A case of delayed postoperative bleeding after excision of endometrial polyp using resectoscope in an infertile woman with von Willebrand disease:a case report and literature review
- PMID: 37853641
- PMCID: PMC10694516
- DOI: 10.5387/fms.2023-04
A case of delayed postoperative bleeding after excision of endometrial polyp using resectoscope in an infertile woman with von Willebrand disease:a case report and literature review
Abstract
Von Willebrand disease (VWD) is a bleeding disorder caused by a congenital quantitative reduction, deficiency, or qualitative abnormality of the von Willebrand factor (VWF). Here, we report a case of delayed postoperative bleeding in an infertile woman with endometrial polyps complicated by VWD. The patient was a 39-year-old infertile woman with type 2A VWD. At 38 years of age, she was referred to our hospital for infertility and heavy menstrual bleeding. Hysteroscopy revealed a 15-mm polyp lesion in the uterus. The patient was scheduled for transcervical resection (TCR) of the endometrial polyp. Gonadotropin-releasing hormone agonists were preoperatively administered to prevent menstruation. The VWF-containing concentrate was administered for 3 days according to guidelines. The patient was discharged on postoperative day 3 after confirming the absence of uterine bleeding. Uterine bleeding began on postoperative day 6. The patient was readmitted on postoperative day 7 and treated with VWF-containing concentrate for 5 days, after which hemostasis was confirmed. TCR surgery for endometrial lesions is classified as a minor surgery, and guidelines recommend short-term VWF-containing concentrate replacement. However, it should be kept in mind that only short-term VWF-containing concentrate replacement may cause rebleeding postoperatively.
Keywords: endometrial polyp; polypectomy; uterine bleeding; von Willebrand disease.
Figures
Similar articles
-
Successful Perioperative Management of Orthotopic Cardiac Transplantation in a Pediatric Patient With Concurrent Congenital von Willebrand Disease and Acquired von Willebrand Syndrome Using Recombinant von Willebrand Factor.J Cardiothorac Vasc Anesth. 2022 Mar;36(3):724-727. doi: 10.1053/j.jvca.2021.01.038. Epub 2021 Jan 27. J Cardiothorac Vasc Anesth. 2022. PMID: 33618961
-
Analysis of current perioperative management with Haemate® P/Humate P® in von Willebrand disease: Identifying the need for personalized treatment.Haemophilia. 2018 May;24(3):460-470. doi: 10.1111/hae.13451. Epub 2018 Mar 24. Haemophilia. 2018. PMID: 29573506
-
Von Willebrand's disease: case report and review of literature.Pan Afr Med J. 2017 Jun 29;27:147. doi: 10.11604/pamj.2017.27.147.12248. eCollection 2017. Pan Afr Med J. 2017. PMID: 28904675 Free PMC article. Review.
-
Abdominoplasty in a Patient With Type 3 von Willebrand Disease: A Case Report.Ann Plast Surg. 2024 Jan 1;92(1):133-136. doi: 10.1097/SAP.0000000000003711. Epub 2023 Oct 23. Ann Plast Surg. 2024. PMID: 37962210
-
[Diagnosis and management of von Willebrand disease].Rinsho Ketsueki. 2018;59(10):2222-2232. doi: 10.11406/rinketsu.59.2222. Rinsho Ketsueki. 2018. PMID: 30305529 Review. Japanese.
References
-
- Laffan M, Sathar J, Johnsen JM. Von Willebrand disease: diagnosis and treatment, treatment of women, and genomic approach to diagnosis. Haemophilia, 27: 66-74, 2021. - PubMed
-
- Harris NS, Pelletier JP, Marin MJ, Winter WE. Von Willebrand factor and disease: a review for laboratory professionals. Crit Rev Clin Lab Sci, 59: 241-256, 2022. - PubMed
-
- Deligeoroglou E, Karountzos V. Abnormal uterine bleeding including coagulopathies and other menstrual disorders. Best Pract Res Clin Obstet Gynaecol, 48: 51-61, 2018. - PubMed
-
- De Wee EM, Knol HM, Mauser-Bunschoten EP, et al. Gynaecological and obstetric bleeding in moderate and severe von Willebrand disease. Thromb Haemost, 106: 885-892, 2011. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous