Eosinophilic Granulomatosis with Polyangiitis (EGPA) - A Case Review
AMINA BEEVI S
, REMYA RAVEENDRAN V , ANISH A L
EGPA, Necrotizing vasculitis, Multiplex Mononeuropathy, Asthma
Eosinophilic granulomatosis with polyangiitis (EGPA) – is a specific variant of the group of diseases characterized by necrotizing vasculitis of small and medium-sized systemic blood vessels. It is highly variable in its presentation and course; the manifestations may range from mild symptoms (asthma, nasal polyps, cutaneous lesions) to life‐threatening conditions (severe gastrointestinal involvement, heart disease, disabling multiplex mononeuropathy).The condition has a male predisposition. Here we discuss a 44 year-old male patient who presented with weakness and numbness of both upper and lower limb and EGPA was diagnosed following a comprehensive workup
"Eosinophilic Granulomatosis with Polyangiitis (EGPA) - A Case Review", IJSDR - International Journal of Scientific Development and Research (www.IJSDR.org), ISSN:2455-2631, Vol.9, Issue 5, page no.382 - 385, May-2024, Available :https://ijsdr.org/papers/IJSDR2405055.pdf
Volume 9
Issue 5,
May-2024
Pages : 382 - 385
Paper Reg. ID: IJSDR_211319
Published Paper Id: IJSDR2405055
Downloads: 000347360
Research Area: Medical Science
Country: Trivandrum, Kerala, India
ISSN: 2455-2631 | IMPACT FACTOR: 9.15 Calculated By Google Scholar | ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 9.15 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator
Publisher: IJSDR(IJ Publication) Janvi Wave