Postoperative radiotherapy

术后放疗
  • 文章类型: Case Reports
    泪腺腺样囊性癌(LGACC)的特点是复发率高,神经周浸润,和远处转移的倾向,导致预后不良。本病例报告旨在强调LGACC的诊断和治疗挑战,强调第一次尽可能彻底切除肿瘤的重要性,坚持术后辅助治疗,并提供有关其手术和诊断管理的详细见解,这些见解可能未在大型病例系列和荟萃分析中广泛涵盖。
    一名34岁男子出现进行性左眼眼球突出4个月。初步评估和成像导致对LGACC的高度怀疑,这是在保留眼睛切除左眶肿瘤后证实的。病人拒绝接受术后放疗,这是手术后推荐的。因此,尽管有手术干预,患者在手术后3个月出现肿瘤复发,导致眼眶放血.病理检查证实存在低分化LGACC。这次病人接受了术后放疗,如推荐。然而,尽管有本地控制,患者在一年内出现颅内转移。
    LGACC由于其隐匿的发作而提出了重大的诊断和治疗挑战,缺乏特定的症状,复发和转移的可能性很高。因此,这个案例强调了早期诊断的必要性,积极治疗,并坚持术后辅助治疗以改善患者预后。未来的研究应该集中在了解LGACC的发病机制和发展标准化的诊断和治疗方案,以提高患者的预后和生存。
    UNASSIGNED: Lacrimal gland adenoid cystic carcinoma (LGACC) is characterized by a high rate of recurrence, perineural invasion, and propensity for distant metastasis, resulting in poor prognosis. This case report aimed to highlight the diagnostic and therapeutic challenges of LGACC, underscore the importance of resectioning the tumor as completely as possible for the first time, adhere to postoperative adjuvant therapy, and provide detailed insights into its surgical and diagnostic management that may not be extensively covered in large case series and meta-analyses.
    UNASSIGNED: A 34-year-old man presented with progressive left eye proptosis for 4 months. Initial evaluation and imaging led to a high suspicion of LGACC, which was confirmed after an eye-sparing excision of the left orbital tumor. The patient declined to undergo postoperative radiotherapy, which was recommended after the surgery. Thus, despite surgical intervention, the patient experienced tumor recurrence 3 months post-surgery, leading to orbital exenteration. Pathological examination confirmed the presence of poorly differentiated LGACC.This time the patient underwent postoperative radiotherapy, as recommended. However, despite local control, the patient developed an intracranial metastasis within a year.
    UNASSIGNED: LGACC presents significant diagnostic and therapeutic challenges owing to its insidious onset, lack of specific symptoms, and high potential for recurrence and metastasis. Thus, this case emphasizes the need for early diagnosis, aggressive treatment, and adherence to postoperative adjuvant therapy to improve patient outcomes. Future research should focus on understanding the pathogenesis of LGACC and on developing standardized diagnostic and treatment protocols to enhance patient prognosis and survival.
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  • 文章类型: Journal Article
    嗅觉神经母细胞瘤(ONB)是一种罕见的恶性肿瘤,通常通过多学科方法治疗,包括手术,放射治疗,和化疗。一名62岁的男性在鼻腔中有肿瘤,并被诊断为KadishA期的ONB。进行前颅底手术作为根治性治疗。由于手术切缘为阴性,未进行术后放疗.手术14年后,发生双侧渗出性中耳炎(OME),我们在双侧咽后淋巴结(RPLN)发现了围绕颈内动脉的复发肿瘤。因为这些是不可切除的,我们计划放化疗为70Gy调强放疗联合两个疗程的卡铂和依托泊苷。肿瘤体积缩小,双侧OME改善。经过抢救治疗,他已经活了3年。尽管ONB的预后相对较好,已知常引起颈淋巴结转移。Hyams分类的III级和IV级被认为是高风险。这个案子,初始肿瘤局限于鼻腔,其临床分类为早期,但Hyams的分类是三级.关于这种情况,考虑到RPLN转移在抢救手术中难以彻底切除,在术后放疗中包括该区域被认为是一种选择.
