Wang H P, Shi J H, Zhang L
Department of Respiratory Medicine, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
Zhonghua Nei Ke Za Zhi. 2017 Jul 1;56(7):490-494. doi: 10.3760/cma.j.issn.0578-1426.2017.07.004.
Pulmonary benign metastasizing leiomyoma (PBML) is a rare entity that leiomyoma of uterus metastasized to the lung. The clinical characteristics of this rare disease were analyzed in this article. The detailed clinical records of 7 patients diagnosed as PBML at Peking Union Medical College Hospital between January 2001 and June 2015 were reviewed. All patients were women with median age of 44 years (range 28-62). Symptoms included dyspnea (2/7), chest pain (1/7), cyanosis (1/7), cough (1/7) and bloody sputum (1/7), while 4/7 cases were asymptomatic. Six patients had the past-history of leiomyoma of uterus 20 months to 14 years ago among whom 5 patients received hysterectomy. Chest CT showed bilateral, random-distributed multiple round solid nodules, or diffuse-distributed miliary nodules, or single solid nodule, even some small cavities. Extra-pulmonary metastasis was found in left superclavicular lymph node (1 case) and right heart (1 case). Histological tissues were obtained by video-assisted thoracic surgery lung biopsy (4/7), mass resection on tricuspid valve (1/7), transbronchil lung biopsy (1/7), and CT-guided percutaneous lung biopsy (1/7). Pathology showed an interlacing pattern by spindle cells having elongated nuclei without cellular atypia. Ki-67 index was less than 1%. Molecules such as smooth muscle antibody, estrogen receptor (ER) and progestrone receptor (PR) were positive in immunohistochemistry staining. Neither letrozole nor zoladex was effective. Two patients responded to bilateral adnexectomy, presenting as shrunk nodules. No relapsed disease was seen in one patient with single nodule after resection. There was only one patient with disease-related mortality, whose chest CT showed milliary nodules. Although CT findings of PBML are similar to malignancies, the clinical outcome is good. Despite the positive expression of ER and PR, the effectiveness of hormone related treatment is limited. And periodical follow up is suggested even to those uneventful patients.
肺良性转移性平滑肌瘤(PBML)是一种罕见的疾病,即子宫平滑肌瘤转移至肺部。本文分析了这种罕见疾病的临床特征。回顾了2001年1月至2015年6月期间在北京协和医院诊断为PBML的7例患者的详细临床记录。所有患者均为女性,中位年龄44岁(范围28 - 62岁)。症状包括呼吸困难(2/7)、胸痛(1/7)、发绀(1/7)、咳嗽(1/7)和咯血(1/7),而4/7的病例无症状。6例患者有20个月至14年前子宫平滑肌瘤病史,其中5例接受了子宫切除术。胸部CT显示双侧、随机分布的多个圆形实性结节,或弥漫分布的粟粒样结节,或单个实性结节,甚至一些小空洞。肺外转移见于左锁骨上淋巴结(1例)和右心(1例)。通过电视辅助胸腔镜肺活检获取组织学标本(4/7)、三尖瓣肿物切除术(1/7)、经支气管肺活检(1/7)和CT引导下经皮肺活检(1/7)。病理显示为梭形细胞呈交错排列,细胞核细长,无细胞异型性。Ki-67指数小于1%。免疫组化染色显示平滑肌抗体、雌激素受体(ER)和孕激素受体(PR)等分子呈阳性。来曲唑和戈舍瑞林均无效。2例患者双侧附件切除术后有反应,表现为结节缩小。1例单个结节切除术后未见疾病复发。只有1例患者死于与疾病相关的原因,其胸部CT显示粟粒样结节。尽管PBML的CT表现与恶性肿瘤相似,但其临床预后良好。尽管ER和PR呈阳性表达,但激素相关治疗的有效性有限。即使是病情平稳的患者也建议定期随访。