Schindler A M, Diaz P, Cuendet A, Sizonenko P C
Department of Pathology, University of Geneva, Switzerland.
Helv Paediatr Acta. 1987 Oct;42(2-3):145-58.
Among a series of 512 boys with an empty scrotum, 495 (96.7%) were found to have cryptorchidism, 4 had ectopia and 13 unilateral anorchia. Cryptorchidism was bilateral in 106 boys (21.4%). The only anomaly consistently associated with cryptorchidism was a detached epididymis, present in 31 patients. A total of 670 biopsies were studied, 441 of which came from cryptorchid and 229 from scrotal testes. Spermatogonial counts, performed according to Mancini's method, showed the germ cell population to be diminished in nearly all cryptorchid testes. The seven boys who still had a well preserved germ cell population were found in a group of 51 patients operated before age three; four of the seven boys with normal counts were below age one. No difference in the mean spermatogonial counts was found between uni- und bilateral cryptorchidism and ectopia, with the exception of bilaterally intraabdominal testes whose spermatogonial cell loss was particularly severe. Mean counts remained constant during childhood, no gradual increase with age having been observed. The scrotal testes in unilateral cryptorchidism showed cell loss in 30.1% of the cases, the germ cell depletion being severe in one out of every six cases. In the remaining scrotal testes, the counts were in the low normal range with a significantly lower mean than that found in scrotal testes associated with anorchia. Control biopsies were performed several months or years after orchidopexy in 18 boys with unilateral and in 24 boys with bilateral cryptorchidism. Orchidopexy does not improve the number of germ cells in either originally cryptorchid or in scrotal testes, the only postoperative change being an increase in tubular diameter. A search for malignant tumours which could have developed in this series has remained negative. According to our data, no optimal time for orchidopexy can be proposed. The damage to germ cells, once established, seems to remain unchanged during childhood at least after age three, and does not warrant special timing for operative correction of cryptorchidism.
在512例阴囊空虚的男孩中,495例(96.7%)被发现患有隐睾症,4例有睾丸异位,13例为单侧无睾症。106例男孩(21.4%)的隐睾症为双侧性。唯一始终与隐睾症相关的异常是附睾分离,31例患者存在该情况。共研究了670份活检标本,其中441份来自隐睾,229份来自阴囊内睾丸。根据曼奇尼方法进行的精原细胞计数显示,几乎所有隐睾的生殖细胞数量均减少。在3岁前接受手术的51例患者中,发现7名男孩的生殖细胞群体仍保存完好;7名计数正常的男孩中有4名年龄在1岁以下。单侧和双侧隐睾症及睾丸异位之间的平均精原细胞计数无差异,但双侧腹腔内睾丸的精原细胞损失尤为严重。童年期平均计数保持不变,未观察到随年龄逐渐增加的情况。单侧隐睾症患者的阴囊内睾丸在30.1%的病例中出现细胞损失,每6例中有1例生殖细胞耗竭严重。在其余阴囊内睾丸中,计数处于正常低范围,平均水平明显低于与无睾症相关的阴囊内睾丸。对18例单侧隐睾症和24例双侧隐睾症男孩在睾丸固定术后数月或数年进行了对照活检。睾丸固定术并未改善原隐睾或阴囊内睾丸的生殖细胞数量,术后唯一的变化是管径增加。对该系列中可能发生的恶性肿瘤进行的搜索结果为阴性。根据我们的数据,无法提出睾丸固定术的最佳时机。一旦生殖细胞受损,至少在3岁以后的童年期似乎保持不变,因此不支持对隐睾症进行手术矫正的特殊时机选择。