| Literature DB >> 9213177 |
N Matsumoto1, H Kagawa, H Ichiyoshi, T Iguchi, Y Yamanaka, Y Kishimoto, S Fukuhara.
Abstract
A 47-year-old woman was referred to our hospital because of severe anemia and polyclonal gammopathy. She developed sicca syndrome after admission. Laboratory data revealed pancytopenia (white blood cells, 2,800/microliter; hemoglobin, 6.4 g/dl; platelets, 6.1 x 10(4)/microliter) and hyper gamma globulinemia (5.2 g/dl), and bone marrow was hypoplastic. Histology of the salivary gland showed infiltration of lymphocytes. We report a good response to immunosuppressive therapy in a rare case of aplastic anemia complicating Sjögren's syndrome.Entities:
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Year: 1997 PMID: 9213177 DOI: 10.2169/internalmedicine.36.371
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271