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A Case of Strangulated Intestinal Obstruction Caused by Acquired Ileal Diverticulum. 获得性回肠憩室致绞窄性肠梗阻1例。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-06-12 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/5634075
Zhong-Yu Wang, Zhe Han, Hong-Fei Pang, Yu-Hang Liu, Ming Wei, Yuan-Yuan Wang
{"title":"A Case of Strangulated Intestinal Obstruction Caused by Acquired Ileal Diverticulum.","authors":"Zhong-Yu Wang, Zhe Han, Hong-Fei Pang, Yu-Hang Liu, Ming Wei, Yuan-Yuan Wang","doi":"10.1155/crgm/5634075","DOIUrl":"10.1155/crgm/5634075","url":null,"abstract":"<p><p><b>Background:</b> Acquired ileal diverticulum is an extremely rare condition that occurs in the ileum and is caused by acquired factors. Strangulated intestinal obstruction, a life-threatening variant of bowel obstruction, is associated with exceedingly high mortality rates. Here, we present a case of acquired ileal diverticulum causing strangulated intestinal obstruction, which was treated at our hospital. <b>Case Report:</b> A 65-year-old female with no previous history of intestinal obstruction presented with acute abdominal pain. An exploratory laparotomy revealed an acquired ileal diverticulum and an internal hernia. <b>Conclusion:</b> Acquired ileal diverticulum leading to strangulated intestinal obstruction is rare. Clinicians should consider the possibility of this disease when encountering intestinal obstruction patients with no history of abdominal surgery.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"5634075"},"PeriodicalIF":0.6,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12178755/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144369396","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 Case of Acute Ischemic Pancreatitis and Duodenitis in the Setting of Cardiogenic Shock. 心源性休克并发急性缺血性胰腺炎和十二指肠炎1例。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-05-29 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/2791133
Binyamin Ravina Abramowitz, Nealansh Embre Gupta, Syeda Maleehah Ali, Bani Chander Roland, Daniel Anthony DiLeo
{"title":"A Rare Case of Acute Ischemic Pancreatitis and Duodenitis in the Setting of Cardiogenic Shock.","authors":"Binyamin Ravina Abramowitz, Nealansh Embre Gupta, Syeda Maleehah Ali, Bani Chander Roland, Daniel Anthony DiLeo","doi":"10.1155/crgm/2791133","DOIUrl":"10.1155/crgm/2791133","url":null,"abstract":"<p><p>Acute ischemic pancreatitis and duodenitis are uncommon diagnoses that can affect patients with shock. As respiratory, cardiac, and neurological manifestations of shock are prioritized, resultant gastrointestinal (GI) related pathologies can be overlooked, leading to underdiagnosis of these conditions. In this report, we highlight the importance of recognizing acute ischemic pancreatitis and duodenitis in our description of a unique patient presenting with GI related complaints with underlying cardiogenic shock.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"2791133"},"PeriodicalIF":0.6,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12140833/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144235435","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
Kaposi Sarcoma Presenting as Upper Gastrointestinal Bleeding in a Patient With Acquired Immune Deficiency Syndrome. 获得性免疫缺陷综合征患者卡波西肉瘤表现为上消化道出血。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-05-27 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/7703200
Karthik Gnanapandithan, Mohammad T Hussain, Daniel Kashani, Philip N Okafor
{"title":"Kaposi Sarcoma Presenting as Upper Gastrointestinal Bleeding in a Patient With Acquired Immune Deficiency Syndrome.","authors":"Karthik Gnanapandithan, Mohammad T Hussain, Daniel Kashani, Philip N Okafor","doi":"10.1155/crgm/7703200","DOIUrl":"10.1155/crgm/7703200","url":null,"abstract":"<p><p>Kaposi sarcoma (KS), an angioproliferative neoplasm driven by human herpesvirus 8, predominantly affects patients with acquired immune deficiency syndrome (AIDS) or those on immunosuppressive therapy. Gastrointestinal involvement in KS is underreported, with limited literature highlighting its clinical significance and morphological diversity on endoscopy. This case report illustrates the complexities of diagnosing and managing gastrointestinal KS in an AIDS patient who presented with upper gastrointestinal bleeding. The diagnosis was established through the characteristic endoscopic appearance of the lesions, supported by histopathological confirmation. This case emphasizes the variable endoscopic manifestations of KS, ranging from linear ulcers to nodular lesions, and underscores the necessity for heightened clinical vigilance and multiple deep biopsies to avoid false-negative results. Treatment options, primarily palliative, include highly active antiretroviral therapy, chemotherapy, and radiation, yet the prognosis remains poor with high short-term mortality. This report contributes to the sparse literature on gastrointestinal KS, advocating for increased awareness and early intervention to potentially improve outcomes in this patient population.