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. 2021 Mar;129(3):250-264.
doi: 10.1055/a-1373-4087. Epub 2021 Mar 9.

First German Guideline on Diagnostics and Therapy of Clinically Non-Functioning Pituitary Tumors

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First German Guideline on Diagnostics and Therapy of Clinically Non-Functioning Pituitary Tumors

Timo Deutschbein et al. Exp Clin Endocrinol Diabetes. 2021 Mar.

Abstract

Although non-functioning pituitary tumors are frequent, diagnostic and therapeutic concepts are not well standardized. We here present the first German multidisciplinary guideline on this topic. The single most important message is to manage the patients by a multidisciplinary team (consisting at least of an endocrinologist, a neurosurgeon, and a (neuro-) radiologist). The initial diagnostic work-up comprises a detailed characterization of both biochemical (focusing on hormonal excess or deficiency states) and morphological aspects (with magnetic resonance imaging of the sellar region). An ophthalmological examination is only needed in presence of symptoms or large tumors affecting the visual system. Asymptomatic, hormonally inactive tumors allow for a 'wait and scan' strategy. In contrast, surgical treatment by an experienced pituitary surgeon is standard of care in case of (impending) visual impairment. Therapeutic options for incompletely resected or recurrent tumors include re-operation, radiotherapy, and observation; the individual treatment plan should be developed multidisciplinary. Irrespective of the therapeutic approach applied, patients require long-term follow-up. Patient with larger pituitary tumors or former surgery/radiotherapy should be regularly counseled regarding potential symptoms of hormonal deficiency states.

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Conflict of interest statement

The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported. A detailed list of all reported potential conflicts of interests is given at https://www.awmf.org/fileadmin/user_upload/Leitlinien/089_D_Ges_fuer_Endokrinologie/089–002i_S2k_Diagnostik-Therapie-hormonaktiver-Hypophsenaddenome_2020–02.pdf

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