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. 2018 Jul 30;119(4):462–470. doi: 10.1038/s41416-018-0191-x

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — a Histopathology of ovarian tumour subtypes (×400): Serous carcinoma. Most frequent ovarian carcinoma. It can be either high grade (type 2) or low grade (type 1). Endometrioid carcinoma. Can be either high grade (type 2) with few glandular spaces, or low grade (type 1) with glandular spaces suggestive of endometrial glands. Clear cell carcinoma. This type 1 carcinoma contains cells with clear cytoplasm. Mucinous carcinoma. Mucin containing cells in this type 1 carcinoma are arranged in a disorderly fashion. Serous borderline. Tumour cells contain eosinophilic or amphophilic cytoplasm and are columnar or cuboidal in shape and line a cystic cavity in an orderly fashion. Mucinous borderline. Tumour cells are orderly in their arrangement, line a cystic cavity, and contain much mucin, which maybe either eosinophilic or basophilic. b Kaplan–Meier survival analysis demonstrates that patient survival depends upon ovarian tumour type, grade, and FIGO stage (p < 0.0001)