首页 > 最新文献

Chest Imaging最新文献

英文 中文
The Immunocompromised Patient: AIDS 免疫功能低下的病人:艾滋病
Pub Date : 2019-07-01 DOI: 10.1093/MED/9780199858064.003.0042
J. Bueno
Acquired immune deficiency syndrome (AIDS) is caused by infection with human immunodeficiency virus (HIV) that results in decreased immunity and favors infectious or neoplastic conditions. The onset of clinical AIDS is defined by a CD4 count of less than 200 cells/mm3 or CD4 cells < 14% of all leukocytes in an HIV-positive patient, even in the absence of opportunistic infections. Imaging abnormalities in HIV(+) should be correlated with the CD4 count to narrow the differential diagnosis. Diffuse ground glass opacities (GGO) on CT in a patient with AIDS and hypoxemia, is virtually diagnostic of Pneumocystis pneumonia (PCP). CT is indicated in HIV(+) patients with respiratory symptoms and normal chest radiographs. Suspect tuberculosis (TB) in patients with advanced AIDS and low CD4 counts presenting with consolidation and lymphadenopathy. Kaposi sarcoma (KS) may simulate cardiogenic pulmonary edema on imaging and should be suspected in patients without clinical evidence of edema.
获得性免疫缺陷综合征(AIDS)是由人类免疫缺陷病毒(HIV)感染引起的,导致免疫力下降,有利于感染性或肿瘤性疾病。临床艾滋病的发病定义为CD4细胞计数低于200个/mm3或CD4细胞<艾滋病毒阳性患者所有白细胞的14%,即使没有机会性感染。影像异常的HIV(+)应与CD4计数相关,以缩小鉴别诊断。艾滋病伴低氧血症患者CT表现弥漫性磨玻璃影(GGO),可作为肺囊虫性肺炎(PCP)的诊断。CT显示在有呼吸道症状的HIV(+)患者和胸片正常的患者。晚期艾滋病患者的疑似结核(TB), CD4计数低,表现为实变和淋巴结病。卡波西肉瘤(KS)在影像学上可能模拟心源性肺水肿,在没有临床水肿证据的患者中应加以怀疑。
{"title":"The Immunocompromised Patient: AIDS","authors":"J. Bueno","doi":"10.1093/MED/9780199858064.003.0042","DOIUrl":"https://doi.org/10.1093/MED/9780199858064.003.0042","url":null,"abstract":"Acquired immune deficiency syndrome (AIDS) is caused by infection with human immunodeficiency virus (HIV) that results in decreased immunity and favors infectious or neoplastic conditions. The onset of clinical AIDS is defined by a CD4 count of less than 200 cells/mm3 or CD4 cells < 14% of all leukocytes in an HIV-positive patient, even in the absence of opportunistic infections. Imaging abnormalities in HIV(+) should be correlated with the CD4 count to narrow the differential diagnosis. Diffuse ground glass opacities (GGO) on CT in a patient with AIDS and hypoxemia, is virtually diagnostic of Pneumocystis pneumonia (PCP). CT is indicated in HIV(+) patients with respiratory symptoms and normal chest radiographs. Suspect tuberculosis (TB) in patients with advanced AIDS and low CD4 counts presenting with consolidation and lymphadenopathy. Kaposi sarcoma (KS) may simulate cardiogenic pulmonary edema on imaging and should be suspected in patients without clinical evidence of edema.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"137 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131131421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lung Cancer: Atelectasis and Consolidation 肺癌:肺不张和实变
Pub Date : 2019-07-01 DOI: 10.1093/MED/9780199858064.003.0047
R. Benson
The chapter titled atelectasis and consolidation discusses these specific manifestations of lung cancer. Patients with lung cancer can present with postobstructive atelectasis and/or pneumonia secondary to centrally obstructive neoplasms. Typical central primary lung cancers are squamous cell and small cell carcinomas. Atelectasis may be sublobar, lobar or may involve the entire lung. Lobar atelectasis may exhibit the S-sign of Golden or the luftsichel sign, which suggest underlying malignancy and require further evaluation with chest CT or bronchoscopy. Central lung cancers may also manifest with postobstructive lipoid pneumonia, typically without active infection. In addition, some adenocarcinomas may manifest with imaging features of consolidation due to replacement of alveolar airspaces by tumor. Therefore, consolidations in adults should be followed to complete radiographic resolution to exclude underlying malignancy.
