Ülseratif Kolit

Yazarlar

Ümit Karabulut
https://orcid.org/0000-0003-3126-2129

Özet

Ülseratif kolit, kolonun mukozal tabakasıyla sınırlı, rektumdan başlayarak proksimale kesintisiz uzanım gösteren, alevlenme ve iyileşme ataklarıyla seyreden kronik inflamatuar bir barsak hastalığıdır. Hastalığın etyopatogenezi tam olarak bilinmemekle birlikte; genetik olarak yatkın bireylerde immunolojik ve çevresel faktörlerin tetiklediği barsak inflamasyonu sonucunda geliştiği kabul edilmektedir. En yüksek insidans ve prevalansı Kuzey Avrupa ile Kuzey Amerika'da görülen hastalık, yetişkinlerde Crohn hastalığına kıyasla daha sık izlenir. Temel klinik semptomu mukuslu veya kanlı ishal olup, süreç içerisinde halsizlik, karın ağrısı ve çeşitli ekstraintestinal bulgular da eşlik edebilir. Tanı, kronik ishal varlığında klinik değerlendirme, laboratuvar testleri, endoskopik ve histopatolojik incelemelerle diğer kolit nedenlerinin dışlanmasıyla konur. Tedavi yaklaşımı, hastalığın yaygınlığına ve ciddiyetine (hafif, orta, ağır) göre değişkenlik göstererek; 5-ASA, lokal/sistemik steroidler, immün modülatörler ve anti-TNF biyolojik ajanları içerir. Medikal tedaviye dirençli olgularda veya displazi/kanser gelişimi gibi komplikasyonlarda total kolektomi küratif bir seçenek olarak uygulanır. Yaşam boyu süren bu hastalıkta mortalite genel popülasyondan yüksek olmasa da toksik megakolon ve uzun vadede artan kolorektal kanser riski yakından takip edilmelidir.

Ulcerative colitis is a chronic inflammatory bowel disease confined to the mucosal layer of the colon, typically presenting with alternating periods of relapse and remission while initiating in the rectum and extending proximally. Although its exact etiopathogenesis remains unknown, it is considered to develop from intestinal inflammation triggered by immunological and environmental factors in genetically susceptible individuals. The highest incidence and prevalence are observed in Northern Europe and North America, and it affects adults more frequently than Crohn's disease. The primary clinical symptom is bloody diarrhea with or without mucus, which can be accompanied by abdominal pain, fatigue, and various extraintestinal manifestations. Diagnosis is established based on clinical assessment, laboratory tests, and endoscopic and histopathological findings showing active inflammation during chronic diarrhea while excluding other causes of colitis. Medical management is tailored to the disease extent and severity, incorporating 5-ASA, topical or systemic steroids, immunomodulators, and biological anti-TNF agents. Surgical intervention, specifically total colectomy, serves as a curative option for patients with medically refractory disease or complications like dysplasia and carcinoma. While mortality is not higher than the general population, toxic megacolon and increased long-term colorectal cancer risks necessitate careful surveillance.

Referanslar

Odras I, Eckmanna L, Talami M et al. Ulcerative Colitis. Lancet 2012;380:1606 – 19.

Cosnes J, Gower- Rosseau C, Seksik P, Cortot A. Epidemiology and Natural History of Inflammatory Bowel Diseases. Gastroenterology 2011;140:1785 – 1794.

Tezel A, Dökmeci G, Eskiocak M, Ümit H, Soylu A.R. Epidemiological Features of Ulcerative Colitis in Trakya – Turkey. J Int Med Res. 2003 Mar-Apr;31(2):141-8.

Scott MM, Ekbom A. Epidemiology of inflammatory bowel disease. Current Opinion in Gastroenterology 2002;18:416-20.

M, F., Sleisenger & Fordtran's gastrointestinal and liver disease. 8th edition. . 2006

Silverberg MS, Satsangi J, Ahmad T, Arnott IDR, Bernstein CN, Brant SR, vd. Toward an integrated clinical, molecular and serological classification of inflammatory bowel disease: report of a Working Party of the 2005 Montreal World Congress of Gastroenterology. Can J Gastroenterol [Internet]. 2005 [kaynak 31 Mart 2021]

Suppl A. Available at: https://pubmed.ncbi.nlm.nih.gov/16151544/ 10. Haskell H, Andrews CW, Ready SI, Dendrinos K, Farraye FA, Stucchi AF, vd. Pathologic features and clinical significance of “backwash” ileitis in ulcerative colitis. Am J Surg Pathol [Internet]. Kasım 2005 [kaynak 01 Nisan 2021];29(11):1472–81. Available at: https://pubmed.ncbi.nlm.nih.gov/16224214/

Ordass I, Eckman L, Taramini M, et al. Ulcerative colitis. Lancet. 2012: 380(9853): 1606-1619.

