Smeenk R M, van Velthuysen M L F, Verwaal V J, Zoetmulder F A N
Department of Surgery, The Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Eur J Surg Oncol. 2008 Feb;34(2):196-201. doi: 10.1016/j.ejso.2007.04.002. Epub 2007 May 23.
Pseudomyxoma peritonei (PMP) is a rare disease with an estimated incidence of 1 per million per year, and is thought to originate usually from an appendiceal mucinous epithelial neoplasm. However it is not known exactly how often these neoplasms lead to PMP. The aim of this study is to investigate the incidence of both lesions and their relation.
The nationwide pathology database of the Netherlands (PALGA) was searched for the incidence of all appendectomies, the incidence of primary epithelial appendiceal lesions and the incidence and pathology history of patients with PMP. All regarded the 10-year period of 1995-2005.
In the 10-year period 167,744 appendectomies were performed in the Netherlands. An appendiceal lesion was found in 1482 appendiceal specimens (0.9%). Nine percent of these patients developed PMP. Coincidentally, an additional epithelial colonic neoplasm was found in 13% of patients with an appendiceal epithelial lesion. A mucinous epithelial neoplasm was identified in 0.3% (73% benign, 27% malignant) of appendiceal specimens and 20% of these patients developed PMP. For mucocele and non-mucinous neoplasm the association with PMP was only 2% and 3%, respectively. From the nationwide database 267 patients (62 men and 205 women) with PMP were identified, which demonstrates an incidence of PMP in the Netherlands approaching 2 per million per year. The primary site was identified in 68% and dominated by the appendix (82%).
Primary epithelial lesions of the appendix are rare. One third of these lesions are mucinous epithelial neoplasms and especially these tumours may progress into PMP. The incidence of PMP seems to be higher than thought before. Furthermore there is a considerable risk of an additional colonic epithelial neoplasm in patients with an epithelial neoplasm at appendectomy.
腹膜假黏液瘤(PMP)是一种罕见疾病,估计年发病率为百万分之一,通常被认为起源于阑尾黏液上皮肿瘤。然而,尚不清楚这些肿瘤导致PMP的确切频率。本研究的目的是调查这两种病变的发病率及其关系。
在荷兰全国病理数据库(PALGA)中搜索所有阑尾切除术的发病率、原发性阑尾上皮病变的发病率以及PMP患者的发病率和病理病史。所有数据均涉及1995 - 2005年这10年期间。
在这10年期间,荷兰共进行了167,744例阑尾切除术。在1482份阑尾标本中发现了阑尾病变(0.9%)。这些患者中有9%发展为PMP。巧合的是,在13%的阑尾上皮病变患者中还发现了另外的结肠上皮肿瘤。在0.3%(73%为良性,27%为恶性)的阑尾标本中鉴定出黏液上皮肿瘤,其中20%的患者发展为PMP。对于黏液囊肿和非黏液性肿瘤,与PMP的关联分别仅为2%和3%。从全国数据库中识别出267例PMP患者(62名男性和205名女性),这表明荷兰PMP的发病率接近每年百万分之二。68%的患者确定了原发部位,其中阑尾占主导(82%)。
阑尾原发性上皮病变罕见。这些病变中有三分之一是黏液上皮肿瘤,尤其是这些肿瘤可能发展为PMP。PMP的发病率似乎比之前认为的要高。此外,阑尾切除术中患有上皮肿瘤的患者发生另外结肠上皮肿瘤的风险相当高。