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29例中线恶性网状细胞增多症的病理及免疫组化观察
引用本文:王淑真. 29例中线恶性网状细胞增多症的病理及免疫组化观察[J]. 皖南医学院学报, 1992, 11(3): 181-183
作者姓名:王淑真
作者单位:厦门市第一医院病理科 361003
摘    要:本文报告29例中线恶性网状细胞增多症,着重对临床、病理形态及,免疫组化观察进行探讨.病理诊断依据是:1、有显著的坏死.2、炎性浸润及异形淋巴细胞(ALC)浸润,并浸润粘膜上皮及缸管壁.3、ALC 的形态分大、中、小3型,数量随临床分期而变化.免疫组化标记结果,病变组织中 ALC 呈 UCHL_1,LCA 膜阳性反应,而 K、λ、Mac_(387)、Lysozymc 均呈阴性反应,提示是 T 细胞来源的恶性淋巴瘤.

关 键 词:中线恶性网状细胞增多症  肉芽肿  败死性中线  T 细胞淋巴瘤

PATHOMORPHOLOGIC AND IMMUNOHISTOCHEMICAL OBSERVATION OF MIDLINE MALIGNANT RETICULOSIS OF 29CASES
Wang shuzhen. PATHOMORPHOLOGIC AND IMMUNOHISTOCHEMICAL OBSERVATION OF MIDLINE MALIGNANT RETICULOSIS OF 29CASES[J]. Acta Academiae Medicinae Wannan, 1992, 11(3): 181-183
Authors:Wang shuzhen
Abstract:In this paper 29 cases of midline malignant reticulosis (MMR) are reported.The enphasis is put on the clinical,histopathologic and immunohistochcmical observation.The pathologic diagnosis was based on the following:1.the significant necrobiosis,2.The infiltration of inflammation and atypical lymphoid cell (ALC),3.the infiltration of ALC onto the mucosa of epithelial and vascular wall.Accordign to the size,ALC were divided into three subtypes:the large,intermediate and small groups.Their amount of ALC changed with the clinical stage.The result of immunohistochemical study showed that UCHL and LCA reactions were positive,while K,λ,Mac_(387)and lysozyme reaction negatiae.It indicates that ALC of MMR belong to one kind of T-cell origin lymphoma.
Keywords:reticulosis  malignant midline  granuloma  lethal midline  lymphoma
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