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"7703200"},"PeriodicalIF":0.6,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12133360/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144217232","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
Peutz-Jeghers Syndrome in a Young Ethiopian Male: A Case Report. 埃塞俄比亚年轻男性Peutz-Jeghers综合征一例报告。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-05-07 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/3667487
Abate Bane Shewaye, Kaleb Assefa Berhane
{"title":"Peutz-Jeghers Syndrome in a Young Ethiopian Male: A Case Report.","authors":"Abate Bane Shewaye, Kaleb Assefa Berhane","doi":"10.1155/crgm/3667487","DOIUrl":"https://doi.org/10.1155/crgm/3667487","url":null,"abstract":"<p><p>Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by hamartomatous polyps in the gastrointestinal (GI) tract, pigmented mucocutaneous lesions, and an increased risk of cancer. We report a case of a 22-year-old male from Ethiopia who presented with recurrent abdominal pain and a history of surgery for bowel obstruction. Endoscopic evaluation revealed multiple polyps in the stomach, ileum, and colon, which were confirmed histopathologically as hamartomatous polyps. Mucocutaneous pigmentation and family history of GI symptoms and maternal breast cancer led to the diagnosis of PJS, despite the unavailability of genetic testing. The patient underwent therapeutic polypectomy and was advised on cancer surveillance. This case highlights the importance of recognizing and managing PJS in resource-limited settings, emphasizing the need for early diagnosis and vigilant surveillance to prevent complications, especially when genetic testing may not be readily available.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"3667487"},"PeriodicalIF":0.6,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12077968/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144081260","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
An Unusual Case of Ileitis and Partial Small Bowel Obstruction Secondary to Mesh Erosion After Totally Extraperitoneal Inguinal Hernia Repair. 腹股沟疝全腹膜外修补术后补片糜烂致回肠炎及部分小肠梗阻1例。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-05-05 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/3047912
Pranesh de Silva, Joseph Do Woong Choi, Craig Lynch, Stephen Pillinger, Saurabh Gupta, Praveen Ravindran
{"title":"An Unusual Case of Ileitis and Partial Small Bowel Obstruction Secondary to Mesh Erosion After Totally Extraperitoneal Inguinal Hernia Repair.","authors":"Pranesh de Silva, Joseph Do Woong Choi, Craig Lynch, Stephen Pillinger, Saurabh Gupta, Praveen Ravindran","doi":"10.1155/crgm/3047912","DOIUrl":"10.1155/crgm/3047912","url":null,"abstract":"<p><p>The objectives were to highlight that: (1) mesh erosion related partial small bowel obstruction after laparoscopic totally extraperitoneal (TEP) inguinal hernia repair (IHR) as an uncommon complication can clinically and radiologically mimic ileocolic Crohn's disease in young adults; and (2) implore clinicians to consider a broad set of differential diagnosis and prompt involvement of other subspecialties, especially if preliminary investigations and treatment yield minimal results. The authors report a 34-year-old male who presented with computed tomography (CT) findings of ileitis, which was initially investigated for Crohns' disease. Due to persisting abdominal pain and negative initial investigations, he underwent a laparotomy demonstrating secondary mesh migration with erosion into distal ileum requiring bowel resection, 2.5 years after an uneventful laparoscopic right TEP IHR. The patient made an uneventful postoperative recovery and at 6 weeks follow-up, he had resolution of abdominal pains, and normal bowel function.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"3047912"},"PeriodicalIF":0.6,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12069841/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143990162","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 Bleeding Unmasking Gastric Metastases From a Primary Breast Malignancy: A Case Report. 胃肠出血揭示原发性乳腺恶性肿瘤胃转移：1例报告。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-05-03 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/2763114
