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1.
Rev. cir. (Impr.) ; 73(6): 744-747, dic. 2021. ilus
Article in Spanish | LILACS | ID: biblio-1388890

ABSTRACT

Resumen Introducción: El síndrome de Wilkie es una causa poco frecuente de obstrucción del tracto digestivo superior, se caracteriza por una disminución del ángulo aorto-mesentérico que resulta en compresión de la tercera porción del duodeno que produce síntomas obstructivos altos. Caso Clínico: Presentamos el caso de una mujer de 64 años, con historia de dolor abdominal, pirosis, saciedad precoz e intolerancia a la vía oral, en quien los estudios iniciales mostraron esofagitis, pero en quien los síntomas no mejoraron con el tratamiento clásico para enfermedad ácido péptica y en quien estudios imagenológicos adicionales sugerían el síndrome de Wilkie como causa de los síntomas. Discusión y Conclusión: Se trata de una patología que debe conocerse y considerar en paciente con historia de pérdida de peso, marcada intolerancia a la vía oral y falta de respuesta al manejo.


Introduction: Wilkie syndrome is a rare cause of upper gastrointestinal tract obstruction, it is characterized by a decrease in the aorto-mesenteric angle that results in a compression of the third portion of the duodenum causing high obstructive symptoms. Case Report: We present the case of a 64-year-old woman, with a history of abdominal pain, heartburn, early satiety, and intolerance to the oral route, in whom initial studies showed esophagitis, but in whom symptoms did not improve with the classic treatment for peptic acid disease, additional imaging studies suggested Wilkie syndrome. Discussion and Conclusión: It is a pathology that must be known and suspected in patients with a history of weight loss, marked intolerance to oral intake, and lack of treatment response.


Subject(s)
Humans , Female , Middle Aged , Superior Mesenteric Artery Syndrome/complications , Duodenal Diseases/etiology , Intestinal Obstruction/etiology , Jejunal Diseases/etiology , Superior Mesenteric Artery Syndrome/surgery , Tomography, X-Ray Computed , Duodenal Diseases/surgery , Abdomen/diagnostic imaging , Jejunal Diseases/surgery
2.
Rev. cir. (Impr.) ; 73(3): 256-261, jun. 2021. ilus, tab
Article in Spanish | LILACS | ID: biblio-1388831

ABSTRACT

Resumen Introducción: La resección duodenal distal (RDD) es una técnica quirúrgica compleja e infrecuente usada para el tratamiento de patologías duodenales o extraduodenales, que no comprometen la papila duodenal mayor, siendo su indicación más frecuente la patología neoplásica. Objetivo: Dar a conocer nuestra experiencia con esta técnica quirúrgica. Materiales y Método: Serie de pacientes sometidos a RDD entre 2009-2020 en el Hospital Clínico UC. Resultados: Total 12 pacientes, mediana de edad 56 años. Diagnóstico preoperatorio: tumores primarios duodenales (4), tumores con compromiso duodenal por contigüidad (5) y patologías de urgencia (3). El abordaje fue abierto en 9 pacientes y laparoscópico en 3 (1 caso convertido). En 9 pacientes se resecó D3-D4, en 1 paciente incluyó parte de D2 y en 2, sólo D4. La anastomosis duodenoyeyunal fue manual en 10 casos, todas con ascenso transmesocólico del asa yeyunal. Hubo 33% (n: 4) de morbilidad, todos Clavien Dindo II y 8% de mortalidad (n: 1). No hubo filtración de la anastomosis duodenoyeyunal. En el seguimiento ninguno presentó complicaciones y 4 pacientes fallecieron por progresión oncológica. Conclusión: La principal indicación quirúrgica fue patología neoplásica y en nuestra serie no hubo morbilidad mayor ni filtración anastomótica.


