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

Adrenocortical carcinoma. Our experience

G Favia1, F Lumachi, P Carraro

  • 1Cattedra Endocrinochirurgia, Istituto Clinica Chirurgica I, Università degli Studi-Padova.

Minerva Endocrinologica
|March 1, 1995
PubMed
Summary

Adrenocortical carcinoma is rare, with surgical outcomes showing a low one-year survival rate below 40% and limited correlation between tumor characteristics and prognosis.

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

The experience of the rigid lockdown in the dental emergency room and urgency care during COVID-19 pandemic: a transnational multicenter observational study.

European review for medical and pharmacological sciences·2024
Same author

Efficacy of guided autofluorescence laser therapy in MRONJ: a systematic review.

European review for medical and pharmacological sciences·2024
Same author

Malignant transformation of oral proliferative verrucous leukoplakia: a series of 48 patients with suggestions for management.

International journal of oral and maxillofacial surgery·2020
Same author

Oral lesions as first clinical manifestations of Crohn's disease in paediatric patients: a report on 8 cases.

European journal of paediatric dentistry·2020
Same author

Noma: a reappraisal in Western countries - are HIV-negative immunocompetent adult patients safe?

Journal of biological regulators and homeostatic agents·2019
Same author

Brain abscess of odontogenic origin in children: a systematic review of the literature with emphasis on therapeutic aspects and a new case presentation.

Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale·2019

Area of Science:

  • Endocrinology
  • Surgical Oncology
  • Oncology

Background:

  • Adrenocortical carcinoma (ACC) is a rare malignancy with a low incidence, leading to limited clinical experience in its management.
  • The study addresses the challenges posed by the rarity of ACC in establishing treatment guidelines.

Purpose of the Study:

  • To analyze the outcomes of surgical treatment for adrenocortical tumors, including malignant cases.
  • To evaluate prognostic factors in patients with adrenocortical carcinoma.

Main Methods:

  • Retrospective analysis of 215 patients treated for adrenal diseases between 1979 and 1993.
  • Focus on 19 patients diagnosed with adrenocortical carcinoma, detailing surgical approaches, adjuvant therapies, and survival data.

Main Results:

  • Of 141 cortical tumors, 19 were malignant ACCs. Surgical intervention was performed on 17 ACC patients.
  • The one-year survival rate for ACC was less than 40%, with only six patients surviving 2-18 months post-surgery.
  • Tumor size and endocrine functionality did not appear to correlate with prognosis in this cohort.

Conclusions:

  • Surgical management of adrenocortical carcinoma in this cohort yielded poor survival rates.
  • Further research is needed to identify effective prognostic markers and treatment strategies for ACC.

Related Experiment Videos