Cargando…

Hepatic Sarcodosis presenting as portal hypertension in a young boy

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, autoi...

Descripción completa

Detalles Bibliográficos
Autores principales: Achakzai, Inamullah Khan, Majid, Zain, Khalid, Muhammad Ali, Khan, Shoaib Ahmed, Laeeq, Syed Mudassir, Luck, Nasir Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849123/
https://www.ncbi.nlm.nih.gov/pubmed/29564070
_version_ 1783305998650310656
author Achakzai, Inamullah Khan
Majid, Zain
Khalid, Muhammad Ali
Khan, Shoaib Ahmed
Laeeq, Syed Mudassir
Luck, Nasir Hassan
author_facet Achakzai, Inamullah Khan
Majid, Zain
Khalid, Muhammad Ali
Khan, Shoaib Ahmed
Laeeq, Syed Mudassir
Luck, Nasir Hassan
author_sort Achakzai, Inamullah Khan
collection PubMed
description 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.
format Online
Article
Text
id pubmed-5849123
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Shaheed Beheshti University of Medical Sciences
record_format MEDLINE/PubMed
spelling pubmed-58491232018-03-21 Hepatic Sarcodosis presenting as portal hypertension in a young boy Achakzai, Inamullah Khan Majid, Zain Khalid, Muhammad Ali Khan, Shoaib Ahmed Laeeq, Syed Mudassir Luck, Nasir Hassan Gastroenterol Hepatol Bed Bench Case Report 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. Shaheed Beheshti University of Medical Sciences 2018 /pmc/articles/PMC5849123/ /pubmed/29564070 Text en ©2018 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Achakzai, Inamullah Khan
Majid, Zain
Khalid, Muhammad Ali
Khan, Shoaib Ahmed
Laeeq, Syed Mudassir
Luck, Nasir Hassan
Hepatic Sarcodosis presenting as portal hypertension in a young boy
title Hepatic Sarcodosis presenting as portal hypertension in a young boy
title_full Hepatic Sarcodosis presenting as portal hypertension in a young boy
title_fullStr Hepatic Sarcodosis presenting as portal hypertension in a young boy
title_full_unstemmed Hepatic Sarcodosis presenting as portal hypertension in a young boy
title_short Hepatic Sarcodosis presenting as portal hypertension in a young boy
title_sort hepatic sarcodosis presenting as portal hypertension in a young boy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849123/
https://www.ncbi.nlm.nih.gov/pubmed/29564070
work_keys_str_mv AT achakzaiinamullahkhan hepaticsarcodosispresentingasportalhypertensioninayoungboy
AT majidzain hepaticsarcodosispresentingasportalhypertensioninayoungboy
AT khalidmuhammadali hepaticsarcodosispresentingasportalhypertensioninayoungboy
AT khanshoaibahmed hepaticsarcodosispresentingasportalhypertensioninayoungboy
AT laeeqsyedmudassir hepaticsarcodosispresentingasportalhypertensioninayoungboy
AT lucknasirhassan hepaticsarcodosispresentingasportalhypertensioninayoungboy