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Hereditary hemorrhagic telangiectasia - Revision history
2026-04-18T16:37:23Z
Revision history for this page on the wiki
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ClaireLewis: Created page with "==Background== *AKA Osler–Weber–Rendu disease *Rare genetic dysfunction of angiogenesis that leads to multiple vascular malformations ==Clinical Features== *Telangiectasi..."
2019-09-19T18:40:19Z
<p>Created page with "==Background== *AKA Osler–Weber–Rendu disease *Rare genetic dysfunction of angiogenesis that leads to multiple vascular malformations ==Clinical Features== *Telangiectasi..."</p>
<p><b>New page</b></p><div>==Background==<br />
*AKA Osler–Weber–Rendu disease<br />
*Rare genetic dysfunction of angiogenesis that leads to multiple vascular malformations<br />
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==Clinical Features==<br />
*Telangiectasias <br />
**Skin/oral mucosa, characteristically on lips, nose, fingers, face (in sun exposed areas)<br />
**Nasal mucosa --> [[epistaxis]] <br />
**GI tract (~20%)--> [[GI bleeding]]<br />
*[[AVM]]s<br />
**Lungs<br />
***Bypassing pulmonary vasculature can --> [[brain abscess]], embolic [[stroke]]<br />
***[[Hemoptysis]], [[hemothorax]], [[dyspnea]], abnormal lung sounds<br />
**Liver<br />
**Brain<br />
***[[Headache]], increased [[seizure]] risk, risk of [[ICH]]<br />
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==Differential Diagnosis==<br />
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==Evaluation==<br />
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==Management==<br />
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==Disposition==<br />
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==See Also==<br />
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==External Links==<br />
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==References==<br />
<references/><br />
[[Category:Vascular]]</div>
ClaireLewis