What are they?
Testicular tumors are rare tumors and occur in 2-3 individuals per 100 thousand. Its highest incidence is in young adults aged 15 to 35 years, which is the phase of increased sexual activity and inícion the professional.
What is it?
Genetic factors are related to the development of testicular tumors, as may occur familial cases (siblings, for example).
Injuries are often cited as possible generators of testicular tumors. What is believed is that the trauma calls attention to the testicular tumor.
The use of estrogens by the mother during pregnancy may result in their
children a higher incidence of testicular tumors, testicular atrophy
(small testes) or cryptorchidism (testicles out of its usual position).
Let me say in passing that patients with cryptorchidism have a 50 times
greater risk of developing testicular tumor than normal patients.
What you feel and how is it diagnosed?
Testicular tumors may present as painless nodules or by increasing the
volume of the organ. Some patients notice the problem by increasing the
weight of the testis. These changes can progress without the patient's
perception. In other cases - about 10% of cases the tumor may have
internal bleeding, causing an acute condition that can be confused with
other benign testicular inflammation (eg, orchitis). In 15% of cases,
there are already metastases and symptoms will emerge as the area
involved as: cough or dyspnea (lung)
back pain (retroperitoneal)
lower extremity edema (vena cava involvement) and other
Breast enlargement (gynecomastia) may also occur in some testicular
tumors. It occurs due to increased production of estrogen deficiency or
by the formation of androgens.
On physical examination, the patient usually palpate the testicle lump
or firm painless.
Other structures of the scrotum (epididymis, vas deferens) are not
involved, except in more advanced cases.
Any acute condition involving the testis in young people and that does
not resolve in 7-10 days of conventional treatment should raise
suspicion by the presence of tumor. In 10% of cases, the patient
presents with signs of metastatic disease such as pain, dyspnea ,
vomiting, gynecomastia, loss of weight
After performing the physical examination, laboratory tests are required
to confirm the diagnosis, such as: alpha fetoprotein and beta-HCG
which is tumor markers, ie, substances produced by tumors and which are
increased in their presence. 8% of seminomas produce beta-HCG whereas 0%
produce alpha feto-protein non-seminomas tumors produce both markers in
about 60% of cases.
testicular ultrasound, which gives us the idea of the volume and
location of the tumor, and gives us the image of the other testicle.
total abdominal tomography, which search the retroperitoneum (area
located behind the abdominal cavity) in search of nodal metastases.
Chest X-ray or CT scan of the chest.
Once confirmed the clinical suspicion, the next step is inguinal
exploration. It holds an incision in the groin of the patient and the
testicle it is pulled. A fragment of the lesion (biopsy) is removed and
sent to the pathologist. If confirmed the presence of malignant tumor,
the testicle is excised (orchiectomy).
The testis is an organ composed of different types of cells, which can
generate different types of tumors, each with a peculiar behavior, with
varying degrees of malignancy.
The tumors can also be composed of different cells. They are mixed
tumors.
It is not the purpose of this article provide detailed knowledge of cell
groups of the testis. However, these can be divided into two major
groups: tumors and seminomas non-seminomas.
Treatment
Knowledge of the cellular component of the tumor and the presence or
absence of metastasis is to guide the tratamentofuturo.
There are several forms of treatment: Radical orchiectomy (OR)
OR + retroperitoneal lymphadenectomy (removal of the retroperitoneal
lymph)
OR + chemotherapy
OR + + chemotherapy lymphadenectomy
OR + radiotherapy (radiation therapy is indicated in seminomas)
The choice of optimal treatment will depend on the extent of disease
(staging) and histological type. There are also the preferences of each
urologist who should also be considered.
What is the prognosis?
The prognosis varies with cell type and tumor extension.
Over the past 25 years due to tumor markers, the diagnostic and
chemotherapy, there was a significant improvement in patient survival,
even in the later stages of the disease.
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