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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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樓主: Stenosis
21#
發(fā)表于 2025-3-25 06:58:54 | 只看該作者
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.
22#
發(fā)表于 2025-3-25 08:16:11 | 只看該作者
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.
23#
發(fā)表于 2025-3-25 12:44:38 | 只看該作者
24#
發(fā)表于 2025-3-25 15:49:48 | 只看該作者
25#
發(fā)表于 2025-3-25 23:56:09 | 只看該作者
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, ..
26#
發(fā)表于 2025-3-26 02:40:54 | 只看該作者
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.
27#
發(fā)表于 2025-3-26 06:00:02 | 只看該作者
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.
28#
發(fā)表于 2025-3-26 08:53:46 | 只看該作者
29#
發(fā)表于 2025-3-26 12:38:53 | 只看該作者
30#
發(fā)表于 2025-3-26 19:29:32 | 只看該作者
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.
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