Case Reports in Dermatological Medicine最新文献

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Oral Isotretinoin Therapy in Recalcitrant Molluscum Contagiosum in an Immunocompromised Patient. 口服异维甲酸治疗免疫功能低下患者的顽固性传染性软疣。
Case Reports in Dermatological Medicine Pub Date : 2021-06-14 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5529382
Vikash Paudel, Deepa Chudal
{"title":"Oral Isotretinoin Therapy in Recalcitrant Molluscum Contagiosum in an Immunocompromised Patient.","authors":"Vikash Paudel,&nbsp;Deepa Chudal","doi":"10.1155/2021/5529382","DOIUrl":"https://doi.org/10.1155/2021/5529382","url":null,"abstract":"<p><p>Molluscum contagiosum is a viral infection caused by the Poxvirus characterized by multiple umbilicated papules. It is common in children and can be present at any body site. Severe molluscum is common in immunocompromised patients. We report a 20-year-old HIV-positive individual with widespread molluscum contagiosum, recalcitrant to topical therapy, under antiretroviral therapy, who was treated with oral isotretinoin and had a dramatic outcome. Although studies are needed to confirm the effectiveness of oral isotretinoin therapy in molluscum contagiosum, its easy availability, cost, and excellent safety profile appear to offer a promising therapeutic option.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"5529382"},"PeriodicalIF":0.0,"publicationDate":"2021-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216825/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39162942","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
New-Onset Bullous Pemphigoid in a COVID-19 Patient. 新发大疱性类天疱疮1例。
Case Reports in Dermatological Medicine Pub Date : 2021-06-07 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5575111
Natalie Olson, David Eckhardt, Angela Delano
{"title":"New-Onset Bullous Pemphigoid in a COVID-19 Patient.","authors":"Natalie Olson,&nbsp;David Eckhardt,&nbsp;Angela Delano","doi":"10.1155/2021/5575111","DOIUrl":"https://doi.org/10.1155/2021/5575111","url":null,"abstract":"<p><p>This manuscript presents a report of bullous pemphigoid rash associated with COVID-19 for the first time. The objective of this manuscript is to present a unique dermatological case in the setting of a COVID-19-positive infection to further recognize the virus symptomatology. A 37-year-old female with a past medical history of class III obesity, type II diabetes mellitus, and hypertension presented to the emergency department in September 2020 with inpatient and outpatient follow-up through to November 2020. The patient denied any personal or family history of skin disorders. The patient tested positive for COVID-19 prior to hospitalization and presented to the hospital with severe, persistent, pruritic rash meeting dermatopathological, serologic, and clinical criteria for bullous pemphigoid diagnosis. Histopathology H&E punch biopsy from her left flexor wrist demonstrated epidermal keratinocyte necrosis, subepidermal vesiculation with eosinophils, gossamer stranding of the papillary dermis, and subepidermal edema. Direct immunofluorescence punch biopsy from her left flexor wrist demonstrated strong linear IgG staining at the dermoepidermal junction, with weaker and focal linear C3 staining. Antigen-specific serology was consistent with bullous pemphigoid. There was no previously reported cutaneous association of COVID-19 infection with bullous pemphigoid making this case an important addition to the body of evidence helping to identify bullous pemphigoid in the setting of viral infection.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"5575111"},"PeriodicalIF":0.0,"publicationDate":"2021-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187076/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39139899","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: 20
Acquired Acrodermatitis Enteropathica in a 28-Year-Old Male with Type 1 Diabetes. 28岁男性1型糖尿病后天性肢端皮炎肠病。
Case Reports in Dermatological Medicine Pub Date : 2021-05-25 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5572583
Owen Ngalamika, Wencilaus M P Selvaraj, Fatima K Yikona, Chibamba Mumba
{"title":"Acquired Acrodermatitis Enteropathica in a 28-Year-Old Male with Type 1 Diabetes.","authors":"Owen Ngalamika,&nbsp;Wencilaus M P Selvaraj,&nbsp;Fatima K Yikona,&nbsp;Chibamba Mumba","doi":"10.1155/2021/5572583","DOIUrl":"https://doi.org/10.1155/2021/5572583","url":null,"abstract":"<p><p>Acrodermatitis enteropathica (AE) is a rare disorder arising from inherited or acquired zinc deficiency. It is mainly characterized by acral dermatitis, periorificial dermatitis, alopecia, and gastrointestinal symptoms in the form of diarrhea. There are many complications of AE including local and systemic infections that may develop as a result of untreated AE. In addition, due to the role of zinc in glucose metabolism, chronic zinc deficiency may pose a challenge in the control of blood glucose levels in diabetics. We report the case of a 28-year-old male with type 1 diabetes who presented with signs and symptoms of AE.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"5572583"},"PeriodicalIF":0.0,"publicationDate":"2021-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169277/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39089185","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
