scholarly journals S2628 Case Report: Hepatic Hydrothorax Without Ascites in Newly Diagnosed Cirrhotic Patient

2021 ◽  
Vol 116 (1) ◽  
pp. S1102-S1103
Author(s):  
Farha N. Ebadi
2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Mehrnosh Aeinfar ◽  
Mehrdad Payandeh ◽  
Mohammad Samadian ◽  
Nasrin Amiryfard ◽  
Mohammaderfan Zare ◽  
...  

2018 ◽  
Vol 12 (5) ◽  
pp. 309-314 ◽  
Author(s):  
Zhaohui Bai ◽  
Xiaozhong Guo ◽  
Xiaodong Shao ◽  
Yingying Li ◽  
Qianqian Li ◽  
...  

Author(s):  
Martino Handoyo ◽  
Titong Sugihartono

Hepatic hydrothorax is a transudative pleural effusion which presents in 5-10% patients with liver cirrhosis. Although fairly uncommon, it is associated with higher morbidity and lower survival rate. The mechanism is yet to be understood fully, but the most widely accepted pathogenesis involves the presence of portal hypertension, diaphragmatic defects, and negative intrathoracal pressure, all of which lead to the formation of unidirectional passage of ascitic fluid from peritoneal cavity into pleural space. Due to its origin, the pleural effusion has similar characteristics to ascitic fluid. We herein report the case of a 60-year-old woman with advanced liver cirrhosis and right-sided moderate hepatic hydrothorax. Treatment given to the patient includes diuretics, sodium restriction, and repeated thoracentesis. Subsequent evaluation of the patient revealed improvement both clinically and radiologically.


Author(s):  
Chumpol Anamnart ◽  
Nanthaya Tisavipat ◽  
Weerapat Owattanapanich ◽  
Metha Apiwattanakul ◽  
Pakawee Savangned ◽  
...  

2020 ◽  
Vol 7 ◽  
Author(s):  
Rachel E. Kinney ◽  
Robert Decker ◽  
Deborah Sundlof ◽  
Muhammad A. Rizvi ◽  
Kelly Schadler

Neuroendocrine tumors (NETs), also known as carcinoid tumors, are a heterogeneous group of neoplasms that arise from cells throughout the neuroendocrine system, most commonly arising from the gastrointestinal (GI) tract, lungs, and bronchi. Myocardial carcinoid metastasis is rare with an incidence among metastatic carcinoid patients of 4%. They are generally asymptomatic and detected incidentally. Infiltrative myocardial metastasis secondary to carcinoid tumor is exceedingly rare with only single-digit cases reported in the literature. We report the case of a 65-years-old female with a newly diagnosed ileal neuroendocrine tumor as well as heart failure due to infiltrative myocardial metastasis.


Sign in / Sign up

Export Citation Format

Share Document