| Literature DB >> 2558888 |
T Momoi1, C Yamanaka, T Yorifuji, H Sasaki, M Kaji, Y Akiyama, Y Inomata, K Tanaka, H Mikawa.
Abstract
Wilms tumour was found in a Japanese boy aged 5 years 9 months with isolated growth hormone (GH) deficiency and some congenital anomalies. He had received pituitary GH replacement therapy from the age of 2 years 1 month to 4 years 7 months and after a 1 year interval he received biosynthetic GH for 2 months until the tumour became clinically apparent. This was the sixth known patient with GH deficiency to develop a malignant neoplasm during or after GH replacement therapy and the first with a solid tumour in Japan since 1975, when treatment with pituitary GH for patients with GH deficiency was introduced.Entities:
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Year: 1989 PMID: 2558888 DOI: 10.1007/BF01958269
Source DB: PubMed Journal: Eur J Pediatr ISSN: 0340-6199 Impact factor: 3.183