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Related Concept Videos

Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
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The Ras Gene02:38

The Ras Gene

The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
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Tumorsphere Derivation and Treatment from Primary Tumor Cells Isolated from Mouse Rhabdomyosarcomas
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Tumorsphere Derivation and Treatment from Primary Tumor Cells Isolated from Mouse Rhabdomyosarcomas

Published on: September 13, 2019

Prostatic stromal sarcoma with rhabdoid features.

Joo Young Kim1, Yong Mee Cho, Jae Y Ro

  • 1Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, 138-736 Seoul, Korea.

Annals of Diagnostic Pathology
|November 16, 2010
PubMed
Summary
This summary is machine-generated.

This report details the first known case of prostatic stromal sarcoma with rhabdoid features in a 31-year-old male. This rare and aggressive tumor exhibited rapid progression and poor prognosis.

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Area of Science:

  • Oncology
  • Pathology
  • Urologic Oncology

Background:

  • Rhabdoid tumors are aggressive neoplasms found in various sites, often as composite tumors.
  • Rhabdoid tumors of the prostate are exceptionally rare, with only one prior report suggesting epithelial origin.
  • Rhabdoid features have not been previously documented in prostatic stromal sarcomas (PSSs).

Observation:

  • A 31-year-old male presented with voiding difficulties and anal pain due to a prostatic mass invading the rectum and bladder.
  • Initial biopsy diagnosed unclassified spindle cell sarcoma; neoadjuvant chemotherapy was administered.
  • Radical prostatectomy revealed a high-grade sarcoma with spindle cells and epithelioid cells exhibiting rhabdoid features.

Findings:

  • Immunohistochemistry showed positivity for vimentin, CD34, and progesterone receptor in both cell types.
  • Desmin and cytokeratin were negative, while INI1 expression was retained in rhabdoid cells.
  • The tumor demonstrated aggressive behavior with recurrence in the bladder and death from sepsis within 7 months.

Implications:

  • This case represents the first description of prostatic stromal sarcoma with rhabdoid features.
  • The findings highlight the potential for rhabdoid differentiation in PSS.
  • This rare entity presents with aggressive clinical behavior and necessitates further investigation into its pathogenesis and treatment strategies.