Barnhart M I, Lusher J M
Am J Hematol. 1976;1(2):243-64. doi: 10.1002/ajh.2830010209.
The three-dimensional world of the spleen was explored by scanning electron microscopy on both arterially perfused and nonperfused specimens, as well as on plastic corrosion casts of splenic vasculatures. Of 25 spleens studied, 18 were examples of hypersplenism. These were contrasted to 7 essentially normal spleens taken from children being staged for treatment of Hodgkin's disease whose spleens proved to be uninvolved in the pathologic process. Splenic sinuses in all 25 spleens were typified by a degree of porosity. RBC were caught in the act of entering sinuses from splenic cords. These sinus windows thus represent one end of an "open" circulation pathway. In casts of microvasculature, direct arteriovenous connections were demonstrated, thus establishing an anatomical basis for an often disputed "closed" circulation pathway. Spleens from 7 patients with hereditary spherocytosis had a super abundance of red pulp. Splenic cords were thickened and crowded with spherocytes, many of which presented slightly wrinkled membranes, as were also noted on the peripheral blood RBC. It is possible that these membrane features are unique for HS and reflect the intrinsic membrane abnormality in protein composition. The 7 spleens from chronic idiopathic thrombocytopenic purpura had white pulp as the predominant region. Germinal centers were frequent. Lymphocytes and plasma cells with well-developed microvilli were suggestive that release of antiplatelet antibody might be occurring in white pulp. Platelets were especially notable in peripheral white pulp and marginal zones. Platelet clumps were observed, generally adjacent to spleenic macrophages.
通过扫描电子显微镜对动脉灌注和未灌注标本以及脾血管系统的塑料腐蚀铸型进行观察,探索脾脏的三维世界。在研究的25个脾脏中,18个是脾功能亢进的例子。将这些与7个基本正常的脾脏进行对比,这些正常脾脏取自正接受霍奇金病分期治疗的儿童,其脾脏未发现有病理改变。所有25个脾脏的脾窦都有一定程度的孔隙率。红细胞正处于从脾索进入脾窦的过程中。这些窦窗因此代表了“开放”循环途径的一端。在微血管铸型中,证实了存在直接动静脉连接,从而为经常存在争议的“封闭”循环途径建立了解剖学基础。7例遗传性球形红细胞增多症患者的脾脏红髓过多。脾索增厚,充满球形红细胞,其中许多红细胞的膜略有褶皱,外周血红细胞也有这种情况。这些膜特征可能是HS所特有的,反映了蛋白质组成方面的内在膜异常。7例慢性特发性血小板减少性紫癜患者的脾脏以白髓为主。生发中心常见。具有发达微绒毛的淋巴细胞和浆细胞提示抗血小板抗体可能在白髓中释放。血小板在外周白髓和边缘区特别明显。观察到血小板团块,通常靠近脾巨噬细胞。