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Biomedical subjects

A Essex-Cater

Publications and source records attributed to A Essex-Cater.

10 recordsLinked to original sources

Continuous arteriovenous haemofiltration in the treatment of tumour lysis syndrome.

The management of tumour lysis syndrome remains problematic despite the rigorous use of preventative measures. Continuous arteriovenous haemofiltration (CAVH) is well suited to its use in both the prevention and treatment of metabolic abnormalities and renal insufficiency associated with tumour lysis. We report the successful use of CAVH in the treatment of a patient with tumour lysis syndrome.

Child↗

Totally implantable venous access systems in paediatric practice.

Forty seven totally implantable venous access systems have been inserted in 45 patients for the management of malignant disease (n = 29), haematological disorders (n = 5), and cystic fibrosis (n = 11). We report our experience with them and discuss the problems we have encountered during the past three years.

Adolescent↗

Relapse of Hodgkin's disease with anaemia and weight loss.

Two children previously treated for Hodgkin's disease had relapse associated with anaemia and weight loss but no other abnormal clinical findings. It was not possible to confirm the diagnosis by bone marrow aspirate or trephine and in each case laparotomy was required in order to establish a histological diagnosis.

Anemia↗

Nasopharyngeal carcinoma in children.

The results of treatment are reviewed in 18 cases of childhood nasopharyngeal carcinoma. Since 1976 adjuvant chemotherapy with cyclophosphamide, methotrexate, and adriamycin has been used in Manchester and Leeds. The outcome is compared in 9 patients treated with radiotherapy alone and 9 patients treated later with both radiotherapy and adjuvant chemotherapy. Relapse-free survival rates were 0% for those treated with radiotherapy alone and 78% at 13-80 months after diagnosis for those treated with both radiotherapy and chemotherapy. It is concluded that adjuvant chemotherapy improves relapse-free survival in childhood nasopharyngeal carcinoma.

Adolescent↗

Fatal congenital varicella syndrome.

A baby with clinical and serological evidence of congenital varicella syndrome died 36 hours after birth. Her mother had developed clinical varicella at 12 weeks gestation. Ultrasound at 37 weeks gestation had shown poor foetal growth and a lacuna within the foetal skull. Varicella-zoster-specific IgM was demonstrated in the baby's serum.

Abnormalities, Multiple↗