与血管免疫母细胞t细胞淋巴瘤相关的Bazex综合征

G. Ugoh, A. Linfante, Allison J. Good, Janice M. Wilson, Kathleen Kroger
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引用次数: 0

摘要

Bazex综合征,也称为副肿瘤性角化术,是一种副肿瘤性疾病,其特征是鼻子、耳朵和肢端部位出现红斑性银屑病样斑块。尽管它通常与上消化道鳞状细胞癌有关,但也有报道称它与腺癌、泌尿生殖系统肿瘤、多发性骨髓瘤有关,很少与外周T细胞淋巴瘤和滤泡性原位淋巴瘤有关。在此,我们介绍了一名Bazex综合征患者,该综合征与血管免疫母细胞T细胞淋巴瘤(AITL)相关,这是一种罕见的文献中未报道的相关性。
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Bazex Syndrome Associated with Angioimmunoblastic T-cell Lymphoma
Bazex syndrome, also known as Acrokeratosis paraneoplastica, is a paraneoplastic disorder characterized by erythematous psoriasiform plaques involving the nose, ears, and acral sites. Although classically associated with squamous cell carcinomas of the upper aerodigestive tract, it has also been reported in association with adenocarcinoma, genitourinary tumors, multiple myeloma, and rarely, peripheral T-cell lymphoma and follicular lymphoma in-situ. Herein, we present a patient with Bazex syndrome associated with angioimmunoblastic T-cell lymphoma (AITL), a rare association not previously reported in the literature.  
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