- 1 Alpha-1-antitrypsin related hepatitis
- 2 Amyloidosis
- 3 Antral pyloric hypertrophy syndrome (pyloric stenosis)
- 4 Cholelithiasis
- 5 Chronic hepatitis
- 6 Chronic idiopathic (lymphocytic-plasmacytic) colitis
- 7 Cleft palate
- 8 Congenital bronchoesophageal fistula
- 9 Congenital polycystic liver disease
- 10 Congenital portosystemic shunts
- 11 Copper storage hepatopathy
- 12 Cricopharyngeal achalasia
- 13 Diarroheal syndrome of Lundehunds
- 14 Dysphagia
- 15 Eosinophilic gastroenteritis, enteritis and enterocolitis
- 16 Exocrine pancreatic insufficiency
- 17 Gastric carcinoma
- 18 Gastric dilatation/volvulus
- 19 Gastric neoplasia
- 20 Gastro-oesophageal intussusception
- 21 Gastrointestinal eosinophilic granuloma
- 22 Gluten-sensitive enteropathy
- 23 Haemangiosarcoma
- 24 Haemorrhagic gastroenteritis
- 25 Hepatic lipidosis
- 26 Hiatal hernia
- 27 Histiocytic colitis
- 28 Hypertrophic gastritis
- 29 Idiopathic hepatic fibrosis
- 30 Immunoproliferative enteropathy of Basenjis
- 31 Intestinal adenocarcinoma
- 32 Lobular dissecting hepatitis
- 33 Lymphangiectasia
- 34 Lymphocytic-plasmacytic enteritis
- 35 Megacolon
- 36 Megaoesophagus
- 37 Microvascular portal dysplasia
- 38 Oral eosinophilic granuloma of the Siberian Husky
- 39 Oropharyngeal neoplasia
- 40 Pancreatic acinar atrophy
- 41 Pancreatic carcinoma
- 42 Pancreatitis
- 43 Parvovirus enteritis
- 44 Perianal fistula (anal furunculosis)
- 45 Portosystemic shunts
- 46 Protein-losing enteropathy
- 47 Pyloric dysfunction
- 48 Pyloric stenosis
- 49 Rectal Prolapse
- 50 Salivary mucocoele
- 51 Selective malabsorption of cobalamin (vitamin B12)
- 52 Small intestinal bacterial overgrowth (SIBO)
- 53 Small-intestinal volvulus
- 54 Tuberculosis (See also Mycobacterial infections under Infectious conditions)
- 55 Vacuolar hepatopathy
- 56 Vascular ring anomaly
A form of chronic progressive hepatitis associated with the accumulation of the acute-phase protein alpha-1-antitrypsin.
Amyloidosis results from the deposition of an insoluble fibrillar protein (amyloid) in a variety of organs, resulting in organ dysfunction. It may occur as an abnormal response to inflammatory or lymphoproliferative disease.
Antral pyloric hypertrophy syndrome (pyloric stenosis)
In this syndrome, gastric-outlet obstruction is caused by hypertrophy of the pyloric muscle, hyperplasia of the antral mucosa or both, and results in persistent vomiting. Congenital hypertrophy of the pyloric muscle is seen in young Boxers and Boston Terriers and may be referred to as congenital pyloric stenosis.
Adult-onset antral pyloric hypertrophy syndrome is seen in older (>6 years) small Oriental canine breeds. In these cases there may be antropyloric mucosal hyperplasia only or a combination of mucosal and muscular hypertrophy.
The development of gallstones. Gallstones are uncommon in the dog and where found are usually asymptomatic.
Inflammatory liver disease which usually progresses to cirrhosis. There are many types of hepatitis, and classification remains controversial, however certain breeds of dog may be predisposed, and individual breeds may demonstrate particular patterns of inflammation.
Chronic idiopathic (lymphocytic-plasmacytic) colitis
Colonic inflammation characterised by the presence of large numbers of lymphocytes and plasma cells in the mucosa. Patients have chronic, intermittent large-bowel-type diarrhoea.
A congenital defect in the hard or soft palate allowing abnormal communication between the oral cavity and the nasal cavity/nasopharynx.
Congenital bronchoesophageal fistula
This is an abnormal communication between the oesophagus and a bronchus resulting from incomplete separation of these structures in the developing embryo. Symptoms of regurgitation and coughing (especially after eating and drinking) are seen.
Congenital polycystic liver disease
Multiple hepatic cysts usually derived from the bile duct epithelium. They may be associated with cysts in other organs (especially the kidneys). Cysts may also be seen as an acquired lesion.
Congenital portosystemic shunts
Failure of foetal venous shunts to close after birth leads to persistent shunting of blood from the gastrointestinal tract to the systemic circulation without hepatic metabolism. Shunts may be single or multiple, intrahepatic or extrahepatic. Large breeds of dog are more likely to have intrahepatic shunts than small breeds.
Copper storage hepatopathy
Copper accumulation in the liver may be the result of a primary defect in copper excretion resulting in hepatic necrosis, as seen in the Bedlington. Alternatively, copper may accumulate as a result of chronic hepatitis and reduced biliary excretion.
Difficulty in swallowing due to failure of the cricopharyngeal sphincter (the upper oesopha-geal sphincter) to relax.
Diarroheal syndrome of Lundehunds
A chronic progressive form of lymphocytic-plasmacytic enteritis specific to this breed.
Eosinophilic gastroenteritis, enteritis and enterocolitis
Chronic inflammatory disease of the stomach and small intestine, small intestine only, or small intestine and colon. Eosinophilic infiltration is a predominant feature of the inflammation and peripheral eosinophilia may also be present.
Exocrine pancreatic insufficiency
Inadequate production of digestive enzymes leading to malabsorption and chronic diarrhoea. This is most commonly due to Pancreatic acinar atrophy, or occasionally due to chronic pancreatitis or pancreatic neoplasia.
A primary, malignant stomach tumour derived from epithelial cells.
Gastric distension due to the rapid accumulation of food, fluid or gas resulting in torsion of the stomach. Usually an acute and severe condition which is rapidly fatal without treatment. Large deep-chested dogs are predisposed.
Primary stomach tumours include gastric carcinomas, lymphosarcoma, leiomyoma/sarcoma, adenomatous polyps, fibroma/fibrosarcoma, plasmacytoma and squamous cell carcinoma.
Invagination of the stomach into the thoracic oesophagus. A rare condition with high mortality.
Gastrointestinal eosinophilic granuloma
Chronic inflammatory masses which may be found anywhere in the gastrointestinal tract. Histologically, the predominant cell type is the eosinophil.
An intolerance to gluten-containing foods, most commonly seen in Irish Setters. Weight loss and chronic diarrhoea due to malabsorption are seen.
See under Neoplastic conditions.
A haemorrhagic diarrhoea syndrome of unknown cause.
A potentially severe liver disease wherein hep-atocyte function is compromised by extensive lipid accumulation. Seen most commonly in anorexic, obese female cats, but occasionally seen in puppies of toy breeds.
Displacement of part of the stomach or other abdominal organs cranially through the oseo-phageal hiatus in the diaphragm. The condition may be congenital or acquired.
Chronic inflammatory disease of the colon characterised histologically by an inflammatory infiltrate with large numbers of histiocytes. Ulceration of the mucosa may be a prominent feature and the disease tends to be refractory to treatment.
A chronic condition of the stomach characterised by hypertrophy of the mucosa. A diffuse form is seen in the Basenji, whereas a focal form affecting primarily the antrum (part of the Antral pyloric hypertrophy syndrome) is seen in small breeds of dog.
Idiopathic hepatic fibrosis
Fibrosis of the liver of unknown cause which is seen without preceeding active inflammation. Various patterns of fibrosis are described. The condition is mostly seen in young dogs. Fibrosis results in portal hypertension, vascular shunting, ascites and hepatic encephalopathy.
