Araki Hironobu, Matsunaga Takuya, Murase Kazuyuki, Kuroda Hiroyuki, Kuribayashi Kageaki, Terui Takeshi, Niitsu Yoshiro
Fourth Dept. of Internal Medicine, School of Medicine, Sapporo Medical University.
Gan To Kagaku Ryoho. 2004 Jun;31(6):965-9.
The patient was a 45-year-old male who had been diagnosed with pancytopenia in 1998 at another hospital, where he continued treatment for idiopathic thrombocytopenic purpura (ITP) as an outpatient. After atypical lymphocytes were detected in his peripheral blood, he was admitted to our hospital for further examination in April 2002. Tests results revealed the additional existence of pancytopenia, splenomegaly, bone marrow fibrosis and erythema nodosum, in addition to the findings of surface marker. Tartrate resistant acid phosphatase (TRAP) staining and scanning electron microscopy of peripheral blood lymphocytes indicated hairy cell leukemia. After administration of cladribine (0.09 mg/kg) for 7 days, complete remission was obtained, with bone marrow fibrosis and erythema nodosum also being completely improved.
该患者为一名45岁男性,1998年在另一家医院被诊断为全血细胞减少症,此后作为门诊患者继续接受特发性血小板减少性紫癜(ITP)的治疗。2002年4月,其外周血中检测到非典型淋巴细胞后,被收治入我院作进一步检查。检测结果显示,除了表面标志物的检查结果外,还存在全血细胞减少、脾肿大、骨髓纤维化和结节性红斑。外周血淋巴细胞的抗酒石酸酸性磷酸酶(TRAP)染色和扫描电子显微镜检查显示为毛细胞白血病。给予克拉屈滨(0.09mg/kg)治疗7天后,实现完全缓解,骨髓纤维化和结节性红斑也完全改善。