摘要
A 42-year-old male presented with generalized massive lymphadenopathy, fever, weight loss and numerous cutaneous nodules. Peripheral blood examination showed lymphocytosis with small lymphocytes, and immunophenotyping revealed B-cell chronic lymphocytic leukemia (CLL). Cytogenetic analysis of bone marrow aspirate revealed a clonal abnormality of chromosome 11. Lymph node biopsies showed a B-immunoblastic lymphoma. A diagnosis of Richter's syndrome (RS) was made. The patient did not respond to doxorubicin, cyclophosphamide, vincristine and prednisolone (CHOP) and died of progressive disease with pneumonia and respiratory failure 9 months later. CLL is not common among Chinese people and RS is extremely rare.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 686-688 |
| 頁數 | 3 |
| 期刊 | Journal of the Formosan Medical Association |
| 卷 | 94 |
| 發行號 | 11 |
| 出版狀態 | 已出版 - 11 1995 |
| 對外發佈 | 是 |
UN SDG
此研究成果有助於以下永續發展目標
-
SDG3 健康與福祉
指紋
深入研究「Richter's syndrome: report of a case.」主題。共同形成了獨特的指紋。引用此
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