期刊文献+

Diffuse intestinal ganglioneuromatosis an uncommon manifestation of Cowden syndrome 被引量:5

Diffuse intestinal ganglioneuromatosis an uncommon manifestation of Cowden syndrome
下载PDF
导出
摘要 Diffuse intestinal ganglioneuromatosis is a hamartomatous polyposis characterized by a disseminated, intramural or transmural proliferation of neural elements involving the enteric plexuses. It has been associated with MEN Ⅱ, neurofibromatosis type 1 and hamartomatous polyposis associated with phosphatase and tensin homolog mutation. We report the case of a female patient with a history of a breast and endometrial tumor who presented in a colonoscopy performed for rectal bleeding diffuse ganglioneuromatosis, which oriented the search for other characteristic findings of Cowden syndrome given the personal history of the patient. The presence of an esophagogastric polyposis was also noted. Cowden syndrome is characterized by skin lesions, but it is rarely diagnosed by these lesions, because they are usually overlooked. Intestinal polyposis is not a major diagnostic criterion but it is very useful for early diagnosis. The combination of colonic polyposis and glucogenic acanthosis should orient the diagnosis to Cowden syndrome. Diffuse intestinal ganglioneuromatosis is a hamartomatous polyposis characterized by a disseminated, intramural or transmural proliferation of neural elements involving the enteric plexuses. It has been associated with MEN Ⅱ, neurofibromatosis type 1 and hamartomatous polyposis associated with phosphatase and tensin homolog mutation. We report the case of a female patient with a history of a breast and endometrial tumor who presented in a colonoscopy performed for rectal bleeding diffuse ganglioneuromatosis, which oriented the search for other characteristic findings of Cowden syndrome given the personal history of the patient. The presence of an esophagogastric polyposis was also noted. Cowden syndrome is characterized by skin lesions, but it is rarely diagnosed by these lesions, because they are usually overlooked. Intestinal polyposis is not a major diagnostic criterion but it is very useful for early diagnosis. The combination of colonic polyposis and glucogenic acanthosis should orient the diagnosis to Cowden syndrome.
出处 《World Journal of Gastrointestinal Oncology》 SCIE CAS 2013年第2期34-37,共4页 世界胃肠肿瘤学杂志(英文版)(电子版)
关键词 Ganglioneuromatosis Gastrointestinal poliposis PHOSPHATASE and TENSIN HOMOLOG Cowden síndrome HAMARTOMA Ganglioneuromatosis Gastrointestinal poliposis Phosphatase and tensin homolog Cowden síndrome Hamartoma
  • 相关文献

参考文献10

  • 1Ken Umemura,Sho Takagi,Yasushi Ishigaki,Masahiro Iwabuchi,Shigeru Kuroki,Yoshitaka Kinouchi,Tooru Shimosegawa.Gastrointestinal polyposis with esophageal polyposis is useful for early diagnosis of Cowden's disease[J].World Journal of Gastroenterology,2008,14(37):5755-5759. 被引量:6
  • 2Robert Pilarski.Cowden Syndrome: A Critical Review of the Clinical Literature[J]. Journal of Genetic Counseling . 2009 (1)
  • 3Kay PS,Soetikno RM,Mindelzun R,Young HS.Diffuse esoph-ageal glycogenic acanthosis: An endoscopic marker of Cowden’s disease. The American journal of Gastroenterology . 1997
  • 4Heald B,Mester J,Rybicki L,Orloff MS,Burke CA,Eng C.Frequent gastrointestinal polyps and colorectal adenocarcinomas in a prospective series of PTEN mutation carriers. Gastroenterology . 2010
  • 5Chambonniere,ML,Porcheron,J,Scoazec,JY,Audigier,JC,Mosnier,JF.Intestinal ganglioneuromatosis diagnosed in adult patients. Gastroenterology Clinics of North America . 2003
  • 6O.T. Chan,P. Haghighi.Hamartomatous polyps of the colon: ganglioneuromatous, stromal, and lipomatous. Archives of Pathology and Laboratory Medicine . 2006
  • 7Farooq A,Walker LJ,Bowling J,Audisio RA.Cowden syn-drome. Cancer Treatment Reviews . 2010
  • 8Nelen MR,Kremer H,Konings IB,Schoute F,van Es-sen AJ,Koch R,Woods CG,Fryns JP,Hamel B,HoefslootLH,Peeters EA,Padberg GW.Novel PTEN mutations inpatients with Cowden disease: absence of clear genotype-phenotype correlations. European Journal of Human Genetics . 1999
  • 9Riegert-Johnson DL,Gleeson FC,Roberts M,Tholen K,Youngborg L,Bullock M,Boardman LA.Cancer and Lher-mitte-Duclos disease are common in Cowden syndromepatients. Hered Cancer Clin Pract . 2010
  • 10Schreibman IR,Baker M,Amos C,McGarrity TJ.The hamar-tomatous polyposis syndromes: a clinical and molecular re-view. The American journal of Gastroenterology . 2005

二级参考文献19

  • 1[1]Lloyd KM 2nd,Dennis M.Cowden's disease.A possible new symptom complex with multiple system involvement.Ann Intern Med 1963; 58:136-142
  • 2[2]Weary PE,Gorlin RJ,Gentry WC Jr,Comer JE,Greer KE.Multiple hamartoma syndrome (Cowden's disease).Arch Dermatol 1972; 106:682-690
  • 3[3]Ushio K,Ishikawa T,Hukutomi T.Cowden's disease (multiple hamartoma syndorome)-Recent knowledge and problems.Clinical oncology 1998; 44:1024-1032
  • 4[4]Salem OS,Steck WD.Cowden's disease (multiple hamartoma and neoplasia syndrome).A case report and review of the English literature.J Am Acad Dermatol 1983; 8:686-696
  • 5[5]Eng C.Will the real Cowden syndrome please stand up:revised diagnostic criteria.J Med Genet 2000; 37:828-830
  • 6[6]Brownstein MH,Wolf M,Bikowski JB.Cowden's disease:a cutaneous marker of breast cancer.Cancer 1978; 41:2393-2398
  • 7[7]Kobayashi T,Tukuda H,Inoue T.A case of Cowden disease diagnosed with the assistance of characteristic findings on gastrointestinal endoscopy.Gastroenterological Endoscopy 1999;41:1438-1444
  • 8[8]Takahashi M,Umeki K,Harada K.A case of Cowden's disease.Clinical Dermatology 1995; 49:736-738
  • 9[9]Starink TM,van der Veen JP,Arwert F,de Waal LP,de Lange GG,Gille JJ,Eriksson AW.The Cowden syndrome:a clinical and genetic study in 21 patients.Clin Genet 1986; 29:222-233
  • 10[10]Sumioka M,Watanabe C,Yamada H,Fujii Y,Koike N,Hata J,Hiraoka T,Hirata K,Imagawa M,Ishida M.[Two cases of Cowden's disease] Nippon Shokakibyo Gakkai Zasshi 1994; 91:2219-2224

共引文献5

同被引文献8

引证文献5

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部