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1.
Endoscopy ; 39(12): 1046-52, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18072054

ABSTRACT

BACKGROUND AND STUDY AIMS: Although capsule endoscopy has become a central diagnostic tool for small-bowel evaluation, retention of a capsule remains a major concern. This study attempted to investigate the incidence and clinical outcomes of capsule retention, and to determine the factors predictive of spontaneous capsule passage after retention. PATIENTS AND METHODS: Through a nationwide multicenter survey, we retrospectively reviewed the records of 1291 patients who had a capsule endoscopy between February 2002 and July 2006 in Korea. Clinical and procedural characteristics and postprocedural outcomes were analyzed for the cases with capsule retention. RESULTS: Capsule retention occurred in 2.5 % of total cases (32/1291). The major diseases accompanying capsule retention were Crohn's disease, malignant tumors, and tuberculous enterocolitis, in decreasing order. In 11 of the 32 patients (34.4 %), early surgical or endoscopic interventions were instituted for diagnosis or treatment of diseases before retention symptoms developed. The remaining 21 (65.6 %) patients initially received medical treatments. Of these, 10 (31.3 %) ultimately underwent surgical intervention due to the development of symptoms of intestinal obstruction or medical treatment failure. The other 11 (34.4 %) eventually passed the capsule. The presence of a larger lumen diameter (greater than two-thirds of the capsule diameter) at the stricture site was associated with spontaneous passage. CONCLUSIONS: Our large-scale study suggests that retention occurs infrequently during capsule endoscopy. Moreover, a retained capsule might indicate the best intervention for the offending pathology, or it may spontaneously pass in the long run, particularly in patients with less small bowel stricture.


Subject(s)
Capsule Endoscopes/adverse effects , Capsule Endoscopy/adverse effects , Foreign Bodies/epidemiology , Intestinal Diseases/diagnosis , Intestinal Obstruction/epidemiology , Intestine, Small , Adult , Aged , Aged, 80 and over , Capsule Endoscopy/methods , Equipment Failure , Female , Foreign Bodies/etiology , Health Care Surveys , Humans , Incidence , Intestinal Obstruction/etiology , Korea , Logistic Models , Male , Middle Aged , Multivariate Analysis , Predictive Value of Tests , Probability , Prognosis , Retrospective Studies , Risk Assessment
2.
Endoscopy ; 36(4): 313-6, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15057680

ABSTRACT

BACKGROUND AND STUDY AIMS: It is not normally difficult to diagnose carcinoid tumors (well-differentiated endocrine neoplasms) of the rectum endoscopically, as they usually have a characteristic appearance. However, little is known about the atypical endoscopic findings in some rectal carcinoids and the present study was performed to analyze these. PATIENTS AND METHODS: The endoscopic findings in 67 consecutive patients with rectal carcinoids (37 men, 30 women; age range 23 - 76) were analyzed retrospectively. RESULTS: Tumor size ranged from 2 mm to 30 mm (average 7.4 mm). Of the 67 patients, 52 (78 %) displayed the characteristic endoscopic findings of smooth, round, sessile elevations covered with normal-appearing or yellow-discolored mucosa; in 15 (22 %) there were one or more atypical endoscopic findings. These included a semipedunculated appearance (n = 6), hyperemia (n = 5), a central depression (n = 6), erosion (n = 5), and ulceration (n = 4). Atypical findings were noted in none of 20 carcinoids &lambda< 5 mm in diameter; in six (20 %) of the 30 carcinoids between 5 mm and 9 mm; in six (43 %) of the 14 carcinoids between 10 mm and 19 mm; and in three (100 %) of the three carcinoids >/= 20 mm in diameter ( P < 0.001). Invasion into the muscularis propria or metastasis to the liver or lymph nodes occurred in three of the four patients with ulceration, but it was confirmed in only one of the 63 patients without ulceration ( P < 0.001). CONCLUSIONS: Atypical endoscopic appearances of rectal carcinoids are observed more frequently as the size of the tumor increases and a finding of ulceration may have a prognostic value.


Subject(s)
Carcinoid Tumor/pathology , Colonoscopy , Rectal Neoplasms/pathology , Adult , Aged , Carcinoid Tumor/surgery , Female , Humans , Male , Middle Aged , Rectal Neoplasms/surgery , Rectum/pathology , Rectum/surgery , Retrospective Studies
3.
Dig Dis Sci ; 45(7): 1405-12, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10961722

ABSTRACT

Recently, several authors have reported that Helicobacter pylori DNA has been found in human bile. The aim of this study is to investigate the presence of H. pylori in the biliary tree of Koreans, including the bile, biliary epithelium, and gallstones. This study analyzed intrahepatic bile, bile duct tissue, and gallstones from 43 patients with hepatobiliary disease (PTCS group), gallbladder bile and tissue from 23 patients with gallbladder disease (CCT group), and eight patients without hepatobiliary disease (control group). H. pylori was examined by PCR with two different primers. PCR was positive in 4/43 (9.3%) by 26 kDa protein antigen primer and in 5/43 (11.6%) by urease A gene primer in bile from the PTCS group. However, in intrahepatic duct tissue, PCR was positive in only one case. PCR of gallbladder bile, tissue, and intrahepatic duct stones was negative. Upon intrahepatic bile analysis, the pH was significantly lower in PCR-positive than in negative cases (P < 0.05). In conclusion, H. pylori DNA may be present in the bile when there are certain environmental changes, such as lowered pH; however, H. pylori does not colonize the bile duct epithelium. We could find no pathogenetic role for H. pylori in the formation of hepatolithiasis.


