Results 161 to 170 of about 8,581 (204)

Autoimmune pulmonary alveolar proteinosis presenting as localized multifocal GGOs: A case report. [PDF]

Radiol Case Rep
Honda K, Koike H, Tsutsui S, Toya R, Matsumoto K, Okano S, Taniguchi H, Ashizawa K.   +7 more
europepmc   +1 more source

Pulmonary fibrosis in patients with autoimmune pulmonary alveolar proteinosis: a retrospective nationwide cohort study. [PDF]

ERJ Open Res
Guirriec Y, Luque-Paz D, Bernard G, Mabo A, Kerjouan M, Ménard C, Monnier D, Nunes H, Uzunhan Y, Reynaud-Gaubert M, Bermudez J, Borie R, Crestani B, Traclet J, Wémeau-Stervinou L, Chenivesse C, Gomez E, Prévot G, Bourdin A, Bondue B, Bergeron A, Cottin V, Lederlin M, Jouneau S, OrphaLung network.   +24 more
europepmc   +1 more source

A case of autoimmune pulmonary alveolar proteinosis responding to oral statin therapy. [PDF]

Respir Med Case Rep
Shimamura S, Morikawa H, Shinohara K, Ohkoshi H, Omori C, Hoshino Y, Uchida Y, Masafumi S, Ikemura S, Ohishi N, Kondo T, Soejima K.   +11 more
europepmc   +1 more source

Pulmonary alveolar proteinosis complicated by lung cancer with favorable prognosis: a case report and literature review. [PDF]

Front Oncol
Wu Y, Guan W, Deng J, Mo W, Xu B, Zhang J, Jiang H, Liu J, Lin X, Zhou C.   +9 more
europepmc   +1 more source

Pulmonary Alveolar Proteinosis During Intensive Immunosuppressive Treatment for Acute Exacerbation of Interstitial Pneumonia: A Case Report and Literature Review. [PDF]

Cureus
Yanagisawa A, Konaka H, Tanaka M, Ihara S, Tachibana I.   +4 more
europepmc   +1 more source

Pulmonary alveolar proteinosis [PDF]

Nature Reviews Disease Primers, 2019
Pulmonary alveolar proteinosis (PAP) is a syndrome characterized by the accumulation of alveolar surfactant and dysfunction of alveolar macrophages. PAP results in progressive dyspnoea of insidious onset, hypoxaemic respiratory failure, secondary infections and pulmonary fibrosis.
Bruce C Trapnell, Koh Nakata, Francesco Bonella   +2 more
exaly   +8 more sources

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Pulmonary alveolar proteinosis

Clinics in Chest Medicine, 2004
Pulmonary alveolar proteinosis (PAP) has been recognized for almost half a century. At least three separate pathophysiologic mechanisms may lead to the characteristic feature of PAP: the excessive accumulation of surfactant lipoprotein in pulmonary alveoli, with associated disturbance of pulmonary gas exchange. The prognosis for adult patients with PAP
Presneill, JJ, Nakata, K, Inoue, Y, Seymour, JF   +3 more
openaire   +5 more sources

Pulmonary Alveolar Proteinosis

Radiology, 1969
Since the original description of pulmonary alveolar proteinosis in 1958 (19), more than 100 cases have been reported. This article indicates the wide spectrum of roentgenographic changes (other than the well known batwing appearance) by reference to 5 patients in the San Francisco area who were examined recently.
J M, Davidson, W M, Macleod
  +7 more sources

Pulmonary Alveolar Proteinosis

Respiration, 1974
A case of alveolar proteinosis of the lungs with sarcoidal reaction of the lymph nodes is reported. The diagnosis was established by histological examination of lung tissue secured during thoracotomy.
J, Kurgan, K, Smigla
openaire   +5 more sources