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口腔黏膜假淋巴瘤性肿胀性红斑狼疮

Pseudolymphomatous tumid lupus erythematosus of the oral mucosa.

作者信息

Tallon Ben, Kaddu Steven, Cerroni Lorenzo, Kerl Helmut, Aberer Elisabeth

机构信息

Department of Dermatology, Medical University of Graz, Austria.

出版信息

Am J Dermatopathol. 2010 Oct;32(7):704-7. doi: 10.1097/DAD.0b013e3181d0d1f9.

Abstract

Oral lesions are frequent complications of systemic lupus erythematosus, but only ulceration is included in the 1982 American College of Rheumatology revised criteria. Because the lack of a uniform classification, a range of ulcerative and keratotic lesions are typically described. In this report we describe a unique progressive irregularly cobblestoned and vegetating plaque of the oral mucosa with clinical and histological features mimicking a cutaneous lymphoma. Despite the papillomatous and extensive nature of the lesions and the dense lymphoid infiltrate with follicle formation suggesting a malignant lymphoproliferative process, the slow progression coupled with a mixed cell infiltrate and polyclonality supported a diagnosis of pseudolymphoma. Recognition of this entity is important to prevent diagnosing them as a malignant lymphoma. As well as with the other mucosal lesions in lupus erythematosus, this pseudolymphomatous variant should be added to the disease spectrum.

摘要

口腔病变是系统性红斑狼疮常见的并发症,但1982年美国风湿病学会修订标准中仅纳入了溃疡。由于缺乏统一分类,通常会描述一系列溃疡性和角化性病变。在本报告中,我们描述了一种独特的、进行性的、不规则鹅卵石样且呈赘生物状的口腔黏膜斑块,其临床和组织学特征类似于皮肤淋巴瘤。尽管病变具有乳头瘤样和广泛性,且有密集的淋巴样浸润并形成滤泡,提示为恶性淋巴增殖性过程,但病变进展缓慢,伴有混合细胞浸润和多克隆性,支持假性淋巴瘤的诊断。认识到这一实体对于防止将其诊断为恶性淋巴瘤很重要。与红斑狼疮中的其他黏膜病变一样,这种假性淋巴瘤变体也应纳入该疾病谱。

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