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<article article-type="case-report" dtd-version="1.0" xml:lang="HR" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML">
<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">LV</journal-id>
<journal-id journal-id-type="nlm-ta">Lijec Vjesn</journal-id>
<journal-title-group>
<journal-title>Lijecnicki Vjesnik</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Lijec. Vjesn.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="ppub">0024-3477</issn>
<issn pub-type="epub">1849-2177</issn>
<publisher><publisher-name>Croatian Medical Association</publisher-name></publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">LV-142-398</article-id>
<article-id pub-id-type="doi">10.26800/LV-142-11-12-59</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Clinical observation</subject></subj-group>
</article-categories>
<title-group>
<article-title>Adenokarcinom dvanaesnika u oboljelog od celijakije: prikaz bolesnika</article-title>
<trans-title-group xml:lang="en">
<trans-title>Duodenal adenocarcinoma in a patient with celiac disease: a case report</trans-title>
</trans-title-group>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6981-7877</contrib-id><name><surname>Bakula</surname><given-names>Branko</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><name><surname>Zori&#x010D;i&#x0107;</surname><given-names>Ivan</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><name><surname>Sever</surname><given-names>Marko</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><name><surname>Maru&#x0161;i&#x0107;</surname><given-names>Marinko</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author"><name><surname>Troskot-Peri&#x0107;</surname><given-names>Rosana</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author"><name><surname>Grbavac</surname><given-names>Martin</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><name><surname>&#x0160;tritof</surname><given-names>Domagoj</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib>
<aff id="aff1"><label>1</label>Klinika za kirurgiju, Medicinski fakultet u Zagrebu, Klini&#x010D;ka bolnica &#x201E;Sveti Duh&#x201C;</aff>
<aff id="aff2"><label>2</label>Zavod za gastroenterologiju, Klinika za internu medicinu, Medicinski fakultet u Zagrebu, Klini&#x010D;ka bolnica &#x201E;Sveti Duh&#x201C;</aff>
</contrib-group>
<author-notes>
<corresp id="cor1">Adresa za dopisivanje: Branko Bakula, dr. med., <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0001-6981-7877">https://orcid.org/0000-0001-6981-7877</ext-link> Klinika za kirurgiju, Klini&#x010D;ka bolnica &#x201E;Sveti Duh&#x201C;, Sveti Duh 64, 10000 Zagreb; e-po&#x0161;ta: <email xlink:href="bakulabranko@gmail.com">bakulabranko@gmail.com</email></corresp></author-notes>
<pub-date pub-type="epub-ppub"><month>12</month><year>2020</year></pub-date>
<volume>142</volume>
<issue>11-12</issue>
<fpage>398</fpage>
<lpage>404</lpage>
<permissions>
<copyright-year>2020</copyright-year>
<copyright-holder>Croatian Medical Association</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by-nc-nd/4.0/" specific-use="CC BY-NC-ND 4.0"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND) 4.0 License.</license-p></license>
</permissions>
<abstract>
<title>SA&#x017D;ETAK</title>
<p>Adenokarcinom dvanaesnika izrazito je rijetka bolest i zaslu&#x017E;an je za samo oko 1,3% gastrointestinalnih tumora odnosno oko 0,2% svih malignih tumora u &#x010D;ovjeka. Naj&#x010D;e&#x0161;&#x0107;i maligni tumori tankog crijeva jesu karcinoid (44%) i adenokarcinom (33%). Ne&#x0161;to vi&#x0161;e od polovine adenokarcinoma tankog crijeva nalazi se u duodenumu. Bolesti koje povisuju rizik od nastanka ovoga rijetkog malignoma jesu obiteljska adenomatozna polipoza (FAP), nasljedni nepolipozni kolorektalni karcinom (HNPCC), Peutz-Jeghersov sindrom, Crohnova bolest te celijakija. Prikazujemo 43-godi&#x0161;njeg mu&#x0161;karca kojemu je jo&#x0161; u djetinjstvu dijagnosticirana celijakija, a primljen je u na&#x0161;u bolnicu zbog intenzivnog povra&#x0107;anja i do 30 puta na dan unatrag nekoliko dana, gubitka te&#x017E;ine od oko 20 kg unatrag godinu dana uz nalaz bla&#x017E;e anemije. Tijekom hospitalizacije rendgenogramom pasa&#x017E;e &#x017E;eludca, MSCT-om, enteroskopijom te PHD-om verificiran je opstruktivni adenokarcinom horizontalnog segmenta dvanaesnika. Tumor je uklonjen Whippleovom operacijom. Adenokarcinom duodenuma, iako rijetka, kobna je komplikacija celijakije. Rizik od razvoja karcinoma vi&#x0161;i je u pacijenata koji se nisu pridr&#x017E;avali bezglutenske dijete, kao i kod onih kojima je bolest otkrivena kasno. Danas smo svjedoci neprihvatljivo malenom postotku rano otkrivenih adenokarcinoma tankog crijeva u pacijenata s celijakijom. &#x017D;elimo naglasiti va&#x017E;nost redovitoga klini&#x010D;kog pra&#x0107;enja bolesnika s celijakijom i njihova educiranja o dijeti, uz nizak prag za indiciranje dodatnih endoskopskih ili slikovnih pretraga pri promjeni klini&#x010D;kog stanja ili slabom odgovoru na primijenjeno lije&#x010D;enje.</p>
