Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

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.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Phenotypic Profile of Microsatellite Stable with Epithelial to Mesenchymal Transition Subtype in Gastric Adenocarcinoma.

International journal of surgical pathology·2025
Same author

Urticarial hypocomplementemic vasculitis syndrome and systemic lupus erythematosus: a case report and review of the literature.

Frontiers in immunology·2025
Same author

A cervical spine metastasis of a hepatocellular carcinoma: a rare presentation.

Future science OA·2025
Same author

Cystic adventitial disease of the popliteal artery: A case report with review of literature.

International journal of surgery case reports·2024
Same author

Supra-sellar granular cell tumor: Report of a case with literature review.

International journal of surgery case reports·2023
Same author

Calcifying pseudoneoplasm of the neuraxis (CAPNON): Unraveling a rare non-neoplastic calcified central nervous system lesion.

International journal of surgery case reports·2023

Related Experiment Video

Updated: Jul 7, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
11:42

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells

Published on: April 7, 2017

[Endometrial adenosarcoma with rhabdomyoblastic differenciation].

Meriem Bel Haj Salah1, Amina Mekni, Chelly Ines

  • 1Service d'Anatomie et de Cytologie Pathologique, obstetrique C. Maternité la Rabta.

La Tunisie Medicale
|February 2, 2008
PubMed
Summary
This summary is machine-generated.

This case report details an uncommon endometrial adenosarcoma in a 59-year-old woman. The study discusses the clinicopathological characteristics and potential causes of this rare neoplasm.

Related Experiment Videos

Last Updated: Jul 7, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
11:42

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells

Published on: April 7, 2017

Area of Science:

  • Gynecologic Oncology
  • Pathology

Background:

  • Mixed Mullerian Tumors (MMTs) are rare endometrial neoplasms with both mesenchymal and epithelial components.
  • Adenosarcoma, a subtype of MMT, features benign glandular elements and low-grade sarcomatous stroma.

Observation:

  • A 59-year-old woman presented with a three-month history of metrorrhagia and an enlarged uterus.
  • Imaging studies (ultrasound and CT) revealed a significant uterine mass without evidence of other tumors.

Findings:

  • Surgical management via hysterectomy with adnexectomy was performed.
  • Pathological examination confirmed an endometrial adenosarcoma, characterized by a mixture of mesenchymal and epithelial elements.

Implications:

  • This case highlights the importance of accurate pathological diagnosis for rare endometrial neoplasms.
  • Understanding the clinicopathological features of adenosarcoma is crucial for appropriate patient management and further research into its etiopathogeny.