Serbian Journal of Dermatology and Venereology最新文献_第6页

Cutaneous Polyarteritis Nodosa: Uncommon and Rare Form of Cutaneous Vasculitis 结节性皮肤多动脉炎:罕见的皮肤血管炎

Serbian Journal of Dermatology and Venereology Pub Date : 2018-06-01 DOI: 10.2478/sjdv-2018-0008

B. Lekić, D. Milčić, M. Popadić, D. Škiljević, Mirjana Milinković Srećković

引用次数: 0

Disseminated Fusarium Infections in Acute Lymphoblastic Leukemia 急性淋巴细胞白血病的播散性镰刀菌感染

Serbian Journal of Dermatology and Venereology Pub Date : 2018-06-01 DOI: 10.2478/sjdv-2018-0007

M. Covington, Juliana Gao, F. Abdulla, V. Rosić

引用次数: 1

Lichen Planus and Hepatitis C Virus Infection: A clinical Evaluation of 168 Cases 扁平苔藓与丙型肝炎病毒感染168例临床分析

Serbian Journal of Dermatology and Venereology Pub Date : 2018-06-01 DOI: 10.2478/sjdv-2018-0006

F. Rad, E. Ghaderi, B. Nikkhoo, M. Rasouli

{"title":"Lichen Planus and Hepatitis C Virus Infection: A clinical Evaluation of 168 Cases","authors":"F. Rad, E. Ghaderi, B. Nikkhoo, M. Rasouli","doi":"10.2478/sjdv-2018-0006","DOIUrl":"https://doi.org/10.2478/sjdv-2018-0006","url":null,"abstract":"Abstract Introduction. Hepatitis C virus (HCV) infection is one of the factors which can lead to a chronic liver disease and hepatocellular carcinoma. There have been several reports on the association of oral lichen planus with hepatic disorders, i.e. hepatitis C infection in particular. Considering the controversies about the association of lichen planus with HCV infection on one hand and considerable impact of hepatitis C on the occurrence of chronic liver disease on the other hand, we investigated the association between lichen planus and HCV infection in Sanandaj City. Methods. This cross sectional study included 168 patients with lichen planus, who were referred to the Dermatology Clinic of Besat Hospital between 2014 and 2016. The diagnosis of lichen planus was made by our dermatologist and HCV antibody titer was determined for every patient. Results. Mean age of the patients was 39.7±13.3 years and mean duration of the disease was 14.8 months. 107 (63.7%) patients were men. The highest frequency of lichen planus was recorded in the housewives (30.4%). In 52 (31%) patients the genital area was involved and it was the most common site. In 6 (3.6%) patients the oral mucosa was involved and it was the least common site in our study. Only 4 (2.7%) patients had family history of lichen planus. None of 168 patients included in this study was found to have HCV infection. Conclusion. In this study, we found no relationship between lichen planus and HCV infection. Yet, the exact mechanism underlying the occurrence of lichen planus in the patients with HCV infection has not been determined. Therefore more studies on this subject are recommended.","PeriodicalId":30659,"journal":{"name":"Serbian Journal of Dermatology and Venereology","volume":"10 1","pages":"37 - 41"},"PeriodicalIF":0.0,"publicationDate":"2018-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46300975","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: 1

Dermoscopy of the Month: Dermoscopy of Primary Cutaneous B-Cell Lymphoma 本月皮肤镜检查：原发性皮肤B细胞淋巴瘤的皮肤镜检查

Serbian Journal of Dermatology and Venereology Pub Date : 2018-06-01 DOI: 10.2478/sjdv-2018-0010

Zorana Kremić, A. Vojvodić, M. Dinić, N. Petrov, O. Tasić, L. K. Sekulovic

引用次数: 0

Allergic Contact Dermatitis Caused by Homemade Slime 自制黏液致过敏性接触性皮炎

Serbian Journal of Dermatology and Venereology Pub Date : 2018-06-01 DOI: 10.2478/sjdv-2018-0009

Bisera Kotevska Trifunova, Z. Demerdjieva, N. Tsankov, J. Kazandjieva

引用次数: 1

Dermoscopy Of The Month: Dermoscopic Finding of Pigment Network in Lesions of Eruptive Syringoma 本月皮肤镜检查:皮肤镜下发现的色素网络病变的爆发性注射器瘤

Serbian Journal of Dermatology and Venereology Pub Date : 2018-03-01 DOI: 10.2478/sjdv-2018-0005

Milana Ivkov Simić, Z. Gajinov, M. Matic, N. Vuckovic, S. Prcic

引用次数: 1

Furuncular Botfly Myiasis – A Case Report 麦地那龙线虫病一例报告

Serbian Journal of Dermatology and Venereology Pub Date : 2018-03-01 DOI: 10.2478/SJDV-2018-0002

Juliana Gao, V. Tesic, Vesna Petronić Rosić

引用次数: 0

Indeterminate Cell Histiocytosis – Case Report and Review of Literature 不确定细胞组织细胞增多症病例报告及文献复习

Serbian Journal of Dermatology and Venereology Pub Date : 2018-03-01 DOI: 10.2478/sjdv-2018-0004