</abstract>
<trans-abstract xml:lang="en">
<title>SUMMARY</title>
<p>Duodenal adenocarcinoma is extremely rare and is responsible for only about 1.3% of gastrointestinal or about 0.2% of all malignant tumors in humans. Most common malignant tumors of the small intestine are carcinoid (44%) and adenocarcinoma (33%). More than half of adenocarcinoma of the small intestine can be found in the duodenum. Diseases that increase the risk of this rare malignancy are familial adenomatous polyposis (FAP), hereditary nonpolyposis colorectal cancer (HNPCC), Peutz-Jeghers syndrome, Crohn&#x2019;s disease and celiac disease. We present the case of a 43-year-old man, in childhood diagnosed with celiac disease, who was admitted to our hospital because of intense vomiting, up to about 30 times a day over the last few days, with weight loss of about 20 kg in a previous year and with the finding of minor anemia. Upper GI series, abdominal MSCT and enteroscopy revealed obstructing adenocarcinoma of horizontal duodenal segment. The tumor was resectable and the Whipple procedure was performed. Duodenal adenocarcinoma, although rare, is a fatal complication of celiac disease. Patients who did not adhere to a gluten-free diet and those with late diagnosis of celiac disease have a greater risk of developing cancer. Today we are witnessing an unacceptably low percantage of early diagnosed patients with small bowel adenocarcinoma. We wish to emphasize the importance of a regular follow-up by experts as well as proper diet education, with low threshold for indicating additional endoscopic and imaging investigations in the case of worsening of symptoms or in the case of a noncompliant patient.</p>
</trans-abstract>
<kwd-group kwd-group-type="author"><kwd>Deskriptori ADENOKARCINOM &#x2013; dijagnoza, kirurgija, komplikacije</kwd><kwd>TUMORI DVANAESNIKA &#x2013; dijagnoza, kirurgija, komplikacije</kwd><kwd>CELIJAKIJA &#x2013; komplikacije</kwd><kwd>PANKREATIKODUODENEKTOMIJA</kwd><kwd>BEZGLUTENSKA DIJETA</kwd></kwd-group>
<kwd-group kwd-group-type="translator" xml:lang="en"><title>Descriptors </title><kwd>ADENOCARCINOMA &#x2013; complications, diagnosis, surgery</kwd><kwd>DUODENAL NEOPLASMS &#x2013; complications, diagnosis, surgery</kwd><kwd>CELIAC DISEASE &#x2013; complications</kwd><kwd>PANCREATICODUODENECTOMY</kwd><kwd>DIET,GLUTEN-FREE</kwd></kwd-group>
</article-meta>
</front>
<body>
<p>Adenokarcinom dvanaesnika izrazito je rijetka bolest i zaslu&#x017E;an je za samo oko 1,3% gastrointestinalnih tumora odnosno oko 0,2% svih malignih tumora u &#x010D;ovjeka. (<xref ref-type="bibr" rid="r1"><italic>1</italic></xref>) Tanko crijevo op&#x0107;enito je rijetko sijelo malignih tumora, &#x0161;to se obja&#x0161;njava br&#x017E;im prolaskom crijevnog sadr&#x017E;aja, kra&#x0107;im djelovanjem karcinogena iz hrane na crijevnu sluznicu, teku&#x0107;om konzistencijom crijevnog sadr&#x017E;aja i manjom koli&#x010D;inom bakterija u crijevu. (<xref ref-type="bibr" rid="r2"><italic>2</italic></xref>) Incidencija adenokarcinoma tankog crijeva u op&#x0107;oj populaciji, prema jednoj je velikoj studiji, 3,7/1.000.000. (<xref ref-type="bibr" rid="r3"><italic>3</italic></xref>) Naj&#x010D;e&#x0161;&#x0107;i maligni tumori tankog crijeva jesu karcinoid (44%) i adenokarcinom (33%). Rje&#x0111;e se mogu na&#x0107;i stromalni karcinomi (17%) te limfomi (8%). (<xref ref-type="bibr" rid="r4"><italic>4</italic></xref>) Ne&#x0161;to vi&#x0161;e od polovine adenokarcinoma tankog crijeva nalazi se u duodenumu, i to ve&#x0107;ina u njegovu drugom segmentu, do oko 7 cm od Vaterove papile, &#x0161;to poti&#x010D;e rasprave o karcinogenosti pankreati&#x010D;no-bilijarnih sokova. (<xref ref-type="bibr" rid="r5"><italic>5</italic></xref>) Bolesti koje povisuju rizik od nastanka ovoga rijetkog malignoma jesu obiteljska adenomatozna polipoza, nasljedni nepolipozni kolorektalni karcinom, Peutz-Jeghersov sindrom, Crohnova bolest i celijakija. (<xref ref-type="bibr" rid="r6"><italic>6</italic></xref>&#x2013;<xref ref-type="bibr" rid="r9"><italic>9</italic></xref>)</p>
