Institute of Endocrinology, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Cancer. 2012 Feb 1;118(3):612-9. doi: 10.1002/cncr.26200. Epub 2011 Jul 12.
Normal adult lungs contain pulmonary neuroendocrine cells (PNECs). PNEC hyperplasia may be either reactive or idiopathic, and the idiopathic type is defined as diffuse idiopathic PNEC hyperplasia (DIPNECH). It is believed that DIPNECH is a neuroendocrine proliferative process associated with carcinoid tumors. The available data regarding this rare condition are very limited. The objective of the current study was to describe the clinical, radiologic, and pathologic characteristics of patients with DIPNECH and the effect of various therapeutic modalities on patient well being.
The authors retrospectively studied 11 consecutive patients with DIPNECH who were followed at 2 referral centers in Israel between 2000 and 2010.
All patients were women, and their median age was 62.8 years. Six patients presented with respiratory symptoms, such as prolonged dyspnea, wheezing, and cough. All patients had carcinoid tumor together with multiple, small pulmonary nodules observed on thoracic high-resolution computerized tomography images. The mean size of the dominant lesion was 19.4 ± 9.6 mm. Nine patients underwent thoracotomy and resection of the dominant lesion. The disease was stable in 5 of 11 patients; in 6 of 10 patients, it progressed, and the patients received treatment with somatostatin analogs, which induced disease stabilization in all patients. Metastatic disease was diagnosed in 3 of 11 patients (36%). All patients were alive at the end of follow-up (mean, 4.63 ± 2.04 years; ongoing).
The association of lung neuroendocrine tumor with multiple nodules in women, together with complains of chronic cough and wheezing, should raise suspicion of DIPNECH. Whenever possible, these patients should undergo surgical excision of the dominant lesion, and somatostatin analogs may be considered for symptomatic or tumor control in patients with progressive disease.
正常成人肺部含有肺神经内分泌细胞(PNEC)。PNEC 增生可能是反应性的或特发性的,特发性类型定义为弥漫特发性 PNEC 增生(DIPNECH)。人们认为 DIPNECH 是一种与类癌肿瘤相关的神经内分泌增殖过程。关于这种罕见疾病的现有数据非常有限。本研究的目的是描述 DIPNECH 患者的临床、放射学和病理学特征,以及各种治疗方式对患者健康状况的影响。
作者回顾性研究了 2000 年至 2010 年在以色列 2 个转诊中心接受治疗的 11 例连续 DIPNECH 患者。
所有患者均为女性,中位年龄为 62.8 岁。6 例患者出现呼吸症状,如长时间呼吸困难、喘息和咳嗽。所有患者均患有类癌肿瘤,胸部高分辨率计算机断层扫描图像上可见多个小结节。主要病变的平均大小为 19.4±9.6mm。9 例患者接受了开胸手术和主要病变切除术。11 例患者中 5 例疾病稳定;10 例患者中有 6 例疾病进展,患者接受了生长抑素类似物治疗,所有患者的疾病均稳定。11 例患者中有 3 例(36%)诊断为转移性疾病。所有患者在随访结束时均存活(平均随访时间 4.63±2.04 年;仍在随访中)。
女性肺部神经内分泌肿瘤伴多个结节,伴有慢性咳嗽和喘息的症状,应怀疑 DIPNECH。只要可能,这些患者应行主要病变切除术,对于进展性疾病的患者,生长抑素类似物可用于症状控制或肿瘤控制。