Regressive Neuroblastoma: Widely Accepted, Underreported Histology

Neuroblastoma accounts for approximately 8% of all pediatric cancers and up to 15% of pediatric cancer-related deaths in malignant cases; neuroblastoma is the most common malignancy in infancy. Notably, up to 50% of tumors may undergo spontaneous regression without treatment. However, detailed histological descriptions of regressed neuroblastoma remain limited in the literature. We report the histological features of a particularly illustrative case, characterized by edema, mild collagen deposition, evidence of prior hemorrhage, and calcifications. Cellularity was minimal, consisting of rare, scattered mature-appearing ganglion cells, without neuropil or neuroblastic clusters. Accurate recognition of these morphological features in surgical specimens is essential for optimal treatment planning.

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Publication Details

Journal
Clinical Case Reports
Published
2026-04-29
DOI
https://doi.org/10.1002/ccr3.72640
Primary Topic
Neuroblastoma Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Regressive Neuroblastoma: Widely Accepted, Underreported Histology

Danai Papangelopoulou, Oliver Sánchez, Anne‐Laure Rougemont, Jim C. H. Wilde et al.
Clinical Case Reports
Neuroblastoma Research and Treatments
article

Regressive Neuroblastoma: Widely Accepted, Underreported Histology

Danai Papangelopoulou, Oliver Sánchez, Anne‐Laure Rougemont, Jim C. H. Wilde, Tom Membrez, Fabienne Gumy‐Pause
article en

Abstract

Neuroblastoma accounts for approximately 8% of all pediatric cancers and up to 15% of pediatric cancer-related deaths in malignant cases; neuroblastoma is the most common malignancy in infancy. Notably, up to 50% of tumors may undergo spontaneous regression without treatment. However, detailed histological descriptions of regressed neuroblastoma remain limited in the literature. We report the histological features of a particularly illustrative case, characterized by edema, mild collagen deposition, evidence of prior hemorrhage, and calcifications. Cellularity was minimal, consisting of rare, scattered mature-appearing ganglion cells, without neuropil or neuroblastic clusters. Accurate recognition of these morphological features in surgical specimens is essential for optimal treatment planning.

Clinical Case ReportsVol. 14(5)
University of Geneva (CH), University Hospital of Geneva (CH), Geneva College (US)
Zero hunger
Openalex Percentile: Top 10%
Neuroblastoma Research and Treatments
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