<p>Celijakija je kroni&#x010D;na autoimunosna bolest uzrokovana preosjetljivo&#x0161;&#x0107;u crijevne sluznice na gluten te je povezana s povi&#x0161;enim rizikom od nastanka ponajprije limfoma tankog crijeva, ali i adenokarcinoma. Malignom kod pacijenata s celijakijom pojavljuje se u ne&#x0161;to ranijoj dobi nego kod op&#x0107;e populacije, a rizik se povisuje kod pacijenata koji se ne pridr&#x017E;avaju bezglutenske dijete. (<xref ref-type="bibr" rid="r10"><italic>10</italic></xref>) Simptomi adenokarcinoma duodenuma nespecifi&#x010D;ni su (bol u trbuhu, mu&#x010D;nina, gubitak te&#x017E;ine, anemija) pa je, na&#x017E;alost, u ve&#x0107;ine bolesnika u trenutku dijagnosticiranja bolest ve&#x0107; u uznapredovalom stadiju (stadij III. i IV. u 58% bolesnika). (<xref ref-type="bibr" rid="r11"><italic>11</italic></xref>) Jedino potencijalno uspje&#x0161;no lije&#x010D;enje jest kirur&#x0161;ka resekcija. Kod operabilnih karcinoma prvog i drugog segmenta duodenuma kirur&#x0161;ko je lije&#x010D;enje jasno &#x2013; cefali&#x010D;na pankreatikoduodenektomija. Kada je rije&#x010D; o operabilnim karcinomima 3. i 4. segmenta duodenuma, treba re&#x0107;i da jo&#x0161; nije dokazana prednost s obzirom na dulje pre&#x017E;ivljenje kod pacijenata s radikalnom operacijom kao &#x0161;to je pankreatikoduodenenktomija u odnosu prema pacijentima sa segmentalnom resekcijom dvanaesnika. (<xref ref-type="bibr" rid="r12"><italic>12</italic></xref>&#x2013;<xref ref-type="bibr" rid="r14"><italic>14</italic></xref>)</p>
<sec sec-type="other1">
<title>Prikaz bolesnika</title>
<p>Prikazujemo 43-godi&#x0161;njeg mu&#x0161;karca koji je primljen u na&#x0161;u bolnicu zbog intenzivnog povra&#x0107;anja i do 30 puta na dan unatrag nekoliko dana, gubitka te&#x017E;ine od oko 20 kg unatrag godinu dana uz nalaz bla&#x017E;e anemije (hemoglobin 110 g/L). Pacijentu je jo&#x0161; u djetinjstvu dijagnosticirana celijakija. U 18. godini prekinuo je s bezglutenskom dijetom te je, budu&#x0107;i da nije imao ve&#x0107;ih tegoba, nastavio s normalnom prehranom. Iz anamneze se doznalo da pacijent nije pu&#x0161;io, alkohol je konzumirao prigodno, a obiteljska mu anamneza nije bila optere&#x0107;ena karcinomom. Godinu dana prije prijma u na&#x0161;u bolnicu zbog simptoma dispepsije obavio je gastroskopiju u privatnoj ustanovi. Uzeta je biopsija s hiperemi&#x010D;ne sluznice antruma &#x017E;eludca koja je upozorila na infekciju bakterijom <italic>Helicobacter Pylori</italic> i kroni&#x010D;an gastritis bez znakova displazije. Endoskopski prikazana sluznica dvanaesnika bila je uredna, a biopsija nije uzeta jer pacijent lije&#x010D;nika nije obavijestio o povijesti celijakije. Nakon provedene propisane trojne terapije za infekciju s <italic>H. Pylori</italic> subjektivno je do&#x0161;lo do ubla&#x017E;avanja simptoma dispepsije.</p>
<p>Tijekom hospitalizacije u na&#x0161;oj je bolnici u&#x010D;injena standardna gastroduodenoskopija do drugog segmenta duodenuma kojom se, osim znakova kroni&#x010D;noga gastritisa, nisu na&#x0161;le druge patolo&#x0161;ke bolesti. Nalaz naknadno uzete biopsije antruma &#x017E;eludca bio je benigan, ali uz perzistiranje infekcije s <italic>H. Pylori</italic>. Rendgenskom obradom (RDG) s peroralno apliciranim kontrastom na&#x0111;eni su izrazito dilatirani &#x017E;eludac te 1. i 2. segment duodenuma uz filiforman prolaz kontrasta kroz mjesto opstrukcije na horizontalnom dijelu duodenuma (<xref ref-type="fig" rid="f1">Figure 1</xref>). Vi&#x0161;eslojna kompjutorizirana tomografija (engl. <italic>Multislice computed tomography</italic> &#x2013; MSCT) abdomena upozorila je na tumor dvanaesnika, veli&#x010D;ine oko 3,7 cm, smje&#x0161;ten ispod gornjih mezenterijskih &#x017E;ila (<xref ref-type="fig" rid="f2">Figure 2 i</xref> <xref ref-type="fig" rid="f3">Figure 3</xref>.. S obzirom na prija&#x0161;nju neuspje&#x0161;nu endoskopsku vizualizaciju tumora, u&#x010D;injena je enteroskopija kojom je u tre&#x0107;em segmentu duodenuma na&#x0111;ena opstruktivna tvorba s koje je uzet bioptat. Patohistolo&#x0161;ka dijagnostika (PHD) upozorila je na