| Autor: |
Barbosa FB; Centro de Ensino Superior do Pará, Belém, PA, Brasil., Callegari A; Santa Casa de Misericórdia, São Paulo, SP, Brasil., Sarinho JC; Santa Casa de Misericórdia, São Paulo, SP, Brasil., Lucena J; Santa Casa de Misericórdia, São Paulo, SP, Brasil., Casagrande R; Santa Casa de Misericórdia, São Paulo, SP, Brasil., de Souza BD; Faculdade de Ciências Médicas da Santa Casa de São Paulo, São Paulo, SP, Brasil. |
| Abstrakt: |
This is a report of a patient who had a previous diagnosis of rheumatoid arthritis, nonerosive, rheumatoid factor negative, that despite the therapeutic approach presented progressive worsening of the articular and general condition. After extensive research, she had a diagnosis of hemochromatosis. Joint symptoms are common manifestations in hemochromatosis. The arthropathy of hemochromatosis may resemble inflammatory arthropathy mimicking RA, particularly in the most common sites as 2nd and 3rd metacarpophalangeal. Radiologically are observed decreased joint space, subchondral sclerosis, cyst formation and chondrocalcinosis. Treatment with disease modifying drugs for rheumatoid arthritis tend to worsen the clinical picture, since the liver is the major site of deposition of iron in hemochromatosis and these medications are known to be hepatotoxic. Phlebotomy treatment for hemochromatosis is apparently ineffective in reversing the articular manifestations, which requires the association with iron chelating drugs. Due to the apparent difficulty in differentiating between the two diseases, a screening profile of iron in patients with rheumatoid arthritis with atypical progression is necessary. |
