Neurological Complications in Eosinophilic Granulomatosis with Polyangiitis (EGPA): The Roles of History and Physical Examinations in the Diagnosis of EGPA

Author:

Oiwa Hiroshi1,Mokuda Sho1,Matsubara Tomoyasu2,Funaki Masamoto1,Takeda Ikuko2,Yamawaki Takemori3,Kumagai Kazuhiko4,Sugiyama Eiji4

Affiliation:

1. Department of Rheumatology, Hiroshima City Hiroshima Citizens Hospital, Japan

2. Department of Clinical Neuroscience and Therapeutics, Hiroshima University, Japan

3. Department of Neurology, Hiroshima City Hiroshima Citizens Hospital, Japan

4. Department of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Reference17 articles.

1. 1. Jennette JC, Falk RJ, Bacon PA, et al. 2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheum 65: 1-11, 2013.

2. 2. Masi AT, Hunder GG, Lie JT, et al. The American College of Rheumatology 1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiitis). Arthritis Rheum 33: 1094, 1990.

3. 3. Adams and Victor's Principles of Neurology, 10th ed. Ropper AH, Samuels MA, Klein JP, Eds. Distribution of the sensory spinal roots on the surface of the body (dermatomes). McGraw-Hill Education, Boston, 2014: beginning of the book.

4. 4. Sinico RA, Bottero P. Churg-Strauss angiitis. Best Pract Res Clin Rheumatol 23: 355-366, 2009.

5. 5. Oiwa H, Nishioka K. Janeway lesions in eosinophilic granulomatosis with polyangiitis. Intern Med 55: 549-550, 2016.

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