Juvenile hyperinsulinism in a Maine Coon kitten

Case summary A 5.5 month-old intact male Maine Coon cat was presented to a referral hospital for a history of muscle fasciculations, lethargy and seizures associated with refractory hypoglycemia. Diagnostic testing for hypothyroidism, hyposomatotropism or hypoadrenocorticism, inborn errors of metabo...

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Main Authors: Matthew Kornya, Anthony Abrams-Ogg, Dominique Comeau, Jeff Caswell
Format: Article
Language:English
Published: SAGE Publishing 2022-11-01
Series:Journal of Feline Medicine and Surgery Open Reports
Online Access:https://doi.org/10.1177/20551169221136473
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author Matthew Kornya
Anthony Abrams-Ogg
Dominique Comeau
Jeff Caswell
author_facet Matthew Kornya
Anthony Abrams-Ogg
Dominique Comeau
Jeff Caswell
author_sort Matthew Kornya
collection DOAJ
description Case summary A 5.5 month-old intact male Maine Coon cat was presented to a referral hospital for a history of muscle fasciculations, lethargy and seizures associated with refractory hypoglycemia. Diagnostic testing for hypothyroidism, hyposomatotropism or hypoadrenocorticism, inborn errors of metabolism (ie, storage diseases and urea cycle disorders), infection or iatrogenic hypoglycemia were negative. An inappropriately high serum insulin level was noted in the face of marked hypoglycemia. The insulin:glucose ratio was 0.44 (<0.3) and the amended insulin:glucose ratio was 1268 (<30). Thoracic radiography and abdominal ultrasonography did not identify a cause for this elevated insulin level. Stabilization with a low, but adequate, blood glucose occurred with corticosteroid therapy, with further significant improvement with the addition of diazoxide. Peripheral neuropathy developed several months later, and concerns for quality of life led to humane euthanasia approximately 1 year after the initial diagnosis. Insulin levels remained high at the time of euthanasia. Necropsy found no gross lesions, though microscopic degeneration of the sciatic nerve and subjectively mildly increased size and number of pancreatic islets was noted. These findings were consistent with a diagnosis of congenital hyperinsulinism. Relevance and novel information This is the first reported case of congenital hyperinsulinism in a cat and may parallel the diffuse form of hypoglycemic hyperinsulinism reported in humans and a single dog. It should be considered a differential diagnosis in kittens presenting for refractory hypoglycemia.
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spelling doaj.art-5c302e17b1244d0396c95c78a19e7bf92022-12-22T04:20:40ZengSAGE PublishingJournal of Feline Medicine and Surgery Open Reports2055-11692022-11-01810.1177/20551169221136473Juvenile hyperinsulinism in a Maine Coon kittenMatthew KornyaAnthony Abrams-OggDominique ComeauJeff CaswellCase summary A 5.5 month-old intact male Maine Coon cat was presented to a referral hospital for a history of muscle fasciculations, lethargy and seizures associated with refractory hypoglycemia. Diagnostic testing for hypothyroidism, hyposomatotropism or hypoadrenocorticism, inborn errors of metabolism (ie, storage diseases and urea cycle disorders), infection or iatrogenic hypoglycemia were negative. An inappropriately high serum insulin level was noted in the face of marked hypoglycemia. The insulin:glucose ratio was 0.44 (<0.3) and the amended insulin:glucose ratio was 1268 (<30). Thoracic radiography and abdominal ultrasonography did not identify a cause for this elevated insulin level. Stabilization with a low, but adequate, blood glucose occurred with corticosteroid therapy, with further significant improvement with the addition of diazoxide. Peripheral neuropathy developed several months later, and concerns for quality of life led to humane euthanasia approximately 1 year after the initial diagnosis. Insulin levels remained high at the time of euthanasia. Necropsy found no gross lesions, though microscopic degeneration of the sciatic nerve and subjectively mildly increased size and number of pancreatic islets was noted. These findings were consistent with a diagnosis of congenital hyperinsulinism. Relevance and novel information This is the first reported case of congenital hyperinsulinism in a cat and may parallel the diffuse form of hypoglycemic hyperinsulinism reported in humans and a single dog. It should be considered a differential diagnosis in kittens presenting for refractory hypoglycemia.https://doi.org/10.1177/20551169221136473
spellingShingle Matthew Kornya
Anthony Abrams-Ogg
Dominique Comeau
Jeff Caswell
Juvenile hyperinsulinism in a Maine Coon kitten
Journal of Feline Medicine and Surgery Open Reports
title Juvenile hyperinsulinism in a Maine Coon kitten
title_full Juvenile hyperinsulinism in a Maine Coon kitten
title_fullStr Juvenile hyperinsulinism in a Maine Coon kitten
title_full_unstemmed Juvenile hyperinsulinism in a Maine Coon kitten
title_short Juvenile hyperinsulinism in a Maine Coon kitten
title_sort juvenile hyperinsulinism in a maine coon kitten
url https://doi.org/10.1177/20551169221136473
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