A Rare Case of Focal Nodular Hyperplasia in a Man With Idiopathic Non-cirrhotic Portal Hypertension

2015 ◽  
Vol 110 ◽  
pp. S369-S370
Author(s):  
Mubeen Khan Mohammed Abdul ◽  
Michael Hsu ◽  
Sheila Eswaran
2021 ◽  
Vol 156 (Supplement_1) ◽  
pp. S124-S125
Author(s):  
A M Alkashash ◽  
S Khan ◽  
R Saxena ◽  
L Nephew ◽  
C Kubal

Abstract Introduction/Objective Non-cirrhotic portal hypertension (NCPH) is uncommon. The underlying pathophysiology appears to lie at the level of intrahepatic portal veins and sinusoids, hence the term “porto-sinusoidal vascular disease” (PSVD). We report a rare case of PSVD with focal nodular hyperplasia (FNH)-like nodules in a patient with neurofibromatosis type 2 (NF2). Methods/Case Report A 57-year-old male with NF2 and type 2 diabetes, presented with a large variceal bleed requiring blood transfusion and subsequent transjugular intrahepatic portosystemic shunt (TIPS). Imaging showed a nodular liver, presumed to be cirrhosis due to non-alcoholic liver disease. Liver biopsy was not done. Thereafter, he had several episodes of hepatic encephalopathy and TIPS was downsized to prevent recurrences. The patient required liver transplantation for intractable portal hypertension and severe hepatic encephalopathy; his liver synthetic function was near normal and MELD was 11. Portal vein was patent. The explanted liver was micronodular, soft and weighed 946 grams. Unencapsulated nodules, a few mm to 1 cm in size, were present. Microscopically, there was diffuse nodularity in the absence of bridging fibrosis. Thin, incomplete curvilinear fibrous septa were present. There were aberrant veins, hypervascular portal tracts, herniated portal veins and rare occluded portal veins. Trichrome and reticulin stains confirmed architectural abnormalities including nodularity, lack of bridging fibrosis and approximation of portal tracts. Immunohistochemistry for glutamine synthetase accentuated architectural distortion and revealed nodules with FNH-like geographic areas of staining. Results (if a Case Study enter NA) NA Conclusion This is a rare case of NCPH due to PSVD in a patient with NF2. Microscopy suggested incomplete septal cirrhosis (ISC), a pattern associated with both PSVD and regression of fibrosis in a cirrhotic liver. Isolated portal hypertension without loss of synthetic function favors primary PSVD over regression of fibrosis. FNH-like nodules are consistent with regenerative changes caused by localized abnormalities of blood flow.


2021 ◽  
Vol 64 ◽  
pp. 101713
Author(s):  
Srinidhi Shanmugasundaram ◽  
Valeria Gioioso ◽  
Mercedes Martinez ◽  
Steven Lobritto ◽  
Jennifer Vittorio ◽  
...  

2010 ◽  
Vol 105 ◽  
pp. S296-S297
Author(s):  
Jonathan Nass ◽  
Teddy N. Winstead ◽  
Nancy Davis ◽  
Justin Levine

2014 ◽  
Vol 44 (10) ◽  
pp. E309-E315 ◽  
Author(s):  
Katsutoshi Sugimoto ◽  
Fukuo Kondo ◽  
Yoshihiro Furuichi ◽  
Hisashi Oshiro ◽  
Toshitaka Nagao ◽  
...  

2000 ◽  
Vol 15 (11) ◽  
pp. 1344-1347 ◽  
Author(s):  
Hideki Kumagai ◽  
Tomoyuki Masuda ◽  
Hiroki Oikawa ◽  
Kaoru Endo ◽  
Mikiya Endo ◽  
...  

Pathology ◽  
2001 ◽  
Vol 33 (3) ◽  
pp. 396-398
Author(s):  
Gerald Langman ◽  
Pauline De La M Hall

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