肺不张和实变一章讨论了肺癌的这些具体表现。肺癌患者可表现为梗阻性肺不张和/或继发于中央阻塞性肿瘤的肺炎。典型的中心性原发性肺癌是鳞状细胞癌和小细胞癌。肺不张可以是大叶下、大叶或累及整个肺。大叶肺不张可表现为金色s征或luftsichel征,提示潜在的恶性肿瘤,需要胸部CT或支气管镜进一步评估。中心性肺癌也可表现为阻塞性后脂质肺炎,通常无活动性感染。此外,一些腺癌可能表现为因肿瘤取代肺泡腔而实变的影像学特征。因此,成人的实变应遵循完整的影像学分辨率,以排除潜在的恶性肿瘤。
{"title":"Lung Cancer: Atelectasis and Consolidation","authors":"R. Benson","doi":"10.1093/MED/9780199858064.003.0047","DOIUrl":"https://doi.org/10.1093/MED/9780199858064.003.0047","url":null,"abstract":"The chapter titled atelectasis and consolidation discusses these specific manifestations of lung cancer. Patients with lung cancer can present with postobstructive atelectasis and/or pneumonia secondary to centrally obstructive neoplasms. Typical central primary lung cancers are squamous cell and small cell carcinomas. Atelectasis may be sublobar, lobar or may involve the entire lung. Lobar atelectasis may exhibit the S-sign of Golden or the luftsichel sign, which suggest underlying malignancy and require further evaluation with chest CT or bronchoscopy. Central lung cancers may also manifest with postobstructive lipoid pneumonia, typically without active infection. In addition, some adenocarcinomas may manifest with imaging features of consolidation due to replacement of alveolar airspaces by tumor. Therefore, consolidations in adults should be followed to complete radiographic resolution to exclude underlying malignancy.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"26 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115590154","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nontraumatic Thoracic Aorta 非创伤性胸主动脉
Pub Date : 2019-07-01 DOI: 10.1093/MED/9780199858064.003.0023
C. Raptis
Chest pain represents one of the most common reasons for emergency department visits. Imaging often plays a key role in the patient’s care. Diseases of the media (aortic dissection, intramural hematoma (IMH) and penetrating atherosclerotic ulcer (PAU)) have been grouped under the term acute aortic syndrome. Other conditions may be seen in patients suspected of an acute aortic syndrome, including thoracic aortic aneurysm, aortic fistula, aortic thrombus and vasculitis. Radiologists must be familiar with the spectrum of these entities to help triage patients appropriately and efficiently. Understanding the imaging findings and proper measurement techniques allow the radiologist to suggest the most appropriate next management step.
