作者: Repatriate 時(shí)間: 2025-3-21 22:45
Mechanisms of Lung Cyst Formation,echanisms of parenchymal loss that occur in common cystic lung diseases such as chronic obstructive pulmonary disease (COPD) with those of rare disorders associated with dysregulation of specific molecular pathways. Four representative cystic lung diseases are described with reference to underlying 作者: Visual-Field 時(shí)間: 2025-3-22 02:37 作者: 離開 時(shí)間: 2025-3-22 06:07
Pathological Evaluation of Pulmonary Cysts,adjacent lung parenchyma, exclusion of cyst mimics, and correlation with clinical and radiographic information. Using this standard approach allows definitive recognition of the etiology of the cystic lesions in most cases. This chapter reviews pathological features of common and uncommon causes of 作者: 群居動(dòng)物 時(shí)間: 2025-3-22 12:11
Pathophysiology of Lymphangioleiomyomatosis,LAM cells that carry bi-allelic loss-of-function mutations in the . or . gene. LAM affects almost exclusively women. LAM occurs in women with tuberous sclerosis complex (TSC) and in women who do not have TSC, which is referred to as sporadic LAM. LAM can result in pneumothorax and oxygen dependency,作者: Thymus 時(shí)間: 2025-3-22 15:34
Smoking-Induced Diffuse Cystic Lung Diseases,uctive pulmonary disease (COPD) and cancer, cigarette smokers may develop diffuse interstitial and bronchiolar disorders. These diffuse lung diseases are referred to as “smoking-related interstitial lung diseases,” a term that recognizes the causal association with cigarette smoking. Several of the 作者: Thymus 時(shí)間: 2025-3-22 17:46 作者: contradict 時(shí)間: 2025-3-22 23:59 作者: exclusice 時(shí)間: 2025-3-23 04:58 作者: DEMUR 時(shí)間: 2025-3-23 06:24 作者: Oratory 時(shí)間: 2025-3-23 12:54 作者: anchor 時(shí)間: 2025-3-23 16:39
Congenital and Developmental Causes of Cystic Lung Disease,ations from diffuse lung disease is essential given the implications for prognosis and treatment. A multidisciplinary approach to these disorders, with clinical, radiographical, pathological, and frequently molecular evaluations, is required to arrive at a specific diagnosis. This chapter reviews th作者: Alienated 時(shí)間: 2025-3-23 19:32
Rare Causes of Cystic Lung Disease,-filled lucencies interfaced with normal lung parenchyma. Commonly encountered DCLDs in clinical practice include lymphangioleiomyomatosis (LAM), pulmonary Langerhans cell histiocytosis (PLCH), lymphoid interstitial pneumonia (LIP), and Birt-Hogg-Dubé syndrome (BHD); these disorders are discussed in作者: anniversary 時(shí)間: 2025-3-23 22:43 作者: expository 時(shí)間: 2025-3-24 04:40
Extrapulmonary Manifestations of Diffuse Cystic Lung Diseases,se extrapulmonary manifestations, although not directly in the purview of management for a practicing pulmonologist, carry significant health implications for patients, factor into the overall management including the decision to start pharmacological therapies, can help ascertain the underlying dis作者: expansive 時(shí)間: 2025-3-24 06:39
Pleural Disease in Diffuse Cystic Lung Diseases,ific disorders. Various disorders belonging to DCLDs, lymphangioleiomyomatosis (LAM), Birt-Hogg-Dubé syndrome (BHDS), and pulmonary Langerhans cell histiocytosis (PLCH) are frequently complicated by a spontaneous pneumothorax. Due to the diffuse nature of underlying pathogenic mechanisms involving v作者: 偉大 時(shí)間: 2025-3-24 13:20
Air Travel in Diffuse Cystic Lung Diseases, due to the diffuse parenchymal lung disease, and the decreased partial pressure of oxygen in the aircraft cabin increases the risk of in-flight hypoxemia. Additionally, in accordance with Boyle’s law, DCLD patients are at increased risk of development of spontaneous pneumothorax due to the expansio作者: 辮子帶來(lái)幫助 時(shí)間: 2025-3-24 18:53 作者: Meager 時(shí)間: 2025-3-24 20:22
Pathological Evaluation of Pulmonary Cysts,finitive recognition of the etiology of the cystic lesions in most cases. This chapter reviews pathological features of common and uncommon causes of DCLDs.?Salient clinical and radiographical features that assist the pathologist are discussed. Finally, pathological features of the cyst mimics are explored.作者: 過(guò)份好問(wèn) 時(shí)間: 2025-3-25 01:52
