Results 31 to 40 of about 665,386 (165)
Evaluation of the Interstitial Histological Lesions in Pulmonary Langerhans Cell Histiocytosis
Objective: Pulmonary Langerhans cell histiocytosis is a cystic lung disease characterized by the proliferation of parenchymal dendritic cells. The disease can become chronic or even cause pulmonary fibrosis.
Halide Nur URER, Hatice DINCER
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IgG4-related disease presenting with combined pulmonary fibrosis and emphysema (CPFE)
A 64-year-old man was admitted to our hospital with an abnormal chest shadow. The patient was a current-smoker and had a past illness of autoimmune pancreatitis with a high serum level of IgG4, 348 mg/dL.
Masato Kono +14 more
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Giant pulmonary bulla causing respiratory compromise in a very low‐birthweight infant
Acquired cystic lung disease in premature infants is a serious respiratory complication, and pulmonary interstitial emphysema (PIE) has been widely reported.
Tamao Shinohara +13 more
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Tobacco smoke exposure causes diverse pulmonary manifestations with involvement of alveolar, interstitial, and vascular diseases due to inflammatory pathology apart from more lethal lung cancer. Combined pulmonary fibrosis and emphysema is a heterogenous
Shital Patil, Gajanan Gondhali
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Pulmonary Interstitial Emphysema
Pulmonary interstitial emphysema (PIE) is a rare, abnormal pathology that occurs more commonly in neonates but can be seen in adults as well. The increased air pressure within the alveoli and alveolar airspaces can disrupt the adjacent lung interstitial ...
Anjum, Fatima, Jalota Sahota, Ruchi
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Airway complications after lung transplantation are a major cause of morbidity and mortality. Bronchial dehiscence presents within a month of lung transplantation and is typically diagnosed radiographically as a sentinel gas pocket at the anastomotic ...
Linda P. Vien +4 more
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Pulmonary air leak syndrome in rheumatoid arthritis patient
Pulmonary air leak syndromes involve dissection of air out of the normal pulmonary airspaces and include pulmonary interstitial emphysema, pneumothorax, pneumomediastinum, pneumopericardium, pneumoperitoneum, subcutaneous emphysema and systemic air ...
Ibtissam El Ouali +5 more
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Myeloperoxidase antineutrophil cytoplasmic autoantibody (MPO-ANCA) is well-known as a serological marker for small-vessel vasculitis. However, when a smoker with interstitial lung disease (ILD) exhibits serum ANCA positivity without systemic vasculitis ...
Masahiro Nemoto +7 more
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Combined Pulmonary Fibrosis and Emphysema: When Scylla and Charybdis Ally
Combined pulmonary fibrosis and emphysema (CPFE) is a recently recognized syndrome that, as its name indicates, involves the existence of both interstitial lung fibrosis and emphysema in one individual, and is often accompanied by pulmonary hypertension.
Marija Gredic +5 more
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Interstitial lung disease (ILD) is a significant cause of morbidity and mortality in patients with inflammatory rheumatic disorders (IRDs). High‐resolution computed tomography (HRCT) is widely considered the gold standard for the noninvasive assessment of ILD; however, its interpretation is constrained by substantial interobserver variability and the ...
Alexander Pfeil +7 more
wiley +1 more source

