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T细胞淋巴瘤中的血液微血管。一项形态学、超微结构和免疫组织化学研究。

The blood microvasculature in T-cell lymphomas. A morphological, ultrastructural and immunohistochemical study.

作者信息

Kittas C, Hansmann M L, Borisch B, Feller A C, Lennert K

出版信息

Virchows Arch A Pathol Anat Histopathol. 1985;405(4):439-52. doi: 10.1007/BF00737170.

Abstract

The microvasculature of lymph nodes of 55 cases of T-cell lymphoma was studied by light microscopy, immunohistochemistry and electron microscopy. A modified peroxidase-antiperoxidase (PAP) method was used for staining paraffin sections with lectin I of Ulex europaeus (UEA-I), which is a specific marker for vascular endothelial cells. The T-cell nature of each case was proven by immunohistochemistry, including immunoperoxidase staining of frozen sections with monoclonal T-cell antibodies. The cases were subclassified according to previously established criteria, but with the addition of a separate group showing a high content of clear cells. For the purpose of the present study, the small blood vessels were separated into two main variants, viz.: high endothelial venules (HEV) and all other types of vessels with flat endothelium (SVFE). The development of each of these variants and the extent of lymphocyte migration through the vascular wall were assessed semiquantitatively. The findings suggest that the blood microvasculature, as a whole, is similar in all types of T-cell lymphoma. There were distinct differences, however, in the development of the two main categories of small vessels between the various types. Chronic lymphocytic leukaemia of T-type (T-CLL) and Sézary's syndrome were poor in SVFE and rich in HEV, and there was considerable lymphocyte traffic through the latter. In contrast, T-immunoblastic and especially T-lymphoblastic lymphocyte traffic. The appearance of the microvasculature varied markedly in the various subtypes of "pleomorphic T-cell lymphoma". In the small cell subtype HEV predominated and SVFE represented only a small or moderate fraction of the microvasculature. As the size of the neoplastic lymphoid cells increased towards the medium-sized and large cell subtype, there was a decrease in the number of HEV and an increase in the number of SVFE accompanied by a decrease in lymphocyte migration. In T-cell lymphoma of the clear cell type the microvasculature showed features between those of T-CLL and the small cell subtype of pleomorphic T-cell lymphoma. Electron microscopy confirmed the light microscopic findings and revealed many similarities in vascular changes between "pleomorphic T-cell lymphomas" and lymphogranulomatosis X.

摘要

采用光学显微镜、免疫组织化学及电子显微镜技术对55例T细胞淋巴瘤淋巴结的微血管系统进行了研究。用改良的过氧化物酶-抗过氧化物酶(PAP)法,以荆豆凝集素I(UEA-I)对石蜡切片进行染色,UEA-I是血管内皮细胞的特异性标记物。通过免疫组织化学,包括用单克隆T细胞抗体对冰冻切片进行免疫过氧化物酶染色,证实了每例的T细胞性质。根据先前确立的标准对病例进行亚分类,但增加了一个显示透明细胞含量高的单独组。为了本研究的目的,小血管被分为两个主要类型,即:高内皮微静脉(HEV)和所有其他具有扁平内皮的血管类型(SVFE)。对这些类型中每一种的发育情况以及淋巴细胞穿过血管壁的迁移程度进行了半定量评估。研究结果表明,总体而言,所有类型的T细胞淋巴瘤的血液微血管系统相似。然而,不同类型之间两种主要小血管类型的发育存在明显差异。T型慢性淋巴细胞白血病(T-CLL)和Sezary综合征的SVFE较少,HEV较多,并且有大量淋巴细胞通过后者。相比之下,T免疫母细胞性淋巴瘤,尤其是T淋巴母细胞性淋巴瘤的淋巴细胞迁移较少。在“多形性T细胞淋巴瘤”的各种亚型中,微血管系统的外观有明显差异。在小细胞亚型中,HEV占主导,SVFE仅占微血管系统的一小部分或中等比例。随着肿瘤性淋巴细胞的大小向中、大细胞亚型增加,HEV数量减少,SVFE数量增加,同时淋巴细胞迁移减少。在透明细胞型T细胞淋巴瘤中,微血管系统表现出介于T-CLL和多形性T细胞淋巴瘤小细胞亚型之间的特征。电子显微镜证实了光学显微镜的发现,并揭示了“多形性T细胞淋巴瘤”和结节病X在血管变化方面有许多相似之处。

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