Case Reports in Dermatological Medicine最新文献

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Partial Excision and Ablative Carbon Dioxide Fractional Laser Therapy for Multiple Apocrine Hidrocystomas on the Periorbital Regions and Cheeks. 部分切除及二氧化碳分割激光消融治疗眼眶周围及面颊多发大汗腺囊肿。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/6318220
Hiroshi Kitagawa, Isao Sugimoto, Toshinori Bito, Keiichi Yamanaka, Hiroto Terashi
{"title":"Partial Excision and Ablative Carbon Dioxide Fractional Laser Therapy for Multiple Apocrine Hidrocystomas on the Periorbital Regions and Cheeks.","authors":"Hiroshi Kitagawa,&nbsp;Isao Sugimoto,&nbsp;Toshinori Bito,&nbsp;Keiichi Yamanaka,&nbsp;Hiroto Terashi","doi":"10.1155/2023/6318220","DOIUrl":"https://doi.org/10.1155/2023/6318220","url":null,"abstract":"<p><p>A 51-year-old Japanese woman presented with translucent papules on the periorbital area and cheeks that had progressively enlarged over five years. She underwent a skin biopsy and was diagnosed with multiple apocrine hidrocystomas. Her lesions became more pronounced and obscured her vision when her body warmed up, such as during bathing. To alleviate her symptoms, we began treatment by partially resecting the tumors on the lower eyelids. After surgery, her vision was no longer obscured. Approximately 1.5 years later, she underwent ablative 10,600 nm carbon dioxide fractional laser therapy for the mildly enlarged apocrine hidrocystomas on her lower eyelids and cheeks. At roughly six months of follow-up, the symptoms had improved, and the cosmetic results were satisfactory, although minor scarring and hypopigmentation were still evident. These case findings underscore the effectiveness of ablative carbon dioxide fractional lasers in treating apocrine hidrocystomas.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"6318220"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353895/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9842457","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
Systemic Sarcoidosis Presenting in a Scar. 系统性结节病表现为疤痕。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/7751754
Amy Xiao, Lauryn M Falcone, Joseph C English Iii
{"title":"Systemic Sarcoidosis Presenting in a Scar.","authors":"Amy Xiao,&nbsp;Lauryn M Falcone,&nbsp;Joseph C English Iii","doi":"10.1155/2023/7751754","DOIUrl":"https://doi.org/10.1155/2023/7751754","url":null,"abstract":"<p><p>While most forms of sarcoidosis of the skin do not require treatment, 40% of patients initially diagnosed with cutaneous sarcoidosis are found to have an asymptomatic disease involving other organ systems. It is the involvement of the lungs, heart, eyes, and nervous system which most often contributes to morbidity/mortality. An early and accurate diagnosis of sarcoidosis is difficult because patients may be asymptomatic, initial presentations may vary, and there is no single reliable diagnostic test except biopsy. We present a case of scar sarcoidosis which led to the diagnosis of stage II pulmonary sarcoidosis in a woman in her 50s. Her scar sarcoidosis presented as well-circumscribed, reddish-brown macules surrounding an atrophic scar from a prior skin graft on the right leg. Biopsy revealed scattered, well-formed, non-necrotizing granulomas of the dermis composed of epithelioid histiocytes and multinucleated giant cells, surrounded by a sparse infiltrate of lymphocytes and histiocytes. A CT chest demonstrated extensive hilar lymphadenopathy, leading to a diagnosis of stage II pulmonary sarcoidosis with cutaneous involvement. This case illustrates the interesting presentation of scar sarcoidosis and underscores the importance of a broad differential including sarcoidosis for skin changes around scars and underscores the need for early biopsy. Prompt cutaneous diagnosis leads to earlier systemic evaluation, therapeutics, and better outcomes.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"7751754"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889162/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9198055","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
Comprehensive Management of Acute Ischemic Stroke in Psoriatic Patient. 银屑病患者急性缺血性脑卒中的综合治疗。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/6580971
Al Rasyid, Taufik Mesiano, Mohammad Kurniawan, Rakhmad Hidayat, Reyhan Eddy Yunus, Endi Novianto, Ocktafiani Ocktafiani, Elvan Wiyarta, Salim Harris
