Literature DB >> 7355854

Prolymphocytic leukemia. An ultrastructural study.

C R Kjeldsberg, R M Bearman, H Rappaport.   

Abstract

The ultrastructural features of the leukemic cells from three patients with prolymphocytic leukemia were examined. In all patients, the prolymphocytes were characterized by a single prominent nucleolus and a chromatin structure intermediate between that of a mature lymphocyte and a lymphoblast. The cytoplasm contained a few short segments of rough endoplasmic reticulum and a poorly-developed Golgi apparatus. Polyribosomes and lysosomes were scarce. These ultrastructural features help in distinguishing prolymphocytic leukemia from other malignant lymphoproliferative disorders. A unique feature of the leukemic cells from one patient was the presence of intracytoplasmic inclusions. These were concentrated in the region of the Golgi zone, were surrounded by a smooth, trilaminar membrane, and had a substructure of parallel lines with a periodicity of approximately 60 A. To the authors' knowledge, similar inclusions have not been previously described in prolymphocytic leukemia.

Entities:  

Mesh:

Year:  1980        PMID: 7355854     DOI: 10.1093/ajcp/73.2.150

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  3 in total

1.  Intracytoplasmic inclusions in B prolymphocytic leukaemia: ultrastructural, cytochemical, and immunological studies.

Authors:  D S Robinson; J V Melo; C Andrews; S A Schey; D Catovsky
Journal:  J Clin Pathol       Date:  1985-08       Impact factor: 3.411

2.  Cytoplasmic inclusions and X-ray microprobe analysis in a case of prolymphocytic leukemia.

Authors:  M Djaldetti; A Eisbruch; J Perek; J Hart
Journal:  J Cancer Res Clin Oncol       Date:  1984       Impact factor: 4.553

3.  Two types of intracytoplasmic inclusions in the cells of a patient with acute lymphoblastic leukemia.

Authors:  M Djaldetti; J Perek; I Zahavi
Journal:  Blut       Date:  1983-07
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.