Li Lin, Zhang Rong, Wu Ling-ying, Bai Ping, Li Shu-min, Li Hong-jun, Li Xiao-guang
Department of Gynecologic Oncology, Cancer Institute and Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100021, China.
Zhonghua Fu Chan Ke Za Zhi. 2012 Oct;47(10):747-50.
To analyze the clinical characteristics, diagnoses, treatments and prognoses of vaginal leiomyosarcoma (LMS).
The clinical and pathological recordings of 9 patients suffering from vaginal leiomyosarcoma from January 1973 to May 2011 were analyzed retrospectively.
The study group constituted 2.7% (9/330) of all the malignant vaginal tumor admitted to our hospital in the same period. The major clinical manifestations were asymptomatic vaginal mass (3/9), bellyache and vaginal bleeding (2/9), vaginal pain (2/9), and difficulty in defecation (1/9) and micturition (1/9). Preoperative diagnosis was highly unreliable. Based on the sample chose, the diagnosis were made in 3 cases by preliminary biopsy before undertaking surgery, while 6 cases were confirmed shortly after simple tumor excision or unexpected recurrence. All the patients were pathologically confirmed diagnosis by tumor resection specimen or biopsy, 5 cases of them were also confirmed by virtue of immunohistochemistry staining. All 9 patients, 8 cases received initial surgery, four of them patients received postoperative adjuvant chemotherapy or radiation therapy, the remaining 1 patients received initial chemotherapy and radiotherapy. Follow-up was performed for all the 9 patients, of which 3 cases were lost, the median follow-up time was 50 months (range 7 - 134). Four patients underwent local recurrence and adjacent organ metastases within two years, with 5 years survival rate 4/9.
Primary vaginal leiomyosarcoma is a rare and difficult to diagnose preoperatively tumor. In this regard, It is strongly recommend preoperative biopsy for definitive diagnosis and perform surgery as the principal approach, in conjunction with radiotherapy or chemotherapy when needed to improve survival.
分析阴道平滑肌肉瘤(LMS)的临床特征、诊断、治疗及预后。
回顾性分析1973年1月至2011年5月间9例阴道平滑肌肉瘤患者的临床及病理记录。
研究组占同期我院收治的所有阴道恶性肿瘤的2.7%(9/330)。主要临床表现为无症状阴道肿物(3/9)、腹痛及阴道出血(2/9)、阴道疼痛(2/9)、排便困难(1/9)及排尿困难(1/9)。术前诊断极不可靠。根据所选样本,3例在手术前行初步活检后确诊,6例在单纯肿瘤切除或意外复发后不久确诊。所有患者均经肿瘤切除标本或活检病理确诊,其中5例还通过免疫组化染色确诊。9例患者中,8例接受了初次手术,4例患者接受了术后辅助化疗或放疗,其余1例患者接受了初次化疗和放疗。对所有9例患者进行了随访,其中3例失访,中位随访时间为50个月(范围7 - 134个月)。4例患者在两年内出现局部复发及邻近器官转移,5年生存率为4/9。
原发性阴道平滑肌肉瘤是一种罕见且术前难以诊断的肿瘤。对此,强烈建议术前行活检以明确诊断,并以手术作为主要治疗方法,必要时联合放疗或化疗以提高生存率。