Case Reports in Pulmonology最新文献

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Brown-Colored Malignant Pleural Fluid With High Bilirubin Levels: A Case Series. 高胆红素水平的棕色恶性胸腔积液:病例系列。
Case Reports in Pulmonology Pub Date : 2024-11-18 eCollection Date: 2024-01-01 DOI: 10.1155/crpu/5807681
Nai-Chien Huan, Larry Ellee Nyanti, Xin Ying Lee, Hema Yamini Ramarmuty, Daniel Theng Sheng Eng, Kunji Kannan Sivaraman Kannan, Yun Chor Gary Lee
{"title":"Brown-Colored Malignant Pleural Fluid With High Bilirubin Levels: A Case Series.","authors":"Nai-Chien Huan, Larry Ellee Nyanti, Xin Ying Lee, Hema Yamini Ramarmuty, Daniel Theng Sheng Eng, Kunji Kannan Sivaraman Kannan, Yun Chor Gary Lee","doi":"10.1155/crpu/5807681","DOIUrl":"10.1155/crpu/5807681","url":null,"abstract":"<p><p>Brown-colored pleural effusion is rare and may result from high bilirubin levels such as bilothorax (often described as a pleural fluid-to-serum bilirubin ratio of > 1.0). We describe four patients with malignant pleural effusion that appeared macroscopically brown with a pleural fluid-to-serum bilirubin ratio between 3.7 and 16.2. All had metastatic adenocarcinomas; three were from lung and one from gastric origin. None demonstrated clear pleurobiliary fistulas on investigations. Postulates for the development of brown effusion include heme oxygenase 1 overexpression in malignant cells situated in the pleura, intrapleural hemolysis, passive movement of bile through microscopic diaphragmatic pores, and drainage of biliary fluid into the pleural lymphatics.</p>","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"2024 ","pages":"5807681"},"PeriodicalIF":0.0,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11599473/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142741216","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 Tracheal Schwannoma Successfully Treated With Endoscopic Resection and Cryoablation Under Rigid Bronchoscopy. 在硬质支气管镜下通过内窥镜切除和冷冻消融成功治疗气管许旺瘤的罕见病例
Case Reports in Pulmonology Pub Date : 2024-10-16 eCollection Date: 2024-01-01 DOI: 10.1155/2024/2961560
Ming Chiu Chan, Cheuk Cheung Derek Leung, Yu Hong Chan, Man Ying Ho, Chun Hoi Chen, Ching Man Ngai, Hiu Ching Christy Chan, Yiu Cheong Yeung
{"title":"A Rare Case of Tracheal Schwannoma Successfully Treated With Endoscopic Resection and Cryoablation Under Rigid Bronchoscopy.","authors":"Ming Chiu Chan, Cheuk Cheung Derek Leung, Yu Hong Chan, Man Ying Ho, Chun Hoi Chen, Ching Man Ngai, Hiu Ching Christy Chan, Yiu Cheong Yeung","doi":"10.1155/2024/2961560","DOIUrl":"https://doi.org/10.1155/2024/2961560","url":null,"abstract":"<p><p>We present a rare case of tracheal schwannoma, the first reported in Hong Kong, emphasizing the diagnostic challenges and treatment outcomes. A 54-year-old woman with respiratory symptoms underwent evaluations revealing a tracheal mass causing luminal narrowing. Emergency operation with rigid bronchoscopy and cryoablation successfully removed the tumor. Follow-up bronchoscopies showed a gradual reduction in residual tumor size, with no evidence of recurrence after 3.5 years postoperation. Tracheal schwannomas are exceedingly rare, often resulting in delayed diagnosis. Clinicians should maintain a high suspicion of tracheal tumors in patients with unexplained respiratory symptoms. Spirometry and flow volume loop analysis aid in identifying upper airway obstruction. Rigid bronchoscopy is preferred for diagnosis and treatment, ensuring airway stability and obtaining tissue samples. Surgical resection remains the mainstay, but observation after endoscopic resection may be considered. This case highlights the successful management of tracheal schwannoma through endoscopic resection and cryoablation, emphasizing the need for further studies and case reports on this rare entity.</p>","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"2024 ","pages":"2961560"},"PeriodicalIF":0.0,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11498987/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142512763","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
Malignant Airway Stenosis Successfully Treated Using a Combination of Interventional Pulmonology, Chemotherapy, and Radiotherapy. 采用介入肺科、化疗和放疗联合疗法成功治疗恶性气道狭窄。
Case Reports in Pulmonology Pub Date : 2024-09-12 eCollection Date: 2024-01-01 DOI: 10.1155/2024/6779155
Jose N Sancho-Chust, Anastasiya Torba, Eusebi Chiner
