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Influence of gastric cancer screening on the stage at diagnosis and survival (Khanderia E. J Clin Gastroenterol 2016)

À§¾Ï °ËÁø È¿°ú¸¦ ºÐ¼®ÇÑ ¿µ±¹ÀÇ ¸ÞŸ¿¬±¸ÀÔ´Ï´Ù. "About 73% of the screened patients were found to have EGC compared with 43% of the nonscreened patients."

³»½Ã°æ¿¡ ºñÇÏ¿© ¹Ù·ý °Ë»ç´Â À§¾ÏÀ» 20% ¹Û¿¡ ¹ß°ßÇÏÁö ¸øÇÑ´Ù°í ÇÕ´Ï´Ù. À§¾Ï °ËÁø¿ë ¹Ù·ý °Ë»ç´Â ºÎµµ´öÇÑ ÀÏ·Î °£ÁֵǾî¾ß ÇÒ °Í °°½À´Ï´Ù.


Association between Helicobacter pylori eradication and gastric cancer incidence (Lee YC. Gastroenterology 2016)

À§¾Ï ¿¹¹æÀ» À§ÇÑ Á¦±ÕÄ¡·áÀÇ È¿°ú¸¦ ºÐ¼®ÇÑ Å¸ÀÌ¿ÏÀÇ ¸ÞŸ¿¬±¸ÀÔ´Ï´Ù. General population ¹× ESD ȯÀÚ±º ¸ðµÎ¿¡¼­ positive resultÀÔ´Ï´Ù. Pooled incidence rate ratio°¡ °¢°¢ 0.62, 0.46À̾ú½À´Ï´Ù.


Endoscopic prediction of recurrence after margin-negative endoscopic resection. (Na HK. JGH 2016)

¼­¿ï¾Æ»êº´¿ø Ãֱ⵷ ±³¼ö´Ô ÆÀ¿¡¼­ À§¾Ï ³»½Ã°æÄ¡·á ÈÄ ±¹¼ÒÀç¹ßÀ» ºÐ¼®ÇÏ¿´½À´Ï´Ù. 1995³âºÎ³Ê 2011³â±îÁö 3,347¿¹ÀÇ Á¶±âÀ§¾Ï ³»½Ã°æÄ¡·á Áß 3,027¿¹(90.7%)°¡ margin-negative EGC¿´½À´Ï´Ù. 22¿¹ÀÇ ±¹¼ÒÀç¹ß°ú 4¹è¼öÀÇ controlÀ» ºñ±³ÇÏ¿´½À´Ï´Ù. Differentiated type EGCÀÇ en-block margin negative resection scar°¡ hyperemic change ¾øÀÌ flat Çϸé Á¶Á÷°Ë»ç¸¦ ÇÒ ÇÊ¿ä°¡ ¾ø´Ù°í °á·ÐÁþ°í ÀÖ½À´Ï´Ù.


[ÀÌÁØÇà comment]

Á¦°¡ ±Ù¹«ÇÏ´Â ±â°ü¿¡¼­´Â °æÇè ¹× ÀÚ·á ÃàÀûÀÌ ÇÊ¿äÇÏ´Ù°í »ý°¢ÇÏ¿© ´çºÐ°£ ±¹¸³¾Ï¼¾ÅÍ ¹× ¼­¿ï¾Æ»êº´¿ø¿¡¼­ Á¦¾ÈÇÑ °Íº¸´Ù Á¶±Ý tightÇÏ°Ô °Ë»çÇÏ´Â Àü·«À» À¯ÁöÇÏ°í ÀÖ½À´Ï´Ù. ¾Æ·¡´Â 2016³â 2¿ù ÇöÀçÀÇ ¹æħÀÔ´Ï´Ù.

1) Á¶±âÀ§¾Ï EMR/ESD: 5³â±îÁö ÃßÀû ³»½Ã°æ¸¶´Ù scar¿¡¼­ Á¶Á÷°Ë»ç (2Á¡) → 5³â ÈĺÎÅÍ´Â Àç¹ß ÀÇ½É ¼Ò°ßÀÌ ÀÖÀ» ¶§¸¸ Á¶Á÷°Ë»ç (´Ü, Á¶±âÀ§¾Ï EMR/ESD ÈÄ Ã¹ ÃßÀû ³»½Ã°æ¿¡¼­´Â H. pylori Á¶Á÷°Ë»çµµ ÇÔ²² ½ÃÇàÇÑ´Ù.)