Introduction: Distal duodenal resection is a complex and infrequent surgical technique used for the treatment of duodenal or extraduodenal pathologies that do not compromise the greater duodenal papilla, the most frequent indication being the neoplastic cause. Aim: To publicize our experience with this surgical technique. Materials and Method: Series of patients undergoing a distal duodenal resection between 2009-2020 at the UC Clinical Hospital. Results: Total 12 patients, median age 56 years. Preoperative diagnosis: primary duodenal tumors (4), tumors with duodenal involvement due to contiguity (5), and emergency pathologies (3). The approach was open in 9 patients and laparoscopic in 3 (1 converted). D3-D4 was resected in 10 patients, 1 included part of D2 and 2 only D4. The duodenojejunal anastomosis was manual in 10 cases, all with transmesocolic ascending of the jejunal loop. There were 33% (n: 4) morbidity, all Clavien Dindo II, and 8% mortality (n: 1). There was no leakage of the duodenojejunal anastomosis. During followup, none presented complications and 4 patients died of oncological progression. Conclusion: The main surgical indication was neoplastic pathology and in our series, there was no major morbidity or anastomotic leak.


Subject(s)
Humans , Male , Female , Duodenal Diseases/surgery , Duodenal Neoplasms/surgery , Treatment Outcome , Duodenal Diseases/diagnosis , Duodenal Diseases/etiology , Duodenal Neoplasms/diagnosis , Perioperative Period
3.
Arch. argent. pediatr ; 119(5): e513-e517, oct. 2021. tab, ilus
Article in Spanish | LILACS, BINACIS | ID: biblio-1292683

ABSTRACT

La enfermedad de injerto contra huésped es una complicación grave que se presenta después del trasplante de médula ósea, con morbilidad y mortalidad elevadas. El patrón de oro para evaluar su compromiso gastrointestinal es la endoscopia digestiva alta y baja con toma de biopsia. El desarrollo de hematoma duodenal intramural es una complicación poco frecuente asociada con este procedimiento .Se presentan dos casos de hematoma duodenal intramural posendoscopia en pacientes con trasplante y sospecha de enfermedad injerto contra huésped que presentaron un cuadro agudo de dolor abdominal y sangrado intestinal. El diagnóstico se realizó por tomografía y recibieron tratamiento conservador, con un resultado favorable. En ambos casos, el diagnóstico de enfermedad injerto contra huésped gastrointestinal se hizo a través de las biopsias colónicas con histología duodenal normal, lo que sugiere evitar la toma de muestras duodenales para prevenir esta grave complicación en pacientes de alto riesgo y, de este modo, disminuir la morbilidad.


Graft versus host disease is a serious complication that occurs following bone marrow transplant with significant morbidity and mortality. The gold standard to diagnose gastrointestinal graft versus host disease is upper and lower gastrointestinal endoscopy with histological validation. The development of intramural duodenal hematoma is a rare complication associated with this procedure. We present two cases of intramural duodenal haematoma after duodenal biopsies in bone marrow transplant patients that presented clinically with severe abdominal pain and intestinal bleeding. In both cases, CT scans confirmed the diagnosis and they were treated conservatively with favorable outcomes.Final diagnosis of gastrointestinal graft versus host disease was based on the colonic samples with normal duodenal histoarchitecture, which could lead to avoiding duodenal samples in future patients in order to prevent this serious complication and thus diminish morbidity.


Subject(s)
Humans , Male , Infant , Child , Duodenal Diseases/diagnosis , Duodenal Diseases/etiology , Graft vs Host Disease/diagnosis , Graft vs Host Disease/etiology , Endoscopy, Gastrointestinal , Hematoma/diagnosis , Hematoma/etiology , Gastrointestinal Hemorrhage
5.
Rev. chil. pediatr ; 91(2): 251-254, abr. 2020. graf
Article in Spanish | LILACS | ID: biblio-1098899

ABSTRACT

Resumen: Introducción: La hemorragia digestiva por hipertensión portal, sin alternativa de tratamiento endos- cópico o quirúrgico por localizaciones ectópicas, no identificadas del sitio de sangrado o caracterís ticas anatómicas, constituye un desafío terapéutico en Pediatría. El tratamiento habitual incluye la infusión de octreótido endovenoso. En los últimos años, la presentación de octreótido de liberación prolongada (OCT-LAR) para administración mensual intramuscular, resulta una alternativa tera péutica atractiva. Objetivo: Reportar el caso de un lactante con hemorragia digestiva por hiperten sión portal que recibió tratamiento exitoso con OCT-LAR. Caso Clínico: Paciente de 8 meses de vida, con malformación de vena porta extrahepática y episodios reiterados de sangrados digestivos con re querimientos transfusionales e infusiones de octréotido, sin posibilidad de tratamiento endoscópico o quirúrgico. Indicamos OCT-LAR intramuscular mensualmente. Después de diez meses de iniciado el tratamiento, el paciente no repitió sangrados digestivos y no presentó efectos adversos relacionados a la medicación. Conclusión: Consideramos que el reporte de este caso puede resultar de utilidad al presentar una nueva alternativa para el tratamiento de pacientes pediátricos con sangrado digestivo por hipertensión portal sin posibilidades terapéuticas convencionales.


