Obliterative portal venopathy
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Hepatoportal sclerosis
Overview
Hepatoportal sclerosis (HPS) is a rare disorder characterized by sclerosis of the intrahepatic portal veins.
Pathophysiology
Pathology
Histopathologic findings are
- Periportal fibrosis
- Sclerosis of the portal venous system
- Proliferation of small vascular channels within/around portal tracts
Causes
- Exposure to toxic substances (arsenic or vinyl chloride)
- autoimmune and connective tissue diseases
- systemic or intra abdominal infections
- Clotting factor abnormalities
Differentiating from other Diseases
Differential diagnosis from liver cirrhosis is crucial and may be difficult. A large liver biopsy specimen, together with expertise and awareness of the examiner, are requested for optimal diagnosis.
Epidemiology and Demographics
The prevalence of this disease is unknown, and the distribution is worldwide, with many cases reported in Asia.
Age
The disease can occur at any age.
Gender
Both males and females are equally affected.
Natural History, Complications and Prognosis
Complications
Prognosis
Current overall prognosis is good (80% survival at ten years after the diagnosis). Male patients and patients with disease onset before 40 years of age show a poorer prognosis.
Diagnosis
Symptoms
Lethargy and in advanced stages symptoms of liver failure
Physical Examination
Eye
Abdomen
- Ascites
- Spleenomegaly
- Signs of portal hypertension
Neurologic
Laboratory Findings
Blood and Biomarker Studies
Endoscopy
Biopsy
- Evidence of sclerosis of portal tract
CT
- Delineates the portal system and helps in the identification of lesions.