胸痛是急诊室就诊最常见的原因之一。成像在病人的护理中往往起着关键作用。介质疾病(主动脉夹层、壁内血肿(IMH)和穿透性动脉粥样硬化性溃疡(PAU))被归为急性主动脉综合征。疑似急性主动脉综合征的患者也可能出现其他情况,包括胸主动脉瘤、主动脉瘘、主动脉血栓和血管炎。放射科医生必须熟悉这些实体的频谱,以帮助适当和有效地对患者进行分类。了解影像学表现和适当的测量技术可以让放射科医生建议最合适的下一步治疗步骤。
{"title":"Nontraumatic Thoracic Aorta","authors":"C. Raptis","doi":"10.1093/MED/9780199858064.003.0023","DOIUrl":"https://doi.org/10.1093/MED/9780199858064.003.0023","url":null,"abstract":"Chest pain represents one of the most common reasons for emergency department visits. Imaging often plays a key role in the patient’s care. Diseases of the media (aortic dissection, intramural hematoma (IMH) and penetrating atherosclerotic ulcer (PAU)) have been grouped under the term acute aortic syndrome. Other conditions may be seen in patients suspected of an acute aortic syndrome, including thoracic aortic aneurysm, aortic fistula, aortic thrombus and vasculitis. Radiologists must be familiar with the spectrum of these entities to help triage patients appropriately and efficiently. Understanding the imaging findings and proper measurement techniques allow the radiologist to suggest the most appropriate next management step.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123946877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hamartoma and Benign Tumor-like Lesions 错构瘤和良性肿瘤样病变
Pub Date : 2019-07-01 DOI: 10.1093/MED/9780199858064.003.0052
T. Ternes
Pulmonary hamartomas are benign neoplasms comprised of various mesenchymal components. The presence of chondroid calcification (popcorn appearance) and/or macroscopic fat can be diagnostic of hamartoma. Very slow growth is an expected finding. Treatment of pulmonary hamartoma is usually conservative. Surgical resection can be considered if the CT findings are nondiagnostic, if biopsy is inconclusive, or if the lesion demonstrates rapid growth. Surgery should also be considered in patients with central lesions and postobstructive atelectasis or infection. Hamartomas account for the majority of benign lung neoplasms. Other benign neoplasms occurring in the lungs and airways include lipoma, chondroma, and leiomyoma and are very rare. If a pulmonary chondroma is diagnosed, additional investigation should be considered to exclude concurrent leiomyosarcoma and extraadrenal paraganglioma (Carney Triad).
肺错构瘤是由多种间质成分组成的良性肿瘤。软骨样钙化(爆米花状)和/或肉眼可见的脂肪可以诊断错构瘤。增长非常缓慢是意料之中的结果。肺错构瘤的治疗通常是保守的。如果CT表现不能诊断,活检结果不确定,或者病变表现出快速增长,则可以考虑手术切除。对于中枢性病变和梗阻性肺不张或感染的患者也应考虑手术。错构瘤占肺良性肿瘤的大多数。其他发生在肺部和呼吸道的良性肿瘤包括脂肪瘤、软骨瘤和平滑肌瘤,这些肿瘤非常罕见。如果诊断为肺软骨瘤,应考虑进行额外的检查,以排除并发平滑肌肉瘤和肾上腺外副神经节瘤(卡尼三联征)。
{"title":"Hamartoma and Benign Tumor-like Lesions","authors":"T. Ternes","doi":"10.1093/MED/9780199858064.003.0052","DOIUrl":"https://doi.org/10.1093/MED/9780199858064.003.0052","url":null,"abstract":"Pulmonary hamartomas are benign neoplasms comprised of various mesenchymal components. The presence of chondroid calcification (popcorn appearance) and/or macroscopic fat can be diagnostic of hamartoma. Very slow growth is an expected finding. Treatment of pulmonary hamartoma is usually conservative. Surgical resection can be considered if the CT findings are nondiagnostic, if biopsy is inconclusive, or if the lesion demonstrates rapid growth. Surgery should also be considered in patients with central lesions and postobstructive atelectasis or infection. Hamartomas account for the majority of benign lung neoplasms. Other benign neoplasms occurring in the lungs and airways include lipoma, chondroma, and leiomyoma and are very rare. If a pulmonary chondroma is diagnosed, additional investigation should be considered to exclude concurrent leiomyosarcoma and extraadrenal paraganglioma (Carney Triad).","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"22 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116628424","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pulmonary Hypertension 肺动脉高压
Pub Date : 2019-07-01 DOI: 10.1093/med/9780199858064.003.0026
C. Raptis
Pulmonary hypertension (PH) is defined as a pulmonary capillary wedge pressure >25 mm Hg. Patients tend to present with nonspecific symptoms centered on worsening dyspnea. The causes of PH are classified according to the Dana Point classification which groups causes of PH based on shared pathophysiology and treatments. In the initial work up of patients with PH, the goal of imaging is determine if there are findings of PH and to look for clues to the underlying cause so that patients are treated appropriately. MRI can be useful in the follow up of patients with PH, as it can evaluate for changes in the right ventricle.
