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Retrograde Balloon-Assisted Deep Enteroscopy in the Diagnosis of Metastatic Melanoma. 逆行球囊辅助深肠镜诊断转移性黑色素瘤。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-06-30 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5572230
William Barge, Mark R Albertini, Christopher Cold, Daniel Abbott, Deepak Gopal
{"title":"Retrograde Balloon-Assisted Deep Enteroscopy in the Diagnosis of Metastatic Melanoma.","authors":"William Barge,&nbsp;Mark R Albertini,&nbsp;Christopher Cold,&nbsp;Daniel Abbott,&nbsp;Deepak Gopal","doi":"10.1155/2021/5572230","DOIUrl":"https://doi.org/10.1155/2021/5572230","url":null,"abstract":"<p><p>A 74-year-old male with a history of metastatic melanoma presents with persistently abnormal small bowel findings on PET-CT scan. The patient had persistent FDG uptake near the ileocolic junction on imaging, concerning for metastatic melanoma. Capsule endoscopy demonstrated ulcerated mucosa in the distal ileum. This area was biopsied and tattooed via retrograde double-balloon enteroscopy to confirm the diagnosis of metastatic melanoma and facilitate subsequent small bowel resection. The case illustrates a unique case of metastatic melanoma to the small bowel and the utility of capsule endoscopy and balloon-assisted enteroscopy to assist in diagnosis and management of metastatic disease.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"5572230"},"PeriodicalIF":0.7,"publicationDate":"2021-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263269/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39220414","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Management of Refractory Gastrointestinal Bleeding in Hereditary Hemorrhagic Telangiectasia with Bevacizumab. 贝伐单抗治疗遗传性出血性毛细血管扩张难治性胃肠道出血。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-06-29 eCollection Date: 2021-01-01 DOI: 10.1155/2021/2242178
Muaaz Masood, Michael Coles, Humberto Sifuentes
{"title":"Management of Refractory Gastrointestinal Bleeding in Hereditary Hemorrhagic Telangiectasia with Bevacizumab.","authors":"Muaaz Masood,&nbsp;Michael Coles,&nbsp;Humberto Sifuentes","doi":"10.1155/2021/2242178","DOIUrl":"https://doi.org/10.1155/2021/2242178","url":null,"abstract":"<p><p>Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder resulting in vascular malformations of several organs including the pulmonary, cerebral, and gastrointestinal systems. One sequela is recurrent gastrointestinal (GI) bleeding. Bevacizumab (Bev) is emerging as an effective treatment of recurrent gastrointestinal bleeding in HHT. Bev is a recombinant monoclonal antibody that inhibits vascular endothelial growth factor (VEGF), an integral part of angiogenesis.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"2242178"},"PeriodicalIF":0.7,"publicationDate":"2021-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263270/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39220413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Chemical Gastroenterocolitis after Dental Root Canal Therapy with Camphorated and Mentholated Chlorophenol. 樟脑和薄荷脑氯酚根管治疗后的化学性胃肠结肠炎。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-06-28 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9918830
Mikheil Kalandarishvili, Ernst-Wolfgang Kolbe, Günther Winde, Michael Kaspari
{"title":"Chemical Gastroenterocolitis after Dental Root Canal Therapy with Camphorated and Mentholated Chlorophenol.","authors":"Mikheil Kalandarishvili,&nbsp;Ernst-Wolfgang Kolbe,&nbsp;Günther Winde,&nbsp;Michael Kaspari","doi":"10.1155/2021/9918830","DOIUrl":"https://doi.org/10.1155/2021/9918830","url":null,"abstract":"<p><p>A 78-year-old man with a history of pancolitis, after the treatment of dental abscess with oral antibiotics and local application of camphorated and mentholated chlorophenol (CMCP), presented with abdominal pain of 4-day duration, as well as hair loss in the area of moustache and finger nail lifting. He was already treated with rectal application of budesonide because of pancolitis, diagnosed 6 weeks ago and interpreted as an allergic reaction to clindamycin. For further investigation, we performed gastroscopy and colonoscopy, which showed the edematous mucosa with polypus-like changes of the whole mucosa of the stomach, duodenum, first part of the jejunum, distal ileum, complete colon, and rectum. The diagnosis was complicated and was achieved in synopsis with anamnestic details, such as endodontic application of camphorated chlorophenol. The patient symptoms abated after he commenced on mesalazine therapy.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"9918830"},"PeriodicalIF":0.7,"publicationDate":"2021-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257390/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39180735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