2) ¼±Á¾ EMR/ESD: 1³â±îÁö ÃßÀû ³»½Ã°æ¸¶´Ù scar¿¡¼­ Á¶Á÷°Ë»ç (2Á¡) → 1³â ÈĺÎÅÍ´Â Àç¹ß ÀÇ½É ¼Ò°ßÀÌ ÀÖÀ» ¶§¸¸ Á¶Á÷°Ë»ç


A randomised trial of EMR versus ESD (Terheqqen G. Gut 2016)

Æò±Õ 16mmÀÇ Á¶±â ¹Ù·¿½Äµµ¾Ï ³»½Ã°æÄ¡·áÀÇ µÎ ¹æ¹ý(EMR°ú ESD)À» ºñ±³ÇÑ µ¶ÀÏ ¿¬±¸ÀÔ´Ï´Ù. ESD´Â R0 resection rate°¡ ³ôÁö¸¸, ½Ã°£ÀÌ ¸¹ÀÌ °É¸®°í ÇÕº´ÁõÀÌ ÈçÇÕ´Ï´Ù. µ¶ÀÏ ¿¬±¸ÀÚµéÀº Ä¡·á È¿°ú°¡ ºñ½ÁÇÏ´Ù´Â ÀÌÀ¯·Î ESD¸¦ °ú¼ÒÆò°¡ÇÏ°í ÀÖ½À´Ï´Ù. Á¦°¡ º¸±â¿¡´Â ESD ¼ú±â¸¦ °¥°í ´Û¾Æ¼­ ÇÕº´Áõ ¾øÀÌ Àß ½Ã¼úÇÏ¸é °á°ú°¡ ´Ù¸¦ °Í °°½À´Ï´Ù.


Which part of a porcine stomach is suitable as an animal training model for ESD? (Horii J. Endoscopy 2016)

ÃÖ±Ù ¿ì¸®³ª¶ó ¸î¸î º´¿ø¿¡¼­ µÅÁö stomachÀ» ÀÌ¿ëÇÑ ESD hands on trainingÀÌ ÁøÇàµÇ°í ÀÖÀ¸¸ç, ´ëÇѼÒÈ­±â³»½Ã°æÇÐȸ ESD ¿¬±¸È¸¿¡¼­µµ Á¶¸¸°£ µ¿ÀÏ ÇÁ·Î±×·¥À» openÇÒ ¿¹Á¤ÀÔ´Ï´Ù.

»ï¼º¼­¿ïº´¿ø 2016³â 2¿ù 1ÀÏ

ÀϺ»¿¡¼­´Â ¿À·¡ ÀüºÎÅÍ µÅÁö stomachÀ» ÀÌ¿ëÇÑ ESD hands on trainingÀÌ ¸Å¿ì È°¹ßÇÏ°Ô ÁøÇàµÇ¾ú½À´Ï´Ù. ¿ì¸®³ª¶ó ¼±»ý´Ôµéµµ ÀϺ»ÀÇ hands on training¿¡ °­»ç·Î ÃʺùµÇ±âµµ ÇÏ¿´½À´Ï´Ù.

2015³â JDDW¿¡¼­ Àü³²´ë ÀÌ¿Ï½Ä ±³¼ö´Ô°ú ÀÎÁ¦´ë ±èÁöÇö ±³¼ö´Ô²²¼­ hands-on training¿¡¼­ ESD ½Ã¼úÀ» demonstration ÇÏ´Â Àå¸é