肺动脉高压(Pulmonary hypertension, PH)定义为肺毛细血管楔压>25 mm Hg,患者往往表现为以呼吸困难加重为中心的非特异性症状。PH的原因根据达纳点分类分类,该分类基于共同的病理生理和治疗方法对PH的原因进行分组。在PH患者的初始工作中,影像学的目标是确定是否有PH的发现,并寻找潜在原因的线索,以便患者得到适当的治疗。MRI在PH患者的随访中很有用,因为它可以评估右心室的变化。
{"title":"Pulmonary Hypertension","authors":"C. Raptis","doi":"10.1093/med/9780199858064.003.0026","DOIUrl":"https://doi.org/10.1093/med/9780199858064.003.0026","url":null,"abstract":"Pulmonary hypertension (PH) is defined as a pulmonary capillary wedge pressure >25 mm Hg. Patients tend to present with nonspecific symptoms centered on worsening dyspnea. The causes of PH are classified according to the Dana Point classification which groups causes of PH based on shared pathophysiology and treatments. In the initial work up of patients with PH, the goal of imaging is determine if there are findings of PH and to look for clues to the underlying cause so that patients are treated appropriately. MRI can be useful in the follow up of patients with PH, as it can evaluate for changes in the right ventricle.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"397 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"123537744","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pleural Neoplasms 胸膜肿瘤
Pub Date : 2019-07-01 DOI: 10.1093/med/9780199858064.003.0032
Christopher M Walker
Pleural neoplasms discusses the radiographic and computed tomography (CT) manifestations of primary and secondary pleural neoplasms. Four CT features suggest malignant pleural thickening including nodular pleural thickening, circumferential pleural thickening, pleural thickening measuring greater than 1 cm in thicknesss, and thickening of the mediastinal pleural surface. The most common pleural malignancy is metastatic disease, generally from adenocarcinomas of the lung, breast, or gastrointestinal tract. Thymoma may spread to the pleura via direct extension or drop metastases. Mesothelioma is uncommon but is the most common primary pleural malignancy and is almost universally associated with asbestos exposure. It manifests with rind-like pleural thickening which may involve interlobar fissures and often causes volume loss in the affected hemithorax. Localized fibrous tumor of the pleura usually arises from the visceral pleural surface and manifests as a lobular or smooth pleural mass usually in the mid or lower hemithorax.
