Journal of dermatological case reports最新文献

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Temporary henna tattoos and hypertrichosis: a case report and review of the literature. 临时指甲花纹身和多毛症:一例报告和文献回顾。
Journal of dermatological case reports Pub Date : 2015-06-30 DOI: 10.3315/jdcr.2015.1204
Constantin El Habr, Hala Mégarbané
{"title":"Temporary henna tattoos and hypertrichosis: a case report and review of the literature.","authors":"Constantin El Habr,&nbsp;Hala Mégarbané","doi":"10.3315/jdcr.2015.1204","DOIUrl":"https://doi.org/10.3315/jdcr.2015.1204","url":null,"abstract":"<p><strong>Background: </strong>Temporary black henna tattooing is highly popular among children and young adults in some regions. The unmonitored addition of different products to darken the color of pure henna has been the cause of many tattoo-associated dermatoses.</p><p><strong>Observation: </strong>Hypertrichosis secondary to henna pseudotattoo is a rare, newly recognized cutaneous manifestation. Only 4 case reports of henna tattooing causing localized hypertrichosis have been reported in the literature. We report a case of hypertrichosis and eczematous reaction to temporary henna tattoo.</p><p><strong>Conclusion: </strong>Hypertrichosis secondary to black henna is independent of the presence of contact dermatitis. The mechanism by which black henna induces hair growth remains unclear.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 2","pages":"36-8"},"PeriodicalIF":0.0,"publicationDate":"2015-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2015.1204","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33891002","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: 13
Photoletter to the editor: Psoriatic erythroderma associated with bullous pemphigoid: clinical appearance and histopathology. 致编辑:银屑病红皮病伴大疱性类天疱疮:临床表现和组织病理学。
Journal of dermatological case reports Pub Date : 2015-03-31 DOI: 10.3315/jdcr.2015.1194
Cristina Garrido Colmenero, Salvador Arias Santiago, Gonzalo Blasco Morente, Israel Pérez López, José Aneiros Fernández
{"title":"Photoletter to the editor: Psoriatic erythroderma associated with bullous pemphigoid: clinical appearance and histopathology.","authors":"Cristina Garrido Colmenero,&nbsp;Salvador Arias Santiago,&nbsp;Gonzalo Blasco Morente,&nbsp;Israel Pérez López,&nbsp;José Aneiros Fernández","doi":"10.3315/jdcr.2015.1194","DOIUrl":"https://doi.org/10.3315/jdcr.2015.1194","url":null,"abstract":"<p><p>Psoriasis and bullous pemphigoid represent two clinically well-characterized, chronic, inflammatory skin conditions. The concomitant occurrence of these two entities in a patient is rare. We report a 62-year-old male with personal history of psoriasis vulgaris who developed disseminated bullous pemphigoid associated with psoriatic erythroderma. Skin histopathology from a scaly plaque was consistent with the diagnosis of psoriasis and showed subepidermal blister with inflammatory infiltrate of eosinophils with some neutrophils. </p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 1","pages":"23-4"},"PeriodicalIF":0.0,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2015.1194","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33146701","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: 6
Recalcitrant oral squamous cell papilloma lesions in two HIV-infected patients successfully treated with topical imiquimod. 顽固性口腔鳞状细胞乳头状瘤病变在两个hiv感染患者成功治疗外用咪喹莫特。
Journal of dermatological case reports Pub Date : 2015-03-31 DOI: 10.3315/jdcr.2015.1192
Lilly Esquivel-Pedraza, Laura Fernández-Cuevas, Marcela Saeb-Lima, Brenda Alicia Guerrero-Ramos, Amparo Hernández-Salazar, Silvia Méndez-Flores
{"title":"Recalcitrant oral squamous cell papilloma lesions in two HIV-infected patients successfully treated with topical imiquimod.","authors":"Lilly Esquivel-Pedraza,&nbsp;Laura Fernández-Cuevas,&nbsp;Marcela Saeb-Lima,&nbsp;Brenda Alicia Guerrero-Ramos,&nbsp;Amparo Hernández-Salazar,&nbsp;Silvia Méndez-Flores","doi":"10.3315/jdcr.2015.1192","DOIUrl":"https://doi.org/10.3315/jdcr.2015.1192","url":null,"abstract":"<p><strong>Background: </strong>Squamous cell papilloma is a benign mucosal disease associated with human papillomavirus. Its presence in human immunodeficiency virus (HIV)-infected patients has rarely been reported. Therapeutic modalities for oral squamous cell papilloma have limited success and recurrences are frequent in HIV-infected subjects. Imiquimod, is a topical immunomodulator successfully used in some human papillomavirus-related oral lesions. However, its use for oral squamous cell papillomas in HIV-infected individuals has never been described.