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1.
J Pediatr Hematol Oncol ; 24(5): 389-93, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12142789

RESUMO

A27-year-old woman presented with back and abdominal pain. She was diagnosed in infancy with Beckwith-Wiedemann syndrome and bilateral multifocal perilobar nephrogenic rests that progressed to diffuse nephroblastomatosis with neoplastic nephroblastomatous rests at 14 months of age and subsequently to a right Wilms tumor at 5 years of age. Computed tomography of the abdomen during the current admission showed multiple obstructed calices. Ureteroscopic inspection of the left kidney revealed severe intrarenal scarring with multiple infundibular stenosis, hydrocalices, and nephrocalcinosis. Renal biopsy showed sclerotic glomeruli with calcification and scarring and persistent subcapsular nodular renal blastema. Electrocautery incision and balloon dilatation provided temporary pain relief. After discharge, the patient has had two or three episodes of recurrent pain associated with new areas of infundibular stenoses and renal cysts. Bilateral nephrectomy and renal transplantation is being considered for management of progressive disease and relief of intractable pain. The potential causes of progressive and severe intrarenal fibrosis, infundibular stenosis and nephrocalcinosis, and renal cysts in this patient may include abnormal renal development secondary to Beckwith-Wiedemann syndrome itself, radiation or chemotherapy damage, or a combination.


Assuntos
Síndrome de Beckwith-Wiedemann/complicações , Cálculos Renais/etiologia , Doenças Renais Císticas/etiologia , Neoplasias Renais/complicações , Rim/patologia , Tumor de Wilms/complicações , Adulto , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Síndrome de Beckwith-Wiedemann/diagnóstico , Síndrome de Beckwith-Wiedemann/terapia , Biópsia por Agulha , Progressão da Doença , Feminino , Fibrose , Humanos , Cálculos Renais/diagnóstico , Cálculos Renais/terapia , Doenças Renais Císticas/diagnóstico , Doenças Renais Císticas/terapia , Neoplasias Renais/diagnóstico , Neoplasias Renais/terapia , Transplante de Rim , Nefrectomia , Radioterapia , Tomografia Computadorizada por Raios X , Tumor de Wilms/diagnóstico , Tumor de Wilms/terapia
2.
J Pediatr ; 140(6): 681-7, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12072870

RESUMO

OBJECTIVES: To examine the body composition of children and adolescents with sickle cell disease (SCD) using bioelectrical impedance analysis and to determine if the impedance parameters resistance, reactance, and phase angle are able to distinguish between subjects with SCD and age- and gender matched controls. STUDY DESIGN: Total body resistance and reactance were obtained for a total of 53 subjects with SCD (27 male and 26 female) between 10 and 18 years of age and 49 control subjects (23 male and 26 female). The fat-free mass, body cell mass, phase angle, and capacitance were also determined. Group comparisons were made using the 2-sample t test. RESULTS: Male subjects with SCD had significantly lower fat-free mass (37.5 +/- 8.8 vs 43.9 +/- 12.3 kg, P =.04), body cell mass (17.4 +/- 4.3 vs 21.7 +/- 5.8 kg,P =.005), and body fat (3.7 +/- 2.6 vs 6.6 +/- 4.7 kg, P =.008) compared with controls. No significant differences in any body composition components were found for the female subjects. Both male and female subjects had significantly lower phase angle measurements (P <.001 and.006, respectively) than their respective controls, indicating possible alterations in cell membrane properties because of an imbalance in membrane composition or function. CONCLUSIONS: Bioelectrical impedance analysis can be used to determine body composition differences in children with SCD. The phase angle may provide a useful method to monitor the efficacy of therapeutic interventions in patients with SCD.


Assuntos
Composição Corporal , Traço Falciforme/fisiopatologia , Adolescente , Índice de Massa Corporal , Criança , Impedância Elétrica , Feminino , Humanos , Masculino
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