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Endocrine Abstracts (2021) 73 OC3.5 | DOI: 10.1530/endoabs.73.OC3.5

ECE2021 Oral Communications Oral Communications 3: Pituitary and Neuroendocrinology (6 abstracts)

Pregnancies after childhood craniopharyngioma – Results of KRANIOPHARYNGEOM 2000/2007

Panjarat Sowithayasakul 1 , 2 , Svenja Boekhoff 1 , Brigitte Bison 3 & Hermann Müller 1


1University Children’s Hospital, Car von Ossietzky University Oldenburg, Department of Pediatrics and Pediatric Hematology/Oncology, Klinikum Oldenburg AöR, Oldenburg, Germany; 2Srinakharinwirot University, Department of Pediatrics, Bangkok, Thailand; 3Augsburg Hospital, Department of Neuroradiology, Augsburg, Germany


Background

Data on female fertility, pregnancy, and outcome of offspring after childhood-onset craniopharyngioma (CP) are rare.

Study design

Observational study on pregnancy rate and outcome of offspring after CP in postpubertal, female patients recruited in KRANIOPHARYNGEOM 2000/2007 since 2000.

Results

451 CP patients (223 female) have been recruited. 269 CP patients (133 female) were postpubertal at study. Six of 133 female CP patients (4.5%) with a median age of 14.9 years at CP diagnosis had 9 pregnancies, giving birth to 10 newborns. Three patients achieved complete surgical resections. No patient underwent postoperative irradiation. Five natural pregnancies occurred in 3 CP patients without pituitary deficiencies. Four pregnancies were achieved in 3 CP with hypopituitarism under assisted reproductive techniques (ART) (after median 4.5 cycles, range: 3–6 cycles). Median maternal age at pregnancy was 30 years (range: 22–41 years). Six babies (60%) were delivered by caesarean section. Median gestational age at delivery was 38 weeks (range: 34–43 weeks); median birth weight was 2, 920 grams (range: 2, 270–3, 520 grams), the rate of preterm delivery was 33%. Enlargements of CP cysts occurred in 2 women during pregnancy. Other severe complications during pregnancy, delivery and postnatal period were not observed.

Conclusions

Pregnancies after CP are rare and achieved in 45% after ART. Close monitoring by an experienced reproductive physician is necessary. Due to a potentially increased risk for cystic enlargement, MRI of cystic CP is recommended during pregnancy. Severe perinatal complications, birth defects, and postnatal morbidity of mothers and offspring were not observed.

Volume 73

European Congress of Endocrinology 2021

Online
22 May 2021 - 26 May 2021

European Society of Endocrinology 

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