نتایج جستجو برای: familial sarcoidosis

تعداد نتایج: 64953  

Journal: :Eurasian Journal of Pulmonology 2017

2014
Wojciech J. Piotrowski Paweł Górski Joanna Duda-Szymańska Sylwia Kwiatkowska

PATIENT Male, 26 FINAL DIAGNOSIS: Sarcoidosis Symptoms: Disseminated lung parenchymal changes Medication: - Clinical Procedure: - Specialty: Pulmonology. OBJECTIVE Rare disease. BACKGROUND Sarcoidosis is a granulomatous inflammatory disease that is induced by unknown antigen(s) in a genetically susceptible host. Although the direct link between Mycobacterium tuberculosis (MTB) infection and...

Journal: :The European respiratory journal 2000
M Luisetti A Beretta L Casali

Sarcoidosis is an immune-mediated, multiorgan, granulomatous disorder thought to be triggered by an intricate combination of environmental and genetic factors. Two robust lines of evidence support the hypothesis of a genetic component in the pathogenesis of sarcoidosis: racial variation in its epidemiology and familial clustering of cases. The relationship between epidemiology and environmental...

Journal: :Postgraduate medical journal 1974
D G James E Neville K H Piyasena A N Walker A N Hamlyn

Five families (three English, one Irish, one West Indian) contained eleven members with sarcoidosis, nine of whom have been investigated and followed. Their multisystem involvement and course was similar to that of other patients attending the Sarcoidosis Clinic at the Royal Northern Hospital. There were three brother-sister and two mother-offspring relations; it was not observed in a father-of...

Journal: :Archives of dermatology 2007
Julie V Schaffer Pranil Chandra Brian R Keegan Patricia Heller Helen T Shin

BACKGROUND Pediatric sarcoidosis has traditionally been divided into 2 distinct groups: (1) school-aged children and adolescents with frequent involvement of the lungs and mediastinal lymph nodes (similar to adult sarcoidosis) and (2) infants and preschoolers with the triad of arthritis, uveitis, and a cutaneous eruption of discrete small papules, referred to as early-onset sarcoidosis. Blau sy...

2014
Joseph E. Rotsinger Wonder P. Drake

Sarcoidosis is an idiopathic multisystem disorder characterized by noncaseating epithelioid granulomas predominately affecting lungs and lymph nodes, but with potential to affect any organ system. Sarcoidosis shares similarities in development to other infectious granulomatous diseases, such as berylliosis and tuberculosis; however, its elusive etiology and non-distinctive histology have provid...

Journal: :Chest 2001
O P Sharma

S arcoidosis is an antigen-driven, multisystem, granulomatous disorder, the cause of which is not known. In a genetically susceptible individual, antigen-presenting cells trap, process, and present the putative antigen, in the context of class II major histocompatibility complex (MHC) molecules, to CD41 lymphocytes. The result of this union is a coordinated release of cytokines and chemokines, ...

Journal: :European Journal of Rheumatology 2017

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