Badhe Bhawana A, Basu Debdatta, Toi Pampa Ch, Dutta T K, Ghotekar L H
Department of Pathology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.
Indian J Pathol Microbiol. 2003 Jul;46(3):484-7.
Plasma cell leukemia, occurring either de novo or in patients with long standing multiple myeloma, is the least common type of plasma cell dyscrasia. Histogenetically plasma cell leukemia is derived from terminally differentiated B cells. It is diagnosed by presence of absolute plasma cell count >2000/cm or >20% circulating plasma cells. Two cases of plasma-cell leukemia are reported here. Clinical spectrum and course of the disease, are discussed. Both cases (of primary plasma cell leukemia) had abrupt onset of disease, poor response to therapy and short survival time. Both presented with fatiguability and weakness. Evidence of organomegaly and radiological and hematological evidence of plasma cell leukemia, with thrombocytopenia and evidence of visceral involvement with leukemic cells, was seen in one case.
浆细胞白血病可原发发生,也可发生于长期患有多发性骨髓瘤的患者,是浆细胞发育异常中最罕见的类型。从组织发生学上讲,浆细胞白血病源自终末分化的B细胞。其诊断依据是绝对浆细胞计数>2000/立方厘米或循环浆细胞>20%。本文报告了两例浆细胞白血病病例,并讨论了该疾病的临床谱和病程。两例(原发性浆细胞白血病)病例均起病急骤,对治疗反应不佳且生存时间短。两例均表现为易疲劳和虚弱。其中一例可见器官肿大的证据以及浆细胞白血病的放射学和血液学证据,伴有血小板减少和白血病细胞内脏受累的证据。