Hurd W W, Katholi R E
Arch Intern Med. 1980 Jun;140(6):844-5. doi: 10.1001/archinte.140.6.844.
A 45-year-old woman who had lower extremity ecchymoses and vague abdominal and back complaints was found to have acquired functional asplenia manifested by Howell-Jolly bodies and poikilocytosis on peripheral blood smear. On spleen scan there was inability to take up radioactive colloid. Shortly thereafter, she was found to have a spontaneous rupture of the spleen. At operation, the spleen, liver, and periaortic lymph nodes were found to be diffusely involved with amyloidosis. Five months later, an acute, serious, intra-abdominal condition developed secondary to spontaneous rupture of the liver, and the patient died. To our knowledge, neither acquired functional asplenia nor spontaneous rupture of the liver has been reported previously in association with amyloidosis.
一名45岁女性,有下肢瘀斑,伴有腹部和背部隐痛,外周血涂片发现有豪-焦小体和异形红细胞,提示获得性功能性无脾。脾脏扫描显示不能摄取放射性胶体。此后不久,她出现脾脏自发性破裂。手术中发现脾脏、肝脏和主动脉旁淋巴结均弥漫性受累于淀粉样变性。五个月后,因肝脏自发性破裂继发急性、严重的腹腔内病变,患者死亡。据我们所知,此前尚未有与淀粉样变性相关的获得性功能性无脾或肝脏自发性破裂的报道。