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Kyoto Prefectural University of Medicine Kyoto 602, Japan
Takaaki Mizutani and Yuuji Nakagaw
Ayabe Municipal Hospital Ayabe 623, Japan
We read with great interest the report of Masuzaki et al. (1), which showed that serum leptin levels were increased in patients with Cushings syndrome. However, serum leptin levels in a patient with pheochromocytoma, another adrenal tumor, were not described.
A 72-yr-old man complaining of episodic headaches, nausea,
palpitations, and perspiration was referred to our department in
October 1997. Physical examination showed that the patient was agitated
and had striking peripheral vasoconstriction. Blood pressure varied
between 240/130 and 80/40 mm Hg; the patient did not have orthostatic
hypotension. Plasma noradrenaline and adrenaline levels were increased
(2.20 ng/mL and 0.86 ng/mL, respectively), although serum cortisol and
aldosterone levels were normal. Twenty-four-hour urinary noradrenaline
and adrenaline were also increased (882 µg/day and 138 µg/day,
respectively). A tentative diagnosis of pheochromocytoma was made.
Computed tomography of the abdomen showed a mass measuring
approximately 4 cm in diameter in the left adrenal gland. Pathological
examination after left-sided adrenalectomy were compatible with
pheochromocytoma. After surgery, the patient had no symptoms and was
normotensive. Although serum leptin levels were low before surgery,
serum leptin levels were increased with diurnal rhythms 1 month after
surgery (Table 1
).
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Footnotes
Address correspondence to: Toshihide Yoshida, First Department of Internal Medicine, Kyoto Prefectural University of Medicine, Kamikyo-ku, Kyoto 602, Japan.
Received December 31, 1997.
References
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