{"title":"Malignant Airway Stenosis Successfully Treated Using a Combination of Interventional Pulmonology, Chemotherapy, and Radiotherapy.","authors":"Jose N Sancho-Chust, Anastasiya Torba, Eusebi Chiner","doi":"10.1155/2024/6779155","DOIUrl":"https://doi.org/10.1155/2024/6779155","url":null,"abstract":"<p><p>Interventional pulmonology can be helpful in cases of malignant airway stenosis. We present a 73-year-old man diagnosed with lung cancer who presented with symptomatic airway stenosis caused by a large endobronchial tumor. Oncological treatment was started with chemotherapy, radiotherapy, and a multimodality bronchoscopic approach using balloon bronchoplasty, electrosurgery, and argon plasma coagulation. Response evaluation showed relief of symptoms, disappearance of the endobronchial tumor, and complete resolution of the airway stenosis.</p>","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"2024 ","pages":"6779155"},"PeriodicalIF":0.0,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11412749/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142300576","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
Acute Myocardial Infarction in the Setting of Pulmonary Hypertension due to a Patent Foramen Ovale and Paradoxical Embolism. 因卵圆孔未闭和矛盾栓塞导致肺动脉高压的急性心肌梗死。
Case Reports in Pulmonology Pub Date : 2024-07-18 eCollection Date: 2024-01-01 DOI: 10.1155/2024/6725308
Madeline Franke, Zeenat Safdar
{"title":"Acute Myocardial Infarction in the Setting of Pulmonary Hypertension due to a Patent Foramen Ovale and Paradoxical Embolism.","authors":"Madeline Franke, Zeenat Safdar","doi":"10.1155/2024/6725308","DOIUrl":"10.1155/2024/6725308","url":null,"abstract":"<p><p>A 67-year-old woman with pulmonary hypertension (PH) presented with a 1-day history of worsening shortness of breath and pleuritic chest pain and was found to have a troponin T level of 3755 ng/L (ref. range 0-19 ng/L). An initial diagnostic workup in the emergency department (ED) led to an urgent left heart catheterization which revealed a 90% occlusive right coronary artery blood clot, even though a recent heart catheterization less than a month prior was completely unremarkable. Further workup led to the discovery of a patent foramen ovale (PFO) and an aneurysmal interatrial septum, suggesting the presence of a paradoxical embolism. While typically asymptomatic, a PFO is an important clinical entity that can lead to irreversible cardiac damage. Suspicion should be high for this finding in the case of an acute myocardial infarction (MI) with no clear cause, especially in a patient with elevated right heart pressures.</p>","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"2024 ","pages":"6725308"},"PeriodicalIF":0.0,"publicationDate":"2024-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11272397/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141762567","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
Endobronchial Infection and Bacterial Lymphadenitis by Gemella morbillorum Leading to Airway Perforation and a Bronchopleural Fistula. 支气管内膜感染和细菌性淋巴结炎导致气道穿孔和支气管胸膜瘘。
Case Reports in Pulmonology Pub Date : 2024-07-17 eCollection Date: 2024-01-01 DOI: 10.1155/2024/8850287
Kaitlin N DePrez, John Ferguson
{"title":"Endobronchial Infection and Bacterial Lymphadenitis by <i>Gemella morbillorum</i> Leading to Airway Perforation and a Bronchopleural Fistula.","authors":"Kaitlin N DePrez, John Ferguson","doi":"10.1155/2024/8850287","DOIUrl":"https://doi.org/10.1155/2024/8850287","url":null,"abstract":"<p><p><b>Introduction:</b> Necrotizing bronchial infection with severe infectious lymphadenitis is infrequently encountered and most commonly ascribed to <i>Aspergillus</i>, <i>Histoplasma</i>, and <i>Mycobacterium</i> species. We present a unique cause of severe airway destruction with lymphadenitis and bronchopleural fistula formation by the bacterium <i>Gemella morbillorum</i>. <b>Case:</b> A 24-year-old man presented with acute symptoms of vomiting, fever, and shoulder pain. A CT of the chest demonstrated a large subcarinal mass encasing the central bronchi. The workup for malignant, fungal, and granulomatous etiologies was unrevealing, while blood cultures identified <i>G. morbillorum</i>. Fiberoptic bronchoscopy revealed a perforation of the right middle lobar bronchus and the formation of a bronchopleural fistula, resulting in a large hydropneumothorax with empyema. Despite antibiotic therapy, surgical intervention to repair the fistula, and ventilatory support, the progression of the bronchopleural fistula led to fatal respiratory failure. <b>Conclusion:</b> In cases of severe mediastinal adenopathy in a young patient, bacterial lymphadenitis should be considered in the differential diagnosis with lymphoma, germ cell tumor, granulomatosis with polyangiitis, sarcoidosis, histoplasmosis, and inflammatory myofibroblastic tumor.</p>","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"2024 ","pages":"8850287"},"PeriodicalIF":0.0,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11268966/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141762568","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
