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1.
Clin Case Rep ; 6(4): 741-744, 2018 04.
Article in English | MEDLINE | ID: mdl-29636951

ABSTRACT

Capsule endoscopy was used to detect intestinal Taenia saginata infection in a 19-year-old man. The patient was initially believed to have Crohn's disease due to a notable family history of the disease. Capsule endoscopy is a valuable tool for diagnosing tapeworm infection even when Crohn's disease is suspected.

2.
World J Hepatol ; 8(30): 1269-1278, 2016 Oct 28.
Article in English | MEDLINE | ID: mdl-27843537

ABSTRACT

AIM: To evaluate the bidirectional association between metabolic syndrome (MS) components and antiviral treatment response for chronic hepatitis C virus (HCV) infection. METHODS: This retrospective cohort study included 119 HCV + patients treated with pegylated-interferon-α and ribavirin. Metabolic characteristics and laboratory data were collected from medical records. Differences in baseline clinical and demographic risk factors between responders and non-responders were assessed using independent samples t-tests or χ2 tests. The effects of sustained viral response (SVR) to antiviral treatment on de novo impairments in MS components, including impaired fasting glucose (IFG) and type 2 diabetes mellitus (T2DM), were assessed using univariable and multivariable logistic regression analysis, while the effect of MS components on SVR was assessed using univariable logistic regression analysis. RESULTS: Of the 119 patients, 80 (67%) developed SVR over the average 54 ± 13 mo follow-up. The cumulative risks for de novo T2DM and IFG were 5.07- (95%CI: 1.261-20.4, P = 0.022) and 3.87-fold higher (95%CI: 1.484-10.15, P = 0.006), respectively for non-responders than responders, when adjusted for the baseline risk factors age, sex, HCV genotype, high viral load, and steatosis. Post-treatment triglyceride levels were significantly lower in non-responders than in responders (OR = 0.27; 95%CI: 0.069-0.962, P = 0.044). Age and HCV genotype 3 were significantly different between responders and non-responders, and MS components were not significantly associated with SVR. Steatosis tended to attenuate SVR (OR = 0.596; 95%CI: 0.331-1.073, P = 0.08). CONCLUSION: SVR was associated with lower de novo T2DM and IFG incidence and higher triglyceride levels. Patients infected with HCV should undergo T2DM screening and antidiabetic treatment.

3.
Harefuah ; 154(10): 617-9, 677, 2015 Oct.
Article in Hebrew | MEDLINE | ID: mdl-26742221

ABSTRACT

BACKGROUND: Adult bronchogenic cysts are rare. Retrogastric bronchogenic cysts are even rarer with only over 30 cases being reported in the English literature. These foregut cysts can be confused with cystic tumors. CASE PRESENTATION: We describe the case of a large gastric bronchogenic cyst in an asymptomatic 61-year-old woman who underwent an abdominal computerized tomography as part of a routine follow-up after lumpectomy due to breast cancer. Final diagnosis was made by endoscopic ultrasound fine needle aspiration (EUS-FNA) which led to conservative management of the patient who has remained asymptomatic over the last 8 years. CONCLUSIONS: Preoperative diagnosis of adult gastric bronchogenic cyst has been difficult to achieve. Our case highlights the importance of EUS in establishing the definitive diagnosis, enabling just follow-up with repeated imaging studies. The relevant literature is discussed.


Subject(s)
Bronchogenic Cyst/diagnosis , Endoscopic Ultrasound-Guided Fine Needle Aspiration/methods , Stomach Diseases/diagnosis , Bronchogenic Cyst/pathology , Bronchogenic Cyst/therapy , Female , Follow-Up Studies , Humans , Middle Aged , Stomach Diseases/pathology , Stomach Diseases/therapy , Tomography, X-Ray Computed
4.
Harefuah ; 154(10): 649-52, 675, 2015 Oct.
Article in Hebrew | MEDLINE | ID: mdl-26742228

ABSTRACT

Common bile duct stones occur in 3%-33% of patients suffering from gallbladder stones. Concurrent gallbladder and common bile duct stones should be treated due to the risk of life-threatening complications such as pancreatitis and cholangitis. There is no consensus regarding the optimal management of common bite duct stones associated with cho[elithiasis. Currently there are variable treatment protocols for concomitant gallstones and common bile duct stones which involve laparoscopic cholecystectomy and laparoscopic bile duct exploration alone, or in combination with preoperative, postoperative, or same session endoscopic retrograde cholangiopancreatography (ERCP). Treatment options depend on local expertise and resources. The aim of this review is to discuss the different treatment options and to assess their utility based on the most recent reports and reviews.


Subject(s)
Cholangiopancreatography, Endoscopic Retrograde/methods , Cholelithiasis/surgery , Gallstones/surgery , Cholecystectomy, Laparoscopic/methods , Cholelithiasis/complications , Gallstones/complications , Humans , Laparoscopy/methods
5.
World J Gastroenterol ; 20(3): 857-62, 2014 Jan 21.
Article in English | MEDLINE | ID: mdl-24574759

ABSTRACT

A 77-year-old man with inflammatory bowel disease (IBD) and who was treated with anti-tumor necrosis factor (TNF), 6-mercaptopurine and corticosteroids, presented with primary effusion lymphoma-like lymphoma (PEL-like lymphoma) with massive ascites. The patient's clinical course was complicated by acute renal insufficiency and hypotension, which led to death within 2 wk. In general, patients with IBD may have an increased risk for development of lymphoma, which is frequently associated with immunosuppressive and/or anti-TNF antibody therapies. PEL is a rare subset of lymphoma localized to serous body cavities, lacks tumor mass or nodal involvement, and is associated with infection by human herpes virus 8 (HHV-8). Primary neoplastic effusion may also be present in patients with large B-cell lymphoma without evidence of human immunodeficiency virus or HHV-8 infections. This type of lymphoma is classified as PEL-like lymphoma. Both PEL and PEL-like lymphoma types have been reported in patients undergoing immunosuppressive therapy, but to the best of our knowledge, the case described herein represents the first PEL-like lymphoma occurring in a patient with IBD.


