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 Experiment Videos

[Pheochromocytomas].

R Mornex1

  • 1Service d'Endocrinologie-diabète-nutrition, Hôpital Edouard Herriot, Lyon, France.

Acta Chirurgica Belgica
|March 1, 1991
PubMed
Summary
This summary is machine-generated.

This study focuses on pheochromocytoma diagnosis and management, highlighting advancements in imaging and surgical outcomes. Early detection and multidisciplinary care improve patient survival rates for this rare adrenal tumor.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

[Étienne Destot (1864-1918) or the other father of French radiology].

Cancer radiotherapie : journal de la Societe francaise de radiotherapie oncologique·2017
Same author

[Jean-Claude Savoie].

Presse medicale (Paris, France : 1983)·2001
Same author

[The 1998 Maurice Dérot Prize. [Diabetology-endocrinology in the same struggle].

Journees annuelles de diabetologie de l'Hotel-Dieu·1998
Same author

[Quality assurance approval in European health care centers training endocrinology, diabetes and metabolism specialists ].

Annales d'endocrinologie·1998
Same author

[Diagnostic strategy for a solitary thyroid nodule. Example of development of recommendations for a practice guideline].

Bulletin de l'Academie nationale de medecine·1997
Same author

[European perspectives of the training of endocrinologists].

Annales d'endocrinologie·1996
Same journal

Tailored surgical planning in TEP inguinal hernia repair: a multivariate analysis of obesity and hernia defect size.

Acta chirurgica Belgica·2026
Same journal

Incidence of tissue-based inguinal hernia repair in Belgium: a web-based national survey.

Acta chirurgica Belgica·2026
Same journal

Breast implant-associated anaplastic large cell lymphoma following prophylactic mastectomy & breast reconstruction: a case report.

Acta chirurgica Belgica·2026
Same journal

Skin bridge versus conventional rods for loop enterostomies: a systematic literature review and meta-analysis.

Acta chirurgica Belgica·2026
Same journal

Risk factors associated with urinary tract infection within 4 days of male rectal cancer surgery in the era of enhanced recovery after surgery (ERAS) programs.

Acta chirurgica Belgica·2026
Same journal

Redo endoscopic assisted coronary artery bypass grafting in an 86-year-old patient: a case report and technical review.

Acta chirurgica Belgica·2026
See all related articles

Area of Science:

  • Endocrinology
  • Oncology
  • Radiology

Context:

  • Pheochromocytoma diagnosis relies on clinical presentation, biochemical tests (catecholamines, metabolites), and imaging (CT, MIBG scintigraphy).
  • Management strategies are evolving, particularly for malignant pheochromocytomas and those associated with Multiple Endocrine Neoplasia type II (MEN II).
  • Familial screening is crucial for MEN II to identify hereditary pheochromocytoma cases.

Purpose:

  • To review key diagnostic and therapeutic advancements in pheochromocytoma management.
  • To emphasize the improved prognosis due to modern diagnostic tools and surgical techniques.
  • To discuss the incidence and management of malignant pheochromocytomas.

Summary:

  • Diagnosis involves clinical assessment, biochemical analysis of catecholamines, and imaging like CT scans and MIBG scintigraphy.

Related Experiment Videos

  • Malignant pheochromocytomas may have a higher incidence than previously reported and require specific management strategies.
  • Surgical resection offers a favorable prognosis with near-zero mortality, though periprocedural morbidity necessitates careful pharmacological management.

    • Impact:

    • Improved diagnostic accuracy leading to earlier detection of pheochromocytoma.
    • Enhanced understanding of malignant pheochromocytoma, potentially increasing survival rates.
    • Surgical advancements have significantly improved patient outcomes and prognosis for pheochromocytoma.