A Case Report of Pseudomyxoma Peritonei Arising From Primary Mucinous Ovarian Neoplasms.
Autor: | Joseph R; Radiology, Chettinad Hospital and Research Institute Chettinad Academy of Research and Education, Chennai, IND., Sathiamoorthy R; Radiology, Chettinad Hospital and Research Institute Chettinad Academy of Research and Education, Chennai, IND., Gnanasekaran R; Radiology, Chettinad Hospital and Research Institute Chettinad Academy of Research and Education, Chennai, IND., Gunasekaran L; Radiology, Chettinad Hospital and Research Institute Chettinad Academy of Research and Education, Chennai, IND., Ilangovan G; Radiology, Chettinad Hospital and Research Institute Chettinad Academy of Research and Education, Chennai, IND. |
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Jazyk: | angličtina |
Zdroj: | Cureus [Cureus] 2022 Sep 19; Vol. 14 (9), pp. e29309. Date of Electronic Publication: 2022 Sep 19 (Print Publication: 2022). |
DOI: | 10.7759/cureus.29309 |
Abstrakt: | Pseudomyxoma peritonei (PMP) is a rare manifestation of primary mucinous neoplasms. We report two rare cases of PMP originating from mucinous primary ovarian neoplasms. The case series discusses the cases of female patients aged 86 and 52 years who presented with worsening dyspepsia, abdominal distension, pelvic pain, and altered bowel habits. Both of the patients underwent evaluation comprising cancer antigen-125 (CA-125) levels, ultrasound (US) examination of the abdomen and the pelvis, tumor markers, cytological evaluation, and contrast-enhanced computed tomography (CECT) of the pelvis and abdomen. Patients were diagnosed to have pseudomyxoma peritonei arising from mucinous ovarian tumors. Patients were referred to the surgical department and were successfully managed with repeated removal of mucinous material. The present case report highlights the significant radio-pathologic characteristics of PMP, which originated from mucinous ovarian tumors. Competing Interests: The authors have declared that no competing interests exist. (Copyright © 2022, Joseph et al.) |
Databáze: | MEDLINE |
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