Background: Hereditary alpha 1-antitrypsin deficiency may be very rarely as
sociated with chronic panniculitis and is therefore often diagnosed only wi
th delay.
Case Report: The typical clinical features of the disease are described in
a 37-year-old woman. This case underlines the importance of determining alp
ha 1-antitrypsin levels in patients with chronic relapsing panniculitis. Th
erapeutic approaches are discussed.