An 18-year-old male patient, Ho Chi Minh City - Date of examination: June 2, 2025 Reason for examination: Epigastric pain Medical history: Gastritis H. PYLORI (+)
Patient history: For the past year, the patient has experienced persistent epigastric pain, treated with multiple courses of gastritis which only provided temporary relief but did not cure the condition. Approximately 3 weeks prior to the examination, the patient experienced severe epigastric pain, worsening in the afternoon, and shortness of breath.
Result of abdominal ultrasound was a pancreatic body tumor.
Lab data:
MSCT confirmed a pancreatic body tumor.
Surgery was performed one year after because the patient has to pass the exam of his study.
- Surgical indications for DP surgery: Pancreatic caudate body tumor
- Surgical method: Scheduled, Laparoscopic
- DP surgical method: Pancreatic caudate resection with splenic preservation (Warshaw style, non-preserving)
- Abdominal examination: Location and size of the tumor.
- Tumor size (length x width x height) cm: 3x3x3
- Intrusion into the retroperitoneal space: Yes
- Exposure of the portal vein behind the pancreas: Yes
- Vascular abnormalities: None
- Pancreatic resection site: Pancreatic neck
- Pancreatic resection instrument: Stapler
- Lymph node dissection: None
- Pancreatic resection margin: None
- Splenic preservation: Warshaw-style splenic preservation
- Post-operative check: Thorough hemostasis, sufficient gauze and instruments
- Drainage placement: Number of drains, location
- Drainage location: Adjacent to the pancreatic resection margin
- Number of drains: 1
- Intraoperative complications: None
- Blood loss: 50ml.
On July 23, 2025, the results of immunohistochemical staining were: Synaptophysin (+), Chromogranin (-), CD56 (+).
Beta-Catenin (+), CD10 (+). CONCLUSION AFTER IMMUNOCHEMICAL STAINING: SOLID PANCREATIC PARAPANCREATIC TUMOR (SOLID)
PSEUDOPAPILLARY TUMOR).
This is a rare clinical case of a solid pseudopapillary neoplasm (SPN) of the pancreas. While SPNs typically occur in young women in their 20s and 30s, their presentation in an 18-year-old male is highly unusual. Studies suggest that SPNs in males can pose specific diagnostic challenges and may carry a slightly higher risk of invasive progression or malignant potential compared to those in females.