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Carney's triad.

S J McLaughlin1, E A Dodge, J Ashworth

  • 1Western General Hospital, Footscray, Melbourne, Victoria.

The Australian and New Zealand Journal of Surgery
|August 1, 1988
PubMed
Summary
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Carney's triad, a rare condition, was partially expressed in a 26-year-old Australian female. Vigilance for complete triad development and surgical considerations are crucial for management.

Area of Science:

  • Medical Genetics
  • Oncology
  • Gastroenterology

Background:

  • Carney's triad is a rare syndrome characterized by the simultaneous occurrence of pulmonary chondroma, gastrointestinal stromal tumors, and functioning extra-adrenal paragangliomas.
  • It predominantly affects young women and is associated with germline mutations in the succinate dehydrogenase genes (SDHx).

Observation:

  • A 26-year-old female presented with symptoms indicative of a partial Carney's triad.
  • This case represents the first documented instance of Carney's triad in Australia.

Findings:

  • The patient exhibited a partial manifestation of Carney's triad, highlighting the condition's variable presentation.
  • The report underscores the importance of recognizing incomplete forms of the triad.

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Implications:

  • Early detection and vigilant monitoring are essential to identify the complete triad and manage potential complications.
  • The role of surgical intervention in managing the tumors associated with Carney's triad requires careful consideration.