Liu Yan-hui, Zhuang Heng-guo, Liao Xin-bo, Luo Xin-lan, Cai Xiu-ling, Luo Dong-lan
Department of Pathology, Guangdong Provincial People's Hospital, Guangzhou 510080, China.
Zhonghua Xue Ye Xue Za Zhi. 2003 Nov;24(11):568-71.
To investigate the diagnosis and differential diagnosis of granulocytic sarcoma (GS).
The morphological and immunological characteristics of 12 cases of GS were studied. FAB classification was made by peripheral blood, bone marrow picture and bone marrow biopsy assay.
All of the 12 cases presented with lymphadenopathy and soft tissue mass. Histologically, the tissue infiltration of GS was composed of blastic cells with round to oval nuclei showing an even, pale chromatin pattern. Some with cleaved or notched nuclei. There were prominent nucleoli and scant cytoplasm in the cells and mitosis was easily found. Immunohistochemically, CD(45) and lysozyme were positive in all of the cases, MPO in 11 (92%), CD(68) in 10 (83%), CD(34) in 5 (42%), and TdT in 2 cases (17%). CD(15) and Mac387 were mainly expressed in mature granulocytes. Examination of bone marrow sections and marrow aspirate smears showed that out of the 11 cases tested 8 were AML-M(2), 2 AML-M(1) and 1 AML-M(0). Only 1 case was nonleukemic, ie. solitary granulocytic sarcoma.
Granulocytic sarcomas are difficult to identify in routine paraffin-embedded tissue sections and usually misdiagnosed as non-Hodgkin's lymphomas. Immunohistochemistry study with a panel of antibodies in combination with bone marrow and peripheral blood examination are helpful in identification of granulocytic sarcoma.
探讨粒细胞肉瘤(GS)的诊断与鉴别诊断。
对12例GS的形态学和免疫学特征进行研究。通过外周血、骨髓涂片及骨髓活检进行FAB分型。
12例均表现为淋巴结肿大和软组织肿块。组织学上,GS的组织浸润由核呈圆形至椭圆形的原始细胞组成,染色质均匀、淡染。部分细胞核有切迹或缺口。细胞中有明显的核仁,胞质稀少,易见核分裂象。免疫组化显示,所有病例CD(45)和溶菌酶均阳性,11例(92%)MPO阳性,10例(83%)CD(68)阳性,5例(42%)CD(34)阳性,2例(17%)TdT阳性。CD(15)和Mac387主要表达于成熟粒细胞。骨髓切片及骨髓穿刺涂片检查显示,11例受检病例中8例为急性髓系白血病M(2)型,2例为急性髓系白血病M(1)型,1例为急性髓系白血病M(0)型。仅1例为非白血病性,即孤立性粒细胞肉瘤。
粒细胞肉瘤在常规石蜡包埋组织切片中难以识别,常被误诊为非霍奇金淋巴瘤。一组抗体的免疫组化研究结合骨髓和外周血检查有助于粒细胞肉瘤的识别。