</p><p><strong>Observations: </strong>We report two male adult patients with HIV-infection, B2 and C3 stage respectively, undergoing antiretroviral therapy, with multiple recalcitrant oral squamous cell papillomas, predominantly affecting the masticatory mucosa. These lesions were successfully treated with daily topical imiquimod 5% cream for a few weeks, with only mild and well-tolerated side effects. No recurrences were observed after a follow-up period of over 20 months.</p><p><strong>Conclusions: </strong>Our cases highlight the value of imiquimod for the non-invasive treatment of multiple persistent oral squamous cell papillomas in two HIV-infected patients.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 1","pages":"19-22"},"PeriodicalIF":0.0,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2015.1192","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33146700","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: 7
Linear psoriasis following the typical distribution of the sciatic nerve. 线性银屑病遵循典型的坐骨神经分布。
Journal of dermatological case reports Pub Date : 2015-03-31 DOI: 10.3315/jdcr.2015.1189
Marco Galluzzo, Marina Talamonti, Alessandro Di Stefani, Sergio Chimenti
{"title":"Linear psoriasis following the typical distribution of the sciatic nerve.","authors":"Marco Galluzzo,&nbsp;Marina Talamonti,&nbsp;Alessandro Di Stefani,&nbsp;Sergio Chimenti","doi":"10.3315/jdcr.2015.1189","DOIUrl":"https://doi.org/10.3315/jdcr.2015.1189","url":null,"abstract":"<p><strong>Background: </strong>Some studies suggest that the nervous system plays a role in the onset of psoriasis and psoriasis flares including the symmetry of lesions, sparing of denervated skin and the role of stress in inducing lesions.</p><p><strong>Main observations: </strong>We describe an unusual case of psoriasis occurring in the same distribution as sciatic pain from a prolapsed intervertebral disc. The patient, a 45-year-old man with plaque psoriasis was treated with ustekinumab for 104 weeks, at a standard dose. During the eight month of therapy he developed an asymptomatic linear eruption on the left lower extremity along the distribution of the sciatic nerve. On examination, erythematous scaly plaques were noted. Histopathology confirmed the diagnosis of psoriasis. The treatment was continued and clobetasol proprionate 0.05% cream was added. At week 12 after the eruption, the patient reported a pain radiating through the buttock and posterior left leg during jogging. Magnetic resonance imaging showed lumbar disc herniation with compression of the L5-S1 spinal nerve roots. The patient stopped running and the psoriasis spontaneously receded, in a slow but complete fashion, without any local treatment.</p><p><strong>Conclusion: </strong>There is substantial evidence that nerves play a key role in the pathogenesis of psoriasis. We hypothesized that local TNF-alpha, neuropeptides and nerve growth factor, which are produced by nerve root compression, played a critical role in this case of psoriasis onset in an area of pain from a bulging lumbar intervertebral disc. To our knowledge, a correlation of psoriasis and nerve root compression has not been described previously.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 1","pages":"6-11"},"PeriodicalIF":0.0,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2015.1189","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33141506","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: 6
Primary cutaneous γ/δ T-cell lymphoma. An atypical case with bone marrow granulomas. 原发性皮肤γ/δ t细胞淋巴瘤。骨髓肉芽肿的不典型病例。
Journal of dermatological case reports Pub Date : 2015-03-31 DOI: 10.3315/jdcr.2015.1191
Guy Shalom, Ronit Gurion, Daniel Benharroch
{"title":"Primary cutaneous γ/δ T-cell lymphoma. An atypical case with bone marrow granulomas.","authors":"Guy Shalom,&nbsp;Ronit Gurion,&nbsp;Daniel Benharroch","doi":"10.3315/jdcr.2015.1191","DOIUrl":"https://doi.org/10.3315/jdcr.2015.1191","url":null,"abstract":"<p><strong>Background: </strong>Primary cutaneous γ/δ T-cell lymphoma is a rare variant of peripheral T-cell lymphoma which has been only recently set apart from subcutaneous panniculitis-like T-cell lymphoma and is known for its aggressive nature.</p><p><strong>Main observation: </strong>We hereby report a case of primary cutaneous γ/δ T-cell lymphoma in a 35-year-old man with bone marrow granulomas, an unexpected feature in this lymphoma. The patient was treated with combination chemotherapy. Partial response was obtained, followed by relapse. Allogeneic stem cell transplantation was then carried out, and full remission was achieved.</p><p><strong>Conclusion: </strong>Bone marrow granulomas can be an accompanying feature in primary cutaneous γ/δ T-cell lymphoma.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 1","pages":"15-8"},"PeriodicalIF":0.0,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2015.1191","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33146699","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