Rare Combined Congenital Pulmonary and Cardiovascular Malformations Revealed by Acute Hemoptysis. 急性咯血揭示的罕见先天性肺部和心血管畸形合并症
Case Reports in Pulmonology Pub Date : 2024-05-09 eCollection Date: 2024-01-01 DOI: 10.1155/2024/1428495
Dima Siblani, Ghassan Abi Chedid, Samir Challita, Sylvana El Zoghbi, Béatrice Le Bon Chami
{"title":"Rare Combined Congenital Pulmonary and Cardiovascular Malformations Revealed by Acute Hemoptysis.","authors":"Dima Siblani, Ghassan Abi Chedid, Samir Challita, Sylvana El Zoghbi, Béatrice Le Bon Chami","doi":"10.1155/2024/1428495","DOIUrl":"https://doi.org/10.1155/2024/1428495","url":null,"abstract":"<p><strong>Background: </strong>Lung sequestration is a subtype of congenital lung malformations; it is infrequently diagnosed in adults and is a rare cause of hemoptysis. The typical management of symptomatic lung sequestration is usually surgical, though intra-arterial embolization is becoming an acceptable alternative. <i>Case Presentation</i>. We report a case of a 36-year-old female patient who presented for an acute onset of hemoptysis. CT chest showed an intralobar sequestration of the right lower lobe lung segment. In addition to the sequestration, the chest imaging also revealed a number of associated abnormalities including double superior vena cava communicating through a bridge, absence of brachiocephalic venous trunk, cardiac dextroposition, and agenesis of the right middle lobe. <i>Outcome and Discussion</i>. The transarterial embolization was selected for being mini-invasive and effective. It successfully controlled the bleed and led to complete regression of the sequestered lung on the follow-up CT chest several months later.</p><p><strong>Conclusion: </strong>Successful management and complete regression are possible with mini-invasive intra-arterial embolization of lung sequestration. Although it is not uncommon to have associated congenital cardiopulmonary abnormalities with lung sequestration, however the exceptional abnormalities described in this case have never been reported before.</p>","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"2024 ","pages":"1428495"},"PeriodicalIF":0.0,"publicationDate":"2024-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11098605/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140960880","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
Rare Combined Congenital Pulmonary and Cardiovascular Malformations Revealed by Acute Hemoptysis 急性咯血揭示的罕见先天性肺部和心血管畸形合并症
Case Reports in Pulmonology Pub Date : 2024-05-09 DOI: 10.1155/2024/1428495
Dima Siblani, Ghassan Abi Chedid, Samir Challita, Sylvana el Zoghbi, Béatrice Le Bon Chami
{"title":"Rare Combined Congenital Pulmonary and Cardiovascular Malformations Revealed by Acute Hemoptysis","authors":"Dima Siblani, Ghassan Abi Chedid, Samir Challita, Sylvana el Zoghbi, Béatrice Le Bon Chami","doi":"10.1155/2024/1428495","DOIUrl":"https://doi.org/10.1155/2024/1428495","url":null,"abstract":"Background Lung sequestration is a subtype of congenital lung malformations; it is infrequently diagnosed in adults and is a rare cause of hemoptysis. The typical management of symptomatic lung sequestration is usually surgical, though intra-arterial embolization is becoming an acceptable alternative. Case Presentation. We report a case of a 36-year-old female patient who presented for an acute onset of hemoptysis. CT chest showed an intralobar sequestration of the right lower lobe lung segment. In addition to the sequestration, the chest imaging also revealed a number of associated abnormalities including double superior vena cava communicating through a bridge, absence of brachiocephalic venous trunk, cardiac dextroposition, and agenesis of the right middle lobe. Outcome and Discussion. The transarterial embolization was selected for being mini-invasive and effective. It successfully controlled the bleed and led to complete regression of the sequestered lung on the follow-up CT chest several months later. Conclusion Successful management and complete regression are possible with mini-invasive intra-arterial embolization of lung sequestration. Although it is not uncommon to have associated congenital cardiopulmonary abnormalities with lung sequestration, however the exceptional abnormalities described in this case have never been reported before.","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":" 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140994261","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}
引用次数: 0
A Rare Case of an Eosinophilic Pleural Effusion and Loculated Ascites Associated with Strongyloides stercoralis Hyperinfection Syndrome in California 加利福尼亚州一例罕见的嗜酸性粒细胞胸腔积液和定位性腹水与斯特龙线虫高感染综合征有关的病例
Case Reports in Pulmonology Pub Date : 2024-04-08 DOI: 10.1155/2024/6652207
A. T. Phan, Luke Buxton, M. W. Choudhery, Henrik Ghantarchyan, Curtis Converse
