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Pseudomyxoma peritonei leading to "jelly belly" abdomen: a case report and review of the literature.
- Source :
-
Journal of medical case reports [J Med Case Rep] 2024 Jun 28; Vol. 18 (1), pp. 296. Date of Electronic Publication: 2024 Jun 28. - Publication Year :
- 2024
-
Abstract
- Background: Pseudomyxoma peritonei is an infrequent condition with a global annual incidence of only one to two cases per million people. Mucinous neoplasms, widespread intraperitoneal implants, and mucinous ascites characterize it. Currently, most clinicians misdiagnose this condition, which leads to delayed management.<br />Case Presentation: A 44-year-old North Indian female presented with a 1.5-month history of an abdominal lump. Physical examination revealed a sizeable abdominopelvic mass at 36 weeks. Contrast-enhanced computed tomography showed a massive multiloculated right ovarian cystic mass measuring 28 × 23 × 13 cm with mild ascites and elevated carcinoembryonic antigen levels (113.75 ng/ml). A provisional diagnosis of ovarian mucinous neoplasm was made, for which the patient underwent laparotomy. Intraoperatively, there were gross mucinous ascites, along with a large, circumscribed, ruptured right ovarian tumor filled with gelatinous material. The appendicular lump was also filled with mucinous material along with the omentum, ascending colon, right lateral aspect of the rectum, splenic surface, and small bowel mesentery. Cytoreductive surgery was performed along with an oncosurgeon, including total abdominal hysterectomy with bilateral salpingoophorectomy, omentectomy, right hemicolectomy, lower anterior resection, ileo-transverse stapled anastomosis with proximal ileal loop diversion stoma, excision of multiple peritoneal gelatinous implants, and peritoneal lavage. Histopathology and immunohistochemistry confirmed the presence of intestinal-type mucinous carcinoma. Postoperatively, the patient was given six cycles of chemotherapy. She tolerated it without any specific morbidity and had an uneventful recovery. Postoperative follow-up at 15 months revealed normal tumor marker levels and abdominal computed tomography findings and no signs suggestive of local recurrence or distal metastases.<br />Conclusions: Pseudomyxoma peritonei is a rare disease that is frequently misdiagnosed in the preoperative phase. Therefore, radiologists and clinicians should maintain a high index of suspicion for accurate diagnosis and multidisciplinary management.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Female
Adult
Tomography, X-Ray Computed
Cytoreduction Surgical Procedures
Ovarian Neoplasms diagnosis
Ovarian Neoplasms surgery
Ovarian Neoplasms pathology
Ovarian Neoplasms diagnostic imaging
Ascites etiology
Hysterectomy
Treatment Outcome
Pseudomyxoma Peritonei diagnosis
Pseudomyxoma Peritonei surgery
Pseudomyxoma Peritonei pathology
Pseudomyxoma Peritonei diagnostic imaging
Peritoneal Neoplasms diagnosis
Peritoneal Neoplasms surgery
Peritoneal Neoplasms diagnostic imaging
Peritoneal Neoplasms pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1752-1947
- Volume :
- 18
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of medical case reports
- Publication Type :
- Academic Journal
- Accession number :
- 38937808
- Full Text :
- https://doi.org/10.1186/s13256-024-04612-1