Woodcock A S, Govan A D, Gowing N F, Langley F A, Anderson M C
Tumori. 1979 Apr 30;65(2):181-9. doi: 10.1177/030089167906500206.
This report deals with 12 cases of gonadoblastoma submitted to the Ovarian Tumour Panel of the Royal College of Obstetricians and Gynaecologists. These tumours are found in children and young adults. Children may present with obvious genital malformation, retarded growth or precocious puberty. In adults the main compliant is amenorrhoea but sometimes there is associated masculinization. Histologically the gonadoblastoma has a distinctive structure, easily recognized in most instances. The most important feature is the instability of the germ cells in these tumours. Nine of these cases showed an associated dysgerminoma, bilateral in 4. In any cases of suspected gonadal dysgenesis presumptive evidence of diagnosis is suggested by the presence of a Y chromosome, raised gonadotrophin output and pelvic calcification on X-ray examination. At operation, streak tissue on both sides must be removed since these tumours are frequently microscopic in size. For the same reason the tissue removed should be serially sectioned.
本报告涉及提交给皇家妇产科学院卵巢肿瘤小组的12例性腺母细胞瘤病例。这些肿瘤见于儿童和年轻成人。儿童可能表现为明显的生殖器畸形、生长发育迟缓或性早熟。在成人中,主要症状是闭经,但有时伴有男性化。从组织学上看,性腺母细胞瘤具有独特的结构,在大多数情况下很容易识别。最重要的特征是这些肿瘤中生殖细胞的不稳定性。其中9例伴有无性细胞瘤,4例为双侧。在任何疑似性腺发育不全的病例中,Y染色体的存在、促性腺激素分泌增加以及X线检查发现盆腔钙化提示有诊断的初步证据。手术时,必须切除双侧的条索状组织,因为这些肿瘤通常体积微小。出于同样的原因,切除的组织应进行连续切片。