adenokarcinom (<xref ref-type="fig" rid="f4">Figure 4</xref>). Eksplorativnom je laparotomijom na&#x0111;en tumor dvanaesnika smje&#x0161;ten ispod gornjih mezenterijskih &#x017E;ila i lijevo od njih. Mezenterijske &#x017E;ile nisu bile zahva&#x0107;ene tumorom. Na&#x0111;ena su i 4 pove&#x0107;ana limfna &#x010D;vora mezenterija proksimalnog jejunuma i ascendentnog mezokolona bez drugih znakova rasadnica (metastaza). S obzirom na operabilan nalaz u&#x010D;injena je klasi&#x010D;na cefali&#x010D;na duodenopankreatektomija (Whippleova operacija), uz uklanjanje i navedenih udaljenih limfnih &#x010D;vorova (<xref ref-type="fig" rid="f5">Figure 5 i</xref> <xref ref-type="fig" rid="f6">Figure 6</xref>). Pacijent je zahvat dobro podnio. Poslijeoperacijski je oporavak, osim prolaznoga dvodnevnog febriliteta, protekao uredno pa je pacijent 11. poslijeoperacijskog dana otpu&#x0161;ten iz bolnice u dobrom op&#x0107;em stanju. Patohistolo&#x0161;ki nalaz potvrdio je da se radi o adenokarcinomu duodenuma koji je dopirao do gu&#x0161;tera&#x010D;e, ali ju nije infiltrirao (T3N2M1). U 2 od 4 uklonjena udaljena limfna &#x010D;vora na&#x0111;eni su dijelovi metastatskog tumora. Tako&#x0111;er, op&#x0161;irnijom analizom sluznice dvanaesnika na&#x0111;ene su znatno izra&#x017E;ena atrofija crijevnih resica, tipi&#x010D;na za nelije&#x010D;enu celijakiju, i povi&#x0161;ena koncentracija intraepitelnih limfocita. Poslijeoperacijski, jo&#x0161; tijekom hospitalizacije, serolo&#x0161;kim su testiranjem na&#x0111;ene znatno povi&#x0161;ene vrijednosti protutijela na tkivnu transglutaminazu (tTg) (47 U/mL). Konzultirali smo gastroenterologa koji je pacijentu indicirao bezglutensku dijetu i educirao ga o bolesti. Nakon otpusta iz bolnice pacijent se javio onkologu koji je indicirao i proveo adjuvantnu kemoterapiju. U okviru onkolo&#x0161;kog pra&#x0107;enja odre&#x0111;ene su vrijednosti tumorskih markera (CEA, CA 19-9, CA 125) dva i &#x0161;est mjeseci poslije operacije, a koje su bile u granicama referentnih vrijednosti. Dva mjeseca poslije operacije obavljena je kolonoskopija &#x010D;iji je nalaz, osim pronalaska ponekog divertikula sigmoidnog kolona, bio uredan. &#x0160;est mjeseci nakon operacije u&#x010D;injen je MSCT abdomena koji je bio bez znakova recidiva tumora ili znakova rasadnica (metastaza). Na kontrolnome kirur&#x0161;kom pregledu 6 mjeseci poslije zahvata pacijent je bio u dobrom op&#x0107;em stanju. Uz pridr&#x017E;avanje bezglutenske dijete i redovite kontrole gastroenterologa pacijent nije imao simptome celijakije, a kontrolne vrijednosti tTg-a u krvi bile su u referentnim vrijednostima.</p>
<fig id="f1" position="float" fig-type="figure"><label>Figure 1</label><caption><p>Contrast X-ray of upper gastrointestinal tract. Considerably dilated stomach and the first two duodenal segments</p></caption><graphic xlink:href="LV-142-398-f1"></graphic></fig>
<fig id="f2" position="float" fig-type="figure"><label>Figure 2</label><caption><p>Abdominal MSCT with peroral contrast &#x2013; frontal plane. Dilated second and third duodenal segment to the level of the superior mesenteric vessels</p></caption><graphic xlink:href="LV-142-398-f2"></graphic></fig>
<fig id="f3" position="float" fig-type="figure"><label>Figure 3</label><caption><p>Abdominal MSCT with peroral contrast administration &#x2013; transversal plane. Dilated horizontal segment of the duodenum to the level of the obstruction located between the superior mesenteric vein and the inferior caval vein</p></caption><graphic xlink:href="LV-142-398-f3"></graphic></fig>
<fig id="f4" position="float" fig-type="figure"><label>Figure 4</label><caption><p>Enteroscopic finding of the obstructing tumor of the horizontal duodenal segment</p></caption><graphic xlink:href="LV-142-398-f4"></graphic></fig>
<fig id="f5" position="float" fig-type="figure"><label>Figure 5</label><caption><p>The entire resected specimen after the Whipple operation</p></caption><graphic xlink:href="LV-142-398-f5"></graphic></fig>
<fig id="f6" position="float" fig-type="figure"><label>Figure 6</label><caption><p>Duodenal tumor &#x2013; posterior view, duodenum and pancreatic head reversed</p></caption><graphic xlink:href="LV-142-398-f6"></graphic></fig>
</sec>
<sec sec-type="other2">
<title>Rasprava</title>
