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[面部恶性肉芽肿与血管中心性T细胞淋巴瘤。结合一例病例的文献综述]

[Malignant granuloma of the face and angiocentric T-cell lymphoma. A review of the literature apropos of a case].

作者信息

Vanrenterghem L, Joly B, de Cordoue X, Montreuil G, Palliez T M, Maillot E, Leleu C, Riviere O, Bosq J

机构信息

Service ORL, Centre Hospitalier de la Région de Saint Omer.

出版信息

Rev Stomatol Chir Maxillofac. 1994;95(1):17-21.

PMID:8153547
Abstract

The authors report the observation of a lethal midline granuloma in a 43 years old man, at first seen with repeated left sinusitis disease, the histo-pathological study of a biopsy of the external middle third of the left side of the nose made the diagnosis of midline lethal granuloma, classically called Stewart granuloma by french authors. General Medical Investigations to find some peripheral extension, done in specialized services were negative, Epstein Barr DNA was not found by the immuno-histochemical investigations and so don't prove the filiation of this case with angiocentric T cell immunoproliferative lesion. By the light of this observation and of a literature review, the authors debate about the difficulty of diagnosis and about the relations with the other granulomatosis lesions of the face, non Hodgkins' lymphoma and angiocentric T cell immuno-proliferative lesions.

摘要

作者报告了一例43岁男性致死性中线肉芽肿的观察病例,该患者最初表现为反复的左侧鼻窦炎。对左侧鼻外侧中三分之一处活检组织进行的组织病理学研究确诊为中线致死性肉芽肿,法国作者通常称其为斯图尔特肉芽肿。在专科科室进行的旨在寻找外周扩散情况的综合医学检查结果为阴性,免疫组织化学检查未发现爱泼斯坦-巴尔病毒DNA,因此无法证实该病例与血管中心性T细胞免疫增殖性病变的关联。基于这一观察结果及文献综述,作者探讨了诊断的困难以及与面部其他肉芽肿性病变、非霍奇金淋巴瘤和血管中心性T细胞免疫增殖性病变的关系。

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