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Hyperpigmentation Due Solely to Increased Plasma β-Melanotropin
Clark T. Sawin, MD;
Kaoru Abe, MD;
David N. Orth, MD
Arch Intern Med. 1970;125(4):708-710.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings. |
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In 1958, Nelson and others 1 described a patient with dark skin, enlargement of the sella turcica, and an elevated level of plasma corticotropin (ACTH), all appearing after adrenalectomy for Cushing's disease. At the time it was not clear whether ACTH or melanocyte-stimulating hormone (MSH) caused the hyperpigmentation. Since such patients have increased levels of MSH as well as of ACTH,2 it has been difficult to state conclusively that one or the other hormone is the responsible substance. We report here a patient with hyperpigmentation after total bilateral adrenalectomy for Cushing's disease, who lacked two of the findings usually found in Nelson's syndrome, namely, an enlarged sella turcica and an elevated plasma level of ACTH, but who did have a high level of β-MSH in his plasma.
Patient Summary
In 1959, a 41-year-old man had typical clinical signs and symptoms of Cushing's syndrome with the level of urinary 17-hydroxycorticosteroids
. . . [Full Text PDF of this Article]
Author Affiliations
Boston; Nashville, Tenn
From the Endocrine Section, Medical Service, Boston Veterans Administration Hospital; and the Department of Medicine, Tufts University School of Medicine, Boston (Dr. Sawin); and the Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tenn (Drs. Abe and Orth).
Footnotes
Received for publication Sept 24, 1969; accepted Nov 7.
Reprint requests to 150 S Huntington Ave, Boston 02130 (Dr. Sawin).
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