IMR Press / CEOG / Volume 31 / Issue 1 / pii/2004008

Clinical and Experimental Obstetrics & Gynecology (CEOG) is published by IMR Press from Volume 47 Issue 1 (2020). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with S.O.G.

Original Research

Giant cell arteritis of the female genital tract

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1 Unit of Gynecologic Oncology, Department of Obstetrics and Gynecology, Beer-Sheva (Israel)
2 Department of Medicine, Soroka Medical Center and Faculty·of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva (Israel)
3 Institute of Pathology, Soroka Medical Center and Faculty·of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva (Israel)
Clin. Exp. Obstet. Gynecol. 2004, 31(1), 31–33;
Published: 10 March 2004
Abstract

Giant cell arteritis (GCAJ of the female genital tract is rare with only 30 cases, including this case, documented in the literature We present a patient who had total abdominal hysterectomy and bilateral salpingo-oophorectomy for an ovarian cyst and on histo­logic examination GCA involving the arteries of the myometrium, cervical stroma, ovaries and tubes was unexpectedly discovered Upon questioning of the patient and further investigations it became clear that the patient did have symptoms and signs suggestive of systemic GCA including fatigue, low-grade fever, weight loss and elevated erythrocyte sedimentation rate (ESR). Treatment with oral corticosteroids resulted in rapid and complete recovery. lt is concluded that an incidental finding of GCA in the genitalia should alert the clinician to the possibility of systemic GCA. If upon questioning of the patient and further investigations the existence of systemic GCA is confirmed, treatment with corticosteroids should be considered.

Keywords
Giant cell arteritis
Temporal arteritis
Polymyalgia rheumatica
Female genital tract
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