Cryptorchidism: Aspects of fertility and neoplasms - A study including data of 1,335 consecutive boys who underwent testicular biopsy simultaneously with surgery for cryptorchidism

被引:154
作者
Cortes, D
Thorup, JM
Visfeldt, J
机构
[1] Univ Copenhagen, Rigshosp, Dept Paediat Surg 4072, Juliane Marie Ctr, DK-2100 Copenhagen O, Denmark
[2] Univ Copenhagen, Rigshosp, Dept Pathol, DK-2100 Copenhagen, Denmark
关键词
cryptorchidism; fertility; infertility; spermatogonia; neoplasia;
D O I
10.1159/000049959
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: An attempt to make a rational strategy for treatment of cryptorchidism. Materials and Methods: 1,335 cryptorchid boys with biopsy at surgery (1,638 specimens). We studied: frequency of no germ cells in biopsies from 698 patients <12 years at surgery; fertility potential of 140 patients who were now adults, and apperance of testicular neoplasia in all biopsies. Results: Lack of germ cells appeared from 18 months. The frequency increased with increasing age. It appeared in 30% (61/202) bilateral, and 18% (88/496) unilateral cases. In men who had undergone bilateral or unilateral orchiopexy, respectively, there was normal sperm count in 19% (14/75) and 83% (54/65), and infertility was suspected in 56% (42/75) and 8% (5/65) (FE, p < 0.00005, p < 0.00005), respectively. The lowest, the mean, and the highest age-matched spermatogonia count per tubule at orchiopexy was associated with sperm count (Spearman test, p < 0.0001, p < 0.005, p < 0.05). Isolated, this was demonstrated for the 75 formerly bilateral (Spearman, p < 0.0001, p < 0.0001, p < 0.0001), but not the 65 formerly unilateral cases (Spearman, p = 1.0). No germ cells at orchiopexy was associated with suspected infertility. Risk was 78-100% in bilateral (dependent on one or both testes affected), and 33% in unilateral cryptorchidism. There was one invasive germ cell tumor, six cases of carcinoma in situ testis, and one Sertoli cell tumor. Three neoplasms were diagnosed in intra-abdominal testes, four in boys with abnormal external genitalia, and two in boys with known abnormal karyotype. Risk of neoplasia was 5% (7/150) in patients with intra-abdominal testis, abnormal external genitalia or diagnosed abnormal karyotype, versus 0% (0/1,185) in patients without these characteristics (FE, p < 0.00005). Conclusion: We recommend surgery for cryptorchidism before 15-18 months of age because: (a) lack of germ cells is very rare before, and (b) lack of germ cells is associated with subsequent risk of infertility. At primary surgery for cryptorchidism, we recommend examination for testicular neoplasia in cases of intra-abdominal testis, abnormal external genitalia or known abnormal karyotype. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:21 / 27
页数:7
相关论文
共 20 条
  • [1] SERUM FSH AND TESTICULAR MORPHOLOGY IN MALE-INFERTILITY
    BERGMANN, M
    BEHRE, HM
    NIESCHLAG, E
    [J]. CLINICAL ENDOCRINOLOGY, 1994, 40 (01) : 133 - 136
  • [2] HISTOLOGY OF TESTICULAR BIOPSIES TAKEN AT OPERATION FOR BILATERAL MALDESCENDED TESTES IN RELATION TO FERTILITY IN ADULTHOOD
    CORTES, D
    THORUP, J
    [J]. BRITISH JOURNAL OF UROLOGY, 1991, 68 (03): : 285 - 291
  • [3] Fertility potential after unilateral orchiopexy: An age independent risk of subsequent infertility when biopsies at surgery lack germ cells
    Cortes, D
    Thorup, JM
    Lindenberg, S
    [J]. JOURNAL OF UROLOGY, 1996, 156 (01) : 217 - 220
  • [4] Is infertility after surgery for cryptorchidism congenital or acquired?
    Cortes, D
    Thorup, JM
    Visfeldt, J
    Schwartz, M
    [J]. PEDIATRIC SURGERY INTERNATIONAL, 1998, 14 (1-2) : 6 - 8
  • [5] Testicular neoplasia in cryptorchid boys at primary surgery: case series
    Cortes, D
    Visfeldt, J
    Moller, H
    Thorup, J
    [J]. BRITISH MEDICAL JOURNAL, 1999, 319 (7214) : 888 - 889
  • [6] CORTES D, 1999, SCAND J UROL NE S196, V32, P1
  • [7] CORTES D, 1996, J UROLOGY, V155, P1096
  • [8] Early orchiopexy:: Prepubertal intratubular germ cell neoplasia and fertility outcome
    Engeler, DS
    Hösli, PO
    John, H
    Bannwart, F
    Sulser, T
    Amin, MB
    Heitz, PU
    Hailemariam, S
    [J]. UROLOGY, 2000, 56 (01) : 144 - 148
  • [9] Absence of microdeletions in the Y chromosome in patients with a history of cryptorchidism and azoospermia or oligospermia
    Fagerli, J
    Schneck, FX
    Lee, PA
    Bellinger, MF
    Witchel, SF
    [J]. FERTILITY AND STERILITY, 1999, 71 (04) : 697 - 700
  • [10] Y chromosome microdeletions in cryptorchidism and idiopathic infertility
    Foresta, C
    Moro, E
    Garolla, A
    Onisto, M
    Ferlin, A
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (10) : 3660 - 3665