scholarly journals Budd-Chiari syndrome: a rare and life-threatening complication of Crohn’s disease

2018 ◽  
pp. bcr-2017-222946 ◽  
Author(s):  
Camila C Simoes ◽  
Yezaz A Ghouri ◽  
Shehzad N Merwat ◽  
Heather L Stevenson
2014 ◽  
Vol 21 (1) ◽  
pp. 31-34 ◽  
Author(s):  
Joana Machado ◽  
Paula Ministro ◽  
Eugénia Cancela ◽  
Ricardo Araújo ◽  
António Castanheira ◽  
...  

2015 ◽  
Vol 69 (3) ◽  
pp. 241-244
Author(s):  
Marta Olbrechtová ◽  
Ondřej Zela ◽  
Petr Vítek

2013 ◽  
Vol 2 (1-2) ◽  
Author(s):  
Banu Kumbak Aygun ◽  
Gulser Goktolga Pinar ◽  
Levent Sahin ◽  
Zehra Sema Ozkan ◽  
Ahmet Kursad Poyraz ◽  
...  

AbstractThe association of Budd-Chiari syndrome (BCS), Crohn’s disease (CD) and pregnancy is extremely rare. The successful medical treatment of BCS in the postpartum period in a woman with CD is presented.A 28-year-old woman with CD presented with fever of 42°C and gross abdominal distention 2 days following delivery. On sonographic examination, massive ascites and hepatosplenomegaly were noted. Color Doppler ultrasonography and contrast-enhanced computed tomography revealed a thrombus in the suprahepatic inferior vena cava causing significant luminal obstruction. She was diagnosed with BCS. Medical treatment with spironolactone, furosemide, imipenem, metronidazole, and enoxaparin improved the clinical picture.In a pregnant woman with CD, extreme thromboembolic events such as BCS might occur. If diagnosed early and treated in the acute phase, prognosis is fair.


Author(s):  
M. Valdés Mas ◽  
C. Martínez Pascual ◽  
J. Egea Valenzuela ◽  
M. C. Martínez Bonil ◽  
A. M. Vargas Acosta ◽  
...  

1989 ◽  
Vol 34 (12) ◽  
pp. 1933-1936 ◽  
Author(s):  
David M. Maccini ◽  
John C. Berg ◽  
Gordon A. Bell

Author(s):  
Esfandiar Shojaei ◽  
Joanna C Walsh ◽  
Nikhil Sangle ◽  
Brian Yan ◽  
Michael S Silverman ◽  
...  

Abstract Disseminated histoplasmosis is a life-threatening disease usually seen in immunocompromised patients living in endemic areas. We present an apparently immunocompetent patient with gastrointestinal histoplasmosis who was initially diagnosed as biopsy-proven Crohn’s disease. Following discontinuation of anti-inflammatory drugs and institution of antifungal therapy, his GI illness completely improved. Specific fungal staining should be routinely included in histopathologic assessment of tissue specimens diagnosed as Crohn’s disease.


2019 ◽  
Vol 2 (1) ◽  
pp. 6-8
Author(s):  
Sith Siramolpiwat ◽  
Tanabute Limprukkasem

Budd-Chiari syndrome (BCS) is a rare, life-threatening disease caused by obstruction of hepatic venous outflow. Common presentations are right upper quadrant pain, ascites, and hepatomegaly. A diagnosis of Budd-Chiari syndrome should be suspected when liver disease occurs in a patient with known risk factors for hypercoagulable state. We report a 22-years old transgender man presented with jaundice, marked ascites and hepatomegaly. Imaging studies showed complete thrombosis of all hepatic veins. Finally, he was diagnosed with Budd-Chiari syndrome with antiphospholipid syndrome.   Figure 1  ภาพ CT upper abdomen แสดงให้เห็น marked ascites with heterogeneous liver enhancement, complete obliteration of all hepatic, caudate lobe hypertrophy, small intrahepatic venous collateral และ small arterial enhancing nodules


1970 ◽  
Vol 3 (2) ◽  
pp. 80-82
Author(s):  
Md. Mukhlesur Rahman ◽  
KMHS Sirajul Haque ◽  
Md. Mahmudur Rahman Siddiqui ◽  
Tanjima Parvin ◽  
Md. Khurshed Ahmed

'Budd Chiari syndrome (BCS)' is an uncommon condition induced by thrombotic or nonthrombotic obstruction to hepatic venous outflow. This disease can be potentially life-threatening but prognosis is more favorable in patient with IVC webs but is extremely poor in malignant and haematological cases. A cooperative collaboration of hepatologist and cardiologist can make the situation easy for diagnosis, even in treatment of some cases. (University Heart Journal 2007; 3 : 80-82)


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