Pitman Sean D, Huang Qin
Division of Pathology, City of Hope National Medical Center, Duarte, California 91010, USA.
Am J Hematol. 2007 Sep;82(9):834-7. doi: 10.1002/ajh.20922.
Authors report a rare case of granular acute lymphoblastic leukemia (ALL) in a 45-year-old woman with a history of multiple myeloma. The patient's lymphoblasts contained large numbers of distinctive cytoplasmic granules closely mimicking heavily granulated myeloblasts in acute myeloid leukemia. These blasts were completely negative for myeloperoxidase but positive for acid phosphatase and Periodic Acid-Schiff reaction by cytochemical staining. Immunophenotype analysis by immunohistochemistry clearly demonstrated precursor B-cell phenotype. Granular ALL occurs approximately 2 to 7% in childhood populations but is extremely rare in adults. Such cases may cause problematic distinction from myeloid differentiation and lead to misdiagnosis of acute myeloid leukemia. Ten cases of adult granular acute lymphoblastic leukemia described to date in the literature were also reviewed.
作者报告了一例罕见的颗粒型急性淋巴细胞白血病(ALL),患者为一名45岁女性,有多发性骨髓瘤病史。患者的淋巴母细胞含有大量独特的胞质颗粒,酷似急性髓系白血病中颗粒粗大的髓母细胞。这些母细胞髓过氧化物酶染色完全阴性,但酸性磷酸酶染色和糖原染色呈阳性。免疫组化免疫表型分析明确显示为前体B细胞表型。颗粒型ALL在儿童人群中发生率约为2%至7%,但在成人中极为罕见。此类病例可能难以与髓系分化相鉴别,从而导致急性髓系白血病的误诊。本文还回顾了文献中迄今报道的10例成人颗粒型急性淋巴细胞白血病病例。