2015年9月2日 星期三
Usual interstitial pneumonia (UIP): lower lobe, honeycombing pattern, fibroblastic foci。
IPF (idiopathic pulmonary fibrosis): pathology UIP without other cause of interstitial lung disease
Desquamative interstitial pneumonitis (DIP)/RB-ILD: DIP is usually more extensive, alveolar macrophages with brown and finely granular pigmentation. The treatment of RB-ILD is smoking cessation .
Lymphoid interstitial pneumonitis (LIP): lymphocytes and plasma cells
Langerhans’-cell histiocytosis: Nodules and cysts, Predominantly upper-lobe disease, Sparing of the costophrenic angles
Organizing Pneumonia: mucopolysacharide-rich matrix, with young fibroblasts,
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