Seminoma

Source: Wikipedia, the free encyclopedia.

Seminoma
Other namesPure seminoma, classical seminoma
Histopathology of classical seminoma, with typical features.[1]
SpecialtyUrology, oncology
Relative incidences of testicular tumors, showing seminoma at bottom left.[2]

A seminoma is a germ cell tumor of the testicle or, more rarely, the mediastinum or other extra-gonadal locations. It is a malignant neoplasm and is one of the most treatable and curable cancers, with a survival rate above 95% if discovered in early stages.[3]

Testicular seminoma originates in the germinal epithelium of the seminiferous tubules.[4] About half of germ cell tumors of the testicles are seminomas.[5] Treatment usually requires removal of one testicle. However, fertility usually isn't affected. All other sexual functions will remain intact.

Signs and symptoms

The average age of diagnosis is between 35 and 50 years. This is about 5 to 10 years older than men with other germ cell tumors of the testes. In most cases, they produce masses that are readily felt on

retroperitoneum.[6]

Some cases of seminoma can present as a primary tumour outside the testis, most commonly in the mediastinum.[6] In the ovary, the tumor is called a dysgerminoma, and in non-gonadal sites, particularly the central nervous system, it is called a germinoma.[5]

Diagnosis

Ultrasound image of a seminoma

alpha fetoprotein.[8] Lactate dehydrogenase (LDH) may be the only marker that is elevated in some seminomas. The degree of elevation in the serum LDH has prognostic value in advanced seminoma.[9]

The cut surface of the tumour is fleshy and lobulated, and varies in colour from cream to tan to pink. The tumour tends to bulge from the cut surface, and small areas of

hemorrhage may be seen. These areas of hemorrhage usually correspond to trophoblastic cell clusters within the tumour.[5]

Microscopic examination shows that seminomas are usually composed of either a sheet-like or lobular pattern of cells with a fibrous

intratubular germ cell neoplasia, and may also show variable spermatocytic maturation arrest.[5]

  • Gross pathology of seminoma
    Gross pathology of seminoma
  • Histopathological image of metastatic seminoma in the inguinal lymph node. Hematoxylin & eosin stain.
    Histopathological image of metastatic seminoma in the inguinal lymph node. Hematoxylin & eosin stain.
  • Histopathological image of metastatic seminoma in the inguinal lymph node. At higher magnification. Hematoxylin & eosin stain.
    Histopathological image of metastatic seminoma in the inguinal lymph node. At higher magnification. Hematoxylin & eosin stain.
  • Micrograph (high magnification) of a seminoma. H&E stain.
    Micrograph (high magnification) of a seminoma. H&E stain.
  • Testicular seminoma, showing a typically prominent lymphocytic infiltrate in the fibrous stroma separating the clusters of tumor cells.
    Testicular seminoma, showing a typically prominent
    stroma
    separating the clusters of tumor cells.
  • Orchidectomy specimen showing seminoma
    Orchidectomy
    specimen showing seminoma
  • The germ cell markers OCT 3/4 and CD117 (positive immunohistochemistry pictured) are useful for diagnosis.[10]
    The germ cell markers
    CD117 (positive immunohistochemistry pictured) are useful for diagnosis.[10]

Relation to spermatocytic tumor

Treatment

Intratesticular masses that appear suspicious on an

nonseminoma elements or that occur with the presence of AFP should be treated as nonseminomas. Abdominal CT or MRI scans as well as chest imaging are done to detect for metastasis. The analysis of tumor markers also helps in staging.[12]

The preferred treatment for most forms of stage 1 seminoma is active surveillance. Stage 1 seminoma is characterized by the absence of clinical evidence of metastasis. Active surveillance consists of periodic history and physical examinations, tumor marker analysis, and radiographic imaging. Around 85-95% of these cases will require no further treatment. Modern radiotherapy techniques as well as one or two cycles of single-agent carboplatin have been shown to reduce the risk of relapse, but carry the potential of causing delayed side effects. Regardless of treatment strategy, stage 1 seminoma has nearly a 100% cure rate.[13]

Stage 2 seminoma is indicated by the presence of retroperitoneal metastasis. Cases require radiotherapy or, in advanced cases, combination chemotherapy. Large residual masses found after chemotherapy may require surgical resection. Second-line treatment is the same as for nonseminomas.[12]

Stage 3 seminoma is characterized by the presence of metastasis outside the retroperitoneum—the lungs in "good risk" cases or elsewhere in "intermediate risk" cases. This is treated with combination chemotherapy. Second-line treatment follows nonseminoma protocols.[12]

References

  1. ^ By Mikael Häggström, MD. Reference for findings: Michelle R. Downes, M.D. "Testis & paratestis - Seminoma". Pathology Outlines. Last author update: 7 January 2020. Last staff update: 19 April 2022
  2. PMID 10851829.{{cite journal}}: CS1 maint: multiple names: authors list (link
    )
  3. ^ "Testicular cancer". Medline Plus. Retrieved 13 December 2012.
  4. ^ "Seminoma" at Dorland's Medical Dictionary
  5. ^ .
  6. ^ .
  7. .
  8. .
  9. )
  10. ^ Michelle R. Downes, M.D. "Testis & epididymis - Germ cell tumors - Seminoma". Pathology Outlines. Topic Completed: 7 January 2020. Minor changes: 26 January 2021
  11. PMID 3583416
    .
  12. ^ a b c "NCCN Testicular Cancer Guidelines". NCCN Clinical Practice Guidelines in Oncology.
  13. PMID 24002502
    .

External links