Case Reports in Otolaryngology最新文献

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Corrigendum to "A Case Report of Complete Resolution of Auricular Mucormycosis in an 18-Month-Old Diabetic Child". 18 个月大糖尿病患儿耳廓黏液瘤病完全治愈的病例报告》更正。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-04-17 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9794624
Mariam Aljehani, Hatem Alahmadi, Mansour Alshamani
{"title":"Corrigendum to \"A Case Report of Complete Resolution of Auricular Mucormycosis in an 18-Month-Old Diabetic Child\".","authors":"Mariam Aljehani, Hatem Alahmadi, Mansour Alshamani","doi":"10.1155/2021/9794624","DOIUrl":"10.1155/2021/9794624","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1155/2021/6618191.].</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"9794624"},"PeriodicalIF":0.6,"publicationDate":"2021-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8088361/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38976194","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
Corrigendum to "A Case of Epistaxis as the First Sign of Acute Idiopathic Thrombocytopenic Purpura". “1例鼻出血是急性特发性血小板减少性紫癜的第一症状”的更正。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-04-12 eCollection Date: 2021-01-01 DOI: 10.1155/2021/9804515
Shori Tajima, Fumihiko Matsumoto, Takashi Anzai, Satoshi Hara, Yo Suzuki, Katsuhisa Ikeda
{"title":"Corrigendum to \"A Case of Epistaxis as the First Sign of Acute Idiopathic Thrombocytopenic Purpura\".","authors":"Shori Tajima,&nbsp;Fumihiko Matsumoto,&nbsp;Takashi Anzai,&nbsp;Satoshi Hara,&nbsp;Yo Suzuki,&nbsp;Katsuhisa Ikeda","doi":"10.1155/2021/9804515","DOIUrl":"https://doi.org/10.1155/2021/9804515","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1155/2021/6612939.].</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"9804515"},"PeriodicalIF":0.6,"publicationDate":"2021-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057897/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38954351","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 Case of Aspiration Pneumonia Caused by Cerebrospinal Fluid Leaks Associated with Delayed Identification of Iatrogenic Skull Base Injury during Endoscopic Sinus Surgery. 内窥镜鼻窦手术中因脑脊液漏致吸入性肺炎伴医源性颅底损伤的延迟诊断1例。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-04-08 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5532194
Takashi Anzai, Akira Baba, Shin Ito, Yo Suzuki, Shori Tajima, Satoshi Hara, Yusuke Takata, Fumihiko Matsumoto, Katsuhisa Ikeda
{"title":"A Case of Aspiration Pneumonia Caused by Cerebrospinal Fluid Leaks Associated with Delayed Identification of Iatrogenic Skull Base Injury during Endoscopic Sinus Surgery.","authors":"Takashi Anzai,&nbsp;Akira Baba,&nbsp;Shin Ito,&nbsp;Yo Suzuki,&nbsp;Shori Tajima,&nbsp;Satoshi Hara,&nbsp;Yusuke Takata,&nbsp;Fumihiko Matsumoto,&nbsp;Katsuhisa Ikeda","doi":"10.1155/2021/5532194","DOIUrl":"https://doi.org/10.1155/2021/5532194","url":null,"abstract":"<p><p>Cerebrospinal fluid (CSF) leaks associated with endoscopic sinus surgery (ESS) are a rare complication affecting approximately 0.09% of patients. Although meningitis is a well-known complication of CSF leaks, the case we present is a rare and cautionary case of CSF leakage associated with ESS leading to aspiration pneumonia. A 43-year-old man with CSF leaks after ESS was referred to our hospital. After the operation, sometimes, he reported having a serous nasal discharge from the right side when he bent over, and he woke up choking on something every day. He also experienced headache, fever, fatigue, and cough. Interestingly, chest computed tomography (CT) showed a consolidation and ground-glass opacity in the posterior segments of the right upper lobes and superior segments of the bilateral lower lobes. These CT imaging findings were similar to those of aspiration pneumonia in bedridden patients who are always in a supine position. These findings suggest that CSF caused aspiration pneumonia. To the best of our knowledge, no case of aspiration pneumonia caused by CSF during endoscopic sinus surgery has been reported until now. If a patient with CSF leakage after ESS experiences fever, cough, or fatigue, physicians should consider aspiration pneumonia in addition to meningitis.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"5532194"},"PeriodicalIF":0.6,"publicationDate":"2021-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052149/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38907845","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
Melanocytic Nevus in the External Auditory Canal with Keratin Accumulation. 外耳道黑色素细胞痣伴角蛋白积累。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-03-24 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5539286