Thilini Delungahawatta, Richard Hum, Stephanie M Woo, Rashmi Samdani, Mark J Real
{"title":"Gastrointestinal Bleeding Unmasking Gastric Metastases From a Primary Breast Malignancy: A Case Report.","authors":"Thilini Delungahawatta, Richard Hum, Stephanie M Woo, Rashmi Samdani, Mark J Real","doi":"10.1155/crgm/2763114","DOIUrl":"https://doi.org/10.1155/crgm/2763114","url":null,"abstract":"<p><p>Metastases to the gastrointestinal tract from primary breast malignancies are rare. Acute gastrointestinal bleeding in patients with history of breast cancer, however, should raise clinical suspicion and warrant further investigation for metastatic disease involving the gastrointestinal tract. We report a case of a 74-year-old female with metastatic breast cancer and provoked thromboembolic events on anticoagulation, who was found to have poorly cohesive gastric carcinoma with immunohistochemistry consistent with primary breast malignancy, after presenting with new-onset melena. Use of anticoagulation may have exacerbated bleeding prompting endoscopic examination. Biopsy and histologic assessment are needed for definitive diagnosis and timely management.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"2763114"},"PeriodicalIF":0.6,"publicationDate":"2025-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12065968/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144019563","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
Celiac Crisis: A Rare Medical Emergency Case Report in Adult Celiac Disease. 乳糜泻危象：成人乳糜泻罕见的医疗急诊病例报告。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-04-28 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/6259846
Mais Musleh, Amani AlMokbel
{"title":"Celiac Crisis: A Rare Medical Emergency Case Report in Adult Celiac Disease.","authors":"Mais Musleh, Amani AlMokbel","doi":"10.1155/crgm/6259846","DOIUrl":"https://doi.org/10.1155/crgm/6259846","url":null,"abstract":"<p><p>Celiac crisis (CC) is a rare but potentially life-threatening complication of celiac disease (CD), characterized by severe diarrhea, electrolyte imbalances, and metabolic disturbances. We report the case of a 32-year-old pregnant woman presented significant dehydration, weight loss, and steatorrheic stools. Diagnosis was confirmed by duodenal biopsy, with rapid improvement following a gluten-free diet (GFD) and corticosteroids. The diagnosis of CC was established based on the acute clinical presentation and rapid improvement following a GFD and corticosteroid therapy. This case highlights the importance of early recognition and prompt management of CC, particularly in undiagnosed or untreated CD, to prevent severe maternal and fetal complications.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"6259846"},"PeriodicalIF":0.6,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12052456/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143991040","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
Giant Mesenteric Cyst in a Young Adult Mimicking Refractory Ascites: A Diagnostic and Surgical Challenge-A Case Report. 巨大肠系膜囊肿的年轻人模仿难治性腹水：诊断和手术的挑战-一个病例报告。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-04-23 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/7405161
Abate Bane Shewaye, Kaleb Assefa Berhane, Amanuel Getu Gebresilassie, Amsalework Daniel Fanta, Megersa Regassa, Fekadu Ayalew, Eyerusalem Fekede, Biruk Demisse Ayalew
{"title":"Giant Mesenteric Cyst in a Young Adult Mimicking Refractory Ascites: A Diagnostic and Surgical Challenge-A Case Report.","authors":"Abate Bane Shewaye, Kaleb Assefa Berhane, Amanuel Getu Gebresilassie, Amsalework Daniel Fanta, Megersa Regassa, Fekadu Ayalew, Eyerusalem Fekede, Biruk Demisse Ayalew","doi":"10.1155/crgm/7405161","DOIUrl":"https://doi.org/10.1155/crgm/7405161","url":null,"abstract":"<p><p>Mesenteric cysts are rare benign intra-abdominal tumors that are usually asymptomatic and diagnosed incidentally while being investigated for other conditions or their complications. Surgical excision remains the primary treatment option. Here we present the case of a 30-year-old male with progressive abdominal distension, initially misdiagnosed with liver disease and refractory ascites, leading to inappropriate diuretic therapy. Subsequent imaging revealed a giant mesenteric cyst, which was successfully managed with complete surgical excision.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"7405161"},"PeriodicalIF":0.6,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12043438/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144020638","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
COVID-19 Challenges in Autoimmune Hepatitis Management: A Successful Outcome With Intravenous Immune Globulin (IVIg). 自身免疫性肝炎管理中的COVID-19挑战：静脉注射免疫球蛋白（IVIg）的成功结果。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-04-07 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/4446896
Amirali Mashhadiagha, Parnian Khalili, Maryam Ataollahi, Fereshteh Karbasian, Ali Arman, Bita Geramizadeh
{"title":"COVID-19 Challenges in Autoimmune Hepatitis Management: A Successful Outcome With Intravenous Immune Globulin (IVIg).","authors":"Amirali Mashhadiagha, Parnian Khalili, Maryam Ataollahi, Fereshteh Karbasian, Ali Arman, Bita Geramizadeh","doi":"10.1155/crgm/4446896","DOIUrl":"https://doi.org/10.1155/crgm/4446896","url":null,"abstract":"<p><p><b>Background:</b> Several autoimmune diseases, such as autoimmune hepatitis (AIH), can arise or become decompensated following COVID-19 infection or vaccination; however, there is a lack of data regarding the management of concurrent COVID-19 infection and autoimmune diseases. <b>Case Summary:</b> In this paper, we present a case of a 9-year-old boy with yellowish discoloration of the skin and sclera, abnormal liver function test, followed by positive qRT-PCR for SARS-CoV-2 and progressive bicytopenia. After a lack of response to corticosteroids, intravenous immune globulin (IVIg) was administrated and a decline in liver enzymes, total bilirubin, and direct bilirubin was observed. <b>Result and Discussion:</b> This case illustrates how IVIg significantly improved the AIH symptoms in the patient with positive qRT-PCR for the SARS-CoV-2 test. We hope our report encourages further research on therapeutic approaches for AIH concomitant with COVID-19.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"4446896"},"PeriodicalIF":0.6,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11996283/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144029673","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
Gallstone Ileus in a 25-Year-Old Female With Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: A Case Report. 25岁女性胆石性肠梗阻伴周期蛋白依赖性激酶样5缺乏症1例报告。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2025-03-23 eCollection Date: 2025-01-01 DOI: 10.1155/crgm/4901433
Hikaru Onoda, Mami Kuroda, Ryo Takeguchi, Ryosuke Tanaka, Daisuke Ishii, Hisayuki Miyagi, Masatoshi Hirasawa, Satoru Takahashi
{"title":"Gallstone Ileus in a 25-Year-Old Female With Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: A Case Report.","authors":"Hikaru Onoda, Mami Kuroda, Ryo Takeguchi, Ryosuke Tanaka, Daisuke Ishii, Hisayuki Miyagi, Masatoshi Hirasawa, Satoru Takahashi","doi":"10.1155/crgm/4901433","DOIUrl":"10.1155/crgm/4901433","url":null,"abstract":"<p><p>Gallstone ileus is an uncommon complication of cholelithiasis and the delayed diagnosis may be associated with increased risk of mortality. When gallstones block the cystic duct, they can lead to cholecystitis. If a fistula forms between the inflamed gallbladder and the adjacent intestine, the gallstones may pass into the intestinal tract and cause obstruction in the intestine. We report a case of 25-year-old female with developmental and epileptic encephalopathy who was intraoperatively diagnosed with gallstone ileus during surgery for small bowel obstruction of unknown origin. The patient had potential risk factors enhancing the formation of cholesterol gallstones, including long-term use of phenobarbital, vagus nerve injury in open gastrostomy and laparoscopic fundoplication, and tube feeding; however, the patient's gallstone had been undiagnosed for a long time. Computed tomography of the abdomen showed small bowel obstruction and pneumobilia. The presence of pneumobilia in a patient without a surgical history of the biliary system should raise suspicion of a bilioenteric fistula. The awareness of this complication of cholelithiasis is important to make an early diagnosis and to initiate the appropriate treatment.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2025 ","pages":"4901433"},"PeriodicalIF":0.6,"publicationDate":"2025-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11955286/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143754936","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
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