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1.
Bull Soc Pathol Exot ; 100(1): 26-7, 2007 Feb.
Article in French | MEDLINE | ID: mdl-17402689

ABSTRACT

The authors report two cases of hydocholecystis causing abdominal pains in the sickle cell child. The patients were two girls aged respectively 4 and 12. Hydrocholecystis is defined by acute distension of the gallbladder The diagnosis was made by scan which allowed to follow the evolution in the two sickle cell children. After two crises, no more recurrence was noted in the first patient, on the other hand in the second child recurrences became more frequent. Some authors indicate surgery systematically while others recommend it only after several recurrences.


Subject(s)
Abdomen, Acute/etiology , Anemia, Sickle Cell/complications , Gallbladder Diseases/etiology , Analgesics/therapeutic use , Anti-Bacterial Agents/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Child , Child, Preschool , Combined Modality Therapy , Dilatation, Pathologic/diagnostic imaging , Dilatation, Pathologic/drug therapy , Dilatation, Pathologic/etiology , Dilatation, Pathologic/therapy , Drug Therapy, Combination , Female , Fluid Therapy , Gallbladder Diseases/diagnostic imaging , Gallbladder Diseases/drug therapy , Gallbladder Diseases/therapy , Hepatitis B, Chronic/complications , Humans , Recurrence , Ultrasonography
2.
Bull Soc Pathol Exot ; 96(2): 101-3, 2003 May.
Article in French | MEDLINE | ID: mdl-12836526

ABSTRACT

The rate of hemoglobin of 71 homozygous sickle cell disease patients from 10 to 18 years was studied, as well as the mean cell volume for 61 of them. Their height, weight and bone age were compared. The rate of hemoglobin in steady state is 6.5 g/dl +/- 2.3 for girls against 7.9 g/dl +/- 1.5 for boys. There's no significant difference between the rate of hemoglobin on sexual maturation state for girls. But the boys from 14 to 18 years old with signs of sexual maturation had higher rate of hemoglobin than those had not (8.5 g/dl +/- 1.3 against 6.3 g/dl +/- 1.5). Eighteen per cent of patients with homozygous sickle cell disease had a MCV superior to 100 mu 3; 57% are between 80 to 100 mu 3 and 25% under 80 mu 3. Patients with higher MCV to 100 mu 3 had low weight and height than those with inferior MCV to 80 mu 3 or 80 and 100 mu 3. Their sexual maturation is delayed with very low bone age and elevated number of hospitalisation and transfusion. Their delay of maturation was very high too. The supplementation with folic acid can lead to reduction of MCV.


Subject(s)
Anemia, Sickle Cell/physiopathology , Growth , Adolescent , Age Determination by Skeleton , Body Height , Body Weight , Child , Congo , Erythrocyte Indices , Female , Hemoglobins/analysis , Humans , Male , Puberty , Sex Characteristics
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