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  Vol. 213 No. 2, July 13, 1970 TABLE OF CONTENTS
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Hyperpigmentation in Thyrotoxicosis

Robert Miller, MD; FUAD S. ASHKAR, MD; Jorge Jacobi, MD

JAMA. 1970;213(2):299.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

To the Editor:—

The signs of thyrotoxicosis have been memorized by medical students for decades; however, changes in skin pigmentation seem to be frequently overlooked. In our experience, alterations in pigmentation have been a useful and interesting physical finding.

Increases in pigmentation are often seen in exophthalmic goiter (Graves' disease) and may be either diffuse or chloasmal in nature. These skin changes can be seen in either exposed or unexposed areas but are rarely seen on the buccal mucosa, nipples, or genitals.

The cause of the pigmentary changes is still speculative; however, it is known that the pigment is melanin. Tyrosine is an amino acid common to both melanin and thyroxine; and it is well established that patients with thyrotoxicosis have tyrosine intolerance with elevated serum tyrosine levels.1

Many theories have been advanced to explain the phenomenon of hyperpigmentation such as elevated levels of adrenocorticotropic hormone (ACTH) or tyrosine, . . . [Full Text PDF of this Article]


Author Affiliations

Miami, Fla



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