The Churg-Strauss syndrome: An unusual presentation

GK Manu; A Mathew; R Rajesh; G Kurian; VN Unni; GS Pillai; KR Hiran

doi:10.4103/0971-4065.109438

Advertisment

About us | Subscription | e-Alerts | Feedback | Login

| | | | |

Users Online:664

Official publication of the Indian Society of Nephrology

~ Next article

~ Previous article

~ Table of Contents

~ Similar in PUBMED

~ Search Pubmed for

~ Search in Google Scholar for

~Related articles

~ Citation Manager

~ Access Statistics

~ Reader Comments

~ Email Alert *

~ Add to My List *

* Requires registration (Free)

Article Access Statistics

Viewed	2693

Printed	58

Emailed	0

PDF Downloaded	110

Comments	[Add]

Cited by others	1

Click on image for details.

CASE REPORT

Year : 2013 | Volume : 23 | Issue : 2 | Page : 133-136

The Churg-Strauss syndrome: An unusual presentation

GK Manu¹, A Mathew¹, R Rajesh¹, G Kurian¹, VN Unni¹, GS Pillai², KR Hiran³
¹ Department of Nephrology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India
² Department of Opthalmology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India
³ Department of Pathology, Amrita Institute of Medical Sciences and Research Centre, Kochi, India

Correspondence Address:
V N Unni
Department of Nephrology, Amrita Institute of Medical Sciences and Research Centre, Kochi - 682 041
India

Source of Support: None, Conflict of Interest: None

Check

DOI: 10.4103/0971-4065.109438

The Churg-strauss syndrome (CSS), also referred to as allergic angiitis and granulomatosis is characterized by asthma, peripheral and tissue eosinophilia, extravascular granuloma formation, and vasculitis of multiple organ systems. It is an uncommon disease with an estimated annual incidence of 1-3 per million. Here, we report a case of CSS with glomerulocentric granulomatous reaction with interstitial eosinophils and involvement of retinal vessels.

[FULL TEXT] [PDF]*