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DOI 10.1097/md.0000000000000011

Медицинская библиотека · Medicine · 2014

Inflammatory arthritis in patients with myelodysplastic syndromes: a multicenter retrospective study and literature review of 68 cases.

Mekinian Arsène, Braun Thorsten, Decaux Olivier, Falgarone Géraldine, Toussirot Eric, Raffray Loic, Omouri Mohamed, Gombert Bruno, De Wazieres Benoit, Buchdaul Anne-Laure, Ziza Jean-Marc, Launay David, Denis Guillaume, Madaule Serge, Rose Christian, Grignano Eric, Fenaux Pierre, Fain Olivier, Club Rhumatismes et Inflammation (CRI), Groupe Francophone des Myélodysplasies (GFM), and Société Nationale Française de Médecine Interne (SNFMI)

Клинический случайСтатьяМногоцентровое исследованиеОбзорПеревод в очереди

Аннотация

We describe the characteristics and outcome of inflammatory arthritis in patients with myelodysplastic syndrome (MDS) in a French multicenter retrospective study. Twenty-two patients with MDS (median age, 77.5 yr [interquartile range, 69-81]; 10 women) were included. Inflammatory arthritis presented as polyarthritis in 17 cases (77%) and with symmetric involvement in 15 cases (68%). At diagnosis, the median disease activity score 28 based on C-reactive protein (DAS28-CRP) was 4.5 [2-6.5]. Two patients had anti-citrullinated protein antibodies (ACPAs), and 1 had radiologic erosions. The median time between the diagnoses of arthritis and MDS was 10 months [6-42], with a median articular symptom duration of 3 months [2-8]. The diagnosis of both diseases was concomitant in 6 cases (27%); arthritis preceded MDS in 12 cases (55%), and occurred after MDS in 4 (18%). While the number of swollen and tender joints significantly decreased during follow-up, as did the median DAS28-CRP (from 4.3 [3.8-4.6] at baseline to 2.9 [1.75-3.3]; p < 0.05), CRP remained elevated (CRP >20 mg/L) in 8 patients (42%). Nevertheless, radiographic progression and new ACPA positivity were not observed during a median follow-up of 29 months [9-76]. While most of the patients were treated with steroids (n = 16) for arthritis, additional treatment was administered in only 4 patients (hydroxychloroquine, n = 2; sulfasalazine [Salazopyrin] and etanercept, n = 1, respectively). Eleven patients died during follow-up from acute myeloid leukemia (n = 5); infections (n = 3); or cerebral bleeding, cardiorespiratory failure, or undetermined cause (n = 1, respectively). Inflammatory arthritis associated with MDS can have various presentations and is often seronegative and nonerosive. Steroids alone are the most common treatment in MDS-associated arthritis, but that treatment is insufficient to control arthritis. Steroid-sparing strategies need to be identified.

Для цитирования: Mekinian Arsène, Braun Thorsten, Decaux Olivier, Falgarone Géraldine, Toussirot Eric, Raffray Loic, Omouri Mohamed, Gombert Bruno, De Wazieres Benoit, Buchdaul Anne-Laure, Ziza Jean-Marc, Launay David, Denis Guillaume, Madaule Serge, Rose Christian, Grignano Eric, Fenaux Pierre, Fain Olivier, Club Rhumatismes et Inflammation (CRI), Groupe Francophone des Myélodysplasies (GFM), and Société Nationale Française de Médecine Interne (SNFMI). Inflammatory arthritis in patients with myelodysplastic syndromes: a multicenter retrospective study and literature review of 68 cases.. Medicine. 2014. DOI: 10.1097/md.0000000000000011.

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