Nakashima Masahiro, Suzuki Kimihiro, Okada Makoto, Takada Kunio, Kobayashi Hiroyuki, Hama Yukihiro
Internal Medicine, Division of Rheumatology, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan.
Clin Rheumatol. 2007 Aug;26(8):1362-4. doi: 10.1007/s10067-006-0383-2. Epub 2006 Nov 15.
Polyarteritis nodosa (PN) occasionally develops in association with malignant disorders. A 71-year-old man suddenly suffered from bleeding due to the rupture of a hepatic artery aneurysm. The ruptured lesion was embolized endovascularly by coiling, and the bleeding was stopped. A biopsy of the right inguinal lymph node demonstrated angioimmunoblastic T cell lymphoma (AITL). He received immunosuppressive treatment with transient response, although he relapsed 4 months later. To our knowledge, this is the first case of which PN was associated with AITL.
结节性多动脉炎(PN)偶尔会与恶性疾病相关联发生。一名71岁男性突然因肝动脉瘤破裂而出血。破裂病变通过血管内栓塞线圈进行了栓塞,出血得以停止。右腹股沟淋巴结活检显示血管免疫母细胞性T细胞淋巴瘤(AITL)。他接受了免疫抑制治疗,有短暂反应,尽管4个月后复发。据我们所知,这是首例PN与AITL相关的病例。