Eosinophilic granulomatosis with polyangiitis (EGPA) is an exceptionally rare systemic necrotizing vasculitis. The disease is clinically characterized by asthma with concomitant blood and tissue eosinophilia, often progressing to eosinophilic vasculitis. From the Onset of asthma, there is usually a three to nine year delay of EGPA diagnosis. We report a case of this highly uncommon disease identified in an early stage.
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All India Inst Med Sci, Dept Dermatol, Gorakhpur, Uttar Pradesh, IndiaAll India Inst Med Sci, Dept Dermatol, Gorakhpur, Uttar Pradesh, India
Shukla, Ratnakar
Kandikatla, Ashwini
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HBT Med Coll, Dept Dermatol, Mumbai, Maharashtra, India
Dr RN Cooper Municipal Gen Hosp, Mumbai, Maharashtra, IndiaAll India Inst Med Sci, Dept Dermatol, Gorakhpur, Uttar Pradesh, India
Kandikatla, Ashwini
Nadkarni, NitinJ
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Dr DY Patil Med Coll, Dept Dermatol, Mumbai, Maharashtra, IndiaAll India Inst Med Sci, Dept Dermatol, Gorakhpur, Uttar Pradesh, India
Nadkarni, NitinJ
Patil, Anant
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Dr DY Patil Med Coll, Dept Pharmacol, Mumbai, Maharashtra, IndiaAll India Inst Med Sci, Dept Dermatol, Gorakhpur, Uttar Pradesh, India
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Ohio State Univ, Dept Internal Med, Div Dermatol, Columbus, OH 43210 USAOhio State Univ, Dept Internal Med, Div Dermatol, Columbus, OH 43210 USA
Korman, Abraham M.
Chung, Catherine G.
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Ohio State Univ, Dept Internal Med, Div Dermatol, Columbus, OH 43210 USA
Ohio State Univ, Dept Pathol, Columbus, OH 43210 USAOhio State Univ, Dept Internal Med, Div Dermatol, Columbus, OH 43210 USA