BONE-MARROW HYPERVASCULARITY IN PATIENTS WITH MYELOFIBROSIS IDENTIFIED BY INFRARED THERMOGRAPHY

被引:0
作者
BAGLIN, TP
CROCKER, J
TIMMINS, A
CHANDLER, S
BOUGHTON, BJ
机构
[1] QUEEN ELIZABETH MED CTR, DEPT NUCL MED, BIRMINGHAM, ENGLAND
[2] E BIRMINGHAM DIST GEN HOSP, DEPT HISTOPATHOL, BIRMINGHAM B9 5ST, W MIDLANDS, ENGLAND
[3] QUEEN ELIZABETH MED CTR, DEPT HAEMATOL, BIRMINGHAM, ENGLAND
[4] QUEEN ELIZABETH MED CTR, DEPT REG RADIAT PHYS & PROTECT SERV, BIRMINGHAM, ENGLAND
来源
CLINICAL AND LABORATORY HAEMATOLOGY | 1991年 / 13卷 / 04期
关键词
MYELOFIBROSIS; VASCULARITY; MARROW BLOOD FLOW; THERMOGRAPHY;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Infra-red thermography was used to assess bone marrow vascularity in six patients with myelofibrosis secondary to myeloproliferative disorders (four primary myelofibrosis and two primary proliferative polycythaemia). The technique was evaluated with conventional static and dynamic radio-isotopic imaging and with immunohistochemical staining of bone marrow biopsies. Infra-red thermography identified increased bone marrow blood flow in patients with established myelofibrosis and correlated with dynamic radio-isotopic studies of blood flow and hypervascularity identified by immunohistochemistry. Increased bone marrow blood flow and vascular proliferation was not confined to the central bone marrow but also extended into the peripheral marrow of the long bones. Endothelial cell proliferation may be an initiating event in the pathogenesis of myelofibrosis but evaluation of bone marrow vascularity and blood flow has hitherto relied on invasive and complicated techniques. This study has identified bone marrow hypervascularity in patients with myelofibrosis and shown infra-red thermography to be a simple non-invasive method of assessing vascularity. This non-invasive technique may be used to study disease progression and response to therapeutic regimens in patients with myelofibrosis and to study bone marrow blood flow in other bone marrow disorders.
引用
收藏
页码:341 / 348
页数:8
相关论文
共 24 条
[1]  
BAGLIN TP, 1988, CLIN LAB HAEMATOL, V10, P25
[2]   POSSIBLE AND UP TO NOW NOT EXPLOITED TREATMENT IN MYELOFIBROSIS [J].
BERANEK, JT .
BRITISH JOURNAL OF HAEMATOLOGY, 1988, 68 (01) :144-144
[3]  
CASTROMALASPINA H, 1981, BLOOD, V57, P781
[4]   QUANTITATION OF THERMOGRAPHY IN ARTHRITIS USING MULTI-ISOTHERMAL ANALYSIS .1. THERMOGRAPHIC INDEX [J].
COLLINS, AJ ;
RING, EFJ ;
COSH, JA ;
BACON, PA .
ANNALS OF THE RHEUMATIC DISEASES, 1974, 33 (02) :113-&
[5]   IMMUNOHISTOCHEMICAL DEMONSTRATION OF LEUKOCYTE ELASTASE IN HUMAN-TISSUES [J].
CROCKER, J ;
JENKINS, R ;
BURNETT, D .
JOURNAL OF CLINICAL PATHOLOGY, 1984, 37 (10) :1114-1118
[6]   VALUE OF FACTOR-VIII RELATED ANTIGEN AS A MEANS OF DEMONSTRATING EXTRAMEDULLARY MEGAKARYOPOIESIS [J].
CROCKER, J ;
SMITH, PJ .
JOURNAL OF CLINICAL PATHOLOGY, 1984, 37 (07) :834-835
[7]   TYPE-IV COLLAGEN IN HODGKINS-DISEASE - AN IMMUNOHISTOCHEMICAL STUDY [J].
CROCKER, J ;
OVERTON, SP ;
SMITH, PJ .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1988, 89 (01) :57-62
[8]  
FARRELL C, 1970, PHYS MED BIOL, V15, P179
[9]   THE PATHOGENESIS OF MYELOFIBROSIS IN MYELOPROLIFERATIVE DISORDERS [J].
GROOPMAN, JE .
ANNALS OF INTERNAL MEDICINE, 1980, 92 (06) :857-858
[10]   ON THE PATHOGENESIS OF ANGIOGENESIS IN IDIOPATHIC MYELOFIBROSIS [J].
HASSELBALCH, H .
AMERICAN JOURNAL OF HEMATOLOGY, 1990, 33 (02) :151-151