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T细胞大颗粒淋巴细胞白血病的骨髓特征性表现。

Characteristic appearances of the bone marrow in T-cell large granular lymphocyte leukaemia.

作者信息

Osuji N, Beiske K, Randen U, Matutes E, Tjonnfjord G, Catovsky D, Wotherspoon A

机构信息

Section of Haemato-oncology, Royal Marsden NHS Foundation Trust, Institute of Cancer Research, Sutton, Surrey, UK.

出版信息

Histopathology. 2007 Apr;50(5):547-54. doi: 10.1111/j.1365-2559.2007.02656.x.

DOI:10.1111/j.1365-2559.2007.02656.x
PMID:17394489
Abstract

AIMS

To augment the limited literature on bone marrow (BM) appearances in T-cell large granular lymphocyte (LGL) leukaemia and to identify a histological signature to aid in diagnosis of this condition.

METHODS AND RESULTS

A descriptive analysis of the histology of the BM in T-cell LGL leukaemia was performed (n = 38). Antibodies against CD3, CD4, CD5, CD8, CD16, CD56, CD57 and CD20 or CD79a were employed. Antibodies against CD68 (macrophages) and CD34 (sinusoids) were also included. BM was normocellular or hypercellular in the majority of cases, with interstitial lymphoid infiltration in 97%. Lymphoid nodules were present in 55% and intrasinusoidal permeation in 58%. Apoptotic figures and haemosiderin deposition were common. All cases showed trilinear haematopoiesis with normal or increased megakaryopoiesis and erythropoiesis, but normal/reduced myelopoiesis. Reticulin was increased (Grade II-III). Immunohistochemistry revealed interstitial infiltration in all cases and helped to identify lymphoid nodules in two-thirds of cases. Preferential localization of CD8+ T lymphocytes to the interstitium and CD4+ T lymphocytes to the periphery of CD20+ B-cell nodules was seen in almost 90% of cases.

CONCLUSIONS

Nodules with non-clonal B-cell centres surrounded by CD4+ cells, with interstitial CD8+ cells, are a characteristic finding in T-cell LGL leukaemia and may represent a histological signature for this condition.

摘要

目的

补充关于T细胞大颗粒淋巴细胞(LGL)白血病骨髓(BM)表现的有限文献,并确定一种组织学特征以辅助诊断该疾病。

方法与结果

对T细胞LGL白血病的骨髓组织学进行了描述性分析(n = 38)。使用了抗CD3、CD4、CD5、CD8、CD16、CD56、CD57和CD20或CD79a的抗体。还包括抗CD68(巨噬细胞)和CD34(血窦)的抗体。大多数病例中骨髓细胞数量正常或增多,97%存在间质淋巴细胞浸润。55%有淋巴小结,58%有血窦内浸润。凋亡小体和含铁血黄素沉积常见。所有病例均显示三系造血,巨核细胞生成和红细胞生成正常或增加,但粒细胞生成正常/减少。网状纤维增加(II-III级)。免疫组化显示所有病例均有间质浸润,三分之二的病例有助于识别淋巴小结。在近90%的病例中可见CD8 + T淋巴细胞优先定位于间质,CD4 + T淋巴细胞定位于CD20 + B细胞小结的周边。

结论

具有被CD4 +细胞包围的非克隆性B细胞中心的小结,伴有间质CD8 +细胞,是T细胞LGL白血病的特征性表现,可能代表该疾病的一种组织学特征。

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