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Solid-pseudopapillary neoplasm of the pancreas in a 12-year-old female: case report.
Ann Med Surg (Lond)
December 2024
Kathmandu Medical College and Teaching Hospital, Kathmandu, Nepal.
Introduction And Importance: A solid-pseudopapillary tumor of the pancreas is a rare solid neoplasm. It is an uncommon exocrine tumor that accounts for 1-3% of exocrine pancreatic tumors.
Case Presentation: The authors have reported two cases of solid-pseudopapillary neoplasm of the pancreas with a median age of 12 years, both in females with abdominal pain.
Solid pseudopapillary neoplasm of the pancreas causing obstructive jaundice: Case report of a rare entity.
Int J Surg Case Rep
November 2024
Institute of Post Graduate Medical Education and Research, Kolkata, West Bengal, India.
Introduction: Solid pseudopapillary neoplasm (SPN) is an extremely rare, low-grade, malignant pancreatic tumour with an excellent prognosis. We describe a case of SPN causing obstructive jaundice in a young female, thus mimicking pancreatic adenocarcinoma clinically and radiologically.
Case Presentation: A 32-year-old female presented with abdominal pain for 12 h, icterus, and an epigastric mass measuring 3 × 3 cm.
Left-sided portal hypertension caused by a solid pseudopapillary neoplasm of pancreas tail: a pediatric case report.
Surg Case Rep
November 2024
Department of Diagnostic Pathology, Institute of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8575, Japan.
Article Synopsis
- Solid pseudopapillary neoplasm (SPN) is a low-grade malignant tumor mostly seen in pediatric cases, where spleen preservation during surgery is critical to prevent infection, though complications like left-sided portal hypertension (LSPH) can complicate this.
- A 12-year-old girl diagnosed with SPN had symptoms like abdominal pain and anemia, and imaging revealed a mass in her pancreas along with signs of LSPH, prompting a surgery that initially aimed to preserve the spleen.
- Despite the initial surgery, the patient faced ongoing abdominal pain due to LSPH-related issues, leading to a splenectomy, which resolved her pain and showed no recurrence after eight years.
Risk and survival outcomes of secondary pelvic neoplasm after radiotherapy in female patients with genital neoplasms: A large Population-Based cohort study.
Radiother Oncol
January 2025
Department of Obstetrics and Gynecology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, Shaanxi Province, China. Electronic address:
Background And Purpose: To investigate the impact of radiotherapy (RT) on the risk of secondary pelvic neoplasms (SPN) and the survival outcomes of patients following a diagnosis of female patients with genital neoplasm(FGN).
Materials And Methods: Utilizing SEER databases, this study involved 102,895 patients from nine oncology centers, spanning 1990 to 2015. We employed the Fine-Gray competing risks regression methodology to chart the trajectory of SPN development and used the Kaplan-Meier method to calculate the 10-year overall survival rates.
Nationwide questionnaire survey on pediatric pancreatic tumors in Japan.
World J Gastrointest Oncol
October 2024
Department of Pediatric Surgery, Shizuoka Children's Hospital, Shizuoka 420-8660, Japan.
Background: Pediatric pancreatic tumors are rare and account for < 0.1% of all childhood cancers. The primary treatment for pancreatic tumors is surgical resection.
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