E Ralfkiaer, K Hou-Jensen, C Geisler, T Plesner, A Henschel, M M Hansen
{"title":"Cytoplasmic inclusions in lymphocytes of chronic lymphocytic leukaemia. A report of 10 cases.","authors":"E Ralfkiaer, K Hou-Jensen, C Geisler, T Plesner, A Henschel, M M Hansen","doi":"10.1007/BF00429615","DOIUrl":null,"url":null,"abstract":"<p><p>Peripheral blood from 90 CLL patients was examined by light-and electron-microscopy for the occurrence of crystalline inclusions in lymphocytes. Inclusions were demonstrated in 10 patients (11%). In these patients the inclusions were present in 5-45% of peripheral blood lymphocytes. In the light microscope the inclusions appeared as rectangular, unstained structures in May-Grünewald Giemsa and PAS stains. In the electron microscope the inclusions appeared as intracytoplasmic, completely partially membrane-bound bodies, which were often associated with dilated profiles of rough endoplasmic reticulum. The ultrastructure of the inclusions was granular. In immunofluorescence staining the inclusions were found to contain immunoglobulin of the same type and class as the surface membrane-bound immunoglobulin of the neoplastic lymphocytes, most frequently IgM-lambda. The lymphocytes of one case with kappa light chains at the cell surface membrane contained inclusions of the same ultrastructural morphology as those of the other cases with lambda light chains. The presence of inclusions was not associated with any specific clinical or prognostic features. the inclusions persisted during antileukaemic therapy. Their formation may be related to a dysfunction in the synthesis of surface membrane-bound immunoglobulins.</p>","PeriodicalId":76799,"journal":{"name":"Virchows Archiv. A, Pathological anatomy and histology","volume":"395 2","pages":"227-36"},"PeriodicalIF":0.0000,"publicationDate":"1982-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/BF00429615","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virchows Archiv. A, Pathological anatomy and histology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/BF00429615","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15
Abstract
Peripheral blood from 90 CLL patients was examined by light-and electron-microscopy for the occurrence of crystalline inclusions in lymphocytes. Inclusions were demonstrated in 10 patients (11%). In these patients the inclusions were present in 5-45% of peripheral blood lymphocytes. In the light microscope the inclusions appeared as rectangular, unstained structures in May-Grünewald Giemsa and PAS stains. In the electron microscope the inclusions appeared as intracytoplasmic, completely partially membrane-bound bodies, which were often associated with dilated profiles of rough endoplasmic reticulum. The ultrastructure of the inclusions was granular. In immunofluorescence staining the inclusions were found to contain immunoglobulin of the same type and class as the surface membrane-bound immunoglobulin of the neoplastic lymphocytes, most frequently IgM-lambda. The lymphocytes of one case with kappa light chains at the cell surface membrane contained inclusions of the same ultrastructural morphology as those of the other cases with lambda light chains. The presence of inclusions was not associated with any specific clinical or prognostic features. the inclusions persisted during antileukaemic therapy. Their formation may be related to a dysfunction in the synthesis of surface membrane-bound immunoglobulins.
用光镜和电镜检查90例CLL患者外周血淋巴细胞中是否存在结晶性包裹体。10例患者(11%)出现夹杂物。在这些患者中,包涵体存在于5-45%的外周血淋巴细胞。在光镜下,包裹体在may - gr newald Giemsa和PAS染色中呈矩形,未染色的结构。在电子显微镜下,包涵体呈胞浆内,完全部分膜结合的小体,通常与粗糙的内质网扩张有关。包裹体的超微结构呈颗粒状。免疫荧光染色发现包涵体含有与肿瘤淋巴细胞表面膜结合免疫球蛋白相同类型和类别的免疫球蛋白,最常见的是IgM-lambda。1例细胞表面有kappa轻链的患者淋巴细胞的超微结构形态与其他有λ轻链的患者相同。夹杂物的存在与任何特定的临床或预后特征无关。这些包涵体在抗白血病治疗期间持续存在。它们的形成可能与表面膜结合免疫球蛋白合成的功能障碍有关。