Retrospective analysis reveals significant differences in age and calcification between craniopharyngioma subtypes, suggesting improved diagnostic strategies.
Objective Although craniopharyngiomas (CPs) are histologically benign, they exhibit significant clinical aggression and subtype-specific biological behavior. This study aims to delineate the clinicopathological heterogeneity between the adamantinomatous (ACP) and papillary (PCP) subtypes using a large-scale cohort of 327 patients to optimize diagnostic accuracy and individualized management strategies. Methods A retrospective analysis was conducted on 327 patients with histologically confirmed CP treated at The First Affiliated Hospital of Sun Yat-sen University between 2005 and 2023. Patients were categorized into ACP, PCP, mixed-type, and unclassified groups. Clinical data, including age at diagnosis and gender, along with histopathological features (microscopic calcification and ossification), were compared using Kruskal-Wallis and Fisher’s exact tests. Results Of the 327 cases, 145 (44.3%) were ACP, 41 (12.5%) were PCP, and 2 (0.6%) were mixed-type. Histological subtyping could not be definitively assigned in 139 cases (42.5%). The mean age at diagnosis was significantly lower in the ACP group compared to the PCP group (32.1 ± 18.9 vs. 42.3 ± 13.9 years; p = 0.018). Microscopic calcification or ossification was identified in 41.4% (60/145) of ACP cases, which was significantly higher than the 4.9% (2/41) observed in the PCP group (p < 0.001). Male patients accounted for 60% (196/327) of the total cohort, but no significant correlation was found between gender and histological subtype (p = 0.3). Conclusion Our results underscore the significant clinicopathological heterogeneity between craniopharyngioma subtypes. In this large-scale cohort, ACP presented at a significantly earlier age and exhibited a markedly higher prevalence of calcification compared to PCP. These findings confirm that age and microscopic calcification remain the most robust indicators for precise histological differentiation.
No takes yet. Share an insight, caveat, or question.
Chen et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: