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Prolactinoma in a Child Showing High MIB-1 Labeling Index : a case report Soichi AKAMINE 1,2 , Tsunehiko MIYAMOTO 1 , Yasushi SUGIURA 1 , Seiya TAKEHARA 1 , Hisaya HIRAMATSU 1 , Shigeru NISHIZAWA 2 , Naoki YOKOTA 2 1Department of Neurosurgery, Seirei Mikatahara General Hospital 2Department of Neurosurgery, Hamamatsu University School of Medicine Keyword: childhood prolactinoma , pituitary adenoma , MIB−1 pp.547-553
Published Date 2000/6/10
DOI https://doi.org/10.11477/mf.1436901905

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  • Abstract
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We report a very rare case of a prolactin secreting, pituitary tumor (prolactinoma) which occurred in a 12-year-old boy. The tumor showed an extremely high MIB-1 index. The clinical implication in the postop-erative management of childhood prolactinoma is discussed. The patient showed right third nerve palsy, and MRI revealed a pituitary tumor invading the right cavernous sinus. Preoperative hormonal evaluation showed a very high prolactin level (2800ng/ml). The patient underwent transsphenoidal surgery, and the third nerve palsy disappeared just after the procedure. MIB-1 index obtained by using immunostaining was 18.9%. Postoperative prolactin level remained high (2200ng/ml), and the patient was treated with 10 mg/day of bromocriptine.

Prolactinomas in children with high MIB-1 index show resistance to treatment with bromocriptine. In the postoperative management of a childhood prolactinoma, it should be considered how to control suffi-ciently high serum prolactin level to expect sexual development while preserving other normal residual pituitary functions. If control with bromocriptine, fails radiation treatment should be adopted with careful observation of the increase in height and the progress of sexual development of the patient.


Copyright © 2000, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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