three-dimensional reconstruction

三维重建
  • 文章类型: Case Reports
    我们介绍了一例特发性奇静脉动脉瘤(AVA),并描述了其放射学特征。临床医生应了解影像学表现,以避免活检引起的出血风险。
    方法:一名无症状的46岁女性在体检中发现胸部计算机断层扫描(CT)扫描有异常阴影。普通CT显示清晰,右主支气管后侧均匀肿块。对比增强CT显示肿块明显增强,指向血管结构。三维重建显示肿块与奇人弓相连,并检测出奇静脉的流入和流出。随后,进行了电视辅助胸腔镜手术。
    特发性AVA患者通常在胸部X光片或CT扫描中意外发现纵隔或肺部肿块,可能会被错误地诊断为气管旁肿瘤,支气管囊肿,或后纵隔肿瘤。由于存在大量出血的风险,应避免进行穿刺活检。在评估胸部恶性肿瘤的过程中,鉴别诊断中应考虑AVAs,特别是在右气管支气管角或右上纵隔或后纵隔区域。三维重建可以帮助外科医生明确疾病诊断。
    结论:影像学表现结合增强CT和三维重建对诊断AVA很有用。
    UNASSIGNED: We present a case of idiopathic azygos vein aneurysm (AVA) and describe its radiological features. Clinicians should be aware of the imaging findings to avoid the risk of bleeding caused by biopsy.
    METHODS: An asymptomatic 46-year-old woman was found to have an abnormal shadow on a chest computed tomography (CT) scan during a medical checkup. Plain CT revealed a well-defined, homogeneous mass on the posterior side of the right main bronchus. Contrast-enhanced CT revealed a mass with marked enhancement pointing to a vascular structure. Three-dimensional reconstruction showed that the mass was connected to the azygos arch, and inflow to and outflow from the azygos vein was detected. Subsequently, video-assisted thoracic surgery was performed.
    UNASSIGNED: Patients with idiopathic AVA often present with accidental findings of a mediastinal or lung mass on a chest radiographs or CT scans, which can be mistakenly diagnosed as a paratracheal tumor, bronchial cyst, or posterior mediastinal tumor. Needle biopsy should be avoided due to the risk of massive bleeding. During the evaluation of thoracic malignancies, AVAs should be considered in the differential diagnosis, especially in area of the right tracheobronchial angle or right upper or posterior mediastinum. Three-dimensional reconstruction can help surgeons to clarify the disease diagnosis.
    CONCLUSIONS: Imaging findings combined with enhanced CT and three-dimensional reconstruction are useful for diagnosing AVAs.
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  • 文章类型: Letter
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  • 文章类型: Case Reports
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  • 文章类型: Review
    背景:随着胸部计算机断层扫描(CT)的日益普及,肺小结节的检测变得越来越普遍,促进肺段切除术的发展。然而,支气管的解剖变异是常见的,特别是在肺的右上叶。
    方法:我们报告一例胸腔镜下右上肺叶后段切除术。术前,结节被认为位于右下叶的上段。然而,术中探查发现结节位于右上叶的后段,进一步显示右肺后段的支气管通向中间支气管。程序顺利完成。术后对肺部CT图像进行回顾性三维(3D)重建,证实右上叶后段的支气管起源于中间支气管。
    结论:这一罕见病例突出了三维重建对于指导解剖变异患者的准确节段切除术的重要性。
    BACKGROUND: With the increasing availability of chest computed tomography (CT), the detection of small pulmonary nodules has become more common, facilitating the development of lung segmental resection. However, anatomical variations of the bronchi are common, particularly in the right upper lobe of the lung.
    METHODS: We report a case of thoracoscopic resection of the posterior segment of the right upper lobe of the lung. Preoperatively, the nodule was believed to be located in the superior segment of the right lower lobe. However, intraoperative exploration revealed that the nodule was located in the posterior segment of the right upper lobe, further showing that the bronchi of the posterior segment of the right lung opened into the bronchus intermedius. The procedure was completed uneventfully. Postoperative retrospective three-dimensional (3D) reconstruction of the lung CT images confirmed that the bronchi of the posterior segment of the right upper lobe originated from the bronchus intermedius.