Abstract: Introduction: Upper gastrointestinal bleeding (UGIB) secondary to portal hypertension (PHT), without endoscopic or surgical treatment options due to an ectopic or unidentified bleeding site or the patient's anatomic characteristics, is challenging in pediatric hepatology. The usual treatment in these cases includes intravenous Octreotide. Recently, the availability of long-acting release Octreo tide (OCT-LAR) for monthly intramuscular administration has become an interesting therapeutic alternative. Objective: To report the case of an infant with UGIB due to PHT who was successfully treated with OCT-LAR. Clinical Case: Eight-month-old patient with repeated episodes of UGIB due to extrahepatic portal vein malformation, requiring blood transfusions, and intravenous octreotide infusions. As neither endoscopic nor surgical treatment were feasible, we decided to start IM OCT- LAR monthly. After ten months of treatment, the patient did not present bleeding episodes. No medication-related events were observed. Conclusion: We consider that this report could help in the management of similar pediatric patients with UGIB due to PHT without conventional therapeutic possibilities.


Subject(s)
Humans , Male , Infant , Gastrointestinal Agents/administration & dosage , Octreotide/administration & dosage , Duodenal Diseases/drug therapy , Gastrointestinal Hemorrhage/drug therapy , Hypertension, Portal/complications , Gastrointestinal Agents/therapeutic use , Octreotide/therapeutic use , Delayed-Action Preparations , Duodenal Diseases/etiology , Gastrointestinal Hemorrhage/etiology , Injections, Intramuscular
6.
São Paulo med. j ; 136(6): 597-601, Nov.-Dec. 2018. tab, graf
Article in English | LILACS | ID: biblio-991695

ABSTRACT

ABSTRACT CONTEXT: Spontaneous intramural duodenal hematoma is uncommon and is usually associated with coagulopathy, anticoagulant therapy and endoscopic procedures. The aim here was to describe a case of intramural duodenal hematoma caused by chronic exacerbation of pancreatitis. CASE REPORT: A 46-year-old male with chronic alcoholic pancreatitis was admitted to hospital due to abdominal pain, melena and low hemoglobin. An intramural duodenal hematoma with active bleeding was detected and selective angioembolization was warranted. The patient evolved with a perforated duodenum and underwent laparotomy with exclusion of the pylorus and Roux-en-Y gastrojejunostomy. He was discharged nine days later. CONCLUSION: Intramural duodenal hematoma is a rare complication of pancreatitis. Selective embolization is the preferred treatment for hemorrhagic complications of pancreatitis. However, the risk of visceral ischemia and perforation should be considered.


Subject(s)
Humans , Male , Middle Aged , Pancreatitis/complications , Duodenal Diseases/etiology , Duodenal Diseases/therapy , Embolization, Therapeutic , Hematoma/etiology , Pancreatitis/diagnostic imaging , Tomography, X-Ray Computed , Acute Disease , Chronic Disease , Endoscopy, Digestive System , Duodenal Diseases/diagnostic imaging , Hematoma/therapy , Gastrointestinal Hemorrhage
7.
Rev. gastroenterol. Perú ; 38(4): 374-376, oct.-dic. 2018. ilus
Article in Spanish | LILACS | ID: biblio-1014112

ABSTRACT

Las lesiones de Dieulafoy se definen como una anomalía vascular que producen un sangrado en la mucosa proveniente de una arteria submucosa anormalmente larga y tortuosa que se ubican principalmente en estómago (80%), con poca frecuencia a nivel duodenal y constituyen el 6% de los sangrados gastrointestinales no asociados a varices y del 1% al 2% de todos los sangrados gastrointestinales. Reportamos el caso de un paciente masculino de 60 años que ingresó por hematemesis, melena y signos de hipovolemia con hemoglobina de 9 g/dl, que luego de realizar su compensación hemodinámica se le realizó una endoscopía alta que evidenció una lesión de Dieulafoy con sangrado activo severo en la segunda porción duodenal realizándosele inyección con adrenalina al 1:10 000 sobre los bordes de la lesión, pero al no lograrse una hemostasia adecuada se le tuvo que realizar la colocación de un clip ovesco con hemostasia efectiva que se corroboró 24 horas después, a través de una segunda endoscopía para poder egresar al paciente sin complicaciones, ni resangrado.