{"title":"Comprehensive Management of Acute Ischemic Stroke in Psoriatic Patient.","authors":"Al Rasyid,&nbsp;Taufik Mesiano,&nbsp;Mohammad Kurniawan,&nbsp;Rakhmad Hidayat,&nbsp;Reyhan Eddy Yunus,&nbsp;Endi Novianto,&nbsp;Ocktafiani Ocktafiani,&nbsp;Elvan Wiyarta,&nbsp;Salim Harris","doi":"10.1155/2023/6580971","DOIUrl":"https://doi.org/10.1155/2023/6580971","url":null,"abstract":"<p><strong>Background: </strong>Stroke is one of the top causes of death and disability in several nations. Patients with psoriasis are susceptible to multiple comorbidities, including stroke. In addition to acute ischemic stroke, psoriasis and chronic inflammation require comprehensive treatment. Here, we present a comprehensive management case of a patient with an acute ischemic stroke and psoriasis. <i>Case Presentation</i>. A 42-year-old man came to the emergency department complaining of sudden left-sided weakness that started two and a half hours before being admitted to the hospital. The patient was treated with cyclosporine from 2013 to 2019 for a history of psoriasis. The patient was then treated for secondary stroke prevention using aspirin, vitamin B6, vitamin B12, folic acid, simvastatin, cyclosporine, and topical treatment. After two days of treatment, the patient's condition improved clinically, and he was discharged without further neurological deficits. As a home medication, the patient's cyclosporine was switched to the initial dose of methotrexate (7.5 mg/week) and titrated weekly to a response dose of 10 mg in the 10<sup>th</sup> week. After three months of follow-up, the patient's condition remained stable, devoid of similar symptoms or sequelae.</p><p><strong>Conclusions: </strong>Cyclosporine should only be used for a maximum of 1 year for stroke management with psoriasis and be substituted for other systemic agents such as methotrexate. In addition, anticoagulants, antihypertensive, antihyperlipidemic, vitamin B6, vitamin 12, and folic acid regimens are highly recommended for comprehensive therapy of cardiovascular comorbidities.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"6580971"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017213/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9145181","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
Acquired Lymphangiectasia of the Scrotum Successfully Treated with Radiofrequency Ablation: A Case Report with Dermoscopic Review. 射频消融术成功治疗阴囊获得性淋巴管扩张:1例皮肤镜回顾报告。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/7111912
Dhan Keshar Khadka, Raksha Pathak, Sudha Agrawal, Sairil Pokharel
{"title":"Acquired Lymphangiectasia of the Scrotum Successfully Treated with Radiofrequency Ablation: A Case Report with Dermoscopic Review.","authors":"Dhan Keshar Khadka,&nbsp;Raksha Pathak,&nbsp;Sudha Agrawal,&nbsp;Sairil Pokharel","doi":"10.1155/2023/7111912","DOIUrl":"https://doi.org/10.1155/2023/7111912","url":null,"abstract":"<p><p>Lymphangiectasia is dilatation of normal superficial lymphatic vessels due to damage or obstruction of deep lymphatic vessels leading to increased lymphatic pressure and engorgement of dermal lymphatics due to varying causes. Lymphangiectasia clinically presents as thick-walled, translucent vesicles and papules with chronic lymphedema rarely involving the scrotum. Here we report a patient with acquired lymphangiectasia of the scrotum secondary to surgery for hydrocele successfully treated with radiofrequency ablation. We highlight the use of dermoscopy as a non-invasive diagnostic tool in lymphangiectasia.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"7111912"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845032/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10550926","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
Topical Nitric Acid Burns: Initial Assessment and Management. 局部硝酸烧伤:初步评估和管理。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9995933
Asmaa Laanaya, Mehdi Ami Ali, Amal Miqdadi, Mostapha Noussair, Mourad Nafaa, Lahcen Belyamani
