Pulmonary Arteriovenous Malformations and Cerebral Abscess Recurrence in a Child With Hereditary Hemorrhagic Telangiectasia

被引:0
|
作者
Giordano, Paola [1 ]
Sangerardi, Maria [1 ]
Suppressa, Patrizia [2 ]
Lastella, Patrizia [2 ]
Attolini, Ettore [4 ]
Valente, Federica [1 ]
Fiorella, Maria L. [3 ]
Lenato, Gennaro M. [2 ]
Sabba, Carlo [2 ]
机构
[1] Univ Hosp Bari, Dept Biomed Sci & Human Oncol, Unit Paediat F Vecchio, I-70124 Bari, Italy
[2] Univ Hosp Bari, Ctr Rare Dis, Unit Internal Med C Frugoni, I-70124 Bari, Italy
[3] Univ Hosp Bari, Unit Otorynolaringol, I-70124 Bari, Italy
[4] Reg Agcy Hlth Apulia, Bari, Italy
关键词
hereditary hemorrhagic telangiectasia; Rendu-Osler-Weber disease; recurrent brain abscess; pulmonary arteriovenous malformation; diagnostic delay; BRAIN-ABSCESS; MANAGEMENT; SEVERITY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A 17-year-old boy was referred to our center with a history of brain abscess (BA) recurring after 9 years. The patient reported 2 previous treatments for pulmonary arteriovenous malformations, sporadic nosebleeds, and familial history for epistaxis. Clinical investigations revealed arteriovenous malformations in lung, brain, and liver, as well as mucocutaneous telangiectases. A definite diagnosis of hereditary hemorrhagic telangiectasia was made based on clinical criteria and confirmed by genetic analysis. This is the first report of BA recurrence at the end of pediatric age. Conclusions: The present case and the literature review of all cases of BA thus far reported highlight the need to raise the suspicion of a pulmonary arteriovenous malformations, both isolated and in the context of a possible hereditary hemorrhagic telangiectasia, for any case of BA of unexplained etiology, in children as well as in adults.
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页码:E200 / E203
页数:4
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