Polymikrobieller Hirnabszess bei hereditärer hämorrhagischer Teleangiektasie (Morbus Osler)

Polák, Pavel; Snopková, Svatava; Husa, Petr

doi:10.1055/s-0032-1305184

Cited by 2 publications

(1 citation statement)

References 14 publications

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“…Vzhledem ke své vzácnosti se pořád stává, že tato choroba zůstane dlouho nerozpoznána. Z toho důvpdu je diagnóza této nemoci někdy stavena až v době vzniku mozkových abscesů, jak popsal v naší literatuře Polák v roce 2012 a Hanoun v roce 2015(16,17).…”

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Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations

Adam¹,

Brančíková²,

Romanová³

et al. 2021

Vnitr Lek

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Hereditární hemoragická teleangiektázie (HHT), známá také jako Osler-Weber-Rendu syndrom, je dědičné onemocnění, způsobující abnormální tvorbu cév. Pacienti mají četné teleangiektázie, z nichž mohou krvácet. S přibývajícím věkem se u nich rozvíjí arteriovenózní malformace, vedoucí k masivním arteriovenózním zkratům a poškození orgánů, v nichž tyto malformace vznikají. U pacientů je nutno provádět skríninková vyšetření s cílem včasné detekce arteriovenózních malformací a v případě jejich detekce jejich specializované obvykle multidisciplinární léčby. Pokroky farmakologické léčby jsou zmíněny v dalším článku.Klíčová slova: hereditární hemoragická teleangiektázie, arteriovenózní malformace.Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is an autosomal dominant disorder that causes abnormal blood vessel formation. Patients with HHT may have telangiectasias and later may develop arteriovenous malformations in various organs. Pacients suffer from many complications caused by the malformations and therefore by patients with HHT must by performed screening of this arteriovenous malformations. Optimal treatment of this malformations is best delivered throught a multidisciplinary approach. Farmacological treatment is described in next paper.

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Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations

Adam¹,

Brančíková²,

Romanová³

et al. 2021

Vnitr Lek

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Streptococcus anginosus group - brief characterization and its contribution to the brain abscess pathogenesis

Bancescu¹,

Băncescu²,

Constantinescu³

2015

EDUJ

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The oral streptococci are microorganisms whose major habitat is the oral cavity and oropharynx. The Streptococcus anginosus group, formerly known as Streptococcus milleri group, comprises the following commensal species: S. anginosus, S. constellatus and S. intermedius. Sometimes these species may produce different oral or extraoral infections, especially oro-maxillo-facial infections and deepseated abscess. Objective: The aim of the present article was to provide the reader with the essential knowledge about S. anginosus group characteristics and a useful updated review of its important contribution to develop brain abscess. Data sources and selection: The most important evidence concerning the recent taxonomical data, main phenotypical features and findings referring to the involvement of these bacteria in causing cerebral abscess in adults and children were collected from PubMed/Medline database. Only articles published between January 2011-November 2015 were selected and the significant data have been presented in a synthesized form, without performing a meta-analysis. Conclusion: The S. anginosus group merits greater attention from both clinicians and microbiologists due to its importance in human pathology, especially in life-threatening infections, like brain abscesses, which often require a multidisciplinary team for proper diagnosis and treatment.

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Polymikrobieller Hirnabszess bei hereditärer hämorrhagischer Teleangiektasie (Morbus Osler)

Cited by 2 publications

References 14 publications

Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations

Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations

Streptococcus anginosus group - brief characterization and its contribution to the brain abscess pathogenesis

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