Weber-Christian disease is a
skin condition that features recurring
inflammation in the
subcutaneous fat layer and systemic symptoms. The
disease is a
diagnosis of exclusion characterized by a lobular
panniculitis without
vasculitis in histopathology. We
report an 80-year-old man with constitutional symptoms and relapsing nonsuppurative nodular
panniculitis. The purpose of the case described is to emphasize that
rare diseases may occur, therefore their
diagnosis can only be made with previous medical
knowledge and the delay, or even the absence, in the
diagnosis of these
pathologies could interfere with the
quality of life of
patients. (AU)