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Giant prolactinoma in children and adolescents: a single-center experience and systematic review

Journal

PITUITARY
Volume 25, Issue 6, Pages 819-830

Publisher

SPRINGER
DOI: 10.1007/s11102-022-01250-y

Keywords

Giant prolactinoma; Prolactinoma; Childhood prolactinoma; Pediatric prolactinoma; Young prolactinoma; Pituitary adenoma

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Giant prolactinoma (GP) in childhood and adolescence is a rare disease characterized by male predominance and frequent delay/arrest of puberty. Dopamine agonist (DA) monotherapy may be preferred as the first-line treatment.
Purpose Giant prolactinoma (GP) in childhood and adolescence is a rare entity with scarce literature. We aimed to describe clinical features, biochemistry, radiology, genetics, management, and outcome in pediatric (<= 20 years) GP. Methods Retrospective record review of 18 pediatric GP patients from our center and systematic review including these and 77 from the literature (total cohort: 95). Results GP constituted 20% of our pediatric prolactinoma cohort. In the total cohort (age: 15.4 +/- 3.5 years), the majority (77, 82.8%) were males. Mass effect symptoms (88.6%), and pubertal delay/arrest in males (82.1%) were frequent. Median basal prolactin was 8649 (3246-17,532) ng/ml and the maximum tumor dimension was 5.5 +/- 1.5 cm. MEN1 and AIP mutations were noted in 7 (21.9%) and 6 (18.8%) patients, respectively. Males with central hypogonadism had baseline bi-testicular volume of 20.2 +/- 8.4 cc, lower LH than FSH (-2.04 +/- 0.9 vs. -0.7 +/- 1.6 SDS, p = 0.0075), and mostly, normal inhibin B. Majority (49/76, 64.5%) received dopamine agonist (DA) as first-line treatment with additional therapy in 35% (17/49). DA monotherapy arm had less frequent central hypothyroidism (42.9% vs 87.1%, p = 0.002) and central adrenal insufficiency (7.1% vs 66.7%, p = 0.0003) than multimodal therapy. A smaller tumor dimension (4.7 vs. 5.7 cm, p = 0.04) was associated with normoprolactinemia on DA monotherapy and AIP mutations (33.3% vs. nil, p = 0.02) with multimodal therapy. Conclusion GP is characterized by male predominance with frequent delay/arrest of puberty (82%), but relative sparing of the FSH-inhibin B axis in boys. DA monotherapy may be preferred as the first-line therapy in pediatric GP.

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