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Autoimmune Hemolytic Anemia in a Patient with Primary Ovarian Non-Hodgkin's Lymphoma

机译:原发性卵巢非霍奇金淋巴瘤患者的自身免疫性溶血性贫血

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摘要

The primary ovarian lymphoma is a rare disease with poor prognosis. The incidence of autoimmune hemolytic anemia in patients with non-Hodgkin's lymphoma is estimated at 3%. However, a substantial portion of the previously reported cases of ovarian lymphoma actually represented ovarian involvement by more diffuse lymphomatous process. If stringent criteria are used for case selection, true primary ovarian lymphoma usually carries a favorable prognosis. We present a primary malignant lymphoma of ovary accompanied by autoimmune hemolytic anemia in a 29-yr-old patient. After ablative surgery, the hemoglobin level and the reticulocyte count were normalized. One year following surgery and chemotherapy, the patient is alive and disease free.
机译:原发性卵巢淋巴瘤是一种罕见的预后较差的疾病。非霍奇金淋巴瘤患者自身免疫性溶血性贫血的发生率估计为3%。然而,在先前报道的卵巢淋巴瘤病例中,很大一部分实际上是通过更弥漫性淋巴瘤突向卵巢受累。如果使用严格的标准进行病例选择,那么真正的原发性卵巢淋巴瘤通常预后良好。我们介绍了一名29岁患者的原发性卵巢恶性淋巴瘤伴自身免疫性溶血性贫血。消融手术后,血红蛋白水平和网织红细胞计数恢复正常。手术和化疗后一年,患者还活着并且没有疾病。

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