Hirnabszess als Komplikation des Morbus Osler mit Lungenbeteiligung [Brain abscess as a complication of Osler's disease with lung involvement].

Détails

ID Serval
serval:BIB_CFFA1FBEACC9
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Titre
Hirnabszess als Komplikation des Morbus Osler mit Lungenbeteiligung [Brain abscess as a complication of Osler's disease with lung involvement].
Périodique
Deutsche Medizinische Wochenschrift
Auteur⸱e⸱s
Schwitter J., Greminger P., Stingl B., Deuel W., Turina M., Siegenthaler W.
ISSN
0012-0472 (Print)
ISSN-L
0012-0472
Statut éditorial
Publié
Date de publication
1991
Volume
116
Numéro
42
Pages
1591-1596
Langue
allemand
Notes
Publication types: Case Reports ; English Abstract ; Journal Article
Résumé
Eight months after sustaining a reversible left motor hemisyndrome, predominantly of the arm, a 47-year-old man known to have hereditary haemorrhagic telangiectasia (Osler's disease) again developed neurological symptoms (headache, vertigo, unsteady gait) with fever (up to 38.5 degrees C). Clinical features and findings on computed tomography indicated a cerebellar abscess. This was resected because it continued to enlarge despite antibiotic treatment with daily 2 g ceftriaxone and twice daily 0.5 g ornidazole. As another manifestation of Osler's disease further tests revealed an arteriovenous malformation (2.5 x 2.0 cm) in the right upper lobe of the lung, presumably the cause of the cerebral abscess. After wedge resection of the anterior upper lobe segment the further course was without complications.
Mots-clé
Arteriovenous Malformations/complications, Arteriovenous Malformations/surgery, Brain Abscess/diagnosis, Brain Abscess/etiology, Humans, Lung/blood supply, Magnetic Resonance Imaging, Male, Middle Aged, Telangiectasia, Hereditary Hemorrhagic/complications, Tomography, X-Ray Computed
Pubmed
Création de la notice
09/10/2011 17:03
Dernière modification de la notice
20/08/2019 16:50
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