Benlemlih Amal, Szableski Vanessa, Bendahou Mouhcine, Rivière Sophie, Villain Max, Costes Valérie
Département de pathologie, université Montpellier 1, hôpital Gui-de-Chauliac, CHU de Montpellier, 80, avenue A-Fliche, 34295 Montpellier cedex 5, France.
Ann Pathol. 2012 Aug;32(4):271-5. doi: 10.1016/j.annpat.2012.06.008. Epub 2012 Jul 24.
Eosinophilic angiocentric fibrosis is a rare fibro-inflammatory disorder of unknown etiology with only 40 cases reported in the literature. It primarily affects the sinonasal tract and more rarely the orbit, the larynx and the gums. This benign disorder is characterized by a slowly progressive process mimicking a tumor, with frequent recurrences after surgical excision and cortico-therapy. The typical histology consists of fibro-inflammatory lesion with numerous eosinophils, arranged in a perivascular pattern. As the lesion matures, inflammation becomes less intense and the fibrosis progresses with an onion-skin type perivascular fibrosis. A recent paper suggests that EAF is part of the spectrum of IgG4-related systemic disease. We report a case of orbital EAF in an 86-year-old woman which sustained this hypothesis.
嗜酸性粒细胞性血管中心性纤维化是一种病因不明的罕见纤维炎症性疾病,文献中仅报道过40例。它主要累及鼻窦,较少累及眼眶、喉和牙龈。这种良性疾病的特点是病程缓慢进展,类似肿瘤,手术切除和皮质激素治疗后常复发。典型的组织学表现为伴有大量嗜酸性粒细胞的纤维炎症性病变,呈血管周围排列。随着病变成熟,炎症减轻,纤维化进展为洋葱皮样血管周围纤维化。最近一篇论文表明,嗜酸性粒细胞性血管中心性纤维化是IgG4相关系统性疾病谱的一部分。我们报告了一例86岁女性眼眶嗜酸性粒细胞性血管中心性纤维化病例,支持了这一假说。