Severe recurrent endometriomas in a young woman with congenital von Willebrand disease
Case report
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This case describes a young woman with von Willebrand disease who developed severe recurrent ovarian endometriomas, suggesting vWD may be a risk factor for aggressive endometriosis.
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Abstract
The pathophysiology of severe endometriosis in young women remains unknown. Menorrhagia, or heavy and prolonged menstrual bleeding, is the most common symptom experienced by women with von Willebrand disease (vWD) and represents a possible risk factor for developing endometriosis. A 17-year-old woman affected by vWD presented with severe dysmenorrhea and heavy menstrual bleeding. After being diagnosed with multiple ovarian endometriomas, the patient underwent repeated surgeries due to suspicious appearance of recurrent pelvic masses. vWD may be a risk factor for developing severe endometriosis, and patients with endometriosis should be screened for vWD and other bleeding disorders. Ovarian endometriomas in such patients might present a more severe progression and unique ultrasound findings, mimicking malignancies.
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Cited by (6)
- Additional file 1 of The effects of coagulation factors on the risk of endometriosis: a Mendelian randomization study 2023
- Additional file 2 of The effects of coagulation factors on the risk of endometriosis: a Mendelian randomization study 2023
- Additional file 1 of The effects of coagulation factors on the risk of endometriosis: a Mendelian randomization study 2023
- Additional file 2 of The effects of coagulation factors on the risk of endometriosis: a Mendelian randomization study 2023
- The effects of coagulation factors on the risk of endometriosis: a Mendelian randomization study 2023
- Age-dependent phenotypes of ovarian endometriomas 2022
Source provenance
- crossref
- last seen: 2026-08-16T06:22:07.882918+00:00
- europepmc
- last seen: 2026-10-15T06:08:49.021275+00:00
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-10-08T21:25:03.247098+00:00
- unpaywall
- last seen: 2026-10-15T06:24:24.424788+00:00
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