    CONCLUSIONS: This rare case highlights the importance of 3D reconstruction to guide accurate segmentectomy in patients with anatomic variations.
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  • 文章类型: Case Reports
    很少报道伴有双下腔静脉(IVC)的腹膜后肿瘤病例。本报告记录了一例伴有双IVC的腹膜后淋巴瘤,并讨论了它的胚胎学,临床和放射学意义。此外,我们回顾了以前的双IVC病例。在本报告中,1例52岁男性患者因腹膜后淋巴瘤和双IVC住院.进行了CT尿路造影,同时还基于CT数据建立了三维可视化模型,显示有双IVC的腹膜后肿瘤.本案涉及双IVC与髂内静脉,左侧IVC为2b型。通过经皮穿刺活检,腹膜后肿瘤被确定为淋巴瘤,尺寸为116x83mm。淋巴瘤一般不推荐手术治疗。因此,根据淋巴瘤治疗指南,该患者被转入血液科接受治疗.在患者的随访期间,化疗后肿瘤的大小减小。总之,三维可视化模型可以直接、准确地呈现双IVC及其周围组织结构的解剖特征。此外,IVC特征的变异可具有重要的临床意义。这对外科医生也很重要,介入放射科医师和临床医师了解此类异常的解剖特征,避免误诊,减少术中严重并发症的发生。
    Cases of a retroperitoneal tumor with double inferior vena cava (IVC) are rarely reported. The present report documents a case of a retroperitoneal lymphoma with double IVC, and discusses its embryological, clinical and radiological significance. In addition, previous cases of a double IVC are reviewed. In the present report, a 52-year-old male patient was hospitalized for a retroperitoneal lymphoma tumor and double IVC. CT urography was performed, whilst a three-dimensional visualization model was also established based on CT data, to reveal a retroperitoneal tumor with double IVC. The present case involved a double IVC with interiliac vein, which was type 2b from the left IVC. The retroperitoneal tumor was identified to be a lymphoma measuring 116x83 mm by percutaneous puncture biopsy. Surgical treatment is generally not recommended for lymphoma. Therefore, this patient was transferred to the Hematology Department for treatment according to the lymphoma management guidelines. The size of the tumor was reduced after chemotherapy during the patient\'s follow-up. In conclusion, the three-dimensional visualization model can directly and accurately present the anatomical features of the double IVC and its surrounding tissue structure. In addition, variations in the features of IVC can have important clinical significance. It is also important for surgeons, interventional radiologists and clinicians to understand such abnormalities in anatomical features to avoid misdiagnosis and reduce the occurrence of serious intraoperative complications.
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  • 文章类型: Review
    背景:Azygos静脉动脉瘤(AVA)极为罕见。多数患者无明显临床症状,所以他们是通过体检或偶然发现的。可参考的临床治疗经验有限,并且没有明确的指南或研究证据来规范手术和介入治疗。这里,我们报道了1例特发性AVA患者,其肿瘤的三维重建在手术前完成.在三维重建的基础上,首次成功完成单孔胸腔镜切除AVA。总结以前报道的病例,为AVA患者的诊断和治疗提供指导。
    方法:一名56岁男子因“吞咽困难”被转院。AVA的诊断是在增强计算机断层扫描后做出的,胃镜检查,纤维支气管镜检查,和三维重建。先天性虚弱或退行性变化导致静脉壁非常薄,AVA有破裂的风险。此外,病人有吞咽困难的症状,他接受了单孔胸腔镜手术。手术后,他的吞咽困难消失了.术后病理证实为血管瘤。患者术后3天出院,无任何并发症。
    结论:AVA是罕见的。术前三维重建可以极大地帮助外科医生明确疾病诊断,制定手术计划,避免损伤周围的重要器官,减少术中出血。胸腔镜手术切除AVA难度大,出血风险高,而微创单孔胸腔镜手术治疗AVA也是安全有效的。
    BACKGROUND: Azygos vein aneurysms (AVAs) are extremely rare. The majority of patients have no obvious clinical symptoms, so they are found by physical examination or by chance. There is limited clinical treatment experience that can be referred to, and there are no clear guidelines or research evidence standardizing the surgical and interventional therapy. Here, we report a patient with idiopathic AVA whose three-dimensional reconstruction of the tumor was completed before surgery. On the basis of three-dimensional reconstruction, single-port thoracoscopic resection of the AVA was successfully completed and reported for the first time. The previously reported cases are summarized to provide guidance for the diagnosis and treatment of patients with AVAs.
