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Demons-Meigs syndrome caused by a giant ovarian fibroma: A case report.
Guelzim, Yousra; Bennasser, Abdallah; Marrakchi, Salma; Houssaini, Abdelkader Sqalli; Idoubba, Salwa; Boujida, Ismail; Jahid, Ahmed; Allali, Nazik; Chat, Latifa; Haddad, Siham El.
Afiliação
  • Guelzim Y; Department of Radiology, Pediatric Teaching Hospital, Rabat, Morocco.
  • Bennasser A; Department of Radiology, Pediatric Teaching Hospital, Rabat, Morocco.
  • Marrakchi S; Department of Radiology, Pediatric Teaching Hospital, Rabat, Morocco.
  • Houssaini AS; Department of Radiology, Pediatric Teaching Hospital, Rabat, Morocco.
  • Idoubba S; Department of Gynecology-Obstetrics and Endoscopy, Maternity Souissi hospital, Rabat, Morocco.
  • Boujida I; Department of Pathology, Ibn Sina Hospital, Rabat, Morocco.
  • Jahid A; Department of Pathology, Ibn Sina Hospital, Rabat, Morocco.
  • Allali N; Department of Radiology, Pediatric Teaching Hospital, Rabat, Morocco.
  • Chat L; Department of Radiology, Pediatric Teaching Hospital, Rabat, Morocco.
  • Haddad SE; Department of Radiology, Pediatric Teaching Hospital, Rabat, Morocco.
Radiol Case Rep ; 19(7): 2585-2589, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38645957
ABSTRACT
Demons-Meigs syndrome is a very rare entity. It combines a benign ovarian "fibroma-like" tumor with ascites and hydrothorax. The notion of benignancy is the key point. CA-125 levels are most of the time normal, but high levels can be observed in rare cases which makes it difficult to have a diagnostic. We present here the case of a 43-year-old female patient who presented with abdominopelvic pain. Imaging discovered a 30 cm large intraabdominal mass with ascites and bilateral pleural effusion. Surgical resection of the tumor was performed, and pathology identified an ovarian fibroma. No postintervention complications were observed, with resorption of the ascites and hydrothorax.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article