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Transient Intussusception Mimicking Acute Coronary Syndrome. 模拟急性冠状动脉综合征的短暂性肠套叠。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-10-09 eCollection Date: 2023-01-01 DOI: 10.1155/2023/7324188
Hiroshi Imamura, Yuichiro Kashima, Yujiro Hamano, Aoi Ogawara
{"title":"Transient Intussusception Mimicking Acute Coronary Syndrome.","authors":"Hiroshi Imamura,&nbsp;Yuichiro Kashima,&nbsp;Yujiro Hamano,&nbsp;Aoi Ogawara","doi":"10.1155/2023/7324188","DOIUrl":"10.1155/2023/7324188","url":null,"abstract":"<p><p>Intussusception in adults is rare and usually associated with organic lesions. However, in the current era of computed tomography (CT), cases of idiopathic and transient intussusceptions are being increasingly diagnosed. Herein, we present a case of ileocecal intussusception with symptoms mimicking those of acute coronary syndrome. A male patient in his 80s with a history of myocardial infarction presented to the emergency department with acute onset of severe precordial and epigastric pain, cold sweating, and vomiting. Coronary angiography did not reveal any significant new lesion, while abdominal CT revealed ileocecal intussusception without bowel obstruction. The pain spontaneously subsided without any intervention, and the patient was discharged on the sixth hospital day. Cases of intussusception may go unnoticed in patients suspected of having chest pain with a normal coronary arteriogram, as idiopathic intussusception is relatively common and subsides spontaneously. Therefore, physicians should note that intussusception is one of the differential diagnoses of acute coronary syndrome.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"7324188"},"PeriodicalIF":0.7,"publicationDate":"2023-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578975/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41239730","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
Aeromonas caviae-Associated Severe Bloody Diarrhea. 豚鼠气单胞菌相关性严重血液性腹泻。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-10-09 eCollection Date: 2023-01-01 DOI: 10.1155/2023/4966879
Xiaolan Tang, Anuoluwa Oyetoran, Tyler Jones, Christopher Bray
{"title":"<i>Aeromonas caviae</i>-Associated Severe Bloody Diarrhea.","authors":"Xiaolan Tang,&nbsp;Anuoluwa Oyetoran,&nbsp;Tyler Jones,&nbsp;Christopher Bray","doi":"10.1155/2023/4966879","DOIUrl":"10.1155/2023/4966879","url":null,"abstract":"<p><p><i>Aeromonas</i> species are capable of inducing severe infections in both immunocompetent and immunocompromised individuals. Gastroenteritis is the most common infection associated with <i>Aeromonas</i> species in humans. We report a rare case of <i>Aeromonas caviae</i> severe gastroenteritis and bloody diarrhea that led to the development of sepsis in a 45-year-old female with no history of immunocompromising conditions. This patient required extensive medical support which included blood transfusions and antibiotics. Fortunately, with appropriate diagnostic measures and targeted antibiotic therapy, her symptoms resolved. <i>Aeromonas</i> species are becoming increasingly frequent among the pathogens isolated from patients suffering from gastroenteritis. As such, it is becoming increasingly important for clinicians to consider this pathogen when working up their patients for diarrhea.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"4966879"},"PeriodicalIF":0.7,"publicationDate":"2023-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578977/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41239729","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
Severe Gastrointestinal Hemorrhage due to Monkeypox Virus-Associated Proctocolitis. 猴痘病毒相关性直结肠炎致严重胃肠道出血。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9981631
Sobaan Taj, Chris Austin, Azhar Hussain, Maryam Salma Babar, Harshavardhan Sanekommu, Steven Imburgio, Anmol Johal, Alejandro CruzPonce, Apurva Vedire, Edward Liu