Immunoproliferative enteropathy of Basenjis
A specific disease of Basenjis, of unknown cause. Several forms of pathology may be identified in the gastrointestinal tract including hypertrophic gastritis and lymphocytic-plasmacytic enteritis resulting in chronic diarrhoea and protein-losing enteropathy.
A malignant tumour found most frequently in the colon of dogs and the jejunum and ileum of cats. Most are locally invasive and metastasise early to the lymph nodes and liver.
Lobular dissecting hepatitis
A form of progressive hepatitis where there is a random pattern of inflammation and fibrosis leading to weight loss and ascites. Seen mostly in young dogs.
Distension of the lymphatic vessels in the intestinal mucosa. It may be a primary congenital disease, or it may be secondary to other disorders including right-sided heart failure or lipogranulomatous inflammation.
A form of inflammatory bowel disease in which the cellular infiltrate of the intestinal mucosa is mainly composed of lymphocytes and plasma cells.
Dilation of the colon which results in constipation.
Oesophageal dilation and reduced motility resulting in regurgitation. Megaoesophagus can be classified as congenital idiopathic megaoesophagus, which presents shortly after weaning, adult-onset idiopathic megaoesophagus which occurs later in life or secondary megaoesophagus where an underlying primary cause can be found.
Microvascular portal dysplasia
Congenital malformation of the intrahepatic portal circulation resulting in vascular shunting and hepatic dysfunction.
Oral eosinophilic granuloma of the Siberian Husky
Raised, ulcerative lesions usually seen on the lateral and ventral areas of the tongue.
The most common canine oropharyngeal tumours are squamous cell carcinomas, malignant melanomas, epulides and fibrosarcomas. The most common feline oropharyngeal tumours are squamous cell carcinomas and fibrosarcomas.
Pancreatic acinar atrophy
A condition where there is spontaneous and progressive loss of pancreatic acinar cells, responsible for the production of digestive enzymes, leading to Exocrine pancreatic insufficiency.
A tumour of the duct cells of the pancreas. Uncommon, but usually highly malignant.
Inflammation of the pancreas.
An infectious viral disease which most commonly causes a severe gastroenteritis, however may also manifest as acute myocarditis or neonatal mortality.
Perianal fistula (anal furunculosis)
Chronically infected and often deep tracts in the soft tissues around the anus.
See Congenital portosystemic shunts.
Excessive loss of plasma proteins via the gastrointestinal tract. It is seen with a number of gastrointestinal and systemic disorders, but particularly with inflammatory enteropathies and lymphangiectasia.
Delayed gastric emptying with no evidence of pyloric stenosis. Seen in Siamese cats.
See Antral pyloric hypertrophy syndrome.
Eversion of the rectum through the anus. Generally seen in young animals.
An accumulation of saliva in the subcutaneous tissues.
Selective malabsorption of cobalamin (vitamin B12)
Malabsorption of vitamin B12 (cobalamin) may occur as a result of an absence of the appropriate receptors in the ileum. The condition is inherited in the Giant Schnauzer and symptoms include inappetance, failure to grow and anaemia.
Small intestinal bacterial overgrowth (SIBO)
Increased numbers of bacteria in the upper small intestine associated with chronic diarrhoea. SIBO is often a secondary condition, however in some cases it may be primary with no evidence of other underlying gastrointestinal disease.
A rare condition where the small intestine rotates about its mesenteric axis resulting in intestinal obstruction and ischaemia. The condition is rapidly fatal.
Tuberculosis (See also Mycobacterial infections under Infectious conditions)
Infection with a species of Mycobacterium. Infection may be gained by the oral, respiratory or percutaneous routes and usually gives rise to granulomas in the affected organs. Infected animals are a public health risk.
A type of liver disease (seen primarily in Miniature Schnauzers with hyperlipidaemia) wherein the hepatocytes appear severely vacuo-lated on biopsy.
Vascular ring anomaly
Congenital abnormalities of the major thoracic arteries leading to entrapment of the oesophagus and clinical signs of regurgitation at or after weaning. Persistent right aortic arch is the most common vascular ring anomaly.