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http://dx.doi.org/10.1016/j.jaip.2024.04.046 | DOI Listing |
J Bras Pneumol
July 2024
Universidade Federal do Rio de Janeiro, Rio de Janeiro (RJ) Brasil.
J Allergy Clin Immunol Pract
July 2024
Department of Medicine, Department of Pediatrics, University of Illinois at Chicago, Chicago, Ill.
J Transl Autoimmun
June 2024
Internal Medicine Department, Health Research Institute Puerta de Hierro-Segovia de Arana (IDIPHIM) Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
Introduction: Patients with sarcoidosis have a lower survival rate than the general population, in part due to cardiovascular disease, infections and neoplasms. Our objective was to evaluate the impact of haematological neoplasms (HN) and lymphomas on sarcoidosis patient mortality in a nation-wide analysis conducted in Spain, a country with a population of 47 million.
Methods: Retrospective and observational comparison of the HN related deaths in sarcoidosis patients and the general Spanish population reported in the Spanish Hospital Discharge Database.
J Hematol
December 2023
Banner Health, Tucson, AZ, USA.
Sarcoidosis is a multisystem disorder characterized by granulomatous inflammation on histopathological evaluation. Diagnosis of sarcoidosis requires thorough elimination of malignancy and alternative causes of noncaseating granulomatous inflammation. Sarcoidosis and several subtypes of lymphoma have similar clinical presentations and can potentially have similar histopathological findings.
View Article and Find Full Text PDFOchsner J
January 2023
Department of Hospital Medicine, Ochsner Clinic Foundation, New Orleans, LA.
Agenesis of the internal carotid artery (ICA) is a rare congenital malformation that is often asymptomatic until the fourth or fifth decade. ICA agenesis is associated with several intracranial pathologies, the most reported being intracranial aneurysms, thought to be attributable to the increased flow in the collateral vessels supplying the anterior circulation. The cause of ICA agenesis is largely unknown and has not been consistently associated with any genetic mutations or syndromes.
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