{"title":"Severe Gastrointestinal Hemorrhage due to Monkeypox Virus-Associated Proctocolitis.","authors":"Sobaan Taj,&nbsp;Chris Austin,&nbsp;Azhar Hussain,&nbsp;Maryam Salma Babar,&nbsp;Harshavardhan Sanekommu,&nbsp;Steven Imburgio,&nbsp;Anmol Johal,&nbsp;Alejandro CruzPonce,&nbsp;Apurva Vedire,&nbsp;Edward Liu","doi":"10.1155/2023/9981631","DOIUrl":"https://doi.org/10.1155/2023/9981631","url":null,"abstract":"<p><p>Monkeypox is primarily a painful cutaneous disease with occasional systemic manifestations. Monkeypox is transmitted predominantly through close physical contact and occasionally sexual contact. The first case was reported in the United States on May 17, 2022, in a recent monkeypox worldwide outbreak. We present a case of severe gastrointestinal bleeding as an atypical manifestation of monkeypox infection in a 40-year-old male with HIV. In our case, monkeypox-induced proctocolitis progressed to severe rectal bleeding requiring one unit of packed red blood cells transfusion despite one week of tecovirimat (TPOXX) therapy. So, patients should be educated about the possibility of unusual complications of monkeypox infection, i.e., bleeding in immunocompromised hosts.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"9981631"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365909/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10233485","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
Gastrointestinal Stromal Tumours (GISTs) with KRAS Mutation: A Rare but Important Subset of GISTs. 伴有KRAS突变的胃肠道间质瘤(gist):一种罕见但重要的胃肠道间质瘤子集。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/4248128
Dorinda Mullen, Rajkumar Vajpeyi, Jose-Mario Capo-Chichi, Klaudia Nowak, Newton Wong, Runjan Chetty
{"title":"Gastrointestinal Stromal Tumours (GISTs) with KRAS Mutation: A Rare but Important Subset of GISTs.","authors":"Dorinda Mullen,&nbsp;Rajkumar Vajpeyi,&nbsp;Jose-Mario Capo-Chichi,&nbsp;Klaudia Nowak,&nbsp;Newton Wong,&nbsp;Runjan Chetty","doi":"10.1155/2023/4248128","DOIUrl":"https://doi.org/10.1155/2023/4248128","url":null,"abstract":"<p><p>Gastrointestinal stromal tumours (GISTs) are the most common mesenchymal tumours of the GI tract, usually found in the stomach, jejunum, and ileum. Typically, they are <i>KIT</i> or <i>PDGFR</i>-mutated, allowing for targetable treatments with tyrosine kinase inhibitors such as imatinib. Here, we present two <i>KRAS</i>-mutated wild-type gastrointestinal tumours (GISTs). Both cases occurred in the small bowel of females. Immunohistochemical studies on both tumours showed KIT and DOG-1 positivity, with SDHB retained. Molecular analysis revealed a <i>KRAS G12D</i> mutation and a <i>KRAS G13D</i> mutation, respectively. Wild-type GISTs are extremely uncommon. They typically occur in the stomach or the small bowel. <i>KRAS</i> is one of the genes implicated in this subset of GIST, with <i>KRAS G12D</i> being the most frequently encountered mutation. GIST <i>KRAS</i> mutations can arise alone or in conjunction with <i>KIT, PDFRA</i>, or <i>BRAF</i> mutations. Identification of these rare molecular subtypes is clinically important due to their resistance to imatinib therapy.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"4248128"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471449/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10153240","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
A Crohn's Disease Patient Found to Have Entamoeba histolytica Infection Causing Pyogenic Liver Abscess. 克罗恩病患者发现有溶组织内阿米巴感染导致化脓性肝脓肿。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9936613
Hannah Saven, Ashton Harmacinski, Andrew Canakis, Uni Wong
{"title":"A Crohn's Disease Patient Found to Have <i>Entamoeba histolytica</i> Infection Causing Pyogenic Liver Abscess.","authors":"Hannah Saven,&nbsp;Ashton Harmacinski,&nbsp;Andrew Canakis,&nbsp;Uni Wong","doi":"10.1155/2023/9936613","DOIUrl":"https://doi.org/10.1155/2023/9936613","url":null,"abstract":"<p><p><i>Entamoeba histolytica</i> is a parasite that typically causes amoebic dysentery but can result in complications such as pyogenic liver abscess. Patients with inflammatory bowel disease often take immunosuppressive therapies that make them more susceptible to such infections. Notably, parasitic infections in this context are rare in nonendemic areas. We describe a 57-year-old man who recently started infliximab therapy for Crohn's disease and presented with fever and right upper quadrant pain. While hospitalized, this patient was diagnosed with <i>Entamoeba histolytica</i> liver abscess. This case demonstrates that parasitic infections should be considered early in immunocompromised patients with inflammatory bowel disease.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"9936613"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406523/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9968635","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
