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August 1957, Vol 75, No. 2 >
ARTICLE | August 1957

Malignant Brenner Tumor

MARGARET MACKINNON, M.D.; MALCOLM B. DOCKERTY, M.D.
AMA Arch Surg. 1957;75(2):282-286. doi:10.1001/archsurg.1957.01280140120022.
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The malignant Brenner tumor is an unusually rare lesion, and thus far only six cases have been reported in the literature. Forty-two cases of Brenner tumor were reported from the Mayo Clinic in 1950, all of which were benign.1 However, a malignant Brenner tumor was seen in 1954. A report of this case is presented herewith.

Report of Case  A 59-year-old white woman (sextigravida, quadripara, two abortions) was first seen at the Clinic in 1938 because of symptoms referable to a duodenal ulcer. Pelvic examination at this time revealed a leiomyoma in the uterus 3 to 4 cm. in diameter.In 1954 the patient returned, complaining of lower abdominal enlargement of two weeks' duration. She reported that the menopause had occurred in 1947. On examination a firm, somewhat nodular mass was found in the left adnexal region. Abdominal hysterectomy and bilateral salpingo-oophorectomy were carried out.The uterus was not

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