    Olfactory neuroblastoma (ONB) is an uncommon malignant tumor and is usually treated by a multidisciplinary approach includes surgery, radiotherapy, and chemotherapy. A 62 years-old male had a tumor in the nasal cavity and diagnosed as ONB with Kadish A stage. Anterior skull base surgery was performed as radical treatment. Since the surgical margin was negative, no postoperative radiotherapy was administered. 14 years after the surgery, bilateral otitis media with effusion (OME) was occurred, we found the recurrence tumor at bilateral retropharyngeal lymph node (RPLN) which surrounded the internal carotid arteries. Since these were unresectable, we planned chemoradiotherapy which was 70Gy of intensity modulated radiotherapy combined with two courses of carboplatin and etoposide. The tumor volume was reduced and bilateral OME were improved. He has been alive for 3 years after salvage treatment. Although ONB has a relatively good prognosis, it is known to often cause cervical lymph node metastasis. Grades III and IV of Hyams classification are considered high risk. This case, initial tumor was limited in the nasal cavity and its clinical classification was early stage, but Hyams classification was grade III. In reference to this case, considering that RPLN metastasis are difficult to radically resect at the salvage surgery, including this area in postoperative radiotherapy was considered an option.
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    文章类型: Journal Article
    目的:探讨自我管理手册结合个案管理模式在鼻咽癌放疗术后管理中的应用价值。
    方法:回顾性纳入2020年5月至2022年4月鹰潭市人民医院收治的84例鼻咽癌患者。分为实验组(接受自我管理手册结合病例管理模式方案,n=42)和对照组(接受常规鼻咽癌放疗后的持续管理,n=42)根据模式差异。癌症相关性疲劳[癌症疲劳量表(CFS)]舒适度状况[一般舒适度问卷(GCQ)],自我管理效能[人们促进健康的中国策略(C-SUPPH)],自我护理能力(自我护理能力测量),疼痛评分[视觉模拟评分(VAS)],放疗4周后,比较两组患者的生活质量[欧洲癌症研究和治疗组织QLQ-C30(EORTCQLQ-C30)]。记录两组患者的不良反应发生情况。结合定期审查和跟踪记录,分析两组患者的预后因素。
    结果:治疗后,身体疲劳评分(12.83±1.10),情绪疲劳(9.78±1.32),认知疲劳(5.62±1.31),实验组CFS总分(28.24±2.26)为12.83±1.10。对照组身体疲劳(13.90±1.25)分,情绪疲劳(10.55±1.40)分,认知疲劳(6.80±1.75)分,两组患者总CFS(31.33±2.59)分均低于治疗前。实验组低于对照组(P<0.05)。生理,心理,精神,社会文化,试验组环境评分高于对照组(均P<0.05)。健康知识的得分,自我护理技能,自我照顾的责任,实验组患者的自我概念评分均高于对照组(均P<0.05)。干预后,实验组VAS评分低于对照组(P<0.05)。干预后,与干预前相比,两组的EORTCQLQ-C30评分均显著升高.实验组评分明显高于对照组[(80.05±10.72)vs(68.11±12.10),P<0.05]。试验组术后(各种)不良反应均低于对照组(均P<0.05)。影响鼻咽癌患者预后的因素有年龄,肿瘤分期,干预模式经Cox模型分析(均P<0.05)。
    结论:自我管理手册结合个案管理模式可缓解癌症疲乏,提高术后自我管理能力,自理能力,鼻咽癌放疗患者的生活质量,减少不良反应的发生,改善患者预后。值得在临床上推广。
    OBJECTIVE: To explore the application value of the self-management manual combined with the case management model in postoperative management of nasopharyngeal carcinoma after radiotherapy.
    METHODS: Eighty-four patients with nasopharyngeal carcinoma admitted to Yingtan People\'s Hospital from May 2020 to April 2022 were retrospectively included in this study. They were divided into the experimental group (receiving self-management manual combined with case management mode scheme, n=42) and the control group (receiving continuous management after conventional nasopharyngeal carcinoma radiotherapy, n=42) according to mode differences. The cancer-related fatigue [Cancer Fatigue Scale (CFS)], comfort status [General Comfort Questionnaire (GCQ)], self-management efficacy [Chinese Strategies Used by People to Promote Health (C-SUPPH)], self-care ability (self-care ability measurement), pain score [Visual analogue scale (VAS)], and quality of life [European Organization for Research and Treatment of Cancer QLQ-C30 (EORTC QLQ-C30)] were compared between the two groups after 4 weeks of radiotherapy. The adverse reactions of the two groups were recorded. Combined with periodic review and follow-up records, the prognostic factors of the two groups of patients were analyzed.
