Ovarian serous tumors belong to ovarian epithelial tumors, and it is widely recognized in recent years that ovarian epithelial tumors originate from the surface epithelium-mesenchyme of the ovary. This epithelium and peritoneal mesothelium both come from coelomic epithelium, and they participate in the formation of the Mullerian duct during the embryonic period. The pathogenesis and metastasis pathways are as follows.
I. Pathogenesis of Ovarian Serous Tumors
1. Serous benign cystadenoma:
① Unilocular serous cystadenoma: Due to its appearance as a unilocular thin-walled cyst, it is often called a simple cyst (simplecyst). The tumor surface is smooth, the wall is thin, and the size ranges from several centimeters to tens of centimeters. The section is a single cystic cavity, with a smooth inner wall, and sometimes flat scattered blunt papillae can also be seen. The fluid in the cyst cavity is transparent, pale yellow, serous, and occasionally contains sticky mucus. The epithelium is a single layer of cuboidal or columnar, often containing a small amount of tubal epithelium.
② Multilocular serous cystadenoma or serous papillary cystadenoma: The cystic cavities are separated by fibrous tissue into multiple chambers, the surface can be nodular, and the size and texture depend on the size of the cyst and the tension of the cyst fluid. Generally, the capsule is slightly thick, grayish-white, and smooth; papillary growth can be seen within the chambers, and the papillae can be endophytic, exophytic, or both. The epithelium is mostly tubal type, with orderly arrangement of cells, uniform size, and no nuclear division. Sand grains can sometimes be seen between the tumor stroma and the papillae.
③ Serous surface papilloma: Less common, characterized by all papillae being exophytic, of unequal size, and under the microscope, ovarian stroma or fibrous tissue can be seen, covered with a single layer of cuboidal or low columnar epithelium, with some cells having cilia. Although these tumors are benign, the epithelial cells can fall off, implant on the surface of the peritoneum or pelvic organs, and even lead to ascites. Clinically, attention should be paid to this.
④ Fibrocystic adenoma and adenofibroma: Derived from the ovarian germinal epithelium and its stroma, adenofibroma is mainly fibrous stroma, mostly solid, with a small amount of scattered small cystic cavities; cystic adenofibroma accounts for half or most of the substance, the rest is larger cystic cavities. Both are benign, with an average size of 9 cm, usually unilateral. Occasionally, there are clusters of polygonal large cells in the stroma, which are flavinized follicular membrane cells, and the cystic cavities are covered with a single layer of cuboidal or columnar epithelium.
2. Borderline serous tumors:Similar to benign serous cystadenoma, but with more papillary protrusions, larger in size, and more opportunities for bilateral occurrence than benign.
Microscopic observation: ① Epithelial hyperplasia does not exceed 3 layers, can also hyperplasia in clusters. There are often papillae formation, with fewer branches, and the surface epithelium does not exceed 3 layers. ② The nuclei are atypical, deeply stained, but limited to below moderate range. ③ Nuclear division is rare, with no more than one in a high-power field. ④ There is no stromal infiltration.
3. Serous carcinoma:① Serous adenocarcinoma, serous papillary adenocarcinoma, and serous papillary cystadenocarcinoma: Serous adenocarcinoma is a malignant tumor of the mucosal epithelium of the Mullerian duct, whose cancer cells are often characterized by the formation of cystic cavities and papillae, but still retain the original tissue morphology to some extent. Some tumors form large and irregular small cystic cavities, and sometimes the epithelium protrudes into the cavity to form epithelial clusters or papillae. ② Malignant adenofibroma and cystic adenofibroma: There is no distinction in appearance from benign adenofibroma, and under the microscope, the epithelial components are malignant, with active nuclear division, or irregularly sized cystic cavities, or solid tumors, etc.
II. Metastatic Routes of Ovarian Serous Tumors
1. Direct Diffusion:Serous papillary cystadenocarcinoma has more opportunities for direct spread and diffusion, such as peritoneum, peritoneal wall peritoneum, and peritoneum of abdominal cavity organs, including diaphragm, omentum, small intestine, rectum, rectouterine pouch, colon, vesicouterine peritoneum, and serous layer of fallopian tube and uterus. About 2/3 of patients have ascites, and the symptoms caused by it have been described as mentioned above. Some patients may have no discomfort at all, just feeling an increase in abdominal circumference. Whether there is ascites is very related to prognosis. Recent reports show that the 5-year survival rate of stage III and IV ovarian cancer without ascites is 5 times higher than that with ascites. The formation of ascites is related to lymphatic obstruction (mainly the right lateral diaphragmatic lymphatic vessels), stimulation of the peritoneum, and unbalanced fluid flow in the abdominal cavity. Cancer cells can not only implant with the flow of fluid, but also the site of abdominal puncture for ascites can appear growth of cancer tumors, forming subcutaneous small nodules or masses. Some patients are misdiagnosed as tuberculous peritonitis and liver cirrhosis due to ascites, and the cancer implantation mass at the puncture site has not yet been able to raise alarm.
2. Lymphatic metastasis:Lymphatic metastasis has the highest incidence in serous papillary carcinoma of the ovary, higher than that of mucinous carcinoma. Pathological grading seems to have little effect, while clinical staging with retroperitoneal lymph node metastasis is classified as stage IIIc. The rate of metastasis in pelvic lymph nodes and para-aortic lymph nodes is similar.
3. Hematogenous spread:In the past, it was thought that there were not many metastases in the lung and liver parenchyma through hematogenous spread, but recent reports are not rare, and even after surgery and chemotherapy for a certain period of time, there are also cases of recurrence of metastasis.