Suppr超能文献

头颈部巨大先天性神经纤维瘤中发生的恶性淋巴瘤。病例报告。

Malignant lymphoma arising in a large congenital neurofibroma of the head and neck. Report of a case.

作者信息

Radi M J, Foucar E, Palmer C H, Gooding R A

机构信息

Department of Surgical Pathology, Stanford University Medical Center, California.

出版信息

Cancer. 1988 Apr 15;61(8):1667-73. doi: 10.1002/1097-0142(19880415)61:8<1667::aid-cncr2820610826>3.0.co;2-9.

Abstract

A lymphoma developed in a large neurofibroma in a young woman who had no other stigmata of neurofibromatosis. The neurofibroma was congenital and extensively involved the soft tissue and bone of the face and neck. Despite multiple attempts to excise the neurofibroma, it persistently recurred. At the age of 30 the patient underwent another resection of the lesion, and a follicular, mixed, small and large cell lymphoma was present within the neurofibroma. Over 3 years the lymphoma transformed into a diffuse large cell type despite the fact that it remained localized to the neurofibroma. After the lymphoma had transformed, the patient received multiagent chemotherapy. She responded well, and a repeat biopsy showed no residual lymphoma. She is alive and well 25 months after completion of chemotherapy. To the best of our knowledge, this is the first report of a lymphoma arising in a soft tissue neoplasm.

摘要

一名年轻女性的巨大神经纤维瘤中发生了淋巴瘤,该女性无神经纤维瘤病的其他体征。神经纤维瘤为先天性,广泛累及面部和颈部的软组织及骨骼。尽管多次尝试切除神经纤维瘤,但它持续复发。患者30岁时再次接受病变切除,神经纤维瘤内存在滤泡性、混合性、小细胞和大细胞淋巴瘤。尽管淋巴瘤仍局限于神经纤维瘤,但在3年多的时间里,它转变为弥漫性大细胞型。淋巴瘤转变后,患者接受了多药化疗。她反应良好,再次活检显示无残留淋巴瘤。化疗结束25个月后,她健在且状况良好。据我们所知,这是关于软组织肿瘤中发生淋巴瘤的首例报告。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验