<p>Najnovija istra&#x017E;ivanja upu&#x0107;uju na to da je incidencija celijakije u porastu te se smatra da od ove bolesti boluje oko 1% op&#x0107;e populacije. (<xref ref-type="bibr" rid="r15"><italic>15</italic></xref>) Sumnja na bolest postavlja se na temelju klini&#x010D;ke slike koja obuhva&#x0107;a simptome kao &#x0161;to su proljev, napuhnutost, bol u trbuhu, malapsorpcija te zaostajanje u rastu kod djece. Nakon postavljene sumnje serolo&#x0161;kim testiranjem krvi te biopsijom sluznice dvanaesnika bolest se i potvr&#x0111;uje. Povi&#x0161;ene vrijednosti protutijela na tkivnu transglutaminazu (anti-tTg) i endomizijskih (EMA) IgA-protutitijela visoko su specifi&#x010D;ne za celija&#x010D;nu bolest, &#x0161;to usmjerava daljnju obradu k biopsiji sluznice dvanaesnika radi kona&#x010D;ne potvrde bolesti. Histolo&#x0161;kom analizom sluznice drugog segmenta duodenuma analiziraju se tipi&#x010D;ni znakovi celijakije kao &#x0161;to su atrofija crijevnih resica i pove&#x0107;an broj endoepitelnih limfocita te se na osnovi tih podataka procjenjuje i te&#x017E;ina bolesti.</p>
<p>Na povezanost celijakije i adenokarcinoma tankog crijeva prvi je upozorio engleski lije&#x010D;nik Simon Kenwright jo&#x0161; 1972. godine objaviv&#x0161;i prikaz 30-godi&#x0161;njeg pacijenta kojemu je dijagnosticirana celijakija. Pacijent se nije pridr&#x017E;avao preporu&#x010D;ene bezglutenske dijete te mu je 5 godina poslije verificiran adenokarcinom po&#x010D;etnog jejunuma tijekom hitnoga kirur&#x0161;kog zahvata zbog ileusa. (<xref ref-type="bibr" rid="r16"><italic>16</italic></xref>)</p>
<p>Prvu ve&#x0107;u seriju pacijenata s adenokarcinomom tankog crijeva u populaciji koja boluje od celijakije prikazao je Swinson sa suradnicima 1983. godine u Engleskoj. (<xref ref-type="bibr" rid="r17"><italic>17</italic></xref>) U svojoj velikoj studiji, koja je analizirala 235 pacijenata s celijakijom u kojih se razvila maligna bolest, na&#x0161;ao je 19 pacijenata s adenokarcinomom tankog crijeva te je relativan rizik od razvoja adenokarcinoma tankog crijeva u pacijenata s celijakijom procijenio na 82,6, &#x0161;to je bilo pribli&#x017E;no jednako riziku od razvoja adenokarcinoma debelog crijeva u op&#x0107;oj populaciji. Iako je jasno dokazao povi&#x0161;en rizik od razvoja adenokarcinoma tankog crijeva u pacijenata s celijakijom, mo&#x017E;da je ova studija taj rizik u nekoj mjeri ipak precijenila budu&#x0107;i da su analizirani podatci samo onih pacijenata u kojih se ve&#x0107; razvila neka maligna bolest te s obzirom na &#x010D;injenicu da se ve&#x0107;ina ispitanika iz 70-ih godina 20. stolje&#x0107;a nije pridr&#x017E;avala bezglutenske dijete.</p>
<p>Na ne&#x0161;to realnije stanje danas upu&#x0107;uje velika metaanaliza iz 2015. godine koju je proveo Han sa suradnicima. (<xref ref-type="bibr" rid="r18"><italic>18</italic></xref>) Oni su analizirali 79.000 pacijenata s celijakijom u 17 razli&#x010D;itih studija provedenih u razdoblju od 1989. do 2015. godine te izra&#x010D;unali omjer izgleda za razvoj adenokarcinoma tankog crijeva kod pacijenata s celijakijom od 14,41 (95%-tni CI 5,53 &#x2013; 37,60).</p>
<p>Patogeneza razvoja adenokarcinoma kod pacijenata s celijakijom nije sasvim jasna, ali najva&#x017E;nijim se &#x010D;imbenicima smatraju: kroni&#x010D;na upala, pove&#x0107;ana propusnost kancerogenih faktora, malapsorpcija za&#x0161;titnih faktora poput vitamina i naru&#x0161;en imunosni sustav. (<xref ref-type="bibr" rid="r19"><italic>19</italic></xref>, <xref ref-type="bibr" rid="r20"><italic>20</italic></xref>)</p>
<p>Zbog histolo&#x0161;ke sli&#x010D;nosti adenokarcinoma tankog crijeva i onoga debelog crijeva, poznata sekvencija adenom &#x2013; karcinom koju vi&#x0111;amo kod debelog crijeva vjerojatno je razvojni put i kod karcinoma tankog crijeva premda takvu tezu ne mo&#x017E;emo sa sigurno&#x0161;&#x0107;u potvrditi s obzirom na rijetkost bolesti i &#x010D;injenicu da je dosad objavljeno samo nekoliko prikaza bolesnika koji opisuju nalaz adenoma u pacijenata s celijakijom. (<xref ref-type="bibr" rid="r21"><italic>21</italic></xref>, <xref ref-type="bibr" rid="r22"><italic>22</italic></xref>)</p>