Trichoscopy findings in loose anagen hair syndrome: rectangular granular structures and solitary yellow dots. 毛发脱落综合征的毛镜检查表现:矩形颗粒状结构和孤立的黄色点。
Journal of dermatological case reports Pub Date : 2015-03-31 DOI: 10.3315/jdcr.2015.1193
Adriana Rakowska, Malgorzata Zadurska, Joanna Czuwara, Olga Warszawik-Hendzel, Marta Kurzeja, Malgorzata Maj, Malgorzata Olszewska, Lidia Rudnicka
{"title":"Trichoscopy findings in loose anagen hair syndrome: rectangular granular structures and solitary yellow dots.","authors":"Adriana Rakowska,&nbsp;Malgorzata Zadurska,&nbsp;Joanna Czuwara,&nbsp;Olga Warszawik-Hendzel,&nbsp;Marta Kurzeja,&nbsp;Malgorzata Maj,&nbsp;Malgorzata Olszewska,&nbsp;Lidia Rudnicka","doi":"10.3315/jdcr.2015.1193","DOIUrl":"https://doi.org/10.3315/jdcr.2015.1193","url":null,"abstract":"<p><strong>Background: </strong>Loose anagen hair syndrome (LAHS) is typically diagnosed in girls older than 2 years who present with hair that \"will not grow\". Hair microscopic examination shows absent inner and outer root sheaths, ruffling of the cuticle on the proximal hair shaft and deformed pigmented anagen bulbs.</p><p><strong>Objective: </strong>The aim of the study was to assess whether there are characteristic trichoscopic features favoring the diagnosis of LAHS.</p><p><strong>Patients and methods: </strong>Eighty nine children patients were included into the study (24 girls with LAHS, 25 with alopecia areata, 20 with telogen effluvium and 20 healthy children). In all groups trichoscopy was performed. Trichoscopy images were analyzed for abnormalities in the hairs shafts, the hair follicle openings and the interfollicular area.</p><p><strong>Results: </strong>Dirty dots were present in all groups. A unique feature of LAHS was the presence of rectangular black granular structures which differs from dense black dots seen in patients with alopecia areata. This feature was observed in 71% of patients with LAHS. Follicular units with single hairs constituted 92,9% of hair units in these patients (65,5% in telogen effluvium and 53% in the control group). Solitary yellow dots were found in 50% of patient with LAHS and in 24% of patients with alopecia areata, but was not found in control group or in patients with telogen effluvium.</p><p><strong>Conclusion: </strong>The trichoscopy features favoring the diagnosis of LAHS are: rectangular black granular structures, solitary yellow dots and major predominance of follicular units with single hairs.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 1","pages":"1-5"},"PeriodicalIF":0.0,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2015.1193","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33141505","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: 19
Photoletter to the editor: Basal cell carcinoma on the vermilion lip. 给编辑的照相信:朱红色唇上的基底细胞癌。
Journal of dermatological case reports Pub Date : 2015-03-31 DOI: 10.3315/jdcr.2015.1195
Ana Batalla, Ana Isabel Encinas-Muñiz, Enrique Gutiérrez-González, Daniel de la Mano
{"title":"Photoletter to the editor: Basal cell carcinoma on the vermilion lip.","authors":"Ana Batalla,&nbsp;Ana Isabel Encinas-Muñiz,&nbsp;Enrique Gutiérrez-González,&nbsp;Daniel de la Mano","doi":"10.3315/jdcr.2015.1195","DOIUrl":"https://doi.org/10.3315/jdcr.2015.1195","url":null,"abstract":"<p><p>The vermilion and vermilion border are rare locations for basal cell carcinoma. We report a case of a 72-year-old woman, who presented with an asymptomatic erosive lesion on the vermilion area of the upper lip. Histopathology examination was consistent with basal cell carcinoma. We suggest that basal cell carcinoma should be included in the differential diagnosis of erosive/ulcerative lesions arising on the vermilion area of the lip. </p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 1","pages":"25-6"},"PeriodicalIF":0.0,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2015.1195","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33146702","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
Photoletter to the editor: Giant cutaneous horn associated with squamous cell carcinoma. 致编辑:与鳞状细胞癌相关的巨大皮肤角。
Journal of dermatological case reports Pub Date : 2015-03-31 DOI: 10.3315/jdcr.2015.1196
Hermann Kneitz, Stephanie Motschenbacher, Marion Wobser, Matthias Goebeler
