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Titlebook: Diffuse Cystic Lung Diseases; Nishant Gupta,Kathryn A. Wikenheiser-Brokamp,Franc Book 2021 Springer Nature Switzerland AG 2021 cystic lung

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发表于 2025-3-21 17:54:59 | 显示全部楼层 |阅读模式
书目名称Diffuse Cystic Lung Diseases
编辑Nishant Gupta,Kathryn A. Wikenheiser-Brokamp,Franc
视频video
概述Comprehensively overviews diffuse cystic lung diseases (DCLDs) starting from basic pathophysiology to state-of-the-art diagnosis and management techniques.Authored by world experts in the diseases, fr
丛书名称Respiratory Medicine
图书封面Titlebook: Diffuse Cystic Lung Diseases;  Nishant Gupta,Kathryn A. Wikenheiser-Brokamp,Franc Book 2021 Springer Nature Switzerland AG 2021 cystic lung
描述.This book is a comprehensive reference on diffuse cystic lung diseases (DCLDs). DCLDs are a group of pathophysiologically heterogenous processes that are characterized by the presence of multiple spherical or irregularly shaped, thin-walled, air-filled spaces within the pulmonary parenchyma. In recent years, tremendous advancements have been made in these diseases leading to improved understanding of the underlying pathophysiology, and improved outcomes with targeted therapies. The authors, who are leading experts in the field, delineate DCLDs as a separate category distinct from other interstitial lung diseases, and have created this textbook specifically dedicated to this disease group.  .This book begins with a chapter introducing the definition and classification of DCLDs. Subsequent chapters address the pathogenic mechanisms underlying pulmonary cyst formation and provide a detailed overview of the radiological and pathological features of DCLDs. The common as well as uncommon 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 culm
出版日期Book 2021
关键词cystic lung diseases; lymphangioleiomyomatosis; LAM; Birt-Hogg-Dubé syndrome; pulmonary Langerhans cell
版次1
doihttps://doi.org/10.1007/978-3-030-63365-3
isbn_softcover978-3-030-63367-7
isbn_ebook978-3-030-63365-3Series ISSN 2197-7372 Series E-ISSN 2197-7380
issn_series 2197-7372
copyrightSpringer Nature Switzerland AG 2021
The information of publication is updating

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发表于 2025-3-21 22:45:32 | 显示全部楼层
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
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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
发表于 2025-3-22 12:11:40 | 显示全部楼层
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,
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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
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