Aubry Marie-Christine, Thomas Charles F, Jett James R, Swensen Stephen J, Myers Jeffrey L
Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA.
Chest. 2007 Jun;131(6):1635-43. doi: 10.1378/chest.06-2788. Epub 2007 Mar 30.
The clinical significance of multiple carcinoid tumorlets in surgical lung specimens has not been systematically analyzed. We reviewed our experience to determine the range of clinical circumstances associated with this finding.
We reviewed clinical records, available imaging, and pathology materials from patients evaluated at Mayo Clinic Rochester (from 1987 to 2000) with two or more carcinoid tumors or tumorlets in lung specimens.
Twenty-eight of 294 patients with a diagnosis of carcinoid tumor or tumorlet had two or more lesions. Twenty-six patients (93%) were women; mean age was 65 years. Patients were categorized into three groups: multiple nodules (n = 17), solitary lung nodules on preoperative imaging (n = 7), and airflow limitation (n = 4). Approximately half of patients with multiple nodules had respiratory complaints; two patients had Cushing syndrome. Ten patients (58.8%) were suspected of having pulmonary metastases, including 7 patients with previously diagnosed malignancies. Intrathoracic lymph node metastases were present in three patients, none of whom had recurrent disease. One patient had a carcinoid tumor resected 8 years later. Extrathoracic metastases developed in another patient 3 years after presentation, and the patient was alive with disease 2 years later. Only one patient with airflow limitation had a syndrome resembling diffuse idiopathic pulmonary neuroendocrine cell hyperplasia.
Our series represents the largest compilation of multiple carcinoid tumors or tumorlets. Our analysis reveals that multiple carcinoid tumors or tumorlets occur most commonly in patients with multiple nodules resembling metastatic disease. Significant airflow limitation is rare. Long-term survival is excellent, although patients have persistent disease.
手术切除的肺标本中多个类癌小结节的临床意义尚未得到系统分析。我们回顾了自身经验,以确定与这一发现相关的临床情况范围。
我们回顾了梅奥诊所罗切斯特院区(1987年至2000年)评估的患者的临床记录、现有影像学资料和病理材料,这些患者的肺标本中有两个或更多类癌肿瘤或类癌小结节。
294例诊断为类癌肿瘤或类癌小结节的患者中,28例有两个或更多病灶。26例患者(93%)为女性;平均年龄为65岁。患者分为三组:多个结节(n = 17)、术前影像学检查发现的孤立性肺结节(n = 7)和气流受限(n = 4)。约一半有多个结节的患者有呼吸道症状;2例患者患有库欣综合征。10例患者(58.8%)被怀疑有肺转移,其中7例患者之前已诊断为恶性肿瘤。3例患者有胸内淋巴结转移,均无疾病复发。1例患者8年后切除了类癌肿瘤。另1例患者在出现症状3年后发生胸外转移,2年后仍带瘤生存。只有1例气流受限的患者有一种类似于弥漫性特发性肺神经内分泌细胞增生的综合征。
我们的系列研究是多个类癌肿瘤或类癌小结节的最大汇编。我们的分析显示,多个类癌肿瘤或类癌小结节最常见于有多个类似转移瘤的结节的患者中。明显的气流受限很少见。尽管患者疾病持续存在,但长期生存率良好。