ÀϺ» ¿¬±¸ÀÚµéÀº µÅÁö stomachÀ¸·Î ¿À·¡ ÈÆ·ÃÇÏ´Ùº¸´Ï ¾î´À ºÎºÐÀÌ ESD ¿¬½À¿¡ ÀûÇÕÇÑÁö ±Ã±ÝÇß´ø ¸ð¾çÀÔ´Ï´Ù. °á·ÐÀûÀ¸·Î greater curvature´Â ÁÁÁö ¾Ê°í Àüº®°ú Èĺ®ÀÌ ÁÁ´Ù´Â À̾߱âÀÔ´Ï´Ù. ¾Æ·¡ »çÁø°ú °°ÀÌ ÁÂÃø greater curvature´Â »ç¶÷°ú µÅÁö°¡ ¿µ ´Ù¸¥µ¥ ¿ìÃø anterior wallÀº »ç¶÷°ú µÅÁö°¡ ºñ½ÁÇÏ´Ù°í ÇÕ´Ï´Ù.

Simulator box¿¡ µÅÁö stomachÀ» °Å²Ù·Î ÀåÂøÇϸé upper stomach Àüº®°ú È宵µ ESD ¿¬½À¿¡ »ç¿ëÇÒ ¼ö ÀÖ´Ù´Â ¾ÆÀ̵ð¾î°¡ Èï¹Ì·Î¿ü½À´Ï´Ù.


Guidelines for endoscopic submucosal dissection and endoscopic mucosal resection for early gastric cancer (Ono H. Digest Endosc 2016)

ÀϺ»¼ÒÈ­±â³»½Ã°æÇÐȸ¿Í ÀϺ»À§¾ÏÇÐȸ°¡ °øµ¿À¸·Î Á¶±âÀ§¾Ï ³»½Ã°æÄ¡·á °¡À̵å¶óÀÎÀ» ³Â½À´Ï´Ù. ÀϺ»ÀÇ ÀïÀïÇÑ ¸â¹öµéÀÌ Ãѵ¿¿ø µÇ¾ú½À´Ï´Ù.

Indication table°ú curability decision criteria tableÀ» µû·Î Á¦½ÃÇß´Ù´Â Á¡¿¡¼­ º¸´Ù ¸í·áÇØÁ³´Ù°í »ý°¢µË´Ï´Ù. Scar¸¦ Æ÷ÇÔÇÑ ulcer findingÀÌ ÀÖ´Â differentiated type Á¡¸·¾Ï 3 cm±îÁö expanded indication¿¡ Æ÷ÇԵǾî ÀÖ½À´Ï´Ù. ±×·¯³ª Á¡¸·ÇϾÏÀ¸·Î ÆÇ´ÜµÈ °æ¿ì(cT1b)´Â Å©±â¿Í ¹«°üÇÏ°Ô expanded indicationÀÌ ¾Æ´Ï¶ó´Â Á¡¿¡ À¯ÀÇÇսôÙ. À§¾Æ·¡ µÎ Ç¥¸¦ ºñ±³ÇÏ¸é ±Ý¹æ ¾Ë ¼ö ÀÖ½À´Ï´Ù.


ACG Clinical Guideline: Diagnosis and Management of Barrett's Esophagus (Shaheen NJ. AJG 2016).

2016³â ¹Ù·¿½Äµµ °¡À̵å¶óÀÎÀÌ ³ª¿Ô½À´Ï´Ù. Á¦°¡ Èï¹Ì·Ó°Ô º» ºÎºÐÀº ¾Æ·¡¿Í °°½À´Ï´Ù.

1 cm ¹Ì¸¸ÀÇ ¹Ù·¿½Äµµ ÀǽɺÎÀ§´Â ¹Ù·¿½Äµµ·Î Áø´ÜÇÏÁö ¾Êµµ·Ï ±ÇÇÏ°í ÀÖ½À´Ï´Ù. Á¶Á÷°Ë»çµµ ÇÏÁö ¸»¶ó°í ÇÕ´Ï´Ù (should not be performed).

Recommendation 2 . Endoscopic biopsy should not be performed in the presence of a normal Z line or a Z line with < 1 cm of variability (strong recommendation, low level of evidence).

