Xie Dong, Jiang Ge-ning, Chen Xiao-feng, Xu Zhi-fei, You Xiao-fang, Ding Jia-an
Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University, Shanghai 200433, China.
Zhonghua Wai Ke Za Zhi. 2012 Feb 1;50(2):120-3.
To investigate the clinicopathological features and surgical treatment of pulmonary sclerosing hemangioma (PSH).
Clinic data of PSH patients admitted by surgical resection from January 1985 to December 2010 was analyzed retrospectively. One hundred and sixty-five patients were enrolled in the study. There were 27 male and 138 female patients with a mean age of (48 ± 13) years. Seventy-nine patients were asymptomatic at the time of diagnosis. Eighty-nine tumors arose in the right lung (27 in right upper lobe, 24 in right middle lobe, 34 in right lower lobe, 2 in right upper lobe with invasion of right middle lobe, 1 in right middle lobe with invasion of right lower lobe, and 1 case with multiple lobe lesions), 75 in the left (33 in left upper lobe, 42 in left lower lobe), and 1 in the bilateral. There were huge mass lesions in 2 cases, endobronchial lesions in 2 cases, and multiple lesions in 6 cases. The mean size of the lesion was (2.6 ± 0.9) cm (ranging from 0.9 to 10.0 cm). Forty-eight cases (29.1%) were misdiagnosed as malignancies preoperatively, and 41 cases (24.8%) were misdiagnosed intraoperatively.
Resections were performed by means of video-assisted thoracoscopy (n = 53) and thoracotomy (n = 112). Surgical resection included pulmonary wedge excision in 61 patients, lobectomy in 89 patients, right bilobectomy in 5 patients, anatomic segmentectomy in 2 patient, enucleation in 6 patients, and synchronous bilateral pulmonary wedge resection in 1 patient. Operative mortality and morbidity occurred in 0 and 2 (4.3%) patients, respectively. Mean follow-up was 34.7 months (ranging from 6 to 62 months). There was no local recurrence or death from PSH.
PSH is a rare benign lung tumor. It is difficult to make accurate diagnosis preoperatively, and sometimes even intraoperative frozen sections can't differentiate it from malignant tumors. Surgical resection is usually indicated for definite diagnosis and treatment. Partial resection is a sufficient treatment in view of uncommon tumor recurrence. Thoracoscopic surgery is recommended for PSH.
探讨肺硬化性血管瘤(PSH)的临床病理特征及外科治疗方法。
回顾性分析1985年1月至2010年12月因手术切除收治的PSH患者的临床资料。本研究共纳入165例患者。其中男性27例,女性138例,平均年龄(48±13)岁。79例患者诊断时无症状。89个肿瘤位于右肺(右上叶27个,右中叶24个,右下叶34个,右上叶侵犯右中叶2个,右中叶侵犯右下叶1个,多叶病变1例),75个位于左肺(左上叶33个,左下叶42个),双侧1例。2例为巨大肿块病变,2例为支气管内病变,6例为多发病变。病变平均大小为(2.6±0.9)cm(范围0.9至10.0 cm)。48例(29.1%)术前误诊为恶性肿瘤,41例(24.8%)术中误诊。
采用电视辅助胸腔镜手术(n = 53)和开胸手术(n = 112)进行切除。手术切除包括61例行肺楔形切除术,89例行肺叶切除术,5例行右双叶切除术,2例行解剖性肺段切除术,6例行肿瘤摘除术,1例行同期双侧肺楔形切除术。手术死亡率为0,手术并发症发生率为2例(4.3%)。平均随访34.7个月(范围6至62个月)。无PSH局部复发或死亡病例。
PSH是一种罕见的肺部良性肿瘤。术前难以做出准确诊断,有时甚至术中冰冻切片也无法将其与恶性肿瘤区分开来。手术切除通常用于明确诊断和治疗。鉴于肿瘤复发不常见,部分切除是一种充分的治疗方法。推荐对PSH行胸腔镜手术。