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Schwannoma of the Adrenal Gland -A case report-
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KMID : 0357919930270040424
Abstract
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Retroperitoneum is often the site of occurrence of schwannoma, but reports on
schwannoma of the adrenal gland is exceptional and only 4 cases have been documented
in the literature.
This report is to add one such case occurred in a 53 year-old male who had anorexia,
nausea and indigestion for one month. Whole body bone scan and abdominal CT scan
resealed a 10 §¯ sifted solid mass at upper pole of the left kidney. Under the impression
of renal cell carcinoma, an operation was performed. The tumor was well encapsulated
and appeared not to involve the kid nay. The cut surfaces were light yellow and
seemed to be composed of several hard lobules with areas of mucoid, cystic and calcific
changes. No adrenal gland was identified grossly. But microscopically, the tumor was
found to be partly surrounded by a small portion of adrenal cortical tissue. Histologically
the tumor was a typical schwannoma with Verocay bodies, although modified in some
extents by mucoid degeneration, cystic change, hyaline change and focal calcification. It
is worthwhile to remember that the retroperitoneal schwannoma commonly had a huge
size, sometimes involving the adjacent structures. (Korean J Pathol 1993; 27: 424¡426)
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Schwannoma; Retroperitoneum; Adrenal gland;
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