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Granulomatose med polyangiitis er en vigtig differentialdiagnose til cancer

Forfatter(e)
Kresten Krarup Keller, Berit Dalsgaard Nielsen, Ellen Margrethe Hauge & Ib Tønder Hansen Reumatologisk Afdeling U, Aarhus Universitetshospital Ugeskr Læger 2015;177:V12140722
Reference: 
Ugeskr Læger 2015;177:V12140722
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Granulomatosis with polyangiitis – a rare but important differential diagnosis
Granulomatosis with polyangiitis (GPA) is a rare disease with inflammation in the small vessels. This is a case report of GPA, where lung cancer was initially suspected. A 54-year-old woman eventually developed manifestations from several organ systems, and a diagnosis of GPA was confirmed. Treatment was initiated, but the neurological manifestations proved to be irreversible. This case illustrates that GPA is important to acknowledge, because timely treatment is crucial to reduce mortality and morbidity.
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