血管免疫母细胞性T细胞淋巴瘤
医学
皮疹
皮肤病科
嗜酸性粒细胞增多
淋巴瘤
嗜酸性粒细胞增多症
病理
免疫学
免疫系统
T细胞
作者
Bartłomiej Wawrzycki,Andrzej Prystupa,Justyna Szumiło,Lech Panasiuk,Dorota Krasowska
摘要
Angioimmunoblastic T-cell lymphoma (AITL) is an uncommon lymphoma of elderly adults with a poor prognosis. AITL patients show systemic symptoms, lymphadenopathy, and not infrequently, skin rash with various dysimmune phenomena rashes. The case is presented of a 68-year-old male with skin rash, lymphadenopathy and hypereosinophilia who, after investigations, was diagnosed with AITL. Despite the treatment used, the patient's condition gradually deteriorated and died due to heart and kidney failure. The diagnosis of AITL is often established only after several weeks or months because of transient physical findings, non-specific symptoms, and a broad range of serologic or radiologic abnormalities. Some patients with AITL experience non-specific dermatitis and eosinophilia. The presented case should raise awareness of the presentations of AITL which is important for physicians to reach an accurate diagnosis.
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