Mucinous cystic neoplasm(MCN)of the pancreas is a rare disease. A 34-year-old female was referred to our hospital for a giant cystic tumor in the left epigastrium, suspected of being a pancreatic MCN. The surgical findings revealed that the tumor originated in the pancreatic tail with the presence of peritoneal dissemination. A distal pancreatectomy and a splenectomy were performed, and the resected specimen histologically revealed an invasive mucinous cystadenocarcinoma of the pancreas. The postoperative computed tomography(CT)scan showed metastatic tumors of the Douglas pouch and the left ovary. Gemcitabine(GEM)was thereafter systemically administered for palliative chemotherapy with a regimen of 1,000 mg/m / 2week for 3 weeks, followed by a week of rest. When assessed by a CT scan after 4 courses of chemotherapy, marked shrinkage of the tumors was identified, and we could not detect the tumors clearly. Moreover, the serum CA19-9 level fell from 341 U/mL to almost normal and there were no severe adverse events. Therefore, systemic chemotherapy with GEM is considered to possibly be an effective treatment against MCN. We describe herein the first case of advanced mucinous cystadenocarcinoma of the pancreas with peritoneal dissemination responding to GEM and a brief review of the literature.

Download full-text PDF

Source

Publication Analysis

Top Keywords

mucinous cystadenocarcinoma
12
cystadenocarcinoma pancreas
12
peritoneal dissemination
12
case advanced
8
advanced mucinous
8
pancreas peritoneal
8
dissemination responding
8
mucinous
4
pancreas
4
responding gemcitabine
4

Similar Publications

Introduction: Mucinous Cystadenocarcinoma (MCA) of the breast remains a relatively rare condition, and to date, there is no systematic summary of its imaging manifestations. Therefore, this report presents a detailed account of the diagnosis and treatment of mucinous cystadenocarcinoma in a 40-year-old woman, with a particular focus on imaging findings. Additionally, we conducted a comprehensive literature review on this disease and summarized its key imaging features.

View Article and Find Full Text PDF
Article Synopsis
  • Appendiceal cancers, particularly mucinous cystadenocarcinoma, are rare and can cause serious complications like pseudomyxoma peritonei, leading to abdominal fluid accumulation called "jelly belly."
  • A case of a young man with a persistent psoas abscess revealed mucinous adenocarcinoma with pseudomyxoma retroperitonei, emphasizing the need to consider malignancy in atypical abscesses.
  • Early and accurate diagnosis is critical because these types of tumors can be misdiagnosed as common issues like abscesses, highlighting the importance of imaging and colonoscopy in identifying them.
View Article and Find Full Text PDF

Primary mucinous cystadenocarcinoma of the breast: A case report and literature review.

Oncol Lett

January 2025

Department of Pathology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, P.R. China.

Article Synopsis
  • - A 51-year-old woman was diagnosed with a rare type of breast cancer called mucinous cystadenocarcinoma (MCA) after presenting with a mass in her left breast, which showed unique features in biopsies, including mucus secretion and papillary structures.
  • - The tumor was identified as basal-like triple-negative breast cancer with mutations in several key genes, including TP53 and MUC6, as highlighted by immunohistochemistry and DNA analysis.
  • - After 26 months of follow-up, the patient showed no signs of cancer recurrence or metastasis, indicating a potential for better understanding and treating this rare breast cancer type through this case study and literature review.
View Article and Find Full Text PDF

Mucinous adenocarcinoma in kidneys with developmental anomalies - a report of two cases.

BMC Urol

November 2024

Department of Urology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India.

Article Synopsis
  • Primary mucinous adenocarcinomas of the kidney are rare and their origins are unclear, with theories including chronic irritation and kidney maldevelopment.
  • Two cases are presented: one involving a 50-year-old male with a duplex collecting system who had invasive mucinous carcinoma, and another case with a 53-year-old male who had a horseshoe kidney and recurrent mucinous adenocarcinoma after previous surgery.
  • Both cases highlight the association between mucinous adenocarcinomas and kidney anomalies, emphasizing the importance of histopathology for diagnosis.
View Article and Find Full Text PDF

Objective: We report the first documented case of concurrent ectopic complete hydatidiform mole (CHM) and high-grade serous carcinoma (HGSC) of the fallopian tube, associated with unique histologic features and mutations in the HGSC.

Case Report: The patient presented with pelvic pain and vaginal bleeding. Laboratory examination revealed a positive urine pregnancy test and high serum beta-human chorionic gonadotropin (β-hCG).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!