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Gallbladder Agenesis in 17 Dogs: 2006–2016

BACKGROUND: Gallbladder agenesis (GBA) is extremely rare in dogs. HYPOTHESIS/OBJECTIVES: To describe the history, clinical signs, diagnosis, treatment, and outcomes of dogs with GBA. ANIMALS: Seventeen client‐owned dogs with GBA. METHODS: Medical records from 2006 through 2016 were retrospectively r...

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Autores principales: Sato, K., Sakai, M., Hayakawa, S., Sakamoto, Y., Kagawa, Y., Kutara, K., Teshima, K., Asano, K., Watari, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787189/
https://www.ncbi.nlm.nih.gov/pubmed/29377355
http://dx.doi.org/10.1111/jvim.15034
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author Sato, K.
Sakai, M.
Hayakawa, S.
Sakamoto, Y.
Kagawa, Y.
Kutara, K.
Teshima, K.
Asano, K.
Watari, T.
author_facet Sato, K.
Sakai, M.
Hayakawa, S.
Sakamoto, Y.
Kagawa, Y.
Kutara, K.
Teshima, K.
Asano, K.
Watari, T.
author_sort Sato, K.
collection PubMed
description BACKGROUND: Gallbladder agenesis (GBA) is extremely rare in dogs. HYPOTHESIS/OBJECTIVES: To describe the history, clinical signs, diagnosis, treatment, and outcomes of dogs with GBA. ANIMALS: Seventeen client‐owned dogs with GBA. METHODS: Medical records from 2006 through 2016 were retrospectively reviewed. Dogs were included when GBA was suspected on abdominal ultrasonography and confirmed by gross evaluation. Signalment, clinical signs, clinicopathological data, diagnostic imaging, histopathology, treatment, and outcome were recorded. RESULTS: Dogs were of 6 different breeds, and Chihuahuas (10 of 17) were most common. Median age at presentation was 1.9 (range, 0.7–7.4) years. Clinical signs included vomiting (5 of 17), anorexia (2 of 17), ascites (2 of 17), diarrhea (1 of 17), lethargy (1 of 17), and seizures (1 of 17). All dogs had increased serum activity of at least 1 liver enzyme, most commonly alanine aminotransferase (15 of 17). Fifteen dogs underwent computed tomography (CT) cholangiography; common bile duct (CBD) dilatation was confirmed in 12, without evidence of bile duct obstruction. Gross evaluation confirmed malformation of the liver lobes in 14 of 17 dogs and acquired portosystemic collaterals in 5 of 17. Ductal plate malformation was confirmed histologically in 16 of 17 dogs. During follow‐up (range, 4–3,379 days), 16 of 17 dogs remained alive. CONCLUSIONS AND CLINICAL IMPORTANCE: Dogs with GBA exhibit clinicopathological signs of hepatobiliary injury and hepatic histopathological changes consistent with a ductal plate abnormality. Computed tomography cholangiography was superior to ultrasound examination in identifying accompanying nonobstructive CBD distention. Computed tomography cholangiography combined with laparoscopic liver biopsy is the preferable approach to characterize the full disease spectrum accompanying GBA in dogs.
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spelling pubmed-57871892018-02-08 Gallbladder Agenesis in 17 Dogs: 2006–2016 Sato, K. Sakai, M. Hayakawa, S. Sakamoto, Y. Kagawa, Y. Kutara, K. Teshima, K. Asano, K. Watari, T. J Vet Intern Med SMALL ANIMAL BACKGROUND: Gallbladder agenesis (GBA) is extremely rare in dogs. HYPOTHESIS/OBJECTIVES: To describe the history, clinical signs, diagnosis, treatment, and outcomes of dogs with GBA. ANIMALS: Seventeen client‐owned dogs with GBA. METHODS: Medical records from 2006 through 2016 were retrospectively reviewed. Dogs were included when GBA was suspected on abdominal ultrasonography and confirmed by gross evaluation. Signalment, clinical signs, clinicopathological data, diagnostic imaging, histopathology, treatment, and outcome were recorded. RESULTS: Dogs were of 6 different breeds, and Chihuahuas (10 of 17) were most common. Median age at presentation was 1.9 (range, 0.7–7.4) years. Clinical signs included vomiting (5 of 17), anorexia (2 of 17), ascites (2 of 17), diarrhea (1 of 17), lethargy (1 of 17), and seizures (1 of 17). All dogs had increased serum activity of at least 1 liver enzyme, most commonly alanine aminotransferase (15 of 17). Fifteen dogs underwent computed tomography (CT) cholangiography; common bile duct (CBD) dilatation was confirmed in 12, without evidence of bile duct obstruction. Gross evaluation confirmed malformation of the liver lobes in 14 of 17 dogs and acquired portosystemic collaterals in 5 of 17. Ductal plate malformation was confirmed histologically in 16 of 17 dogs. During follow‐up (range, 4–3,379 days), 16 of 17 dogs remained alive. CONCLUSIONS AND CLINICAL IMPORTANCE: Dogs with GBA exhibit clinicopathological signs of hepatobiliary injury and hepatic histopathological changes consistent with a ductal plate abnormality. Computed tomography cholangiography was superior to ultrasound examination in identifying accompanying nonobstructive CBD distention. Computed tomography cholangiography combined with laparoscopic liver biopsy is the preferable approach to characterize the full disease spectrum accompanying GBA in dogs. John Wiley and Sons Inc. 2018-01-28 2018 /pmc/articles/PMC5787189/ /pubmed/29377355 http://dx.doi.org/10.1111/jvim.15034 Text en Copyright © 2018 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle SMALL ANIMAL
Sato, K.
Sakai, M.
Hayakawa, S.
Sakamoto, Y.
Kagawa, Y.
Kutara, K.
Teshima, K.
Asano, K.
Watari, T.
Gallbladder Agenesis in 17 Dogs: 2006–2016
title Gallbladder Agenesis in 17 Dogs: 2006–2016
title_full Gallbladder Agenesis in 17 Dogs: 2006–2016
title_fullStr Gallbladder Agenesis in 17 Dogs: 2006–2016
title_full_unstemmed Gallbladder Agenesis in 17 Dogs: 2006–2016
title_short Gallbladder Agenesis in 17 Dogs: 2006–2016
title_sort gallbladder agenesis in 17 dogs: 2006–2016
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787189/
https://www.ncbi.nlm.nih.gov/pubmed/29377355
http://dx.doi.org/10.1111/jvim.15034
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