    METHODS: A 56-year-old man was transferred to our hospital due to \"dysphagia\". The diagnosis of AVA was made after enhanced computed tomography, gastroscopy, fiberoptic bronchoscopy, and three-dimensional reconstruction. Congenital weakness or degenerative changes causes the vein walls to be extremely thin that the AVA had the risk of ruptur. Furthermore, the patient had symptoms of dysphagia, he received single-port thoracoscopic surgery. After the operation, his dysphagia disappeared. The postoperative pathology confirmed hemangioma. The patient was discharged 3 days after surgery without any complications.
    CONCLUSIONS: AVAs are rare. Preoperative three-dimensional reconstruction can greatly help surgeons clarify the disease diagnosis, formulate the surgical plan, avoid damage to the surrounding vital organs, and reduce intraoperative bleeding. Thoracoscopic surgery to remove AVAs is difficult and has a high risk of bleeding, while more minimally invasive single-port thoracoscopic surgery is also safe and effective for the treatment of AVAs.
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  • 文章类型: Case Reports
    背景:中国多原发肺癌(MPLC)的发病率为0.52%-2.45%。大多数原发性肺癌病例在罕见病例中报告有两个或三个病变。我们报告了一种罕见的病例,双侧同时发生四种不同基因型的多原发性肺腺癌。
    方法:一名58岁的女性于2021年6月29日入院,经体检,在双肺中发现4个多发肺结节.进一步的计算机断层扫描(CT)图像显示毛玻璃结节的存在,通过人工智能预测为高危癌症病变。在术前CT图像三维重建的指导下,在胸腔镜下切除结节。术后病理检查显示结节类型为原位腺癌,浸润性肺泡腺癌,和微浸润性腺癌。使用26个肺癌基因的高通量测序(半导体测序方法)对切除的结节进行进一步测序,以确认这四个病变不是同源的。患者在术后第8天出院,即2021年7月15日一个月后,她返回医院接受随访和复查。胸部CT检查显示她恢复良好,两个胸膜腔均未见明显的渗出和积液。术后肺功能评估显示,她的用力肺活量为1.40L(术前值,2.27L)和用力呼气量为1.24L(术前值,2.23L)。
    结论:对于多发肺结节的手术方案应慎重考虑。对于精心挑选的双肺同时发生多个肺结节的患者,同时双侧切除病灶是安全可行的方案。基因测序是MPLC诊断和治疗的必要条件。
    BACKGROUND: The incidence of multiple primary lung cancer (MPLC) in China is 0.52%-2.45%. Most primary lung cancer cases have reported two lesions or three in rare cases. We report a rare case of bilateral simultaneous multiple primary lung adenocarcinoma of four different genotypes.
    METHODS: A 58-year-old woman was admitted to our hospital on June 29, 2021, and upon physical examination, four multiple pulmonary nodules were identified in both lungs. Further computed tomography (CT) images revealed the presence of ground glass nodules, predicted to be high-risk cancer lesions by artificial intelligence. With the guidance of three-dimensional reconstruction of preoperative CT images, the nodules were resected under thoracoscopy. Postoperative pathological investigation revealed that the nodule types were adenocarcinoma in situ, invasive alveolar adenocarcinoma, and microinvasive adenocarcinoma. The excised nodules were further sequenced using high-throughput sequencing (semiconductor sequencing method) of 26 lung cancer genes to confirm that the four lesions were not homologous. The patient was discharged on postoperative day 8, that is, on July 15, 2021. One month later, she returned to the hospital for follow-up and reexamination. Chest CT examination showed that she had recovered well, and no obvious exudation and effusion were found in both pleural cavities. Evaluation of postoperative pulmonary function showed that her forced vital capacity was 1.40 L (preoperative value, 2.27 L) and forced expiratory volume was 1.24 L (preoperative value, 2.23 L).
