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The triad of paragangliomas, gastric stromal tumours and pulmonary chondromas (Carney triad), and the dyad of paragangliomas and gastric stromal sarcomas (Carney-Stratakis syndrome): molecular genetics and clinical implications.

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Updated: Jun 22, 2026

Screening of Axonal Degeneration in Carpal Tunnel Syndrome Using Ultrasonography and Nerve Conduction Studies
06:40

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Published on: January 11, 2019

Incomplete Carney triad--a review of two cases.

S A Sawhney1, A D Chapman, J A Carney

  • 1Department of Respiratory Medicine, Aberdeen Royal Infirmary, Foresterhill, Aberdeen, UK AB25 2ZD. simonsawhney@nhs.net

QJM : Monthly Journal of the Association of Physicians
|June 30, 2009
PubMed
Summary
This summary is machine-generated.

Carney's triad is a rare condition involving three distinct tumors. This report details two new cases of incomplete Carney's triad, highlighting variations in tumor presentation.

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Last Updated: Jun 22, 2026

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06:40

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Published on: January 11, 2019

Area of Science:

  • Oncology
  • Rare Diseases
  • Genetics

Background:

  • Carney's triad, first described in 1977, is a rare neoplastic syndrome.
  • It characteristically comprises multifocal pulmonary chondroma, gastric stromal sarcoma, and extra-adrenal paraganglioma.
  • The syndrome can manifest as complete or incomplete forms, with varying tumor combinations.

Observation:

  • This report presents two new cases of patients with incomplete Carney's triad.
  • These cases illustrate the diverse clinical presentations of this rare condition.
  • The patients exhibited a subset of the three characteristic tumors.

Findings:

  • The study focuses on the incomplete expression of Carney's triad.
  • It contributes to understanding the spectrum of this rare disease.
  • Detailed case reports provide insights into the clinical course and management.

Implications:

  • Understanding incomplete Carney's triad is crucial for accurate diagnosis and timely intervention.
  • These findings may aid in refining diagnostic criteria and management strategies for rare tumor syndromes.
  • Further research into the genetic and molecular underpinnings of Carney's triad is warranted.