TY  - CHAP
M1  - Book, Section
TI  - Chapter 34. Eosinophilic Granulomatosis with Polyangiitis (Churg-Strauss Syndrome)
A1  - Seo, Philip
A1  - Stone, John H.
A2  - Imboden, John B.
A2  - Hellmann, David B.
A2  - Stone, John H.
Y1  - 2013
N1  - 
T2  - CURRENT Diagnosis & Treatment: Rheumatology, 3e
AB  - Asthma,  eosinophilia,  and  systemic  vasculitis  are  the  hallmarks  of  eosinophilic  granulomatosis  with  polyangiitis  (EGPA;  Churg-Strauss  syndrome).Classic  clinical  features  include  the  following:Allergic  rhinitis  and  nasal  polyposis.Reactive  airway  disease.Peripheral  eosinophilia  (10–60%  of  all  circulating  leukocytes).Fleeting  pulmonary  infiltrates  and  occasional  alveolar  hemorrhage.Vasculitic  neuropathy.Congestive  heart  failure.Approximately  50%  of  patients  with  EGPA  have  antineutrophil  cytoplasmic  antibodies  (ANCAs),  usually  with  a  specificity  for  myeloperoxidase  (MPO).  
SN  - 
PB  - The McGraw-Hill Companies
CY  - New York, NY
Y2  - 2024/04/19
UR  - accessmedicine.mhmedical.com/content.aspx?aid=57273337
ER  -