Mitotically active cellular fibroma of the ovary: a case report and literature review

Abstract

Background

The ovarian cellular fibrous tumor with mitotic figure >4 per 10 high power field without moderate to severe atypia is defined as mitotically active cellular fibroma according to the 2014 World Health Organization classification. As this category is new and rare now, we described here a case of MACF and reviewed the literature.

Case

We present a case of mitotically active cellular fibroma of the ovary with 10-year history that was treated with laparoscopic surgery.

Methods

We reviewed the relevant literature using PubMed search system and analyzed the previous cases.

Results

To date, only 5 cases of mitotically active cellular fibroma have been reported. Our patient is the first case of mitotically active cellular fibroma of the ovary treated with laparoscopic surgery.

Conclusion

MACF of the ovary is a newly defined category and few cases have been reported, while prognostic factors have also not yet been fully characterized. Long-term clinical follow-up is necessary.

Background

The ovarian cellular fibrous tumors with mitotic figures >4 per 10 high-power fields (HPF) had been defined as fibrosarcoma [1]. In 2014 World Health Organization (WHO) histological classification, mitotic activity of >4 per 10 HPF in an ovarian cellular fibromatous neoplasm in the absence of moderate to severe atypia is defined as mitotically active cellular fibroma (MACF). As this category is new and rare now, we described here a case of MACF and reviewed systematically the literature for the appropriate treatment.

Materials and methods

We treated a case of MACF, a new diagnostic category, with a long term history. And we searched previous cases using PubMed search system from 1966 to July 2015 with the terms “mitotically active cellular fibroma”, “ovary”, and “fibrosarcoma”. Then we analyzed and clarified that data of the cases have been recorded for finding important factors.

Results

Case description

A 36-year-old woman (gravida 3, para 3) consulted a doctor for further examination of an ovarian tumor. She had been diagnosed with a right-sided 6-cm ovarian tumor 10 years previously, since her first pregnancy at another hospital. Pelvic examination showed an adnexal hard mass without tenderness on the right side. Vaginal echography and pelvic computed tomography (CT) showed a 6-cm ovarian solid tumor. Magnetic resonance imaging (MRI) revealed a 61-mm solid tumor with heterogeneous low signal intensity in the pelvis. As such, a benign tumor such as a fibroma/fibrothecoma or malignant tumor such as a germ cell tumor or lymphoma was suspected (Fig. 1). Serum levels of tumor markers were negative for carcinoembryonic antigen (CEA), CA125, CA19–9, squamous cell carcinoma (SCC), human chorionic gonadotropin (HCG) and alpha fetoprotein (AFP). Laparoscopic surgery was performed to confirm diagnosis and direct treatment after 8 months from the third delivery. Laparoscopic observation revealed that the tumor in the Douglas pouch protruded from the right ovary without adhesion (Fig. 2). Subsequently, right salpingo-oophorectomy was performed. The tumor was cut into small pieces in the bag, which was then extracted from the laparoscopic wound at the umbilicus without scattering in the abdominal cavity. The sectioned surface of the tumor was solid, light-yellow and without hemorrhagic necrosis (Fig. 3). Intraoperative cytology of ascitic fluid was negative, and intraoperative diagnosis of a frozen section revealed benign fibrous tumor as atypical cells were not observed.

Fig. 1

MRI appearance of the tumor. Axial T2-weighted MR image showed a well-circumscribed mass (white arrows) including cystic component (arrowhead) adjacent to the right ovary (black arrow) as having inhomogeneous low signal intensity. Small amount of ascites was noted (*)

Fig. 2

Laparoscopic findings of the tumor. The tumor (white arrows) in the Douglas pouch protruded from right ovary (black arrow) without adhesion

Fig. 3

Macroscopic appearance of resected right oophorosalpinx. The sectioned surface of the tumor was solid and light-yellow without hemorrhagic necrosis. (right ovary: black arrow)

In paraffin sections, the tumor cells were spindle shaped and arranged in intersecting bundles (Fig. 4). They had ill-defined cytoplasmic borders and spindled to ovoid hyperchromatic nuclei with a moderate mitotic rate (10 per 10 HPF) but without significant nuclear atypia (Fig. 5). The cystic lesion was unclear. On immunohistochemistry, vimentin, progesterone receptor (PR), CD10, CD56 and Wilms tumor gene (WT-1) were positive, alpha-inhibin was focally positive, and pan cytokeratin (AE1/AE3), estrogen receptor (ER), calretinin and epithelial membrane antigen (EMA) were negative. Ki-67 index was 8.7 %. Pathologic findings and the case’s long-term clinical history led to the diagnosis of MACF of the ovary. She had a good clinical course after surgery for 6 months.

Fig. 4

Macroscopic appearance of the tumor. The cells are spindle shaped and arranged in intersecting bandles. (bar = 200 μm)

Fig. 5

Macroscopic appearance of the tumor. The cells having spindled to ovoid shaped nuclei with moderate mitotic rate (mitoses: white arrows) but without significant nuclear atypia. (bar = 50 μm)

Review the literature

In connection with ovarian tumor, five cases were found by a PubMed search system and shown in Table 1 [2–6]. Laparotomy was selected in all cases. Long-term local recurrence has also been seen in one case but all cases were alive at time of publication. However, there was no specific tumor marker or immunochemical staining.

Table 1 Cases of mitotically active cellular fibroma of the ovary

Discussion

In the 2003 WHO histological classification, ovarian cellular fibrous tumors with mitotic figures 3 or less per 10 HPF and no severe nuclear atypia were defined as cellular fibroma, while the fibrous tumors with mitotic figures >4 per 10 HPF and severe nuclear atypia were defined as fibrosarcoma. However, ovarian tumors with mitotic figures >4 per 10 HPF but no severe nuclear atypia were not categorized. These kinds of tumors were mostly diagnosed as ovarian fibrosarcoma. However, the clinicopathologic characteristic of this tumor is that it is significantly different from the malignant behaviors of ovarian fibrosarcoma. In 2006, Irving et al. first defined these kind of ovarian tumors as ‘MACF’ [7]. In the 2014 WHO histological classification, a new definition was described: “mitotic activity of 4 per 10 HPFs in an ovarian cellular fibromatous neoplasm in the absence of moderate to severe atypia does not signify a fibrosarcoma. In such cases, a diagnosis of MACF is made.”

To date, only five cases of MACF of the ovary have been reported in the literature. All cases were alive at time of publication. However, there were no specific diagnostic or prognostic factors.

Our patient is the first case of MACF of the ovary treated with laparoscopic surgery. Ovarian benign fibrous tumors such as fibroma/fibrothecomas are often misdiagnosed as uterine myomas and malignant ovarian tumors preoperatively. However, laparoscopic surgery has been used for the management of ovarian fibroma/fibrothecomas [8, 9] and uterine myomas [10]. Histological diagnosis should be very important and include intraoperative consultation. Even if many mitoses are observed, it is imperative that we do not misdiagnose fibrosarcoma, in order to avoid excessive treatment. In our case, the tumor was benign both historically and histologically.

Conclusions

We report a case of MACF with a long term history treated by laparoscopic surgery. MACF of the ovary is a newly defined category and few cases have been reported, while prognostic factors have also not yet been fully characterized. Treatment is still not well established therefore long-term clinical follow-up including image processing, such as echography, CT, MRI etc., is necessary.

Consent

Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.