Difference between revisions of "Lymphangiectasia"

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{{review}}
 
  
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==Introduction==
{{cat}}
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'''Lymphangiectasia''' is a disease of the [[Lymphatic Vessels - Anatomy & Physiology|lymphatic vessels]] that results in the leakage of protein-rich [[Lymph - Anatomy & Physiology|lymph]].  The term is usually taken to mean intestinal lymphangiectasia (in which lymph is lost into the intestinal lumen, producing a [[Protein Losing Enteropathy|protein-losing enteropathy]](PLE) and severe lipid malabsorption) but thoracic and generalised lymphangiectasia have been reported. 
  
 +
Lymphangiectasia can be classified into a primary or secondary disease.  '''Primary lymphangiectasia''' usually only affects the intestine but it occasionally involves a concurrent [[Chylous Effusion|chylothorax]].  It occurs due to a congenital defect of the lymphatic vessels but it may be associated with inflammation of the lymphatics, so-called '''lipogranulomatous lympangitis'''.  The relationship between lymphangiectasia and lipogranulomatous lymphangitis is currently unclear and it is possible that either condition could result in the development of the other.  '''Secondary lymphangiectasia''' occurs with any pathological process that causes lymphatic obstruction, of which the most common are:
 +
*Direct damage to the lymphatics
 +
**'''Inflammation''' and subsequent fibrosis of the lymphatics, obstructing the lumina of the vessels.
 +
**'''Neoplastic infiltration or erosion''' of the walls of lymphatic vessels.
 +
**'''Obstruction of the thoracic duct''', the major lymphatic vessel that runs through the chest.  This may occur due to traumatic rupture or due to the presence of a neoplastic mass.
 +
*Increased pressure in the systemic veins reducing the pressure gradient from the thoracic duct to the subclavian veins
 +
**'''[[Heart Failure, Right-Sided|Right-sided heat failure]]''' due to [[Cardiomyopathy|cardiomyopathy]], [[Cardiac Tamponade|cardiac tamponade]] or [[Tricuspid Valve Dysplasia|tricuspid dysplasia]], [[Cor Pulmonale]] or Cor Triatriatum Dexter. 
 +
**Obstruction to venous return by '''intra-thoracic masses''' including thymoma and thymic lymphoma.
  
 
==Signalment==
 
==Signalment==
*Breed predisposition:
+
The disease is relatively common in dogs but rare in cats.  Yorkshire terriers, Rottweilers and Norwegian Lundehunds are predisposed to the development of disease.
**Yorkshire Terrier
 
**Rottweiler
 
**Soft Coated Wheaten Terriers
 
**Lundehund
 
 
 
<gallery>
 
Image:Yorkshire_Terrier.jpg|'''Yorkshire Terrier'''<p>WikiCommons
 
Image:Rottweiler.jpg|'''Rottweiler'''<p>WikiCommons
 
Image:Soft_coated_wheaten_terrier.jpg|'''Soft Coated Wheaten Terrier'''<p>WikiCommons
 
</gallery>
 
 
 
==Description==
 
'''Lymphangiectasia''' is characterised by dilation and dysfunction of the [[Lymphatic Vessels - Anatomy & Physiology|lymphatic vessels]] of the intestines.  Consequently, protein rich [[Lymph - Anatomy & Physiology|lymph]] leaks into the intestinal lumen, causing a [[Protein Losing Enteropathy|
 
protein-losing enteropathy]] and severe lipid malabsorption.  It is relatively common in dogs but rare in cats.   
 