Junhui Jeong, Kyuin Lee, Hyun Seung Choi
{"title":"Melanocytic Nevus in the External Auditory Canal with Keratin Accumulation.","authors":"Junhui Jeong,&nbsp;Kyuin Lee,&nbsp;Hyun Seung Choi","doi":"10.1155/2021/5539286","DOIUrl":"https://doi.org/10.1155/2021/5539286","url":null,"abstract":"<p><p>Nevus is a benign melanocytic neoplasm and the most common type of skin tumor. It may occur anywhere on the skin, but it is rare in the external auditory canal (EAC). We present a case of melanocytic nevus in the EAC with keratin accumulation. In microscopic surgery, the mass was excised completely, and the wax and keratin material medial portion of the EAC behind the mass was removed. In this patient, a melanocytic nevus in the EAC caused symptoms of hearing loss and wax and keratin buildup. For melanocytic nevus in the EAC, excision and pathologic confirmation should be performed if there are symptoms or when malignant transformation is suspected.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"5539286"},"PeriodicalIF":0.6,"publicationDate":"2021-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8012142/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25575734","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
Concomitant Obstructive Sleep Apnoea in Patients with Meniere's Disease: A Case Report and Literature Review. 梅尼埃病患者伴发阻塞性睡眠呼吸暂停1例报告及文献复习
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-03-23 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5592611
Wong Kein Low, Esther Jiayi Lim
{"title":"Concomitant Obstructive Sleep Apnoea in Patients with Meniere's Disease: A Case Report and Literature Review.","authors":"Wong Kein Low,&nbsp;Esther Jiayi Lim","doi":"10.1155/2021/5592611","DOIUrl":"https://doi.org/10.1155/2021/5592611","url":null,"abstract":"<p><p>Meniere's disease (MD) is a condition characterised by fluctuating and progressive hearing loss, aural fullness, tinnitus, and intermittent attacks of vertigo. The disabling vertigo symptoms can be controlled in most patients by lifestyle changes and medications such as diuretics. Should standard medical therapy fail, the patient may require surgery in order to control the disease, but such surgical procedures can be functionally destructive. Obstructive sleep apnoea syndrome (OSAS) is common, especially in people who are grossly overweight. Up to 15% of patients with MD may have concomitant OSA. Unless the OSA is well controlled, such patients may continue to experience MD symptoms despite receiving adequate standard medical therapy for MD. Moreover, MD patients may experience insomnia as a result of vertigo and/or tinnitus where sedatives are indicated. The use of sedatives with muscle relaxant properties may inadvertently further aggravate OSA resulting in a vicious cycle of symptoms. Symptoms suggestive of concomitant OSA must be proactively sought as these patients do not necessarily exhibit the obvious phenotypic features of OSA. This is especially so in Asians where OSAS is commonly observed in people who are not overly obese. We report a case of a female patient who presented with recalcitrant MD disease and was later found to have concomitant OSA. The relevant literature will be reviewed, and learning points will be discussed from the perspective of the otologist/neurotologist. The clinician must always be mindful of the existence of concomitant \"silent\" OSAS as this impacts the management of patients with MD.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"5592611"},"PeriodicalIF":0.6,"publicationDate":"2021-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009700/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38883916","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 Uncommon Cause of Dysphagia: Postpneumonectomy Syndrome. 吞咽困难的一个不常见原因:肺切除术后综合征。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-03-08 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6658690
Erica Rego, Ahmed Abdelmeguid, Yuqi Kevin Wang, Karuna Dewan
