Testicular tumors: Pathology review

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Testicular tumors: Pathology review

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A 5-year-old boy is brought to the pediatrician by his parents for evaluation of testicular pain and fullness, which have been ongoing for the last 3 weeks. A physical examination is performed and reveals the presence of a mass on the left testicle that does not transilluminate with light. Imaging and tumor marker analysis are performed, confirming the diagnosis of testicular cancer. He subsequently undergoes a radical orchiectomy. Post-operative pathological analysis of the testicle reveals a 6-mm tumor containing strands of hair and keratinous material. Which of the statements is most likely to be true regarding this type of malignancy?

Transcript

Content Reviewers:

Yifan Xiao, MD

25-year-old Kyle comes to the office after palpating a lump on his left testicle while showering this morning.

On physical examination, there is a nontender, round, firm, rubbery mass in the left testicle that does not transilluminate with light.

Scrotal ultrasound shows a 1.4-cm solid mass with no cystic components.

Laboratory tests reveal normal serum human chorionic gonadotropin or hCG level, and normal α-fetoprotein or AFP level.

Later that day, 32-year-old William comes to the physician's office complaining of heat intolerance, excessive sweating, palpitations, frequent bowel movements and recent weight loss despite increased appetite.

His past medical history is insignificant.

On examination, the thyroid gland is normal with no signs of goiter or nodules.

However, a hard nodule is palpated in the right testicle which does not transilluminate with light and appears solid on scrotal ultrasound.

Laboratory studies show increased serum T4 and T3 levels as well as extremely elevated hCG levels.

Based on the initial presentation, Kyle and William both have some form of testicular mass.

In fact, testicular tumors are the most common solid malignancy in males between 20 and 35 years old.

Okay, now, for your exams, it’s important to know that the main risk factors for developing testicular cancer, especially the germ cell variety, include cryptorchidism, which is when the testicles fail to descend to the scrotum or get stuck in the inguinal canal, as well as Klinefelter syndrome, where biological male individuals inherit more than one X chromosome leading to small, undeveloped testicles.

For symptoms, a testicular tumor most often comes up as a small, firm lump that is typically painless, but can sometimes cause a sharp or dull pain in the testicles and lower abdomen.

In more severe cases, symptoms may arise from a malignant tumor metastasizing to other organs.

This is most commonly hematogenous to the lungs, leading to dyspnea or hemoptysis, which is the coughing of blood, or to the brain, leading to headache, nausea, vomiting or seizures.

Another way for the cancer cells to metastasize is by the testicular lymphatic system that drains into retroperitoneal lymph nodes.

Metastasis to these lymph nodes leads to symptoms like lower back pain.

Now, once a lump has been palpated in the testis, diagnosis can be confirmed with an ultrasound.

Also remember that in a transillumination test solid tumors do not transilluminate with light, while hydrocele and cysts do.

Imaging with CT or MRI scan can then be done to look for evidence of metastasis if carcinoma is suspected.

Next, lab tests are used to measure levels of tumor markers like PALP, hCG, and AFP. LDH could also be measured, but it’s not very specific.

Based on the type of testicular tumor, these markers rise in a different pattern.

And that’s a popular way for examiners to clue you in a particular type of tumor.

Another very high-yield fact that you should absolutely remember is that testicular tumors should not be biopsied.

That’s because the lymph from the scrotum is drained by the superficial inguinal lymph nodes and not the retroperitoneal ones.

So cutting into the scrotum would open an additional route for the cancer cells to escape and metastasize.

Treatment involves surgical removal of the whole testicle called radical orchiectomy, followed by chemotherapy and radiotherapy if the tumor has spread.

After the removal a histopathological work up can be done, involving gross and microscopic examination, to determine the type of the tumor.

Alright, now, there are two types of testicular tumors: germ cell tumors, which derive from primordial germ cells which are the cells that can give rise to all other tissues and organs, and non-germ cell tumors or sex cord-stromal tumors which arise from Sertoli cells, which are supportive cells inside the seminiferous tubules, or Leydig cells which lie outside the tubules and secrete sex hormones.

Starting with germ cell tumors, a high-yield fact is that they comprise almost 95% of all testicular tumors.

They can be classified into seminoma tumors, and non-seminoma tumors, which include yolk sac tumors, choriocarcinomas, teratomas and embryonal carcinomas.

The reason behind this classification is that a seminoma, in general, has a slow growth, metastasizes late, responds very well to radiotherapy and has an excellent prognosis.

In contrast, non-seminoma tumors are overall more aggressive, metastasize early, have a variable response to treatment and a variable prognosis.

However, it’s important to know that the majority of germ cells tumors are mixed and the prognosis is based on the worst component.

Okay, so seminoma is the most common type of germ cell tumor.

For your exams, remember that gross examination of this tumor typically shows a homogenous mass with no hemorrhage or necrosis.

On microscopic examination, tumor cells are large with central nuclei surrounded by clear cytoplasm.

A key word for that is a “fried-egg appearance”.

Another high-yield thing to know is that this is the testicular analogue of ovarian dysgerminoma. Now, lab tests may show increased PALP levels, however, remember that AFP levels are always normal. hCG is usually also normal, but in rare cases, it might be increased.

Moving on to non-seminomatous tumors, let’s start with yolk sac tumors, also known as endodermal sinus tumors.

What’s high-yield here is that these are the most common testicular tumor in children.

So, if a test question is about a child, particularly younger than 3 years old, with a firm, painless testicular mass, think of yolk sac tumor at the top of your differentials.

On gross examination, this type of tumor is typically yellow and mucinous.

A key thing to keep in mind is that, under the microscope they form glomeruloid structures or Schiller-Duval bodies, which are rings of malignant cells around the central blood vessel.

Lab tests classically show elevated AFP levels, with normal PALP and normal or increased hCG.

Next, there’s choriocarcinoma.

Sources
  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Sternberg's Diagnostic Surgical Pathology" LWW (2009)
  4. "Medical Treatment of Advanced Testicular Cancer" JAMA (2008)
  5. "Testicular Cancer: A Prototypic Tumor of Young Adults" Seminars in Oncology (2009)
  6. "Testicular Choriocarcinoma Presenting as Hyperthyroidism" The American Journal of Medicine (2013)