Subject(s)
Biological Products/adverse effects , Immunocompromised Host , Immunosuppressive Agents/adverse effects , Inflammatory Bowel Diseases/drug therapy , Lymphoma, Primary Effusion/chemically induced , Aged , Ascites/chemically induced , Biomarkers, Tumor/analysis , Fatal Outcome , Humans , Immunohistochemistry , Inflammatory Bowel Diseases/diagnosis , Inflammatory Bowel Diseases/immunology , Lymphoma, Primary Effusion/chemistry , Lymphoma, Primary Effusion/diagnostic imaging , Lymphoma, Primary Effusion/immunology , Male , Tomography, X-Ray Computed , Tumor Necrosis Factor-alpha/antagonists & inhibitors
6.
World J Hepatol ; 5(11): 649-53, 2013 Nov 27.
Article in English | MEDLINE | ID: mdl-24303094

ABSTRACT

Wilson's disease is a rare disorder of copper transport in hepatic cells, and may present as cholestatic liver disease; pancreatitis and cholangitis are rarely associated with Wilsons's disease. Moreover, cases of Wilson's disease presenting as pigmented gallstone pancreatitis have not been reported in the literature. In the present report, we describe a case of a 37-year-old man who was admitted with jaundice and abdominal pain. The patient was diagnosed with acute pancreatitis, cholangitis, and obstructive jaundice caused by pigmented gallstones that were detected during retrograde cholangiopancreatography. However, because of his long-term jaundice and the presence of pigmented gallstones, the patient underwent further evaluation for Wilson's disease, which was subsequently confirmed. This patient's unique presentation exemplifies the overlap in the clinical and laboratory parameters of Wilson's disease and cholestasis, and the difficulties associated with their differentiation. It suggests that Wilson's disease should be considered in patients with pancreatitis, cholangitis, and severe protracted jaundice caused by pigmented gallstones.

7.
Eur J Pediatr ; 168(5): 633-5, 2009 May.
Article in English | MEDLINE | ID: mdl-18762978

ABSTRACT

Pylephlebitis, a septic thrombophlebitis of the portal vein, is a life-threatening complication of intraabdominal infections, commonly associated with acute appendicitis in children, and diverticulitis in adults. A 13-year-old boy was admitted for high fever and jaundice. On the fifth day of hospitalization, ultrasound Doppler flow and Computer Tomography scan studies showed thrombosis of the portal vein and acute appendicitis. The patient was treated with antibiotics, anticoagulation and laparotomy with appendectomy. No thrombophilic risk factors were diagnosed. Our aim is to improve physicians' awareness of this complication and emphasize the importance of early diagnosis and appropriate therapy in children in order to reduce serious complications and long-term sequels.


Subject(s)
Appendicitis/complications , Sepsis/complications , Sepsis/etiology , Thrombophlebitis/complications , Thrombophlebitis/etiology , Adolescent , Anticoagulants/therapeutic use , Appendicitis/diagnosis , Heparin, Low-Molecular-Weight/therapeutic use , Humans , Male , Prothrombin/metabolism , Thrombophlebitis/drug therapy , Ultrasonography, Doppler
8.
Rheumatol Int ; 25(6): 401-5, 2005 Aug.
Article in English | MEDLINE | ID: mdl-15098137

ABSTRACT

OBJECTIVE: The aim of this study was to describe arthritis or vasculitis as initial manifestations of Crohn's disease (CD). METHODS: We describe three cases in which the rheumatological manifestations preceded the bowel disease and one with rheumatological manifestation and asymptomatic gut inflammation. The information on clinical manifestations, laboratory examination results, imaging procedures, and histological data were gathered from the patients' medical charts. A MEDLINE search for the associations of extraintestinal manifestations of inflammatory bowel disease was performed. RESULTS: Arthritis or vasculitis preceded the bowel disease by 3 to 15 months. In one case, the bowel disease remained asymptomatic throughout the follow-up period. CONCLUSION: Rheumatological presentations of CD such as arthritis and vasculitis are uncommon. The diagnosis of CD without evident bowel symptoms might offer explanations and treatment options for puzzling symptoms and signs. Recognition, early diagnosis, and treatment of the underlying gut disease might prove useful for both the bowel disease and the rheumatological manifestations.


Subject(s)
Arthritis/diagnosis , Crohn Disease/diagnosis , Vasculitis/diagnosis , Adolescent , Adult , Arthritis/etiology , Crohn Disease/complications , Diagnosis, Differential , Female , Humans , Inflammatory Bowel Diseases/complications , Inflammatory Bowel Diseases/diagnosis , Male , Middle Aged , Time Factors , Vasculitis/etiology
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