The anatomical position of the ovaries and the delayed onset of symptoms in ovarian cancer are the main reasons for the high mortality rate. The application of vaginal sonography alone or in combination with Ca125 does not seem to reduce the OC mortality rate significantly, while it increases the number of unnecessary laparoscopies/laparotomies [2, 3]. Hence, the need for a better method of detection of OC at an early stage is necessary. At this stage, the application of an OC detection screening program looks remote. Studies have shown that the application of vaginal sonography and Ca125 serum levels is more efficient for this special group of patients [2], but, again, in order to establish the diagnosis at least with a biopsy implies an invasive procedure with anesthesia with a substantial financial cost and psychological distress for the patient.
Imaging procedures like 3D-ultrasound, color Doppler studies, computerized tomography scanning or magnetic resonance imaging give excellent resolution and are very helpful in identifying an ovarian lesion. However, for the final diagnosis an open biopsy is still necessary. Recently, the fractal dimensions of outlines of sonographically depicted solid components in 160 ovarian tumors were measured using a box-counting method. This study showed that the surface of solid components in cystic epithelial ovarian cancers has a fractal structure and may require different treatment strategies [8]. Of course, there is still the question whether ovarian cancer initiates from the ovarian core or from the surface. The two basic theories generally accepted by the majority of gynecologists worldwide are: (1) the theory of “incessant ovulation,” i.e., the switching on and off of cell growth inducing the potential of uncontrolled growth [9] and (2) the theory of “ovulatory age,” the more ovulations the greater the risk of developing ovarian cancer [10]. Both theories support the fact that OC initiates from the ovarian cortex surface. The chance to depict ovarian lesions at a very early stage, before even stage I, by imaging techniques has not been tried because it seems unrealistic.
Recently, Leeper et al. reported an increased frequency of occult ovarian carcinomas after prophylactic oophorectomy specimens in high-risk women and concluded that (1) the fallopian tubes and the ovaries should be entirely submitted for histopathological serial sections and (2) that laparoscopy and laparotomy are the surgical modalities of choice to allow inspection of the peritoneal surfaces at the time of prophylactic oophorectomy and collection of fluid for cytologic evaluation [11].
Under these circumstances TVL seems to be an attractive method for examining the adnexae, but also the whole pelvis of women at high risk of OC. In TVL the tissues inspected are floating in normal saline, providing better and more accurate visualization since pelvic lesions can be demonstrated that could not be identified by laparoscopy or laparotomy. Brosens et al. in 2001 reported the diagnosis of micro, filmy adhesions and endometriosis foci within the fallopian tubes and the ovaries that could not be diagnosed by laparoscopy [5].
The problem of spreading the disease after biopsy of a lesion suspected of OC during TVL is of primary importance. However, frozen section or a switch to laparotomy in these cases can be an option. In this case report we can conclude that the method of trans-vaginal laparoscopy enabled direct visualization of the ovaries and pelvis, whereby the cytology obtained excluded pelvic/ovarian malignancies.