Skip to content
← Childhood Astrocytomas, Other Gliomas, and Glioneuronal/Neuronal Tumors

HEALTH PROFESSIONAL · SOURCE READING

Second Surgery

Source: Childhood Astrocytomas, Other Gliomas, and Glioneuronal/Neuronal Tumors Treatment (PDQ®)–Health Professional Version, National Cancer Institute.

Source updated: April 14, 2025 · Captured 2026-09-09.

Selected source text with whitespace normalised. This Triangle page is not an NCI PDQ summary.

Context: Treatment of Recurrent Pediatric-Type Diffuse High-Grade Gliomas

The use of surgical intervention must be individualized based on the following:

Initial tumor type.

Length of time between initial treatment and the reappearance of the mass lesion.

Location of the recurrent tumor.

Consideration of therapeutics based on the requirement for fresh tumor tissue or to deliver therapy to the operative bed.

In most cases of diffuse midline gliomas centered in the pons (diffuse intrinsic pontine glioma [DIPG]), biopsy at the time of clinical or radiological progression is neither necessary nor recommended. Biopsy may be considered for confirmation of relapse when treatment-related brain stem damage, which may be clinically indistinguishable from tumor recurrence, is in the differential diagnosis. Other tests, including positron emission tomography, magnetic resonance spectroscopy, and single-photon emission computed tomography, are not reliable in distinguishing necrosis from tumor recurrence in previously irradiated patients with DIPG.

Preserved source evidence · Not medical advice