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1
Gardner's syndrome: a case report and review of the literature.加德纳综合征:一例病例报告及文献综述
World J Gastroenterol. 2005 Sep 14;11(34):5408-11. doi: 10.3748/wjg.v11.i34.5408.
2
The challenge of extraabdominal desmoid tumour management in patients with Gardner's syndrome: radiofrequency ablation, a promising option.加德纳综合征患者腹外硬纤维瘤治疗面临的挑战:射频消融,一种有前景的选择。
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3
[Long-term experience with therapy of a female patient with Gardner's syndrome, first presenting with extra-abdominal desmoid tumor, and review of the literature].[一名以腹外硬纤维瘤首次就诊的加德纳综合征女性患者的长期治疗经验及文献复习]
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4
[Gardner's syndrome, a rare disease].[加德纳综合征,一种罕见疾病]
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Gardner syndrome and desmoid tumors.加德纳综合征与硬纤维瘤
Acta Chir Belg. 1993 Sep-Oct;93(5):230-2.
6
[Desmoid tumor in a male breast in the context of Gardner's syndrome. Case report].[加德纳综合征背景下男性乳腺硬纤维瘤。病例报告]
Ann Chir. 2005 Jan;130(1):40-3. doi: 10.1016/j.anchir.2004.10.011.
7
Familial polyposis coli: clinical manifestations, evaluation, management and treatment.家族性腺瘤性息肉病:临床表现、评估、管理与治疗
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[A rare case of Gardner's syndrome complicated with rectal carcinoma].[1例罕见的加德纳综合征合并直肠癌病例]
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The role of the ET nurse in managing Gardner's syndrome.造口治疗师护士在管理加德纳综合征中的作用。
J Wound Ostomy Continence Nurs. 1996 Mar;23(2):73-9. doi: 10.1016/s1071-5754(96)90064-9.
10
[Gardner's syndrome].[加德纳综合征]
Dtsch Z Mund Kiefer Gesichtschir. 1990 Mar-Apr;14(2):106-10.

引用本文的文献

1
Surgical dilemmas in Gardner syndrome: infiltrative basal cell carcinoma and total knee prosthesis failure.加德纳综合征的外科难题:浸润性基底细胞癌与全膝关节假体失败
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Gardner's Syndrome: Vigilance Better than Negligence - A Case Report.加德纳综合征:警惕优于疏忽——一例报告
Ann Maxillofac Surg. 2024 Jul-Dec;14(2):240-243. doi: 10.4103/ams.ams_105_24. Epub 2024 Nov 29.
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Rare Germline Variants in the Adenomatous Polyposis Coli Gene Associated with Dental and Osseous Anomalies.腺瘤性结肠息肉病基因中的罕见种系变异与牙齿和骨骼异常有关。
Int J Mol Sci. 2024 Jul 26;25(15):8189. doi: 10.3390/ijms25158189.
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A rare case of Gardner syndrome in an African adult male: A case report.一名非洲成年男性患加德纳综合征的罕见病例:病例报告。
Clin Case Rep. 2024 Apr 3;12(4):e8735. doi: 10.1002/ccr3.8735. eCollection 2024 Apr.
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Extracolonic manifestations of Gardner syndrome: A case report.加德纳综合征的结肠外表现:一例报告。
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Gardner's syndrome: Simultaneous diagnosis and treatment in monozygotic twins.加德纳综合征:单卵双胞胎的同步诊断与治疗
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Osteoma of the Jaw as First Clinical Sign of Gardner's Syndrome: The Experience of Two Italian Centers and Review.颌骨骨瘤作为加德纳综合征的首发临床症状:两个意大利中心的经验及文献综述
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Parosteal lipoma of the radius with posterior interosseous nerve palsy.桡骨骨旁脂肪瘤伴骨间后神经麻痹。
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Gardner syndrome with a giant mass in the thoracic cavity: a case report and analysis of the related complications.胸腔巨大肿物的加德纳综合征:一例病例报告及相关并发症分析
Int J Clin Exp Pathol. 2020 Aug 1;13(8):2158-2162. eCollection 2020.
10
Importance of Extraintestinal Manifestations in Early Diagnosis of Gardner Syndrome.肠外表现对Gardner综合征早期诊断的重要性。
Case Rep Gastrointest Med. 2020 Aug 4;2020:7394928. doi: 10.1155/2020/7394928. eCollection 2020.

