由非小细胞肺癌继发的下腔静脉肿瘤血栓引起的急性布-恰里综合征

Kohei Fujita, Young Hak Kim, Mitsuru Yoshino, Masataka Ichikawa, Tadashi Mio, Michiaki Mishima
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引用次数: 1

摘要

继发于肺癌的布-恰利综合征非常罕见。这种疾病的临床特征尚未得到很好的描述,因为在过去的30年里只有少数病例被报道。我们分析了5例这样的病例,包括本病例,并确定了肺癌的某些特征可能在这种综合征中起作用。所有病例均起源于右肺,其中4例为非小细胞肺癌。由于肝功能衰竭进展迅速,该综合征的预后非常差,化疗和/或放疗的效果有限。然而,最近,新的治疗方法,如支架置入术,已经被证明可以缓解疼痛和延长生命。我们报告一例罕见的由肺癌继发的下腔静脉肿瘤血栓引起的急性布-恰里综合征。此外,我们还讨论了过去30年报道的类似病例以及支架置入术的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acute Budd–Chiari syndrome caused by tumor thrombus of the inferior vena cava secondary to non-small cell lung cancer

Budd–Chiari syndrome secondary to lung cancer is very rare. The clinical features of this disease have not been well described, as only a few cases have been reported in the past 3 decades. We analyzed 5 such cases, including the present case, and have identified certain features of lung cancer that may play a role in this syndrome. All cases had cancers originating in the right lung, and 4 cases were patients with non-small cell lung cancers. Because of the rapid progression of liver failure, the prognosis for this syndrome is very poor, and the effects of chemotherapy and/or radiotherapy are limited. Recently, however, new treatments, such as stent placement therapy, have been shown to relieve pain and prolong life. We describe a rare case of acute Budd–Chiari syndrome caused by tumor thrombus of the inferior vena cava secondary to lung cancer. In addition, we discuss similar cases reported in the past 3 decades and the effectiveness of stent placement therapy.

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