<p>Iako se ve&#x0107;ina istra&#x017E;ivanja o adenokarcinomima tankog crijeva u pacijenata s celijakijom bazira na malenom broju bolesnika prikazanih u obliku pojedina&#x010D;nih slu&#x010D;ajeva, prou&#x010D;avanje literature ipak jasno upu&#x0107;uje na to da se bolest javlja uglavnom kod pacijenata koji se nisu pridr&#x017E;avali preporu&#x010D;ene bezglutenske dijete ili u pacijenata s neotkrivenom celijakijom do trenutka dijagnoze adenokarcinoma. Tako isti&#x010D;emo istra&#x017E;ivanje Caioa i suradnika, objavljeno 2019. godine, koje je jedna od najve&#x0107;ih studija provedenih u okviru jedne institucije. Oni su, naime, retrospektivno analizirali 770 pacijenata koji su zbog celijakije obra&#x0111;ivani u njihovoj bolnici u Bologni izme&#x0111;u 1995. i 2015. godine, a me&#x0111;u njima je prona&#x0111;eno i analizirano 5 pacijenata s adenokarcinomom tankog crijeva. (<xref ref-type="bibr" rid="r23"><italic>23</italic></xref>) Prosje&#x010D;na dob oboljelih bila je 41,3 godine. &#x010C;etiri su pacijenta imala tumor lociran u jejunumu, a samo jedan u drugom segmentu dvanaesnika. Kod 3 od 5 pacijenata celijakija je otkrivena istodobno s adenokarcinomom tankog crijeva, jedan se pacijent 30 godina nije pridr&#x017E;avao bezglutenske dijete unato&#x010D; celijakiji otkrivenoj na vrijeme i preporu&#x010D;enoj dijeti, a kod jednoga je, unato&#x010D; pridr&#x017E;avanju bezglutenske dijete od trenutka dijagnoze celijakije (2 godine prije dijagnoze adenokarcinoma), perzistirao histolo&#x0161;ki nalaz sluznice duodenuma koji upu&#x0107;uje na aktivnu celijakiju (slab odgovor bolesti na bezglutensku dijetu). Svih 5 pacijenata u trenutku otkrivanja adenokarcinoma tankog crijeva imalo je povi&#x0161;ene vrijednosti protutijela na tTg i EMA u krvi, a nalaz biopsije sluznice dvanaesnika pokazivao je znakove uznapredovale celijakije (4 pacijenta sa suptotalnom atrofijom crijevnih resica &#x2013; stupanj 3. C prema Marsh-Oberh&#x00FC;berovoj klasifikaciji, 1 pacijent sa stupnjem o&#x0161;te&#x0107;enja 3. A prema Marsh-Oberh&#x00FC;berovoj klasifikaciji). Zanimljivo je da su samo dva pacijenta imala klasi&#x010D;ne simptome celijakije, dok je njih troje imalo nespecifi&#x010D;ne simptome u obliku sideropeni&#x010D;ne anemije, konstipacije ili neredovitih menstruacija.</p>
<p>Ova je studija jasno upozorila na problem neadekvatne prevencije adenokarcinoma tankog crijeva u pacijenata s celijakijom. Iako danas postoje brojne pretrage za evaluaciju tankog crijeva i eventualno rano otkrivanje karcinoma, kao &#x0161;to su enteroskopija dvostrukim balonom (engl. <italic>Double balloon enteroscopy</italic> &#x2013; DBE), enteroskopija videokapsulom (engl. <italic>Video capsule endoscopy</italic> &#x2013; VCE), enterografija magnetskom rezonancijom (MR enterografija), MSCT s peroralnim kontrastom, pozitronska emisijska tomografija &#x2013; CT (PET-CT) te ultrazvuk tankog crijeva, ipak se ne uo&#x010D;ava smanjenje incidencije adenokarcinoma tankog crijeva ni pobolj&#x0161;anje prognoze u pacijenata s tom bolesti. (<xref ref-type="bibr" rid="r24"><italic>24</italic></xref>) Smisao prevencije adenokarcinoma tankog crijeva bilo bi otkrivanje bolesti u fazi adenoma sli&#x010D;no kao &#x0161;to se to ve&#x0107; desetlje&#x0107;ima prili&#x010D;no uspje&#x0161;no provodi kod tumora debelog crijeva. Na&#x017E;alost, praksa je pokazala da to nije mogu&#x0107;e. Razlog tomu vjerojatno jesu &#x010D;injenice da se najprikladnija pretraga za rano otkrivanje adenoma tankog crijeva, poput enteroskopije dvostrukim balonom, obavlja samo u visokospecijaliziranim centrima, iziskuje veliku vje&#x0161;tinu lije&#x010D;nika, a malen se broj gastroenterologa bavi time zbog &#x010D;ega je trenuta&#x010D;no nerealno o&#x010D;ekivati da se u svih pacijenata s celijakijom ova pretraga provodi redovito. S druge strane, manje invazivne pretrage poput enteroskopije videokapsulom, MR enterografije, MSCT-a ili ultrazvuka tankog crijeva nisu toliko specifi&#x010D;ne za otkrivanje adenoma, a neke od njih i relativno su skupe, &#x0161;to zasigurno smanjuje njihovu pristupa&#x010D;nost.</p>
<p>Do danas, na&#x017E;alost, ne postoje jasne me&#x0111;unarodne smjernice za rano otkrivanje adenokarcinoma tankog crijeva u pacijenata s celijakijom, kao ni kod op&#x0107;e populacije. (<xref ref-type="bibr" rid="r25"><italic>25</italic></xref>) Ipak, uzimaju&#x0107;i u obzir dosada&#x0161;nje spoznaje o ovoj temi koje idu u prilog &#x010D;injenici da se adenokarcinom tankog crijeva kod pacijenata s celijakijom uglavnom javlja u onih s neadekvatno lije&#x010D;enom ili nelije&#x010D;enom celijakijom, ve&#x0107;ina se stru&#x010D;njaka sla&#x017E;e da je za prevenciju adenokarcinoma tankog crijeva klju&#x010D;no izdvojiti pacijente s povi&#x0161;enim rizikom od nastanka te bolesti