THE COINCIDENCE OF MEDITERRANEAN ANEMIA AND PERNICIOUS ANEMIA IN A YOUNG SICILIAN

Author:

CROSBY WILLIAM H.1,SACKS HARRY J.1

Affiliation:

1. Medical and Laboratory Services, Brooke General Hospital, Fort Sam Houston, Texas.

Abstract

Abstract 1. Coincidental Mediterranean anemia and pernicious anemia were found in a 26 year old soldier of Sicilian parentage. 2. The diagnosis of pernicious anemia was made on the finding of achlorhydria after histamine, glossitis, megaloblastic bone marrow and macrocytic anemia which responded to liver extract on two occasions. 3. The diagnosis of mild Mediterranean anemia was made by finding the target-oval-cell trait in the patient and in five members of his family. 4. It is of interest that target cells were not found in the peripheral blood until treatment with liver was begun. While pernicious anemia dominated, the character of the peripheral blood picture was macrocytic. Liver therapy corrected this, whereupon "hypochromic polycythemia" characteristic of mild Mediterranean anemia was found.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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1. Punctate Basophilia in the Erythrocyte with Especial Reference to Rietti-Greppi-Micheli's Anemia;Acta Medica Scandinavica;2009-04-24

2. FOLIC ACID IN THE MANAGEMENT OF beta-THALASSAEMIA MINOR DURING PREGNANCY;BJOG: An International Journal of Obstetrics and Gynaecology;1974-02

3. VITAMIN B12METABOLISM IN THALASSEMIA MAJOR;Annals of the New York Academy of Sciences;1969-11

4. BETA-THALASSAEMIA MINOR DURING PREGNANCY, WITH PARTICULAR REFERENCE TO IRON STATUS;BJOG: An International Journal of Obstetrics and Gynaecology;1969-05

5. Lactate Dehydrogenase in the Diagnosis and Assessment of Response to Treatment of Megaloblastic Anaemia;British Journal of Haematology;1966-11

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