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

Primary hepatic carcinoid tumor.

T Asakawa1, T Tomioka, K Abe

  • 1Department of Surgery II, Nagasaki University School of Medicine, Japan.

Journal of Gastroenterology
|April 16, 1999
PubMed
Summary
This summary is machine-generated.

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

Different thresholds of HSP70 and HSC70 heat shock mRNA induction in post-ischemic gerbil brain.

Brain research·1992
Same author

[Mechanism of renin release and cellular action of angiotensin II].

Nihon Naibunpi Gakkai zasshi·1992
Same author

Ras (CXXX) and Rab (CC/CXC) prenylation signal sequences are unique and functionally distinct.

The Journal of biological chemistry·1992
Same author

Isolation of complementary DNAs for heat shock protein (HSP) 70 and heat shock cognate protein (HSC) 70 genes and the expressions in post-ischaemic gerbil brain.

Neurological research·1992
Same author

[DNA typing of HLA-class II genes in idiopathic nephropathy].

Nihon rinsho. Japanese journal of clinical medicine·1992
Same author

Effect of slow release nifedipine tablets in patients with essential hypertension.

Arzneimittel-Forschung·1992

This case report details a rare primary hepatic carcinoid tumor in a 49-year-old woman. Despite surgical intervention and chemoembolization, the patient succumbed to the disease five years post-diagnosis.

Area of Science:

  • Hepatobiliary Medicine
  • Surgical Oncology
  • Gastrointestinal Pathology

Background:

  • Primary hepatic carcinoid tumors are exceptionally rare, posing diagnostic challenges.
  • Carcinoid tumors typically arise from neuroendocrine cells in the gastrointestinal tract or lungs.

Observation:

  • A 49-year-old woman presented with multiple liver tumors.
  • Histopathological examination revealed a large, necrotic mass with satellite nodules.
  • Tumor cells exhibited characteristic neuroendocrine morphology and positive staining for chromogranin A.

Findings:

  • Ultrastructural analysis confirmed duct-like formations and neurosecretory granules, consistent with carcinoid tumors.
  • Immunohistochemistry was positive for chromogranin A and negative for other markers.

Related Experiment Videos

  • The tumor was definitively diagnosed as a primary hepatic carcinoid tumor.

    • Implications:

    • This case highlights the importance of considering rare diagnoses in liver pathology.
    • Effective treatment strategies for primary hepatic carcinoid tumors remain an area for further research.
    • Early diagnosis and multidisciplinary management are crucial for improving patient outcomes.