scholarly journals Hereditary hemorrhagic telangiectasia with liver cirrhosis: a case report

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Linxia Xu ◽  
Feng Xu ◽  
Qizhi Wang ◽  
Xiquan Ke

Abstract Background Hereditary hemorrhagic telangiectasia is an autosomal dominant hereditary hemorrhagic disease. Its main feature is an abnormal structure of the blood vessel wall. Cirrhosis of the liver is a common chronic progressive disease with one or more causes in which diffuse liver damage occurs after long-term or repeated injury. Liver cirrhosis can cause dilation of gastrointestinal capillaries. Many patients with hereditary hemorrhagic telangiectasia accompanied by gastrointestinal vascular malformations and liver cirrhosis may be diagnosed only with liver cirrhosis if the clinician does not pay attention to physical examination findings and family history. Moreover, general treatment measures, such as blood transfusion, iron supplementation, and application of hemostatic drugs, are less effective for bleeding in patients with hereditary hemorrhagic telangiectasia than in those with liver cirrhosis alone. Case presentation Here, we report the rare case of a 75-year-old Chinese man who was admitted to the hospital with repeated melena and epistaxis. He was diagnosed with unexplained liver cirrhosis, which was later confirmed as hereditary hemorrhagic telangiectasia. Subsequently, we implemented the treatment intervention of oral thalidomide combined with gastrointestinal argon plasma coagulation. A follow-up of more than 8 months showed that the treatment effect was excellent. Conclusions If patients with liver cirrhosis and gastrointestinal vascular malformations also have a family history of epistaxis, special attention should be paid to targeted physical examination results, and the possibility of hereditary hemorrhagic telangiectasia should be considered. Moreover, for patients with hereditary hemorrhagic telangiectasia and both gastrointestinal bleeding caused by gastrointestinal capillaries and repeated epistaxis, when other general treatment measures are ineffective, thalidomide combined with gastrointestinal argon plasma coagulation may be an effective intervention.

1999 ◽  
Vol 109 (1) ◽  
pp. 15-20 ◽  
Author(s):  
Wolfgang Bergler ◽  
Frank Riedel ◽  
Antonio Baker-Schreyer ◽  
Cathrin Juncker ◽  
Karl Hörmann

2012 ◽  
Vol 133 (2) ◽  
pp. 174-180 ◽  
Author(s):  
Fabio Pagella ◽  
Elina Matti ◽  
Francesco Chu ◽  
Alessandro Pusateri ◽  
Carmine Tinelli ◽  
...  

2006 ◽  
Vol 20 (4) ◽  
pp. 421-425 ◽  
Author(s):  
Fabio Pagella ◽  
Lucia Semino ◽  
Carla Olivieri ◽  
Sabrina Corno ◽  
Roberto Dore ◽  
...  

2014 ◽  
Vol 7 ◽  
pp. CGast.S17667
Author(s):  
Amir Abadir

Periampullary bleeding is an uncommon cause of upper gastrointestinal (GI) hemorrhage, which is typically iatrogenic in origin occurring as the result of endoscopic intervention of the papilla. Spontaneous, non-iatrogenic periampullary bleeding is extraordinarily rare with only a few cases reported in the literature to date. Vascular malformations, including angiodysplasia and Dieulafoy's lesions, have been implicated in several reports as the etiology but endoscopic intervention is often unsuccessful in achieving durable hemostasis with surgery being required for definitive management in many cases. Herein is reported the case of a 67-year-old male on anticoagulation for atrial fibrillation who presented with severe upper GI bleeding determined to be arising from underneath the hood of the major papilla. No distinct lesion was seen endoscopically but the presumed etiology was an unidentified vascular malformation. Successful treatment was achieved with argon plasma coagulation (APC) applied circumferentially around the papilla. No subsequent endoscopic or surgical intervention was required for durable hemostasis and the patient was able to resume anticoagulation shortly after the procedure. This is the first reported case of spontaneous periampullary bleeding successfully treated with APC.


VASA ◽  
2006 ◽  
Vol 35 (4) ◽  
pp. 258-261
Author(s):  
Katsinelos ◽  
Chatzimavroudis ◽  
Zavos ◽  
Kamperis ◽  
Triantafillidis ◽  
...  

Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease is an autosomal-dominant disorder that frequently presents with epistaxis and gastrointestinal bleeding which may be a diagnostic and therapeutic challenge. We describe a 48-year-old monk with familiar history of HHT, who presented with frequent epistaxes and symptoms of ferropenic anemia. Upper gastrointestinal endoscopy revealed innumerable telangiectasias in the stomach. The patient underwent three sessions with argon plasma coagulation treatment but the results were poor. We also review the literature on the pathophysiology of the disease and discuss the suggested treatment.


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