 
 
Lymphangiectasia can be classified into a primary or a secondary lymphangiectasia.  '''Primary lymphangiectasia''' may form part of a localised or a more widespread lymphatic abnormality.  '''Secondary lymphangiectasia''' results from lymphatic obstruction, which may be caused by:
 
*[[Inflammation - Pathology|inflammation]],[[Neoplasia - Pathology|neoplastic]] infiltration or fibrosis
 
*thoracic duct obstruction
 
*[[Right-Sided Heart Failure - WikiClinical|right sided cardiac failure]]
 
*caval obstruction
 
*hepatic disease
 
 
 
Lymphangiectasia often accompanies a lipogranulomatous [[Inflammation - Pathology|inflammation]], but it is not clear which is the primary event.  [[Oedema - Pathology#Lymphatic oedema|Lymphangitis]] can cause lymphatic obstruction but the leakage of [[Lymph - Anatomy & Physiology|lymph]] can also cause a [[Chronic Inflammation  - Pathology#Granulomatous Inflammation|granuloma]] to form.
 
 
 
  
 
==Diagnosis==
 
==Diagnosis==
 
===Clinical Signs===
 
===Clinical Signs===
*Weight loss
+
Clinical signs are related to the loss of lymph and the resultant protein-losing enteropathy and fat malabsorption.  The following signs are therefore common:
*Chronic [[Diarrhoea|diarrhoea]]; steatorrhoea
+
*'''Weight loss''' in the face of '''polyphagia''' due to loss of fat and protein.
*Ascites, oedema or chylothorax may result if there is severe hypoproteinaemia or lymphatic obstruction
+
*'''Chronic [[Diarrhoea|diarrhoea]]''' or '''steatorrhoea''', the latter occurring due to the high fat content of the faeces.  The presence of large quantities of fat in the intestinal lumen provides a substrate for bacteria which produce hydroxy-fatty acids as by-products.  Bacterial proliferation may result in concurrent [[Antibiotic Responsive Diarrhoea|small intestinal bacterial overgrowth]] (SIBO) and the hydroxy-fatty acids act as potent secretagogues in the colon, leading to the production of diarrhoeic faeces.
*Increased appetite
+
*[[:Category:Effusions|'''Effusions''']] may develop for a number of reasons in animals with lymphangiectasia.  Ascites composed of a [[Transudate|transudate]] may develop in severely [[Hypoalbuminaemia|hypoproteinaemic]] animals but, in animals that develop secondary lymphangiectasia due to right-sided heart failure, a [[Modified Transudate|modified transudate]] may form due to portal hypertension.  If the major lymphatic vessels of the abdomen are disrupted (by a neoplastic mass), [[Chylous Effusion|chylous ascites]] may develop, although this is very rare.  In animals with congenital lymphangiectasia or in those with disruption of the thoracic duct, chylothorax has also been described.
*[[Stomach and Abomasum Consequences of Gastric Disease - Pathology|Vomiting]], lethargy and anorexia (less common)
+
*[[Vomiting|Vomiting]], lethargy and anorexia are uncommon clinical signs.
 
 
  
 
===Laboratory Tests===
 
===Laboratory Tests===
 +
Several parameters may be altered on haematological or biochemical analysis of blood samples.
 
====Haematology====
 
====Haematology====
*'''Panhypoproteinaemia'''
+
'''[[Lymphopenia|Lymphopaenia]]''' occurs as lymphocytes are the major type of cell present in lymph and they are therefore lost into the intestinal lumen in large numbers.  If an inflammatory process (such as lipogranulomatous lymphangitis) has developed, there may be a '''monocytosis''' or '''neutrophilia'''.
*'''[[Changes in Inflammatory Cells Circulating in Blood - Pathology #Lymphopenia|Lymphopaenia]]'''
 
  
 
====Biochemistry====
 
====Biochemistry====
*'''Hypocholesterolaemia'''
+
Changes on biochemistry mainly reflect the loss of lymph into the intestine:
*[[Hypocalcaemia - Small Animal|Hypocalcaemia]] due to hypoproteinaemia, vitamin D and calcium malabsorption
+
*'''Panhypoproteinaemia''' occurs in most forms of protein-losing enteropathy and suggests that both plasma albumin and globulin are being lost. 
*Hypomagnesaemia
+
*'''Hypocholesterolaemia''' and a reduction in the circulating concentration of triglycerides occur as these nutrients are lost into the intestinal lumen.
 
