Abstract
Since its first reported use in humans in 1981 [1], 131I-meta-iodobenzylguanidine (MIBG) has been used with success for the scintigraphic diagnosis of a variety of neuroendocrine tumours [2]. Derived from the neural crest, many of these tumours maintain the characteristic features of these cells, such as an active uptake-1 mechanism at the cell membrane and neurosecretory storage granules in the cytoplasm, which are responsible for the specific uptake and retention of MIBG.
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Further Reading
Hoefnagel, C.A. (1989) The Clinical Use of 131 I-metaiodobenzylguanidine (MIBG) for the diagnosis and treatment of neural crest tumors. Thesis, University of Amsterdam, ISBN 90–9003051–4.
Mazzaferri, L. and Samaan, N.A. (eds) (1993) Endocrine Tumors, Blackwell, Oxford.
Moertel, C.G. (1987) Karnofsky memorial lecture. An Odyssey in the land of small tumors. J. Clin. Oncol., 5, 1502–22.
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Voûte, P.A., de Kraker, J. and Hoefnagel, C.A. (1992) Tumours of the sympathetic nervous system. Neuroblastoma, ganglioneuroma and phaeocnromocytoma, in Cancer in children: Clinical management (eds P.A. Voûte, A. Barrett and J. Lemerle), Springer, Berlin, pp. 226–43.
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Hoefnagel, C.A. (1998). Neuro-ectodermal tumours. In: Maisey, M.N., Britton, K.E., Collier, B.D. (eds) Clinical Nuclear Medicine. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-3356-0_3
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DOI: https://doi.org/10.1007/978-1-4899-3356-0_3
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