• Title of article

    Hepatic Sarcodosis presenting as portal hypertension in a young boy

  • Author/Authors

    Achakzai, Inamullah Khan Sindh Institute of Urology and Transplantation - Pakistan , Majid, Zain Sindh Institute of Urology and Transplantation - Pakistan , Ali Khalid, Muhammad Sindh Institute of Urology and Transplantation - Pakistan , Ahmed Khan, Shoaib Sindh Institute of Urology and Transplantation - Pakistan , Laeeq, Mudassir Sindh Institute of Urology and Transplantation - Pakistan , Luck, Nasir Hassan Sindh Institute of Urology and Transplantation - Pakistan

  • Pages
    9
  • From page
    220
  • To page
    228
  • Abstract
    A 13-year-old boy, known case renal stone disease came with the complaints of abdominal pain along with low grade fever. On examination, hepatosplenomegaly was noted while his lab reports showed a low hemoglobulin with a raised ESR. His blood and urine cultures showed no growth. Viral markers, autoimmune profile, C and p ANCA were all negative apart from a raised serum IgG level. Ultrasound abdomen showed a hyperechoic liver with an enlarged spleen along with splenic varices and minimum ascites. Ultrasound hepatic doppler was normal. Serum AFP levels were normal while workup for Wilson’s disease was negative. Fibroscan showed F4 fibosis. CT scan abdomen showed an enlarged left lobe of the liver along with an enlarged spleen. His EGD revealed varices. So liver biopsy was done that was suggestive of chronic granulomatous disease with ZN stain testing negative for TB.PPD, urine for AFB were both negative. Serum ACE levels were raised. He started ATT therapy but his condition did not improve. So, on the suspicion of hepatic sarcoidosis, he started on steroids and had a drastic improvement in his condition.
  • Keywords
    Hepatic sarcoidosis , chronic granulomatous disease , steroids , Serum ACE levels
  • Journal title
    Astroparticle Physics
  • Serial Year
    2018
  • Record number

    2479678