Anton-Lamprecht I, Kotzur B, Schopf E
Fertil Steril. 1976 Jun;27(6):685-93. doi: 10.1016/s0015-0282(16)41900-x.
Ultrastructural investigation of two cases of round-headed spermatozoa from human ejaculates revealed the existence of two different pathomorphogenetic types. Case 1 represented round-headed spermatozoa of the Schirren and Holstein type caused by loss of the abnormally formed acrosome during spermiogenesis and the missing nuclear transformation. In case 2 a primary maturing inhibition was responsible for the round-headed feature of the spermatozoa; the normally flattened, conical nucleus and acrosomal cap were surrounded by huge droplets of ample cytoplasm. Secondary degenerative changes contributed to the decreased motility of these round-headed spermatozoa. Therapeutic trials for this oligospermic patient showed that an increase in cell count to values in the low-normal range and a drastic reduction in the percentage of round-headed cells (from 80% to 47%) could be achieved. The Schirren and Holstein type, however, must be regarded as absolutely infertile due to the absence of an acrosome and its intrinsic enzymes.
对两例人类射精中圆头精子的超微结构研究揭示了两种不同的病理形态发生类型。病例1表现为Schirren和Holstein型圆头精子,是由于精子发生过程中异常形成的顶体丢失以及核转化缺失所致。病例2中,原发性成熟抑制是精子圆头特征的原因;正常扁平的锥形细胞核和顶体帽被大量细胞质的巨大液滴包围。继发性退行性变化导致这些圆头精子的活力下降。对这名少精子症患者的治疗试验表明,可以将细胞计数增加到低正常范围的值,并大幅降低圆头细胞的百分比(从80%降至47%)。然而,由于顶体及其内在酶的缺失,Schirren和Holstein型必须被视为绝对不育。