Link
http://www.casereports.in/articles/4/1/A-Rare-Case-of-Carcinoma-of-Ovary-with-Carcinoma-of-Cervix.html
http://www.casereports.in/articles/4/1/A-Rare-Case-of-Carcinoma-of-Ovary-with-Carcinoma-of-Cervix.html
Rajshree D. Katke, Shruti Gadekar, Priyanka Pagare
From
the Department of Obstetrics & Gynecology, Grant Government Medical
College & Sir J. J. Group of Hospitals, Mumbai, Maharashtra,
India.
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Introduction:
Synchronous
genital tract malignancies are rare. The most frequently observed
synchronous neoplasms are those of the ovary together with the
endometrium constituting 40% of all and carries favorable prognosis
because of its low malignant potential [1]. Overall incidence of
synchronous female genital tract malignancies is 0.63% [2,3]. Cervical
and ovarian malignancies are still rare and if they occur they have
similar histopathology due to direct spread of cervical malignancy to
ovary. The literature on both the spread of cervical carcinoma and
metastatic tumors to the ovary indicates that ovarian involvement by
cervical carcinoma is rare if cases of direct spread are excluded. An
important category of cervical carcinomas that may show ovarian spread
is adenocarcinoma and related tumors, including adenosquamous carcinoma
and glassy cell carcinoma [4]. We are presenting a rare case report of
synchronous squamous cell carcinoma of cervix and serous papillary
cyst-adenocarcinoma of ovary.
Case Report:
A
40 year female with foul smelling discharge per vaginum and postcoital
bleeding since 3 months was referred to us. She was diagnosed as a case
of ovarian malignancy with moderately differentiated squamous cell
carcinoma of cervix, histopathologically proved on cervical biopsy. Her
Tumor marker cancer antigen were evaluated and CA-125 was found to be
raised (CA 125: 774 U/mL); whereas other tumor markers were normal
[Alpha fetoprotein (AFP) was 3.37 ng/mL, ß HCG < 1.2 IU/mL, CA 19.9
< 2 IU/mL, LDH: 320U/L]. Fine needle aspiration cytology (FNAC) of
right ovarian mass was suggestive of carcinoma; whereas cervical biopsy
showed presence of squamous cell carcinoma. Per abdomen examination
revealed solid, non-mobile palpable mass of approximately 8x8x7 cm
arising from pelvis. On per speculum examination cervical erosion,
hypertrophied cervix and biopsy mark were noted. After getting
anesthetic fitness patient was posted for surgery. In situ findings
revealed ascites, 15x10x10 cm necrotic hemorrhagic, cystic, friable
tumor mass arising from right ovary. Mass was adherent to rectum and
adjacent pelvic structures. It was separated from bowel and surrounding
structures by blunt and sharp dissection. Total abdominal hysterectomy
with removal of right sided ovarian tumor with left sided
salpingo-oophorectomy with bilateral internal iliac, external iliac,
obturator and para-aortic lymph nodes dissection and omentectomy was
done. Uterus, tumor mass, cervix with dissected lymph nodes were sent
for histopathological examination [Fig.1]. Vault closure was done with
vicryl number 1 continuous interlocking suture. After achieving complete
hemostasis abdomen was closed in layers.
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Patient
withstood the procedure well. Postoperative period of patient was
uneventful. Stich removal was done on day 11. Histopathology report
revealed squamous cell carcinoma of cervix and high grade serous
papillary cystadenocarcinoma of ovary [Fig.3,4]. Chemotherapy was given
to the patient post-operatively and patient is on regular follow-up.
Discussion:
Simultaneous
occurring genital tract malignancies can be synchronous or
metachronous. Primary malignancies of the genital tract seem to occur
synchronously more often than one would expect as it was seen in our
case [5]. The prognoses in both the groups differs; those with
synchronous malignancies have better prognosis when compared to
metastatic lesions of individual tumors [6,7]. While the etiology of
this phenomenon remains unclear, it has been postulated that
embryologically similar tissues of the female genital tract, when
simultaneously subjected to carcinogen may develop synchronous neoplasm.
