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面部肉芽肿:10例患者的临床、形态学及免疫组化特征

Granuloma faciale: clinical, morphological and immunohistochemical aspects in a series of 10 patients.

作者信息

Oliveira Cristiano Claudino, Ianhez Pedro Eugênio de Carvalho, Marques Silvio Alencar, Marques Mariângela Esther Alencar

机构信息

Universidade Estadual Paulista "Júlio de Mesquita Filho" (Unesp) - Botucatu (SP), Brazil.

Hospital Ipiranga - São Paulo (SP), Brazil.

出版信息

An Bras Dermatol. 2016 Nov-Dec;91(6):803-807. doi: 10.1590/abd1806-4841.20164628.

Abstract

Granuloma faciale is a chronic, benign, cutaneous vasculitis with well-established clinical and morphological patterns, but with an unknown etiology. This study describes clinical and pathologic aspects of patients diagnosed with granuloma faciale. The authors analyzed demographic, clinical, morphological and immunohistochemical data from patients with a final diagnosis of granuloma faciale, confirmed between 1998 and 2012. There was a proportional and mixed inflammatory infiltrate, Grenz zones were present in almost all the samples. Immunophenotyping confirmed a higher intensity of T lymphocytes than B lymphocytes in thirteen samples, with a predominance of T CD8 lymphocytes in 64% of cases, in contrast to the literature, which indicates that the major component is T CD4 lymphocytes. All cases were positive for IgG4 but the majority (12/14) had less than 25% of stained cells. The pathogenesis of granuloma faciale remains poorly understood, making studies of morphological and immunohistochemical characterization important to better understand it.

摘要

面部肉芽肿是一种慢性、良性皮肤血管炎,具有明确的临床和形态学特征,但病因不明。本研究描述了诊断为面部肉芽肿患者的临床和病理特征。作者分析了1998年至2012年间最终诊断为面部肉芽肿患者的人口统计学、临床、形态学和免疫组化数据。存在比例性和混合性炎性浸润,几乎所有样本中均有无细胞区。免疫表型分析证实,13个样本中T淋巴细胞的强度高于B淋巴细胞,64%的病例中T CD8淋巴细胞占优势,这与文献报道的主要成分是T CD4淋巴细胞相反。所有病例IgG4均呈阳性,但大多数(12/14)染色细胞少于25%。面部肉芽肿的发病机制仍知之甚少,因此对其进行形态学和免疫组化特征研究对于更好地理解该病很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88f4/5193193/35538c6a36bf/abd-91-06-0803-g01.jpg

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