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Case Reports

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Primary fallopian tube carcinoma - case report

  • V. Pažin1,2
  • A. Dobrosavljevic2,*,
  • L. Nejkovic1,2

1Medical faculty University of Belgrade, Belgrade, Serbia

2Clinic of Obstetrics and Gynecology “Narodni Front”, Belgrade, Serbia

DOI: 10.12892/ejgo4417.2019 Vol.40,Issue 1,February 2019 pp.163-165

Accepted: 14 September 2017

Published: 10 February 2019

*Corresponding Author(s): A. Dobrosavljevic E-mail: dobrosavljevical@gmail.com

Abstract

Primary fallopian tube carcinoma is a rare gynecological malignancy and it accounts for about 1% of all gynecological malignancies. Etiological factors are not sufficiently known, but most commonly specified are infertility, nulliparity, and pelvic inflammatory disorder. It is most often asymptomatic, although, a triad reported by Latzko including a vaginal watery discharge, colic like pelvic pain, presence of tumor mass in pelvis, is mentioned as pathognomonic. In the present case, it was primary fallopian tube carcinoma, in FIGO Stage IA. After complete abdominal hysterectomy with lymph node dissection, in line with the expert council’s decision, no adjuvant chemotherapy was administered. PET CT in June 2017, two years after the surgical treatment, presented both some metastatic changes in lungs and enlarged retroperitoneal lymph nodes and after this finding, and chemotherapy with carboplatin was begun. The therapy implies surgical treatment being hysterectomy with adnexectomy, but also retroperitoneal lymph node dissection as well, considering that it more often affects lymphatic glands than epithelial ovarian cancer (EOC). It can be misinterpreted with EOC in a pathological sense. In addition to a surgical treatment, the most common form of chemotherapy is platinum-combined with taxanes.

Keywords

Fallopian tube carcinoma; Epithelial ovarian cancer, Pelvic inflammatory disorder; Chemotherapy; Platinum; Taxanes

Cite and Share

V. Pažin,A. Dobrosavljevic,L. Nejkovic. Primary fallopian tube carcinoma - case report. European Journal of Gynaecological Oncology. 2019. 40(1);163-165.

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