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December 1987, Volume 37, Issue 12

Case Reports


Fazle Raziq  ( Department of Pathology, Ayub Medical College, Abbottabad. )
Muhammad Tariq Khan  ( Department of Pathology, Ayub Medical College, Abbottabad. )
Wali Muhammad  ( Department of Paediatric ward, DHQ Hospital, Abbottabad. )
Abdur Rashid  ( Department of Methcaj ward, DHQ Hospital, Abbottabad. )

A case of primary choriocarcinoma in the fallopian tube of a 30 year-old woman is presen­ted.


The patient left against medical advise therefore further investigations like HCG titre, X-ray chest and liver scan to determine the extent of disease could not be done. The patient is lost to follow up.
A 30 years old female, gravida 3, para 2, was admitted to DHQ Hospital, Abbottabad with amenorrhoea for 55 days, painful abdominal mass and irregular vaginal bleeding for 15 days. On examination, the mass was tender, fixed about 24 week size gestation and was arising from pelvis. Provisional diagnosis of twisted ovarian cyst ectopic tubal pregnancy was made. Exploratory laparotomy showed a large haemorrhagic friable mass in the pelvis which was obliterating the right adnexal ara. The mass was separate from the uterus but was adherent to the right ovary and parts of small intestine. Both ovaries were cystically enlarged to approximately 10.0 x 8.0 cm size. On manipulation of the growth, heavy bleeding started. Gentle attempts were made to separate the mass from the adjacent structures, which separated quite easily and no raw areas were left behind. About 200ml of blood, present in the peritoneal cavity was also removed.
The tumour alongwith the affected tube and right ovary, removed at operation, were sent for histopathological examination.
The histologic diagnosis of (1) choriocar­cinoma of the right fallopian tube and (2) corpus luteum and theca lutein cysts of the right ovary was made. Section of the tubal growth showed tumour made up of cytotrophoblast and synci­tiotrophoblast. The cytotrophoblast consisted of large round to polyhedral shaped cells with distinct cell borders. The cells were having pale cytoplasm and large round vesicular nuclei with prominent nucleoli. The syncitiotrophoblast consisted of columns of large pleomorphic cells having basophiic cytoplasm and large multiple nuclei.


Choriocarcinoma of the fallopian tube is a rare occurrance. According to Fedele et al1 only 77 such cases have been reported till 1985.
The diagnosis of choriocarcinoma of the fallopian tube is difficult to make before operation and is rarely suspected on gross exa­mination2. The same happened in the present case. The diagnosis was first made on histology.
The histogonesis of tubal choriocarcinoma is not clear.2 Primary choriocarcinoma of the fallopian tube may arise either from an ectopic tubal pregnancy, an intrauterine pregnancy that has spread to the tube (via embolic spread of cherionic villi to the tube), or from teratogénous change within the tube i.e. unrelated to pregnancy. In the opinion of Riggs et al1 with whom we agree, tubal choriocarcinoma most probably arises in the trophoblastic tissue of the ectopic tubal gestation.
An unusual characteristic of tubal chorio­carcinoma is that it is almost never preceded by a hydatidiform mole.


1. Fedele, M., Lanza, A., Olivero, F., Fessia, L.A. and Addeto, F. Primary choriocarcinoma of the fallopian tube; report of a case. Eur. J. Gynecol. Oncol., 1985;6:230.
2. Riggs, LA., Wainer, A.S., Hahn, G.A. and Farell, D 3sf. Extrauterine tubal choriocarcinoma; a case report and review of recent literature. Am. J. Obstet.Gynecol., 1964;88: 637.

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