胸膜肿瘤讨论了原发性和继发性胸膜肿瘤的影像学和CT表现。4项CT表现提示恶性胸膜增厚,包括结节性胸膜增厚、环状胸膜增厚、厚度大于1cm的胸膜增厚、纵隔胸膜表面增厚。最常见的胸膜恶性肿瘤是转移性疾病,通常来自肺、乳腺或胃肠道的腺癌。胸腺瘤可通过直接延伸或下降转移扩散到胸膜。间皮瘤不常见,但却是最常见的原发性胸膜恶性肿瘤,几乎普遍与石棉暴露有关。它表现为皮状胸膜增厚,可累及叶间裂隙,常导致受影响的半胸体积减少。胸膜的局限性纤维性肿瘤通常起源于内脏胸膜表面,表现为小叶状或平滑的胸膜肿块,通常位于中胸或下半胸。
{"title":"Pleural Neoplasms","authors":"Christopher M Walker","doi":"10.1093/med/9780199858064.003.0032","DOIUrl":"https://doi.org/10.1093/med/9780199858064.003.0032","url":null,"abstract":"Pleural neoplasms discusses the radiographic and computed tomography (CT) manifestations of primary and secondary pleural neoplasms. Four CT features suggest malignant pleural thickening including nodular pleural thickening, circumferential pleural thickening, pleural thickening measuring greater than 1 cm in thicknesss, and thickening of the mediastinal pleural surface. The most common pleural malignancy is metastatic disease, generally from adenocarcinomas of the lung, breast, or gastrointestinal tract. Thymoma may spread to the pleura via direct extension or drop metastases. Mesothelioma is uncommon but is the most common primary pleural malignancy and is almost universally associated with asbestos exposure. It manifests with rind-like pleural thickening which may involve interlobar fissures and often causes volume loss in the affected hemithorax. Localized fibrous tumor of the pleura usually arises from the visceral pleural surface and manifests as a lobular or smooth pleural mass usually in the mid or lower hemithorax.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"17 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128846333","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chest Trauma: Nonvascular Injuries 胸部创伤:非血管损伤
Pub Date : 2019-07-01 DOI: 10.1093/MED/9780199858064.003.0022
C. Raptis
In the setting of trauma, thoracic injuries are third in frequency after injuries to the head and extremities. While the greatest source of mortality in the setting of thoracic trauma is vascular injury, nonvascular injuries are much more common and can result in substantial morbidity and mortality, complicating overall case management. This section will focus on non vascular injuries that may be seen in the setting of trauma involving the lungs, diaphragm, mediastinum, thoracic skeleton, heart and pleura. Findings in both blunt and penetrating trauma will be highlighted.
在创伤的情况下,胸部损伤是继头部和四肢损伤之后的第三常见损伤。虽然胸外伤中最大的死亡来源是血管损伤,但非血管损伤更为常见,可导致大量发病率和死亡率,使整体病例管理复杂化。本节将着重于非血管性损伤,可能在涉及肺、隔膜、纵隔、胸骨、心脏和胸膜的创伤设置中看到。钝性和穿透性创伤的结果将被强调。
{"title":"Chest Trauma: Nonvascular Injuries","authors":"C. Raptis","doi":"10.1093/MED/9780199858064.003.0022","DOIUrl":"https://doi.org/10.1093/MED/9780199858064.003.0022","url":null,"abstract":"In the setting of trauma, thoracic injuries are third in frequency after injuries to the head and extremities. While the greatest source of mortality in the setting of thoracic trauma is vascular injury, nonvascular injuries are much more common and can result in substantial morbidity and mortality, complicating overall case management. This section will focus on non vascular injuries that may be seen in the setting of trauma involving the lungs, diaphragm, mediastinum, thoracic skeleton, heart and pleura. Findings in both blunt and penetrating trauma will be highlighted.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"114 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117309969","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mediastinal Lymphadenopathy 纵隔淋巴结病
Pub Date : 2019-07-01 DOI: 10.1093/med/9780199858064.003.0083
B. Carter
Lymphadenopathy represents the pathologic enlargement of lymph nodes. Within the chest, the mediastinum is the most commonly affected region. Mediastinal lymphadenopathy may result in loss of normal mediastinal contours or thickening of lines and stripes. On computed tomography (CT), lymph nodes measuring greater than 1 cm in short-axis dimension are typically considered enlarged. Although many disease process may result in mediastinal lymphadenopathy, including lymphoma, metastatic disease, infections, and sarcoidosis, specific characteristics such as attenuation, enhancement, and calcification help narrow the differential diagnosis. PET/CT demonstrates the metabolic activity of structures such as lymph nodes and may help in identifying pathologic lymphadenopathy. However, PET/CT cannot reliably differentiate between lymphadenopathy due to active malignancy and certain benign processes such as active infection or sarcoidosis.