Loftus EV Jr. Clinical epidemiology of inflammatory bowel disease: incidence, prevalence, and environmental influences. Gastroenterlogy. 2004; 126(6): 1504-1517.

Pai RK, Jairath V, Vande Casteele N, Rieder F, Parker CE, Lauwers GY. The emerging role of histologic disease activity assessment in ulcerative colitis. Gastrointest Endosc. 2018 Dec;88(6):887-898. [PubMed] [Reference list]

Satsangi J, Silverberg M. S, Vermeire, et al. The Montreal classification of inflammatory bowel disease: Controversies, consensus, and implications. Gut. 2006 Jun;55(6):749-753.

Danese S, Fiocchi C. Ulcerative Colitis. New England Journal of Medicine.2011; 365(18), 1713–1725.

Loddenkemper C. Diagnostic standards in the pathology of inflammatory bowel disease. Dig Dis 2009; 27: 576-583.

Nikolaus S, Schreiber S. Diagnostics of Inflammatory Bowel Disease. Gastroenterology [Internet]. 2007 [kaynak 01 Nisan 2021];133(5):1670–89. Available at: https://pubmed.ncbi.nlm.nih.gov/17983810/)

Jobling J.C, Lindley K.J, Yousef Y, et al. Investigating inflammatory bowel disease--white cell scanning, radiology, and colonoscopy. Arch. Dis. Child.1996; 74(1): 22–26

Kim B, Barnett J.L, Kleer C.G, et al. Endoscopic and histological patchiness in treated ulcerative colitis. Am J Gastroenterol 1999; 94:3258.

Davies, N.M., Toxicity of nonsteroidal anti-inflammatory drugs in the large intestine. Diseases of the Colon & Rectum, 1995. 38(12): p. 1311-1321.

Jess T, Simonsen J, Jorgensen K.T, et al. Decreasing risk of colorectal cancer in patients with inflammatory bowel disease over 30 years. Gastroenterology 2012; 143(2): 375-381.

Danese S, Banerjee R, Cummings JF, Dotan I, Kotze PG, Leong RWL, Paridaens K, Peyrin-Biroulet L, Scott G, Assche GV, Wehkamp J, Yamamoto-Furusho JK. Consensus recommendations for patient-centered therapy in mild-to-moderate ulcerative colitis: the i Support Therapy-Access to Rapid Treatment (iSTART) approach. Intest Res. 2018 Oct;16(4):522-528. [PMC free article] [PubMed] [Reference list])

Ko CW, Singh S, Feuerstein JD, Falck-Ytter C, Falck-Ytter Y, Cross RK, vd. AGA Clinical Practice Guidelines on the Management of Mild- 51 to-Moderate Ulcerative Colitis. Gastroenterology [Internet]. 01 Şubat 2019 [kaynak 02 Nisan 2021];156(3):748–64. Available at: /pmc/articles/PMC6858922/)

Hanauer, S.B., et al., Delayed-release oral mesalamine 4.8 g/day (800 mg tablets) compared with 2.4 g/day (400 mg tablets) for the treatment of mildly to moderately active ulcerative colitis: the ASCEND I trial. Canadian Journal of Gastroenterology and Hepatology, 2007. 21(12): p. 827-834.)

Probert CSJ, Hearing SD, Schreiber S, Kühbacher T, Ghosh S, Arnott IDR, vd. Infliximab in moderately severe glucocorticoid resistant ulcerative colitis: A randomised controlled trial. Gut [Internet]. 01 Temmuz 2003 [kaynak 02 Nisan 2021];52(7):998–1002. Available at: https://pubmed.ncbi.nlm.nih.gov/12801957/

Sandborn WJ, Van Assche G, Reinisch W, Colombel J, D’Haens G, Wolf DC, vd. Adalimumab induces and maintains clinical remission in patients with moderate-to-severe ulcerative colitis. Gastroenterology [Internet]. 2012 [kaynak 02 Nisan 2021];142(2). Available at: https://pubmed.ncbi.nlm.nih.gov/22062358/

Sandborn WJ, Feagan BG, Marano C, Zhang H, Strauss R, Johanns J, vd. Subcutaneous golimumab induces clinical response and remission in patients with moderate-to-severe ulcerative colitis. Gastroenterology [Internet]. 2014 [kaynak 02 Nisan 2021];146(1):85–95. Available at: https://pubmed.ncbi.nlm.nih.gov/23735746/

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6 Nisan 2022

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