- Case report
- Open Access
Relevance of frozen sections and serum markers in invasive squamous cell carcinoma arising from ovarian mature cystic teratoma: two case reports
Journal of Medical Case Reports volume 10, Article number: 20 (2016)
Ovarian mature cystic teratoma (MCT) is a common neoplasm in women. While malignant transformation of MCT is relatively rare, squamous cell carcinoma is the most frequent malignant neoplasm arising from MCT. Some tumor markers have been reported to be useful for prediction of MCT malignant transformation prior to operation. However, widely accepted use of these markers remains to be established. In the present study, we report the usefulness of frozen section assessment during operation, as well as preoperative measurement of tumor marker levels.
We present two cases of squamous cell carcinoma arising from ovarian MCT. The first case was a 45-year-old Asian woman referred to our hospital after her periodical company medical checkup, due to possible ovarian tumor. Image analysis suggested a dermoid cyst, and left salpingo-oophorectomy was performed. Because the cyst was histologically diagnosed as an invasive squamous cell carcinoma arising from an MCT, our patient underwent an additional preventative operation. The TNM classification and FIGO stage were T1aNXM0 and Ia, respectively. The second case was a 53 -year-old Asian woman who visited our hospital due to complaints of abdominal pain and urinary retention. Image analysis and laboratory data showing high serum levels of SCC antigen (normal range: < 1.5 ng/mL) and CA19-9 (normal range: < 37 U/mL), which strongly suggested malignant transformation of MCT. Frozen sections obtained during the operation were histologically analyzed to confirm malignancy, and our patient underwent an additional operation. The TNM classification and FIGO stage were T1aNXM0 and Ia, respectively.
We report the usefulness of frozen section assessment during operation, as well as preoperative measurement of tumor marker levels.
Ovarian mature cystic teratoma (MCT) is a common neoplasm in women. While malignant transformation of MCT is relatively rare [1, 2], squamous cell carcinoma (SCC) is the most frequent malignant neoplasm arising from MCT [3, 4]. Preoperative levels of tumor markers, such as SCC antigen, are useful for identifying the presence of SCC arising from MCT [5, 6]. However, there have been previously reported cases of other types of malignancies arising from MCT, such as neuroendocrine carcinoma [7–11], which are unable to be identified by preoperative evaluation of SCC antigen. The prognoses of patients with such secondary malignancies depend on their International Federation of Gynecology and Obstetrics (FIGO) stage [4, 7, 12, 13]. To improve patient quality of life, we investigated the usefulness of frozen section assessment during operation for confirmation of MCT malignant transformation.
A 45-year-old Asian woman was referred to the gynecology and obstetrics department of our hospital after a periodical company medical checkup, due to possible ovarian tumor. Ultrasound and magnetic resonance imaging (MRI) scans revealed an intra-abdominal cyst, approximately 44 mm in diameter. Periodical follow-up imaging later revealed a hairball in the cyst, leading to diagnosis of dermoid cyst. Five years after initial presentation, the size of the cyst measured 59 x 59 mm (Fig. 1a), and serum levels of SCC antigen and cancer antigen (CA)125 (normal range: < 35 U/mL) were 1.4 ng/mL and 10.8 U/mL, respectively. Follow-up biochemical analysis revealed that the level of SCC antigen gradually increased over a period of 6 months, to 4.8 ng/mL. Our patient subsequently underwent left salpingo-oophorectomy due to suspicion of malignant transformation of the ovarian cyst. At laparotomy, bloody ascites in the peritoneal cavity were observed, and the cytological analysis of the ascites fluid during the operation revealed no malignant cells. On gross examination, the resected ovarian cyst contained a number of mature hair shafts intermingled with abundant atheromic material. Frozen section analysis was not performed because the cyst was macroscopically diagnosed as a dermoid cyst. After fixation by formaldehyde, the cyst walls were observed to be thickened, with protruding, irregular nodules partially filling the cyst (Fig. 2a). The cut surface of the thickened cyst wall was yellowish and solid (Fig. 2b). Histologically, the multilocular cystic space was lined by mature squamous epithelium, and many carcinomatous foci were observed. Invasive growth of SCC was pronounced in the cyst wall (Fig. 2c). These findings led to a diagnosis of invasive SCC (well-differentiated SCC) arising from MCT. No vascular invasion was identified. One month after the first operation, our patient underwent an additional preventive operation (a simple abdominal hysterectomy and right salpingo-oophorectomy). Lymphadenectomy and omentectomy were not performed due to our patient’s wish for limited surgery. Pathological analysis revealed no residual carcinoma in the uterus, right ovary, or right fallopian tube. The TNM classification and FIGO stage were T1aNXM0 and Ia, respectively. Our patient was started on paclitaxel and carboplatin chemotherapy postoperatively; 22 months later, she remained free of any clinically identifiable recurrence.
