- Case report
- Open Access
A case of ovarian adenosquamous carcinoma arising from endometrioid adenocarcinoma: a case report and systematic review
© The Author(s). 2016
- Received: 28 November 2015
- Accepted: 19 July 2016
- Published: 11 August 2016
The aims of this report were to describe a case of ovarian adenosquamous carcinoma and to systematically review the pertinent literature.
We describe a case in which a 57-year-old woman had stage IC ovarian cancer histologically diagnosed as adenosquamous carcinoma. We also systematically reviewed the literature using the PubMed database.
Preoperative computed tomography and magnetic resonance imaging showed a tumor measuring 14 cm in diameter and containing solid areas. Tumor marker levels were as follows: CA125, 42.6 U/mL; CA 19–9, 134.1 U/mL; CEA, 0.9 ng/mL; and SCC, 1.6 ng/mL. The patient underwent multiple surgeries including total abdominal hysterectomy, bilateral salpingo-oophorectomy, pelvic lymph node dissection, para-aortic lymph node biopsy, and total omentectomy. Based on the cytological features of the ascitic fluid, the tumor was diagnosed as a squamous cell carcinoma. Histological examination of an excised specimen showed the transition of an endometrioid adenocarcinoma to a squamous cell carcinoma. There was no evidence of any teratomas or endometriosis-related features. We considered the tumor to be an adenosquamous carcinoma, with the squamous cell carcinoma component arising from the endometrioid adenocarcinoma component. After surgery, the patient underwent 6 cycles of paclitaxel and carboplatin chemotherapy. There has been no recurrence to date, 66 months after the initial treatment.
Histologically, the 8 adenosquamous carcinomas reported in the literature either arose from the mature cystic teratoma (4 cases) or endometriosis (3 cases) or were pure adenosquamous carcinomas (1 case). Our literature search uncovered no cases of ovarian adenosquamous carcinomas originating from endometrioid adenocarcinomas.
This is the first reported case of an adenosquamous carcinoma arising from an endometrioid adenocarcinoma. Because such tumors are rare, their standard management is unclear.
- Ovarian cancer
- Adenosquamous carcinoma
- Endometrioid adenocarcinoma
- Squamous mataplasia
Various types of primary and metastatic tumors occur in the ovaries. Squamous cell carcinoma of the ovary is, however, rare, and adenosquamous carcinomas account for less than 1 % of all ovarian malignancies . Conditions leading to the development of an adenosquamous carcinoma include malignant transformation of a preexisting ovarian teratoma [2, 3] and endometriosis . In addition, endometrioid adenocarcinomas contain squamous components, which may become malignant. Herein we report a case of adenosquamous carcinoma that did not involve a preexisting teratoma or endometriosis. Based on the histopathological findings, we believe this tumor arose from the squamous metaplasia of an endometrioid adenocarcinoma. We describe this tumor and its histology in the context of previously reported cases obtained from a systematic review of the literature [1–7].
Methods of literature review
We present an usual case of ovarian adenosquamous carcinoma. A primary hospital referred a 57-year-old Japanese woman (gravida 0, para 0) to our hospital because a pelvic tumor was suspected. At the primary hospital, the woman had complained of abdominal fullness.
During longitudinal laparotomy, we detected a left ovarian tumor 14 cm in size and a small amount of yellow transparent ascitic fluid in the abdominal cavity. Fluid samples were submitted for cytology, left salpingo-oophorectomy was performed, and biopsy samples were obtained and frozen. The cytology of the ascitic fluid suggested squamous cell carcinoma, while the biopsy indicated adenosquamous carcinoma. Ovarian cancer was diagnosed, and the patient underwent total abdominal hysterectomy, right salpingo-oophorectomy, pelvic lymph node dissection, para-aortic lymph node biopsy, and total omentectomy.
The postoperative recovery was unremarkable. The levels of all tumor markers were within the normal range immediately after surgery. The patient received 6 cycles of paclitaxel (175 mg/m2) and carboplatin (area under the curve, 6 mg/mL per min) every 3 weeks. In the five and a half years since chemotherapy, she has remained recurrence-free.
