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1.
J Pediatr ; 132(6): 1016-22, 1998 Jun.
Article in English | MEDLINE | ID: mdl-9627596

ABSTRACT

Stenotic aorto-arteriopathy is an uncommon vascular lesion characterized by segmental arterial stenoses. We reviewed the experience with several management algorithms to define the most effective management course. The clinical records of 14 pediatric patients with acquired SAA who presented over a 16-year period were reviewed. Most patients presented with a mid-thoracoabdominal coarctation and were diagnosed with Takayasu arteritis. Differentiating between Takayasu arteritis and fibromuscular dysplasia was difficult on clinical grounds or by angiography. Medical management of the end-organ disease and renovascular hypertension was only palliative. Selective percutaneous transluminal balloon angioplasty of the stenotic renal arteries had only transient benefits; renal autotransplantation had slightly better success. Dilation of stenosed aortic segments with balloon-expandable endovascular stents and subsequent renal autotransplantation proved useful. Distinguishing SAA resulting from fibromuscular dysplasia caused by Takayasu arteritis in the chronic vaso-occlusive phase may be unnecessary for effective treatment. Therapy should focus on interventions to minimize the end-organ damage caused by the vaso-occlusive manifestations of the disorders.


Subject(s)
Aortic Diseases/diagnosis , Aortic Diseases/therapy , Fibromuscular Dysplasia/diagnosis , Fibromuscular Dysplasia/therapy , Takayasu Arteritis/diagnosis , Takayasu Arteritis/therapy , Adolescent , Algorithms , Angioplasty, Balloon , Aorta, Abdominal , Aorta, Thoracic , Aortic Coarctation/diagnosis , Aortic Coarctation/therapy , Aortography , Child , Child, Preschool , Diagnosis, Differential , Female , Humans , Male , Retrospective Studies , Stents , Treatment Outcome
2.
J Pediatr ; 122(3): 366-71, 1993 Mar.
Article in English | MEDLINE | ID: mdl-8441089

ABSTRACT

Pulmonary function tests in adults with sickle cell disease have shown a restrictive pattern that has been attributed to the sequelae of acute chest syndrome (ACS). We compared pulmonary function test results in 37 children with sickle cell anemia (20 with SS hemoglobin (HbSS), 14 with SC hemoglobin, and 3 with S beta hemoglobin) with those in 22 control subjects matched for sex, race, and height and compared pulmonary function in patients with and without a history of ACS. Of the 10 patients with a history of ACS, all but one had HbSS. Pulmonary function tests measured forced vital capacity (FVC), the diffusion capacity of carbon monoxide, and the plethysmographic determination of lung volumes. The FVC and forced expiratory volume in 1 second (FEV1), expressed as the percentage of the predicted value, were significantly less for those with HbSS with or without a history of ACS than for control subjects (p < 0.05), but the FEV1/FVC ratio, an index of airway obstruction, was normal in all groups. Total lung capacity was also significantly lower in patients with HbSS with or without a history of ACS than in control subjects (p < 0.05), but the ratio of residual volume to total lung capacity, another index of airway obstruction, was normal. We conclude that children with sickle cell disease, particularly those with HbSS, may have abnormally small lungs that function normally relative to their size; clustering of ACS episodes is not specifically associated with the observed abnormality.


Subject(s)
Anemia, Sickle Cell/physiopathology , Forced Expiratory Flow Rates , Total Lung Capacity , Adolescent , Anemia, Sickle Cell/complications , Child , Female , Humans , Male , Reference Values
3.
Early Hum Dev ; 15(2): 103-11, 1987 Mar.
Article in English | MEDLINE | ID: mdl-3036463

ABSTRACT

Routine full blood counts and serum ferritin determinations were carried out after admission to hospital in 112 children which included a white caucasian group (n = 65) and two ethnic minority groups of West Indians (n = 24) and Asians (n = 23). In these 3 groups those children between the ages of 1 week and 6 months were found to have similar haemoglobin, mean corpuscular volume, and ferritin levels. In the remaining children (aged from 7 months to 14 years 5 months) serum ferritin levels were lower in the ethnic minority groups than in white caucasians, but the haemoglobin and mean corpuscular volume were not significantly different. Children with lower height centiles had reduced ferritin levels, irrespective of their ethnic origins. A nutritional survey between the ages of 7 months and 14 years 5 months showed that mean daily dietary intakes of energy, protein, and iron in white caucasions were similar to those in West Indian and Asian children. The differences noted were in larger phytate and fibre intakes in the ethnic minority groups. Asian diets appeared to differ in containing meat less often as a source of iron, while pulses and chapattis provided more phytate and fibre. It is suggested that dietary intakes of phytate and fibre are important in causing lower ferritin levels by reducing iron absorption.


Subject(s)
Dietary Fiber/administration & dosage , Iron Deficiencies , Phytic Acid/administration & dosage , Adolescent , Anemia, Hypochromic/etiology , Asia/ethnology , Child , Child, Preschool , Ethnicity , Female , Ferritins/blood , Humans , Infant , Infant, Newborn , Male , West Indies/ethnology
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