淋巴结病是指淋巴结的病理性肿大。在胸部,纵隔是最常见的受累部位。纵隔淋巴结病可导致正常纵隔轮廓的丧失或线条和条纹的增厚。在计算机断层扫描(CT)上,淋巴结短轴尺寸大于1cm通常被认为是肿大。虽然许多疾病过程可能导致纵隔淋巴结病,包括淋巴瘤、转移性疾病、感染和结节病,但特异性特征如衰减、增强和钙化有助于缩小鉴别诊断范围。PET/CT显示了淋巴结等结构的代谢活动,可能有助于识别病理性淋巴结病。然而,PET/CT不能可靠地区分由活动性恶性肿瘤引起的淋巴结病和某些良性病变,如活动性感染或结节病。
{"title":"Mediastinal Lymphadenopathy","authors":"B. Carter","doi":"10.1093/med/9780199858064.003.0083","DOIUrl":"https://doi.org/10.1093/med/9780199858064.003.0083","url":null,"abstract":"Lymphadenopathy represents the pathologic enlargement of lymph nodes. Within the chest, the mediastinum is the most commonly affected region. Mediastinal lymphadenopathy may result in loss of normal mediastinal contours or thickening of lines and stripes. On computed tomography (CT), lymph nodes measuring greater than 1 cm in short-axis dimension are typically considered enlarged. Although many disease process may result in mediastinal lymphadenopathy, including lymphoma, metastatic disease, infections, and sarcoidosis, specific characteristics such as attenuation, enhancement, and calcification help narrow the differential diagnosis. PET/CT demonstrates the metabolic activity of structures such as lymph nodes and may help in identifying pathologic lymphadenopathy. However, PET/CT cannot reliably differentiate between lymphadenopathy due to active malignancy and certain benign processes such as active infection or sarcoidosis.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"33 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133448440","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Upper and Middle Lobe Atelectasis 上、中肺叶不张
Pub Date : 2019-07-01 DOI: 10.1093/MED/9780199858064.003.0017
Christopher M Walker
Upper and middle lobe atelectasis discusses the radiographic and computed tomography (CT) manifestations of upper and middle lobe atelectasis. The most common radiographic signs of right upper lobe atelectasis include upward and medial displacement of the minor fissure, superior displacement of adjacent structures such as the hilum and main bronchus, and ipsilateral shift of the mediastinal structures. The S sign of Golden results from a centrally obstructing lung cancer as the cause of the atelectasis and manifests as a reverse S configuration of the minor fissure outlined by atelectatic lung and central mass. Left upper lobe atelectasis manifests with a veil-like opacity on frontal radiography with leftward shift of upper mediastinal structures such as the trachea and upward shift of the left main bronchus and left hemidiaphragm. The Luftsichel sign or air crescent sign may be seen and represents the hyperexpanded superior segment of the left lower lobe outlining the transverse aortic arch. Lobar atelectasis in the inpatient setting is most commonly secondary to an obstructing mucus plug. Lobar atelectasis in the outpatient setting is often a heralding sign of a centrally obstructing lung cancer and should be further evaluated with contrast-enhanced CT and/or bronchoscopy.
