骨髓增生异常综合征患者的behet病

Clinical Lymphoma and Myeloma Pub Date : 2009-12-01 DOI:10.3816/CLM.2009.n.090

Erzsebet Kovacs , Hajnalka Nemeth , Bela Telek , Aniko Ujfalusi , Erzsebet Balogh , Eva Pasztor , Gyorgy Pfliegler

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引用次数: 7

摘要

75岁男性，口腔及腹股沟溃疡疼痛。没有任何感染和溃疡的位置表明是behaperet病。随后出现全血细胞减少症，骨髓检查显示骨髓增生异常综合征。细胞遗传学检查显示7q -和20q -，但没有8+。环孢素和皮质类固醇免疫抑制治疗可显著改善临床症状和血液学异常。

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Behçet's Disease in a Patient With Myelodysplastic Syndrome

A 75-year-old man presented with painful oral and groin ulcers. The lack of any infections and the location of the ulcers suggested Behçet's disease. Subsequently, pancytopenia developed and bone marrow examination revealed myelodysplastic syndrome. Cytogenetic examination revealed 7q— and 20q— but not 8+. Immunosuppressive therapy with cyclosporine and corticosteroid resulted in a dramatic improvement in both clinical signs and hematologic abnormalities.

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Clinical Lymphoma and Myeloma

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