+
*'''Hypocalcaemia''' occurs due to hypoproteinaemia (reducing the total but not ionised calcium concentration) and due to vitamin D and calcium malabsorption.  Hypocalcaemic tetany may be observed in animals which are severely hypocalcaemic and which then become stressed or excited.
[[Image:Lymphangiectasia.jpg|thumb|right|300px|Lymphangiectasia Endoscopy- Copyright Karin Allenspach's lecture RVC]]
+
*'''Hypomagnesaemia''' may also develop due to malabsorption but this is rarely recognised in clinical practice.
 +
*[[Antibiotic Responsive Diarrhoea|Changes associated with SIBO are discussed here]].
  
 
====Other Tests====
 
====Other Tests====
*Faecal α1-proteinase inhibitor concentrations or chromium 51-labelled albumin may be used to confirm [[Protein Losing Enteropathy|protein-losing enteropathy]].
+
Further tests may be used to confirm the presence of [[Protein Losing Enteropathy|protein-losing enteropathy]], including measurement of '''faecal alpha-1 protease inhibitor concentration''' and '''faecal 51-Chromium albumin concentration''' after intra-venous injection.
 
 
  
 
===Diagnostic Imaging===
 
===Diagnostic Imaging===
====Ultrasound====
+
====Ultrasonography====
Abdominal ultrasonography may reveal pleural fluid or ascites as well as helping to narrow down other differential diagnosesMucosa of intestinal loops may appear thickened due to oedema.
+
Ultrasound scans may reveal the presence of effusions (pleural fluid or ascites) and may be used to rule out other causes of PLEThe mucosa of affected intestinal loops may appear to be thickened and may also appear to have 'tiger stripes', although the latter finding is an unreliable indicator of lymphangiectasia.  
  
 
====Endoscopy====
 
====Endoscopy====
Grossly, multiple white lipid droplets with prominent mucosal blebs can be seen.
+
[[Image:Lymphangiectasia.jpg|thumb|right|300px|Endoscopy of a dog with lymphangiectasia, showing protrusion of lipid droplets into the intestinal lumen.<br><small>Copyright Karin Allenspach 2007 RVC]]</small>
 
+
Grossly, multiple white lipid droplets can be seen to protrude from prominent mucosal blebs in the intestine (see image).  The mucosa is frequently oedematous.
  
 
===Histopathology===
 
===Histopathology===
Preferably, a full thickness biopsy is needed for a definitive diagnosis.
+
Preferably, a full thickness intestinal biopsy should be taken to achieve a definitive diagnosis. Care should be taken as hypoproteinaemic animals are at much greater risk of dehiscence at the biopsy sites, potentially leading to an acute septic [[Peritonitis - Cats and Dogs|peritonitis]].  On histological examination of the biopsy sample, accumulation of lipid-laden macrophages may be detected together with a granulomatous response around distended lymphatics.
 
 
Refer to [[Lymphangiectasia|Lymphangiectasia]] for pathology
 
 
 
It is essential to distinguish a true lymphangiectasia from a secondary lacteal dilation due to [[Inflammatory Bowel Disease|Inflammatory Bowel Disease ]] (IBD)In the case of IBD, inflammatory infiltrate will be seen in the lamina propria, but the degree of infiltration may be underestimated if [[Oedema - Pathology|oedema]] is present.
 
  
 +
It is essential to distinguish a true lymphangiectasia from secondary lacteal dilation that occurs with [[Inflammatory Bowel Disease|Inflammatory Bowel Disease]] (IBD).  In the case of IBD, an inflammatory infiltrate will be seen in the lamina propria but the degree of infiltration may be underestimated if [[Oedema|oedema]] is present.
  
 
==Treatment==
 
==Treatment==
*Identify and treat the underlying cause if it is a secondary lymphangiectasia
+
If the lymphangiectasia is secondary to another disease, the underlying cause should be treated.  Otherwise, the following elements should be considered in designing a treatment plan.
 
