Churg-Strauss syndrome historical perspective
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Krzysztof Wierzbicki M.D. [3]Chandrakala Yannam, MD [4]
Overview
Two pathologists Churg and Strauss first described disease in 1951. They named it as allergic granulomatosis with angiitis. Over the years, they called the disease by the name of Churg-Strauss syndome. In 2010, American college of rheumatology changed this name to eosinophilic granulomatosis with polyangiitis based on histopathology.
Historical Perspective
- In 1951, Russian born American pathologist Jacob Churg along with German born, American pathologist Lotte Strauss first described the disease as allergic granulomatosis, allergic angiitis, and periarteritis nodosa.[1][2][3]
- The name 'Churg-Strauss syndrome has' been changed to 'Eosinophilic granulomatosis with polyangiitis' in 2010 by the American College of Rheumatology, and the European League Against Rheumatism. The name has been changed to characterize the pathology of the disease rather than having it remain as a historical reference. [4]
References
- ↑ CHURG J, STRAUSS L (1951). "Allergic granulomatosis, allergic angiitis, and periarteritis nodosa". Am J Pathol. 27 (2): 277–301. PMC 1937314. PMID 14819261.
- ↑ Template:WhoNamedIt
- ↑ Churg J, Strauss L (1951). "Allergic granulomatosis, allergic angiitis, and periarteritis nodosa". Am. J. Pathol. 27 (2): 277–301. PMID 14819261.
- ↑ Falk RJ, Gross WL, Guillevin L, Hoffman GS, Jayne DR, Jennette JC; et al. (2011). "Granulomatosis with polyangiitis (Wegener's): an alternative name for Wegener's granulomatosis". Arthritis Rheum. 63 (4): 863–4. doi:10.1002/art.30286. PMID 21374588.