Summary of the main results
On the basis of 280 cases of primary fallopian tube cancer, this study reveals, for the first time, that abdominal pain and/or distension are the primary clinical manifestations of primary tubal carcinoma, surpassing the incidence of painless vaginal discharge. Ultrasound imaging revealed that nearly 30% of patients presented with intrauterine fluid accumulation. In cases where the lesion is located primarily in the fallopian tubes, the lesion diameter and serum CA-125 levels are significantly lower than those in cases where the lesion is located primarily in metastasis sites such as the ovaries, demonstrating a characteristic pattern of “small primary lesion, large metastatic lesion.”
Results in the context of published literature
To the best of our knowledge, this study is currently the largest sample size study describing the clinical and ultrasonic characteristics of fallopian tube carcinoma [
16‐
19]. There has been only one comprehensive retrospective study on the clinical and ultrasound characteristics of tubal tumors, which included a sample size of 79 [
17]. This study expands the sample size to more than three times that of previous studies, thereby enhancing the reliability of the data. On the basis of previous research [
17], we summarized the clinical features and ultrasound imaging characteristics of fallopian tube cancer. Most findings, including age, postmenopausal status, anamnestic data, serum CA125 concentration, and histological type, were consistent with those of previous reports. However, some differences were discovered.
First, we observed a lower proportion of asymptomatic patients (approximately 42%) than that reported earlier (approximately 62%) [
17]. Additionally, we found that patients presenting with abdominal pain or bloating constituted approximately 35% of the total population, ranking as the most common symptom among patients, rather than the textbook summary of abnormal vaginal bleeding or discharge [
20]. The abdominal symptoms may be due to local fallopian tube dilation and fluid accumulation caused by lesion proliferation in the early stages. Severe secretions from lesions that accumulate in the uterine cavity may also cause lower abdominal discomfort. In advanced stages, abdominal discomfort may be due primarily to the formation of ascites, accompanied by some gastrointestinal symptoms.
Second, in terms of sonographic feature findings, we noted that significantly more patients with bilateral lesions (32.12%) than previously reported (11.24%) [
17]; however, most patients reported unilateral carcinomas. The lesion morphology of the sonographic images was consistent with that in a previous report [
17] and varied from sausage shaped and irregular to oval. However, in this previous report, a “sausage-shaped” appearance, including a sausage-shaped cystic structure with solid tissue protruding into it such as a papillary projection and with a larger solid component filling part of the cyst cavity, accounted for a significant proportion of fallopian tube carcinomas (39%). In the present study, with more cases included, we found that such a “sausage-shaped” appearance was rather rare and constituted less than 10% of primary fallopian tube carcinomas. Even in cases where the fallopian tube was the predominant site of the lesion, sonographic manifestations could appear as ovoid or irregular configurations. All lesions presented at least G2 blood flow signals on color Doppler imaging. These findings underscore the marked heterogeneity in sonographic presentations of fallopian tube carcinomas, highlighting the need for clinicians to remain vigilant regarding non-sausage-shaped, highly vascularized lesions, which may also represent malignant pathologies of tubal origin.
Third, we identified nearly 30% of primary tubal carcinoma patients whose endometrial fluid was reported via ultrasonic examination. This feature has not been well described in previous clinical and sonographic studies regarding primary fallopian tube carcinoma. However, it was clearly described in imaging studies of primary fallopian tube cancer via pelvic MR [
21,
22]. Owing to the characteristic serous fluid secretion of serous tumors, intrauterine fluid accumulation can be effectively attributed to the serous fluid secreted by cancerous cells being decompressed via the isthmus of the fallopian tubes into the uterine cavity. This feature is absent in primary ovarian cancer, making it a good feature for differentiating primary fallopian tube cancer from primary ovarian cancer.
Furthermore, we also demonstrated that the ultrasonic diagnosis of fallopian tube cancer reveals a characteristic pattern of "small primary lesion, large metastatic lesion." Specifically, lesion size is greater in the ovary or other pelvic metastasis locations than in the fallopian tube. Serum CA125 levels are significantly higher in cases where the primary lesions are located at metastatic sites than in those where the primary lesions are found in the fallopian tubes. These findings can be explained by the fact that fallopian tube carcinomas originate from epithelial lesions at the fimbriated end of the tube. Larger metastatic lesions may emerge at secondary sites even when primary lesions remain inconspicuous. In clinical practice, when mild elevations in serum CA-125 levels are observed alongside suspicious pelvic masses, ultrasound specialists must assess multiple ultrasound findings carefully to evaluate the likelihood of tubal cancer, with the exception of benign and malignant ovarian tumors [
23]. As one of the most conventional screening methods, CA125 is the most sensitive tumor marker and prognostic factor for primary fallopian tube carcinoma in high-grade serous carcinoma [
24]. Recent advances in high-grade serous carcinoma research have led to the development of more precise detection methods [
25]. These include blood tests for tumor DNA, glycoproteins, autoantibodies, and microRNAs, along with cervical/uterine sampling for tumor cell analysis and tubal cytology. While these techniques show promise, most remain in the experimental stage owing to challenges in standardization and practical implementation. The CA125 level remains one of the most easily accessible and useful clinical screening indicators.
In the context of this study, only 67.15% of the ultrasound reports accurately described the location of the primary fallopian tube cancer lesions, which was consistent with the intraoperative observations. We propose that the results may be attributed to several factors. First, differentiating the origin of adnexal masses is challenging, as fallopian tube and ovarian lesions often share similar ultrasonographic features and are anatomically close in position. Additionally, concurrent benign conditions such as uterine fibroids, benign ovarian cysts, and hydrosalpinx can obscure the accurate identification of the lesion’s origin. Furthermore, the characteristic “small primary tumor and large metastasis” presentation of fallopian tube cancer often leads to widespread abdominal metastasis. Particularly in the presence of ascites, the lesions tend to be more dispersed, and similar-sized lesions may be present with no distinct primary lesion. These findings indicate that when a pelvic malignancy is suspected, sonographers should meticulously examine all suspicious areas of the abdominal cavity and accurately detail their relationships with surrounding tissues.