A 53-year-old Japanese woman presented at the gynecology and obstetrics department of our hospital due to complaint of abdominal pain and urinary retention. A computed tomography (CT) scan revealed an intra-abdominal cyst measuring 130 x 135 mm, and an MRI scan showed focal thickening of the cyst wall. Laboratory analysis revealed high serum levels of SCC antigen (6.2 ng/mL) and CA19-9 (344 U/mL). The possibility of malignant transformation of the dermoid cyst was thought to be low, and systemic CT suggested no distant metastasis. Forty-two days after initial presentation, our patient underwent surgery. At laparotomy, yellowish ascites was observed in the peritoneal cavity, and gross examination revealed that the cyst wall was thickened and attached to the left fallopian tube, small intestines, posterior wall of the uterus, and retroperitoneum. Frozen sections of the thickened wall of the cyst were prepared and histologically analyzed, revealing invasive SCC in the cyst wall. Cytological analysis of the ascites fluid during the operation revealed no malignant cells. Thus, malignant transformation was diagnosed, and our patient underwent a total abdominal hysterectomy, bilateral salpingo-oophorectomy, and omentectomy. However, lymphadenectomy was not performed due to the firm attachment of the cyst wall to the surrounding lymph nodes. Focal and irregular thickening of the cyst wall was observed after fixation by formaldehyde (Fig. 3a). The cut surface of the thickened cyst wall appeared yellowish and solid, and was connected directly to the inner surface of the cyst (Fig. 3b). Histological analysis revealed a unilocular cystic space lined by mature squamous epithelium. Malignant transformation was identified in the epithelial lining (Fig. 3c). These findings led to a diagnosis of SCC (well-differentiated SCC) arising from MCT. No definite vascular invasion was identified. The TNM classification and FIGO stage were T1aNXM0 and Ia, respectively. Twenty-one months postoperatively, our patient remained free of any clinically identifiable recurrence.
The etiology of malignant transformation in MCT has not yet been elucidated. Approximately 75 % of malignant transformations are categorized as SCCs . Iwasa et al. speculated that SCC may arise from metaplastic squamous epithelium located within the MCT . It has also been suggested that long-term presence of MCT without removal may be associated with malignant transformation . We have experienced another case of MCT with focal nodular hyperplasia of the squamous epithelium lining, similar in appearance to ‘seborrheic keratosis’ and with a preoperative SCC serum level of over 1.0 ng/mL (data not shown). Furthermore, the internal lining of the squamous epithelium of the mature cystic teratoma may also have potential for growth.
Some tumor markers have been reported to be useful for MCT characterization and prediction of malignant transformation . Hackethal et al. analyzed the age, presence of tumor markers, symptoms, and FIGO stages of 277 cases described in the literature from 1978 to 2007 . Kataoka et al. reported that the level of CA125 and CA19-9, but not SCC antigen, was significantly correlated with MCT tumor diameter . The significance of high SCC antigen serum levels has been reported in several cases of malignant MCT transformation [5, 6, 17, 18], with a SCC cutoff level of 2.0 ng/mL [6, 17, 18], and Mori et al. utilized a SCC antigen cutoff level of 2.5 ng/mL in patients aged over 40 years old . Furthermore, Kikkawa et al. demonstrated that patient age and ovarian tumor size are important factors in predicting SCC arising from ovarian MCT . Choi et al. reported an average SCC antigen level of 1.5 ng/mL in patients with FIGO stage Ia tumors . Futagami et al. assessed malignant transformation risk by tumor size and marker levels . Suzuki et al. proposed the use of a combination of two serum markers, macrophage colony-stimulating factor (M-CSF) and SCC antigen, to preoperatively diagnose SCC arising from ovarian MCT .
