Results 91 to 100 of about 8,530 (199)

The Paradox of Metachronous Lipoid Pneumonia

open access: yesRespirology Case Reports, Volume 13, Issue 9, September 2025.
This is a case of recurrent exogenous lipoid pneumonia in a single patient caused by multiple unrelated substances. This case underscores the diagnostic value of radiologic patterns, the significance of meticulous exposure history, and the necessity of contemplating alternative aetiologies in patients with new infiltrates during cancer therapy ...
Haruki Kobayashi
wiley   +1 more source

Neumonía lipídica endógena en 2 gatos de raza Persa [PDF]

open access: yes, 2006
En este trabajo se describen dos casos de neumonía lipídica endógena en dos gatos de raza persa. En ambos se llegó al diagnóstico por necropsia. Se describen los tratamientos aplicados y se discute el diagnóstico y tratamientos de elección, así como ...
Avellaneda, Ana, Font Utset, Artur
core  

Niche signals and transcription factors involved in tissue-resident macrophage development [PDF]

open access: yes, 2018
Tissue-resident macrophages form an essential part of the first line of defense in all tissues of the body. Next to their immunological role, they play an important role in maintaining tissue homeostasis. Recently, it was shown that they are primarily of
Bonnardel, Johnny   +2 more
core   +2 more sources

Macrophages: Subtypes, Distribution, Polarization, Immunomodulatory Functions, and Therapeutics

open access: yesMedComm, Volume 6, Issue 8, August 2025.
Macrophages originate from the yolk sac, fetal liver, and bone marrow, differentiating into two main subtypes: M1‐like (proinflammatory) and M2‐like (anti‐inflammatory). These subtypes exhibit high plasticity, allowing them to transform in response to environmental cues or therapeutic interventions.
Mengyuan Peng   +10 more
wiley   +1 more source

A case of uncomplicated pulmonary alveolar proteinosis evolving to pulmonary fibrosis

open access: yesMonaldi Archives for Chest Disease, 2016
Pulmonary alveolar proteinosis (PAP) is a rare syndrome characterised by intra-alveolar accumulation of surfactant components and cellular debris, with minimal interstitial inflammation or fibrosis.
A. Chroneou   +4 more
doaj   +1 more source

CLINICAL APPLICABILITY OF PROPOSED ALGORITHM FOR IDENTIFYING INDIVIDUALS AT RISK FOR HEREDITARY HEMATOLOGIC MALIGNANCIES [PDF]

open access: yes, 2017
Over the past decade, more than 12 genes have been identified to cause hereditary predispositions to hematologic malignancies. These syndromes are characterized by an increased risk to develop myelodysplastic syndrome (MDS), acute myeloid leukemia (AML),
Clifford, Maggie
core   +1 more source

Venoarterial extracorporeal membrane oxygenation (ECMO) for support during whole lung lavage for pulmonary alveolar proteinosis. [PDF]

open access: yes, 2012
INTRODUCTION ECMO as support during whole lung lavage (WLL) for pulmonary alveolar proteinosis is reserved for severe cases where oxygenation is inadequate to support the patient using the ventilator alone.
Cavarocchi, Nicholas C   +4 more
core   +2 more sources

Therapy options in pulmonary alveolar proteinosis

open access: yesTherapeutic Advances in Respiratory Disease, 2010
Pulmonary alveolar proteinosis is a rare condition characterized by the accumulation of lipoproteinaceous material within the airspaces, resulting in impaired gas transfer, and clinical manifestations ranging from asymptomatic to severe respiratory ...
Maurizio Luisetti   +5 more
doaj   +1 more source

Synovial tissue macrophages: friend or foe? [PDF]

open access: yes, 2017
Healthy synovial tissue includes a lining layer of synovial fibroblasts and macrophages. The influx of leucocytes during active rheumatoid arthritis (RA) includes monocytes that differentiate locally into proinflammatory macrophages, and these produce ...
Alivernini, Stefano   +1 more
core   +2 more sources

Lung surfactant in subacute pulmonary disease

open access: yesRespiratory Research, 2002
Pulmonary surfactant is a surface active material composed of both lipids and proteins that is produced by alveolar type II pneumocytes. Abnormalities of surfactant in the immature lung or in the acutely inflamed mature lung are well described.
Spragg Roger G, Devendra Gehan
doaj   +1 more source

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