Mu-heavy chain disease associated with systemic amyloidosis.

Mu-heavy chain disease associated with systemic amyloidosis.
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DOI:
10.1080/10245330410001671561
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发表时间:
2004-04-01
期刊:
Hematology (Amsterdam, Netherlands)
影响因子:
--
通讯作者:
Kanamaru, Akihisa
Kanamaru, Akihisa
中科院分区:
其他
文献类型:
--
作者:
Kinoshita, Koji;Yamagata, Toshiaki;Kanamaru, Akihisa

文献摘要

被引文献

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mu-重链病 (HCD) 非常罕见,文献报道仅 30 例。我们报告了一名与系统性淀粉样变性相关的 mu-HCD 患者。 mu-HCD 的诊断基于血清中 mu-重链片段、Bence Jones 蛋白尿和骨髓中空泡浆细胞的发现。据我们所知,这是第三例系统性淀粉样变性导致患者死亡的病例。
mu-heavy chain disease (HCD) is very rare, with only 30 cases reported in the literature. We report a patient with mu-HCD associated with systemic amyloidosis. The diagnosis of mu-HCD was based on findings of mu-heavy chain fragments in the serum, Bence Jones proteinuria and vacuolated plasma cells in the bone marrow. To our knowledge, this is the third case in which systemic amyloidosis led to the patient's death.