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Angioimmunoblastic T-cell lymphoma-associated pure red cell aplasia with abdominal pain

机译:血管免疫母细胞性T细胞淋巴瘤相关的纯红细胞发育不良伴腹痛

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摘要

Angioimmunoblastic T-cell lymphoma (AITL) is a unique type of peripheral T-cell lymphoma with a constellation of clinical symptoms and signs, including weight loss, fever, chills, anemia, skin rash, hepatosplenomegaly, lymphadenopathy, thrombocytopenia and polyclonal hypergammaglobulinemia. The histological features of AITL are also distinctive. Pure red cell aplasia is a bone marrow failure characterized by progressive normocytic anemia and reticulocytopenia without leucopenia or thrombocytopenia. However, AITL with abdominal pain and pure red cell aplasia has rarely been reported. Here, we report a rare case of AITL-associated pure red cell aplasia with abdominal pain. The diagnosis was verified by a biopsy of the enlarged abdominal lymph nodes with immunohistochemical staining.
机译:血管免疫母细胞性T细胞淋巴瘤(AITL)是一种独特的外周性T细胞淋巴瘤,具有一系列临床症状和体征,包括体重减轻,发烧,发冷,贫血,皮疹,肝脾肿大,淋巴结病,血小板减少症和多克隆高铁球蛋白血症。 AITL的组织学特征也很独特。纯红细胞发育不全是一种骨髓衰竭,其特征是进行性正常红细胞性贫血和网状细胞减少,无白细胞减少症或血小板减少症。然而,极少有腹痛和纯红细胞发育不良的AITL报告。在这里,我们报道了极少一例AITL相关的纯红细胞发育不良并伴有腹痛。通过对扩大的腹部淋巴结进行活检并进行免疫组织化学染色证实了诊断。

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