Warning: mkdir(): Permission denied in /home/virtual/lib/view_data.php on line 81

Warning: fopen(upload/ip_log/ip_log_2024-11.txt): failed to open stream: No such file or directory in /home/virtual/lib/view_data.php on line 83

Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 84
Non-cirrhotic Portal Hypertension in Idiopathic Myelofibrosis: A case report.
Skip Navigation
Skip to contents

J Pathol Transl Med : Journal of Pathology and Translational Medicine

OPEN ACCESS
SEARCH
Search

Articles

Page Path
HOME > J Pathol Transl Med > Volume 34(5); 2000 > Article
Case Report Non-cirrhotic Portal Hypertension in Idiopathic Myelofibrosis: A case report.
Sung Eun Kim, Young Nyun Park, Woo Ick Yang, Jin Sup Choi, Chanil Park
Journal of Pathology and Translational Medicine 2000;34(5):386-388
DOI: https://doi.org/
1Departments of Pathology, Yonsei University College of Medicine, Seoul 120-752, Korea.
2Departments of Surgery, Yonsei University College of Medicine, Seoul 120-752, Korea.
prev next
  • 1,760 Views
  • 18 Download
  • 0 Crossref
  • 0 Scopus

We report a case of non-cirrhotic portal hypertension in a 73 year-old woman, who had 19-year history of idiopathic myelofibrosis. There were esophageal varix, splenomegaly, and ascites. The biopsied liver showed irregular sinusoidal/ perisinusoidal fibrosis and occasional central-to-central fibrous connection. In areas with extensive fibrosis, coarse collagen fibers filled the sinusoidal spaces and compressed hepatocytes. However, nodular regeneration was absent. Double immunohistochemical stain for smooth muscle actin and proliferation cell nuclear antigen (PCNA) revealed diffusely activated stellate cells, some of which showed nuclear PCNA staining. There was also extramedullary hematopoiesis with bizarre megakaryocytes. The portal vein and its branches were patent. Idiopathic myelofibrosis is a rare cause of non-cirrhotic portal hypertension: the portal hypertension was considered to be the result of sinusoidal/perisinusoidal fibrosis in this case.

Related articles

J Pathol Transl Med : Journal of Pathology and Translational Medicine
TOP