Neoplasms That Present as Multicystic Lung Disease,onary metastases including mesenchymal and epithelial tumors, lymphomas, and various sarcomas. The radiological and pathological features are reviewed along with discussion of the clinical features of a number of these conditions that can present as isolated, multifocal, or diffuse cystic lesions in the lung.作者: 高興一回 時(shí)間: 2025-3-25 06:58
Congenital and Developmental Causes of Cystic Lung Disease,h clinical, radiographical, pathological, and frequently molecular evaluations, is required to arrive at a specific diagnosis. This chapter reviews the spectrum of congenital and developmental entities presenting as cystic lung disease in children including discussion of proposed pathogenesis as well as genetic and neoplastic implications.作者: 不感興趣 時(shí)間: 2025-3-25 08:16
Rare Causes of Cystic Lung Disease,onary Langerhans cell histiocytosis (PLCH), lymphoid interstitial pneumonia (LIP), and Birt-Hogg-Dubé syndrome (BHD); these disorders are discussed in detail in individual chapters of this book. However, the etiology of DCLDs may include other particularly rare etiologies, some of which are addressed in this chapter.作者: 仇恨 時(shí)間: 2025-3-25 12:44 作者: bromide 時(shí)間: 2025-3-25 15:49 作者: 混合,攙雜 時(shí)間: 2025-3-25 23:56
Reconstruction of the Knee Jointdistinguish these disorders from the more indolent chronic DCLDs. This review describes infectious etiologies of cystic lung disease as well as the mechanisms of cyst development, the clinical and radiographic presentations, and the clinical management, with a special focus on the prototypical DCLD-associated infection, ..作者: fetter 時(shí)間: 2025-3-26 02:40
https://doi.org/10.1007/978-3-319-52280-7 of patients with DCLDs includes prevention and treatment of complications such as spontaneous pneumothorax. This chapter reviews the key aspects of clinical, radiological, and other diagnostic modalities as well as the currently available treatment options that can help physicians in managing DCLD patients.作者: prosperity 時(shí)間: 2025-3-26 06:00
Chen Peng,Chuanliang Cheng,Ling Wangnt with DCLD. The operating principle for this book is that the presentation, differential diagnosis, and management for the DCLDs differ from the interstitial lung diseases, and should be classified separately.作者: mitral-valve 時(shí)間: 2025-3-26 08:53 作者: 季雨 時(shí)間: 2025-3-26 12:38 作者: 按時(shí)間順序 時(shí)間: 2025-3-26 19:29
https://doi.org/10.1007/978-3-319-52280-7CLDs, thus underscoring the need to pay careful attention to these conditions when evaluating a patient with DCLD. This chapter comprises a detailed discussion of a variety of common conditions, which mimic DCLDs. In the course of our discussion, we consider the radiographical and clinical nuances which can help to differentiate these conditions.作者: 昆蟲 時(shí)間: 2025-3-26 23:23
Definition and Classification of Diffuse Cystic Lung Diseases,nt with DCLD. The operating principle for this book is that the presentation, differential diagnosis, and management for the DCLDs differ from the interstitial lung diseases, and should be classified separately.作者: AV-node 時(shí)間: 2025-3-27 04:18
Radiological Evaluation of Cystic Lung Disease,sis include cyst distribution and shape. In addition, ancillary lung and extrapulmonary findings can suggest the diagnosis. Chest CT in conjunction with clinical and laboratory information often allow establishment of the diagnosis without further invasive testing.作者: 精致 時(shí)間: 2025-3-27 06:42 作者: 期滿 時(shí)間: 2025-3-27 13:07 作者: 碎石頭 時(shí)間: 2025-3-27 13:46 作者: 泥土謙卑 時(shí)間: 2025-3-27 17:49
Pathophysiology of Lymphangioleiomyomatosis,tic chest computed tomography (CT) scan. Here, we review the clinical and genetic features of LAM, the pathophysiology of LAM, and animal models of LAM, highlighting key clinical and translational unknowns.作者: yohimbine 時(shí)間: 2025-3-28 00:41 作者: ear-canal 時(shí)間: 2025-3-28 05:00 作者: ICLE 時(shí)間: 2025-3-28 07:20
https://doi.org/10.1057/9781137428837finitive recognition of the etiology of the cystic lesions in most cases. This chapter reviews pathological features of common and uncommon causes of DCLDs.?Salient clinical and radiographical features that assist the pathologist are discussed. Finally, pathological features of the cyst mimics are explored.作者: endoscopy 時(shí)間: 2025-3-28 10:58 作者: 拋媚眼 時(shí)間: 2025-3-28 17:35