{"title":"An Uncommon Cause of Dysphagia: Postpneumonectomy Syndrome.","authors":"Erica Rego,&nbsp;Ahmed Abdelmeguid,&nbsp;Yuqi Kevin Wang,&nbsp;Karuna Dewan","doi":"10.1155/2021/6658690","DOIUrl":"https://doi.org/10.1155/2021/6658690","url":null,"abstract":"<p><strong>Objective: </strong>Dysphagia after pneumonectomy is uncommon but concerning. The purpose of this paper is to present a case of dysphonia secondary to postpneumonectomy syndrome. <i>Case Report</i>. A 66-year-old female with stage IIIa adenocarcinoma of the lung was treated with a left pneumonectomy. Three years later, she presented with severe dysphagia, dyspnea, and dysphonia. Esophagram demonstrated severely deviated esophagus to the left of midline, attributed to prior left-sided pneumonectomy, without clear evidence of any external compression. Chest CT scan showed associated leftward mediastinal shift. This patient was treated with voice therapy and an exclusion diet, as the patient elected not to have surgery.</p><p><strong>Conclusion: </strong>This is the first reported case of dysphonia accompanying severe dysphagia following left pneumonectomy. While postpneumonectomy syndrome is rare, a high degree of clinical suspicion is recommended when treating patients with history of pneumonectomy.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"6658690"},"PeriodicalIF":0.6,"publicationDate":"2021-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7960023/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25501563","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
Nasopharyngeal Carcinoma Ex Pleomorphic Adenoma: Case Report and Comprehensive Literature Review. 鼻咽癌多形性腺瘤1例报告及综合文献复习。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-02-26 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8892280
Ellen L Tokarz, Adian A Ong, Mark S Burke
{"title":"Nasopharyngeal Carcinoma Ex Pleomorphic Adenoma: Case Report and Comprehensive Literature Review.","authors":"Ellen L Tokarz,&nbsp;Adian A Ong,&nbsp;Mark S Burke","doi":"10.1155/2021/8892280","DOIUrl":"https://doi.org/10.1155/2021/8892280","url":null,"abstract":"<p><p>Carcinoma ex pleomorphic adenoma (CXPA) is an epithelial malignancy that transforms from benign pleomorphic adenomas (PA) at a rate of 1.5% after 5 years and 10% after 15 years. The average age of reported nasopharyngeal CXPA is 56.7 years. However, the present case describes a 19-year-old making this case exceptionally rare. Standard treatment is wide local excision with adjuvant treatment. We report the demographics, presentation, treatment, and outcomes of 8 cases of nasopharyngeal CXPA. While surgical excision is the mainstay of treatment, negative margins can be difficult to obtain at the skull base, and we report a recurrence rate of 50% in nasopharyngeal primaries. Due to the aggressive nature of the disease and high rate of recurrence, the majority of patients in our review received adjuvant radiation with some receiving adjuvant chemotherapy in addition.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"8892280"},"PeriodicalIF":0.6,"publicationDate":"2021-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7935586/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25495762","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
Exuberant Intratracheal Granuloma. 气管内大量肉芽肿。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-02-22 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6697478
Emelia Stuart, Michael Armaneous, David Bracken, Kayva Crawford, Andrew M Vahabzadeh-Hagh
{"title":"Exuberant Intratracheal Granuloma.","authors":"Emelia Stuart,&nbsp;Michael Armaneous,&nbsp;David Bracken,&nbsp;Kayva Crawford,&nbsp;Andrew M Vahabzadeh-Hagh","doi":"10.1155/2021/6697478","DOIUrl":"https://doi.org/10.1155/2021/6697478","url":null,"abstract":"<p><strong>Background: </strong>Upper airway granulomas are commonly encountered benign masses and are a result of pronounced tissue reactivity to localized respiratory mucosal trauma. The mechanism of injury to respiratory epithelium is most commonly iatrogenic and associated with intubation or indwelling tracheostomy. <i>Case Report</i>. A 40-year-old obese female with a history of multiple intubations, poorly controlled diabetes mellitus type II, and history of tracheal stenosis presented with sudden onset respiratory distress requiring intubation at an outside hospital. Direct laryngoscopy revealed a rapidly forming transglottic tissue mass, measuring 5.0 × 2.2 × 0.8 cm. The following case represents an unusual exception to our experience with granulomas given its rapidity of onset and migration of tissue around the endotracheal tube. Discussion. Laryngeal erythema and granulation formation are expected postintubation findings in most patients; however, the large size of granuloma tissue and rapid onset of symptoms in this case make it remarkable. Our patient had multiple risk factors for postintubation stenosis: female sex, poorly controlled diabetes, hypertension, obesity, and multiple prior intubations for periods lasting longer than forty-eight hours.</p><p><strong>Conclusion: </strong>Our case highlights a rare laryngeal finding of a large granulation tissue mass causing sudden onset airway obstruction.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"6697478"},"PeriodicalIF":0.6,"publicationDate":"2021-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920715/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25452818","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 Case Report of Complete Resolution of Auricular Mucormycosis in an 18-Month-Old Diabetic Child. 18月龄糖尿病患儿耳毛霉菌病完全治愈1例报告。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-02-20 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6618191
