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Thickened but unclear: Clinical course of isolated pituitary stalk thickening in the pediatric age group
Hannah K Miller1, Vikram P Rajan2, Christopher Blunden3,4
1Children's Hospital of Michigan, Detroit, Michigan (H.K.M.).
Insights
Pituitary stalk thickening (PST) in children often remains stable, indicating that serial MRI monitoring is a safe approach. Not all cases require immediate biopsy, allowing for careful observation and reduced invasive procedures.
Area of Science:
- Pediatric Endocrinology
- Neuroradiology
- Oncology
Background:
- Pituitary stalk thickening (PST) incidence is rising due to increased brain MRI utilization.
- The clinical significance and diagnostic workup for PST are not well-established.
- This study addresses the need for clarity on PST's clinical course in pediatric patients.
Purpose of the Study:
- To investigate the clinical significance and natural history of isolated pituitary stalk thickening in pediatric patients.
- To determine appropriate diagnostic pathways and management strategies for pediatric PST.
- To evaluate the safety and efficacy of serial MRI monitoring versus upfront biopsy.
Main Methods:
- Retrospective review of pediatric tumor board and endocrinology clinic records (2003-2024).
- Identification and selection of pediatric patients with PST, excluding those with additional MRI findings.
- Clinical course data collection, including serial MRIs, diagnostic workup, and outcomes.
Main Results:
- 18 pediatric patients with isolated PST were analyzed.
- No neoplasms were diagnosed with initial workup (CBC, metabolic panel, tumor markers, skeletal survey).
- Five patients (27.7%) showed PST progression requiring biopsy (diagnoses: 2 germinomas, 2 Langerhans cell histiocytosis).
- Ten patients (55.5%) had stable PST, and 3 (16.7%) experienced complete resolution during follow-up.
Conclusions:
- Isolated PST in pediatric patients is frequently stable over time.
- Serial MRI monitoring is a safe and effective strategy for managing pediatric PST.
- Upfront biopsy is not always necessary for isolated PST, supporting a watchful approach.
Background:
The incidence of pituitary stalk thickening (PST) has increased in recent years due to the increased utilization of diagnostic MRI of the brain. The clinical significance of PST, appropriate diagnostic workup, and clinical course for these patients is not well documented.
Methods:
After Institutional Review Board approval, we reviewed the pediatric tumor board and pediatric endocrinology clinic records between 2003 and 2024 to identify patients with PST. We followed the clinical course of these patients to collect applicable data.
Results:
A total of 29 patients were identified with PST; 11 were excluded due to additional MRI findings, and out of 18 selected patients, 9 were females (50%). Initial diagnostic workup included complete blood count (CBC), basic metabolic panel, serum and cerebrospinal fluid (CSF) tumor markers (AFP, β-hCG), and skeletal survey. With the initial workup, no patient was diagnosed with neoplasm. Patients were followed with serial MRIs. Five patients (27.7%) displayed progression of PST, warranting biopsy (2 germinomas, 2 Langerhans cell histiocytosis, and 1 inconclusive). The median time to biopsy was 8 months (range 4-26 months). All the patients diagnosed with neoplasm had central diabetes insipidus at presentation, and 3 went on to develop additional endocrine abnormalities. Ten patients had stable PST over a median follow-up period of 19 months (range 0-81 months), and 3 patients had complete resolution of PST during the follow-up period.
Conclusion:
Most isolated PST among pediatric patients remain stable over time. Serial monitoring of patients with isolated PST can be safe, and not all cases of PST warrant upfront biopsy.
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