{"title":"A Rare Case of an Eosinophilic Pleural Effusion and Loculated Ascites Associated with Strongyloides stercoralis Hyperinfection Syndrome in California","authors":"A. T. Phan, Luke Buxton, M. W. Choudhery, Henrik Ghantarchyan, Curtis Converse","doi":"10.1155/2024/6652207","DOIUrl":"https://doi.org/10.1155/2024/6652207","url":null,"abstract":"Introduction. Strongyloides stercoralis causes a helminthic infection that occurs via penetration of the skin with migration to the bloodstream, tracheobronchial tree, and gastrointestinal system. Pulmonary manifestations are rare and are typically seen in immunosuppressed patients who have Strongyloides stercoralis hyperinfection syndrome. Eosinophilic pleural effusions are rare in strongyloidiasis and only cited in a few case reports. Case Presentation. A 45-year-old male with a past medical history of diabetes mellitus, alcoholic cirrhosis, and end-stage renal disease presented to the emergency department with abdominal pain and dyspnea. Imaging studies demonstrated large bilateral pleural effusions, and he subsequently underwent an ultrasound-guided thoracentesis on the right hemithorax, yielding an exudative eosinophilic pleural effusion. An extensive hematology, gastroenterology, and infectious work-up was pursued. Strongyloides immunoglobulin G was positive, and he was successfully treated with ivermectin. Discussion. Eosinophilic pleural effusions related to strongyloidiasis are exceedingly rare. Clinicians should consider Strongyloides stercoralis infection as a part of the differential diagnosis when evaluating immunosuppressed patients with eosinophilic pleural effusions. Loculated abdominal fluid may also be a rare manifestation of Strongyloides stercoralis hyperinfection syndrome.","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"36 20","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140732091","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}
引用次数: 0
A Fatal Case of Legionella bozemanii Pneumonia in an Immunocompetent Patient 一名免疫力低下患者的博兹曼军团菌肺炎死亡病例
Case Reports in Pulmonology Pub Date : 2024-04-02 DOI: 10.1155/2024/7571380
A. Siddiqui
{"title":"A Fatal Case of Legionella bozemanii Pneumonia in an Immunocompetent Patient","authors":"A. Siddiqui","doi":"10.1155/2024/7571380","DOIUrl":"https://doi.org/10.1155/2024/7571380","url":null,"abstract":"Legionella bozemanii pneumonia is a rare form of Legionnaires' disease caused by the bacterium Legionella bozemanii. It is well known to cause pneumonia in immunocompromised patients and has rarely been reported in immunocompetent hosts. We describe a case of a 59-year-old immunocompetent female presented with pneumonia, acute respiratory failure, acute respiratory distress, and septic shock, who was treated with azithromycin, goal-directed resuscitation, and extracorporeal membrane oxygenation (ECMO) but did not survive. Clinicians should have high suspicion of rare legionella pathogens as causative agents for pneumonia.","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"13 24","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140754286","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}
引用次数: 0
Severe Atelectasis due to Aspirated Valproic Acid Tablet 吸入丙戊酸片导致严重气胸
Case Reports in Pulmonology Pub Date : 2024-03-18 DOI: 10.1155/2024/6650141
T. Tanigaki, Takunori Ogawa, S. Nomura, Koki Ito, Yuhei Kurata, Akira Matsukida, Morio Ishihara, A. Yoshino, Akihiko Kawana, Y. Kimizuka
{"title":"Severe Atelectasis due to Aspirated Valproic Acid Tablet","authors":"T. Tanigaki, Takunori Ogawa, S. Nomura, Koki Ito, Yuhei Kurata, Akira Matsukida, Morio Ishihara, A. Yoshino, Akihiko Kawana, Y. Kimizuka","doi":"10.1155/2024/6650141","DOIUrl":"https://doi.org/10.1155/2024/6650141","url":null,"abstract":"A 60-year-old man treated with valproic acid (VPA) for epilepsy developed atelectasis and respiratory failure after an accidentally aspirated VPA tablet-induced mucus hypersecretion. Following bronchoscopic removal of the aspirated tablet, his respiratory status improved and massive sputum production did not recur. We hypothesized that the aspirated VPA tablet increased the expression of mucin-related genes, thereby increasing mucus production. Our in vitro experiments using a human respiratory epithelial cell line revealed that VPA directly upregulates the airway mucin-related genes. We believe that this is the first case report of aspirated VPA-induced severe atelectasis and respiratory failure, which were successfully treated with the bronchoscopic removal of the VPA tablet.","PeriodicalId":52364,"journal":{"name":"Case Reports in Pulmonology","volume":"325 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140233183","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}
引用次数: 0
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