Alpha-fetoprotein-producing ovarian clear cell adenocarcinoma with fetal gut differentiation: a rare case report and literature review

Epithelial ovarian carcinoma (EOC) rarely secretes alpha-fetoprotein (AFP) in postmenopausal women, especially for clear cell type. We report a 55-year-old postmenopausal woman with AFP-producing clear cell type EOC with fetal gut differentiation, FIGO (International Federation of Gynecology and Obstetrics) IIIC, and conducted a systematic literature review for published cases of AFP-producing clear cell type EOC. To our knowledge, this is the first literature review of AFP-producing clear cell type EOC.

A 52-year-old menopausal woman complained of intermittent vaginal spotting for 1 month. She denied any systemic disease, dysmenorrhea, menorrhagia, body weight loss, abdominal pain, or abdominal fullness. Gynecologic history was gravida 2 and para 2. Transvaginal ultrasound revealed a 10-cm multi-lobular cystic pelvic mass containing the mixed heterogeneous solid component, fluid and papillary growth in the inner surface of cystic wall Significant venous flow was detected in the solid part and papillary growth lesion. Serum AFP (< 20 ng/ml), cancer antigen (CA)-125 (< 35 U/ml), and carcinoembryonic antigen (< 5 ng/ml), and CA19–9 (< 37 U/ml) were 60,721, 38.1, 84, and 97 ng/ml, respectively. All of these tumor markers from serum have their own specific cut off values and sensitivities, and they come from the same assay methods and from the same laboratory. All are elevated. Computed tomography (CT) showed a 9-cm heterogenous mass probably developed from the left adnexa (Fig. 1a, b) and a 4-cm well-defined mass located at the right subphrenic region (Fig. 1c, d), suggesting the diagnosis of left ovarian carcinoma with peritoneal seeding.

The patient underwent optimal debulking surgery, including total hysterectomy, bilateral salpingo-oophorectomy, omentectomy, pelvic lymphadenectomy, and para-aortic lymphadenectomy (Fig. 2a, b). All gross tumors were almost completely resected. Histologically, sections of the left ovarian tumor showed a clear cell carcinoma (Fig. 3a). The tumor is composed of polygonal, cuboidal to columnar cells with clear cytoplasm arranged in solid nests and tubule-cystic growth patterns. Numerous hyaline globules are present. Some tumor cells also showed high-grade anaplastic nuclear features. Right ovarian tumor showed metastatic clear cell carcinoma (Fig. 3b). Typical yolk sac tumor differentiation and Shiller-Duval body were absent. Sal-like protein 4 (SALL4) was strongly positive (Fig. 3c). Immunohistochemically, the tumor cells were positive for glypican-3 (GPC3) and AFP and negative for CD30. Meanwhile, the tumor cells showed weak positive staining for hepatocyte nuclear factor1-beta (HNF-1beta) (Fig. 4). The tumor cells were focally positive for cytokeratin (CK) 20 and Cdx2 (caudal type homeobox 2) and negative for CK7 (Fig. 4). To rule out potential artifacts due to antibody issues, we titrated the antibody used for AFP staining (Fig. 5a). For every immunohistochemical stain, positive controls were included. As a negative control, we also stained the classical clear cell carcinoma (Fig. 5b). Combination of all made a diagnosis of AFP-producing clear cell type EOC with fetal gut differentiation, FIGO (International Federation of Gynecology and Obstetrics) IIIc.

After surgery, the patient received adjuvant multi-agent chemotherapy (carboplatin and paclitaxel). After treatment, CT showed a 2-cm hypodense nodule at the right subphrenic region and wedge-shaped hypoperfusion over segment 7 of the liver, suspicious tumor seeding, and liver metastasis (Fig. 6a) and serum level of AFP was 1831 ng/ml. Tumor excision for liver metastasis was done. Dose-intensity chemotherapy with weekly paclitaxel was given. CT scan, 1 year later, showed a lobulated mixed solid and cystic lesion at the right paracolic gutter measuring 5 cm in size in favor of peritoneal seeding (Fig. 6b). Exploratory laparotomy was done, including the use of Cavitron Ultrasonic Surgical Aspirator. After operation, chemotherapy was given through intraperitoneal route. After additional 18 months, tumor recurrence was found, including persistent liver metastases (Fig. 6c, d), with increasing serum level of AFP of 330,014 ng/ml. The patient finally died of disease.