Although there have been previous studies assessing the association between clinical findings and malignant transformation of MCT [3, 14], specific symptoms for malignant transformation remain to be identified. The present results suggested the usefulness of analyzing frozen sections during operation to identify malignant transformation of MCT. Furthermore, this technique provides the opportunity to detect malignancies other than SCC, which may also arise from ovarian MCT. If preoperative imaging reveals unnatural nodular areas within the cyst wall, histological analysis of frozen sections during the initial operation may avoid the need for a secondary operation for complete removal of the malignancy. Although prognosis depends on the FIGO stage [4, 7, 12, 13] and malignancy may not be identified in all cases , avoiding a secondary operation has been demonstrated to increase the patient’s quality of life.
In summary, we report two cases of SCC arising from ovarian MCT. We emphasize the usefulness of frozen section assessment during operation, as well as preoperative measurement of tumor marker levels. These methods facilitated detection of both SCC and other malignancies arising from MCT.
Malignant transformation of mature cystic teratoma is rare. However, such transformation is difficult to identify prior to operation, if serum levels of tumor markers are near the cutoff level. The present results suggested the usefulness of frozen section assessment during operation, which may aid in increasing patient quality of life.
Written informed consent was obtained from the patients for publication of both the case reports and any accompanying images. Copies of written consent are available for review by the Editor-in-Chief of this journal.
International Federation of Gynecology and Obstetrics
Macrophage-colony stimulating factor
Mature cystic teratoma
Magnetic resonance imaging
Squamous cell carcinoma
Iwasa A, Oda Y, Kaneki E, Ohishi Y, Kurihara S, Yamada T, et al. Squamous cell carcinoma arising in mature cystic teratoma of the ovary: an immunohistochemical analysis of its tumorigenesis. Histopathol. 2007;51:98–104.
Hackethal A, Brueggmann D, Bohlmann MK, Franke FE, Tinneberg HR, Münstedt K. Squamous-cell carcinoma in mature cystic teratoma of the ovary: systematic review and analysis of published data. Lancet Oncol. 2008;9:1173–80.
Tangjitgamol S, Manusirivithaya S, Sheanakul C, Leelahakorn S, Thawaramara T, Jesadapatarakul S. Squamous cell carcinoma arising from dermoid cyst: case reports and review of literature. Int J Gynecol Cancer. 2003;13:558–63.
Dos Santos L, Mok E, Iasonos A, Park K, Soslow RA, Aghajanian C, et al. Squamous cell carcinoma arising in mature cystic teratoma of the ovary: a case series and review of the literature. Gynecol Oncol. 2007;105:321–4.
Mori Y, Nishii H, Takabe K, Shinozaki H, Matsumoto N, Suzuki K, et al. Gynecol Oncol. 2003;90:338–41.
Yamanaka Y, Tateiwa Y, Miyamoto H, Umemoto Y, Takeuchi Y, Katayama K, et al. Preoperative diagnosis of malignant transformation in mature cystic teratoma of the ovary. Eur J Gynaecol Oncol. 2005;26:391–2.
Sakuma M, Otsuki T, Yoshinaga K, Utsunomiya H, Nagase S, Takano T, et al. Malignant transformation arising from mature cystic teratoma of the ovary: a retrospective study of 20 cases. Int J Gynecol Cancer. 2010;20:766–71.
Miyamoto M, Takano M, Goto T, Kato M, Sasaki N, Furuya K. Large cell neuroendocrine carcinoma arising in mature cystic teratoma: a case report and review of the literature. Eur J Gynaecol Oncol. 2012;33:414–8.
Kajo K, Masák L, Sorkovská D, Vallová M, Kajo M, Macháleková K, et al. Mucinous carcinoma (non-intestinal type) arising in the ovarian mature cystic teratoma - a case report. Cesk Patol. 2013;49:141–5.