    CONCLUSIONS: The surgical plan for multiple pulmonary nodules should be carefully considered. For carefully selected patients with concurrently occurring multiple lung nodules in both lungs, sublobectomy is a safe and feasible plan for concurrent bilateral resection of the lesions. Genetic sequencing is necessary for MPLC diagnosis and treatment.
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  • 文章类型: Case Reports
    原发性胸腺小细胞神经内分泌癌(SCNEC),具有更具侵略性的生物学行为,包括近端结构的侵入,局部复发,和远处转移,极为罕见。根据以前的文献报道,只有少数患有这种疾病的患者被报道,与骨远处转移的患者相比,肺,脾,脾肝脏,和肾上腺(1,2)。报告数据表明,与人体的大多数其他肿瘤相比,SCNEC是一种高度恶性的肿瘤。在这项研究中,我们介绍了一个患者的案例,该患者在手术前接受了三维重建建模的指导下进行了手术。我们已经为使用三维重建模型切除该肿瘤做好了充分准备,即使在阅读计算机断层扫描(CT)图像后,显示与心包的密切关系,右中肺叶的静脉,和膈神经.所有这些特征表明SCNEC是高度恶性的。迄今为止,没有关于恶性胸腺肿瘤三维重建建模的程序性报告。
    Primary thymic small cell neuroendocrine carcinoma (SCNEC), which possesses a more aggressive biological behaviour, including invasion of proximal structures, local recurrence, and distant metastasis, is extremely rare. According to a previous literature report, only a few patients with this disease have been reported, compared to patients with distant metastasis of bones, lungs, spleen, liver, and adrenal glands (1, 2). The report data suggest that SCNEC is a highly malignant tumour compared to most other tumours of the human body. In this study, we presented the case of a patient who underwent surgery guided by three-dimensional reconstruction modelling before the operation. We were fully prepared for the resection of this tumour using three-dimensional reconstruction modelling, even after reading the computed tomography (CT) images that showed a closed relationship with the pericardium, the vein of the right middle lung lobe, and the phrenic nerve. All these features demonstrate that SCNEC is highly malignant. To date, there are no procedural reports for three-dimensional reconstruction modelling in malignant thymus tumours.
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  • 文章类型: Case Reports
    上颌第一前磨牙通常有一个或两个根管;很少有三个根管的存在。这些根管在治疗过程中很容易被遗漏,导致根管治疗失败。本报告描述了一种情况,其中通过锥形束计算机断层扫描诊断了上颌第一前磨牙中的三个根管。使用三维重建技术来确定根管的曲率的形式和方向,成功地治疗了本文所述的患者。
    The maxillary first premolar commonly has one or two root canals; the presence of three canals is rare. These root canals are easily missed during treatment, resulting in failure of root canal therapy. The present report describes a case in which three root canals in the maxillary first premolar were diagnosed by cone-beam computed tomography. The herein-described patient was successfully treated using three-dimensional reconstruction technology to determine the form and direction of curvature of the root canals.
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  • 文章类型: Case Reports
    背景:与部分肺静脉回流异常(PAPVR)结合的奇生叶(AL)在右肺癌的根治性手术中相对少见。
    方法:我们在此介绍一例极为罕见的肺癌合并AL和无症状PAPVR,术前造影三维重建诊断,胸腔镜根治术。在手术过程中,我们成功保留了奇静脉,并在右上肺静脉发现了一个分裂型PAPVR。
    结论:AL合并PAPVR可能会导致右肺门血管分离和断开的混乱。然而,术前三维重建更有利于该类手术的正确进行。
    BACKGROUND: The azygos lobe (AL) combined with partial anomalous pulmonary venous return (PAPVR) is comparatively uncommon as well as in radical surgery for right lung cancer.
    METHODS: We herein present an extremely rare case of lung cancer coexisting with AL and asymptomatic PAPVR, which was diagnosed with preoperative contrast three-dimensional reconstruction and received radical surgery by thoracoscopy. During the surgery, we preserved azygos vein successfully and found a split type of PAPVR in right upper pulmonary vein.
    CONCLUSIONS: AL combined with PAPVR may cause confusion on the vascular separation and disconnection of the right pulmonary hilar. However, preoperative 3D reconstruction is more conducive to the correct performing of this type of surgery.
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