Abstract/References

Ovarian strumal carcinoid: a case report

Masaru Kanasugi, Hiroshi Nishiyama, Minoru Sanpei, Shigeyuki Asano, Tsuyoshi Honda

Author information
  • Masaru Kanasugi

    Department of Obstetrics and Gynecology, Iwaki Kyouritsu Hospital

  • Hiroshi Nishiyama

    Department of Obstetrics and Gynecology, Iwaki Kyouritsu Hospital

  • Minoru Sanpei

    Department of Obstetrics and Gynecology, Iwaki Kyouritsu Hospital

  • Shigeyuki Asano

    Department of Pathology, Iwaki Kyouritsu Hospital

  • Tsuyoshi Honda

    Department of Obstetrics and Gynecology, Iwaki Kyouritsu Hospital

Abstract

Background:Carcinoid tumors of the ovary are rare tumors, histopathologically classified as monodermal teratomas and somatic-type tumors arising from dermoid cysts. Their malignancy varies from borderline to malignant. Carcinoid tumors can occur in young and elderly women, and are sometimes seen in mature teratoma, struma ovarii, or mucinous cystadenoma as a nodule or tumor. Strumal carcinoid and mucinous carcinoid present as special types of carcinoid tumors of the ovary.


Case report:This report describes a 56-year-old woman who presented with a large pelvic mass on abdominal ultrasonography during a medical examination. The diameter of the pelvic tumor was approximately 11 cm and was suspected to be ovarian cancer. The values of CA125 and CEA were above their reference intervals on preoperative examination. Abdominal total hysterectomy and bilateral salpingo-oophorectomy were performed. Intraoperative frozen-section histopathology suggested a diagnosis of mucinous adenocarcinoma; therefore, partial omentectomy and pelvic lymphadenectomy were also performed. Permanent-section histopathology led to a final diagnosis of strumal carcinoid of the ovary, stage IA (FIGO 2014). Six years post-operation, the patient had no sign of recurrence.

The cintent of reseach paper

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