Trueblood H W, Gustafson J R, Williams D K
Am Surg. 1978 Aug;44(8):517-22.
The five-year experience with 75 consecutive splenectomies has been reviewed. Special detail was given to eight critically ill hypersplenic patients. Their diagnoses included Hodgkin's disease, lymphoma, leukemia, myelofibrosis and Felty's syndrome. Three presented with sepsis, two with anemia not responsive to transfusion, three had pathologic bleeding and two could not receive additional needed therapy of underlying disease because of low counts. All cases responded to splenectomy favorably. Hypersplenism is primarily a loss of balance between the splenic destruction-sequestration and bone marrow production. The demonstrated rapid consumption of transfused cells and some degree of functional reserve of the bone marrow is the prerequisite and clue for splenectomy response in critically ill patients.
回顾了连续75例脾切除术的五年经验。特别详细地研究了8例重症脾功能亢进患者。他们的诊断包括霍奇金病、淋巴瘤、白血病、骨髓纤维化和费尔蒂综合征。3例出现败血症,2例输血无效的贫血,3例有病理出血,2例因血细胞计数低而无法接受基础疾病的额外所需治疗。所有病例脾切除术后反应良好。脾功能亢进主要是脾破坏-潴留与骨髓生成之间的平衡失调。所证实的输入细胞的快速消耗和一定程度的骨髓功能储备是重症患者脾切除术后反应的前提和线索。