上、中肺叶不张讨论上、中肺叶不张的影像学和CT表现。右上肺叶不张最常见的影像学征象包括小裂的向上和内侧移位,邻近结构如肺门和主支气管的上移位,以及纵膈结构的同侧移位。金的S征象是由肺不张引起的中央阻塞性肺癌引起的,表现为肺不张和中央肿块所勾勒的小裂隙的反S形。左侧上肺叶不张表现为额片上的面纱样不透明,上纵隔结构如气管向左移位,左主支气管和左膈向上移位。可见Luftsichel征或气月牙征,表示左下叶上段过度扩张,显示主动脉弓横切面。住院患者肺叶不张最常继发于阻塞的粘液塞。门诊大叶肺不张通常是中央阻塞性肺癌的前兆,应进一步通过增强CT和/或支气管镜检查进行评估。
{"title":"Upper and Middle Lobe Atelectasis","authors":"Christopher M Walker","doi":"10.1093/MED/9780199858064.003.0017","DOIUrl":"https://doi.org/10.1093/MED/9780199858064.003.0017","url":null,"abstract":"Upper and middle lobe atelectasis discusses the radiographic and computed tomography (CT) manifestations of upper and middle lobe atelectasis. The most common radiographic signs of right upper lobe atelectasis include upward and medial displacement of the minor fissure, superior displacement of adjacent structures such as the hilum and main bronchus, and ipsilateral shift of the mediastinal structures. The S sign of Golden results from a centrally obstructing lung cancer as the cause of the atelectasis and manifests as a reverse S configuration of the minor fissure outlined by atelectatic lung and central mass. Left upper lobe atelectasis manifests with a veil-like opacity on frontal radiography with leftward shift of upper mediastinal structures such as the trachea and upward shift of the left main bronchus and left hemidiaphragm. The Luftsichel sign or air crescent sign may be seen and represents the hyperexpanded superior segment of the left lower lobe outlining the transverse aortic arch. Lobar atelectasis in the inpatient setting is most commonly secondary to an obstructing mucus plug. Lobar atelectasis in the outpatient setting is often a heralding sign of a centrally obstructing lung cancer and should be further evaluated with contrast-enhanced CT and/or bronchoscopy.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"56 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131680702","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Silicosis and Coal Worker’s Pneumoconiosis 矽肺病和煤工尘肺病
Pub Date : 2019-07-01 DOI: 10.1093/MED/9780199858064.003.0067
J. Azok
Silicosis and coal-workers pneumoconiosis (CWP) are fibrotic lung diseases secondary to the inhalation of free silica and coal dust. Exposure is typically occupational and occurs over many years before symptoms develop. Cough and shortness of breath are the most common presenting symptoms. Imaging features of silicosis and CWP are similar and often indistinguishable. Both silicosis and CWP result in upper lobe predominant disease. Pulmonary nodules are the most common imaging feature which may coalesce into progressive massive fibrosis. Lymphadenopathy and emphysema are additional findings seen in patients with silicosis and CWP. Silicosis has a higher incidence of tuberculosis and both pneumoconioses have a higher incidence of lung cancer.
矽肺病和煤工尘肺病(CWP)是继发于吸入游离二氧化硅和煤尘的纤维化肺部疾病。暴露通常是职业性的,并且在出现症状之前已发生多年。咳嗽和气短是最常见的症状。矽肺和CWP的影像学特征相似,通常无法区分。矽肺和CWP都会导致上叶为主的疾病。肺部结节是最常见的影像学特征,可合并为进行性大块纤维化。淋巴结病和肺气肿是矽肺病和 CWP 患者的额外发现。矽肺病的肺结核发病率较高,而这两种尘肺病的肺癌发病率也较高。
{"title":"Silicosis and Coal Worker’s Pneumoconiosis","authors":"J. Azok","doi":"10.1093/MED/9780199858064.003.0067","DOIUrl":"https://doi.org/10.1093/MED/9780199858064.003.0067","url":null,"abstract":"Silicosis and coal-workers pneumoconiosis (CWP) are fibrotic lung diseases secondary to the inhalation of free silica and coal dust. Exposure is typically occupational and occurs over many years before symptoms develop. Cough and shortness of breath are the most common presenting symptoms. Imaging features of silicosis and CWP are similar and often indistinguishable. Both silicosis and CWP result in upper lobe predominant disease. Pulmonary nodules are the most common imaging feature which may coalesce into progressive massive fibrosis. Lymphadenopathy and emphysema are additional findings seen in patients with silicosis and CWP. Silicosis has a higher incidence of tuberculosis and both pneumoconioses have a higher incidence of lung cancer.","PeriodicalId":415668,"journal":{"name":"Chest Imaging","volume":"40 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128156576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
期刊
Chest Imaging
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1