These neoplasms may represent metaplasia.
Incidence
of synchronous genital tract malignancy is 0.63%. Out of this
endometrioid carcinoma of ovary and endometrium constitutes 40% [2].
Literature shows very few case reports on synchronous cervical and
ovarian malignancy. Earlier reported cases were of ovarian endometrioid
adenocarcinoma and frank squamous cell carcinoma of cervix in 1996 by
Jawornik and colleagues [8]. Only one similar case with ovarian
cyst-adenocarcinoma and squamous cell carcinoma of cervix has been
reported by K.Srivastav and colleagues in 2009 [2]. In 2006, Huang YD
and colleagues reported ovarian endometrioid adenocarcinoma and
endocervical mucinous adenocarcinoma [9]. Our patient had squamous cell
carcinoma of cervix along with high grade ovarian serous
cysadenocarcinoma. While these cases represent synchronous involvement, a
case study conducted by Elishaev E showed that endocervical
adenocarcinomas, including some qualifying as microinvasive, can
metastasize to the ovaries and simulate primary ovarian surface
epithelial neoplasms [10]. The literature on both the spread of cervical
carcinoma and metastatic tumors to the ovary indicates that ovarian
involvement by cervical carcinoma is rare if cases of direct spread are
excluded. An important category of cervical carcinomas that may show
ovarian spread is adenocarcinoma and related tumors, including
adenosquamous carcinoma and glassy cell carcinoma [11]. HPV staining may
be used in demonstrating metastatic involvement on ovary by cervical
malignancy.
Based
on our case report we need to keep in mind that even if patient
presents with symptoms pertaining to a single malignancy; still the rare
possibility of synchronous malignancies should be looked for by doing
proper investigations. In our case, patient had symptoms pertaining to
cervical malignancy; whereas ovarian malignancy was diagnosed after
investigating the patient. Histologic examination should be done
properly as the prognosis depends on the malignancies being metastatic
or synchronous ones; the latter group having better prognosis as shown
by earlier studies [2,8,9]. Surgical management should be offered in
all such cases as it greatly aids in diagnosis and also helps in
improving overall survival. Long term follow up of such patients should
be maintained to determine the prognosis.
References:
- Ayhan A, Yalçin OT, Tuncer ZS, Gürgan T, Küçükali T. Synchronous primary malignancies of the female genital tract. Eur J Obstet Gynecol Reprod Biol. 1992;45(1):63-66.
- Srivastava K, Zahra F. Synchronous primary malignancy of ovary and cervix with different histopathology: a rare presentation. The Internet Journal of Gynecology and Obstetrics 2009; Volume 12 Number 2.
- Kambi DP, Mallikarjuna M, Santosh C, Abhishek V. Synchronous malignancies of ovary, fallopian tube and cervix: A rare case. International Journal of Biomedical and Advance Research 2013;4(9):676-679.
- Young RH, Gersell DJ, Roth LM, Scully RE. Ovarian Metastases from Cervical Carcinomas Other than Pure Adenocarcinomas. Cancer J 1993;71(2):407-416.
- Desai R, Darad D, Chugh A, Patel H. A case report of 2 synchronous tumors of female genital tract – rare finding. National journal of Medical Research 2012;2(1):102.
- Matloch DL, Salem FA, Charles EH, Save EW. Synchronous multiple primary neoplasms of the upper female genital tract. Gynec Oncol 1982;13:271.
- Eifel P, Henricksen M, Ross W, Ballon S, Martines A, Kempson R. Simultaneous presentation of carcinoma involving the ovary and the uterine corpus. Cancer 1982;50:163.
- Pitynski K, Bogdanowicz M, Jawornik M. Coexistence of endometrioid ovarian tumor and squamous cell carcinoma of the cervix. Ginekol Pol 1996;67(12):629-631.
- Huang YD, Hung YC, Yeh LS, Chiang IP, Zeng GC, Chang WC. Synchronous ovarian endometrioid adenocarcinoma and endocervical mucinous adenocarcinoma. Taiwan J Obstet Gynecol. 2006;45(3):264-267.
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