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Has anyone experienced a ruptured endometrioma?
Almost 2 years ago just before I was diagnosed with endometriosis I had an episode of bad pain and ended up in hospital. I was misdiagnosed at the time. After surgery proved their initial diagnosis was wrong, doctors told me I had endometriosis but they were not able to explain what actually caused the episode.
I found case studies that fit my symptoms very closely. It makes me believe that was initially sent me to Hospital was a ruptured… read more
@A MyEndometriosisTeam Member I read that also but my gynaecologist at the time recommended medication as first line treatment, fearing more harm than benefit from further surgery after my diagnostic laparoscopy. My symptoms are fairly well controlled but I want to feel good again.
@A MyEndometriosisTeam Member the pain started low in my pelvis then moved up and expanded quickly to low abdomen/pelvis, much worse on the right. After 24 hours trying heat and otc remedies, my abdomen was noticeably distended and the pain was unbearable so I went to the ER. Ketorolac provided immense relief whereas morphine really didn’t help. IV antibiotics, one night in ER and two nights on the ward and I was well enough to go home. They thought it was pelvic inflammatory disease, then ovarian cancer, but later ruled out both conditions.
An endometrioma larger than 4 cm must be surgically removed and is an emergency.
I have 2 endometrioma left and right. Though yours is really huge…. Not really sure about ruptured but where was the pain when you were rushed to ER?
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