Hepatic sarcoidosis in patients presenting with liver dysfunction: imaging appearance, pathological correlation and disease evolution.

Objectives: We hypothesize that hepatic sarcoidosis is a dynamic process that can lead to cirrhosis and portal hypertension, independent of the course of thoracic disease. Therefore, we assess the imaging appearance and progression of hepatic sarcoidosis in subjects presenting with hepatic dysfuncti...

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Publicado en:European Radiology Vol. 26; no. 9; pp. 3129 - 3138
Autores principales: Fetzer, David, Rees, Mitchell, Dasyam, Anil, Tublin, Mitchell, Fetzer, David T, Rees, Mitchell A, Dasyam, Anil K, Tublin, Mitchell E
Formato: diagnostic images research tables/charts Journal Article
Publicado: Springer Nature Sep2016
Acceso en línea:Ver este registro en EBSCOhost
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      pub: Springer Nature
      place: New York, New York
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        atl: Hepatic sarcoidosis in patients presenting with liver dysfunction: imaging appearance, pathological correlation and disease evolution.
      aug:
        au:
          Fetzer, David
          Rees, Mitchell
          Dasyam, Anil
          Tublin, Mitchell
          Fetzer, David T
          Rees, Mitchell A
          Dasyam, Anil K
          Tublin, Mitchell E
        affil: Department of Radiology , UT Southwestern Medical Center , 5323 Harry Hines Blvd Dallas 75390-8896 USA
      sug:
        subj:
          Liver Diseases Diagnosis
          Magnetic Resonance Imaging Methods
          Multidetector Computed Tomography Methods
          Sarcoidosis Diagnosis
          Liver
          Middle Age
          Prospective Studies
          Disease Progression
          Liver Diseases Etiology
          Retrospective Design
          Female
          Aged
          Biopsy
          Male
          Sarcoidosis Complications
          Hypertension, Portal Pathology
          Adult
          Human
          Middle Aged: 45-64 years
          Aged: 65+ years
          Adult: 19-44 years
          Female
          Male
      ab: Objectives: We hypothesize that hepatic sarcoidosis is a dynamic process that can lead to cirrhosis and portal hypertension, independent of the course of thoracic disease. Therefore, we assess the imaging appearance and progression of hepatic sarcoidosis in subjects presenting with hepatic dysfunction.Methods: An IRB-approved, HIPAA-compliant, single-institution retrospective review identified 39 subjects with sarcoidosis-related liver dysfunction. Clinical information was collected. Two abdominal radiologists analyzed baseline and follow-up imaging studies, scoring features of cirrhosis. Chest CT was also analyzed.Results: At presentation, 23 subjects (59.0 %) exhibited >3 cirrhotic features and 15 (38.5 %) >2 findings of portal hypertension. Of subjects with available follow-up, 57.9 % (19 subjects; mean interval 4.7 years) showed worsening of >3 cirrhotic features (Pearson rho = 0.58; p = 0.009). Parenchymal nodules were uncommon (25.6 %), and most regressed. Although 87.2 % of subjects were diagnosed with thoracic sarcoidosis, there was poor correlation between severity of hepatic and chest disease (Pearson rho = 0.30; p = 0.119). A mean of 7.2 years elapsed between diagnosis of pulmonary and liver involvement.Conclusion: Sarcoidosis may present as liver dysfunction, cirrhosis or portal hypertension. Sarcoid-related liver disease may progress and can manifest without, alongside or significantly after a diagnosis of pulmonary disease.Key Points: • Patients often present with elevated liver function tests indicating cholestasis. • Patients may present with portal hypertension, and some progress to cirrhosis. • Though biopsy can be considered for focal liver lesions, most will regress. • Extent of intra-abdominal involvement may not correlate with severity of thoracic disease. • Liver disease may manifest alongside, prior to or significantly after initial diagnosis.
      pubtype: Academic Journal
      doctype:
        diagnostic images
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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