Difference between revisions of "Hepatic Microvascular Dysplasia"
Jump to navigation
Jump to search
JamesSwann (talk | contribs) |
|||
Line 18: | Line 18: | ||
*Higher MCV, serum postprandial bile acid concentrations, serum albumin and cholesterol concentrations when PSS and HMD together, compared to HMD alone. | *Higher MCV, serum postprandial bile acid concentrations, serum albumin and cholesterol concentrations when PSS and HMD together, compared to HMD alone. | ||
[[Category:Liver_-_Developmental_Pathology]] | [[Category:Liver_-_Developmental_Pathology]] | ||
− | [[Category:To_Do_- | + | |
+ | [[Category:To_Do_-_James]] |
Revision as of 19:46, 8 July 2010
- Small intrahepatic portal vessels and portal endothelial hyperplasia which allows abnormal communication between portal and systemic circulation.
- Can develop as a separate entity or in conjunction with a portosystemic shunt.
- Can cause c/s similar to those of PSS.
- Vomiting, diarrhoea, urinary tract changes associated with ammonium biurate urolithiasis, stunted growth, prolonged recovery from anesthesia.
- Average age of presentation =3yrs.
- Mainly small dogs, esp. Yorkies
- Females>males
Histology
- Arteriolarization of central veins
- smooth muscle proliferation (segmental) within the walls of central veins
- random distribution of small calibre vessels
- endothelial hyperplasia within portal triads
- dilation of periacinar vascular spaces.
- May also see decreased diameter of intrahepatic veins.
- Can’t be accurately distinguished from PSS alone.
- Seen in older dogs than PSS
- Higher MCV, serum postprandial bile acid concentrations, serum albumin and cholesterol concentrations when PSS and HMD together, compared to HMD alone.