From an Incidental Finding to an Emergent Treatment: A Case Report of a Hepatic Adenomatosis and Large Ruptured Hepatic Adenoma. 从偶然发现到紧急治疗:1例肝腺瘤病和大破裂的肝腺瘤。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-06-19 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9963440
Maria Mironova, Mohammed K Mahdi, Jyoti Bhatia, Rosemarie C Nielson, Cataldo Doria
{"title":"From an Incidental Finding to an Emergent Treatment: A Case Report of a Hepatic Adenomatosis and Large Ruptured Hepatic Adenoma.","authors":"Maria Mironova,&nbsp;Mohammed K Mahdi,&nbsp;Jyoti Bhatia,&nbsp;Rosemarie C Nielson,&nbsp;Cataldo Doria","doi":"10.1155/2021/9963440","DOIUrl":"https://doi.org/10.1155/2021/9963440","url":null,"abstract":"<p><p><i>Introduction</i>. Hepatic adenoma is an uncommon benign liver tumor presenting as solitary lesions or even rarely as hepatic adenomatosis. Large lesions carry a risk of rupture, hemorrhage, and malignant transformation. This case report aims to increase awareness about risk factors for hepatic adenomas, considering the increasing prevalence of obesity and the widespread use of oral contraceptive pills. <i>Case Presentation</i>. A 20-year-old obese female who was taking oral contraceptive pills for seven years presented to the emergency department with vomiting and abdominal pain caused by gastroenteritis. On imaging, multiple hepatic adenomas, including two lesions 6 and 9 cm in diameter, were incidentally found. During the hospitalization, the patient suddenly developed acute anemia and rupture of the largest lesion, which was promptly treated with arterial embolization. <i>Discussion</i>. Obesity and exposure to hormones are well-known risk factors for hepatic adenomas. The incidence of hepatic adenomas is steadily increasing because of the prevalence of obesity, especially among females. Lifestyle interventions for weight loss and discontinuation of oral contraceptive pills are considered a conservative treatment of hepatic adenomas. Large lesions possess the risk of malignant transformation and rupture and require surgical excision.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"9963440"},"PeriodicalIF":0.7,"publicationDate":"2021-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238616/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39167277","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Adult Intestinal Intussusception Caused by the Gastrojejunostomy Tube: An Endoscopically Treatable Phenomenon. 由胃空肠造口管引起的成人肠套叠:一种内镜下可治疗的现象。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-06-11 eCollection Date: 2021-01-01 DOI: 10.1155/2021/4325443
Kermit S Zhang, Jash Bansal, Anmol Bansal, Vikas Chitnavis
{"title":"Adult Intestinal Intussusception Caused by the Gastrojejunostomy Tube: An Endoscopically Treatable Phenomenon.","authors":"Kermit S Zhang,&nbsp;Jash Bansal,&nbsp;Anmol Bansal,&nbsp;Vikas Chitnavis","doi":"10.1155/2021/4325443","DOIUrl":"https://doi.org/10.1155/2021/4325443","url":null,"abstract":"<p><p>Adult duodenoduodenal intussusception is extremely rare due to the retroperitoneal fixation of the second, third, and fourth parts of the duodenum. A majority of clinically significant intussusception with identifiable etiologies is typically neoplastic with more rare causes including retained food and indwelling enteral tubes, specifically with gastrojejunostomy (GJ) tubes. Herein, we discuss the case of a 23-year-old male who developed duodenoduodenal intussusception upon a PEGJ placement with associated gastroduodenal dilation and telescope phenomenon. To the best of our knowledge, there are no reports of intussusception found to be caused by GJ tubes in the adult population. The reported patient was found to have a 4-cm enteroenteric intussusception without obstruction or ischemia with bowel thickening proximal to the pathology. Although adult intussusception cases are typically managed surgically, we were able to reduce the intussusception via endoscopy due to rapid diagnosis upon presentation and intervention before the bowel wall could be compromised.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"4325443"},"PeriodicalIF":0.7,"publicationDate":"2021-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213475/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39148220","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Massive Hematochezia from a Large Bleeding Duodenal Diverticulum. 十二指肠憩室大量出血导致大量便血。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-06-08 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5585264