Dieulafoy's lesions are vascular anomalies that produce gastrointestinal bleeding of the mucosa from an abnormally long and tortuous submucosal artery. It is found predominately in the stomach (80%) and less frequently in the duodenum. They constitute the 6% of all non-variceal bleeding and the 1 to 2% of all gastrointestinal bleeding source. We report a case of a 60-year-old man with hematemesis, melena and signs of hypovolemic shock with a hemoglobin level of 9 g/dL. After adequate fluid resuscitation, an upper endoscopy showed an actively bleeding Dieulafoy lesion in the second portion of the duodenum. After epinephrine injection over lesion borders, an adequate hemostasis was not achieved. An over-the-scope clip was placed. Follow-up endoscopy 24 hours later showed an effective hemostasis and the patient was discharged without complications or re-bleeding.


Subject(s)
Humans , Male , Middle Aged , Arteries/abnormalities , Hemostasis, Endoscopic/instrumentation , Duodenal Diseases/therapy , Duodenum/blood supply , Gastrointestinal Hemorrhage/therapy , Intestinal Mucosa/blood supply , Duodenal Diseases/etiology , Equipment Design , Gastrointestinal Hemorrhage/etiology
8.
J. bras. nefrol ; 40(3): 266-272, July-Sept. 2018. tab
Article in English | LILACS | ID: biblio-975906

ABSTRACT

ABSTRACT Introduction: The incidence of gastrointestinal disorders among patients with chronic kidney disease (CKD) is high, despite the lack of a good correlation between endoscopic findings and symptoms. Many services thus perform upper gastrointestinal (UGI) endoscopy on kidney transplant candidates. Objectives: This study aims to describe the alterations seen on the upper endoscopies of 96 kidney-transplant candidates seen from 2014 to 2015. Methods: Ninety-six CKD patients underwent upper endoscopic examination as part of the preparation to receive kidney grafts. The data collected from the patients' medical records were charted on Microsoft Office Excel 2016 and presented descriptively. Mean values, medians, interquartile ranges and 95% confidence intervals of the clinic and epidemiological variables were calculated. Possible associations between endoscopic findings and infection by H. pylori were studied. Results: Males accounted for 54.17% of the 96 patients included in the study. Median age and time on dialysis were 50 years and 50 months, respectively. The most frequent upper endoscopy finding was enanthematous pangastritis (57.30%), followed by erosive esophagitis (30.20%). Gastric intestinal metaplasia and peptic ulcer were found in 8.33% and 7.30% of the patients, respectively. H. pylori tests were positive in 49 patients, and H. pylori infection was correlated only with non-erosive esophagitis (P = 0.046). Conclusion: Abnormal upper endoscopy findings were detected in all studied patients. This study suggested that upper endoscopy is a valid procedure for kidney transplant candidates. However, prospective studies are needed to shed more light on this matter.