Use of Reflectance Confocal Microscopy for Hidrocystomas: An Emerging, Cost-Effective, and Powerful Tool. 使用反射共聚焦显微镜对汗液囊肿:一个新兴的,具有成本效益的,强大的工具。
Case Reports in Dermatological Medicine Pub Date : 2021-04-09 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5543803
Amanda Walker, Vikram Nath Sahni, Dev Ram Sahni, Julia Curtis
{"title":"Use of Reflectance Confocal Microscopy for Hidrocystomas: An Emerging, Cost-Effective, and Powerful Tool.","authors":"Amanda Walker,&nbsp;Vikram Nath Sahni,&nbsp;Dev Ram Sahni,&nbsp;Julia Curtis","doi":"10.1155/2021/5543803","DOIUrl":"https://doi.org/10.1155/2021/5543803","url":null,"abstract":"<p><p>Reflectance confocal microscopy (RCM) is an emerging and noninvasive imaging tool in dermatological practice. Benefits of this modality include differentiation between benign and malignant skin lesions, prevention of unnecessary biopsies, and cost effectiveness. However, RCM findings for benign lesions are rarely reported in the literature. We describe a case of reflectance confocal microscopy findings of a hidrocystoma and review potential applications of this imaging technique in everyday clinical practice.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"5543803"},"PeriodicalIF":0.0,"publicationDate":"2021-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052164/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38907843","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
Halo Nevi Are Not Trivial: About 2 Young Patients of Regressed Primary Melanoma That Simulates Halo Nevi. 光环痣不是微不足道的:关于两个年轻的退化原发性黑色素瘤患者,模拟光环痣。
Case Reports in Dermatological Medicine Pub Date : 2021-03-22 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6672528
S De Schrijver, I Theate, O Vanhooteghem
{"title":"Halo Nevi Are Not Trivial: About 2 Young Patients of Regressed Primary Melanoma That Simulates Halo Nevi.","authors":"S De Schrijver,&nbsp;I Theate,&nbsp;O Vanhooteghem","doi":"10.1155/2021/6672528","DOIUrl":"https://doi.org/10.1155/2021/6672528","url":null,"abstract":"<p><strong>Background: </strong>Halo nevi are often considered benign, and the possibility of malignancy is not always clear to practitioners. We present two case reports suggesting that a halo nevus appearance can be seen in melanoma, even in young adults. A literature search for halo nevi revealing melanoma shows that this is a very rare condition. <i>Case presentation</i>. This report of two young patients indicates the importance of obtaining a detailed history to detect warning signs such as itching, pain, spontaneous bleeding, and previous alterations according to the patient, including a previously totally black colour in an already fully regressed melanoma.</p><p><strong>Conclusions: </strong>The risk of a halo nevus being malignant is higher if there is only one unique halo nevus and no personal or familial history of vitiligo. We postulate that a regressing atypical nevus or a regressing melanoma may be induced by an immunologic reaction as halo nevus type of clinical picture.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"6672528"},"PeriodicalIF":0.0,"publicationDate":"2021-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009706/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38878263","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: 2
Long-Term Medical Follow-Up (for More than 15 Years) of a Patient with Stage IA Mycosis Fungoides Originally Presenting in Childhood: Remission for >15 Years with Localised Electron Beam Therapy. 长期医学随访(超过15年)1例儿童期出现的IA期蕈样真菌病患者:局部电子束治疗缓解>15年。
Case Reports in Dermatological Medicine Pub Date : 2021-03-13 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5541246
Eric Bessell, Martin Dalton, John David Parry
