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阿姆斯特丹阳性家族患者的手术模式。

Patterns of surgery in patients belonging to amsterdam-positive families.

作者信息

Van Dalen Ralph, Church James, McGannon Ellen, Fay Susan, Burke Carole, Clark Brian

机构信息

David G. Jagelman Inherited Colorectal Cancer Registries, Department of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, Ohio, USA.

出版信息

Dis Colon Rectum. 2003 May;46(5):617-20. doi: 10.1007/s10350-004-6619-9.

Abstract

INTRODUCTION

The phenotype of hereditary nonpolyposis colorectal cancer includes an 80 percent lifetime risk of colorectal cancer, a predominance of lesions proximal to the splenic flexure, and a high incidence of synchronous and metachronous neoplasia. Although prophylactic colectomy is rarely advised for patients with a hereditary nonpolyposis colorectal cancer genotype and a normal colon, the presence of advanced neoplasia in the context of a qualifying family history or a hereditary nonpolyposis colorectal cancer genotype has led to such recommendations. We performed this study to document the patterns of colorectal surgery performed for cancer-bearing patients who are part of an Amsterdam criteria-positive family and to compare rates of metachronous cancers that follow index total or segmental colectomy.

METHODS

Family trees fulfilling the classic Amsterdam criteria for hereditary nonpolyposis colorectal cancer were identified, and all patients for whom surgical and pathology records were available were included in the study. Type of surgery and the outcome of subsequent follow-up were abstracted. Patients were divided into those treated at the Cleveland Clinic and those treated elsewhere.

RESULTS

There were 39 families with 93 affected patients. These patients had 127 colorectal cancers, 76 (60 percent) of which were right sided (proximal to the splenic flexure). Median age at diagnosis of the index cancer was 47 (range, 26-81) years. Sixteen patients (17 percent) had metachronous cancers and multiple surgeries, whereas four (4 percent) had synchronous cancers. Median follow-up for patients who underwent surgery at the Cleveland Clinic was 13 (range, 4-49) years, whereas that for those who underwent surgery elsewhere was 14 (range, 1-42) years. Sixteen (48 percent) of the 33 patients who underwent surgery at the Cleveland Clinic had a total colectomy vs. 7 (12 percent) of the 60 who had surgery elsewhere (Fisher's exact test, P < 0.001). Only one patient who had surgery at the Cleveland Clinic had a second operation for a metachronous cancer (1/17 patients having a segmental resection). Fifteen patients who underwent surgery elsewhere needed a second resection for metachronous cancer (15/53 patients having a segmental resection; Fisher's exact test, P = 0.094).

CONCLUSION

We conclude that there is high risk of metachronous colorectal cancer if an index cancer in a hereditary nonpolyposis colorectal cancer patient (defined according to Amsterdam criteria) is treated by partial colectomy. However, this risk can be lowered by performing a total colectomy at the time of index surgery, or possibly by effective postoperative surveillance.

摘要

引言

遗传性非息肉病性结直肠癌的表型包括一生中患结直肠癌的风险为80%,病变多位于脾曲近端,同时性和异时性肿瘤的发生率较高。尽管很少建议对具有遗传性非息肉病性结直肠癌基因型且结肠正常的患者进行预防性结肠切除术,但在符合条件的家族史或遗传性非息肉病性结直肠癌基因型背景下出现晚期肿瘤已导致了此类建议。我们进行这项研究是为了记录为符合阿姆斯特丹标准阳性家族中患癌患者实施的结直肠手术模式,并比较初次全结肠或节段性结肠切除术后异时性癌的发生率。

方法

识别符合遗传性非息肉病性结直肠癌经典阿姆斯特丹标准的家族谱系,纳入所有有手术和病理记录的患者。提取手术类型和后续随访结果。将患者分为在克利夫兰诊所接受治疗的患者和在其他地方接受治疗的患者。

结果

有39个家族,93名受影响患者。这些患者共患127例结直肠癌,其中76例(60%)位于右侧(脾曲近端)。初次癌症诊断时的中位年龄为47岁(范围26 - 81岁)。16例患者(17%)发生异时性癌症并接受了多次手术,而4例(4%)患有同时性癌症。在克利夫兰诊所接受手术的患者中位随访时间为13年(范围4 - 49年),而在其他地方接受手术的患者中位随访时间为14年(范围1 - 42年)。在克利夫兰诊所接受手术的33例患者中有16例(48%)接受了全结肠切除术,而在其他地方接受手术的60例患者中有7例(12%)接受了全结肠切除术(Fisher精确检验,P < 0.001)。在克利夫兰诊所接受手术的患者中只有1例因异时性癌症进行了二次手术(1/17例接受节段性切除术的患者)。在其他地方接受手术的15例患者因异时性癌症需要二次切除(接受节段性切除术的53例患者中有15例;Fisher精确检验,P = 0.094)。

结论

我们得出结论,如果对遗传性非息肉病性结直肠癌患者(根据阿姆斯特丹标准定义)的初次癌症采用部分结肠切除术治疗,发生异时性结直肠癌的风险很高。然而,通过在初次手术时进行全结肠切除术或可能通过有效的术后监测可以降低这种风险。

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