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Updated: Oct 8, 2026

Isolation, Enrichment, and Maintenance of Medulloblastoma Stem Cells
Published on: September 1, 2010
A case of Cushing ulcer in an 8-month-old patient with medulloblastoma
Walavan Sivakumar1, Heather S Spader1, Eric Scaife1
11 Department of Neurosurgery, Division of Pediatric Neurosurgery, 2 Department of Surgery, Division of Pediatric Surgery, Primary Children's Hospital, University of Utah, Salt Lake City, Utah, USA.
Insights
This case report details the first infant with medulloblastoma to develop a Cushing ulcer. Despite prophylaxis, corticosteroid use worsened the ulcer, requiring surgical repair.
Area of Science:
- Pediatric Oncology
- Gastroenterology
- Neurosurgery
Background:
- Medulloblastoma is a common pediatric brain tumor.
- Cushing ulcers are stress-induced gastric ulcers often associated with central nervous system lesions.
- Corticosteroids are frequently used in neuro-oncology but can increase gastrointestinal risks.
Observation:
- An 8-month-old boy with medulloblastoma received dexamethasone preoperatively.
- The infant developed melanotic stools postoperatively, indicating gastrointestinal bleeding.
- Endoscopic evaluation revealed two duodenal ulcers.
Findings:
- The patient presented with a Cushing ulcer, a rare complication in infants with medulloblastoma.
- Stress ulcer prophylaxis was insufficient to prevent ulceration during corticosteroid therapy.
- Surgical repair of the duodenal ulcers was necessary.
Implications:
- This case highlights the critical need for vigilant gastrointestinal monitoring in infants with brain tumors receiving corticosteroids.
- It underscores the potential for severe gastrointestinal complications like Cushing ulcers in this vulnerable population.
- Further research may be warranted to optimize ulcer prophylaxis strategies in pediatric neuro-oncology patients.
Abstract:
The authors present the first case of a Cushing ulcer in an infant with medulloblastoma who, despite being administered stress ulcer prophylaxis, worsened after corticosteroids were initiated. An 8-month-old boy presented with progressive vomiting, lethargy, and decreased oral intake. Imaging revealed a heterogeneous fourth ventricular mass. Preoperatively, the patient was started on dexamethasone. The patient underwent an uncomplicated external ventricular drain placement and suboccipital craniotomy for resection of the lesion. The results of the pathological analysis were consistent with medulloblastoma. Postoperatively, the patient had melanotic stools, which were reported to be occurring for months prior to presentation. Two proximal duodenal bulb ulcers were found and required definitive surgical repair. The patient recovered from the acute postsurgical course after continued stress ulcer prophylaxis and is currently undergoing chemotherapy.
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