    RESULTS: After treatment, the scores of physical fatigue (12.83±1.10), emotional fatigue (9.78±1.32), cognitive fatigue (5.62±1.31), and total score of CFS (28.24±2.26) in the experimental group were 12.83±1.10. The control group physical fatigue (13.90±1.25) points, emotional fatigue (10.55±1.40) points, cognitive fatigue (6.80±1.75) points, and total CFS (31.33±2.59) points in both groups were lower than before treatment. The experimental group was lower than the control group (ALL P<0.05). The physiological, psychological, spiritual, socio-cultural, and environmental scores of the experimental group were higher than those of the control group (all P<0.05). The scores of health knowledge, self-care skills, self-care responsibility, and self-concept score of patients in the experimental group were higher than the control group (all P<0.05). After intervention, the VAS score of the experimental group was lower than that of the control group (P<0.05). After intervention, the EORTC QLQ-C30 score of both groups increased significantly as compared with pre-intervention. The score in the experimental group was significantly higher than that in the control group [(80.05±10.72) vs (68.11±12.10), P<0.05]. Postoperative (various) adverse reactions in the experimental group were lower than the control group (all P<0.05). The factors influencing the prognosis of nasopharyngeal carcinoma patients were age, tumor stage, and intervention mode by Cox model analysis (all P<0.05).
    CONCLUSIONS: The self-management manual combined with the case management mode can alleviate cancer fatigue, improve postoperative self-management ability, self-care ability, and quality of life of patients with nasopharyngeal cancer radiotherapy, reduce the occurrence of adverse reactions and improve the prognosis of patients. It is worth promoting in clinical settings.
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  • 文章类型: Case Reports
    黏液纤维肉瘤是老年人的恶性间叶性肿瘤和成纤维细胞肉瘤。粘液纤维肉瘤可以是低级或高级,取决于细胞特征。有或没有放疗和化疗的广泛手术切除是其治疗的基础。有时候,肿瘤细胞分泌胰岛素或胰岛素样物质并引起低血糖发作。这里,我们打算证明早期手术在终止低血糖发作和预防复发和转移方面的作用.我们还打算显示切开活检在区分低级和高级粘液纤维肉瘤方面的不足。一名82岁的男性患者来到我们的诊所,左肩胛骨后区域的肿块迅速增长,每天都有几次低血糖发作。成像和初次活检后,在组织病理学检查中,肿瘤分级是不确定的;因此,手术切除了肿块。病理检查导致高度粘液纤维肉瘤,而最初的活检无法详细说明其等级。手术后低血糖发作停止。总剂量为60Gy的辅助局部放疗分30次给予手术区域,术后无并发症。没有新的质量,复发,或在3年随访中发现低血糖发作.总之,低血糖发作可能是恶性肿瘤存在的标志,并且在开始和随访期间可能是复发和肿瘤肿块侵袭性的线索。因为活检可以显示诊断,但不能显示肿瘤的分级,需要早期手术干预.
    Myxofibrosarcoma is a malignant mesenchymal tumor and a fibroblastic sarcoma of the elderly. Myxofibrosarcoma can be low-grade or high-grade depending on the cell characteristics. Wide surgical resection with or without radiotherapy and chemotherapy is the basis of its treatment. Sometimes, tumor cells secrete insulin or insulin-like substances and cause hypoglycemia attacks. Here, we intend to demonstrate the role of early surgery to end hypoglycemia attacks and prevent recurrence and metastases. We also intend to show the insufficiency of tru-cut biopsy to distinguish between low- and high-grade myxofibrosarcoma. An 82-year-old male patient visited our clinic with a rapidly growing giant mass in the left retroscapular area and suffered from hypoglycemic attacks several times a day. After imaging and initial biopsy, the tumor grade was indeterminate on histopathological examination; hence, the mass was removed surgically. The pathological examination resulted in high-grade myxofibrosarcoma whereas the initial biopsy could not elaborate on the grade. The hypoglycemia attacks ceased after the surgery. Adjuvant local radiotherapy at a total dose of 60 Gy was administered in 30 fractions to the surgery area with no complications after the surgery. No new mass, recurrence, or hypoglycemia attack was detected in the three-year follow-up. In conclusion, hypoglycemia attacks may be a marker of malignant tumor presence and may be a clue at the beginning and in the follow-up period both for recurrence and the aggressiveness of the tumoral mass. Because a biopsy may show the diagnosis but not the grade of the tumor, early surgical intervention is needed.