{"title":"Topical Nitric Acid Burns: Initial Assessment and Management.","authors":"Asmaa Laanaya,&nbsp;Mehdi Ami Ali,&nbsp;Amal Miqdadi,&nbsp;Mostapha Noussair,&nbsp;Mourad Nafaa,&nbsp;Lahcen Belyamani","doi":"10.1155/2023/9995933","DOIUrl":"https://doi.org/10.1155/2023/9995933","url":null,"abstract":"<p><p>Nitric acid (NA) is corrosive. On contact with the skin, liquid splashes with nitric acid and may produce severe burns. These burns usually take on a characteristic yellowish hue. We report the case of a 54-year-old man presenting a nitric acid burn with a pathognomonic skin lesion and perfect healing. NA is a chemical that is important in industry, and it is a very strong acid that is used for engraving, metal refining, electroplating, and fertilizer manufacturing. Skin contact with NA leads to severe burns. The pathophysiology depends on the type of concentration, the strength, quality, and duration of contact, and the penetration power of the acids concerned. The early and abundant irrigation with water or sterile isotonic saline solution, the use of panthenol-containing creams and covering with silver sulphadiazine dressing, carefully monitoring wounds, keeping wounds clean and moist, and preventing and managing secondary infection allow the healing.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"9995933"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412252/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10050703","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
Confluent and Reticulated Papillomatosis Successfully Treated with Topical Vitamin A Derivative. 局部维生素A衍生物成功治疗汇合性网状乳头状瘤病。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9467084
Manal Alsulami, Bader Alharbi, Yaser Alotaibi, Fadi Alghamdi, Adel Alsantali
{"title":"Confluent and Reticulated Papillomatosis Successfully Treated with Topical Vitamin A Derivative.","authors":"Manal Alsulami,&nbsp;Bader Alharbi,&nbsp;Yaser Alotaibi,&nbsp;Fadi Alghamdi,&nbsp;Adel Alsantali","doi":"10.1155/2023/9467084","DOIUrl":"https://doi.org/10.1155/2023/9467084","url":null,"abstract":"<p><p>Confluent and reticulated papillomatosis (CARP) is a rare dermatosis that typically develops in adolescents and young adults. Clinical characteristics include hyperkeratotic papules that coalesce centrally with a reticulated pattern peripherally on the central and upper trunk, neck, and axilla. Its etiology is not precisely known, and disordered keratinization has been postulated as one of the etiologies. Treatment options of the disease include systemic (such as antibiotics, antifungals, and retinoids) and topical treatments (such as lactic acid, antifungals, retinoids, salicylic acid, urea, tacrolimus, and vitamin D analogs). We report a case of a 17-year-old boy, otherwise healthy, presented with a new onset of asymptomatic, persistent, and slowly progressing brownish skin lesions over the trunk for 6 months. The diagnosis was revised to CARP based on clinical and histopathological examination. Treatment with topical tretinoin 0.025% cream once daily was begun. There was complete resolution of his lesions at the end of 8 weeks of therapy. There has been no relapse at 2 months follow-up. The effectiveness of tretinoin in this patient supports the theory that CARP is a keratinization disorder. Initiating treatment with topical tretinoin when no limitations for its use would be reasonable as it can provide a safer alternative to systemic therapy.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"9467084"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010871/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9123253","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 and Literature Review of Bilateral Cervical Chondrocutaneous Branchial Remnants. 双侧颈椎软骨皮鳃裂残余1例并文献复习。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/8475270
Yuehua He, Huiling Zhu, Hang Ji, Weining Huang, Zhongrong Liu
{"title":"A Case Report and Literature Review of Bilateral Cervical Chondrocutaneous Branchial Remnants.","authors":"Yuehua He,&nbsp;Huiling Zhu,&nbsp;Hang Ji,&nbsp;Weining Huang,&nbsp;Zhongrong Liu","doi":"10.1155/2023/8475270","DOIUrl":"https://doi.org/10.1155/2023/8475270","url":null,"abstract":"<p><p>Chondrocutaneous branchial remnants (CCBRs) are rare congenital heterotopic tissue formations originating from the first or second embryonic branchial arches. Clinically, CCBRs are characterized predominantly by unilateral and solitary cartilaginous nodules found on the lower neck region. Herein, we present a case of CCBRs in a 9-year-old male patient who presented with horn-shaped projecting masses on either side of the anterior border of the sternocleidomastoid muscle. The pathological report following surgical resection revealed that the lesion was located in the dermis and consisted primarily of hyaline cartilage tissue enclosed by a fibrous capsule, with few local vascular proliferations. Based on the clinical and pathological features, the patient was ultimately diagnosed with congenital bilateral cervical chondrocutaneous branchial remnants.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"8475270"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10279493/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9707686","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