Production of AFP in tumors us often found in the germ cell tumors, particularly yolk sac tumor [4, 5]. AFP is also secreted in other tumors such as hepatocellular carcinoma and testicular carcinoma [6]. Epithelial ovarian cancers had been rarely reported to secrete AFP [7, 8], and AFP-producing EOCs are also extremely rare. Meguro et al. reported a comprehensive review addressing the topic of AFP-producing ovarian tumors with germ cell differentiation in postmenopausal women [9]. A total of 18 cases were included, and all patients were middle-aged (57–76 years). Histopathological findings were varied as follows: 9 hepatoid carcinoma [10‐16], 4 endometrioid adenocarcinoma [8, 17‐19], 3 mucinous adenocarcinoma [7, 20, 21], 2 serous adenocarcinoma [22, 23], 1 clear cell carcinoma [1], and 1 uncertain [24].

Histopathological examination in the current case showed tumors largely comprising clear cells and lacking the germ cell tumor component. The tumor was composed of polygonal, cuboidal to columnar cells with fetal gut differentiation. The CK7/CK20 pattern of the tumors is the most helpful immunochemical marker because the CK7-/CK20+ pattern is typical of the diagnosis of colorectal adenocarcinomas [25]. Cdx2, a critical nuclear transcription factor for intestinal development, is expressed in intestinal epithelium and adenocarcinomas [26]. The presence of Cdx2 in the current case report was indicative of fetal gut differentiation. These cells in the current case were positive for GPC3 and SALL4, which are known as oncofetal proteins expressed in germ cell tumors [3, 27], contributing to the need of additional immunohistochemical staining for differentiating germ cell tumors from clear cell type EOC in the current case. HNF-1 beta is a transcription activator that regulates genes expressed specifically in the liver-specific, such as albumin and AFP [28]. HNF-1 beta is reported to serve as clear cell type EOC marker with a high sensitivity [29‐31], especially when the diffuse and strong HNF-1 beta expression pattern is found [30]. In the current case, the diagnosis of clear cell type EOC is based on this finding. Taken together, the combination of morphological and immunohistochemical findings confirmed the diagnosis of AFP-producing ovarian clear cell carcinoma with fetal gut differentiation.

AFP-producing clear cell type EOC has two characteristics: an ovarian clear cell carcinoma with and without typical germ cell tumor. AFP production in some EOCs is attributed to the foci of yolk sac tumors, such as endometrioid adenocarcinoma with a yolk sac component, mucinous adenocarcinoma with a yolk sac component, clear cell adenocarcinoma with a serous adenocarcinoma component, and endometrioid adenocarcinoma with a clear cell component [1, 8, 17, 19, 27].

However, the current case was largely composed of clear cells that lacked the germ cell tumor component. The elevation of serum tumor markers, such as CA-125 and AFP in the current case has been found in previous studies [1, 2]. Similar to Dr. Cetin’s report [1], AFP seemed to be more sensitive for tumor follow-up compared to CA-125. Meanwhile, Takahashi et al. presented a case in which CA-125 elevation was correlated with ovarian clear cell malignancy, and AFP elevation was due to hepatoid differentiation or neometaplasia from clear cell carcinoma [2]. By contrast, Morimoto et al. reported a case of ovarian clear cell adenocarcinoma with elevated AFP without elevated CA-125 [3].

Extensive surgery is the primary treatment modality due to diagnosis of EOC in the current case. Although we followed the current concept to use the combination of platinum and paclitaxel in the management of this patient, which has been shown by Takahashi et al. [2] and Morimoto et al. [3], the patient still died of disease. The possible reason might be related to advanced disease status (FIGO IIIC) [32], clear cell type [33], and AFP-producing component, and all of them might contribute to worse outcome of the current case.

Histopathological and advanced immunohistochemical examination, such as for GPC3, SALL4, and HNF-1 beta are crucial for the current diagnosis of AFP-producing clear cell type EOC with gut differentiation. Due to rarity of similar cases, an optimal treatment, especially for the regimen of chemotherapy is still uncertain.