Abstract |
Behçet's disease (BD) is a multisystem inflammatory vasculitis of unknown etiology and pathogenesis. Coexistence of BD along with hematological malignancies is extremely rare. We describe a patient diagnosed with BD and chronic myelomonocytic leukaemia (CMML) with trisomy 8. This case suggests that trisomy 8 may be involved in the concurrent manifestation of myelodysplastic syndrome (MDS) and BD with gastrointestinal ulcers.
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Authors | M G Mantzourani, K Chantziara, I Thanopoulou, H Variami, G Vaiopoulos, G A Pangalis |
Journal | Clinical and experimental rheumatology
(Clin Exp Rheumatol)
Vol. 27
Issue 2 Suppl 53
Pg. S85-7
( 2009)
ISSN: 0392-856X [Print] Italy |
PMID | 19796540
(Publication Type: Case Reports, Journal Article)
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Topics |
- Aged
- Behcet Syndrome
(complications)
- Chromosomes, Human, Pair 8
- Humans
- Karyotyping
- Leukemia, Myelomonocytic, Chronic
(complications, genetics)
- Male
- Trisomy
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