Difference between revisions of "Enteritis, Lymphocytic - Plasmacytic"

From WikiVet English
Jump to navigation Jump to search
m (Text replace - 'Lymphocytes - WikiBlood' to 'Lymphocytes')
(15 intermediate revisions by 2 users not shown)
Line 1: Line 1:
 +
{{unfinished}}
 +
 +
{{dog}}
 +
{{cat}}
 +
 +
 
==Signalment==
 
==Signalment==
 
*Often affects older animals but kittens of 16 weeks old and puppies of 20 weeks old have been reported.  
 
*Often affects older animals but kittens of 16 weeks old and puppies of 20 weeks old have been reported.  
Line 5: Line 11:
  
 
==Description==
 
==Description==
'''Lymphocytic - plasmacytic enteritis (LPE)''' is the most common form of [[Inflammatory Bowel Disease|Inflammatory Bowel Disease]] (IBD).  As its name suggests, the predominant cell type in the intestinal mucosa is [[Lymphocytes - Introduction|'''lymphocytes''']] and '''plasma cells'''.  Enteric parasites, bacteria in dogs and [[Toxoplasma gondii|''Toxoplasma'']] in cats have been reported to associated with LPE.  This disorder in cats have also been shown to associate with concurrent disease of the pancreas and liver such as [[Pancreatitis|pancreatitis]], [[Cholangitis|cholangitis]] and [[Hepatic Lipidosis|hepatic lipidosis]].  LPE is believed to be caused by an abnormal [[Regional Lymphoid Tissue - Anatomy & Physiology|mucosal associated lymphoid tissue (MALT)]] response to luminal bacterial, dietary or self-antigens.   
+
'''Lymphocytic - plasmacytic enteritis (LPE)''' is the most common form of [[Inflammatory Bowel Disease - WikiClinical|Inflammatory Bowel Disease]] (IBD).  As its name suggests, the predominant cell type in the intestinal mucosa is [[Lymphocytes|'''lymphocytes''']] and '''plasma cells'''.  Enteric parasites, bacteria in dogs and [[Toxoplasma|''Toxoplasma'']] in cats have been reported to associated with LPE.  This disorder in cats have also been shown to associate with concurrent disease of the pancreas and liver such as [[Pancreatitis - WikiClinical|pancreatitis]], [[Cholangitis/Cholagiohepatitis- WikiClinical|cholangitis]] and [[Hepatic Lipidosis - WikiClinical|hepatic lipidosis]].  LPE is believed to be caused by an abnormal [[Regional Lymphoid Tissue - Anatomy & Physiology|mucosal associated lymphoid tissue (MALT)]] response to luminal bacterial, dietary or self-antigens.   
  
The [[Small Intestine Overview - Anatomy & Physiology|small intestines]] are affected to a variable degree of severity.  It has also been known to affect other parts of the gastrointestinal tract such as the [[:Category:Stomach and Abomasum - Pathology|stomach]] and the [[Colon - Anatomy & Physiology|colon]].  In severely affected animals, this will result in a protein-losing enteropathy (PLE).
+
The [[Small Intestine - Anatomy & Physiology|small intestines]] are affected to a variable degree of severity.  It has also been known to affect other parts of the gastrointestinal tract such as the [[:Category:Stomach and Abomasum - Pathology|stomach]] and the [[Colon - Anatomy & Physiology|colon]].  In severely affected animals, this will result in a protein-losing enteropathy (PLE).
  
 
==Diagnosis==
 
==Diagnosis==
Line 23: Line 29:
 
*abdominal discomfort
 
*abdominal discomfort
 
*ascites or subcutaneous oedema if severe PLE resulting in hypoproteinaemia
 
*ascites or subcutaneous oedema if severe PLE resulting in hypoproteinaemia
*concurrent systemic immune-mediated response and [[Thromboembolism|thromboembolism]] (rare)
+
*concurrent systemic immune-mediated response and [[Thrombosis - Pathology#Thromboembolism|thromboembolism]] (rare)
  
 
===Laboratory Tests===
 
===Laboratory Tests===
Line 33: Line 39:
  
 
====Other Tests====
 
====Other Tests====
*Serum trypsin-like immunoassay (TLI) to rule out [[Exocrine Pancreatic Insufficiency|exocrine pancreatic insufficiency (EPI)]].
+
*Serum trypsin-like immunoassay (TLI) to rule out [[Exocrine Pancreatic Insufficiency - WikiClinical|exocrine pancreatic insufficiency (EPI)]].
 
*Faecal analysis to rule out endoparasite and pathogenic bacteria.
 
