# Contemporary series of transsphenoidal microsurgery in pediatric patients

**Authors:** Stefanie Ott, Nora Ramdani, Lasse Dührsen, Franz L. Ricklefs, Roman Rotermund, Jörg Flitsch, Alice Ryba

PMC · DOI: 10.1007/s10143-025-04019-6 · 2026-01-23

## TL;DR

This study examines transsphenoidal microsurgery in children, showing that craniopharyngiomas are more common in younger kids while pituitary adenomas are more frequent in older children.

## Contribution

The study presents one of the largest series of pediatric transsphenoidal surgeries, highlighting age-related differences in tumor types and surgical outcomes.

## Key findings

- Craniopharyngiomas were most common in children under 10 years old.
- Pituitary adenomas were more prevalent in older children.
- Surgical duration was longer in younger patients and correlated inversely with sphenoid sinus pneumatization.

## Abstract

Pituitary tumors are rare in the pediatric population, accounting for less than 10% of childhood tumors. Craniopharyngiomas are the most common pediatric sellar lesions, but pituitary adenomas/PitNETs also occur, representing 2–8% of all sellar lesions. This study explores a decade of transsphenoidal microsurgery on pediatric patients, examining perioperative features including complications, clinical outcomes and anatomical peculiarities. This retrospective study included a total of 147 transsphenoidal surgeries performed by a single surgeon on 122 pediatric patients under the age of 18 between 2013 and 2023. Parameters assessed included age, gender, clinical hormone production, histopathological and radiographic parameters, surgical features, postoperative complications and recurrences rate. Among 122 pediatric patients with pituitary lesions, we found that craniopharyngiomas were the most common entity (34.4%), especially in children under 10 years old (58.6%). Pituitary adenomas/PitNETs accounted for 31.1% and were more prevalent in older children, with corticotrophic and lactotrophic adenomas being the most common subtypes. Younger patients needed significantly more time for surgery, with the longest durations observed in the 3–9 years age group and the shortest in the 16–17 years age group. Additionally, sphenoid sinus pneumatization increased with age and was inversely correlated with the duration of surgery. The current study is one of the largest to date on pediatric pituitary region lesions shedding light on demographic, clinical and histopathological features. The age-dependent distribution pattern highlights the prominence of craniopharyngiomas in younger patients, while PPAs became increasingly prevalent in those older than 10 years.

The online version contains supplementary material available at 10.1007/s10143-025-04019-6.

## Full-text entities

- **Genes:** PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, STH (saitohin) [NCBI Gene 246744] {aka MAPTIT}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}
- **Diseases:** Sellar lesions (MESH:D009059), ACTH-secreting adenoma (MESH:D049913), vascular injury (MESH:D057772), polyuria (MESH:D011141), meningitis (MESH:D008580), arginine vasopressin disorder (MESH:D020790), hyperprolactinemia (MESH:D006966), Headaches (MESH:D006261), infertility (MESH:D007246), SIADH (MESH:D007177), pituitary dysfunction (MESH:D010900), Craniopharyngioma (MESH:D003397), CSF fistula (MESH:D002559), Pituitary insufficiency (MESH:D007018), DI (MESH:D003919), Tumor (MESH:D009369), epistaxis (MESH:D004844), growth arrest (MESH:D006130), GH-secreting adenomas (MESH:D049912), pan (MESH:C537931), TSH-secreting adenomas (MESH:D006964), hyponatremia (MESH:D007010), postoperative (MESH:D019106), hypotension (MESH:D007022), bleeding (MESH:D006470), STH-cell adenomas (MESH:D000236), primary amenorrhea (MESH:D000568), Pituitary neuroendocrine tumor (MESH:D018358), CSF leak (MESH:D065634), germ cell tumors (MESH:D009373), PPA (MESH:D010911), Rathke's cleft cysts (MESH:D020863), visual disturbances (MESH:D014786), endocrine dysfunction (MESH:D004700), corticotrophic and lactotrophic adenomas (MESH:D015175), delayed puberty (MESH:D011628)
- **Chemicals:** testosterone (MESH:D013739), Cerebro (MESH:D013468), PPA (-), T4 (MESH:D013974), estradiol (MESH:D004958), dopamine (MESH:D004298), cortisol (MESH:D006854)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** V600E

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12827427/full.md

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Source: https://tomesphere.com/paper/PMC12827427