A report describes a case of a 35-year-old woman, para 3, who presented with acute menorrhagia. She described a history of three prior cesarean sections, with the latest one a year earlier. Before this episode, she reported regular menstrual cycles.
The examination was unremarkable, with a bulky uterus. Investigations revealed a negative urine pregnancy test, a hemoglobin level of 5.3 g/dL with normal platelet counts, and a normal pelvic ultrasound along with a follicle.
She reported a similar episode of menorrhagia two weeks before demanding admission to a local hospital, where she underwent curettage and received five units of packed cells.
Histology demonstrated benign endometrial cells. The menorrhagia episode recurred a week later, and she was readmitted, transfused four units of packed cells, and given an intrauterine balloon tamponade to arrest bleeding. She then got transferred to another hospital, where she received intramuscular progesterone 100 mg, maintenance oral progesterone, and intravenous antibiotics, along with packed cells and platelets. Her menorrhagia, however, persisted.
Investigations for hematological causes were negative. CT-pelvis revealed no arteriovenous malformation. She was initiated intravenous tranexamic acid and subsequently on oral estrogen when the bleeding persisted. Despite that, the bleeding continued, prompting pelvic angiogram and embolization of bilateral uterine arteries, which settled the bleeding, and then she received combined oral contraceptives (COC) before her discharge.
However, the patient presented again to the hospital a year later with prolonged heavy vaginal bleeding for 5 days. Before this, her menses were regular with normal menstrual flow. Adenomyosis was ruled-out. She received oral progesterone and got discharged the next day. Her hemoglobin on discharge was 12 g/dL.
She then re-presented the next day with severe menorrhagia complicated by symptomatic anemia. Her hemoglobin level saw a drop of 3 g/dL. She received blood transfusions, oral estrogen, and intravenous tranexamic acid. Despite these conservative measures, her vaginal bleeding persisted.
She underwent a pelvic angiogram and embolization of bilateral uterine arteries. Intraoperatively, she showed a tortuous right uterine artery with no arteriovenous malformation. Her bleeding settled, and she got discharged.
After discharge, the patient experienced an elective hysteroscopy with dilation and curettage, which revealed a normal endocervical and endometrial cavity. Histologic study of the endometrial curetting showed late secretory endometrium without hyperplasia or malignancy. The patient is now considering a hysterectomy.
Kho CL, Mathur M. Uterine artery embolisation for acute dysfunctional uterine bleeding with failed medical therapy: a novel approach to management. BMJ Case Rep. 2015 Jan 16;2015:bcr2014204446. doi: 10.1136/bcr-2014-204446. PMID: 25596287; PMCID: PMC4307078.
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