Necrotizing Pancreatitis Infected with Stenotrophomonas maltophilia: An Emerging Rare Multidrug-Resistant Organism. 坏死性胰腺炎感染嗜麦芽窄养单胞菌:一种新兴的罕见多重耐药生物。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/8071158
Sophia Dar, Nooraldin Merza, Maryam Haider, Yousaf Zafar, Noren Din, Rosario Ligresti, Rani Sebti
{"title":"Necrotizing Pancreatitis Infected with <i>Stenotrophomonas maltophilia</i>: An Emerging Rare Multidrug-Resistant Organism.","authors":"Sophia Dar,&nbsp;Nooraldin Merza,&nbsp;Maryam Haider,&nbsp;Yousaf Zafar,&nbsp;Noren Din,&nbsp;Rosario Ligresti,&nbsp;Rani Sebti","doi":"10.1155/2023/8071158","DOIUrl":"https://doi.org/10.1155/2023/8071158","url":null,"abstract":"<p><p><i>Stenotrophomonas maltophilia</i> (SM) is a multidrug-resistant, Gram-negative (GN) bacillus that is an increasingly recognized nosocomial and environment pathogen. It is intrinsically resistant to carbapenems, a drug commonly utilized in the management of necrotizing pancreatitis (NP). We report a 21-year-old immunocompetent female with NP complicated by pancreatic fluid collection (PFC) infected with SM. One-third of patients with NP will develop infections by GN bacteria, while broad-spectrum antibiotics, including carbapenems, cover most infections, trimethoprim-sulfamethoxazole (TMP-SMX) is the first-line treatment antibiotic for SM. This case is critical because it highlights a rare pathogen that should be considered a causal pathogen in patients who do not respond to their care plan.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"8071158"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313464/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9801313","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
Gastric Pneumatosis in the Setting of Diabetic Ketoacidosis. 糖尿病酮症酸中毒背景下的胃肺病。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/6655536
Mohammed Rifat Shaik, Chet Ranabhat, Nishat Anjum Shaik, Akshay Duddu, Zaid Bilgrami, Guofeng Xie
{"title":"Gastric Pneumatosis in the Setting of Diabetic Ketoacidosis.","authors":"Mohammed Rifat Shaik,&nbsp;Chet Ranabhat,&nbsp;Nishat Anjum Shaik,&nbsp;Akshay Duddu,&nbsp;Zaid Bilgrami,&nbsp;Guofeng Xie","doi":"10.1155/2023/6655536","DOIUrl":"https://doi.org/10.1155/2023/6655536","url":null,"abstract":"<p><p>Gastric pneumatosis, an uncommon radiologic finding characterized by the presence of gas within the gastric wall, presents a diagnostic challenge due to its association with both benign gastric emphysema and more severe emphysematous gastritis. The contrasting outcomes and management approaches for these conditions underscore the necessity for accurate diagnosis and appropriate intervention. We present a case of a 29-year-old female with a medical history significant for type 1 diabetes mellitus who presented with abdominal pain, nausea, and vomiting. Initial evaluation revealed elevated blood glucose levels, an anion gap metabolic acidosis, and evidence of gastric pneumatosis on imaging. The patient was managed with aggressive fluid resuscitation and intravenous insulin therapy per diabetic ketoacidosis protocol. General surgery evaluation ruled out the need for acute surgical intervention and attributed the gastric pneumatosis to increased intragastric pressures from prolonged vomiting. The patient was managed with conservative measures, including nasogastric tube decompression and antibiotics. Over the course of a few days, the patient showed signs of clinical and radiologic improvement, with a resolution of symptoms. This case highlights the importance of accurate diagnosis and appropriate management strategies tailored to the underlying pathology to optimize patient outcomes in cases of gastric pneumatosis.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"6655536"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362984/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10220862","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
Ectopic Cecal Varices as a Cause of Lower Gastrointestinal Bleeding. 盲肠异位静脉曲张是下消化道出血的原因之一。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/7005565