Mariam Aljehani, Hatem Alahmadi, Mansour Alshamani
{"title":"A Case Report of Complete Resolution of Auricular Mucormycosis in an 18-Month-Old Diabetic Child.","authors":"Mariam Aljehani,&nbsp;Hatem Alahmadi,&nbsp;Mansour Alshamani","doi":"10.1155/2021/6618191","DOIUrl":"https://doi.org/10.1155/2021/6618191","url":null,"abstract":"<p><strong>Background: </strong>One of the most rare but deadly types of infectious fungal infection is Mucormycosis. All the cases reported with this type of infection are immunocompromised individuals. The challenge of early detection and intervention makes it one of the high mortality rates among other infectious diseases. <i>Case Report</i>. We report an 18-month-old girl with undiagnosed diabetes presented with a very aggressive form of necrotic infection of the ear auricle with facial nerve palsy. Using a series of magnetic resonance imaging, antibiotics, and high clinical suspicion, a diagnosis was established, and the patient was sent to the operation theatre for surgical debridement. Monthly follow-ups showed improvement of the facial palsy, and a plan for artificial auricle is set to occur in the following months before the age of five. <i>Discussion</i>. Mucormycosis is considered a very fatal and aggressive infection that has a very high mortality rate in immunocompromised patients. Early detection of such cases with an array of magnetic resonance imaging (MRI) and computed tomography (CT) is crucial in early treatment. Early aggressive surgical debridement and empirical coverage of bacterial, viral, and fungal infections can also alleviate the chances of preventing any secondary infection to develop in such cases.</p><p><strong>Conclusion: </strong>A combination of antifungal, antibiotic, and antiviral with timely surgical intervention improved the patient with complete resolution of the facial nerve palsy and no further recurrence of the infection.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"6618191"},"PeriodicalIF":0.6,"publicationDate":"2021-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8068535/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38954350","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: 4
A Case of Epistaxis as the First Sign of Acute Idiopathic Thrombocytopenic Purpura. 鼻出血为急性特发性血小板减少性紫癜的先兆1例。
IF 0.6
Case Reports in Otolaryngology Pub Date : 2021-02-06 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6612939
Shori Tajima, Fumihiko Matsumoto, Takashi Anzai, Satoshi Hara, Yo Suzuki, Katsuhisa Ikeda
{"title":"A Case of Epistaxis as the First Sign of Acute Idiopathic Thrombocytopenic Purpura.","authors":"Shori Tajima,&nbsp;Fumihiko Matsumoto,&nbsp;Takashi Anzai,&nbsp;Satoshi Hara,&nbsp;Yo Suzuki,&nbsp;Katsuhisa Ikeda","doi":"10.1155/2021/6612939","DOIUrl":"https://doi.org/10.1155/2021/6612939","url":null,"abstract":"<p><p>Idiopathic thrombocytopenic purpura (ITP) is an acquired thrombocytopenia caused by the action of autoantibodies against platelet antigens. It is traditionally defined by a platelet count of less than 10 × 10<sup>4</sup>/<i>μ</i>L. Most patients with ITP are asymptomatic; however, symptoms have been confirmed in some cases. Conversely, it is very rare to find epistaxis as the first sign of ITP. We report the case of an 84-year-old man who came to the ear, nose, and throat department with severe and repeated epistaxis. We decided to keep him hospitalized as it was very difficult to stop the nasal bleeding. A full blood count showed a platelet level of only 1000/<i>μ</i>L. Hematologic results confirmed the diagnosis of ITP. The patient underwent treatment with intravenous gamma-globulin, platelet transfusions, and romiplostim with a favorable response.</p>","PeriodicalId":45872,"journal":{"name":"Case Reports in Otolaryngology","volume":"2021 ","pages":"6612939"},"PeriodicalIF":0.6,"publicationDate":"2021-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884150/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25402880","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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