Difference between revisions of "Gastric Neoplasia - Dog and Cat"
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+ | ==Introduction== | ||
+ | Gastric [[Neoplasia - Pathology|neoplasia]] is uncommon and represents less than 1% of neoplasia in small animals. Aetiology is largely idiopathic though long term ingestion of dietary carcinogens may have some responsibility. In humans, ''[[Helicobacter]] pylori'' can induce gastric carcinomas and lymphomas. Its role in gastric tumours in dogs and cats has not yet been fully established though it is known to cause [[Gastritis, Acute|gastritis]] and [[Gastric Ulceration - all species|ulceration]]. Belgian Shepherd dogs may have a genetic predisposition to gastric carcinomas. Cats with gastric lymphomas are usually [[Feline Leukemia Virus|FeLV]] positive. | ||
+ | '''Malignant''' tumours include: | ||
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* [[Adenocarcinoma|Adenocarcinoma]] - 70-80% of all canine gastric neoplasms | * [[Adenocarcinoma|Adenocarcinoma]] - 70-80% of all canine gastric neoplasms | ||
* [[Squamous Cell Carcinoma|Squamous Cell Carcinoma]] | * [[Squamous Cell Carcinoma|Squamous Cell Carcinoma]] | ||
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* Mast cell | * Mast cell | ||
* Gastrointestinal stromal tumours (GIST tumours) - 20% of these tumours occur in the canine stomach | * Gastrointestinal stromal tumours (GIST tumours) - 20% of these tumours occur in the canine stomach | ||
− | Benign tumours include: | + | |
+ | '''Benign''' tumours include: | ||
* Polyps | * Polyps | ||
* [[Leiomyoma|Leiomyoma]] | * [[Leiomyoma|Leiomyoma]] | ||
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==Signalment== | ==Signalment== | ||
Male dogs are more commonly affected than female: e.g male:female ratio in those with carcinoma 2.5:1 | Male dogs are more commonly affected than female: e.g male:female ratio in those with carcinoma 2.5:1 | ||
− | The mean age of dogs with | + | The mean age of dogs with carcinomas is 8 years and cats with carcinomas are usually over 10 years. For benign tumours the mean age of affected dogs is 15 years. |
+ | |||
+ | ==Diagnosis== | ||
+ | ===History and Clinical Signs=== | ||
+ | Clinical signs may be mild or non-specific early on in the disease process. | ||
+ | Often a history of Chronic [[Vomiting|vomiting} - blood tinged/'coffee grounds' appearance (partially digested blood, weight loss, asnorexia and maleana/occult faecal blood. | ||
+ | Anterior abdominal pain may or may not be present. | ||
+ | '''Adenocarcinomas''': frequently [[Neoplasia - Pathology#The Process of Metastasis| metastasise]] to the regional [[Lymph Nodes - Anatomy & Physiology|lymph nodes]] (gastroduodenal and splenic lymph nodes), also the [[Liver - Anatomy & Physiology |liver]] and sometimes the [[Lungs - Anatomy & Physiology|lungs]]. They are also locally aggressive and can cause stomach wall perforation resulting in [[Peritonitis|peritonitis]]. Other complications include pyloric outflow obstruction and ischaemic necrosis where tumour plugs develop in the surrounding vasculature. | ||
− | + | '''Leiomyosarcomas''': rarely metastasise. | |
− | + | ||
− | + | '''Lymphoma''': may be limited to the stomach, may affect lymph nodes and other abdominal organs or may be multicentric. | |
− | + | ||
− | + | '''Plasmacytoma''': metastasis is frequently evident in local lymph nodes. | |
===Haematology and biochemistry=== | ===Haematology and biochemistry=== | ||
− | + | A Regenerative anaemia may be present due to gastric haemorrhage. [[:Category:Electrolytes|Electrolyte]] disturbances will be evident following vomiting and also elevated [[Urea|BUN]] and [[Creatinine|creatinine]] levels due to [[Dehydration|dehydration]]. | |
− | + | ||
− | + | If hepatic metastasis has occurred or if there is [[Biliary Tract Obstruction|obstruction to the common bile duct]] hepatic enzymes will also be increased. | |
− | + | ||
+ | ====Paraneoplastic Syndromes==== | ||
+ | Hypercalcaemia may be evident if lymphoma is present. Hypoglycaemia can also be associated with leiomyomas and leiomyosarcomas and is potentially reversibe following tumour resection. | ||
===Positive Contrast Radiography=== | ===Positive Contrast Radiography=== | ||
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===Surgical Biopsy=== | ===Surgical Biopsy=== | ||
Alternatively, biopsies can be taken via gastrotomy at the time of surgical treatment (see below). If a GIST is susptected a CD117 immunohistochemical stain can be used for diagnosis (in half of all dogs affected GIST tumours express CD117 (c-kit), a tyrosine kinase receptor). | Alternatively, biopsies can be taken via gastrotomy at the time of surgical treatment (see below). If a GIST is susptected a CD117 immunohistochemical stain can be used for diagnosis (in half of all dogs affected GIST tumours express CD117 (c-kit), a tyrosine kinase receptor). | ||
