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黑人患者的家族性结肠息肉病

Familial polyposis coli in black patients.

作者信息

Leffall L D, Chung E B, Dewitty R L, Cornwell E E, Blakey T M

出版信息

Ann Surg. 1977 Sep;186(3):324-33. doi: 10.1097/00000658-197709000-00010.

DOI:10.1097/00000658-197709000-00010
PMID:889375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1396334/
Abstract

We have presented our experience with 19 black patients who had familial polyposis coli, seven of whom had associated cancer. Four of the seven had multiple cancers. Seventeen of the 19 patients were female but most of the patients at risk in our series were female. Sixteen of the 19 had extracolonic manifestations which have been described as part of Gardner's syndrome. Although our series was quite small, larger series do not report as high an incidence of extracolonic manifestations. Follow-up was too short to make any statements concerning the development of cancer in the retained rectal stump.

摘要

我们介绍了19例患有家族性结肠息肉病的黑人患者的情况,其中7例伴有癌症。7例中有4例患有多发性癌症。19例患者中有17例为女性,但在我们的系列研究中,大多数有患病风险的患者是女性。19例中有16例有结肠外表现,这些表现被描述为加德纳综合征的一部分。尽管我们的系列研究规模很小,但更大规模的系列研究并未报告如此高的结肠外表现发生率。随访时间过短,无法就保留的直肠残端发生癌症的情况发表任何声明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/19d0ef89aaf2/annsurg00368-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/ee7ccf008cc0/annsurg00368-0101-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/0b829428f383/annsurg00368-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/be93803b73fe/annsurg00368-0102-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/d372b91fca3a/annsurg00368-0103-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/76c05a168da2/annsurg00368-0103-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/e2afe6c8b9c3/annsurg00368-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/d751b809a3c5/annsurg00368-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/b3b210c4b796/annsurg00368-0105-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/14c2a8909407/annsurg00368-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/19d0ef89aaf2/annsurg00368-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/ee7ccf008cc0/annsurg00368-0101-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/0b829428f383/annsurg00368-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/be93803b73fe/annsurg00368-0102-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/d372b91fca3a/annsurg00368-0103-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/76c05a168da2/annsurg00368-0103-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/e2afe6c8b9c3/annsurg00368-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/d751b809a3c5/annsurg00368-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/b3b210c4b796/annsurg00368-0105-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/14c2a8909407/annsurg00368-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ee/1396334/19d0ef89aaf2/annsurg00368-0107-a.jpg

相似文献

1
Familial polyposis coli in black patients.黑人患者的家族性结肠息肉病
Ann Surg. 1977 Sep;186(3):324-33. doi: 10.1097/00000658-197709000-00010.
2
Surgical management of familial polyposis and Gardner's syndrome.家族性腺瘤性息肉病和加德纳综合征的外科治疗
Am J Surg. 1979 Jan;137(1):54-6. doi: 10.1016/0002-9610(79)90010-2.
3
Lymphoid polyposis associated with familial polyposis and Gardner's syndrome.
Ann Surg. 1974 Sep;180(3):319-22. doi: 10.1097/00000658-197409000-00011.
4
Periampullary malignancy in Gardner's syndrome.加德纳综合征中的壶腹周围恶性肿瘤。
Ann Surg. 1977 May;185(5):565-73. doi: 10.1097/00000658-197705000-00009.
5
[Gardner's syndrome. Familial colonic polyposis diagnosed after extracolonic manifestations].[加德纳综合征。结肠外表现后诊断出的家族性结肠息肉病]
Ugeskr Laeger. 1980 Jul 7;142(28):1829-30.
6
Familial polyposis.家族性息肉病
Cancer. 1977 Jan;39(1):267-73. doi: 10.1002/1097-0142(197701)39:1<267::aid-cncr2820390141>3.0.co;2-x.
7
Familial polyposis coli associated with bile duct cancer.
Am J Surg. 1981 Mar;141(3):378-80. doi: 10.1016/0002-9610(81)90201-4.
8
Familial polyposis of the colon in the Bantu.班图人中的结肠家族性息肉病。
S Afr Med J. 1972 Sep 2;46(35):1241-6.
9
Unfamiliar aspects of familial polyposis coli.
Am J Surg. 1986 Jul;152(1):81-6. doi: 10.1016/0002-9610(86)90147-9.
10
[Mesenteric fibromatosis following total colectomy for familial polyposis. A rare case of Gardner's syndrome].
Minerva Chir. 1982 Feb 15;37(3):183-6.

引用本文的文献

1
Colorectal carcinoma in young persons: experience at Howard University Hospital, 1955--1977.青年人大肠癌:霍华德大学医院的经验,1955 - 1977年
J Natl Med Assoc. 1979 May;71(5):449-51.

本文引用的文献

1
Hereditary pattern for multiple osteomas in a family group.一个家族群体中多发性骨瘤的遗传模式。
Am J Hum Genet. 1952 Mar;4(1):31-6.
2
Surgical management of multiple polyposis. The problem of cancer in the retained bowel segment.多发性息肉病的外科治疗。保留肠段内的癌症问题。
Arch Surg. 1970 Apr;100(4):521-6. doi: 10.1001/archsurg.1970.01340220197033.
3
Adenocarcinoma of the duodenum and the Gardner syndrome.十二指肠腺癌与加德纳综合征。
JAMA. 1973 Mar 12;223(11):1229-32.
4
The evolution of cancer of the colon and rectum.结肠直肠癌的演变
Cancer. 1975 Dec;36(6):2251-70. doi: 10.1002/cncr.2820360944.
5
Surgical treatment of hereditary adenomatosis of the colon and rectum in Sweden during the last 20 years. Part II. Patients with prophylactic operations, primary and late results. Discussion and summary.
Acta Chir Scand. 1975;141(3):228-37.
6
Inherited gastrointestinal-polyposis syndromes.遗传性胃肠道息肉综合征。
N Engl J Med. 1976 May 13;294(20):1101-4. doi: 10.1056/NEJM197605132942007.