===Dietary modification===
 
===Dietary modification===
*Fat-restricted diet
+
The diet should have a '''low fat content''' to reduce the production of lymph but should have a high calorie content to allow the animal to regain weight.  The fat soluble vitamins (K, E, D and A) should be supplemented and additional calcium should be added if hypocalcaemia is documented.
*The diet needs to be calorific and highly digestible
 
*Supplementation of fat soluble vitamins
 
*Anecdotal report of glutamine supplementation
 
  
 
===Immunosuppressive===
 
===Immunosuppressive===
*[[Steroids|Prednisolone]]
+
Immunosuppressive agents are a key element in the treatment of lymphangiectasia.  Corticosteroids such as [[Steroids|prednisolone]] are used most commonly for this pupose at an immunosuppressive dose (of 1-2 mg/kg/day in dogs).  These drugs are likely to be of most benefit in those animals that have evidence of inflammatory pathology, such as lipogranulomatous lymphangitis and inflammatory infiltration of the lamina propria. If further immunosuppression is considered necessary or if adverse effects occur with corticosteroid therapy, azathioprine or ciclosporin could also be used.
*[[Anti-Inflammatory Drugs|Anti-inflammatory]] and immunosuppressive effect may be beneficial.
 
*This is particularly true if there is associated lymphangitis, lipogranulomas or a [[Lymphocytic - Plasmacytic Enteritis - WikiClinical|lymphocytic-plasmacytic]] infiltration of the lamina propria.
 
*Azathioprine or Ciclosporin can also be considered
 
  
 
===Antimicrobials===
 
===Antimicrobials===
*[[Nitroimidazoles|Metronidazole]] or [[Macrolides and Lincosamides|tylosin]] can be given
+
[[Nitroimidazoles|Metronidazole]] or [[Macrolides and Lincosamides|tylosin]] may be used to control any secondary [[Antibiotic Responsive Diarrhoea|SIBO]]. Antibiotics are thought to have effects on both the intestinal immune system and the normal enteric flora.
*This may be beneficial due to their potential immunomodulatory effect and modulation of the enteric flora
 
*Diuretics such as [[Treatment of Heart Failure - WikiClinical #C. Pharmacological|frusemide]] and [[Treatment of Heart Failure - WikiClinical #C. Pharmacological|spironolactone]] are used to manage effusions.
 
  
 
===Fluid therapy===
 
===Fluid therapy===
*Short term treatment with [[Plasma - WikiBlood|plasma]] or [[Colloids|colloids]] can be given for plasma expansion.
+
Short term treatment with plasma or [[Colloids|colloids]] can be instituted in severely hypoproteinaemic animals that have begun to develop clinical signs.  Diuretics such as [[Heart Failure, Treatment#C. Pharmacological|frusemide and spironolactone]] may also be used to manage effusions.
 
 
  
 
==Prognosis==
 
==Prognosis==
Guarded.  The response to treatment is generally poor although some dogs may do well.  Dogs  may be in remission for several years but the disease eventually progress to fulminant hypoproteinaemia.
+
The long-term prognosis is guarded as, although animals may respond to medical therapy initially, they frequently relapse and develop clinical signs associated with hypoproteinaemia.
 
 
==From pathology==
 
 
 
===Pathology===
 
 
 
====Gross====
 
 
 
* Small and [[Large Intestine - Anatomy & Physiology|large intestine]]s may be affected.
 
* Dilation of lacteals.
 
* Oedema of intestinal mucosa.
 
* Distension of mesenteric lymphatics and lymph nodes.
 
 
 
====Histological====
 
 
* Accumulation of lipid-laden macrophages and granulomatous response around distended lymphatics.
 
