Meigs's syndrome
Meigs's syndrome is a rare medical condition that involves a triad of ascites, pleural effusion, and benign ovarian tumor (fibroma, fibrothecoma, Brenner tumours, and occasionally granulosa cell tumours). The syndrome was named after Joe Vincent Meigs, an American obstetrician and gynecologist.
Symptoms[edit | edit source]
The symptoms of Meigs's syndrome include shortness of breath due to pleural effusion, abdominal swelling or distension due to ascites, and pelvic mass due to ovarian fibroma. Other symptoms may include weight loss, nausea, vomiting, and constipation.
Diagnosis[edit | edit source]
The diagnosis of Meigs's syndrome is typically made based on the presence of the triad of symptoms. Imaging studies such as ultrasound, CT scan, or MRI may be used to identify the presence of ascites, pleural effusion, and ovarian tumor. A biopsy of the ovarian tumor may be performed to confirm the diagnosis.
Treatment[edit | edit source]
The treatment for Meigs's syndrome typically involves surgical removal of the ovarian tumor. Following surgery, the ascites and pleural effusion usually resolve within a few weeks. In some cases, diuretics may be used to help reduce the ascites and pleural effusion.
Prognosis[edit | edit source]
The prognosis for Meigs's syndrome is generally good, as the ovarian tumors associated with this condition are usually benign. However, regular follow-up is necessary to monitor for potential recurrence of the tumor.
See also[edit | edit source]
References[edit | edit source]
Meigs's syndrome Resources | |
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