[Acute pancreatitis and spontaneous rupture of pancreatic pseudocyst in systemic lupus erythematosus].

Autor: Campos CF; Médica residente do Serviço de Clínica Médica do HUGV-UFAM., Scrignoli JA, de Almeida LP, Ferreira BL, Ribeiro SL, de Lima DS, Passos LF
Jazyk: portugalština
Zdroj: Acta reumatologica portuguesa [Acta Reumatol Port] 2010 Apr-Jun; Vol. 35 (2), pp. 236-40.
Abstrakt: Systemic Lupus Erythematosus (SLE) is an autoimmune disease, with multisystemic involvement. Gastrointestinal symptoms are common, like nausea, vomiting and dyspepsia. Acute pancreatitis is an unusual manifestation of SLE, being an important differential diagnosis in evaluation of abdominal pain. The patients usually presents with pain of variable intensity, some occasions simulating acute abdomen. Several factors have been implicated in the pathogenesis of this condition, such as vasculitis, drugs and antiphospholipid antibodies. The role of corticosteroids as etiologic factor remains controversial. Due to the rarity of SLE associated to pancreatitis, we report two cases of patients with severe inflammatory process. In one case, it was used corticosteroids in high doses during treatment, with good outcome. In another, the patient died because of pancreatic pseudocyst rupture and its postoperative hemodynamic complications. In the reported cases, predisposing factors for acute pancreatitis were not verified, so it was considered a primary manifestation of SLE activity.
Databáze: MEDLINE