 
 
 
 
  
 +
{{Learning
 +
|Vetstream = [https://www.vetstream.com/canis/Content/Disease/dis02922.asp, Canine lymphatic diseases]
 +
|literature search = [http://www.cabdirect.org/search.html?rowId=1&options1=AND&q1=Lymphangiectasia&occuring1=title&rowId=2&options2=AND&q2=&occuring2=freetext&rowId=3&options3=AND&q3=&occuring3=freetext&x=54&y=14&publishedstart=yyyy&publishedend=yyyy&calendarInput=yyyy-mm-dd&la=any&it=any&show=all Lymphangiectasia publications]
 +
}}
  
 
==References==
 
==References==
Line 122: Line 79:
 
*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''.
  
 +
 +
{{review}}
 +
 +
==Webinars==
 +
<rss max="10" highlight="none">https://www.thewebinarvet.com/gastroenterology-and-nutrition/webinars/feed</rss>
  
 
[[Category:Intestine_-_Inflammatory_Pathology]]
 
[[Category:Intestine_-_Inflammatory_Pathology]]
[[Category:To_Do_-_Clinical]]
+
 
 +
[[Category:Intestinal Diseases - Dog]][[Category:Intestinal Diseases - Cat]]
 +
[[Category:Expert_Review]]

Latest revision as of 14:13, 9 January 2023

Introduction

Lymphangiectasia is a disease of the lymphatic vessels that results in the leakage of protein-rich lymph. The term is usually taken to mean intestinal lymphangiectasia (in which lymph is lost into the intestinal lumen, producing a protein-losing enteropathy(PLE) and severe lipid malabsorption) but thoracic and generalised lymphangiectasia have been reported.

Lymphangiectasia can be classified into a primary or secondary disease. Primary lymphangiectasia usually only affects the intestine but it occasionally involves a concurrent chylothorax. It occurs due to a congenital defect of the lymphatic vessels but it may be associated with inflammation of the lymphatics, so-called lipogranulomatous lympangitis. The relationship between lymphangiectasia and lipogranulomatous lymphangitis is currently unclear and it is possible that either condition could result in the development of the other. Secondary lymphangiectasia occurs with any pathological process that causes lymphatic obstruction, of which the most common are:

  • Direct damage to the lymphatics
    • Inflammation and subsequent fibrosis of the lymphatics, obstructing the lumina of the vessels.
    • Neoplastic infiltration or erosion of the walls of lymphatic vessels.
    • Obstruction of the thoracic duct, the major lymphatic vessel that runs through the chest. This may occur due to traumatic rupture or due to the presence of a neoplastic mass.
  • Increased pressure in the systemic veins reducing the pressure gradient from the thoracic duct to the subclavian veins

Signalment

The disease is relatively common in dogs but rare in cats. Yorkshire terriers, Rottweilers and Norwegian Lundehunds are predisposed to the development of disease.

Diagnosis

Clinical Signs

Clinical signs are related to the loss of lymph and the resultant protein-losing enteropathy and fat malabsorption. The following signs are therefore common:

  • Weight loss in the face of polyphagia due to loss of fat and protein.
  • Chronic diarrhoea or steatorrhoea, the latter occurring due to the high fat content of the faeces. The presence of large quantities of fat in the intestinal lumen provides a substrate for bacteria which produce hydroxy-fatty acids as by-products. Bacterial proliferation may result in concurrent small intestinal bacterial overgrowth (SIBO) and the hydroxy-fatty acids act as potent secretagogues in the colon, leading to the production of diarrhoeic faeces.
  • Effusions may develop for a number of reasons in animals with lymphangiectasia. Ascites composed of a transudate may develop in severely hypoproteinaemic animals but, in animals that develop secondary lymphangiectasia due to right-sided heart failure, a modified transudate may form due to portal hypertension. If the major lymphatic vessels of the abdomen are disrupted (by a neoplastic mass), chylous ascites may develop, although this is very rare. In animals with congenital lymphangiectasia or in those with disruption of the thoracic duct, chylothorax has also been described.
  • Vomiting, lethargy and anorexia are uncommon clinical signs.

Laboratory Tests

Several parameters may be altered on haematological or biochemical analysis of blood samples.

