Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease

EGPA, previously known as Churg-Strauss Syndrome (CSS), is a rare, non-transmissible, medium and small vessel autoimmune vasculitis. We report a case of a 45-year-old lady whose initial presentation was left foot drop, which later on progressed to a sudden onset of vasculitic skin rashes at the back...

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Main Authors: Mak, Woh Wei, Masnammany, Adrian Mark, Wan Azman, Siti Sanaa, Abdullah, Hilmi
Format: Proceeding Paper
Language:English
Published: 2017
Subjects:
Online Access:http://irep.iium.edu.my/59911/
http://irep.iium.edu.my/59911/7/59911-EGPA.pdf
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author Mak, Woh Wei
Masnammany, Adrian Mark
Wan Azman, Siti Sanaa
Abdullah, Hilmi
author_facet Mak, Woh Wei
Masnammany, Adrian Mark
Wan Azman, Siti Sanaa
Abdullah, Hilmi
author_sort Mak, Woh Wei
building IIUM Repository
collection Online Access
description EGPA, previously known as Churg-Strauss Syndrome (CSS), is a rare, non-transmissible, medium and small vessel autoimmune vasculitis. We report a case of a 45-year-old lady whose initial presentation was left foot drop, which later on progressed to a sudden onset of vasculitic skin rashes at the background of longstanding poorly controlled bronchial asthma
first_indexed 2025-11-14T16:52:31Z
format Proceeding Paper
id iium-59911
institution International Islamic University Malaysia
institution_category Local University
language English
last_indexed 2025-11-14T16:52:31Z
publishDate 2017
recordtype eprints
repository_type Digital Repository
spelling iium-599112018-01-03T03:15:05Z http://irep.iium.edu.my/59911/ Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease Mak, Woh Wei Masnammany, Adrian Mark Wan Azman, Siti Sanaa Abdullah, Hilmi RC582 Specialities of Internal Medicine- Immunologic Diseases EGPA, previously known as Churg-Strauss Syndrome (CSS), is a rare, non-transmissible, medium and small vessel autoimmune vasculitis. We report a case of a 45-year-old lady whose initial presentation was left foot drop, which later on progressed to a sudden onset of vasculitic skin rashes at the background of longstanding poorly controlled bronchial asthma 2017 Proceeding Paper NonPeerReviewed application/pdf en http://irep.iium.edu.my/59911/7/59911-EGPA.pdf Mak, Woh Wei and Masnammany, Adrian Mark and Wan Azman, Siti Sanaa and Abdullah, Hilmi (2017) Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease. In: Pahang Research Day 2017, 12th October 2017, Kuantan, Pahang. (Unpublished)
spellingShingle RC582 Specialities of Internal Medicine- Immunologic Diseases
Mak, Woh Wei
Masnammany, Adrian Mark
Wan Azman, Siti Sanaa
Abdullah, Hilmi
Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease
title Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease
title_full Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease
title_fullStr Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease
title_full_unstemmed Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease
title_short Eosinophilic Granulomatosis with Polyangitis (EGPA) with foot drop. A rare presentation of a rare disease
title_sort eosinophilic granulomatosis with polyangitis (egpa) with foot drop. a rare presentation of a rare disease
topic RC582 Specialities of Internal Medicine- Immunologic Diseases
url http://irep.iium.edu.my/59911/
http://irep.iium.edu.my/59911/7/59911-EGPA.pdf