Hypopigmented Mycosis Fungoides in an 11-Year-Old Palestinian Boy. 11岁巴勒斯坦男孩的蕈样霉菌病。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/4310796
Duha Rabi, Balqis Shawer, Ahmad Rabee, Mohammad Qudaimat, Mohammad Milhem, Izzeddin Bakri
{"title":"Hypopigmented Mycosis Fungoides in an 11-Year-Old Palestinian Boy.","authors":"Duha Rabi,&nbsp;Balqis Shawer,&nbsp;Ahmad Rabee,&nbsp;Mohammad Qudaimat,&nbsp;Mohammad Milhem,&nbsp;Izzeddin Bakri","doi":"10.1155/2023/4310796","DOIUrl":"https://doi.org/10.1155/2023/4310796","url":null,"abstract":"<p><p>Cutaneous T-cell lymphoma (CTCL) is a lymphoproliferative disorder of the skin. The most common subtype of CTCL in pediatrics is mycosis fungoides (MF). There are multiple variants of MF. The hypopigmented variant represents more than 50% of MF cases in pediatrics. Misdiagnosis of MF can occur because it may resemble other benign skin pathologies. This is a case of an 11-year-old Palestinian boy presented with generalized nonpruritic hypopigmented maculopapular patches with progressive course for 9-months. Biopsy samples from a hypopigmented patch revealed appearances diagnostic of MF. Immunohistochemical staining was positive for CD3 and CD7 (partial) and a mixture of CD4 and CD8 positive cells. The patient's case was managed with narrowband ultraviolet B (NBUVB) phototherapy. After a few sessions, the hypopigmented lesions improved significantly.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"4310796"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949951/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10792925","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
Granulosis Rubra Nasi: A Case Report and Brief Review of the Literature. 红斑性颗粒病1例报告及文献综述。
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/3927244
Girum T Assefa
{"title":"Granulosis Rubra Nasi: A Case Report and Brief Review of the Literature.","authors":"Girum T Assefa","doi":"10.1155/2023/3927244","DOIUrl":"https://doi.org/10.1155/2023/3927244","url":null,"abstract":"<p><p>Granulosis rubra nasi is a rare autosomal dominant disease of the eccrine glands. It is clinically characterized by mid-face hyperhidrosis, most prominent at the tip of the nose, and dark erythematous papules on the nose, cheeks, chin, and upper lip. Although it commonly occurs in childhood, it can also occur in adults. This is a case report of two female granulosis rubra nasi patients. This report, to the best of my knowledge, has not before been described in Ethiopian individuals and is hence being reported due to its rarity.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"3927244"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9897907/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10652543","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
LEOPARD Syndrome with a Sporadic PTPN11 Mutation in a Saudi Patient. 豹综合征伴散发性PTPN11突变的沙特患者
Case Reports in Dermatological Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/4161574
Hussein M Alshamrani, Luai M Assaedi, Jumanah A Bahattab, Abdulrahman M Mohammad, Magdy R Abdulghani
{"title":"LEOPARD Syndrome with a Sporadic <i>PTPN11</i> Mutation in a Saudi Patient.","authors":"Hussein M Alshamrani,&nbsp;Luai M Assaedi,&nbsp;Jumanah A Bahattab,&nbsp;Abdulrahman M Mohammad,&nbsp;Magdy R Abdulghani","doi":"10.1155/2023/4161574","DOIUrl":"https://doi.org/10.1155/2023/4161574","url":null,"abstract":"<p><p>LEOPARD syndrome (LS) is a rare autosomal dominant inherited or sporadic genetic disorder caused commonly by missense mutations in the protein-tyrosine phosphatase-nonreceptor type 11 (<i>PTPN11</i>) gene. Due to its rarity and a high chance of misdiagnosis, the epidemiological profile of LS is poorly established. To the best of our knowledge, this is the second report with a documented <i>PTPN11</i> gene mutation in Saudi Arabia.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2023 ","pages":"4161574"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229248/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9567771","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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