Rheumatoid arthritis in patient with homozygous haemoglobin C disease
作者： Sanae Ali Ou Alla , Fadoua Allali , Najia Hajjaj-Hassouni
DOI: 10.1007/S00296-009-1230-Y
关键词:
摘要: To date, few cases of hemoglobinopathies in patients with rheumatoid arthritis (RA) have been reported (Marino and Mcdonald J Rheumatol 17:970–972, 1990; Gladman Bombardier Arthritis Rheum 30:1065–1068, 1987; Michel et al. Semin 38:228–240, 2008). These haemoglobin diseases are associated characteristics abnormalities the skeleton. Haemoglobin C disease is a benign hemoglobinopathy rarely skeletal disorders [Pieron la semaine des hopitaux 57(1–2):22–25, 1981]. We report case RA 60-year-old woman homozygous disease. This coexistence may be pure coincidence, although we discuss difficulties treatment this due to unknown effect anti-rheumatic drugs on progression
springer.com
sci-hub.se 参考文章(13)
M Sadat-Ali, A H Al Elq, Sickle cell anaemia: is it a cause for secondary osteoporosis? West African journal of medicine. ,vol. 26, pp. 134- 137 ,(2007)
P.A. Tyler, G. Madani, R. Chaudhuri, L.F. Wilson, E.A. Dick, The radiological appearances of thalassaemia. Clinical Radiology. ,vol. 61, pp. 40- 52 ,(2006) , 10.1016/J.CRAD.2005.07.006
M. Michel, A. Habibi, B. Godeau, D. Bachir, A. Lahary, F. Galacteros, A. Fifi-Mah, S. Arfi, Characteristics and Outcome of Connective Tissue Diseases in Patients with Sickle-Cell Disease: Report of 30 Cases Seminars in Arthritis and Rheumatism. ,vol. 38, pp. 228- 240 ,(2008) , 10.1016/J.SEMARTHRIT.2007.10.003
Redonda G Miller, Jodi B Segal, Bimal H Ashar, Sophia Leung, Shamim Ahmed, Shabina Siddique, Tasha Rice, Sophie Lanzkron, None, High prevalence and correlates of low bone mineral density in young adults with sickle cell disease American Journal of Hematology. ,vol. 81, pp. 236- 241 ,(2006) , 10.1002/AJH.20541
Dafna D. Gladman, Claire Bombardier, Sickle cell crisis following intraarticular steroid therapy for rheumatoid arthritis. Arthritis & Rheumatism. ,vol. 30, pp. 1065- 1068 ,(1987) , 10.1002/ART.1780300916
Jacques Simpore, Salvatore Pignatelli, Sergio Barlati, Salvatore Musumeci, BIOLOGICAL AND CLINICAL PRESENTATION OF PATIENTS WITH HEMOGLOBINOPATHIES ATTENDING AN URBAN HOSPITAL IN OUAGADOUGOU: CONFIRMATION OF THE MODIFICATION OF THE BALANCE BETWEEN Hb S AND Hb C IN BURKINA FASO Hemoglobin. ,vol. 26, pp. 121- 127 ,(2002) , 10.1081/HEM-120005449
C. Montecucco, R. Caporali, S. Rossi, O. Epis, RHEUMATOID ARTHRITIS IN BETA-THALASSAEMIA TRAIT Rheumatology. ,vol. 38, pp. 1021- 1022 ,(1999) , 10.1093/RHEUMATOLOGY/38.10.1021
G. Castellino, M. Govoni, F. Trotta, Rheumatoid arthritis in β‐thalassaemia trait Rheumatology. ,vol. 39, pp. 1286- 1287 ,(2000) , 10.1093/RHEUMATOLOGY/39.11.1286
Kevin J. Murray, Kiran Nistala, Co-existent sickle cell disease and juvenile rheumatoid arthritis. Two cases with delayed diagnosis and severe destructive arthropathy. The Journal of Rheumatology. ,vol. 28, pp. 2125- 2128 ,(2001)
Xanthi Giakoumi, Maria Tsironi, Charalampos Floudas, Evangelos Polymeropoylos, Efstathios Papalambros, Athanassios Aessopos, None, Rheumatoid arthritis in thalassemia intermedia: coincidence or association? Israel Medical Association Journal. ,vol. 7, pp. 667- 669 ,(2005)