Marcus Juan Esteban, Amit Sureen, Daniel Herlihy, Sherif Elhanafi, Marc J Zuckerman
{"title":"Massive Hematochezia from a Large Bleeding Duodenal Diverticulum.","authors":"Marcus Juan Esteban,&nbsp;Amit Sureen,&nbsp;Daniel Herlihy,&nbsp;Sherif Elhanafi,&nbsp;Marc J Zuckerman","doi":"10.1155/2021/5585264","DOIUrl":"https://doi.org/10.1155/2021/5585264","url":null,"abstract":"<p><strong>Background: </strong>Duodenal diverticula are a rare cause of gastrointestinal (GI) bleeding despite being a common finding in the GI tract. We present a case of a patient who had massive hematochezia due to a complex duodenal diverticulum. <i>Case Presentation.</i> A 74-year-old Hispanic female presented initially with generalized weakness. During admission, the patient had an episode of a large amount of hematochezia and had to be transferred to the intensive care unit (ICU). Upper endoscopy was done using a forward-viewing endoscope which revealed a bleeding complex duodenal diverticulum. Successful hemostasis was achieved through epinephrine injection followed by placement of hemostatic clips.</p><p><strong>Conclusion: </strong>Although rare, gastroenterologists need to be aware of duodenal diverticulum as a possible cause of gastrointestinal bleed. It could be life-threatening, and thus, prompt diagnosis and management is necessary.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"5585264"},"PeriodicalIF":0.7,"publicationDate":"2021-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208870/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39139900","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Suggestive Diagnostic Process in a Case of Multiple Myeloma with Gastrointestinal Immunoglobulin Light-Chain Amyloidosis Accompanied by Protein-Losing Enteropathy. 多发性骨髓瘤合并胃肠道免疫球蛋白轻链淀粉样变伴蛋白丢失性肠病1例的提示诊断过程。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-05-27 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5533993
Katsuya Endo, Takehito Ito, Jun Nomura, Keigo Murakami, Shiho Kondo, Tomonori Satoh, Daisuke Fukushi, Yuki Yoshino, Yoshiteru Sasaki, Atsuko Takasu, Takayuki Kogure, Morihisa Hirota, Takayoshi Meguro, Kazuhiro Murakami, Junichi Kameoka, Kennichi Satoh
{"title":"Suggestive Diagnostic Process in a Case of Multiple Myeloma with Gastrointestinal Immunoglobulin Light-Chain Amyloidosis Accompanied by Protein-Losing Enteropathy.","authors":"Katsuya Endo,&nbsp;Takehito Ito,&nbsp;Jun Nomura,&nbsp;Keigo Murakami,&nbsp;Shiho Kondo,&nbsp;Tomonori Satoh,&nbsp;Daisuke Fukushi,&nbsp;Yuki Yoshino,&nbsp;Yoshiteru Sasaki,&nbsp;Atsuko Takasu,&nbsp;Takayuki Kogure,&nbsp;Morihisa Hirota,&nbsp;Takayoshi Meguro,&nbsp;Kazuhiro Murakami,&nbsp;Junichi Kameoka,&nbsp;Kennichi Satoh","doi":"10.1155/2021/5533993","DOIUrl":"https://doi.org/10.1155/2021/5533993","url":null,"abstract":"<p><p>Multiple myeloma is a type of plasma cell neoplasm that produces monoclonal immunoglobulin. Multiple myeloma is known to cause immunoglobulin light-chain (AL) amyloidosis, which frequently involves the kidney and heart. Bone pain or fractures caused by osteolytic lesions and physical disorders related to renal or cardiac AL amyloidosis are major initial symptoms in multiple myeloma. Multiple myeloma diagnosed from the gastrointestinal symptoms is rare. We report a case of an 80-year-old man with multiple myeloma accompanied by gastrointestinal AL amyloidosis and secondary protein-losing enteropathy. The diagnostic process was suggestive, in that diarrhea and refractory leg edema related to protein-losing enteropathy were the primary symptoms and the trigger for making a sequential diagnosis of gastrointestinal AL amyloidosis and underlying multiple myeloma. This case is highly suggestive, in that multiple myeloma with gastrointestinal AL amyloidosis should be considered one of the background diseases of protein-losing enteropathy.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"5533993"},"PeriodicalIF":0.7,"publicationDate":"2021-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177977/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39238500","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Rare Twist of the Forgotten Disease: A Case of Fusobacterium necrophorum Sepsis with Portomesenteric Thrombosis and a Review of the Literature. 罕见的被遗忘疾病:坏死性梭杆菌脓毒症合并肠系膜血栓形成1例并文献复习。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-05-27 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6699867
