Abstract

Pregnancies are rare in women with pituitary adenomas, which may relate to hormone excess from secretory subtypes such as prolactinomas or corticotroph adenomas. Decreased fertility may also result from pituitary hormone deficiencies due to compression of the gland by large tumours and/or surgical or radiation treatment of the lesion. Counselling premenopausal women with pituitary adenomas about their chance of conceiving spontaneously or with assisted reproductive technology, and the optimal pre-conception treatment, should start at the time of initial diagnosis. The normal physiological changes during pregnancy need to be considered when interpreting endocrine tests in women with pituitary adenomas. Dose adjustments in hormone substitution therapies may be needed across the trimesters. When medical therapy is used for pituitary hormone excess, consideration should be given to the known efficacy and safety data specific to pregnant women for each therapeutic option. In healthy women, pituitary gland size increases during pregnancy. Since some pituitary adenomas also enlarge during pregnancy, there is a risk of visual impairment, especially in women with macroadenomas or tumours near the optic chiasm. Pituitary apoplexy represents a rare acute complication of adenomas requiring surveillance, with surgical intervention needed in some cases. This guideline describes the choice and timing of diagnostic tests and treatments from the pre-conception stage until after delivery, taking into account adenoma size, location and endocrine activity. In most cases, pregnant women with pituitary adenomas should be managed by a multidisciplinary team in a centre specialised in the treatment of such tumours.

Highlights

  • The pituitary gland and endocrine milieu in pregnancyPregnancy changes the morphology and function of the pituitary gland

  • We recommend that women of reproductive age with a diagnosis of a pituitary adenoma be counselled about their potential fertility and pregnancy outcomes as early as possible

  • We recommend that women and their partners be provided with education for glucocorticoid stress dose adjustment and measures on how to prevent or manage adrenal crisis during pregnancy

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Summary

A Luger and others

A Luger, L H A Broersen, N R Biermasz, B M K Biller, M Buchfelder, P Chanson 6, J O L Jorgensen 7, F Kelestimur, S Llahana, D Maiter, G Mintziori, F Petraglia, R Verkauskiene, S M Webb 14 and O M Dekkers 15,16,17. Netherlands, 4Neuroendocrine & Pituitary Tumor Clinical Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA, 5Department of Neurosurgery, University Hospital Erlangen, Erlangen, Germany, 6Université Paris-Saclay, Inserm, Physiologie et Physiopathologie Endocriniennes, Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Service d’Endocrinologie et des Maladies de la Reproduction et Centre de Réference des Maladies Rares de l’Hypophyse, Le Kremlin-Bicêtre, France, 7Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark, 8Department of Endocrinology, Yeditepe. University, Istanbul, Turkey, 9School of Health Sciences, City, University of London, London, UK, 10Department of Endocrinology and Nutrition, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium, 11Unit of Reproductive. Investigación Biomédica en Red de Enfermedades Raras (CIBER-ER, Unit 747), ISCIII, Barcelona, Spain, 15Department should be addressed of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands, 16Department of Clinical to A Luger. Endocrinology, Leiden University Medical Center, Leiden, The Netherlands, and 17Department of Clinical Epidemiology, Aarhus University, Aarhus, Denmark

Overview of recommendations
Introduction
Guideline working group
Target group
Aims
Summary of methods used for guideline development
Description of search and selection of literature
Review process and endorsement of other societies
Clinical question I
Clinical question II
Clinical question III
Clinical question IV
Clinical question V
General recommendations
Prolactinomas
Acromegaly
Cushing’s disease
Findings
Suggestions for future research
Full Text
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