Haematology

Lymphopaenia occurs as lymphocytes are the major type of cell present in lymph and they are therefore lost into the intestinal lumen in large numbers. If an inflammatory process (such as lipogranulomatous lymphangitis) has developed, there may be a monocytosis or neutrophilia.

Biochemistry

Changes on biochemistry mainly reflect the loss of lymph into the intestine:

  • Panhypoproteinaemia occurs in most forms of protein-losing enteropathy and suggests that both plasma albumin and globulin are being lost.
  • Hypocholesterolaemia and a reduction in the circulating concentration of triglycerides occur as these nutrients are lost into the intestinal lumen.
  • Hypocalcaemia occurs due to hypoproteinaemia (reducing the total but not ionised calcium concentration) and due to vitamin D and calcium malabsorption. Hypocalcaemic tetany may be observed in animals which are severely hypocalcaemic and which then become stressed or excited.
  • Hypomagnesaemia may also develop due to malabsorption but this is rarely recognised in clinical practice.
  • Changes associated with SIBO are discussed here.

Other Tests

Further tests may be used to confirm the presence of protein-losing enteropathy, including measurement of faecal alpha-1 protease inhibitor concentration and faecal 51-Chromium albumin concentration after intra-venous injection.

Diagnostic Imaging

Ultrasonography

Ultrasound scans may reveal the presence of effusions (pleural fluid or ascites) and may be used to rule out other causes of PLE. The mucosa of affected intestinal loops may appear to be thickened and may also appear to have 'tiger stripes', although the latter finding is an unreliable indicator of lymphangiectasia.

Endoscopy

Endoscopy of a dog with lymphangiectasia, showing protrusion of lipid droplets into the intestinal lumen.
Copyright Karin Allenspach 2007 RVC

Grossly, multiple white lipid droplets can be seen to protrude from prominent mucosal blebs in the intestine (see image). The mucosa is frequently oedematous.

Histopathology

Preferably, a full thickness intestinal biopsy should be taken to achieve a definitive diagnosis. Care should be taken as hypoproteinaemic animals are at much greater risk of dehiscence at the biopsy sites, potentially leading to an acute septic peritonitis. On histological examination of the biopsy sample, accumulation of lipid-laden macrophages may be detected together with a granulomatous response around distended lymphatics.

It is essential to distinguish a true lymphangiectasia from secondary lacteal dilation that occurs with Inflammatory Bowel Disease (IBD). In the case of IBD, an inflammatory infiltrate will be seen in the lamina propria but the degree of infiltration may be underestimated if oedema is present.

Treatment

If the lymphangiectasia is secondary to another disease, the underlying cause should be treated. Otherwise, the following elements should be considered in designing a treatment plan.

Dietary modification

The diet should have a low fat content to reduce the production of lymph but should have a high calorie content to allow the animal to regain weight. The fat soluble vitamins (K, E, D and A) should be supplemented and additional calcium should be added if hypocalcaemia is documented.

Immunosuppressive

Immunosuppressive agents are a key element in the treatment of lymphangiectasia. Corticosteroids such as prednisolone are used most commonly for this pupose at an immunosuppressive dose (of 1-2 mg/kg/day in dogs). These drugs are likely to be of most benefit in those animals that have evidence of inflammatory pathology, such as lipogranulomatous lymphangitis and inflammatory infiltration of the lamina propria. If further immunosuppression is considered necessary or if adverse effects occur with corticosteroid therapy, azathioprine or ciclosporin could also be used.

Antimicrobials

Metronidazole or tylosin may be used to control any secondary SIBO. Antibiotics are thought to have effects on both the intestinal immune system and the normal enteric flora.

Fluid therapy

Short term treatment with plasma or colloids can be instituted in severely hypoproteinaemic animals that have begun to develop clinical signs. Diuretics such as frusemide and spironolactone may also be used to manage effusions.

Prognosis

The long-term prognosis is guarded as, although animals may respond to medical therapy initially, they frequently relapse and develop clinical signs associated with hypoproteinaemia.


Lymphangiectasia Learning Resources
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Lymphangiectasia publications


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.



Webinars

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