i prikladno ih obraditi prije navedenim specifi&#x010D;nim dijagnosti&#x010D;kim pretragama. U takve rizi&#x010D;ne skupine me&#x0111;u pacijentima oboljelima od celijakije spadaju: svi novootkriveni pacijenti s celijakijom stariji od 45 godina, oni s prije dijagnosticiranom celijakijom koji se dugo nisu pridr&#x017E;avali preporu&#x010D;ene bezglutenske dijete, pacijenti sa simptomima &#x201E;crijevnog alarma&#x201C; (mu&#x010D;nina, povra&#x0107;anje, gubitak te&#x017E;ine, pozitivan test na okultno krvarenje), oni s atipi&#x010D;nom klini&#x010D;kom slikom celijakije (sideropeni&#x010D;na anemija, konstipacija, bol u trbuhu) te pacijenti kod kojih unato&#x010D; pridr&#x017E;avanju bezglutenske dijete perzistira aktivna bolest potvr&#x0111;ena pozitivnim serolo&#x0161;kim testovima na protutijela (tTg i EMA) i histolo&#x0161;kim nalazom sluznice dvanaesnika. Valja naglasiti da se i svi ostali pacijenti s celija&#x010D;nom bolesti koji ne spadaju u navedene posebno rizi&#x010D;ne skupine moraju redovito kontrolirati u skladu s jasnim me&#x0111;unarodnim smjernicama koje je, me&#x0111;u ostalima, izdalo i Europsko dru&#x0161;tvo za istra&#x017E;ivanje celijakije (engl. <italic>European Society for the Study of Coeliac Disease</italic>). Posljednje izdane smjernice iz 2019. godine sa&#x017E;eto su prikazane na <xref ref-type="table" rid="t1">Table 1</xref>. (<xref ref-type="bibr" rid="r26"><italic>26</italic></xref>)</p>
<table-wrap id="t1" position="float">
<label>Table 1</label><caption><title>European Society for the Study of Coeliac Disease 2019 guidelines for patients with coeliac disease</title>
</caption>
<table frame="hsides" rules="groups">
<col width="19.6%"/>
<col width="13.61%"/>
<col width="14.04%"/>
<col width="16.16%"/>
<col width="16.17%"/>
<col width="20.42%"/>
<thead>
<tr>
<th valign="middle" align="left" scope="col" style="border-left: solid 0.75pt; border-top: solid 0.75pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">Prvi pregled<break/><italic>/First visit</italic></th>
<th valign="middle" align="left" scope="col" style="border-left: solid 0.50pt; border-top: solid 0.75pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">Prvi kontrolni pregled<break/><italic>/The first follow-up visit</italic></th>
<th valign="middle" align="left" scope="col" style="border-left: solid 0.50pt; border-top: solid 0.75pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">Drugi kontrolni pregled<break/><italic>/The second follow-up visit</italic></th>
<th valign="middle" align="left" scope="col" style="border-left: solid 0.50pt; border-top: solid 0.75pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">Tre&#x0107;i kontrolni pregled<break/><italic>/The third follow-up visit</italic></th>
<th valign="middle" align="left" scope="col" style="border-left: solid 0.50pt; border-top: solid 0.75pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">&#x010C;etvrti kontrolni pregled<break/><italic>/The fourth follow-up visit</italic></th>
<th valign="middle" align="left" scope="col" style="border-left: solid 0.50pt; border-top: solid 0.75pt; border-right: solid 0.75pt; border-bottom: solid 0.50pt">Peti i svi sljede&#x0107;i pregledi<break/><italic>/The fifth follow-up visit and all future visits</italic></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left" style="border-left: solid 0.75pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt" scope="row">Pri postavljanju dijagnoze<break/><italic>/At diagnosis</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">Nakon 3 &#x2013; 4 mjeseca<break/><italic>/After 3-4 months</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">Nakon 6 mjeseci<break/><italic>/After 6 months</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">Nakon 12 mjeseci<break/><italic>/After 12 months</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.50pt">Nakon 24 mjeseca<break/><italic>/After 24 months</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.75pt; border-bottom: solid 0.50pt">Nakon 36 mjeseci i dalje jedanput na godinu<italic>/After 36 months and thereafter once a year</italic></td>
</tr>
<tr>