*Faecal analysis to rule out endoparasite and pathogenic bacteria.
  
Line 57: Line 63:
 
*Hall, E.J, Simpson, J.W. and Williams, D.A. (2005) '''BSAVA Manual of Canine and Feline Gastroenterology (2nd Edition)''' ''BSAVA''
 
*Hall, E.J, Simpson, J.W. and Williams, D.A. (2005) '''BSAVA Manual of Canine and Feline Gastroenterology (2nd Edition)''' ''BSAVA''
 
*Nelson, R.W. and Couto, C.G. (2009) '''Small Animal Internal Medicine (Fourth Edition)''' ''Mosby Elsevier''.
 
*Nelson, R.W. and Couto, C.G. (2009) '''Small Animal Internal Medicine (Fourth Edition)''' ''Mosby Elsevier''.
 
==Lymphocytic - Plasmacytic Enteritis==
 
 
====Pathology====
 
 
* Hypersensitivity reaction results in increased GIT permeablility and recruitment of inflammatory cells.
 
* Histologically:
 
** Mucosal epithelial-glandular alterations.
 
** Variably increased mucosal infiltrate of lymphocytes and plasma cells.
 
*** In these dogs there is an increase in the number of [[IgA]] and [[IgG]] containing cells and CD3+ T-cells.
 
**** Can develop into lymphoma.
 
*** Changes in the relative and absolute numbers of plasma cells and lymphocytes have been  associated with IBD in humans.
 
 
{{unfinished}}
 
 
[[Category:Intestine_-_Inflammatory_Pathology_by_Type]][[Category:To_Do_-_Alimentary]][[Category:To Do - Medium]]
 

Revision as of 12:37, 12 June 2010



Category:WikiClinical CanineCow
Category:WikiClinical FelineCow


Signalment

  • Often affects older animals but kittens of 16 weeks old and puppies of 20 weeks old have been reported.
  • Basenjis have been reported to suffer from a severe form known as immunoproliferative disease.


Description

Lymphocytic - plasmacytic enteritis (LPE) is the most common form of Inflammatory Bowel Disease (IBD). As its name suggests, the predominant cell type in the intestinal mucosa is lymphocytes and plasma cells. Enteric parasites, bacteria in dogs and Toxoplasma in cats have been reported to associated with LPE. This disorder in cats have also been shown to associate with concurrent disease of the pancreas and liver such as pancreatitis, cholangitis and hepatic lipidosis. LPE is believed to be caused by an abnormal mucosal associated lymphoid tissue (MALT) response to luminal bacterial, dietary or self-antigens.

The small intestines are affected to a variable degree of severity. It has also been known to affect other parts of the gastrointestinal tract such as the stomach and the colon. In severely affected animals, this will result in a protein-losing enteropathy (PLE).

Diagnosis

Clinical Signs

Most common:

  • small intestinal diarrhoea
  • weight loss
  • protein - losing enteropathy in severe cases
  • chronic vomiting (more common presentation in cats compared to the other signs)
  • thickened small intestinal loops and mesenteric lymphadenopathy may be detected on physical examination in cats

Others:

  • appetite changes
  • excessive borborygmi
  • abdominal discomfort
  • ascites or subcutaneous oedema if severe PLE resulting in hypoproteinaemia
  • concurrent systemic immune-mediated response and thromboembolism (rare)

Laboratory Tests

Haematology

  • Panhypoproteinaemia (non-specific)

Biochemistry

  • Leucocytosis (non-specific)

Other Tests

Diagnostic Imaging

  • Abdominal radiography is unremarkable, but it can be used to eliminate other differential diagnosis.
  • Abdominal ultrasonography may reveal thickened intestinal walls, mesenteric lymphadenopathy or abdominal effusion.

Histopathology

Intestinal biopsy is needed for a definitive diagnosis once all the other differential diagnoses have been eliminated.

Refer to Lymphocytic - Plasmacytic Enteritis for pathology.


Treatment

Refer to IBD

Prognosis

Refer to IBD


References

  • Ettinger, S.J. and Feldman, E. C. (2000) Textbook of Veterinary Internal Medicine Diseases of the Dog and Cat Volume 2 (Fifth Edition) W.B. Saunders Company.
  • Hall, E.J, Simpson, J.W. and Williams, D.A. (2005) BSAVA Manual of Canine and Feline Gastroenterology (2nd Edition) BSAVA
  • Nelson, R.W. and Couto, C.G. (2009) Small Animal Internal Medicine (Fourth Edition) Mosby Elsevier.