Proye C A, Vix M, Jansson S, Tisell L E, Dralle H, Hiller W
Clinique Chirurgicale Adultes Est, Service de Chirurgie Générale et Endocrinienne, CHU de Lille, Hôpital Huriez, France.
World J Surg. 1994 Jul-Aug;18(4):467-72. doi: 10.1007/BF00353738.
This study aims to examine the frequency of the pheochromocytoma (pheo), defined as a "benign, intra-adrenal, hypertensive, sporadic, unilateral tumor." Three large series amounting to 310 subphrenic chromaffin tumors operated over periods of 17, 23, and 41 years, respectively, have been reviewed. Among those combined 310 pheos, 48 (15.5%) were malignant (i.e., metastatic) and 262 (84.5%) were benign; 42 (13.5%) were ectopic (35% of malignant tumors versus 9.5% of benign tumors); 230 (74.2%) were hypertensive (74% of benign tumors versus 73% of malignant tumors); 29 (9.4%) were bilateral, including 23 patients with a family history; 41 (13.2%) of patients had MEN II type A or B syndrome; and 20 (6.5%) occurred in a phacomatosis setting. Some of the patients had a non-MEN family history of pheo (n = 5), seemingly sporadic hyperparathyroidism (n = 4), or other associated neuroendocrine tumor (n = 9). Sometimes several of these features were combined. Finally 125 (40.3%) cases fitted the classic description of the tumor, 47.0% at the time of initial presentation and 40.3% at the end of follow-up. Late occurrence of metastases or metachronous diagnosis of familial disease make lifelong follow-up mandatory. Genetic studies may be indicated in pheochromocytoma patients.
本研究旨在调查嗜铬细胞瘤(pheo)的发病频率,嗜铬细胞瘤被定义为“良性、肾上腺内、高血压、散发性、单侧肿瘤”。我们回顾了三个大型系列研究,分别涉及在17年、23年和41年期间接受手术的310例膈下嗜铬细胞瘤。在这310例嗜铬细胞瘤中,48例(15.5%)为恶性(即转移性),262例(84.5%)为良性;42例(13.5%)为异位性(恶性肿瘤的比例为35%,良性肿瘤的比例为9.5%);230例(74.2%)有高血压(良性肿瘤的比例为74%,恶性肿瘤的比例为73%);29例(9.4%)为双侧性,其中23例有家族病史;41例(13.2%)患者患有A型或B型多发性内分泌腺瘤病(MEN II)综合征;20例(6.5%)发生于错构瘤病背景下。部分患者有嗜铬细胞瘤的非MEN家族病史(n = 5)、看似散发性甲状旁腺功能亢进(n = 4)或其他相关神经内分泌肿瘤(n = 9)。有时这些特征会合并出现。最终,125例(40.3%)病例符合该肿瘤的经典描述,初始就诊时为47.0%,随访结束时为40.3%。转移的晚期发生或家族性疾病的异时诊断使得终身随访成为必要。嗜铬细胞瘤患者可能需要进行基因研究。