Partial splenectomy in homozygous beta thalassaemia. 1990

M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
Département de Pédiatrie, Hôpital des Enfants Malades, Paris.

Partial splenectomy was performed on 30 patients with homozygous beta thalassaemia to reduce blood requirements and to avoid the risk of overwhelming postsplenectomy infections; 24 patients had thalassaemia major and six thalassaemia intermedia. Five patients received a high transfusion regimen before and after surgery and 25 a lower one. Follow up after surgery ranged from one to four years. Partial splenectomy improved the long term haematological state in the six patients with thalassaemia intermedia. Recurrence of hypersplenism occurred in nine of the 24 patients with thalassaemia major, however, and complete splenectomy was required. Serum IgM concentrations were not significantly modified by surgery. The mean (SD) residual spleen after surgery was 4.45 (2.36) cm measured by scintigraphy. No severe infections occurred after surgery; however, most patients were routinely treated with phenoxymethylpenicillin and the protective effect of the remaining spleen could not be exactly determined. Because of the possibility of recurrence of hypersplenism, routine partial splenectomy when splenectomy is needed in thalassaemia major is not advised, except in children under 5 years whose risk of overwhelming postsplenectomy infection is greatest.

UI MeSH Term Description Entries
D006971 Hypersplenism Condition characterized by splenomegaly, some reduction in the number of circulating blood cells in the presence of a normal or hyperactive bone marrow, and the potential for reversal by splenectomy. Anemia, Splenic,Anemias, Splenic,Splenic Anemia,Splenic Anemias
D010976 Platelet Count The number of PLATELETS per unit volume in a sample of venous BLOOD. Blood Platelet Count,Blood Platelet Number,Platelet Number,Blood Platelet Counts,Blood Platelet Numbers,Count, Blood Platelet,Count, Platelet,Counts, Blood Platelet,Counts, Platelet,Number, Blood Platelet,Number, Platelet,Numbers, Blood Platelet,Numbers, Platelet,Platelet Count, Blood,Platelet Counts,Platelet Counts, Blood,Platelet Number, Blood,Platelet Numbers,Platelet Numbers, Blood
D011183 Postoperative Complications Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery. Complication, Postoperative,Complications, Postoperative,Postoperative Complication
D012008 Recurrence The return of a sign, symptom, or disease after a remission. Recrudescence,Relapse,Recrudescences,Recurrences,Relapses
D001803 Blood Transfusion The introduction of whole blood or blood component directly into the blood stream. (Dorland, 27th ed) Blood Transfusions,Transfusion, Blood,Transfusions, Blood
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
August 1985, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
November 1975, British journal of haematology,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
June 1978, Journal of clinical pathology,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
July 1978, British journal of haematology,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
June 1975, Journal of medical genetics,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
January 1974, Acta haematologica,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
January 1981, Hereditas,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
November 1994, British journal of haematology,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
February 1984, The Australian & New Zealand journal of obstetrics & gynaecology,
M de Montalembert, and R Girot, and Y Revillon, and D Jan, and L Adjrad, and F Z Ardjoun, and M Belhani, and Y Najean
June 1977, The Journal of tropical pediatrics and environmental child health,
Copied contents to your clipboard!