V. Soria, J. Pizzala, M. Mahler, Dante Manazzoni, S. Durán, Santiago Rinaudo, M. L. González, M. Marcolongo
Single balloon enteroscopy allows a non-surgical therapeutic approach in patients with small bowel polyps. In patients with Peutz Jeghers Syndrome (SPJ) resection of hamartomatous polyps with this method is safe and effective. Although complications are rare, if they occur, they can be managed conservatively. We present a 16-year-old patient with a history of PJS who underwent an enteroscopy for small bowel polyps. Endoscopic resection of a 3 cm jejunum polyp was performed, and a full thickness intestinal perforation was immediately noticed after the resection. We were able to close the gap with hemo clips. The patient had an excellent clinical outcome.
{"title":"Cierre de perforación de intestino delgado posterior a polipectomía de pólipo hamartomatoso","authors":"V. Soria, J. Pizzala, M. Mahler, Dante Manazzoni, S. Durán, Santiago Rinaudo, M. L. González, M. Marcolongo","doi":"10.52787/DPRA8893","DOIUrl":"https://doi.org/10.52787/DPRA8893","url":null,"abstract":"Single balloon enteroscopy allows a non-surgical therapeutic approach in patients with small bowel polyps. In patients with Peutz Jeghers Syndrome (SPJ) resection of hamartomatous polyps with this method is safe and effective. Although complications are rare, if they occur, they can be managed conservatively. We present a 16-year-old patient with a history of PJS who underwent an enteroscopy for small bowel polyps. Endoscopic resection of a 3 cm jejunum polyp was performed, and a full thickness intestinal perforation was immediately noticed after the resection. We were able to close the gap with hemo clips. The patient had an excellent clinical outcome.","PeriodicalId":35700,"journal":{"name":"Acta Gastroenterologica Latinoamericana","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46113055","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Irene Andaluz García, J. P. Cordón, Rubén Fernández Martos
Splenosis is an uncommon entity resulting from the spread of splenic tissue to different body compartments. Although it is usually asymptomatic, it can cause a variety of symptoms and must be suspected in patients with a traumatic history of the spleen, including splenectomy. Nevertheless the diagnostic tool of choice to confirm it is the scintigraphy with denatured red blood cells marked with Tc-99.We report the case of an 18-year-old male with a personal history of splenectomy admitted for asthenia, jaundice and abdominal discomfort. An ultrasound identifies multiple abdominal masses predominantly on the left flank, being finally diagnosed of splenosis after CT and scintigraphy with red blood cells marked with Tc-99.
{"title":"Esplenosis abdominal: un diagnóstico infrecuente","authors":"Irene Andaluz García, J. P. Cordón, Rubén Fernández Martos","doi":"10.52787/OEYW6995","DOIUrl":"https://doi.org/10.52787/OEYW6995","url":null,"abstract":"Splenosis is an uncommon entity resulting from the spread of splenic tissue to different body compartments. Although it is usually asymptomatic, it can cause a variety of symptoms and must be suspected in patients with a traumatic history of the spleen, including splenectomy. Nevertheless the diagnostic tool of choice to confirm it is the scintigraphy with denatured red blood cells marked with Tc-99.We report the case of an 18-year-old male with a personal history of splenectomy admitted for asthenia, jaundice and abdominal discomfort. An ultrasound identifies multiple abdominal masses predominantly on the left flank, being finally diagnosed of splenosis after CT and scintigraphy with red blood cells marked with Tc-99.","PeriodicalId":35700,"journal":{"name":"Acta Gastroenterologica Latinoamericana","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-03-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45317728","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hepatic tumors are infrequent. Sarcomas represent less than 2% of them, and Leiomyosarcoma (LMS) is a certain rarity. The frequency grows from primitive tumors to metastatic tumors and in the last years, in relation with different immunodeficiencies. A case of a patient diagnosed in the postoperative and assisted in two relapses until her death, is reported. The possible aetiologies are analyzed in the hepatic gland that does not have muscle of its own, as well as in diagnostic and therapeutic modalities, insisting in the lack of rules, because of the low number of publications. Morphologic variations between the primitive tumor and its relapses are also shown.
{"title":"[Liver leiomyosarcoma].","authors":"J. R. Usandivaras","doi":"10.32388/gpfan1","DOIUrl":"https://doi.org/10.32388/gpfan1","url":null,"abstract":"Hepatic tumors are infrequent. Sarcomas represent less than 2% of them, and Leiomyosarcoma (LMS) is a certain rarity. The frequency grows from primitive tumors to metastatic tumors and in the last years, in relation with different immunodeficiencies. A case of a patient diagnosed in the postoperative and assisted in two relapses until her death, is reported. The possible aetiologies are analyzed in the hepatic gland that does not have muscle of its own, as well as in diagnostic and therapeutic modalities, insisting in the lack of rules, because of the low number of publications. Morphologic variations between the primitive tumor and its relapses are also shown.","PeriodicalId":35700,"journal":{"name":"Acta Gastroenterologica Latinoamericana","volume":"32 2 1","pages":"91-4"},"PeriodicalIF":0.0,"publicationDate":"2020-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42527172","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"[Prevention of cancer colorectal. From stone age to the cornerstone].","authors":"Roque Sáenz, Edison Salazar","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":35700,"journal":{"name":"Acta Gastroenterologica Latinoamericana","volume":"46 2","pages":"127-30"},"PeriodicalIF":0.0,"publicationDate":"2016-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35164927","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ana García García de Paredes, Javier Martínez González, Laura Crespo Pérez
Ménétrier disease is a rare condition of an unknown origin, with a wide spectrum of clinical signs and symptoms at presentation. Diagnosis is made through the combination of clinical, analytical, endoscopic and histological data. Surgery is the classical treatment. However, new medical approaches have emerged.
{"title":"[An infrequent cause of iron-deficiency\u0000anemia: Ménétrier disease].","authors":"Ana García García de Paredes, Javier Martínez González, Laura Crespo Pérez","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Ménétrier disease is a rare condition of an unknown origin,\u0000with a wide spectrum of clinical signs and symptoms at\u0000presentation. Diagnosis is made through the combination of\u0000clinical, analytical, endoscopic and histological data. Surgery\u0000is the classical treatment. However, new medical approaches\u0000have emerged.</p>","PeriodicalId":35700,"journal":{"name":"Acta Gastroenterologica Latinoamericana","volume":"46 2","pages":"118-21"},"PeriodicalIF":0.0,"publicationDate":"2016-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35164299","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}