{"title":"Long-Term Medical Follow-Up (for More than 15 Years) of a Patient with Stage IA Mycosis Fungoides Originally Presenting in Childhood: Remission for >15 Years with Localised Electron Beam Therapy.","authors":"Eric Bessell,&nbsp;Martin Dalton,&nbsp;John David Parry","doi":"10.1155/2021/5541246","DOIUrl":"https://doi.org/10.1155/2021/5541246","url":null,"abstract":"<p><p>A man now aged 80 years has received specialist care for stage 1A mycosis fungoides for 58 years. The disease developed in childhood. Long-term follow-up (>30 years) of patients with mycosis fungoides is infrequently described in the world literature. The disease in this patient was limited to 5 areas, but these were large (up to 25 cm in diameter). The rest of the skin was normal clinically. All 5 areas were treated separately with electron beam therapy (3-4 MeV) to a dose of 30 Gy in 15 fractions over 3 weeks between 2000 and 2005. Complete regression was obtained in all 5 areas, and the patient has been in complete remission for 15 years after living with the disease previously for over 40 years.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"5541246"},"PeriodicalIF":0.0,"publicationDate":"2021-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7984908/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25537132","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
Cutaneous Lymphadenoma: A Case of Recurrence after Shave Excision. 皮肤淋巴结瘤:剃须切除后复发1例。
Case Reports in Dermatological Medicine Pub Date : 2021-03-10 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5543404
Fateme Rajabi, Kambiz Kamyab, Alireza Firooz
{"title":"Cutaneous Lymphadenoma: A Case of Recurrence after Shave Excision.","authors":"Fateme Rajabi,&nbsp;Kambiz Kamyab,&nbsp;Alireza Firooz","doi":"10.1155/2021/5543404","DOIUrl":"https://doi.org/10.1155/2021/5543404","url":null,"abstract":"<p><p>Cutaneous lymphadenoma (CL) is a rare skin tumor supposedly derived from the pilosebaceous unit. Since its description in 1987, fewer than 60 cases have been documented. Herein we report a case of CL presenting as a small nodule on the forehead of a young female. The lesion recurred two years after shave excision of a similar lesion. The histopathological examination revealed interconnected islands, sheets, and trabeculae consisting of two distinct types of cells within a sclerotic stroma, a peripheral rim of palisading basophilic cells, and central epithelial cells with eosinophilic to clear cytoplasm. A dense infiltration with prominent lymphocytes and few plasma cells dominated the stroma and permeated the epithelial nests. This case represents the recurrence of this type of skin tumor after shave excision and thus highlights the importance of complete margin-free excision of such lesions.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"5543404"},"PeriodicalIF":0.0,"publicationDate":"2021-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969119/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25525087","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: 2
Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact. 利什曼原虫和皮肤真菌引起的混合皮肤感染:罕见的巧合或免疫学事实。
Case Reports in Dermatological Medicine Pub Date : 2021-03-08 eCollection Date: 2021-01-01 DOI: 10.1155/2021/5526435
Amresh Kumar Singh, Ankur Kumar, Jayesh Pandey, Vivek Gaur, Pratima Tripathi, Indra Prasad Adhikari
{"title":"Mixed Cutaneous Infection Caused by Leishmania and Dermatophytes: A Rare Coincidence or Immunological Fact.","authors":"Amresh Kumar Singh,&nbsp;Ankur Kumar,&nbsp;Jayesh Pandey,&nbsp;Vivek Gaur,&nbsp;Pratima Tripathi,&nbsp;Indra Prasad Adhikari","doi":"10.1155/2021/5526435","DOIUrl":"https://doi.org/10.1155/2021/5526435","url":null,"abstract":"<p><p>Leishmaniasis was first described in 1824, in the Jessore district of Bengal (now Bangladesh) and more prevalent in Bihar, Uttar Pradesh, Jharkhand, and West Bengal. The disease is associated with depressed cellular immunity. Tinea is a fungal infection of the skin, which can become more extensively pathogenic particularly in patients with depressed cell-mediated immunity. Regulatory T cells and Th17 cells have been shown to be responsible for post-kala-azar dermal leishmaniasis (PKDL). We present a rare case of a 52-year-old house wife with a history of recurrent itching, depigmentation of the skin of extremities, and loss of appetite for 2-3 months followed by progressive spread of such lesion all over the body in an apparently healthy female. On examination, there were many hypopigmented scaly lesions mainly over the extensor aspect of the body. Skin lesions were characteristics of tinea infection with or without PKDL. A diagnosis of PKDL with tinea was made based on the history of kala-azar and on the skin slit smear for amastigote forms, <i>rK39</i> test, and KOH mount. Routine blood investigations showed negative serology for HIV and lower normal CD4+T counts. The patient was advised for treatment on systemic antifungal therapy with antihistaminics and later with miltefosine. We have highlighted that PKDL, although uncommon, is a distinct manifestation of VL. In our case study, we also tried to find the reason of coinfection; this was probably due to the depressed cellular immunity, skin abruptions, and acquired dermatophytic infection which is prevalent and associated with lower CD4+ T cell count.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"5526435"},"PeriodicalIF":0.0,"publicationDate":"2021-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7963913/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25514483","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 Porocarcinoma and Trichoblastoma Arising in a Nevus Sebaceus of Jadassohn. 皮脂腺痣中出现的罕见的多孔癌和毛母细胞瘤1例。
