scholarly journals A case report of hereditary hemorrhagic telangiectasia (HHT) with recurrent gastric bleeding

2015 ◽  
Vol 86 (1) ◽  
pp. 138-139 ◽  
Author(s):  
Maiko Suzuki ◽  
Osamu Kobayashi ◽  
Kazuki Ohta ◽  
Yasuhiro Hayashi ◽  
Takuto Kojima ◽  
...  
2008 ◽  
pp. 106-114
Author(s):  
Vesna Supak ◽  
Lidija Bilic-Zulle ◽  
Antica Duletic-Nacinovic ◽  
Elizabeta Fisic

Chirurgia ◽  
2018 ◽  
Vol 113 (6) ◽  
pp. 837
Author(s):  
Mihnea-Ioan Ionescu ◽  
Ian David Edwin Nesbitt ◽  
Colin Hugh Wilson ◽  
Samantha Erica Saikia ◽  
David Talbot

2010 ◽  
Vol 3 (3) ◽  
pp. 463-470 ◽  
Author(s):  
Ahmad Amanzada ◽  
Gwen-Jana Töppler ◽  
Silke Cameron ◽  
Harald Schwörer ◽  
Giuliano Ramadori

2017 ◽  
Vol 20 (2) ◽  
pp. 164-169 ◽  
Author(s):  
Abbas Rattani ◽  
Michael C. Dewan ◽  
Vickie Hannig ◽  
Robert P. Naftel ◽  
John C. Wellons ◽  
...  

The authors present a case of monozygotic twins with hereditary hemorrhagic telangiectasia (HHT) who experienced cerebral arteriovenous malformation (AVM) hemorrhage at a very young age. The clinical variables influencing HHT-related AVM rupture are discussed, and questions surrounding the timing of screening and intervention are explored. This is only the second known case of monozygotic HHT twins published in the medical literature, and the youngest pair of first-degree relatives to experience AVM-related cerebral hemorrhage. Evidence guiding the screening and management of familial HHT is lacking, and cases such as this underscore the need for objective and validated protocols.


2016 ◽  
Vol 11 (3) ◽  
pp. 2137-2139 ◽  
Author(s):  
YUICHIRO YOSHIOKA ◽  
HIROAKI NOZAWA ◽  
JUNICHIRO TANAKA ◽  
TAKESHI NISHIKAWA ◽  
TOSHIAKI TANAKA ◽  
...  

2020 ◽  
Vol 4 (3) ◽  
pp. 417-420
Author(s):  
Jodi Spangler ◽  
Bjorn Watsjold ◽  
Jonathan Ilgen

Introduction: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterized by arteriovenous malformations (AVM). HHT can have neurological manifestations. Case Report: A 32-year-old woman with a history of HHT presented to the emergency department with acute partial paralysis of the right leg, urinary retention, and right-sided back and hip pain. Magnetic resonance imaging of the spine demonstrated multiple, dilated blood vessels along the cervical spine, diffuse AVMs in the lumbar and thoracic spine, and a new arteriovenous fistula at the twelfth thoracic (T12) vertebral level. Her symptoms improved after endovascular embolization of the fistula. Conclusion: Spinal AVMs are thought to be more prevalent in patients with HHT. Given the high morbidity of arteriovenous fistulas, early recognition and intervention are critical.


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