RESUMO Introdução: A incidência de doenças gastrointestinais altas em pacientes com doença renal crônica é elevada, porém não há boa correlação entre achados endoscópicos e sintomas. Assim, muitos serviços preconizam a realização de Endoscopia Digestiva Alta (EDA) nos candidatos a transplante renal. Objetivos: Descrever alterações endoscópicas presentes em 96 candidatos a transplante renal no período de 2014 a 2015. Métodos: Noventa e seis pacientes renais crônicos submetidos à EDA como preparo para transplante renal. Prontuários médicos dos pacientes foram revisados, os dados tabulados no programa Microsoft Office Excel 2016 e apresentados de maneira descritiva. Calculou-se média, mediana, intervalo interquartílico e intervalo de confiança de 95% das variáveis utilizadas. Alterações endoscópicas foram apresentadas quanto ao número, intervalo de confiança e valor de P, e correlacionadas com a presença ou ausência de infecção por Helicobacter pylori. Resultados: Dos 96 pacientes, 54,17% eram homens e 45,83% mulheres. As medianas de idade e tempo em diálise foram 50 anos e 50 meses, respectivamente. O achado mais comum na EDA foi pangastrite enantematosa (57,30%), seguida de esofagite erosiva (30,20%). Metaplasia intestinal gástrica e úlcera péptica foram encontradas em 8,33% e 7,30% dos pacientes, respectivamente. Pesquisa para H. pylori foi positiva em 49 pacientes, e somente houve correlação entre infecção por H. pylori e esofagite não erosiva (P = 0,046). Conclusão: Afecções gastrointestinais foram detectadas em todos os pacientes estudados. Os achados deste estudo sugerem que a realização de EDA em candidatos a receber transplante renal é desejável. Entretanto, estudos prospectivos são necessários para responder a esta questão.


Subject(s)
Humans , Male , Female , Adult , Middle Aged , Stomach Diseases/etiology , Duodenal Diseases/etiology , Esophageal Diseases/etiology , Renal Insufficiency, Chronic/complications , Stomach Diseases/diagnosis , Cross-Sectional Studies , Endoscopy, Gastrointestinal , Kidney Transplantation , Duodenal Diseases/diagnosis , Esophageal Diseases/diagnosis , Renal Insufficiency, Chronic/surgery
10.
Rev. chil. cir ; 68(4): 316-318, jul. 2016. ilus
Article in Spanish | LILACS | ID: lil-788900

ABSTRACT

Objetivo Presentar un caso de GIST con presentación clínica poco usual. Caso clínico Presentamos una paciente de género femenino, de 70 años, con 5 días de dolor en hemiabdomen superior y vómitos; se le diagnóstica por TC de abdomen y pelvis con contraste una intususcepción gastroduodenal. Se ingresa a pabellón; confirmando diagnóstico, se realiza gastrectomía subtotal más Y de Roux. La biopsia diferida con inmunohistoquímica confirma un GIST gástrico con 2 mitosis cada 50 campos. Se decide manejo conservador y control anual con endoscopia digestiva alta. Buena evolución.


Aim To present a case of GIST with unusual clinical presentation. Case report We present a 70-year old female patient with 5 days of upper abdominal pain and vomiting, being diagnosed with a gastroduodenal intussusceptions by contrasted CT scan. She was admitted to the operating room, confirming the diagnosis and a subtotal gastrectomy with Roux-en-Y reconstruction was performed. A deferred biopsy with immunohistochemical confirmed GIST with 2 mitoses/50 high-powerfields. Conservative management was proposed and annual control with upper endoscopy decided. Satisfactory evolution.


Subject(s)
Humans , Female , Aged , Gastrointestinal Stromal Tumors/surgery , Gastrointestinal Neoplasms/surgery , Gastrointestinal Neoplasms/diagnosis , Intussusception/etiology , Stomach Diseases/etiology , Endometrial Stromal Tumors/diagnosis , Gastrointestinal Stromal Tumors/complications , Duodenal Diseases/etiology , Gastrectomy , Gastrointestinal Neoplasms/complications , Intussusception/surgery
11.
The Korean Journal of Internal Medicine ; : 101-105, 2014.
Article in English | WPRIM | ID: wpr-155073

ABSTRACT

A 71-year-old male patient was readmitted to our hospital 1 month after discharge because of relapse of abdominal pain. He had been diagnosed with hepatocellular carcinoma (HCC) 1 year prior and had undergone repeated transcatheter arterial chemoembolization and radiotherapy. During the last hospitalization, he was diagnosed with a liver abscess complicated by previous treatments for HCC and was treated with intravenous antibiotics and abscess aspiration. Follow-up abdominal computed tomography revealed a liver abscess with a duodenal fistula, which was successfully treated with endoscopic Histoacryl injection into the fistula. Liver abscesses with duodenal fistulas rarely occur, but they are intractable and possibly fatal in patients with HCC. In the literature, they have frequently been managed only with abscess treatment without fistula management. We herein report the first case of a patient with a liver abscess complicated by a fistula between the duodenum and the abscess, which was treated with endoscopic Histoacryl injection.