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==Treatment== | ==Treatment== | ||
===Surgery=== | ===Surgery=== | ||
− | Prior to any surgical intervention thoracic radiography should be performed for evidence of metastasis. Regional lymph nodes should also be examined at the start of surgery along with the rest of the abdominal cavity. For tumours that have not metastasised, resection is the treatment of choice (wide partial gastrectomy or antrectomy with gastroduodenostomy | + | Prior to any surgical intervention thoracic radiography should be performed for evidence of metastasis. Regional lymph nodes should also be examined at the start of surgery along with the rest of the abdominal cavity. For tumours that have not metastasised, resection is the treatment of choice (wide partial gastrectomy or antrectomy with gastroduodenostomy. However, frequently there are difficulties as tumours are often in an advanced stage at time of presentation. |
+ | |||
+ | Excision with large margins whilst maintaining the ability to successfully reconstruct the stomach without post-operative complications can be problematic. Furthermore, pylorectomy and gastroduodenostomy or gastrojejunostomy for antral tumours risk iatrogenic trauma to the local blood supply as well as to the pancreas and extrahepatic biliary system. | ||
+ | |||
+ | Neoplasia associated with the lesser curvature is generally non-resectable. | ||
===Chemotherapy=== | ===Chemotherapy=== | ||
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===Other Medical Management=== | ===Other Medical Management=== | ||
− | Symptomatic therapy of for example vomiting may improve quality of life in the short term. Treatment options include anti-emetics such as metocolpramide and H2 blockers including ranitidine and cimetidine | + | Symptomatic therapy of for example vomiting may improve quality of life in the short term. Treatment options include [[Emetics and Anti-Emetic Drugs|anti-emetics]] such as metocolpramide and H2 blockers including ranitidine and cimetidine. |
==Prognosis== | ==Prognosis== | ||
Variable: | Variable: | ||
− | + | Benign tumours are frequently cured by surgical resection and hence have a good prognosis. | |
− | + | Lymphoma often has a poor response to chemotherapy and survival rates are low. | |
− | + | Most malignant tumours are associated with recurrent or metastatic cancer. Prognosis therefore usually poor despite surgical resection. Survival time up to six months. | |
− | + | Extramedullary plasmacytomas can have a very good prognosis following surgery and chemotherapy. | |
+ | |||
+ | {{Learning | ||
+ | |Vetstream = [https://en.wikivet.net/Gastric_Neoplasia_-_Dog_and_Cat, Gastric neoplasia] | ||
+ | |literature search = [http://www.cabdirect.org/search.html?q=title%3A%28%22gastric+neoplasia%22%29 Gastric neoplasia publications] | ||
+ | }} | ||
==References== | ==References== | ||
− | + | Morris J, Dobson J (2001) '''Gastrointestinal Tract, in Small Animal Oncology''', ''Blackwell Science'', pp 127-130 | |
− | + | Liptak J. M, Withrow S.J, (2007), '''Cancer of the Gastrointestinal Tract, in Withrow and MacEwen's Small Animal Clinical Oncology''', fourth edition. ''Saunders Elsevier'', pp 480-482 | |
− | [[Category:Stomach_and_Abomasum_-_Proliferative_Pathology | + | |
+ | |||
+ | {{review}} | ||
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+ | {{OpenPages}} | ||
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+ | [[Category:Stomach_and_Abomasum_-_Proliferative_Pathology]] | ||
[[Category:Neoplasia]] | [[Category:Neoplasia]] | ||
− | [[Category:Dog]][[Category:Cat]] | + | [[Category:Gastric Diseases - Dog]][[Category:Gastric Diseases - Cat]] |
+ | [[Category:Expert_Review - Small Animal]] |
Latest revision as of 13:55, 6 September 2015
Introduction
Gastric neoplasia is uncommon and represents less than 1% of neoplasia in small animals. Aetiology is largely idiopathic though long term ingestion of dietary carcinogens may have some responsibility. In humans, Helicobacter pylori can induce gastric carcinomas and lymphomas. Its role in gastric tumours in dogs and cats has not yet been fully established though it is known to cause gastritis and ulceration. Belgian Shepherd dogs may have a genetic predisposition to gastric carcinomas. Cats with gastric lymphomas are usually FeLV positive.
Malignant tumours include:
- Adenocarcinoma - 70-80% of all canine gastric neoplasms
- Squamous Cell Carcinoma
- Lymphoma - the most common feline gastric neoplasm
- Fribrosarcoma
- Plasmacytoma
- Leiomyosarcoma
- Mast cell
- Gastrointestinal stromal tumours (GIST tumours) - 20% of these tumours occur in the canine stomach
Benign tumours include:
- Polyps
- Leiomyoma
Signalment
Male dogs are more commonly affected than female: e.g male:female ratio in those with carcinoma 2.5:1 The mean age of dogs with carcinomas is 8 years and cats with carcinomas are usually over 10 years. For benign tumours the mean age of affected dogs is 15 years.
