scholarly journals Minimally invasive percutaneous endovascular therapies in the management of complications of non-alcoholic fatty liver disease (NAFLD): A case report

2015 ◽  
Vol 9 (9) ◽  
Author(s):  
Keith Pereira ◽  
Jason Salsamendi ◽  
Kyungmin Kang ◽  
Ji Fan
2005 ◽  
Vol 48 (2) ◽  
pp. 195-198 ◽  
Author(s):  
Pierre-Henri Bernard ◽  
Cécile Ged ◽  
Evelyne Faivre ◽  
Gérald Legac ◽  
Paulette Bioulac-Sage ◽  
...  

2021 ◽  
Vol 156 (Supplement_1) ◽  
pp. S60-S61
Author(s):  
H Sonani ◽  
A C Srivastava ◽  
N Varshney

Abstract Introduction/Objective Trisomy 21 (Down syndrome) is the most common chromosomal disorder. Among trisomy 21 patients in the pediatric setting, obesity is one of the most common conditions, with prevalence ranging from 23% to 70%. Trisomy 21 has several risk factors for obesity, including increased unfavorable dietary patterns, lower levels of physical activity, and other comorbidities. Epidemiologic studies found this increase in pediatric obesity along with an increased prevalence of non-alcoholic fatty liver disease (NAFLD). Furthermore, children with trisomy 21 have a higher prevalence of NAFLD than children without trisomy 21, even in the absence of obesity. As per literature, NAFLD is present in 64.3 percent of patients with Trisomy 21. Methods/Case Report We present a case of a 17-year-old female with trisomy 21 who was diagnosed with B-cell acute lymphoblastic leukemia (B-ALL) after being admitted due to abdominal pain and decreased appetite. The patient was found to have elevated liver enzymes with abnormal ultrasonography findings. MR images showed fatty liver infiltration with a hepatic fat fraction of 47%. Subsequently, a percutaneous liver biopsy was obtained. Microscopic examination showed minimal hepatic parenchyma with collapsed architecture replaced by abundant steatosis (approximately 90%). Portal triads showed mild lymphocytic inflammation and presence of neutrophils. No fibrosis was confirmed with the trichrome stain. She was then enrolled on AALL1731, a clinical trial for a therapy to treat B-ALL. A 4-month follow-up MR image showed hepatic steatosis. After 9 months, liver biopsy revealed cirrhotic liver along with portal lymphoplasmacytic inflammation, bile duct proliferation and mild macro vesicular steatosis. Results (if a Case Study enter NA) NA Conclusion This case report signifies the importance of histological evaluation of liver abnormalities to provide better treatment. It is vital to schedule close follow-ups in Trisomy 21 patient polpulation, because NAFLD can transform rapidly into a completely cirrhotic liver escpecially with acute lymphoblastic leukemia on chemotherapy. We also emphasizes early lifestyle modifications, including weight loss and proper diet.


2020 ◽  
Vol 41 (5) ◽  
pp. 740-744
Author(s):  
Gi-hyeon Gwon ◽  
Seo-hye Oh ◽  
Geum-ju Song ◽  
Sang-beom Kim ◽  
Hyung-woo Lee ◽  
...  

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