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Canine pancreatic islet cell tumours secreting insulin‐like growth factor type 2: a rare entity
Authors:R. Finotello  L. Ressel  M. Arvigo  G. Baroni  V. Marchetti  G. Romanelli  R. Burrow  D. Mignacca  L. Blackwood
Affiliation:1. Small Animal Teaching Hospital, School of Veterinary Sciences, University of Liverpool, Liverpool, UK;2. Section of Veterinary Pathology, School of Veterinary Sciences, University of Liverpool, Liverpool, UK;3. Department of Internal Medicine and Medical Specialities, University of Genova, Genova, Italy;4. Division of Pathological Anatomy, Department of Surgery and Translational Medicine, University of Florence, Florence, Italy;5. Department of Veterinary Sciences, Veterinary Teaching Hospital, University of Pisa, Pisa, Italy;6. Clinica Veterinaria Nerviano, Milan, Italy;7. Clinica Veterinaria Roma Sud, Rome, Italy
Abstract:Insulin‐like growth factor type II (IGF‐II) is the main cause of non‐islet cell tumour hypoglycaemia (NICTH) and insulin is thought to be the only factor causing hypoglycaemia in insulinomas. However, two case reports of pancreatic neuroendocrine tumours (PNETs) producing IGF‐II have been previously published: a human and a canine patient. In this study, we investigated clinical, histopathological, immunohistochemical and ultrastructural features, and biological behaviour of canine pancreatic IGF‐II‐omas, a subgroup of PNETs that has not been previously characterized. Case records of 58 dogs with confirmed PNETs and hypoglycaemia were reviewed: six patients were affected by IGF‐II‐omas. Surgery was performed in all cases and two dogs had metastases. Four patients remained alive and in remission at 370, 440, 560 and 890 days post‐diagnosis; two died of non‐tumour‐related causes. IGF‐II‐omas can be differentiated from insulinomas through hypoinsulinaemia, IGF‐II positive and insulin negative immunostaining. The prevalence of this neoplasia is low, accounting for just 6% of PNETs.
Keywords:dog  hypoglycaemia  IGF‐II  insulin growth factor‐II  insulinoma  islet cell tumour
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