BE has been traditionally defined as the presence of at least 1 cm of metaplastic columnar epithelium that replaces the stratifi ed squamous epithelium normally lining the distal esophagus. The reason why such segments < 1 cm have been classifi ed as "specialized IM of the esophagogastric junction" (SIM-EGJ) and not BE is because of high interobserver variability as well as the low risk for EAC. Patients with SIM-EGJ have not demonstrated an increase in the development of dysplasia or EAC in large cohort studies aft er long-term follow-up, in contrast with patients with segments of IM >1 cm.

¹Ù·¿½Äµµ¶óµµ dysplasia°¡ ¾øÀ¸¸é ³»½Ã°æÀ» ³Ê¹« ÀÚÁÖ ÇÏÁö´Â ¾Êµµ·Ï ±ÇÇÏ°í ÀÖ½À´Ï´Ù.

Acknowledging recent data on the low risk of malignant progression in patients with nondysplastic BE, endoscopic surveillance intervals are attenuated in this population; patients with nondysplastic BE should undergo endoscopic surveillance no more frequently than every 3-5 years. Neither routine use of biomarker panels nor advanced endoscopic imaging techniques (beyond high-definition endoscopy) is recommended at this time. Endoscopic ablative therapy is recommended for patients with BE and high-grade dysplasia, as well as T1a esophageal adenocarcinoma. Based on recent level 1 evidence, endoscopic ablative therapy is also recommended for patients with BE and low-grade dysplasia, although endoscopic surveillance continues to be an acceptable alternative. Given the relatively common recurrence of BE after ablation, we suggest postablation endoscopic surveillance intervals.

ChomopreventionÀ¸·Î PPI »ç¿ëÀ» ±ÇÇÏ°í ÀÖ½À´Ï´Ù.

Recommendation 26 . Patients with BE should receive once-daily PPI therapy. Routine use of twice-daily dosing is not recommended, unless necessitated because of poor control of refl ux symptoms or esophagitis (strong recommendation, moderate level of evidence).

PPI therapy is common in patients with BE, in part because of the high proportion of those patients who also have symptomatic GERD. In these cases, the use of PPIs is substantiated by the need for symptom control, making consideration of chemoprevention secondary. However, even in patients without refl ux symptoms, in whom BE is incidentally found during evaluation of other symptoms and/or signs, the use of PPIs deserves consideration. Several cohort studies now suggest that subjects with BE maintained on PPI therapy have a decreased risk of progression to neoplastic BE compared with those with either no acid suppressive therapy or those maintained on H2RA therapy. In addition, the risk profi le of these medications is favorable in most patients, and the cost of this class of drugs has diminished substantially in recent years because of the availability of generic forms of the medications.

These factors, combined with the theoretical consideration that the same infl ammation that may be in part be responsible for pathogenesis of BE may also promote progression of BE, make the use of PPIs in this patient population appear justifi ed, even in those without GERD symptoms. Given the low probability of a randomized study of PPI use in BE, decisions regarding this intervention will likely rely on these retrospective data and expert opinion.


Clinical impact of second-look endoscopy after ESD (Jee SR. EJGH 2016)

ºÎ»ê´ë¿Í °í½Å´ë°¡ Çù·ÂÇÏ¿© ESD ÈÄ second-look endoscopyÀÇ Àǹ̸¦ ºÐ¼®ÇÏ¿´½À´Ï´Ù. ÀüüÀûÀ¸·Î negative studyÀÔ´Ï´Ù. Áï routineÇÏ°Ô second-look endoscopy¸¦ ÇÒ ÇÊ¿ä°¡ ¾ø´Ù´Â °ÍÀÔ´Ï´Ù. ¿ÀÈ÷·Á second-look endoscopy¸¦ ¹ÞÀº ȯÀÚ¿¡¼­ ÃâÇ÷·üÀÌ ³ô¾Ò½À´Ï´Ù. ÀúÀÚµéÀº second-look endoscopy ÀÚü°¡ ÃâÇ÷À» ÀÏÀ¸Å³ À§ÇèÀÌ ÀÖ´Ù´Â Á¡À» ÁöÀûÇÏ¿´½À´Ï´Ù.