A. Vojvodić, Z. Mijuskovic, L. Kandolf Sekulovič

{"title":"Indeterminate Cell Histiocytosis – Case Report and Review of Literature","authors":"A. Vojvodić, Z. Mijuskovic, L. Kandolf Sekulovič","doi":"10.2478/sjdv-2018-0004","DOIUrl":"https://doi.org/10.2478/sjdv-2018-0004","url":null,"abstract":"Abstract Introduction. Indeterminate cell histiocytosis is a rare proliferative disorder of indeterminate dendritic cells, reported in only 50 case reports so far. It is clinically presented as yellow, red or brown papules and nodules that appear in otherwise healthy adult individuals. Indeterminate cells are distinct dendritic cells of the skin that have ultrastructural similarities to the epidermal Langerhans cells but do not contain the characteristic Birbeck’s granules and they are also langerin-negative, unlike LCH. Indeterminate cell histiocytosis is an exceptional entity with variable clinical, histopathologic or immunohistochemical findings, sharing morphologic and immunophenotypic features with both Langerhans- and non-Langerhans cell histiocytoses. Case Report. We present a case of indeterminate histiocytosis in a 77-year-old man with 3-year history of asymptomatic, multiple reddish and brown papules and nodules over the entire body, including the oral mucosa. Skin biopsy was done, and histopathological analysis with immunohistochemistry was performed. The positive ICH staining of cells for CD68, CD1a, and S-100 enabled us to diagnose ICH in our patient. Also, BRAF V600E mutation was detected in tumor tissue. The treatment was started with methotrexate that was effective for 6 months, but due to the disease recurrence, further therapy with thalidomide was advised, without effect. Conclusion. Indeterminate histiocytosis is a rare disease, therefore no standardized treatment has been established and the treatment options are limited.","PeriodicalId":30659,"journal":{"name":"Serbian Journal of Dermatology and Venereology","volume":"10 1","pages":"18 - 24"},"PeriodicalIF":0.0,"publicationDate":"2018-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41339144","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

Possible Influence of Oxidative Stress on Development of Raynaud Phenomenon in Patients With CREST Scleroderma Syndrome 氧化应激对CREST硬皮病综合征患者雷诺现象发展的可能影响

Serbian Journal of Dermatology and Venereology Pub Date : 2018-03-01 DOI: 10.2478/sjdv-2018-0001

H. Kocic, B. Stamenkovic, D. Popović, Zorana Zlatanović, T. Markovic, D. Tiodorovic

{"title":"Possible Influence of Oxidative Stress on Development of Raynaud Phenomenon in Patients With CREST Scleroderma Syndrome","authors":"H. Kocic, B. Stamenkovic, D. Popović, Zorana Zlatanović, T. Markovic, D. Tiodorovic","doi":"10.2478/sjdv-2018-0001","DOIUrl":"https://doi.org/10.2478/sjdv-2018-0001","url":null,"abstract":"Abstract CREST syndrome represents a form of scleroderma where the progressive autoimmune reaction is mainly manifested by the main symptoms, which make this acronym: calcinosis cutis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly and teleangiectasia. Among the first affected organs is the skin followed by the excessive fibrosis manifested by the deposition of collagen in dermis. Reactive oxygen species (ROS) theory has been underlined as one of the main pathogenetic mechanisms and triggering factor in development of scleroderma. The present study was aimed at estimating the marker of lipid peroxidation products (MDA) in plasma of patients with CREST syndrome having manifested symptoms of both Raynaud syndrome and positive ANA antibodies. The lipid peroxidation (MDA) level was significantly higher in the patients who had CREST syndrome and Raynaud syndrome for less than 10 years compared to the patients suffering from Raynoud syndrome for more than 10 years (p<0.05). Both groups were found to have a significant MDA level increase (p<0.001) compared to the control healthy subjects. In conclusion, the relationship between lipid peroxidation (MDA level) and Raynaud syndrome appearance may emphasize the role of ROS produced by the ischemia-reperfusion injury as an early pathogenetic mechanism in CREST scleroderma syndrome.","PeriodicalId":30659,"journal":{"name":"Serbian Journal of Dermatology and Venereology","volume":"10 1","pages":"3 - 7"},"PeriodicalIF":0.0,"publicationDate":"2018-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44011123","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

Inherited Epidermolysis Bullosa – A Case Report of Several Family Members in Three Generations 遗传性大疱性表皮松解症——几代家族成员的一例报告

Serbian Journal of Dermatology and Venereology Pub Date : 2018-03-01 DOI: 10.2478/sjdv-2018-0003

L. Vujanović, M. Jovanović, Z. Golušin, Svetlana Kovačić Dukić, Sanja Jakovljević, Milos Nisavic

{"title":"Inherited Epidermolysis Bullosa – A Case Report of Several Family Members in Three Generations","authors":"L. Vujanović, M. Jovanović, Z. Golušin, Svetlana Kovačić Dukić, Sanja Jakovljević, Milos Nisavic","doi":"10.2478/sjdv-2018-0003","DOIUrl":"https://doi.org/10.2478/sjdv-2018-0003","url":null,"abstract":"Abstract Inherited epidermolysis bullosa (IEB) is a genodermatosis transmitted in either autosomal dominant or autosomal recessive manner. The disease is characterized by the development of blisters, erosions, scars, nail dystrophy and scalp abnormalities. Our case report has included four members of one family in three generations with manifested disease. Our 25-year-old female patient presented with a few eroded, crusted, nummular lesions localized on the dorsal plate of interphalangeal joints of fingers, elbow and knee skin, while anonychia was found on her digits. Our youngest patient (her 3.5-year-old son) presented with the lesions in the form of blisters filled with serous fluid, erosions, recent scars and atrophy. Some atrophic scars on the elbow and knee skin were found in our patient′s younger brother, aged 16. The 46-year-old mother of our female patient had nail dystrophy on her hands accompanied by the toenails absence. Pediatric geneticist created the pedigree chart which showed autosomal dominant inheritance pattern with complete expressivity and penetrance. Further diagnostics was not done because the family was not interested.","PeriodicalId":30659,"journal":{"name":"Serbian Journal of Dermatology and Venereology","volume":"10 1","pages":"12 - 17"},"PeriodicalIF":0.0,"publicationDate":"2018-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47849208","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