Case Reports in Dermatological Medicine Pub Date : 2021-03-03 eCollection Date: 2021-01-01 DOI: 10.1155/2021/7598086
Drew C Mitchell, Gina J Kuehn, Glynis A Scott, Timothy D Doerr, Francisco Tausk
{"title":"A Rare Case of Porocarcinoma and Trichoblastoma Arising in a Nevus Sebaceus of Jadassohn.","authors":"Drew C Mitchell,&nbsp;Gina J Kuehn,&nbsp;Glynis A Scott,&nbsp;Timothy D Doerr,&nbsp;Francisco Tausk","doi":"10.1155/2021/7598086","DOIUrl":"https://doi.org/10.1155/2021/7598086","url":null,"abstract":"<p><p>Nevus sebaceus of Jadassohn, or \"organoid nevus,\" is a common, benign hamartoma of the skin consisting of epithelial and adnexal components. Its natural history and association with neoplastic growths is well documented. The majority of concomitant neoplasms are benign-trichoblastoma and syringocystadenoma papilliferum are most frequently discovered-but malignant tumors have been described. We present the case of a 58-year-old male with a congenital nevus sebaceus of Jadassohn on his left parietal scalp that had been enlarging, changing color, and bleeding over the prior year. Clinical exam and histology disclosed the presence of a trichoblastoma and porocarcinoma arising within the nevus sebaceus. Porocarcinoma is a rare, intermediately aggressive, malignant eccrine gland tumor that is frequently metastasized at presentation. Otolaryngology performed wide local resection with sentinel lymph node biopsy. This case highlights the diversity of tumors associated with nevus sebaceus of Jadassohn, potential for malignant expansion, and necessity for close monitoring and maintaining a low threshold for biopsy in evolving lesions.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"7598086"},"PeriodicalIF":0.0,"publicationDate":"2021-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7946472/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25514484","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: 2
Cutaneous Metastasis vs. Isolated Skin Recurrence of Invasive Breast Carcinoma after Modified Radical Mastectomy. 浸润性乳腺癌改良根治术后皮肤转移与孤立性皮肤复发的比较。
Case Reports in Dermatological Medicine Pub Date : 2021-02-16 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6673289
Reza Hosseinpour, Mohammad Javad Yavari Barhaghtalab
{"title":"Cutaneous Metastasis vs. Isolated Skin Recurrence of Invasive Breast Carcinoma after Modified Radical Mastectomy.","authors":"Reza Hosseinpour,&nbsp;Mohammad Javad Yavari Barhaghtalab","doi":"10.1155/2021/6673289","DOIUrl":"https://doi.org/10.1155/2021/6673289","url":null,"abstract":"<p><strong>Background: </strong>Five to ten percent of the patients with operable breast cancer develop a chest wall recurrence within 10 years following the mastectomy. One of the most distressing presentations of locally recurrent breast cancer is the appearance of cutaneous metastases. To the best of authors' knowledge, there is no study distinguishing skin metastasis from local recurrence, so the main aim of this report was to elucidate if these two features are important in the prognosis and management of the disease. <i>Case Presentation</i>. A 51-year-old woman referred to the breast clinic due to a painful mass in the left breast. The patient underwent the modified radical mastectomy (MRM) and left axillary lymph node dissection followed by 30 sessions of radiotherapy and 8 sessions of chemotherapy (T3N1M0, ER-, and HER2+). About 15 months after the surgery, she presented with redness and eruptive lesions over the mastectomy scar that increased in size within a three-month follow-up.</p><p><strong>Conclusion: </strong>Mastectomy is not an absolute cure in the treatment of an invasive breast cancer because almost always, there is a recurrence risk and possibility of metastasis. It is vital to differentiate between local recurrence and skin metastasis because it would alter the overall treatment decision, prognosis, and patient outcomes.</p>","PeriodicalId":9630,"journal":{"name":"Case Reports in Dermatological Medicine","volume":"2021 ","pages":"6673289"},"PeriodicalIF":0.0,"publicationDate":"2021-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7902130/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25414834","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: 2
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