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Przeglad Lekarski 2010

[Long-term endocrine complications after brain tumor treatment--own experience].

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Małgorzata Wójcik
Katarzyna Dolezal-Ołtarzewska
Małgorzata Kumorowicz-Czoch
Anna Kalicka-Kasperczyk
Dominika Januś
Agata Zygmunt-Górska
Joanna Wojtyś
Elzbieta Korab-Chrzanowska
Stanisław Kwiatkowski
Jerzy Starzyk

Sleutelwoorden

Abstract

BACKGROUND

Long-term endocrine complications affect approximately 40% of childhood cancer survivors.

OBJECTIVE

The retrospective analysis of parameters of the endocrine system function up to 10 years after head radiotherapy (RT) and chemotherapy (CT) due to malignant solid tumor of the central nervous system.

METHODS

The analysis included 30 patients (15 girls; 15 boys) followed in Endocrine Outpatient Department, University Children's Hospital of Krakow for 1-10 years (mean 5.8 years) after completion of cancer therapy.

RESULTS

There was no endocrinopathy in 11 patients (34%), but only five of them were followed for longer than 5 years. A single endocrine disorder was seen in patients (28%), two independent disorders in six (20%), three in three children (10%), and four in two (6.7%). The most common endocrine disorder was growth hormone deficiency (GHD) (13 patients, 46.6%). Primary and secondary hypothyroidism were observed in seven (23%) and two patients (6.7%), respectively, secondary adrenal insufficiency in two (6.7%), hypogonadotropic or hypergonadotropic hypogonadism in seven (23%) and two patients (6.7%), respectively. Obesity without any hormone deficiency was present in five patients (16.6%) patients, in one case, the condition was complicated by glucose intolerance, in four children, by a high level of triglycerides and low HDL cholesterol.

CONCLUSIONS

1. Late endocrine complications after malignant brain tumor treatment affect 66% of patients followed for 1-10 years after completion of RT. That points to the necessity of long-term, regular followup of the patients after cancer treatment. 2. The most common endocrinopathy is GHD, followed by hypothyroidism, hypogonadism and adrenal insufficiency. 3. In patients after head RT and CT in childhood, there is noted secondary obesity, with complications typical for metabolic syndrome.

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