Mixed gangliocytoma-silent somatotroph pituitary adenoma: a rare variant with pregnancy-associated growth

We report a case of mixed gangliocytoma-pituitary adenoma in a woman in the early 30s who presented with an incidental pituitary macroadenoma that demonstrated significant pregnancy-related growth. Initially discovered during investigation for joint pains, the lesion remained stable under surveillance until pregnancy, when it increased in size from 18 mm to 30 mm. Following successful endoscopic transsphenoidal resection, histological examination revealed the characteristic biphasic pattern of a mixed gangliocytoma-pituitary adenoma with a sparsely granulated somatotroph adenoma component. Despite the growth hormone-producing adenomatous component confirmed on histology, the patient remained clinically silent for acromegaly throughout. This case highlights the rare occurrence of silent growth hormone adenoma within a mixed gangliocytoma which represents less than 1% of all pituitary tumours and the challenges in managing such tumours during pregnancy.

Authors

Institutions

Publication Details

Journal
BMJ Case Reports
Published
2025-12-01
DOI
https://doi.org/10.1136/bcr-2025-270262
Primary Topic
Pituitary Gland Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Mixed gangliocytoma-silent somatotroph pituitary adenoma: a rare variant with pregnancy-associated growth

Joe M Das, Alistair J. Lawrence, Ramesh Nair, Joshua J Hon et al.
BMJ Case Reports
Pituitary Gland Disorders and Treatments
article

Mixed gangliocytoma-silent somatotroph pituitary adenoma: a rare variant with pregnancy-associated growth

Joe M Das, Alistair J. Lawrence, Ramesh Nair, Joshua J Hon, Yigit Ercetin
article en

Abstract

We report a case of mixed gangliocytoma-pituitary adenoma in a woman in the early 30s who presented with an incidental pituitary macroadenoma that demonstrated significant pregnancy-related growth. Initially discovered during investigation for joint pains, the lesion remained stable under surveillance until pregnancy, when it increased in size from 18 mm to 30 mm. Following successful endoscopic transsphenoidal resection, histological examination revealed the characteristic biphasic pattern of a mixed gangliocytoma-pituitary adenoma with a sparsely granulated somatotroph adenoma component. Despite the growth hormone-producing adenomatous component confirmed on histology, the patient remained clinically silent for acromegaly throughout. This case highlights the rare occurrence of silent growth hormone adenoma within a mixed gangliocytoma which represents less than 1% of all pituitary tumours and the challenges in managing such tumours during pregnancy.

BMJ Case ReportsVol. 18(12)
Imperial College Healthcare NHS Trust (GB), National Hospital for Neurology and Neurosurgery (GB), University College London (GB), Imperial College London (GB)
Good health and well-being
Openalex Percentile: Top 29%
Pituitary Gland Disorders and Treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.