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  • 文章类型: Journal Article
    一些头颈癌外科医生发现,许多未经术后放疗(PORT)的局部晚期头颈鳞状细胞癌(LA-HNSCC)患者也具有良好的预后。这项研究的目的是确定PORT对LA-HNSCC患者生存率的影响。
    在两个机构对LA-HNSCC患者进行病例匹配队列分析。仅接受手术的患者与接受手术加PORT治疗的患者病例匹配1:1,pN,肿瘤亚位点等.结果:114例患者配对为57对,中位随访期为40.2个月。总生存期无差异(OS,HR0.88;95%CI0.50-1.58;P=0.79)或疾病特异性生存率(DFS,0.86;95%CI0.50-1.50;P=0.76)观察到无PORT。
    对于首次接受治疗的LA-HNSCC患者,只要头颈部癌症外科医生坚持适当的手术理念,就不需要PORT。LA-HNSCC患者PORT的适应症需要进一步讨论。
    Some head and neck cancer surgeons found that many patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC) without postoperative radiotherapy (PORT) also have a good prognosis. The purpose of this study was to determine the effect of PORT on survival in patients with LA-HNSCC.
    A case-match cohort analysis was performed at two institutions on patients with LA-HNSCC. Patients who received surgery alone were case-matched 1: 1 with patients treated by surgery plus PORT based on pT, pN, tumor subsite etc. RESULTS: 114 patients were matched into 57 pairs, with a median follow-up period of 40.2 months. No difference in overall survival (OS, HR 0.88; 95% CI 0.50-1.58; P = 0.79) or disease-specific survival (DFS, 0.86; 95% CI 0.50-1.50; P = 0.76) was observed with no PORT.
    PORT isn\'t necessary for patients with LA-HNSCC who are treated for the first time as long as the head and neck cancer surgeon adhere to appropriate surgical concepts. The indications of PORT for patients with LA-HNSCC need to be further discussed.
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  • 文章类型: Case Reports
    瘢痕疙瘩是横向生长的纤维增生性皮肤病。严重瘢痕疙瘩广泛传播,有时在关节上,从而显著限制了运动功能。它们与复发有关,非常痛苦的引流感染。这里,我们报告了一例巨大瘢痕疙瘩,该病例通过联合治疗成功治疗,包括手术(部分切除,然后进行局部皮瓣移位)以及随后的放疗和类固醇石膏疗法。当患者7岁时,在婴儿期接受左肩BacilleCalmette-Guérin疫苗接种的部位首次发现了瘢痕疙瘩。成年后瘢痕疙瘩迅速而广泛地生长。另一家医院怀疑有恶性肿瘤,但45岁时的活检显示病变是瘢痕疙瘩。稍后,瘢痕疙瘩从肩膀生长到胸部和背部,并在前腋下。62岁时,病人被转介到我们医院。在全身麻醉下,瘢痕疙瘩被部分切除,伤口被局部皮瓣覆盖。术后1周后进行放疗。用类固醇胶带治疗残留的瘢痕疙瘩18个月。手术后18个月,未观察到瘢痕疙瘩复发。患者没有疼痛或运动受限。她对结果非常满意,并认为治疗改善了她的生活质量。虽然严重瘢痕疙瘩的标准策略仍有待建立,联合治疗包括手术,术后放疗,和类固醇石膏疗法,旨在减少炎症和皮肤紧张可能是一种选择。
    Keloids are laterally growing fibroproliferative skin disorders. Severe keloids spread widely, sometimes over joints, thus significantly limiting motor function. They are associated with recurrent, very painful draining infections. Here, we report a case of a giant keloid that was successfully treated by combination therapy comprising surgery (partial resection followed by local flap transposition) and subsequent radiotherapy and steroid-plaster therapy. The keloid was first noticed when the patient was 7 years old at the site of a Bacille Calmette-Guérin vaccination she had received on her left shoulder in infancy. The keloid grew rapidly and widely after adulthood. A malignant tumor was suspected at another hospital, but a biopsy at age 45 years indicated the lesion was a keloid. Later, the keloid grew from the shoulder onto the chest and back and over the anterior axilla. At age 62 years, the patient was referred to our hospital. Under general anesthesia, the keloid was partially resected and the wound was covered with a local flap. Postoperative radiotherapy was performed 1 week later. The residual keloid was treated for 18 months with steroid tape. At 18 months after surgery, no recurrence of the keloid was observed. The patient had no pain or movement restriction. She was extremely satisfied with the results and considered the treatment to have improved her quality of life. While a standard strategy for severe keloid remains to be established, combination therapy comprising surgery, postoperative radiotherapy, and steroid-plaster therapy that aims to reduce inflammation and skin tension may be an option.
