Submucous uterine adenosarcoma—minimally invasive treatment

Early diagnosis in uterine adenosarcoma is essential because patients’ survival is correlated to the tumour stage. Preoperative physical examination combined with transvaginal ultrasound is not suspicious in most of the cases [2]. Usually, definitive diagnosis of adenosarcoma is achieved only after surgical specimen analysis. Only diagnostic hysteroscopy with intrauterine biopsy or resection allows the histological evaluation of the tumour before definitive hysterectomy and thus a subsequent correct oncologic approach in case of a malignant process. Therefore, especially when hysterectomy with electric morcellation is planned, a hysteroscopy with biopsy could be performed in case of premenopausal submucous lesions in order to differ malignant lesions from benign polyps or myomas. Gonzalez-Bosquet et al. reported one case of hysteroscopic detection of a uterine adenosarcoma in a postmenopausal woman [3] and the diagnosis of an endometrial stromal sarcoma in a 41-year-old woman who presented with bleeding disorders and polypoid masses in ultrasound [4]. Shveiky et al. [5] reported six cases of unexpected malignant uterine mesenchymal tumours. In all cases, the initial hysteroscopic diagnosis erroneously was endometrial polyp or submucous myoma: only pathology revealed the malignancy of the lesions, and thus, all patients underwent complete staging by laparotomy. None of the patients had extrauterine spread of the disease, and at mean follow-up of 21.5 months, all patients were asymptomatic. It plays an important role if the adenosarcoma shows a sarcomatous overgrowth or not. A sarcomatous overgrowth is diagnosed when more than 25 % of the tumour volume is sarcomatous tissue. Gallardo reported that sarcomatous overgrowth was found in 33 % of uterine adenosarcomas. Six out of 29 patients with adenosarcoma developed metastasis. Four of these six patients had adenosarcomas with sarcomatous overgrowth [1]. Schroeder et al. described a systemic therapy in advanced uterine adenosarcoma with sarcomatous overgrowth [6]. Tissue with sarcomatous overgrowth can be detected by immunohistochemical analysis, while the differentiation between adenosarcomas without sarcomatous overgrowth and benign adenofibromas can be difficult. However, a standardized therapeutic approach for adenosarcoma is not yet established. Usually, the treatment is analogue to the therapy of the endometrial stromal sarcoma. In postmenopausal women, the hysterectomy with bilateral adnexectomy and peritoneal staging is the treatment of first choice. In comparison, in premenopausal women, it is possible to save the ovaries. The lymphadenectomy is not established, due to the low rate of lymphatic metastasis. In addition, the lymphatic node status would have no consequence for the adjuvant treatment, as a specific chemotherapy does not exist. Clement et al. reported that radiotherapy has no benefit for the patient in case of adenosarcomas [7]. However, Kaku et al. described that in 31 % of all cases, an extrauterine manifestation of the tumour can be found in the vagina, the lymphatic nodes, the peritoneal cytology or the ovary [8]. In this case of low-grade adenosarcoma without adenosarcomatous overgrowth, we preferred the minimally invasive approach for hysterectomy and staging, as laparotomy has many well-known disadvantages but no benefit in order to carry out a simple hysterectomy with adnexectomy and peritoneal staging. Further studies must show if there is a difference in the prognosis of the disease comparing laparoscopy to laparotomy when staging is realized. It also remains unclear if bilateral adnexectomy should be part of the surgical staging in uterine adenosarcoma. However, in low-grade and high-grade endometrial stromal sarcoma, the bilateral adnexectomy is recommended [9], but ovary-sparing procedures could be considered for young women [10]. In this case of a premenopausal woman, we decided to preserve one ovary and thus the hormonal function. A representative laparoscopic ovarian biopsy did not show any remaining microscopic disease. A second-look laparoscopy after 4 month for ovarian tumour revealed a benign functional cyst.

The main risk factors for recurrence and metastasis in uterine sarcomas are the myometrial infiltration, the tumour size, the extrauterine appearance, the histological tumour type and the presence of sarcomatous overgrowth [8]. The recurrence rate in adenosarcoma without sarcomatous overgrowth is estimated to be 15–25 % respectively and 45–70 % in cases with sarcomatous overgrowth. On a multivariate analysis, Carroll et al. [11] showed that sarcomatous overgrowth and lymphovascular space invasion were predictors of worse progression-free survival and overall survival. Another important prognostic factor is the complete resection (R0) of the sarcoma without intra-abdominal morcellation of the sarcoma. In modern gynaecological minimally invasive surgery, the electric morcellation of uterine tissue in laparoscopic myomectomy or total and subtotal hysterectomy plays an important technical role. The risk of accidental morcellation of occult sarcoma is currently under discussion [12‐14]. The incidence of this rare complication has to be shown by further studies but is estimated to be under 1 %. The steering committee on fibroid morcellation of the European Society of Gyneacological Endoscopy (ESGE) concluded that the prevalence of uterine sarcoma in presumed fibroids is 0.14 % with a range from 0.49 to 0.014 % [15]. However, the patients should be informed about this risk when the use of morcellation is planned and alternative surgical approaches should be discussed. While the intraperitoneal morcellation of submucous uterine sarcomas influences the prognosis of the disease, the role of intrauterine biopsy or resection of adenosarcoma in hysteroresectoscopy on the prognosis of the disease so far remains unclear. In comparison, in endometrial cancer, the diagnostic hysteroscopy with biopsy or curettage is a standard procedure and the eventual diversion of cancer cells with the distension medium through the fallopian tubes to the peritoneal cavity is not seen as a risk factor [16]. As adenosarcomas are rare tumours, it will be difficult to achieve reliable prospective data in studies. A second-look laparoscopy after 6 to 12 months could be an option in order to offer the maximal surgical safety to the patient. It is very important to avoid perforation of the uterine wall in the diagnostic or operative hysteroscopy as a peritoneal metastasis could be the result in case of a malignant lesion.