Subject(s)
Aged , Humans , Male , Abscess/complications , Carcinoma, Hepatocellular/radiotherapy , Chemoembolization, Therapeutic/adverse effects , Cholangiopancreatography, Endoscopic Retrograde , Duodenal Diseases/etiology , Enbucrilate/administration & dosage , Intestinal Fistula/etiology , Liver Diseases/etiology , Radiotherapy/adverse effects
12.
The Korean Journal of Gastroenterology ; : 372-376, 2012.
Article in Korean | WPRIM | ID: wpr-33540

ABSTRACT

The gastrointestinal stromal tumor (GIST) is a mesenchymal tumor of the digestive tract showing differentiation along the line of interstitial cell of Cajal. The most GISTs in the stomach generally show the appearance of submucosal tumors. It is rare for GISTs to appear as a pedunculated polypoid lesion on endoscopy. We experienced a case of a 51-year-old man who had a pedunculated polypoid GIST. He was admitted to our hospital for nausea, vomiting, melena and severe anemia (hemoglobin 3.4 g/dL, hematocrit 10.8%). An upper endoscopy showed gastroduodenal intussusception due to a pedunculated polypoid mass. This report presents a rare case of endoscopically proven gastroduodenal intussusceptions due to pedunculated polypoid GIST in the stomach.


Subject(s)
Humans , Male , Middle Aged , Duodenal Diseases/etiology , Gastrointestinal Hemorrhage , Gastrointestinal Neoplasms/complications , Gastrointestinal Stromal Tumors/complications , Gastroscopy , Intussusception/etiology , Tomography, X-Ray Computed
14.
Korean Journal of Radiology ; : 275-278, 2008.
Article in English | WPRIM | ID: wpr-46417

ABSTRACT

Eosinophilic gasteroenteritis is an uncommon disease with variable clinical features characterized by eosinophilic infiltration. Clinical manifestations range from non-specific gastrointestinal complaints such as nausea, vomiting, crampy abdominal pain, and diarrhea to specific findings such as malabsorption, protein loosing enteropathy, luminal obstruction, eosinophilic ascites and effusion. We report here on a case of eosinophilic gastroenteritis causing enterobiliary fistula which is an extremely unusual complication.


Subject(s)
Aged , Humans , Male , Biliary Fistula/diagnosis , Cholangiopancreatography, Magnetic Resonance , Duodenal Diseases/etiology , Eosinophilia/complications , Gastroenteritis/complications , Intestinal Fistula/diagnosis
15.
The Korean Journal of Gastroenterology ; : 336-340, 2007.
Article in Korean | WPRIM | ID: wpr-82666

ABSTRACT

Duodenal varix is a rare cause of hemorrhage in patients with portal hypertension, however their rupture is serious and often life threatening. Treatments for duodenal variceal bleeding include endoscopic procedures, surgery, or interventional radiologic procedures. We report a case of duodenal varices rupture in a 45-year-old man with alcoholic liver cirrhosis who presented with melena and dizziness. Emergent upper endoscopy revealed large nodular varices with a ruptured erosion on the top in the distal second portion of duodenum. Two consecutive injections with 1.0 mL of n-butyl-2-cyanoacrylate (Histoacryl; Braun-Melsungen, Germany) mixed with 1.0 mL of lipiodol (Laboratoire-Guerbet, France) were performed intravariceally and achieved successful hemostasis. This suggests that endoscopic injection sclerotherapy with histoacryl may be an effective therapeutic option for the control of ruptured duodenal variceal bleeding.


Subject(s)
Humans , Male , Middle Aged , Duodenal Diseases/etiology , Duodenoscopy , Duodenum/blood supply , Enbucrilate/analogs & derivatives , Gastrointestinal Hemorrhage/etiology , Liver Cirrhosis, Alcoholic/complications , Rupture , Sclerosing Solutions/therapeutic use , Sclerotherapy , Tissue Adhesives/therapeutic use , Tomography, X-Ray Computed , Varicose Veins/complications
17.
Article in English | IMSEAR | ID: sea-124858

ABSTRACT

Primary mesenteric fibromatosis is a rare condition. The aggressive nature of these tumors and the potential for major morbidity secondary to resection makes it a challenging disease for the surgeon. We report a case of mesenteric fibromatosis with involvement of small bowel.


