Context: Carney complex (CNC) is a syndrome characterized by hyperplasia of endocrine organs and may present with clinical features of Cushing syndrome and acromegaly due to functional adrenal and pituitary gland tumors. CNC has been linked to mutations in the regulatory subunit of protein kinase A type I-alpha () gene.
Design: Tissue samples were taken from the hypothalamus or thalamus or tumors of patients with pituitary adenomas seen and operated on by neurosurgeon Harvey Cushing between 1913 and 1932. Following DNA extraction, sequencing for genes of interest was attempted, including , , , , and , to explore the possibility that these mutations associated with acromegaly, CNC, and Cushing syndrome have been conserved over time.
Results: We report a patient described by Dr. Cushing in 1914 with a clinical presentation and postmortem findings suggestive of CNC. Genetic sequencing of the hypothalamus and pituitary adenoma revealed a germline heterozygous p.Arg74His mutation in the gene, a codon previously described as mutated in CNC, but with a novel amino acid change.
Conclusions: This patient is, to our knowledge, the first molecularly confirmed individual with CNC. This case demonstrates the power of modern genetics in studying archived tissues and the importance of recording detailed clinical notes in the diagnosis of disease.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686675 | PMC |
http://dx.doi.org/10.1210/js.2017-00283 | DOI Listing |
Ann Med Hist
May 1929
305 Walnut Street, Brookline, Mass.
Ann Med Hist
September 1919
Peter Bent Brigham Hospital, Boston, Mass.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!