Anémie Polyglobulique Hypochrome
作者:
Lefevre De ArricM.,
期刊:
Acta Clinica Belgica
(Taylor Available online 1946)
卷期:
Volume 1,
issue 2
页码: 160-167
ISSN:1784-3286
年代: 1946
DOI:10.1080/17843286.1946.11716366
出版商: Taylor&Francis
数据来源: Taylor
摘要:
SummaryIn a 55 years old man repeated blood tests detected a haemologic syndrom characterized by :1°Polyglobulia ;2°Very low haemoglobin ;3°Definite microcytosis ;4°Numerous abnormalities of the red cells.The patient had achlorhydrie and his bone marrow showed only a slight erythroblastic reaction. Liver extracts exagerated the tendancy to polyglobulia. Martial treatment increased the haemoglobin content of the blood.It is difficult to classify this syndrome in the group of microcytic anaemias. The hyperglobulia may be the characteristic pecularity of this case; but it may as well be the consequence of an exagerated blood regeneration.
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