icon fsr

文献詳細

雑誌文献

胃と腸38巻4号

2003年04月発行

文献概要

特集 全身性疾患と消化管病変 総論

1. 消化管疾患にみられる他臓器病変

著者: 大島忠之1 横山善文1 伊藤恵介1 谷田諭史1 片岡洋望1 佐々木誠人1 佐野仁1 妹尾恭司1 大原弘隆1 城卓志1 伊藤誠1 森田明理2

所属機関: 1名古屋市立大学大学院臨床機能内科学 2名古屋市立大学大学院加齢・環境皮膚科学

ページ範囲:P.415 - P.426

文献購入ページに移動
 消化管疾患では消化管自体の病変のみならず,消化管以外の他臓器にも特有な病変を発現することがある.これら消化管外病変は,消化管病変より先行して発見されることも多く,消化管疾患に併存・合併する他臓器病変を理解しておくことは臨床上重要である.なかでも内臓病変に合併する皮膚病変はデルマドロームと言われ,日常臨床でしばしば遭遇するので重要な概念である.本稿では,家族性大腸腺腫症,Gardner症候群,Turcot症候群,Peutz-Jeghers症候群,Cronkhite-Canada症候群,Cowden病,潰瘍性大腸炎,Crohn病,腸管Behçet病,Wipple病に合併する他臓器病変を中心に概説した.

