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Khan, J., McClennan, B.L., Qureshi, S., Martell, M., Lyer, A. and Bokhari, S.J. (2005) Meigs syndrome and gliomatosis peritonei: A case report and review of literature. Gynecologic Oncology, 98, 313-317. doi:10.1016/j.ygyno.2005.03.048

has been cited by the following article:

• TITLE: Pseudo-Meigs syndrome in association with primitive peritoneal tumor

  AUTHORS: Auriane De Neef, Jean-Christophe Noel, Frédéric Buxant

  KEYWORDS: Ovarian and Tubal Neoplasms; Peritoneal Neoplasm

  JOURNAL NAME: Open Journal of Obstetrics and Gynecology, Vol.2 No.2, June 27, 2012

  ABSTRACT: We report the case of a 61-year old woman presented with a voluminous centro-pelvic mass (22 × 17 cm), hydrothorax and ascites. Serum CA-125 was high (11,000 UI/ml). An explorative laparotomy located the mass between the rectum and the posterior wall of the uterus. The histological examination showed a primitive peritoneal tumor with serous and endometrioid differentiations. There was a left ovarian metastasis and both peritoneal and pleural liquids revealed no sign of malignancy. After the incomplete surgery, the hydrothorax and ascites decreased considerably. This association of Pseudo-Meigs’ syndrome with primitive peritoneal tumor is uncommon. To our knowledge this is the first case described through a Medline search.