Department of Gynecologic Oncology, Medical University Pleven, 5800 Pleven, Bulgaria.
Department of Surgical Oncology, Medical University Pleven, 5800 Pleven, Bulgaria.
Medicina (Kaunas). 2020 Jan 18;56(1):37. doi: 10.3390/medicina56010037.
Adenosquamous cancer of the uterine cervix is a rare type of cervical cancer with both malignant squamous and glandular components. A very rare subtype is mucoepidermoid carcinoma (MEC), which was first described as a salivary gland tumor. It has been described as having the appearance of a squamous cell carcinoma without glandular formation and contains intracellular mucin. The postoperative evolution of this tumor and the potentially poorer prognosis may indicate an intensification of the follow-up. The objective of our study was to analyze the frequency of mucoepidermoid carcinoma in hospitalized women with cervical cancer, clinical characteristics and prognosis. A retrospective study of all cases of mucoepidermoid carcinoma of the cervix at Department of Gynecologic Oncology,University Hospital-Pleven, Pleven Bulgaria between 1 January 2007 and 31 December 2016 was performed. All patients were followed-up till December 2019. We analyzed certain clinical characteristics of the patients; calculated the frequency of mucoepidermoid carcinoma of the cervix from all patients with stage I cervical cancer; and looked at the overall survival rate, correlation between overall survival, lymph node status and the size of the tumor. The frequency of MEC was 1.12% of all patients with stage I cervical cancer in this study. The median age of the patients with MEC was 46.7 years (range 38-62). Four patients (57.1%) were staged as FIGO IB1, and three patients (42.8%) were FIGO IB2. The size of the primary tumor was <2 cm in 2 patients (28.57%), 2-4 cm in 2 patients (28.57%) and >4 cm in 3 patients (42.8%). Metastatic lymph nodes were found in two patients (28.57%), and nonmetastatic lymph nodes were found in five patients (71.43%). There were two (28.57%) disease-related deaths during the study period. The five-year observed survival in the MEC group was 85.7% and in the other subtypes of adenosquamous cancer group was 78.3%. MEC of the uterine cervix is a rare entity diagnosis. As a mucin-producing tumor, it is frequently regarded as a subtype with worse clinical behavior and patients' outcomes. Nevertheless, our data did not confirm this prognosis. New molecular markers and better stratification are needed for better selection of patients with CC, which may benefit more from additional treatment and new target therapies.
宫颈的腺鳞癌是一种罕见的宫颈癌类型,具有恶性鳞状和腺体成分。一种非常罕见的亚型是黏液表皮样癌(MEC),它最初被描述为一种唾液腺肿瘤。它的外观表现为没有腺体形成的鳞状细胞癌,但含有细胞内黏液。这种肿瘤的术后演变和潜在的较差预后可能表明需要加强随访。我们的研究目的是分析在保加利亚普列文大学医院妇科肿瘤学系住院的宫颈癌患者中 MEC 的频率、临床特征和预后。 对 2007 年 1 月 1 日至 2016 年 12 月 31 日期间在保加利亚普列文大学医院妇科肿瘤科诊断为宫颈 MEC 的所有病例进行了回顾性研究。所有患者均随访至 2019 年 12 月。我们分析了患者的某些临床特征;计算了 MEC 在所有 I 期宫颈癌患者中的频率;并观察了总生存率、总生存率与淋巴结状态和肿瘤大小的相关性。 在本研究中,MEC 在所有 I 期宫颈癌患者中的频率为 1.12%。MEC 患者的中位年龄为 46.7 岁(范围 38-62 岁)。4 名患者(57.1%)分期为 FIGO IB1,3 名患者(42.8%)分期为 FIGO IB2。原发肿瘤大小<2cm 者 2 例(28.57%),2-4cm 者 2 例(28.57%),>4cm 者 3 例(42.8%)。2 例(28.57%)患者发现转移性淋巴结,5 例(71.43%)患者发现非转移性淋巴结。研究期间有 2 例(28.57%)与疾病相关的死亡。MEC 组的 5 年观察生存率为 85.7%,其他腺鳞癌组的 5 年观察生存率为 78.3%。 宫颈 MEC 是一种罕见的实体诊断。作为一种产生黏液的肿瘤,它常被认为是一种具有更差临床行为和患者预后的亚型。然而,我们的数据并未证实这一预后。需要新的分子标志物和更好的分层,以便更好地选择宫颈癌患者,这些患者可能受益于额外的治疗和新的靶向治疗。