参考文献

1)Nishisho I, Nakamura Y, Miyoshi Y, et al. Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science 253 : 665-669, 1991
2)Bertario L, Russo A, Sala P, et al. Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis. Int J Cancer 95 : 102-107, 2001
3)Parisi ML. Congenital hypertrophy of the retinal pigment epithelium serves as a clinical marker in a family with familial adenomatous polyposis. J Am Optom Assoc 66 : 106-112, 1995
4)Iwama T, Mishima Y, Utsunomiya J. The impact of familial adenomatous polyposis on the tumorigenesis and mortality at the several organs. Its rational treatment. Ann Surg 217 : 101-108, 1993
5)Baughman FA Jr, List CF, Williams JR, et al. The glioma-polyposis syndrome. N Engl J Med 281 : 1345-1346, 1969
6)Turcot J. Malignant tumors of the central nervous system associated with familial polyposis of the colon : report of two cases. Dis Colon Rectum 2 : 465-468, 1959
7)Paraf F, Jothy S, Van Meir EG. Brain tumor-polyposis syndrome : two genetic diseases? J Clin Oncol 15 : 2744-2758, 1997
8)Todd DW, Christoferson LA, Leech RW, et al. A family affected with intestinal polyposis and gliomas. Ann Neurol 10 : 390-392, 1981
9)Miyaki M, Nishio J, Konishi M, et al. Drastic genetic instability of tumors and normal tissues in Turcot syndrome. Oncogene 15 : 2877-2881, 1997
10)Chan TL, Yuen ST, Chung LP, et al. Germline hMSH2 and differential somatic mutations in patients with Turcot's syndrome. Genes Chromosomes Cancer 25 : 75-81, 1999
11)Miyaki M, Iijima T, Shiba K, et al. Alterations of repeated sequences in 5' upstream and coding regions in colorectal tumors from patients with hereditary nonpolyposis colorectal cancer and Turcot syndrome. Oncogene 20 : 5215-5218, 2001
12)Westerman AM, Entius MM, de Baar E, et al. Peutz-Jeghers syndrome : 78-year follow-up of the original family. Lancet 353 : 1211-1215, 1999
13)Hemminki A, Markie D, Tomlinson I, et al. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 391 : 184-187, 1998
14)妹尾恭司,横山善文,伊藤誠.不全型Peutz-Jeghers症候群の1例.胃と腸 28 : 1397- 1402, 1993
15)Giardiello FM, Brensinger JD, Tersmette AC, et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 119 : 1447-1453, 2000
16)Cronkhite LW Jr, Canada WJ. Generalized gastrointestinal polyposis, an unusual syndrome of polyposis, pigmentation, alopecia and onychotrophia. N Engl J Med 252 : 1011-1015, 1955
17)Lloyd KM, Dennis M. Cowdens's disease. A possible new symptom complex with multiple system involvement. Ann Intern Med 58 : 136-142, 1963
18)Marsh DJ, Kum JB, Lunetta KL, et al. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Hum Mol Genet 8 : 1461-1472, 1999
19)Liaw D, Marsh DJ, Li J, et al. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet 16 : 64-67, 1997
20)Nelen MR, Padberg GW, Peeters EA, et al. Localization of the gene for Cowden disease to chromosome 10q22-23. Nat Genet 13 : 114-116, 1996
21)Marsh DJ, Dahia PL, Zheng Z, et al. Germline mutations in PTEN are present in Bannayan-Zonana syndrome. Nat Genet 16 : 333-334, 1997
22)Olschwang S, Serova-Sinilnikova OM, Lenoir GM, et al. PTEN germ-line mutations in juvenile polyposis coli. Nat Genet 18 : 12-14, 1998
23)Oka M, Berking C, Nesbit M, et al. Interleukin-8 overexpression is present in pyoderma gangrenosum ulcers and leads to ulcer formation in human skin xenografts. Lab Invest 80 : 595-604, 2000
24)Shpiro D, Gilat D, Fisher-Feld L, et al. Pyoderma gangrenosum successfully treated with perilesional granulocyte-macrophage colony stimulating factor. Br J Dermatol 138 : 368-369, 1998
25)原田敬志.潰瘍性大腸炎.潰瘍性大腸炎の消化管外合併症 眼疾患.日本臨牀 57 : 2575-2579, 1999
26)Raby O, Salvanet-Bouccara A, Forestier F. The eye and chronic inflammatory diseases of the intestines. Immunopathological and genetic aspects. Apropos of 3 cases. J Fr Ophtalmol 10 : 683-698, 1987
27)Gravallese EM, Kantrowitz FG. Arthritic manifestations of inflammatory bowel disease. Am J Gastroenterol 83 : 703-709, 1988
28)Wiesner RH. Current concepts in primary sclerosing cholangitis. Mayo Clin Proc 69 : 969-982, 1994
29)Olsson R, Danielsson A, Jarnerot G, et al. Prevalence of primary sclerosing cholangitis in patients with ulcerative colitis. Gastroenterology 100 : 1319-1323, 1991
30)Duerr RH, Targan SR, Landers CJ, et al. Neutrophil cytoplasmic antibodies : a link between primary sclerosing cholangitis and ulcerative colitis. Gastroenterology 100(5 Pt 1) : 1385-1391, 1991
31)Lam A, Borda IT, Inwood MJ, et al. Coagulation studies in ulcerative colitis and Crohn's disease. Gastroenterology 68 : 245-251, 1975
32)Collins CE, Cahill MR, Newland AC, et al. Platelets circulate in an activated state in inflammatory bowel disease. Gastroenterology 106 : 840-845, 1994
33)Orchard TR, Chua CN, Ahmad T, et al. Uveitis and erythema nodosum in inflammatory bowel disease : clinical features and the role of HLA genes. Gastroenterology 123 : 714-718, 2002
34)Fielding JF, Cooke WT. Finger clubbing and regional enteritis. Gut 12 : 442-444, 1971
35)Ohno S, Ohguchi M, Hirose S, et al. Close association of HLA-Bw51 with Behcet's disease. Arch Ophthalmol 100 : 1455-1458, 1982
36)森伸一,徳富研二,日下洋,他.〔ベーチェット病1988〕腸管ベーチェット病.最新医学 43 : 329-334, 1988
37)Whipple GH. A hitherto undescribed disease characterized anatomically by deposits of fat and fatty acid in the intestinal and mesenteric lymphatic tissues. Bull. Johns Hopkins Hosp 18 : 382-391, 1907
38)Relman DA, Schmidt TM, MacDermott RP, et al. Identification of the uncultured bacillus of Whipple's disease. N Engl J Med 327 : 293-301, 1992
39)Baisden BL, Lepidi H, Raoult D, et al. Diagnosis of Wihipple disease by immunohistochemical analysis : a sensitive and specific method for the detection of Tropheryma whipplei (the Whipple bacillus)in paraffinembedded tissue. Am J Clin Pathol 118 : 742- 748, 2002
40)Schmitt BP, Richardson H, Smith E, et al. Encephalopathy complicating Whipple's disease : failure to respond to antibiotics. Ann Intern Med 94 : 51-52, 1981

掲載誌情報

出版社:株式会社医学書院

電子版ISSN:1882-1219

印刷版ISSN:0536-2180

雑誌購入ページに移動
icon up
あなたは医療従事者ですか?