https://doi.org/10.1007/978-981-10-6138-7h clinical, radiographical, pathological, and frequently molecular evaluations, is required to arrive at a specific diagnosis. This chapter reviews the spectrum of congenital and developmental entities presenting as cystic lung disease in children including discussion of proposed pathogenesis as well as genetic and neoplastic implications.作者: 含水層 時(shí)間: 2025-3-28 22:03 作者: heirloom 時(shí)間: 2025-3-29 00:15
Lequan Yu,Xin Yang,Jing Qin,Pheng-Ann Hengions for patients, factor into the overall management including the decision to start pharmacological therapies, can help ascertain the underlying disease diagnosis, and enable a comprehensive evaluation of patients presenting with diffuse cystic lung disease.作者: 種族被根除 時(shí)間: 2025-3-29 03:50
Smoking-Induced Diffuse Cystic Lung Diseases,cigarette smoking-induced diffuse lung diseases are associated with pulmonary parenchymal cystic change. This chapter focuses on the mechanisms of cigarette smoking-induced cystic lung disease development and clinical characterization and management of smoking-induced cystic lung disease.作者: Jejune 時(shí)間: 2025-3-29 08:35 作者: BARB 時(shí)間: 2025-3-29 14:37
Approach to the Diagnosis and Management of Diffuse Cystic Lung Diseases, of patients with DCLDs includes prevention and treatment of complications such as spontaneous pneumothorax. This chapter reviews the key aspects of clinical, radiological, and other diagnostic modalities as well as the currently available treatment options that can help physicians in managing DCLD patients.作者: 揭穿真相 時(shí)間: 2025-3-29 16:33 作者: 親屬 時(shí)間: 2025-3-29 22:26
Mechanisms of Lung Cyst Formation, of the BRAF/MEK/ERK pathway in dendritic cells interacts with cigarette smoke to cause a destructive bronchiolitis. In Birt-Hogg-Dubé syndrome (BHD), loss of the tumour suppressor folliculin leads to defects in cell-cell interactions and shear-mediated lung damage. Finally, we discuss the poorly un作者: nominal 時(shí)間: 2025-3-30 02:20 作者: 證實(shí) 時(shí)間: 2025-3-30 06:58 作者: flammable 時(shí)間: 2025-3-30 08:43 作者: FAZE 時(shí)間: 2025-3-30 14:10 作者: Surgeon 時(shí)間: 2025-3-30 17:56 作者: ENACT 時(shí)間: 2025-3-30 23:50
Lecture Notes in Computer Sciencesion complicated by LAM. Chylothorax used to be managed by chemical or surgical pleurodesis, but due to its high effectiveness, sirolimus therapy is currently recommended to manage various lymphatic problems associated with LAM.作者: Monocle 時(shí)間: 2025-3-31 01:47
https://doi.org/10.1007/978-3-319-52280-7r travel in DCLDs along with the available literature concerning risk assessment for flying in this patient population. We also briefly mention the potential physiologic consequences that underwater diving could have for DCLD patients.作者: 涂掉 時(shí)間: 2025-3-31 07:15
2197-7372 ncommon causes of DCLDs are comprehensively reviewed in individual chapters, as are the varied clinical presentations and extrapulmonary manifestations, and approaches to management and treatment. The book culm978-3-030-63367-7978-3-030-63365-3Series ISSN 2197-7372 Series E-ISSN 2197-7380 作者: 犬儒主義者 時(shí)間: 2025-3-31 10:02
Diffuse Cystic Lung Diseases978-3-030-63365-3Series ISSN 2197-7372 Series E-ISSN 2197-7380 作者: 失誤 時(shí)間: 2025-3-31 14:00 作者: medium 時(shí)間: 2025-3-31 21:00 作者: Extort 時(shí)間: 2025-4-1 01:40 作者: LAPSE 時(shí)間: 2025-4-1 03:28 作者: 編輯才信任 時(shí)間: 2025-4-1 07:40 作者: Scintillations 時(shí)間: 2025-4-1 13:13 作者: BRINK 時(shí)間: 2025-4-1 16:30
Chen Peng,Chuanliang Cheng,Ling Wanginterface with normal lung. Emphysema, bronchiectasis, fibrotic lung disease, and cavitary lung diseases can also produce parenchymal lucencies that can mimic true DCLDs. A variety of low-grade or high-grade metastasizing neoplasms, polyclonal or monoclonal lymphoproliferative disorders or plasma ce作者: Delirium 時(shí)間: 2025-4-1 21:19
Chen Peng,Chuanliang Cheng,Ling Wangechanisms of parenchymal loss that occur in common cystic lung diseases such as chronic obstructive pulmonary disease (COPD) with those of rare disorders associated with dysregulation of specific molecular pathways. Four representative cystic lung diseases are described with reference to underlying
