环状弹性溶解性巨细胞肉芽肿的临床病理特征

H. Erdogan, D. Arık, Ersoy Acer, E. Yılmaz, Z. N. Saraçoğlu
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摘要

目的:环状弹性溶解性巨细胞肉芽肿(AEGCG)是一种罕见的肉芽肿性疾病,以环状斑块为特征。在本研究中,我们旨在描述诊断为AEGCG的患者的临床和病理特征。方法:回顾性记录确诊为AEGCG患者的人口学、临床及病理特征。结果:纳入10例AEGCG患者(女性9例,男性1例)。患者平均年龄60±9.53岁。平均病程24.2±36.30个月。在皮肤科检查中,所有患者均可见多发、界限清晰、边界升高和中央萎缩性红斑环形斑块。在大多数患者中(90%)病变位于阳光照射的区域。其中6名患者伴有其他疾病。穿刺组织病理检查显示真皮内有异物型多核巨细胞及淋巴细胞浸润。巨细胞内可见弹性纤维碎片,显示有弹性吞噬作用。结论:egcg是一种罕见的肉芽肿性疾病,可伴发多种疾病。关于该病的术语、分类和发病机制存在争议。需要进一步的研究来阐明未知因素。
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Clinicopathological Features of Annular Elastolytic Giant Cell Granuloma Patients
Objective: Annular elastolytic giant cell granuloma (AEGCG) is a rare granulomatous disease characterized by annular plaques. In this study, we aimed to describe the clinical and pathological features of the patients diagnosed with AEGCG. Methods: The demographic, clinical and pathological features of patients who diagnosed with AEGCG were recorded retrospectively. Results: Ten patients with AEGCG included in the study (nine females and one male). The mean age of the patients was 60±9.53 years. The mean duration of disease was 24.2±36.30 months. On dermatologic examination, multiple, well-demarcated, elevated borders and central atrophic erythematous annular plaques were seen in all patients. In the most of the patients (90%) lesions were on the sun-exposed regions. Six of the patients had accompanying diseases. Histopathologic examination of the punch biopsies revealed foreign body type multinucleated giant cells and lymphocytic cell infiltration in the dermis. There were intracellular elastic fiber fragments as sign of elastophagocytosis in the giant cells. Conclusion: AEGCG is a rare granulomatous disease which can accompany various diseases. There is debate on the terminology, classification and pathogenesis. Further studies are required to elucidate the unknowns.
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