Progress in the diagnosis and classification of pituitary adenomas

Luis V. Syro*, Fabio Rotondo, Alex Ramirez, Antonio Di Ieva, Aydin Sav, Lina M. Restrepo, Carlos A. Serna, Kalman Kovacs

*Corresponding author for this work

    Research output: Contribution to journalReview article

    33 Citations (Scopus)
    75 Downloads (Pure)

    Abstract

    Pituitary adenomas are common neoplasms. Their classification is based upon size, invasion of adjacent structures, sporadic or familial cases, biochemical activity, clinical manifestations, morphological characteristics, response to treatment and recurrence. Although they are considered benign tumors, some of them are difficult to treat due to their tendency to recur, despite standardized treatment. Functional tumors present other challenges for normalizing their biochemical activity. Novel approaches for early diagnosis as well as different perspectives on classification may help to identify subgroups of patients with similar characteristics, creating opportunities to match each patient with the best personalized treatment option. In this paper we present the progress in the diagnosis and classification of different subgroups of patients with pituitary tumors that may be managed with specific considerations according to their tumor subtype.

    Original languageEnglish
    Article number97
    Pages (from-to)1-8
    Number of pages8
    JournalFrontiers in Endocrinology
    Volume6
    DOIs
    Publication statusPublished - 12 Jun 2015

    Bibliographical note

    Copyright the Author(s) 2015. Version archived for private and non-commercial use with the permission of the author/s and according to publisher conditions. For further rights please contact the publisher.

    Keywords

    • diagnosis
    • genetics
    • pathology
    • acromegaly
    • multiple endocrine neoplasia type 1
    • pituitary adenoma
    • familial isolated
    • Carney complex

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