Subject(s)
Bile Duct Diseases/microbiology , Bile Ducts, Intrahepatic , Biliary Tract/microbiology , Cholelithiasis/microbiology , DNA, Bacterial/metabolism , Helicobacter pylori/genetics , Adult , Aged , Base Sequence/genetics , Bile/chemistry , Bile Duct Diseases/metabolism , Biliary Tract/metabolism , Cholelithiasis/metabolism , Female , Helicobacter Infections/complications , Helicobacter pylori/enzymology , Humans , Male , Middle Aged , Polymerase Chain Reaction , Urease/genetics
5.
Gastrointest Endosc ; 49(6): 743-7, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10343220

ABSTRACT

BACKGROUND: Although several reports have claimed that the appendix can be involved as a skip lesion in ulcerative colitis, they do not exclude the possibility that this skip lesion occurs as a result of medical therapy. Also, little is known about the relation between the presence of appendiceal orifice inflammation and the extent of the disease. METHODS: The presence of appendiceal orifice inflammation was prospectively assessed both endoscopically and histologically in 94 patients with active ulcerative colitis, the extent of whose disease had not been beyond the hepatic flexure. To evaluate the effect of prior medical therapy on the prevalence of appendiceal orifice inflammation, all cases were divided into two groups. Group A consisted of 66 patients who had been treated before inclusion; group B was composed of 28 patients newly diagnosed at inclusion. RESULTS: Appendiceal orifice inflammation was diagnosed in 24 (26%) of 94 patients with active subtotal ulcerative colitis, with no statistical difference observed between group A (23%) and group B (32%). In all 94 patients, the frequency of appendiceal orifice inflammation decreased significantly as the extent of disease increased, i.e., 37% in proctitis (n = 49), 17% in left-sided colitis (n = 36), and 0% in extensive colitis (n = 9) (p < 0.05). CONCLUSIONS: Appendiceal orifice inflammation as a skip lesion of ulcerative colitis is not rare, is more frequently observed in patients with less extensive disease, and is not the result of patchy improvement due to medical therapy.


Subject(s)
Appendicitis/pathology , Colitis, Ulcerative/pathology , Adult , Appendicitis/epidemiology , Appendicitis/etiology , Biopsy, Needle , Chi-Square Distribution , Colitis, Ulcerative/complications , Colitis, Ulcerative/therapy , Colonoscopy , Diagnosis, Differential , Female , Humans , Incidence , Male , Middle Aged , Prospective Studies , Risk Factors , Severity of Illness Index , Software
6.
Acta Haematol ; 97(4): 231-5, 1997.
Article in English | MEDLINE | ID: mdl-9158668

ABSTRACT

Primary renal non-Hodgkin's lymphoma (NHL) with acute renal failure is a very rare condition, which frequently occurs in bilateral renal involvement. We report a 26-year-old male with primary bilateral renal NHL presenting with acute renal failure. A CT scan of the abdomen showed markedly enlarged kidneys with multinodularity and para-aortic lymphadenopathy. A percutaneous renal biopsy demonstrated 'follicular center lymphoma, diffuse, small cell'. Thirteen cycles of systemic chemotherapy with cyclophosphamide-doxorubicin-vincristine-prednisolone (CHOP) and ifosfamide-methotrexate-etoposide-bleomycin (IMVP-Bleo) regimens were administered, which resulted in normalization of renal function with improvement of renal lymphoma. Since there was no further change of renal lesions after initial partial remission, a follow-up renal biopsy was performed 10 months after diagnosis, and no residual lymphoma was found.


Subject(s)
Acute Kidney Injury/etiology , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Kidney Neoplasms/complications , Lymphoma, Follicular/complications , Neoplasms, Multiple Primary/complications , Adult , Bleomycin/administration & dosage , Cyclophosphamide/administration & dosage , Doxorubicin/administration & dosage , Etoposide/administration & dosage , Humans , Ifosfamide/administration & dosage , Kidney Neoplasms/drug therapy , Kidney Neoplasms/pathology , Lymphoma, Follicular/drug therapy , Male , Methotrexate/administration & dosage , Neoplasms, Multiple Primary/drug therapy , Neoplasms, Multiple Primary/pathology , Prednisone/administration & dosage , Remission Induction , Vincristine/administration & dosage
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