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Behcet’s Disease Multiple Faces - Observation on a Case
Authors: Alina Dobroş , Marius Irimie
Number of views: 814
Behcet’s disease is a chronic, inflammatory multisystemic condition of unknown aetiology. It is
clinically characterized by recurrent orogenital ulcera
tions and skin eruptions, ocular manifestations, arthri-
tis, vasculitis and in some cases neurological and large
vessel involvement. Aetiology has not been defined,
but genetic, environmental, viral, bacterial and im
munological factors have been proposed as causative
agents.
We present the case of a 32-year-old male patient
that was admitted in our hospital with fever, recur-
rent oral and scrotal aphthous ulcerations, erythemato
us painful nodules on his calves and forearms, arthral-
gias and superficial migratory thrombophlebitis on the
lower limbs. Papulo-pustular lesions were developing
on the venous punction on the right forearm. Laboratory investigations showed an elevated ESR and leuko-
cytosis, and the histopatologic examination of a cutaneous biopsy specimen revealed a perivascular neutro-
philic inflammatory infiltrate on the upper dermis. Di
agnosis of Behcet’s disease was made. Treatment con-
sisted in oral prednisone 1 mg/kgc/day, dapsone 100 mg/day and pentoxiphylline 400 mg/day associated
with topical antiseptics and anaesthetics for oral ulcera
tions, followed by fever remission after 48 hours and
oral ulcerations healing after one week.