Acquired C1-Esterase Inhibitor Deficiency Associated with Burkitt Lymphoma

J. Prichard, Delilah D Coconubo, M. Gero, B. Noorbehesht, Michelle B Azimov
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引用次数: 0

Abstract

C1-esterase inhibitor deficiency results in recurrent episodes of angioedema. Acquired deficiency has been associated with B-cell lymphoproliferative disorders, rheumatologic diseases or, in a small proportion of patients, the cause remains unknown. Of the malignancies associated with acquired C1-esterase deficiency, indolent lymphomas and plasma cell disorders are the most common. Aggressive lymphomas are rarely reported in such cases. We report the association of Burkitt lymphoma, a highly aggressive B-cell malignancy, which evolved seven months after the initial symptoms of acquired angioedema in a fifty-five year old man. Following treatment of the lymphoma, episodes of angioedema ceased. An association of acquired angioedema with Burkitt lymphoma has not previously been reported.
获得性c1 -酯酶抑制剂缺乏与伯基特淋巴瘤相关
c1 -酯酶抑制剂缺乏导致血管性水肿的反复发作。获得性缺乏与b细胞淋巴细胞增生性疾病、风湿病有关,在一小部分患者中,其原因尚不清楚。在与获得性c1酯酶缺乏相关的恶性肿瘤中,惰性淋巴瘤和浆细胞疾病是最常见的。侵袭性淋巴瘤在这类病例中很少报道。我们报告的关联伯基特淋巴瘤,一种高度侵袭性b细胞恶性肿瘤,在获得性血管性水肿的最初症状七个月后发展在一个55岁的男人。淋巴瘤治疗后,血管性水肿发作停止。获得性血管性水肿与伯基特淋巴瘤的相关性此前未见报道。
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