Previously reported cases with adenosquamous carcinoma of the ovary
Mature cystic teratoma
Carboquone + Futraful
Died 6 months
Mature cystic teratoma
CDDP + Epi + CPA
Alive well 3 years
Mature cystic teratoma
Alive well 11 months
Mature cystic teratoma
Recurrence 12 months
CDDP + 5-Fu
Died 3 months
Alive well 5.5 years
Many types of malignant tumors occur in the ovaries. The most common primary malignant ovarian tumors are adenocarcinomas, whereas squamous cell carcinomas are rare and adenosquamous carcinomas are even rarer. Most reported squamous cell carcinomas presumably originated from benign cystic teratomas  or Brenner tumors . There are few reports of pure squamous cell carcinomas of the ovary .
Ovarian endometriosis is a frequent cause of squamous cell carcinoma . Endometrioid adenocarcinomas contain squamous elements and were previously classified as adenoacanthomas or adenosquamous carcinomas depending on whether the squamous element was benign or malignant, respectively. They have more recently been termed “endometrioid adenocarcinomas with squamous differentiation” .
The tumor in our case was composed of intermixed endometrioid adenocarcinoma and squamous cell carcinoma components in almost equal parts. Differentiation of the endometrioid adenocarcinoma component from the squamous cell component was also observed. We therefore believe that the endometrioid adenocarcinoma developed first, after which squamous metaplasia led to the formation of the squamous cell carcinoma. It seems reasonable to describe this case as an adenosquamous carcinoma rather than an endometrioid adenocarcinoma with squamous differentiation because nearly half of the tumor consisted of malignant squamous cells. In support, in the 76 cases recently revaluated by Lim, squamous differentiation was observed in 50 cases (76 %) .
Cytological examination of the ascitic fluid from patients with ovarian cancer usually reveals adenocarcinoma cells. Most previous reports of ovarian adenosquamous carcinomas did not discuss the cytology of the ascitic fluid, presumably because most cytological examinations indicate adenocarcinoma. One report, however, did note the presence of numerous clusters of adenocarcinoma cells and a few squamous cells in the ascitic fluid . In contrast, in our case, the ascitic fluid contained malignant squamous cells but not adenocarcinoma cells, perhaps because squamous cell carcinoma was the predominant component of the tumor. This observation strongly suggests that the squamous cell carcinoma component arose from the adenocarcinoma component.
Although the prognosis of patients with adenosquamous carcinoma merits discussion, the low number of reported cases limits such discussion. The reported 5-year survival rate was 90 % for patients with stage I or II endometrioid adenoacanthoma, but was only 36 % for patients with stage I or II endometrioid adenocarcinoma . Furthermore, of the 7 reported patients with adenosquamous carcinomas arising from benign cystic teratomas, the 3 with stage Ia disease remained alive and recurrence-free for 9 months to 5 years after surgery, while the 4 with stage Ic disease were resistant to therapy and died within 13 months . Karateke described a patient with stage Ic adenosquamous carcinoma who relapsed 13 months after surgery . These outcome results indicate that adenosquamous carcinoma has a very poor prognosis and that clinical stage is an important determinant of outcome.
No effective treatments for adenosquamous carcinoma have yet been established. We administered paclitaxel and carboplatin because they are the standard chemotherapeutic agents for ovarian endometrioid adenocarcinoma and squamous cell carcinoma, respectively. Since her first treatment, the patient in our case has remained alive without recurrence for 66 months. Despite the reportedly poor prognosis of patients with adenosquamous carcinomas, chemotherapy consisting of paclitaxel and carboplatin was effective in our case and merits further study.
Because ovarian adenosquamous carcinomas are extremely rare, effective chemotherapeutic regimens should be established once sufficient numbers of patients can be recruited for statistical analysis. We hope that international organizations such as the Gynecologic Oncology Group will aid in this endeavor.
We presented a rare case of an ovarian adenosquamous carcinoma in which the squamous cell carcinoma component originated from the endometrioid adenocarcinoma component. Histologically, the 8 adenosquamous carcinomas reported in the literature arose from either the mature cystic teratoma (4 cases) or endometriosis (3 cases) or were pure adenosquamous carcinomas (1 case). To our knowledge, we are the first report a case of an ovarian tumor consisting of intermixed squamous cell carcinoma and endometrioid adenocarcinoma components. Because there is no established chemotherapy regimen for adenosquamous carcinoma, we administered the agents (paclitaxel and carboplatin) routinely used to treat epithelial ovarian cancers to our patient. Although ovarian adenosquamous carcinoma is rare, efforts should be made to recruit a sufficient number of patients for clinical trials aimed at identifying effective treatment protocols.
