tumor was located in the head in 22 (27%) cases, while the neck area accounted for 53 (65%) cases. General description without precise location was shown in 6 (7%) cases. All patients underwent complete surgical excision. Post surgical recurrence was noted in 6% clinical cases in the analyzed articles.
    CONCLUSIONS: Lipoblastoma is characterized by a rapidly growing predominantly adipose mass. The treatment of choice is complete surgical excision. In selected cases when the pathology is hard to reach, as a consequence of the extensive penetration of the mass, we recommend performing the procedure with an interdisciplinary team. Endoscopy assistance and microdebrider significantly facilitated the removal of pathology in the described advanced case of lipoblastoma. This is the only case reported in the pediatric literature of a head and neck lipoblastoma, where due to extensive involvement and location of the disease the cranial nerves V2 and inferior alveolar branch of V3 could not be spared. Long-term follow-up even to 10 years is required because there is a reported tendency for these tumors to recur.
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  • 文章类型: Review
    背景和目的:迷走神经鞘瘤的临床处理是一个真正的诊断和治疗挑战,因为病史和临床检查通常是非特异性的,手术切除后的迷走神经损伤仍然是一个未解决的问题。本文的目的是提供一系列病例以及头颈部迷走神经鞘瘤的诊断和治疗算法,结合我们的经验和文献中的临床证据。材料和方法:我们回顾性分析了2000年至2020年接受治疗的一系列迷走神经鞘瘤患者。此外,对迷走神经鞘瘤治疗的文献进行了综述.根据所描述的案例和文献综述,我们制定了迷走神经鞘瘤的诊断和治疗算法。结果:我们能够识别出10例受迷走神经鞘瘤影响的患者,并在2000年至2020年之间进行了治疗。所有患者都出现了无痛的,mobile,颈部外侧肿块生长缓慢,发病时间从几个月到几年不等。术前诊断检查包括9例超声(US),6例患者的计算机断层扫描(CT)增强扫描,7例患者的颈部磁共振成像(MRI)。本研究中包括的所有患者均接受手术治疗。结论:迷走神经鞘瘤的治疗对临床医生来说是一个真正的挑战,手术是目前最有效的治疗策略。通过耳鼻喉科医师与其他专家的合作的多学科方法期望为患者制定量身定制的治疗计划。
    Background and Objectives: Clinical management of vagal schwannoma is a real diagnostic and therapeutic challenge because the medical history and clinical examination are often non-specific and vagal nerve injury following surgical resection still represents an unsolved problem. The aim of this paper is to provide a case series along with a diagnostic and therapeutic algorithm for vagal schwannoma of the head and neck, combining our experience with clinical evidence available in the literature. Materials and Methods: We retrospectively analyzed a series of patients affected by vagal schwannoma who were treated between 2000 and 2020. In addition, a review of the literature on vagal schwannoma management was conducted. Based on the cases described and the literature review, we made a diagnostic and therapeutic algorithm for the management of vagal schwannoma. Results: We were able to identify 10 patients affected by vagal schwannoma and treated between 2000 and 2020. All patients presented with a painless, mobile, slow-growing lateral neck mass with onset varying from a few months to years. The preoperative diagnostic workup included ultrasound (US) in nine cases, computed tomography (CT) with contrast in six patients and magnetic resonance imaging (MRI) of the neck in seven cases. All patients included in this study were surgically treated. Conclusions: Vagal schwannoma management represents a true challenge for clinicians and surgery is currently the most effective therapeutic strategy. A multidisciplinary approach through the collaboration of otolaryngologist with other specialists is desirable to develop a tailored treatment plan for the patient.
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  • 文章类型: Case Reports
    乳头状癌是最常见的分化型甲状腺癌。通常,转移发生在中央隔室的淋巴途径和颈静脉链。然而,咽旁间隙(PS)淋巴结转移是一种罕见但可能的事件。事实上,已经确定了连接甲状腺上极和PS的淋巴途径。我们描述了一名45岁的男子,有两个月的右颈部肿块病史。他接受了完整的诊断路径,强调了与怀疑是恶性的甲状腺结节相关的咽旁肿块的存在。患者接受了手术(甲状腺切除术并切除PS肿块,发现该肿块是甲状腺乳头状癌的转移淋巴结)。这种情况的目的是强调检测这类病变的重要性。来自甲状腺癌的PS中的淋巴结转移是一种罕见的发生,在转移达到相当大的尺寸之前,通过临床检查不容易检测到。计算机断层扫描(CT)和磁共振成像(MRI)允许早期识别,但不幸的是,这些技术通常不作为甲状腺癌患者的一级成像技术.选择的治疗方法是通过宫颈入路手术,可以更好地控制疾病和解剖结构。非手术治疗通常保留给晚期疾病患者,结果令人满意。
    Papillary carcinoma is the most frequently encountered differentiated thyroid carcinoma. Usually, metastasis occurs along lymphatic pathways in the central compartment and along the jugular chain. Nevertheless, lymph node metastasis in the parapharyngeal space (PS) is a rare but possible event. In fact, a lymphatic pathway has been identified that connects the upper pole of the thyroid and the PS. We describe the case of a 45-year-old man with a two-month history of a right neck mass. He underwent a complete diagnostic path that highlighted the presence of a parapharyngeal mass associated with the presence of a thyroid nodule suspected to be malignant. The patient underwent surgery (thyroidectomy and removal of the PS mass that was found to be a metastatic node of papillary thyroid carcinoma). The aim of this case is to underline the importance of detecting these kinds of lesions. Nodal metastasis in PS from thyroid cancer is a rare occurrence that is not easily detectable by a clinical examination until the metastasis reaches a considerable dimension. Computed tomography (CT) and magnetic resonance imaging (MRI) permit early identification, but unfortunately, these are not usually employed as a first-level imaging technique in patients with thyroid cancer. The treatment of choice is surgery with a transcervical approach that allows for better control of the disease and of the anatomical structures. Non-surgical treatments are usually reserved for patients with advanced disease, with satisfactory results.
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  • 文章类型: Review
    Synchronous pleomorphic adenoma in the parotid gland and parapharyngeal space are rare. We report a case of simultaneous pleomorphic adenoma in parotid gland and parapharyngeal space in a 65-year-old male presenting to the ENT outpatient department at Northwest General Hospital, Peshawar. The patient presented with a left parotid lump, intra oral examination of which revealed the left palatine tonsil to have been pushed medially. CT of the neck showed a completely separate lump in the left parapharyngeal space, and FNAC of the parotid lump was suggestive of mucoepidermoid carcinoma. The superficial parotid lump was excised first, and the parapharyngeal growth was accessed intraorally and excised. Histopathology revealed both the growths to be pleomorphic adenomas. It is important to raise awareness of synchronous salivary gland tumours, which are a rare occurrence, to highlight its optimal investigation to ensure complete surgical excision, and appropriate management.
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