<td valign="top" align="left" style="border-left: solid 0.75pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.75pt" scope="row">Fizikalni pregled, indeks tjelesne mase, edukacija o celijakiji, serologija (tTg, EMA), osnovna laboratorijska obrada krvi uklju&#x010D;uju&#x0107;i i &#x017E;eljezo, vitamin B12, hormoni &#x0161;titnja&#x010D;e, jetreni enzimi, kalcij, vitamin D; denzitometrija kosti kod starijih od 35 godina<break/><italic>/Physical examination, body mass index, dietary counselling, serology (tTg, EmA), routine blood tests including iron status, vitamin B12, thyroid function</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.75pt">evaluacija simptoma, evaluacija pridr&#x017E;avanja dijete, serologija (tTg, EMA)<break/><italic>/assess symptoms, dietary review, serology (tTg, EmA)</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.75pt">evaluacija simptoma, evaluacija pridr&#x017E;avanja dijete, serologija (tTg, EMA),<break/>ponoviti laboratorijske nalaze (kao kod prvog pregleda)<break/><italic>/assess symptoms, dietary review, serology (tTg, EmA), repeat laboratory tests (as at the first visit)</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.75pt">evaluacija simptoma, evaluacija pridr&#x017E;avanja dijete, serologija (tTg, EMA),<break/>ponoviti laboratorijske nalaze (kao kod prvog pregleda), fizikalni pregled, biopsija dvanaesnika<break/><italic>/assess symptoms, dietary review, serology (tTg, EmA), repeat laboratory tests (as at the first visit), physical examination, duodenum biopsy</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.50pt; border-bottom: solid 0.75pt">evaluacija simptoma, evaluacija pridr&#x017E;avanja dijete, serologija (tTg, EMA),<break/>hormoni &#x0161;titnja&#x010D;e,<break/>ponoviti biopsiju dvanaesnika pri pozitivnoj serologiji<break/><italic>/assess symptoms, dietary review, serology (tTg, EmA), thyroid function</italic><break/><italic>tests,repeatduodenum biopsy in case of positive serology</italic></td>
<td valign="top" align="left" style="border-left: solid 0.50pt; border-top: solid 0.50pt; border-right: solid 0.75pt; border-bottom: solid 0.75pt">evaluacija simptoma, evaluacija pridr&#x017E;avanja dijete, serologija (tTg, EMA),<break/>hormoni &#x0161;titnja&#x010D;e,<break/>ponoviti biopsiju dvanaesnika pri pozitivnoj serologiji,<break/>denzitometrija kostiju (kod starijih od 35 godina)<break/><italic>/assess symptoms, dietary review, serology (tTg, EmA),thyroid function</italic><break/><italic>tests,repeat duodenum biopsy in case of positive serology,bone densitometry in patients older than 35</italic></td>
</tr>
</tbody></table></table-wrap>
<p>U na&#x0161;eg se pacijenta adenokarcinom tankog crijeva razvio zbog dugogodi&#x0161;njeg nepridr&#x017E;avanja preporu&#x010D;ene bezglutenske dijete. Slu&#x010D;aj je dobar primjer &#x201E;zamke&#x201C; u koju mogu upasti pacijenti kod kojih nakon puberteta unato&#x010D; nepridr&#x017E;avanju dijete tipi&#x010D;ni simptomi celijakije oslabe ili nestanu, &#x0161;to ih uvjeri da su ozdravili i ohrabri za daljnje nepridr&#x017E;avanje dijete. (<xref ref-type="bibr" rid="r21"><italic>21</italic></xref>) Prvi simptomi bolesti u na&#x0161;eg pacijenta bili su posljedica razvoja okluzije duodenuma. Ve&#x0107;ina karcinoma duodenuma smje&#x0161;tena je u periampularnoj regiji ili na njegovu silaznom kraku. U takvim slu&#x010D;ajevima zbog blizine Vaterove ampule, odnosno distalnog dijela koledohusa, relativno brzo u tijeku bolesti dolazi do pojave prvih simptoma u obliku opstruktivnog ikterusa koji pacijenta dovedu lije&#x010D;niku. Kod na&#x0161;eg pacijenta karcinom dvanaesnika pojavio se na izrazito rijetkoj lokaciji, horizontalnom (tre&#x0107;em) segmentu duodenuma. Tumori tog segmenta nisu vidljivi tijekom standardne gastroduodenoskopije. Zbog ve&#x0107;e udaljenosti od Vaterove ampule prvi specifi&#x010D;niji simptomi pojavili su se tek kada je do&#x0161;lo do opstrukcije dvanaesnika, &#x0161;to je, na&#x017E;alost, ve&#x0107; znak uznapredovalog stadija bolesti.</p>
</sec>
<sec sec-type="other3">
<title>Zaklju&#x010D;ak</title>
<p>Adenokarcinom dvanaesnika, iako rijetka, kobna je komplikacija celijakije. Danas svjedo&#x010D;imo neprihvatljivo malenom postotku rano otkrivenih adenokarcinoma tankog crijeva kod pacijenata s celijakijom. &#x017D;elimo naglasiti va&#x017E;nost redovitoga klini&#x010D;kog pra&#x0107;enja bolesnika s celijakijom, njihova educiranja o dijeti te niskog praga za indiciranje dodatnih endoskopskih ili slikovnih pretraga pri promjeni klini&#x010D;kog stanja ili slabom odgovoru na primijenjeno lije&#x010D;enje.</p>
</sec>
</body>
<back>
<ref-list>
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