The authors thank Uesugi N and Anbo J for administrative assistance in preparation of this manuscript.
TS who dealt with the case and drafted the manuscript. ET, KM and YK assisted in histo pathological report of the sample and ST, AK and TS carried out all the documentary and article work out. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Ethics approval and consent to participate
This study was approved by the Ethical Committee of Iwate Medical University School of Medicine (H28-56).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Lee JY, Noo SM, Cho NH, Choi YM, Yim GW, Lee M, et al. A rare case of primary adenosquamous carcinoma arising from ovary. J Women’s Med. 2010;3(3):126–9.View ArticleGoogle Scholar
- Iwaoki Y, Katsube Y, Toyota N. Adenosquamous carcinoma arising in a mature cystic teratoma of the ovary: a case report and review of the literature. Asia Oceania J Obstet Gynaecol. 1994;20(3):237–43.View ArticlePubMedGoogle Scholar
- Maeyama M, Miyazaki K, Oka M, Higashi K, Nakayama M, Iwamasa T. Malignant degeneration of benign cystic teratomas of the bilateral ovaries: adenosquamous carcinoma in the right tumor and squamous carcinoma in the left tumor. Nihon Sanka Fujinka Gakkai Zasshi. 1983;35(3):331–4.PubMedGoogle Scholar
- Terada T. Adenosquamous carcinoma of the ovary arising from endometriosis: two case reports. Cases J. 2009;4(2):6661.View ArticleGoogle Scholar
- Hsu CY, Yang CF, Chen WY, Chiang H. Adenosquamous carcinoma and schneiderian papilloma-like lesion in a mature cystic teratoma of the ovary: a case report. Zhonghua Yi Xue Za Zhi. 1996;57(5):375–9.PubMedGoogle Scholar
- Karateke A, Gurbuz A, Kir G, Haliloglu B, Kabaca C, Devranoglu B, Yakut Y. Mucoepidermoid variant of adenosquamous carcinoma arising in ovarian dermoid cyst: a case report and review of the literature. Int J Gynecol Cancer. 2006;16(1):379–84.View ArticlePubMedGoogle Scholar
- Rodríguez Moguel L, Huerta Bahena J, Zepeda del Rio G, Lira Puerto V. Dermatomyositis and adenosquamous carcinoma of the ovary. Report of a case. Gynecol Obstet Mex. 1992;60:296–8.Google Scholar
- Selim MA, Razi A, Lankerani M. Squamous cell carcinoma arising from ovarian benign cystic teratoma. Am J Obstet Gynecol. 1984;150(6):790–2.View ArticlePubMedGoogle Scholar
- Idelson MG. Malignancy in Brenner tumor of the ovary, with comments on histogenesis and possible estrogen production. Obstet Gynecol Survey. 1963;18:246–67.View ArticleGoogle Scholar
- Ben-Baruch G, Menashe Y, Herczeg E, Menczer J. Pure primary ovarian squamous cell carcinoma. Gynecol Oncol. 1988;29(2):257–62.View ArticlePubMedGoogle Scholar
- Naresh KN, Ahuja VK, Rao CR, Mukherjee G, Bhargava MK. Squamous cell carcinoma arising in endometriosis of the ovary. J Clin Pathol. 1991;44(11):958–9.View ArticlePubMedPubMed CentralGoogle Scholar
- The International Agency for Research on Cancer, Tavassoéli FA, Devilee P. WHO classification of tumours. Pathology and genetics, Tumours of the breast and female genital organs. Ryon: IARC press; 2003.Google Scholar
- Lim D, Murali R, Murray MP, Veras E, Park KJ, Soslow RA. Morphological and immunohistochemical reevaluation of tumors initially diagnosed as ovarian endometrioid carcinoma with emphasis on high-grade tumors. Am J Surg Pathol. 2016;40(3):302–12.View ArticlePubMedGoogle Scholar
- Tsukamoto N, Matsukuma K, Daimaru Y, Ota M. Cytologic presentation of ovarian adenosquamous carcinoma in ascitic fluid. Acta Cytol. 1983;28(6):703–5.Google Scholar
- Fu YS, Stock RJ, Reagan JW, Storaasli JP, Wentz WB. Significance of squamous components in endometrioid carcinoma of the ovary. Cancer. 1979;44(2):614–21.View ArticlePubMedGoogle Scholar