Kar A, Kar T, Pattnaik K, Biswal P. Carcinosarcoma in dermoid cyst of ovary: an extremely rare malignant transformation. Indian J Pathol Microbiol. 2013;56:176–7.
Ting WH, Hsiao SM, Lin HH, Wei MC. Primary carcinoid tumor of the ovary arising in a mature cystic teratoma: a case report. Eur J Gynaecol Oncol. 2014;35:100–2.
Ulker V, Numanoglu C, Akbayir O, Akyol A, Tuncel A, Akca A, et al. Malignant transformation arising from mature cystic teratoma of the ovary: a report of six cases. J Obstet Gynaecol Res. 2012;38:849–53.
Zakkouri FA, Ouaouch S, Boutayeb S, Rimani M, Gamra L, Mrabti H, et al. Squamous cell carcinoma in situ arising in mature cystic teratoma of the ovary: a case report. J Ovarian Res. 2011;4:5.
Spannuth WA, Rocconi RP, Kirby TO, Huh WK, Conner MG. Gamma mode of infiltration associated with poor prognosis in malignant teratoma of the ovary: a case report. Gynecol Oncol. 2005;98:155–7.
Rim SY, Kim SM, Choi HS. Malignant transformation of ovarian mature cystic teratoma. Int J Gynecol Cancer. 2006;16:140–4.
Kataoka T, Watanabe Y, Hoshiai H. Retrospective evaluation of tumor markers in ovarian mature cystic teratoma and ovarian endometrioma. J Obstet Gynaecol Res. 2012;38:1071–6.
Suzuki M, Kobayashi H, Sekiguchi I, Konnai K, Terao T, Sato I. Clinical evaluation of squamous cell carcinoma antigen in squamous cell carcinoma arising in mature cystic teratoma of the ovary. Oncology. 1995;52:287–90.
Suzuki M, Tamura N, Kobayashi H, Ohwada M, Terao T, Sato I. Clinical significance of combined use of macrophage colony-stimulating factor and squamous cell carcinoma antigen as a selective diagnostic marker for squamous cell carcinoma arising in mature cystic teratoma of the ovary. Gynecol Oncol. 2000;77:405–9.
Kikkawa F, Nawa A, Tamakoshi K, Ishikawa H, Kuzuya K, Suganuma N, et al. Diagnosis of squamous cell carcinoma arising from mature cystic teratoma of the ovary. Cancer. 1998;82:2249–55.
Choi EJ, Koo YJ, Jeon JH, Kim TJ, Lee KH, Lim KT. Clinical experience in ovarian squamous cell carcinoma arising from mature cystic teratoma: a rare entity. Obstet Gynecol Sci. 2014;57:274–80.
Futagami M, Yokoyama Y, Mizukami H, Shigeto T, Mizunuma H. Can malignant transformation in mature cystic teratoma be preoperatively predicted? Eur J Gynaecol Oncol. 2012;33:662–5.
Zorlu CG, Kuscu E, Soysal ME, Caglar T, Aydogdu T, Cobanoglu O, et al. Malignant degeneration of mature cystic teratomas. Aust N Z J Obstet Gynaecol. 1996;36:221–2.
We thank Ms. Mariko Ogi, Ms. Tomoko Yoshii, Ms. Maiko Kohara, and Ms. Natsuki Hata for preparing the histological material and performing the immunohistochemical staining.
We do not report any competing interests for our manuscript.
YT performed the operations, assessed clinical precautions, and drafted the manuscript. HY performed histopathological diagnosis, designed the study, and completed the manuscript. TS, NK, and YY performed the operations and assessed clinical precautions. TO performed the image analysis. All authors read and approved the final manuscript.
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Tazo, Y., Yoshimura, Y., Shoda, T. et al. Relevance of frozen sections and serum markers in invasive squamous cell carcinoma arising from ovarian mature cystic teratoma: two case reports. J Med Case Reports 10, 20 (2016). https://doi.org/10.1186/s13256-015-0783-5
- Squamous cell carcinoma
- Mature cystic teratoma
- Immunohistochemical analysis