2021, Number 04
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Ginecol Obstet Mex 2021; 89 (04)
Endometrial osseous metaplasia: a rare differential diagnosis of translocated IUD: hysteroscopic management. Case Report
Jiménez-Bonola A, Valencia-Torres MÁ, Olivares-Montano AK
Language: Spanish
References: 18
Page: 336-342
PDF size: 219.46 Kb.
ABSTRACT
Background: Endometrial osseous metaplasia has an estimated incidence of 3
cases per 10,000 women and there are few reported cases. Symptoms are nonspecific:
chronic pelvic pain, abnormal uterine bleeding, dysmenorrhea and dyspareunia. Most
patients suffer from primary or secondary infertility. There are different theories of its
pathophysiology. Two-dimensional endovaginal pelvic ultrasound plays a decisive role
in the diagnosis; most cases are an incidental finding with a typical structure mimicking
an intrauterine device.
Clinical case: 47-year-old female patient, in perimenopause, with chronic pelvic
pain and abnormal uterine bleeding. She came for consultation with a translocated
intrauterine device, noticed in the routine gynecological ultrasonography, with an
apparent history of having had it removed 21 years ago. During the examination the
reins of the IUD were not observed. Office hysteroscopy showed endometrial bone
metaplasia; the bone fragments were removed, and her symptoms subsided. She
continued to be followed up in the climacteric clinic for treatment of perimenopausal
symptoms.
Conclusions: Endometrial bone metaplasia is rare, with very few cases reported
worldwide, perhaps because it is underdiagnosed. The pathophysiology is still unclear,
although its different theories are accepted. It should be suspected in patients without
an intrauterine device, in the presence of ultrasonographic findings compatible with its
location, associated with abnormal uterine bleeding and chronic pelvic pain. Most of
the reported cases are associated with infertility. The definitive diagnosis and treatment
is with office hysteroscopy, with grasper or hysteroscopic resectoscope.
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