A rapidly progressive orbital tumor in a seven-year-old girl revealing a primitive systemic vasculitis

被引:0
|
作者
Picard, Cecile [1 ]
Borgnat, Florent [2 ]
Chastang, Marie-Caroline [3 ]
Fleury, Aude [4 ]
Guibaud, Laurent [5 ]
Dijoud, Frederique [1 ]
机构
[1] Grp Hosp Est, Ctr Pathol Est, F-69500 Bron, France
[2] Grp Hosp Est, Serv Chirurg Maxillofaciale & Stomatol Pediat, F-69677 Lyon, France
[3] Grp Hosp Est, Serv Rhumatol Pediat, F-69677 Lyon, France
[4] Grp Hosp Est, Serv Otorhinolaryngol Pediat, F-69677 Lyon, France
[5] Grp Hosp Est, Serv Imagerie, F-69677 Lyon, France
关键词
Orbital pseudo-tumor; ANCA vasculitis; Granulomatosis with polyangiitis; (wegener's granulomatiosis); Children; WEGENER GRANULOMATOSIS; CHILDHOOD; CLASSIFICATION; CRITERIA;
D O I
10.1016/j.annpat.2014.09.007
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Orbital tumor lesions in pediatric population encompass a wide range of pathological processes, which are very different in etiology and prognosis. They usually require an emergency in histological diagnosis because of their quick growth. Beside malignant and benign tumors, the inflammatory pseudo-tumors group included dysimmune orbital involvement secondary to systemic vasculitis such as granulomatosis with polyangiitis (ex-Wegener's granulomatosis). We report the case of a seven-year-old girl suffering from a severe primitive ANCA vasculitis, revealed by an orbital mass. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:469 / 473
页数:5
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