Literature DB >> 15809476

Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-DOPA.

Maria-João Ribeiro1, Pascale De Lonlay, Thierry Delzescaux, Nathalie Boddaert, Francis Jaubert, Sandrine Bourgeois, Frédéric Dollé, Claire Nihoul-Fékété, André Syrota, Francis Brunelle.   

Abstract

UNLABELLED: Hyperinsulinism (HI) of infancy is a neuroendocrine disease secondary to either focal adenomatous hyperplasia or a diffuse abnormality of insulin secretion of the pancreas. HI with focal lesions can revert by selective surgical resection in contrast to the diffuse form, which requires subtotal pancreatectomy when resistant to medical treatment. Neuroendocrine diseases are a heterogeneous group of entities with the ability to take up amine precursors and to convert them into biogenic amines. Therefore, the aim of this study was (a) to evaluate the use of PET with 18F-fluoro-L-dihydroxyphenylalanine (18F-fluoro-L-DOPA) and (b) to distinguish between focal and diffuse HI.
METHODS: Fifteen patients (11 boys, 4 girls) with neonatal HI were enrolled in this study. All patients fasted for at least 6 h before the PET examination and their medication was discontinued for at least 72 h. The examination was performed under light sedation (pentobarbital associated with or without chloral). The dynamic acquisition started 45-65 min after the injection of 18F-fluoro-L-DOPA (4.0 MBq/kg weight). Four or 6 scans of 5 min each (2 or 3 steps according to the height of the patient) were acquired from the neck to the upper legs.
RESULTS: An abnormal focal pancreatic uptake of 18F-fluoro-L-DOPA was observed in 5 patients, whereas a diffuse uptake of the radiotracer was observed in the pancreatic area of the other patients. All patients with focal radiotracer uptake and also 4 of 10 patients with pancreatic diffuse radiotracer accumulation, unresponsive to medical treatment, underwent surgery. The histopathologic results confirmed the PET findings--that is, focal versus diffuse HI.
CONCLUSION: The results of this study suggest that 18F-fluoro-L-DOPA could be an accurate noninvasive technique to distinguish between focal and diffuse forms of HI.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15809476

Source DB:  PubMed          Journal:  J Nucl Med        ISSN: 0161-5505            Impact factor:   10.057


  34 in total

1.  18F-FDOPA PET/CT imaging of insulinoma revisited.

Authors:  Alessio Imperiale; Frédéric Sebag; Michel Vix; Frédéric Castinetti; Laurence Kessler; François Moreau; Philippe Bachellier; Benjamin Guillet; Izzie-Jacques Namer; Olivier Mundler; David Taïeb
Journal:  Eur J Nucl Med Mol Imaging       Date:  2014-11-01       Impact factor: 9.236

Review 2.  Role of 18F-DOPA PET/CT imaging in congenital hyperinsulinism.

Authors:  Dunia Ismail; Khalid Hussain
Journal:  Rev Endocr Metab Disord       Date:  2010-09       Impact factor: 6.514

Review 3.  Pancreatic β-cell KATP channels: Hypoglycaemia and hyperglycaemia.

Authors:  Kate Bennett; Chela James; Khalid Hussain
Journal:  Rev Endocr Metab Disord       Date:  2010-09       Impact factor: 6.514

4.  Ability of (18)F-DOPA PET/CT and fused (18)F-DOPA PET/MRI to assess striatal involvement in paediatric glioma.

Authors:  Giovanni Morana; Matteo Puntoni; Maria Luisa Garrè; Michela Massollo; Egesta Lopci; Merhdad Naseri; Mariasavina Severino; Domenico Tortora; Andrea Rossi; Arnoldo Piccardo
Journal:  Eur J Nucl Med Mol Imaging       Date:  2016-02-25       Impact factor: 9.236

5.  Pancreatic head resection and Roux-en-Y pancreaticojejunostomy for the treatment of the focal form of congenital hyperinsulinism.

Authors:  Pablo Laje; Charles A Stanley; Andrew A Palladino; Susan A Becker; N Scott Adzick
Journal:  J Pediatr Surg       Date:  2012-01       Impact factor: 2.545

6.  The radiation response of cells from 9L gliosarcoma tumours is correlated with [F18]-EF5 uptake.

Authors:  Cameron J Koch; Anne L Shuman; Walter T Jenkins; Alexander V Kachur; Joel S Karp; Richard Freifelder; William R Dolbier; Sydney M Evans
Journal:  Int J Radiat Biol       Date:  2009-12       Impact factor: 2.694

7.  Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism.

Authors:  C Saint-Martin; Q Zhou; G M Martin; C Vaury; G Leroy; J-B Arnoux; P de Lonlay; S-L Shyng; C Bellanné-Chantelot
Journal:  Clin Genet       Date:  2014-06-06       Impact factor: 4.438

Review 8.  Diagnostic performance of fluorine-18-dihydroxyphenylalanine positron emission tomography in diagnosing and localizing the focal form of congenital hyperinsulinism: a meta-analysis.

Authors:  Giorgio Treglia; Paoletta Mirk; Alessandro Giordano; Vittoria Rufini
Journal:  Pediatr Radiol       Date:  2012-08-12

9.  Pancreatic head resection preserving the main pancreatic duct for congenital hyperinsulinism of infancy.

Authors:  Masayuki Obatake; Kyoko Mochizuki; Yasuaki Taura; Yukio Inamura; Akiko Nakatomi; Fumiko Kinoshita; Takeshi Nagayasu
Journal:  Pediatr Surg Int       Date:  2012-09       Impact factor: 1.827

Review 10.  Dosimetry of FDG PET/CT and other molecular imaging applications in pediatric patients.

Authors:  Michael J Gelfand
Journal:  Pediatr Radiol       Date:  2008-12-16
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.