Abdulrahman Qatomah, Sulaiman Almushir, Faisal Aljohani
{"title":"Ectopic Cecal Varices as a Cause of Lower Gastrointestinal Bleeding.","authors":"Abdulrahman Qatomah,&nbsp;Sulaiman Almushir,&nbsp;Faisal Aljohani","doi":"10.1155/2023/7005565","DOIUrl":"https://doi.org/10.1155/2023/7005565","url":null,"abstract":"<p><p>Ectopic varices account for 1%-5% of all variceal bleeding episodes in patients with portal hypertension. They can be found at any part of gastrointestinal tract including the small intestines, colon, or rectum. We report a case of a 59-year-old man who presented with bleeding per rectum 2 days after a routine colonoscopy, in which 2 lesions were biopsied. Gastroscopy was negative for bleeding, and he was not stable enough to undergo colonoscopy. CT angiography showed a large portosystemic shunt with multiple collaterals in the right lower quadrant. These findings were clues for a diagnosis of ectopic cecal varices.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"7005565"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287515/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9770468","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
The First Case of Cribriform-Morular Thyroid Carcinoma and FAP with APC Gene Mutation in China: A Case Report and Brief Review. 中国首例筛状-摩粒型甲状腺癌伴APC基因突变的FAP病例报告及简要回顾。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/6222432
Sucong Lyu, Guoqiang Zhong, Hui Chen, Jin Li, Mingsong Li
{"title":"The First Case of Cribriform-Morular Thyroid Carcinoma and FAP with APC Gene Mutation in China: A Case Report and Brief Review.","authors":"Sucong Lyu,&nbsp;Guoqiang Zhong,&nbsp;Hui Chen,&nbsp;Jin Li,&nbsp;Mingsong Li","doi":"10.1155/2023/6222432","DOIUrl":"https://doi.org/10.1155/2023/6222432","url":null,"abstract":"<p><p>The cribriform-morular variant of papillary thyroid carcinoma (CMV-PTC) is now designated as morular cribriform thyroid carcinoma (CMTC) according to the 5<sup>th</sup> edition of the World Health Organization (WHO) Classification of Thyroid Tumors. CMTC can appear within a familial adenomatous polyposis (FAP) or be sporadic. We report the first case of a young female patient in China who was diagnosed with FAP and CMTC with a mutation in exon 16 of the APC gene underlying the disease. The main purpose of this case report is to provide a special pathological type of thyroid tumors, which is expected to be helpful for clinical work in the future.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"6222432"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10212671/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9917531","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
Perigastric Hematoma Masquerading as a Gastric Tumor. 胃周围血肿伪装成胃肿瘤。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9568983
Kevin Yang, Nariman Hossein-Javaheri, Naren Nallapeta, Mayada Ismail
{"title":"Perigastric Hematoma Masquerading as a Gastric Tumor.","authors":"Kevin Yang,&nbsp;Nariman Hossein-Javaheri,&nbsp;Naren Nallapeta,&nbsp;Mayada Ismail","doi":"10.1155/2023/9568983","DOIUrl":"https://doi.org/10.1155/2023/9568983","url":null,"abstract":"<p><p>Perigastric and intramural gastric hematomas rarely occur, with most cases associated with trauma, coagulopathy, and peptic ulcer disease. Furthermore, hematomas in the upper gastrointestinal tract are commonly located in the esophagus and duodenum. In this case report, we describe a hematoma masquerading as a gastric tumor on esophagogastroduodenoscopy (EGD) in a 54-year-old male presenting with melena. Initial computed tomography (CT) imaging suggested gastrointestinal stromal tumor (GIST) as the probable cause. We performed endoscopic ultrasound (EUS) with findings consistent with a perigastric hematoma, which aligned with the patient's diagnosis of splenic vein thrombosis (SVT) and numerous collateral vessels communicating with the hematoma. Interventional radiology (IR) was consulted for further management, although we ultimately chose a conservative approach.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"9568983"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462448/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10120537","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
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