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Systemic medium-sized vessel vasculitis associated with chronic myelomonocytic leukemia.
- Source :
-
Seminars in arthritis and rheumatism [Semin Arthritis Rheum] 2001 Oct; Vol. 31 (2), pp. 119-26. - Publication Year :
- 2001
-
Abstract
- Objective: To determine the clinical aspects of systemic vasculitis associated with chronic myelomonocytic leukemia (CMML).<br />Methods: In this retrospective study, 8 patients suffering from systemic vasculitis associated with CMML are described. The French and English literature on systemic vasculitis associated with myelodysplasia was reviewed.<br />Results: All 8 patients had a systemic medium-sized vessel vasculitis which fulfilled the American College of Rheumatology criteria for polyarteritis nodosa in the setting of active CMML. Antineutrophil cytoplasmic antibodies (ANCA) were negative in 7 patients. One patient had cytoplasmic ANCA by indirect immunofluorescence without antiproteinase 3 or antimyeloperoxydase antibodies on the enzyme-linked immunosorbent assay. At presentation, 6 patients had fever of unknown origin, 5 had polymyalgia rheumatica, 3 had sensory hearing loss, and 4 had eosinophilia. None had viral infection or drug-associated vasculitis. Diagnostic procedures included renal or hepatic angiography in 6 patients which showed microaneurysms in 4, skin and temporal artery biopsy in 2 which showed vasculitis, and 1 postmortem examination which showed gastroduodenal arteritis. All patients were treated with corticosteroids, and 7 received immunosuppressive drugs. Death was attributable to vasculitis in 2 cases, infection in 3, and other vasculitis-related causes in 2. In a review of the French-English literature, we found 11 similar cases of ANCA-negative systemic vasculitis, generally associated with refractory anemia, with or without blast excess.<br />Conclusions: Systemic ANCA-negative polyarteritis nodosa-type vasculitis seems closely associated to CMML. Clinical presentation is nonspecific, and systemic vasculitis should be suspected when a patient with myelodysplasia develops atypical manifestations. Renal, gastrointestinal, or hepatic angiography are useful diagnostic procedures when more invasive biopsies should be avoided because of low platelet count. The prognosis of CMML-associated systemic vasculitis is poor.<br /> (Copyright 2001 by W.B. Saunders Company)
- Subjects :
- Aged
Aneurysm diagnosis
Antibodies, Antineutrophil Cytoplasmic blood
Drug Therapy, Combination
Enzyme-Linked Immunosorbent Assay
Fatal Outcome
Female
Fluorescent Antibody Technique, Indirect
Glucocorticoids therapeutic use
Humans
Immunosuppressive Agents therapeutic use
Leukemia, Myelogenous, Chronic, BCR-ABL Positive blood
Leukemia, Myelogenous, Chronic, BCR-ABL Positive drug therapy
Leukemia, Myelogenous, Chronic, BCR-ABL Positive pathology
Male
Middle Aged
Retrospective Studies
Vasculitis blood
Vasculitis drug therapy
Vasculitis pathology
Leukemia, Myelogenous, Chronic, BCR-ABL Positive complications
Vasculitis etiology
Subjects
Details
- Language :
- English
- ISSN :
- 0049-0172
- Volume :
- 31
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Seminars in arthritis and rheumatism
- Publication Type :
- Academic Journal
- Accession number :
- 11590581
- Full Text :
- https://doi.org/10.1053/sarh.2001.27717