fertility potential in adulthood. A recent study
evaluating fertility potential in 65 men with ac-
quired and congenital UDT who had undergone
orchiopexy at puberty found abnormal testicular
consistency, smaller testes, lower sperm concentra-
tions and fewer motile sperm than in controls, por-
tending worse fertility potential, although without
evaluation of paternity.
19
In another study evalu-
ating long-term fertility potential via semen pa-
rameters in 78 men 18 to 26 years old who had
undergone orchiopexy during the first 2 years of
life 96% of men had normal total sperm count
and motility if orchiopexy had been done within the
first year of life, in contrast to 66% to 75% of those
who had undergone orchiopexy in the second year
of life, further supporting early intervention.
20
The number of germ cells per seminiferous tubule
is used as an indicator of fertility potential in
the developing testis. A recent study examining
testis samples from boys 5 to 25 months old using
germ and Sertoli cell markers demonstrated a
clear decrease in germ cell number with increasing
age at orchiopexy, suggesting a lasting impact on
fertility.
21
Overall, however, the fertility potential
of the cryptorchid testis is difficult to determine
using single variables or even a combination of
variables. Recent work linking the number of adult
dark spermatogonia, which differentiate into pri-
mary spermatocytes, to other known fertility pa-
rameters,
including
serum
gonadotropin
and
inhibin B levels, and number of tubular germ cells,
has allowed further insight into the determination
of fertility potential in boys with a history of cryp-
torchidism. However, limiting the significance of
this analysis was the fact that no evaluation of
pregnancy rates was available.
22
CRYPTORCHIDISM IN ADULTS
Early work demonstrated a higher risk of testicular
cancer in men with intra-abdominal testis but this
risk has been revised to 0.05% to 1%. Furthermore,
recent studies have demonstrated a lower risk of
cancer in boys undergoing orchiopexy before pu-
berty, with no increased risk of malignancy in a
contralateral normal testis.
23,24
However, fewer
studies have examined the role and risks of orchio-
pexy in postpubertal men. Given that the risk of
perioperative mortality has continued to decrease
and is now less than the risk of mortality from
germ cell tumors, some advocate for orchiectomy
postpubertally until age 50 years, at which point
observation
would
become
preferable
due
to
increased risk of perioperative morbidity.
25
Unfortunately, there is currently no consensus
and bilateral cryptorchidism in adults appears to
be rare, with few reports addressing management
in this situation. However, having an improved
understanding of the approach to such patients,
particularly with regard to balancing risk of malig-
nancy, fertility and endocrine function, should be
considered in the future.
In summary, the new AUA guideline is a signifi-
cant step forward in synthesizing the existing data
on the diagnosis and management of cryptorchidism,
a daunting task in light of the volume of research
of variable quality performed in the last several de-
cades. Nevertheless, as evidenced by our findings,
continued progress in the field is inevitable, with
numerous findings in the last year further contrib-
uting to our knowledge of the diagnosis and man-
agement of cryptorchidism, and largely supporting
the findings of the AUA guideline panel. Future
research remains necessary to better understand
numerous important aspects of cryptorchidism,
including the effects of the condition in adults.
Alexander W. Pastuszak and Larry I. Lipshultz
Scott Department of Urology
Center for Reproductive Medicine
Baylor College of Medicine
Houston, Texas
REFERENCES
1. van der Plas E, Zijp G, Froeling F et al:
Orchidopexy in late childhood often associated
with previously normal testicular position. Eur
J Pediatr Surg 2013;
23:
276.
2. Sekaran P, O
Toole S, Flett M et al: Increased
occurrence of disorders of sex development,
prematurity and intrauterine growth restriction
in children with proximal hypospadias associated
with undescended testes. J Urol 2013;
189:
1892.
3. Kistamas K, Ruzsnavszky O, Telek A et al:
Expression of anti-Mullerian hormone receptor
on the appendix testis in connection with uro-
logical disorders. Asian J Androl 2013;
15:
400.
4. Wongprasert H, Somanunt S, De Filippo R et al:
A novel mutation of anti-Mullerian hormone
gene in Persistent Mullerian Duct Syndrome
presented with bilateral cryptorchidism: a case
report. J Pediatr Urol 2013;
9:
e147.
5. Quinonez SC, Park JM, Rabah R et al: 9p
partial monosomy and disorders of sex devel-
opment: review and postulation of a pathoge-
netic mechanism. Am J Med Genet A 2013;
161A:
1882.
6. Lottrup G, Jorgensen A, Nielsen JE et al:
Identification of a novel androgen receptor
mutation in a family with multiple components
compatible
with
the
testicular
dysgenesis
syndrome. J Clin Endocrinol Metab 2013;
98:
2223.
7. Agopian AJ, Lupo PJ, Canfield MA et al:
Case-control study of maternal residential atra-
zine exposure and male genital malformations.
Am J Med Genet A 2013;
161A:
977.
8. Rantakokko P, Main KM, Wohlfart-Veje C et al:
Association of placenta organotin concentrations
with congenital cryptorchidism and reproductive
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DIAGNOSIS AND TREATMENT OF CRYPTORCHIDISM