A 58-year-old woman presented speech impairment, mental confusion, and left hemiparesis after being found unconscious. Brain magnetic resonance imaging (MRI) showed pyogenic abscess and multiple vascular malformations in the cerebral hemispheres (Figures 1 and 2), resulting in suspicion of Rendu-Osler-Weber disease, i.e., hereditary hemorrhagic telangiectasia (HHT). Chest computed tomography (CT) revealed pulmonary arteriovenous malformation. Ectoscopy detected multiple telangiectasia in the lips, tongue, face, and nasosinusal mucosa (Figure 3). HHT is a rare systemic fibrovascular dysplasia (prevalence rate: 1:50000-100000)11. Fuchizaki U, Miyamori H, Kitagawa S, Kaneko S, Kobayashi K. Hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease). Lancet. 2003 Nov;362(9394):1490-4. https://doi.org/10.1016/S0140-6736(03)14696-X
https://doi.org/https://doi.org/10.1016/...
, and brain abscess is an acute and easily forgotten complication that occurs in 1% of patients with considerable mortality, i.e., death rate of 40%22. Dong SL, Reynolds SF, Steiner IP. Brain abscess in patients with hereditary hemorrhagic telangiectasia: case report and literature review. J Emerg Med. 2001 Apr;20(3):247-51. https://doi.org/10.1016/S0140-6736(03)14696-X
https://doi.org/https://doi.org/10.1016/...
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Brain MRI in axial FLAIR (A), T2-weighted (B), B1000 diffusion (C), and ADC map (D). A pyogenic abscess surrounded by vasogenic edema (arrows) in the right superior temporal gyrus is detected.
Brain MRI in axial, post-gadolinium volumetric T1 (A to C) and MIP (D) sequences. A pyogenic abscess surrounded by vasogenic edema (arrows) in the right superior temporal gyrus is detected (arrows in A and B). Dashed circles of images A to D highlight multiple tiny vascular malformations in both cerebral hemispheres (capillary malformations and microMAVs), more conspicuous in the MIP sequence.
Face ectoscopy (A) and rhinoscopy exam (B); CT of the chest in the lung (C) and soft tissue (D) windows. Other systemic changes in the spectrum of the syndrome: multiple tiny cutaneous telangiectasia on the face, tongue, and labial mucosa (A), as well as on the nasal mucosa (B) and pulmonary vascular malformation compatible with arteriovenous malformation (AVM) (arrows on C and D).
References
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1Fuchizaki U, Miyamori H, Kitagawa S, Kaneko S, Kobayashi K. Hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease). Lancet. 2003 Nov;362(9394):1490-4. https://doi.org/10.1016/S0140-6736(03)14696-X
» https://doi.org/https://doi.org/10.1016/S0140-6736(03)14696-X -
2Dong SL, Reynolds SF, Steiner IP. Brain abscess in patients with hereditary hemorrhagic telangiectasia: case report and literature review. J Emerg Med. 2001 Apr;20(3):247-51. https://doi.org/10.1016/S0140-6736(03)14696-X
» https://doi.org/https://doi.org/10.1016/S0140-6736(03)14696-X
Publication Dates
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Publication in this collection
25 Mar 2022 -
Date of issue
Feb 2022
History
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Received
19 Sept 2021 -
Reviewed
20 Oct 2021 -
Accepted
21 Oct 2021