{"title":"Photoletter to the editor: Giant cutaneous horn associated with squamous cell carcinoma.","authors":"Hermann Kneitz,&nbsp;Stephanie Motschenbacher,&nbsp;Marion Wobser,&nbsp;Matthias Goebeler","doi":"10.3315/jdcr.2015.1196","DOIUrl":"https://doi.org/10.3315/jdcr.2015.1196","url":null,"abstract":"<p><p>A 90-year-old patient presented with a large cutaneous horn (cornu cutaneum) of nine-year duration arising at her right cheek. The lesion was removed by surgery. Histology was reported as cornu cutaneum with a well-differentiated squamous cell carcinoma at its base. Cutaneous horn is morphological designation for protuberant mass of keratin that resembles the horn of an animal. Such lesions appear on sun-exposed skin areas like upper parts of the face and ears in elderly patients. Large cutaneous horns (> 1 cm) tend to be more commonly associated with squamous cell carcinoma compared to smaller cutaneous horns, particularly when present on the face. </p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 1","pages":"27-8"},"PeriodicalIF":0.0,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2015.1196","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33146703","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: 8
Symmetrical drug-related intertriginous and flexural exanthema (Baboon syndrome) associated with infliximab. 与英夫利昔单抗有关的对称性药物相关三叉神经间和挠曲性红斑(狒狒综合征)。
Journal of dermatological case reports Pub Date : 2015-03-31 DOI: 10.3315/jdcr.2015.1190
Isil Bulur, Havva Ozge Keseroglu, Zeynep Nurhan Saracoglu, Müzeyyen Gönül
{"title":"Symmetrical drug-related intertriginous and flexural exanthema (Baboon syndrome) associated with infliximab.","authors":"Isil Bulur, Havva Ozge Keseroglu, Zeynep Nurhan Saracoglu, Müzeyyen Gönül","doi":"10.3315/jdcr.2015.1190","DOIUrl":"10.3315/jdcr.2015.1190","url":null,"abstract":"<p><strong>Background: </strong>Symmetrical drug related intertriginous and flexural exanthema (SDRIFE or Baboon syndrome) is a symmetrical contact dermatitis on inverse regions of the body. The disorder is easily differentiated from other drug eruptions by its typical appearance and lack of other concurrent findings.</p><p><strong>Observation: </strong>A 50-year-old male patient presented to our clinic complaining of a rash that had developed two days after the tenth infliximab infusion for psoriasis and reoccurred after consecutive infusions. The physical examination revealed a bilateral intergluteal, inguinal, abdominal, axillary, antecubital and neck region macular erythematous rash. There were no other systemic findings. The laboratory values were within normal range. The patient was diagnosed with symmetrical drug-related intertriginous and flexural exanthema associated with infliximab treatment based on dermatological findings, histopathology and the results of the provocation test. The lesions resolved permanently after the patient was swiched from infliximab to adalimumab.</p><p><strong>Conclusion: </strong>Various cutaneous adverse events of anti-tumor necrosis factor alpha treatment have already been reported. The increased use of these agents can lead to a wider variety of drug-induced skin lesions, such as the reported Baboon syndrome.</p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"9 1","pages":"12-4"},"PeriodicalIF":0.0,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410885/pdf/jdcr-09-012.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33146698","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
Photoletter to the editor: Acquired idiopathic generalized anhidrosis. 给编辑的信:获得性特发性全身性无汗症。
Journal of dermatological case reports Pub Date : 2014-12-31 DOI: 10.3315/jdcr.2014.1187
Uwe Wollina
{"title":"Photoletter to the editor: Acquired idiopathic generalized anhidrosis.","authors":"Uwe Wollina","doi":"10.3315/jdcr.2014.1187","DOIUrl":"https://doi.org/10.3315/jdcr.2014.1187","url":null,"abstract":"<p><p>Anhidrosis is a failure in sweat production in response to physiological thermal or chemical stimuli. Acquired idiopathic generalized anhidrosis is a rare disorder without sweat gland pathology and without neurologic symptoms. Most cases have been reported from Far East. We report a case of a 58-year-old Caucasian male who suffered from heat intolerance, heat-induced cutaneous burning and failed to sweat even in sauna for five years. A skin biopsy disclosed no pathologies. He had no neurologic disorders. The diagnosis of acquired idiopathic generalized anhidrosis was confirmed and treatment with methylprednisolone initiated. This led to improvement of heat tolerance, remission of burning and partial remission of sweating. </p>","PeriodicalId":15601,"journal":{"name":"Journal of dermatological case reports","volume":"8 4","pages":"120-1"},"PeriodicalIF":0.0,"publicationDate":"2014-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3315/jdcr.2014.1187","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33327865","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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