本文引用的文献

1
Familial adenomatous polyposis. Surgical treatment: when and how.家族性腺瘤性息肉病。外科治疗:时机与方式。
Tech Coloproctol. 2004 Dec;8 Suppl 2:s309-14. doi: 10.1007/s10151-004-0183-0.
2
Familial polyposis coli: clinical manifestations, evaluation, management and treatment.家族性腺瘤性息肉病:临床表现、评估、管理与治疗
Mt Sinai J Med. 2004 Nov;71(6):384-91.
3
Chemoprevention of carcinogenesis in familial tumors.家族性肿瘤致癌作用的化学预防
Int J Clin Oncol. 2004 Aug;9(4):299-303. doi: 10.1007/s10147-004-0417-1.
4
Simple and complex genetics of colorectal cancer susceptibility.结直肠癌易感性的简单与复杂遗传学
Am J Med Genet C Semin Med Genet. 2004 Aug 15;129C(1):35-43. doi: 10.1002/ajmg.c.30023.
5
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.
6
A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum.一项关于肠道息肉病的遗传学与临床研究,肠道息肉病是结肠癌和直肠癌的一个诱发因素。
Am J Hum Genet. 1951 Jun;3(2):167-76.
7
Treatment of desmoids and mesenteric fibromatosis in familial adenomatous polyposis with raloxifene.雷洛昔芬治疗家族性腺瘤性息肉病中的硬纤维瘤和肠系膜纤维瘤病。
Tumori. 2003 Jul-Aug;89(4):391-6. doi: 10.1177/030089160308900408.
8
Multiple cutaneous and subcutaneous lesions occurring simultaneously with hereditary polyposis and osteomatosis.多发性皮肤和皮下病变与遗传性息肉病和骨瘤病同时出现。
Am J Hum Genet. 1953 Jun;5(2):139-47.
9
Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome.遗传性非息肉病性结直肠癌、家族性腺瘤性息肉病、幼年性息肉病和黑斑息肉综合征的胃肠道监测指南。
Gut. 2002 Oct;51 Suppl 5(Suppl 5):V21-7. doi: 10.1136/gut.51.suppl_5.v21.
10
Diagnosis and management of hereditary colon cancer.遗传性结肠癌的诊断与管理
Gastroenterol Clin North Am. 2002 Jun;31(2):537-49, x. doi: 10.1016/s0889-8553(02)00009-2.

加德纳综合征:一例病例报告及文献综述

Gardner's syndrome: a case report and review of the literature.

作者信息

Fotiadis C, Tsekouras D-K, Antonakis P, Sfiniadakis J, Genetzakis M, Zografos G-C

机构信息

8 Tripoleos Street, Melissia, Athens 15721, Greece.

出版信息

World J Gastroenterol. 2005 Sep 14;11(34):5408-11. doi: 10.3748/wjg.v11.i34.5408.

DOI:10.3748/wjg.v11.i34.5408
PMID:16149159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4622822/
Abstract

Gardner's syndrome is an autosomal dominant disease characterized by the presence of colonic polyposis, osteomas and a multitude of soft tissue tumors. The syndrome may present at any age from 2 mo to 70 years with a variety of symptoms, either colonic or extracolonic. We present a case of a 11-year-old female patient with Gardner's syndrome who presented with a lumbar area desmoid tumor and treated with resection of the desmoid, restorative proctocolectomy and ileal pouch anal anastomosis, A review of the current literature has been performed.

摘要

加德纳综合征是一种常染色体显性疾病,其特征为存在结肠息肉病、骨瘤和多种软组织肿瘤。该综合征可在2个月至70岁的任何年龄出现,伴有各种症状,包括结肠或结肠外症状。我们报告一例11岁加德纳综合征女性患者,该患者出现腰部硬纤维瘤,并接受了硬纤维瘤切除术、全直肠系膜切除及回肠储袋肛管吻合术治疗。同时对当前文献进行了综述。