2例滤泡性淋巴瘤伴MYC基因异常,表现为骨髓坏死。

Yuri Miyazawa, Hisashi Takei, Nobuhiko Kobayashi, Naoki Akashi, Yukiko Sairenji, Manato Sugisaki, Chiaki Naito, Tetsuya Ishikawa, Hiroaki Shimizu, Takuma Ishizaki, Akihiko Yokohama, Norifumi Tsukamoto, Yuka Yoshida, Nozomi Matsumura, Yoshiyasu Takayama, Hiroshi Handa
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引用次数: 0

摘要

骨髓坏死(BMN)最常见于血液系统恶性肿瘤,有时也见于非血液系统疾病。引起坏死的淋巴性疾病被认为是高级别疾病。b淋巴母细胞白血病/淋巴瘤是BMN最常见的恶性病因。在此,我们报告了两例滤泡性淋巴瘤(FL)和MYC基因异常并发BMN的患者。在一例骨髓性神经网络中,化疗后坏死消失,患者完全缓解。另一例患者化疗后BMN仍然存在,由于造血抑制无法给予有效的化疗,导致淋巴瘤恶化,患者死亡。惰性淋巴瘤,如FL,在这些病例中,有发展成BMN的潜力。由于严重的BMN使患者无法得到有效的治疗,因此早期发现BMN的发展并给予化疗对改善患者预后非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Two cases of follicular lymphoma with MYC gene abnormalities that presented with bone marrow necrosis.

Bone marrow necrosis (BMN) occurs most frequently in hematological malignancies and sometimes in non-hematological disorders. Lymphoid diseases causing necrosis are regarded as high-grade disease. B-lymphoblastic leukemia/lymphoma is the most common malignant cause of BMN. Here, we present two patients with follicular lymphoma (FL) and MYC gene abnormalities who developed BMN. In one case of BMN, the necrosis disappeared in response to chemotherapy, and the patient survived with complete remission. In the other case, BMN remained even after chemotherapy, and effective chemotherapy could not be administered due to suppressed hematopoiesis, which led to the lymphoma worsening and the patient's death. Indolent lymphomas, such as FL, as in these cases, have the potential to develop BMN. It is important to detect the development of BMN and administer chemotherapy early to improve patient prognosis, since severe BMN prevents patients from receiving effective treatment.

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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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