ÀüÀûÀ¸·Î µ¿ÀÇÇÕ´Ï´Ù. ²À ÇÊ¿äÇÏÁö ¾ÊÀº °Ë»ç´Â ºÎÀÛ¿ë, ÇÕº´Áõ¸¸ ÀÏÀ¸Å³ »ÓÀÔ´Ï´Ù.


»óºÎÀ§Àå°ü ³»½Ã°æ ½Ã¼úÀÇ ±¹°¡°£ Â÷ÀÌ (Uedo N. Digest Endosc 2016 - Epub)

ÀϺ»°ú ÀϺ»ÀÌ ¾Æ´Ñ ´Ù¸¥ ³ª¶ó(ŸÀÌ¿Ï, ŸÀÌ, ¸»·¹ÀÌÁö¾Æ, Çѱ¹, Áß±¹, ÀÌÅ»¸®¾Æ, ¹Ì±¹, È£ÁÖ µî)ÀÇ ¿©·¯ ¼±»ý´ÔµéÀÇ ³»½Ã°æ style¿¡ ´ëÇÑ survey °á°ú°¡ ¹ßÇ¥µÇ¾ú½À´Ï´Ù. Çѱ¹¿¡¼­´Â Àú¸¦ Æ÷ÇÔÇÏ¿© 5ºÐÀÌ ¼³¹®¿¡ Âü¿©ÇÏ¿´½À´Ï´Ù.

International groupÀÇ ´ëÇ¥¼ºÀÌ ¶³¾îÁö´Â ÀÚ·áÀÌÁö¸¸ ÀϺ»ÀÇ ³»½Ã°æ ÇöȲÀ» »ìÆ캼 ¼ö ÀÖ´Â ÁÁÀº ±âȸ¶ó°í »ý°¢µË´Ï´Ù. SurveyÀÎ °ü°è·Î Çö½Ç°ú´Â ¾à°£ ´Ù¸¦ ¼ö ÀÖ´Ù´Â Á¡À» °¨¾ÈÇØ ÁÖ¼¼¿ä.

ÀϺ»À̳ª ±âŸ ³ª¶ó ¸ðµÎ¿¡¼­ antispasmodics¸¦ »ç¿ëÇÏÁö ¾Ê´Â °æ¿ì°¡ ¸¹¾Ò½À´Ï´Ù. Àú´Â Ưº°ÇÑ ±Ý±âÁõÀÌ ¾øÀ¸¸é °ÅÀÇ Ç×»ó »ç¿ëÇߴµ¥¿ä... °í¹ÎÇØ º¼ À̽´ÀÔ´Ï´Ù. Antispasmodics¸¦ »©°í °Ë»çÇصµ °á°ú¿¡ Â÷ÀÌ°¡ ¾ø´Ù¸é ¾öû ÆíÇØÁú °Í °°½À´Ï´Ù.

ÀϺ»¿¡¼­´Â mucolytics/deforming agents¸¦ °ÅÀÇ Ç×»ó »ç¿ëÇϴ±º¿ä.

ÀϺ»ÀÇ clinic¿¡¼­´Â transnasal endoscopy¸¦ »ó´çÈ÷ ¸¹ÀÌ ÀÌ¿ëÇÏ°í ÀÖ±º¿ä. ¿ì¸®³ª¶ó¿¡¼­´Â ¸Å¿ì µå¹°°Ô ÀÌ¿ëµË´Ï´Ù¸¸...

»óºÎÀ§Àå°ü ³»½Ã°æÀÇ °Ë»ç ½Ã°£Àº ¿ª½Ã 5ºÐ ÀüÈÄ°¡ °¡Àå ¸¹Àº °Í °°½À´Ï´Ù. 3ºÐÀº ºÐ¸íÈ÷ ºÎÁ·ÇÑ ½Ã°£ÀÔ´Ï´Ù.

ÀϺ»»ç¶÷µéÀº º´¼Ò ´ç Á¶Á÷°Ë»ç ¼ö°¡ ¸Å¿ì Àû½À´Ï´Ù. ÇÑ°³ ȤÀº µÎ°³ Á¤µµ target biopsy ÇÏ´Â °ÍÀÌ ÀϺ» ½ºÅ¸ÀÏÀÔ´Ï´Ù.


