Primary Bilateral Fallopian Tube Carcinoma The Report of a Single Case with Review of the Literature

• Main Authors: Prajna Hariprasad, Hariprasad S, Teerthanath Srinivas, Jayrama Shetty K.
• Format: Article
• Language: English
• Published: JCDR Research and Publications Private Limited 2013-05-01
• Series: Journal of Clinical and Diagnostic Research
• Subjects: primary fallopian tube carcinoma; serous adenocarcinoma
• Online Access: https://jcdr.net/articles/PDF/2980/38-%205483_E(C)_PF1(M)_F(P)_PF1(P)_PF1(P)_PFA(N)_OLF_PF1(PP)_PF2(PP).pdf

Primary fallopian tube carcinoma is an extremely uncommon neoplasm of the female genital tract. Primary Fallopian Tube Carcinoma (PFTC) has a clinical and a histological resemblance to Epithelial Ovarian Cancer (EOC). We are reporting a case of PFTC in a 55 year old tubectomized, postmenopausal woman with the non-specific complaints of a watery vaginal discharge and lower abdominal pain. The clinical and radiological findings suggested a bilateral tubo-ovarian abscess. On laprotomy, a bilateral fallopian tube tumour was seen, with a focal extension to the surface of the right ovary from the right fallopian tube. Total abdominal hysterectomy, bilateral adnexectomy andomentectomy, along with excision of the draining lymph nodes, was done. The histopathological examination revealed a bilateral papillary serous carcinoma of the fallopian tube. The patient was treated with adjuvant chemotherapy with Paclitaxel. There was no evidence of any recurrence, after 2 years of regular follow up. The clinical signs and symptoms of fallopian tube neoplasms are usually non-specific. The primary treatment remains a surgical resection, followed by adjuvant chemotherapy or radiation. The prognosis is poor, although long-term survivors have been reported.