Small F chromosome in myelo- and lymphoproliferative diseases

J. Whang-Peng, H. R. Gralnick, T. Knutsen, H. Brereton, P. Chang, G. P. Schechter, L. Lessin

研究成果: 雜誌貢獻文章

13 引文 (Scopus)

摘要

A deleted F group chromosome was observed in five patients with myeloproliferative and lymphoproliferative diseases. Three patients had a small F chromosome with both arms deleted, 19p-q-. Each of these patients had a different disease, acute myelomonocytic leukemia (AMML), lymphosarcoma (LSA), and erythroleukemia, respectively. One patient had a hyperplastic marrow and erythroid hyperplasia for a year prior to the development of acute myelogenous leukemia (AML), and had a small F chromosome with del(20)(q12) which is similar to the small F chromosome reported in patients with polycythemia vera. No banding studies were available on one patient with sideroblastic anemia and possible erythroleukemia. These cytogenetic findings lead us to believe that: (1) there is a high incidence of F chromosome abnormalities in cases with abnormal erythropoiesis; (2) erythroid diseases may be predisposed to the small F chromosome abnormality, which is enhanced by treatment, such as irradiation; and (3) the cells with a small F chromosome are rather stable and can gradually replace cytogenetically normal cells without affecting the clinical course of the diseases, and it is the emergence of additional chromosomal abnormalities in these cells which signal a poor prognosis.
原文英語
頁(從 - 到)19-30
頁數12
期刊Leukemia Research
1
發行號1
DOIs
出版狀態已發佈 - 一月 1 1977
對外發佈Yes

指紋

Chromosomes, Human, 19-20
Chromosome Aberrations
Leukemia, Erythroblastic, Acute
Sideroblastic Anemia
Leukemia, Myelomonocytic, Acute
Polycythemia Vera
Erythropoiesis
Acute Myeloid Leukemia
Cytogenetics
Non-Hodgkin's Lymphoma
Hyperplasia
Bone Marrow
Incidence

ASJC Scopus subject areas

  • Hematology
  • Oncology
  • Cancer Research

引用此文

Whang-Peng, J., Gralnick, H. R., Knutsen, T., Brereton, H., Chang, P., Schechter, G. P., & Lessin, L. (1977). Small F chromosome in myelo- and lymphoproliferative diseases. Leukemia Research, 1(1), 19-30. https://doi.org/10.1016/0145-2126(77)90061-3

Small F chromosome in myelo- and lymphoproliferative diseases. / Whang-Peng, J.; Gralnick, H. R.; Knutsen, T.; Brereton, H.; Chang, P.; Schechter, G. P.; Lessin, L.

於: Leukemia Research, 卷 1, 編號 1, 01.01.1977, p. 19-30.

研究成果: 雜誌貢獻文章

Whang-Peng, J, Gralnick, HR, Knutsen, T, Brereton, H, Chang, P, Schechter, GP & Lessin, L 1977, 'Small F chromosome in myelo- and lymphoproliferative diseases', Leukemia Research, 卷 1, 編號 1, 頁 19-30. https://doi.org/10.1016/0145-2126(77)90061-3
Whang-Peng J, Gralnick HR, Knutsen T, Brereton H, Chang P, Schechter GP 等. Small F chromosome in myelo- and lymphoproliferative diseases. Leukemia Research. 1977 1月 1;1(1):19-30. https://doi.org/10.1016/0145-2126(77)90061-3
Whang-Peng, J. ; Gralnick, H. R. ; Knutsen, T. ; Brereton, H. ; Chang, P. ; Schechter, G. P. ; Lessin, L. / Small F chromosome in myelo- and lymphoproliferative diseases. 於: Leukemia Research. 1977 ; 卷 1, 編號 1. 頁 19-30.
@article{27a97fb5f38c43ed85f7830cc7f64d67,
title = "Small F chromosome in myelo- and lymphoproliferative diseases",
abstract = "A deleted F group chromosome was observed in five patients with myeloproliferative and lymphoproliferative diseases. Three patients had a small F chromosome with both arms deleted, 19p-q-. Each of these patients had a different disease, acute myelomonocytic leukemia (AMML), lymphosarcoma (LSA), and erythroleukemia, respectively. One patient had a hyperplastic marrow and erythroid hyperplasia for a year prior to the development of acute myelogenous leukemia (AML), and had a small F chromosome with del(20)(q12) which is similar to the small F chromosome reported in patients with polycythemia vera. No banding studies were available on one patient with sideroblastic anemia and possible erythroleukemia. These cytogenetic findings lead us to believe that: (1) there is a high incidence of F chromosome abnormalities in cases with abnormal erythropoiesis; (2) erythroid diseases may be predisposed to the small F chromosome abnormality, which is enhanced by treatment, such as irradiation; and (3) the cells with a small F chromosome are rather stable and can gradually replace cytogenetically normal cells without affecting the clinical course of the diseases, and it is the emergence of additional chromosomal abnormalities in these cells which signal a poor prognosis.",
author = "J. Whang-Peng and Gralnick, {H. R.} and T. Knutsen and H. Brereton and P. Chang and Schechter, {G. P.} and L. Lessin",
year = "1977",
month = "1",
day = "1",
doi = "10.1016/0145-2126(77)90061-3",
language = "English",
volume = "1",
pages = "19--30",
journal = "Leukemia Research",
issn = "0145-2126",
publisher = "Elsevier Limited",
number = "1",