Diagnosis
History and Clinical Signs
Clinical signs may be mild or non-specific early on in the disease process. Often a history of Chronic [[Vomiting|vomiting} - blood tinged/'coffee grounds' appearance (partially digested blood, weight loss, asnorexia and maleana/occult faecal blood.
Anterior abdominal pain may or may not be present.
Adenocarcinomas: frequently metastasise to the regional lymph nodes (gastroduodenal and splenic lymph nodes), also the liver and sometimes the lungs. They are also locally aggressive and can cause stomach wall perforation resulting in peritonitis. Other complications include pyloric outflow obstruction and ischaemic necrosis where tumour plugs develop in the surrounding vasculature.
Leiomyosarcomas: rarely metastasise.
Lymphoma: may be limited to the stomach, may affect lymph nodes and other abdominal organs or may be multicentric.
Plasmacytoma: metastasis is frequently evident in local lymph nodes.
Haematology and biochemistry
A Regenerative anaemia may be present due to gastric haemorrhage. Electrolyte disturbances will be evident following vomiting and also elevated BUN and creatinine levels due to dehydration.
If hepatic metastasis has occurred or if there is obstruction to the common bile duct hepatic enzymes will also be increased.
Paraneoplastic Syndromes
Hypercalcaemia may be evident if lymphoma is present. Hypoglycaemia can also be associated with leiomyomas and leiomyosarcomas and is potentially reversibe following tumour resection.
Positive Contrast Radiography
The following abnormalities may be observed:
- Apparent mass extending into the gastric lumen
- Delayed gastric emptying
- Changes in motility in certain areas of the stomach
- Thickening of the gastric wall or ulceration
- Filling defects
- Loss of rugal folds
Ultrasonography and Biopsy
Characteristic features of gastric neoplasia are a thickened gastric wall along with disruption of the wall layers. Enlarged lymph nodes may be observed. The rest of the abdominal organs should be checked for metastases. Ulceration appears as a localised outpouching of the luminal (inner) surface with accompanying gas bubbles which become trapped. Definitive diagnosis requires histopathology of samples. Guided fine-needle or core biopsies may be taken at this time.
Endoscopy and Biopsy
This allows direct visualisation of the lesion. Several biopsies can be taken via grab biopsy, however the samples may be unrepresentative.
Surgical Biopsy
Alternatively, biopsies can be taken via gastrotomy at the time of surgical treatment (see below). If a GIST is susptected a CD117 immunohistochemical stain can be used for diagnosis (in half of all dogs affected GIST tumours express CD117 (c-kit), a tyrosine kinase receptor).
Treatment
Surgery
Prior to any surgical intervention thoracic radiography should be performed for evidence of metastasis. Regional lymph nodes should also be examined at the start of surgery along with the rest of the abdominal cavity. For tumours that have not metastasised, resection is the treatment of choice (wide partial gastrectomy or antrectomy with gastroduodenostomy. However, frequently there are difficulties as tumours are often in an advanced stage at time of presentation.
Excision with large margins whilst maintaining the ability to successfully reconstruct the stomach without post-operative complications can be problematic. Furthermore, pylorectomy and gastroduodenostomy or gastrojejunostomy for antral tumours risk iatrogenic trauma to the local blood supply as well as to the pancreas and extrahepatic biliary system.
Neoplasia associated with the lesser curvature is generally non-resectable.
Chemotherapy
For lymphoma only. There is an associated risk of gastric perforation.
Radiotherapy
Unreported. Surrounding tissues including the liver and intestine show poor tolerance.
Other Medical Management
Symptomatic therapy of for example vomiting may improve quality of life in the short term. Treatment options include anti-emetics such as metocolpramide and H2 blockers including ranitidine and cimetidine.
Prognosis
Variable: Benign tumours are frequently cured by surgical resection and hence have a good prognosis. Lymphoma often has a poor response to chemotherapy and survival rates are low. Most malignant tumours are associated with recurrent or metastatic cancer. Prognosis therefore usually poor despite surgical resection. Survival time up to six months. Extramedullary plasmacytomas can have a very good prognosis following surgery and chemotherapy.
Gastric Neoplasia - Dog and Cat Learning Resources | |
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Literature Search Search for recent publications via CAB Abstract (CABI log in required) |
Gastric neoplasia publications |
References
Morris J, Dobson J (2001) Gastrointestinal Tract, in Small Animal Oncology, Blackwell Science, pp 127-130 Liptak J. M, Withrow S.J, (2007), Cancer of the Gastrointestinal Tract, in Withrow and MacEwen's Small Animal Clinical Oncology, fourth edition. Saunders Elsevier, pp 480-482
This article has been peer reviewed but is awaiting expert review. If you would like to help with this, please see more information about expert reviewing. |
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