Anesthetic challenges in a child with hereditary hemorrhagic telangiectasia with coexisting pulmonary and cerebral arteriovenous malformations for intracerebral hematoma evacuation: A case report

2021 ◽  
Vol 74 ◽  
pp. 110430
Author(s):  
Aishvarya Shree Nedunchezhian ◽  
Ranganatha Praveen ◽  
Manikandan Sethuraman ◽  
Salini Varma
Keyword(s):  
Case Report ◽  
Hereditary Hemorrhagic Telangiectasia ◽  
Arteriovenous Malformations ◽  
Intracerebral Hematoma ◽  
Cerebral Arteriovenous Malformations ◽  
Hematoma Evacuation

Development of multiple cerebral arteriovenous malformations documented in an adult by serial angiography

2003 ◽  
Vol 98 (1) ◽  
pp. 190-193 ◽  
Author(s):  
Yoshio Miyasaka ◽  
Kuniaki Nakahara ◽  
Hiroshi Takagi ◽  
Hiroyuki Hagiwara
Keyword(s):  
Subarachnoid Hemorrhage ◽  
Cerebral Angiography ◽  
Arteriovenous Malformations ◽  
Intracerebral Hematoma ◽  
Cerebral Arteriovenous Malformations ◽  
Content Type ◽  
Hematoma Evacuation ◽  
Cerebral Avms ◽  
Fine Print

✓ A 50-year-old woman with a parietal intracerebral hematoma was initially treated by hematoma evacuation. Initial preoperative and follow-up angiograms obtained 6 months later demonstrated no pial arteriovenous malformations (AVMs). She suffered a subarachnoid hemorrhage 8 years later. Results of follow-up cerebral angiography revealed the development of previously undetected multiple cerebral AVMs. This appears to be the first reported case of the development of multiple cerebral AVMs in an adult, demonstrated on serial angiography.

scholarly journals Multiple Cerebral Arteriovenous Malformations —Case Report—

1993 ◽  
Vol 33 (1) ◽  
pp. 24-27 ◽  
Author(s):  
Kohsuke YAMASHITA ◽  
Yoichi SUZUKI ◽  
Hideyuki YOSHIZUMI ◽  
Jun TAKAHASHI ◽  
Tokuji NOGAWA
Keyword(s):  
Case Report ◽  
Arteriovenous Malformations ◽  
Cerebral Arteriovenous Malformations

scholarly journals Osler-Weber-Rendu Disease Uncovered by Preeclampsia in a Case Report

2020 ◽  
Vol 2020 ◽  
pp. 1-4
Author(s):  
Jamal Ouachaou ◽  
Hamza Mimouni ◽  
Mohammed Maarad ◽  
Yassine Mellagui ◽  
Asmae Oulad Amar ◽  
...  
Keyword(s):  
Case Report ◽  
Disease Management ◽  
Hereditary Hemorrhagic Telangiectasia ◽  
Arteriovenous Malformations ◽  
Symptomatic Treatment ◽  
Patient Experiences ◽  
Associated Symptoms ◽  
Genetic Illness

Osler-Weber-Rendu disease (OWRD), called hereditary hemorrhagic telangiectasia, is an uncommon genetic illness with the dominant autosomal transmission. It cannot be easily or quickly diagnosed because of both its infrequency and its various associated symptoms. As far as its symptoms are concerned, the patient experiences recurring epistaxis, mucocutaneous telangiectasia, and arteriovenous malformations that can lead to severe undesirable symptoms. In our case, we report a 32-year-old female that was diagnosed with postpartum preeclampsia and whose paraclinical examinations showed that she suffers from hereditary hemorrhagic telangiectasia disease. Management of OWRD includes systematic diagnosis of visceral arteriovenous malformations (AVMs) in regular intervals, measures to prevent complications, and symptomatic treatment.

Multiple cerebral arteriovenous malformations associated to rostral hypoplasia of the superior sagittal sinus: a case report

2020 ◽  
Vol 64 (3) ◽  
Author(s):  
Ramon Torné ◽  
Felipe A. Molina Jaque ◽  
Ana Rodríguez-Hernández ◽  
Fuat Arikan ◽  
Diego López Bermeo ◽  
...  
Keyword(s):  
Case Report ◽  
Arteriovenous Malformations ◽  
Superior Sagittal Sinus ◽  
Cerebral Arteriovenous Malformations ◽  
Sagittal Sinus
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