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PITUITARY ONCOCYTOMA:A CLINICAL AND, LIGHT AND ELECTRON MICROSCOPICAL OBSERVATION WITH SPECIAL REFERENCE TO THE PATHOLOGICAL CRITERIA AND SECRETORY FUNCTION Kunio Shirataki 1 , Hiromitsu Sumiyoshi 1 , Norihiko Tamaki 1 , Satoshi Matsumoto 1 , Junji Iwasaki 2 , Kazuo Chihara 2 , Yoshio Yoshimoto 2 , Takuo Fujita 2 , Satoshi Okada 3 1Department of Neurological Surgery, Kobe University School of Medicine 2Third Division, Department of Medicine, Kobe University School of Medicine 3Department of Pathology,Kobe University,School of Medicine pp.679-689
Published Date 1982/7/1
DOI https://doi.org/10.11477/mf.1406204967
  • Abstract
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Hamperl (1931), for the first time, proposed the term "oncocyte " for a large epithelial cell with extreme cytoplasmic granularity and acidophilia in human salivary glands. Thereafter oncocytes or oncocytoma composed of oncocytes have been found also in thyroid, parathyroid, pancreas, etc.. Electron microscopy has shown that oncocytes contain ex-cessive accumulations of mitochondria since 1959. In anterior lobe of the hypophysis, Hamperl (1936) also described oncocytes, but the regular light and electron microscopical study on pituitary oncocy-toma has been started far later since about 1970. Although several pituitary oncocytomas have been reported in these years, many problems still remain unanswered.

As we experienced an attractive case of pituitary oncocytoma recently, we dscribed his clinical course and, light and electron microscopical findings of the tumor, and, in particular, discussed the pathologi-cal criteria for pituitary oncocytoma and its hormonal function.

A 57-year-old man was admitted on May 28, 1975, because of nausea, loss of appetite and faint-ing. On investigation, serum Na value was 102 mEq/1, K 3. 4 mEq/l, Cl 74 mEq/l, on the contrary urinary Na and CI high. His axillary and pubic hair were scant. About a month later he had delirium and abnormal behavior, and further 2 months later he complained bilateral failing vision. Plain skull X-ray revealed the cellar enlargement and destruction. With the diagnosis of non-func-tioning pituitary adenoma. operation was performed on September 22. The solid, jellied mass was partially extirpated. In April, 1979, he was read-mitted because of persistency of a large mass with supra- and parasellar extension, confirmed by CT. Hormonal examination showed that GH, prolactin and ACTH had no responses to various test stimuli as well as they were very low levels in baseline, on the other hand, LH, FSH and TSH responded normally or to some extent as well as their basal values were normal or somewhat lower. On June 18, the patient had reoperation, accompanied by irradiation therapy with the total doses of 4,000 rads.

Light microscopy of the tissue removed during first operation demonstrated the tumor composed of granular eosinophilic cells with organoid arrange-ment. But the granularity and eosinophilia was diminished in the tumor from second operation.

Electron microscopically, the findings between specimens from the first and second operation were thought to be almost the same. The striking feature was the presence of a great many mitochon-dria in most tumor cells. Most mitochondria were normal, but some were condensed or swollen. A few secretory granules with an average diameter of 109 nm were also noted.

Accordingly, it is concluded that numerous mitochondria cause the oncocytic granularity of cytoplasm observed by light microscopy. We agree to the thought that pituitary oncocytoma should be correctly identified after they had been studiedby electron microscopy. Pituitary oncoytoma derived from common pituitary adenoma, aside from oncocytoma only composed of fully developed oncocytes without secretory granules. Although it is difficult to define precisely the pituitary ade-noma which is composed predominantly of transi-tional oncocytes ultrastructurally, such a tumor is also thought to be a type of pituitary oncocytoma.


Copyright © 1982, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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