Subject(s)
Adult , Duodenal Diseases/etiology , Fibromatosis, Abdominal/complications , Humans , Intestinal Fistula/etiology , Male , Mesentery , Peritoneal Neoplasms/complications , Tomography, X-Ray Computed
18.
Bol. Hosp. San Juan de Dios ; 52(4): 229-233, jul.-ago. 2005. ilus, tab
Article in Spanish | LILACS | ID: lil-423547

ABSTRACT

La fístula duodeno-cólica es una entidad de presentación inusual, descrita en la literatura sólo como reportes de casos aislados. Las FDC benignas son una rara complicación de numerosas enfermedades gastro-intestinales, siendo la causa más frecuente la secundaria a la enfermedad de Crohn. Dolor abdominal, signos de malabsorción (diarrea, baja de peso), asociados eventualmente a náuseas y vómitos son la forma de presentación más frecuentes. El enema baritado es el mejor método diagnosticado. El manejo debe ser integral, considerando tanto el manejo de la enfermedad de base, como el soporte nutricional y la resolución quirúrgica de la fístula. Se presenta un caso clínico de esta patología.


Subject(s)
Male , Humans , Middle Aged , Duodenal Diseases/etiology , Duodenal Diseases/therapy , Colonic Diseases/etiology , Colonic Diseases/therapy , Duodenal Diseases/physiopathology , Colonic Diseases/physiopathology , Intestinal Fistula/etiology
19.
Bol. venez. infectol ; 15(1): 12-17, ene.-jun. 2004. tab, graf
Article in Spanish | LILACS | ID: lil-721135

ABSTRACT

Los objetivos del presente trabajo fueron: establecer la seroprevalencia de la infección por Helicobacter pylori en población venezolana y su asociación con trastornos gastroduodenales y evaluar la presencia del gen cagA mediante la reacción en cadena de la polimerasa y su asociación con trastornos gastroduodenales. Para el estudio de seroprevalencia se evaluaron un total de 1041 personas de distintos estados del país, 370 adultos sintomáticos, 406 asintomáticos, 27 niños sintomáticos y 238 asintomáticos. La determinación de anticuerpos IgG específicos se realizó mediante ELISA comercial. La presencia del gen CagA fue evaluada en 133 pacientes del área metropolitana y el Centro de Cáncer Gástrico de San Cristóbal. Las biopsias se analizaron por diferentes métodos de diagnóstico para H. pylori: cultivo, prueba de ureasa, reacción en cadena de la polimerasa. En la población infantil el porcentaje de niños con valores de anticuerpos IgG específicos anti-H. pylori varía de 30 por ciento a 60 por ciento. En adultos sintomáticos la seroprevalencia varía entre un 68 por ciento a 93 por ciento según el área geográfica estudiada. Una disminución de anticuerpos IgG anti- H. pylori se observó en pacientes con gastritis antral difusa asociada con metaplasia tipo II. En el grupo de pacientes de San Cristóbal se observaron títulos elevados en pacientes con gastritis antral difusa. Un 46 por ciento de las cepas de H. pylori aisladas de pacientes del Area Metropolitana presentaron el gen cagA a diferencia de grupo de San Cristóbal donde se observó una frecuencia menor (26,41 por ciento).


Subject(s)
Humans , Male , Female , Child , Epithelial Cells/pathology , Duodenal Diseases/etiology , Helicobacter pylori/pathogenicity , Biomarkers/blood , Biopsy/methods , Seroepidemiologic Studies
20.
Article in English | IMSEAR | ID: sea-64054

ABSTRACT

We report a 42-year-old man who developed coloduodenal fistula secondary to hepatic flexure tuberculosis. Initially, feeding jejunostomy and ileostomy were done; subsequently, after antitubercular therapy, right hemicolectomy and excision of the fistula with a sleeve of duodenal wall was performed.


Subject(s)
Adult , Colonic Diseases/etiology , Duodenal Diseases/etiology , Humans , Intestinal Fistula/etiology , Male , Tuberculosis, Gastrointestinal/complications
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