Nicholas Lazar, Kamil Sardarli, Zaid Imam, Majd Khasawneh, Ismail Hader
{"title":"A Rare Twist of the Forgotten Disease: A Case of <i>Fusobacterium necrophorum</i> Sepsis with Portomesenteric Thrombosis and a Review of the Literature.","authors":"Nicholas Lazar,&nbsp;Kamil Sardarli,&nbsp;Zaid Imam,&nbsp;Majd Khasawneh,&nbsp;Ismail Hader","doi":"10.1155/2021/6699867","DOIUrl":"https://doi.org/10.1155/2021/6699867","url":null,"abstract":"<p><p>Abdominal variants of Lemierre's syndrome presenting with pylephlebitis are rare, and the role of anticoagulation in treatment is controversial. We hereby report a case of pylephlebitis secondary to <i>F. necrophorum</i> bacteremia in a 57-year-old female originating from bacterial translocation secondary to colitis, who developed a favorable outcome with prompt treatment with antibiotics and anticoagulation. We also perform a literature review on similar cases in the literature and discuss management options of this rare but potentially fatal complication.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"6699867"},"PeriodicalIF":0.7,"publicationDate":"2021-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177980/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39238501","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Erratum to "Esophageal Pemphigus Vulgaris: A Rare Etiology of Upper Gastrointestinal Hemorrhage". “食道寻常型天疱疮:一种罕见的上消化道出血病因”的勘误。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-05-26 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9871312
Jennifer Rose F Del Castillo, Muhammad Nadeem Yousaf, Fizah S Chaudhary, Nahar Saleh, Lawrence Mills
{"title":"Erratum to \"Esophageal Pemphigus Vulgaris: A Rare Etiology of Upper Gastrointestinal Hemorrhage\".","authors":"Jennifer Rose F Del Castillo,&nbsp;Muhammad Nadeem Yousaf,&nbsp;Fizah S Chaudhary,&nbsp;Nahar Saleh,&nbsp;Lawrence Mills","doi":"10.1155/2021/9871312","DOIUrl":"https://doi.org/10.1155/2021/9871312","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1155/2021/5555961.].</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"9871312"},"PeriodicalIF":0.7,"publicationDate":"2021-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179773/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39238502","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Patient with Eosinophilic Esophagitis and Herpes Simplex Esophagitis: A Case Report and Literature Review. 嗜酸性粒细胞性食管炎合并单纯疱疹性食管炎1例报告并文献复习。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-05-25 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5519635
Hemnishil K Marella, Jiten P Kothadia, Nasir Saleem, Bilal Ali, Yousef Abdel-Aziz, Vamsee Mupparaju, Twisha Oza, Abdallah Azouz, Colin W Howden
{"title":"A Patient with Eosinophilic Esophagitis and Herpes Simplex Esophagitis: A Case Report and Literature Review.","authors":"Hemnishil K Marella,&nbsp;Jiten P Kothadia,&nbsp;Nasir Saleem,&nbsp;Bilal Ali,&nbsp;Yousef Abdel-Aziz,&nbsp;Vamsee Mupparaju,&nbsp;Twisha Oza,&nbsp;Abdallah Azouz,&nbsp;Colin W Howden","doi":"10.1155/2021/5519635","DOIUrl":"https://doi.org/10.1155/2021/5519635","url":null,"abstract":"<p><p>Acute herpes simplex esophagitis (HSE) is common in immunocompromised patients. Eosinophilic esophagitis (EoE) is characterized by immune-mediated eosinophil-predominant esophageal inflammation. We report a patient with human immunodeficiency virus infection who presented with dysphagia and odynophagia and was found to have HSE and EoE. The combination of these two relatively rare conditions suggests possible predisposition.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"5519635"},"PeriodicalIF":0.7,"publicationDate":"2021-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169267/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39090598","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
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