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  • 文章类型: Case Reports
    Pigmented villonodular synovitis (PVNS) is a benign proliferative disorder of the synovium that usually involves joints, tendon sheaths, and bursae. It presents rarely, however, in the temporomandibular joints (TMJs). This paper reports a 59-year-old female patient with PVNS of the TMJ and its clinico-pathologic features are discussed. The patient was treated with surgery and postoperative radiotherapy (PORT). Follow-up was conducted, and there were no recurrences, metastases, skin changes or joint stiffness noted. The main treatment of PVNS is surgical resection. However, postoperative radiotherapy is important for local control of extensive tumors or positive margins. We conducted a literature review for postoperative radiotherapy case reports related to PVNS of the TMJ.
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  • 文章类型: Comparative Study
    The purpose of this study was to determine the effect of postoperative radiotherapy (PORT) on recurrence and survival in patients with oral squamous cell carcinoma (OSCC) of intermediate recurrence risk.
    Intermediate risk patients, defined as pT1, pT2, pN0, or pN1 with at least one adverse pathological feature (eg, lymphovascular/perineural invasion), were identified from the head and neck databases of the Liverpool Head and Neck Cancer Unit and the Sydney Head and Neck Cancer Institute. Patients who received surgery and PORT were case matched with patients treated by surgery alone based on pN, pT, margins, and pathological features.
    Ninety patients were matched into 45 pairs. There was significant improvement (P = .039) in locoregional control with PORT (84%) compared with surgery alone (60%), which was concentrated in the pN1 subgroup (P = .036), but not the pN0 subgroup (P = .331).
    PORT significantly improves locoregional control for intermediate risk OSCC.
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  • 文章类型: Case Reports
    原发性血管肉瘤是一种罕见的疾病,预后不良。它最常见于头颈部;在颈部深层软组织中的定位极为罕见。我们在此介绍一例源自右颈内静脉的血管肉瘤。一名79岁的男子有1个月的右颈部肿块病史。计算机断层扫描,磁共振成像,正电子发射断层扫描-计算机断层扫描,细针穿刺细胞学检查发现不明原因的恶性肿瘤。右颈淋巴结清扫术用于诊断和治疗。切除的肿瘤细胞的免疫染色显示CD31,CD34,VIII因子相关抗原,和D2-40,可以明确诊断血管肉瘤。术后右颈部放疗(66Gy),包括手术床和上纵隔。患者随访10个月,无复发。英语文献中仅报道了6例颈部深层软组织中出现的血管肉瘤。本报告是第一个描述由颈内静脉引起的血管肉瘤的报告。
    Primary angiosarcoma is a rare disease with a poor prognosis. It most commonly arises in the head and neck region; localization in the deep soft tissue of the neck is extremely rare. We herein present a case of angiosarcoma derived from the right internal jugular vein. A 79-year-old man presented with a 1-month history of a growing right neck mass. Computed tomography, magnetic resonance imaging, positron emission tomography-computed tomography, and fine-needle aspiration cytology revealed a malignant tumor of unknown origin. Right neck dissection was performed for both diagnosis and therapy. Immunostaining of the resected tumor cells revealed positivity for CD31, CD34, factor VIII-related antigen, and D2-40, which allowed for a definitive diagnosis of angiosarcoma. Postoperative radiotherapy (66Gy) was performed on the right neck, including the surgical bed and upper mediastinum. The patient was followed up for 10 months with no recurrence. Only six cases of angiosarcoma arising in the deep soft tissue of the neck have been reported in the English-language literature. The present report is the first to describe angiosarcoma arising from the internal jugular vein.
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    文章类型: Case Reports
    A whistle deformity is defined as a deficiency in the vertical length of the lip so that the free margins of the upper and lower lips do not meet normally, giving the appearance of whistling. This is a common secondary deformity of the vermilion in patients with cleft lip. A case involving a 61-year-old man who developed a whistle deformity as a result of two wedge resections and postoperative radiotherapy for treatment of squamous cell carcinoma of the lower lip is presented. Hyaluronic acid-based tissue filler and autologous microfat transplantation to the lower lip were used for definitive management of the patient\'s whistle deformity. After one year of follow-up, the patient was pleased with the overall result and noted marked improvement of his oral competence and overall appearance of the lip. The present case demonstrates that microfat transplantation is a viable option for correcting a whistle deformity, not only after surgery, but also following adjuvant radiotherapy - both of which potentially reduce graft viability secondary to decreased vascularity of the recipient site.
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