À§¾Ï ¿µ¿ª¿¡¼­ °¡Àå ¿µÇâ·ÂÀÌ ³ôÀº ³í¹® 100°³ (Powell AG. Int J Surg 2016)

À§¾Ï ¿µ¿ª¿¡¼­ °¡Àå ¿µÇâ·ÂÀÌ ³ôÀº ³í¹® 100°³°¡ ¹ßÇ¥µÇ¾ú½À´Ï´Ù. 1µîÀº ParsonnetÀÇ 1991³â NEJM ³í¹® Helicobacter pylori infection and the risk of gastric carcinoma À̾ú½À´Ï´Ù. 100À§ ³»¿¡ ¿ì¸®³ª¶ó ³í¹®ÀÌ 3°³ ÀÖ¾ú½À´Ï´Ù

7À§. ¼­¿ï´ë ³»°ú ¹æ¿µÁÖ ±³¼ö´ÔÀÇ 2010³â Lancet ³í¹® Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): a phase 3, open-label, randomised controlled trial

50À§. ÇѸ²´ë¿¡ °è¼Ì°í NCI ¿¬¼ö Áß ¹Ú±ÙÄ¥ ±³¼ö´ÔÀÌ ÀÛ¼ºÇÑ 1994³â Proc Natl Acad Sci U S A ³í¹® Genetic changes in the transforming growth factor beta (TGF-beta) type II receptor gene in human gastric cancer cells: correlation with sensitivity to growth inhibition by TGF-beta

61À§. ¿¬¼¼´ë ¿Ü°ú 2000³â Br J Surg ³í¹® Recurrence following curative resection for gastric carcinoma


Å©·Ðº´ ȯÀÚÀÇ À§³»½Ã°æ ¼Ò°ß

Intestinal Research 2016³â ùȣ¿¡ ½Ç¸° Gastric lesions in patients with Crohn¡¯s disease in Korea: a multicenter study¸¦ ¼Ò°³ÇÕ´Ï´Ù. Å©·Ð ȯÀÚ¿¡¼­ gastric noncaseating granuloma°¡ prognostic value¸¦ °¡Áú ¼ö ÀÖ´Ù´Â °á·ÐÀÌ ½Å¼±Çß½À´Ï´Ù.

Methods: Among 492 patients with CD receiving upper gastrointestinal (GI) endoscopic evaluation in 19 Korean hospitals, we evaluated the endoscopic findings and gastric histopathologic features of 47 patients for our study. Histopathologic classification was performed using gastric biopsy tissues, and H. pylori infection was determined using the rapid urease test and histology. Results: There were 36 men (76.6%), and the median age of patients at the time of upper GI endoscopy was 23.8 years (range, 14.2-60.5). For CD phenotype, ileocolonic disease was observed in 38 patients (80.9%), and non-stricturing, nonpenetrating disease in 31 patients (66.0%). Twenty-eight patients (59.6%) complained of upper GI symptoms. Erosive gastritis was the most common gross gastric feature (66.0%). Histopathologically, H. pylori-negative chronic active gastritis (38.3%) was the most frequent finding. H. pylori testing was positive in 11 patients (23.4%), and gastric noncaseating granulomata were detected in 4 patients (8.5%). Gastric noncaseating granuloma showed a statistically significant association with perianal abscess/fistula (P=0.0496).


Àεµ¿¡¼­ ¸¸¼º ¼ÒÀå ¼³»çÀÇ ¿øÀÎ

Intestinal Research 2016³â ùȣ¿¡ ½Ç¸° Spectrum of chronic small bowel diarrhea with malabsorption in Indian subcontinent: is the trend really changing?À» ¼Ò°³ÇÕ´Ï´Ù. Àεµ¿¡¼­´Â »ý°¢º¸´Ù ±â»ýÃæÁõÀÌ ¾ÆÁ÷µµ Áß¿äÇÑ ºÎºÐÀ» Â÷ÁöÇÏ°í ÀÖ¾ú½À´Ï´Ù. ºÐ¼±Ãæ (Strongyloides stercoralis)µµ Èï¹Ì·Ó±º¿ä.



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