98%
921
2 minutes
20
Systemic lupus erythematosus (SLE) is a complex autoimmune disease with multiorgan manifestations, including pleuropulmonary involvement (20-90%). The precise mechanism of pleuropulmonary involvement in SLE is not well-understood; however, systemic type 1 interferons, circulating immune complexes, and neutrophils seem to play essential roles. There are eight types of pleuropulmonary involvement: lupus pleuritis, pleural effusion, acute lupus pneumonitis, shrinking lung syndrome, interstitial lung disease, diffuse alveolar hemorrhage (DAH), pulmonary arterial hypertension, and pulmonary embolism. DAH has a high mortality rate (68-75%). The diagnostic tools for pleuropulmonary involvement in SLE include chest X-ray (CXR), computed tomography (CT), pulmonary function tests (PFT), bronchoalveolar lavage, biopsy, technetium-99m hexamethylprophylene amine oxime perfusion scan, and (18)F-fluorodeoxyglucose positron emission tomography. An approach for detecting pleuropulmonary involvement in SLE includes high-resolution CT, CXR, and PFT. Little is known about specific therapies for pleuropulmonary involvement in SLE. However, immunosuppressive therapies such as corticosteroids and cyclophosphamide are generally used. Rituximab has also been successfully used in three of the eight pleuropulmonary involvement forms: lupus pleuritis, acute lupus pneumonitis, and shrinking lung syndrome. Pleuropulmonary manifestations are part of the clinical criteria for SLE diagnosis. However, no review article has focused on the involvement of pleuropulmonary disease in SLE. Therefore, this article summarizes the literature on the epidemiology, pathogenesis, diagnosis, and management of pleuropulmonary involvement in SLE.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9698564 | PMC |
http://dx.doi.org/10.3390/jcm11226714 | DOI Listing |
Biomedicines
July 2025
Department of Pulmonology, Mother and Child Health Care Institute of Serbia, 11070 Beograd, Serbia.
: Primary malignant lung tumors in children are rare and diagnostically challenging. This study presents a single-center experience in the diagnosis and treatment of these tumors, emphasizing the role of histopathological and genetic profiling in informing individualized therapeutic strategies. : We retrospectively reviewed records of seven pediatric patients (ages 2-18) treated from 2015 to 2025.
View Article and Find Full Text PDFCureus
August 2025
Chest Diseases, Alexandria University Faculty of Medicine, Alexandria, EGY.
Amyloidosis is an uncommon disease characterized by the buildup of misfolded protein fibrils outside cells in various tissues. Its diagnosis relies on tissue biopsy confirmation. Due to its diverse clinical presentations, diagnosis is often delayed.
View Article and Find Full Text PDFJ Thorac Dis
June 2025
Department of Thoracic Surgery, National Institute of Respiratory Diseases "Ismael Cosío Villegas", Mexico City, Mexico.
Background: It has been reported that up to 30% of patients with empyema require surgical intervention, with procedures such as the Clagett pleural window or the Eloesser flap being the last resort. The objective of this study was to compare the postoperative outcomes of patients undergoing a conventional thoracic window versus a modified technique.
Methods: We conducted a retrospective cohort study between 2012 and 2023 of patients who underwent a conventional or modified thoracic window.
Discov Oncol
July 2025
Department of Thoracic Surgery, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, NO.9 Jinsui Road, Tianhe District, Guangzhou, 510000, China.
Background: Pleuropulmonary blastoma (PPB) is a rare pediatric sarcoma often associated with DICER1 mutations. However, additional genetic factors may influence disease progression and prognosis. This study identifies a novel mutation in the GPC3 gene and evaluates its potential as a prognostic biomarker in PPB.
View Article and Find Full Text PDFRev Mal Respir
July 2025
Centre de lutte antituberculeuse de Nice, Hôpital Pasteur, 30, voie Romaine, 06000 Nice, France. Electronic address:
Introduction: Ruxolitinib is a Janus kinase 2 inhibitor (JAK2i) used in patients with primary myelofibrosis. This treatment is a risk factor for bacterial and viral infections, and can reactivate latent infections, such as tuberculosis.
Observation: We report the case of a 80-year-old patient hospitalized for disseminated tuberculosis.