}

TY - JOUR

T1 - Small F chromosome in myelo- and lymphoproliferative diseases

AU - Whang-Peng, J.

AU - Gralnick, H. R.

AU - Knutsen, T.

AU - Brereton, H.

AU - Chang, P.

AU - Schechter, G. P.

AU - Lessin, L.

PY - 1977/1/1

Y1 - 1977/1/1

N2 - A deleted F group chromosome was observed in five patients with myeloproliferative and lymphoproliferative diseases. Three patients had a small F chromosome with both arms deleted, 19p-q-. Each of these patients had a different disease, acute myelomonocytic leukemia (AMML), lymphosarcoma (LSA), and erythroleukemia, respectively. One patient had a hyperplastic marrow and erythroid hyperplasia for a year prior to the development of acute myelogenous leukemia (AML), and had a small F chromosome with del(20)(q12) which is similar to the small F chromosome reported in patients with polycythemia vera. No banding studies were available on one patient with sideroblastic anemia and possible erythroleukemia. These cytogenetic findings lead us to believe that: (1) there is a high incidence of F chromosome abnormalities in cases with abnormal erythropoiesis; (2) erythroid diseases may be predisposed to the small F chromosome abnormality, which is enhanced by treatment, such as irradiation; and (3) the cells with a small F chromosome are rather stable and can gradually replace cytogenetically normal cells without affecting the clinical course of the diseases, and it is the emergence of additional chromosomal abnormalities in these cells which signal a poor prognosis.

AB - A deleted F group chromosome was observed in five patients with myeloproliferative and lymphoproliferative diseases. Three patients had a small F chromosome with both arms deleted, 19p-q-. Each of these patients had a different disease, acute myelomonocytic leukemia (AMML), lymphosarcoma (LSA), and erythroleukemia, respectively. One patient had a hyperplastic marrow and erythroid hyperplasia for a year prior to the development of acute myelogenous leukemia (AML), and had a small F chromosome with del(20)(q12) which is similar to the small F chromosome reported in patients with polycythemia vera. No banding studies were available on one patient with sideroblastic anemia and possible erythroleukemia. These cytogenetic findings lead us to believe that: (1) there is a high incidence of F chromosome abnormalities in cases with abnormal erythropoiesis; (2) erythroid diseases may be predisposed to the small F chromosome abnormality, which is enhanced by treatment, such as irradiation; and (3) the cells with a small F chromosome are rather stable and can gradually replace cytogenetically normal cells without affecting the clinical course of the diseases, and it is the emergence of additional chromosomal abnormalities in these cells which signal a poor prognosis.

UR - http://www.scopus.com/inward/record.url?scp=49349130335&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=49349130335&partnerID=8YFLogxK

U2 - 10.1016/0145-2126(77)90061-3

DO - 10.1016/0145-2126(77)90061-3

M3 - Article

AN - SCOPUS:49349130335

VL - 1

SP - 19

EP - 30

JO - Leukemia Research

JF - Leukemia Research

SN - 0145-2126

IS - 1

ER -