Polycytemie bij een patiënte met een uterusmyoom

Translated title of the contribution: Polycythaemia in a patient with uterus myomatosus Background

Jolien P. De Boer*, Gerjo Velders, Riena Aliredjo, Eduard Scheenjes, Thijs W.H. Flinsenberg

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Myomatous erythrocytosis syndrome (MES) is characterised by a combination of polycythaemia, uterus myomatosus and the normalisation of erythrocyte count after hysterectomy. Case description A 58yearold postmenopausal woman was referred to the gynaecologist with symptoms of vaginal blood loss, increased abdominal circumference and pollakiuria. Physical examination indicated her uterus was enlarged to the size of a 24week gestation. Endometrial malignancy was excluded and ultrasound showed a myoma. In consultation with the patient a hysterectomy was planned. Preoperative blood tests showed increased haemoglobin levels (14.2 mmol/l). No indications of polycythaemia vera or secondary polycythaemia were found after which the diagnosis of MES was made. Haemoglobin levels normalised after hysterectomy without any further intervention. Conclusion MES is common, although relatively unknown. Its pathophysiology is most likely based on ectopic production of erythropoietin by leiomyoma tissue. The combination of polycythaemia and uterus myomatosus should alert clinicians to this syndrome, especially as polycythaemia normalises after hysterectomy.

Translated title of the contributionPolycythaemia in a patient with uterus myomatosus Background
Original languageDutch
Article numberD1161
JournalNederlands Tijdschrift voor Geneeskunde
Volume161
Issue number29
Publication statusPublished - 2017

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