Pub Date : 2020-01-01DOI: 10.5336/dermato.2020-78969
I. Erturan, P. Basak, Gonca Meriç Biçici, M. Atay, Selma Korkmaz, M. Yıldırım, H. Ayvaz
{"title":"Neglected Victims of Psoriasis","authors":"I. Erturan, P. Basak, Gonca Meriç Biçici, M. Atay, Selma Korkmaz, M. Yıldırım, H. Ayvaz","doi":"10.5336/dermato.2020-78969","DOIUrl":"https://doi.org/10.5336/dermato.2020-78969","url":null,"abstract":"","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"30 1","pages":"95-101"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70756818","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}
Pub Date : 2020-01-01DOI: 10.5336/dermato.2019-65403
A. Yalçınkaya İyidal, Kadir Balaban, F. Kılıç
26 iken planus (LP); deri, muköz membran, saçlı deri ve tırnakları tutan, etiyolojisi tam olarak bilinmeyen edinsel inflamatuar bir dermatozdur. Lezyonların yeri, dağılım şekli ve morfolojisine göre çok sayıda klinik tipleri bulunmaktadır. Bunlar içerisinde lineer LP (LLP), LP’nin nadir bir varyantıdır.1-12 Bu çalışmada, sol üst ekstremitesinde yanık sonrası LLP ortaya çıkan erişkin kadın olgunun, nadir görülmesi nedeni ile sunulması amaçlanmıştır. OLGU SUNUMU
26 iken planus（LP）；皮肤、粘膜、头发和指甲是一种完全未知的皮肤病。根据激光的位置、分布和形态，有许多临床类型。在这些情况下，LP（LLP）是LP.1-12的一个罕见变量。在本研究中，它的出现是出于一个罕见的原因，即火灾后左上角出现了一名可用的女性。文件名
{"title":"Linear Lichen Planus After Burn","authors":"A. Yalçınkaya İyidal, Kadir Balaban, F. Kılıç","doi":"10.5336/dermato.2019-65403","DOIUrl":"https://doi.org/10.5336/dermato.2019-65403","url":null,"abstract":"26 iken planus (LP); deri, muköz membran, saçlı deri ve tırnakları tutan, etiyolojisi tam olarak bilinmeyen edinsel inflamatuar bir dermatozdur. Lezyonların yeri, dağılım şekli ve morfolojisine göre çok sayıda klinik tipleri bulunmaktadır. Bunlar içerisinde lineer LP (LLP), LP’nin nadir bir varyantıdır.1-12 Bu çalışmada, sol üst ekstremitesinde yanık sonrası LLP ortaya çıkan erişkin kadın olgunun, nadir görülmesi nedeni ile sunulması amaçlanmıştır. OLGU SUNUMU","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70753729","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}
Pub Date : 2020-01-01DOI: 10.5336/dermato.2019-65094
Ömer Kutlu, T. Karadeniz, Pınar Özdemir Çetinkaya, F. Kutlu, Hatǐce Ünverdǐ, H. Ekşioğlu
22 ranüloma anülare (GA); sıklıkla kendini sınırlayan, benign seyirli, dermis ve subkütan dokunun granülomatöz hastalığı olup, ilk kez 1895 yılında Colcott-Fox tarafından tanımlanmıştır.1,2 Hastalığın etiyolojisi tam olarak bilinmemektedir. GA’nın lokalize, jeneralize (dissemine), subkutanöz, perfore, papüler ve yama (interstisyel) tip olmak üzere alt grupları vardır.1,3 Yama form GA, daha çok gövde ve ekstremiteleri tutan; papül ve skuamların eşlik etmediği eritemli-viyolase, asemptomatik yamalarla karakterize bir GA alt tipidir.4 Kalsinörin inhibitörleri (takrolimus, pimekrolimus), steroidler, imikimod, dapson ve anti-tümör nekrozis faktör (TNF) ajanlar GA’nın farklı tiplerinde değişen başarı oranlarında kullanılan tedaviler arasında yer almaktadır.5 Pentoksifilin, fosfodiesteraz inhibitörü olup hücre içinde ikincil haberci olan “siklik adenozin monofosfatın (cAMP)” yükselmesine neden olPentoksifilin Tedavisine Yanıt Veren Yama Form Granüloma Anülare Olgusu
22 ranüloma anülare（GA）；1895年，Colcott-Fox被普遍诊断为视觉、皮肤和皮下组织肉芽肿。1.2这种疾病的病因尚不清楚。GA的位置分为一般型、皮下型、穿孔型、乳头型和亚马型；Phytoxyline是GA的一种亚型，其特征是存在红斑、无症状炎症，与丘疹和骨骼不匹配。4钙化抑制剂（他克莫司、吡美洛林）、类固醇、酰亚胺、dapson和抗肿瘤坏死因子（TNF）用于不同类型的GA，为什么磷酸二酯酶抑制剂会增加次级细胞的“环磷酸腺苷（cAMP）”，并建议治疗olPentoxifilin Veren Yama Form Granüloma Anülare Olgus
{"title":"A Case of Patch Form Granuloma Annulare Respond to Pentoxifylline Treatment","authors":"Ömer Kutlu, T. Karadeniz, Pınar Özdemir Çetinkaya, F. Kutlu, Hatǐce Ünverdǐ, H. Ekşioğlu","doi":"10.5336/dermato.2019-65094","DOIUrl":"https://doi.org/10.5336/dermato.2019-65094","url":null,"abstract":"22 ranüloma anülare (GA); sıklıkla kendini sınırlayan, benign seyirli, dermis ve subkütan dokunun granülomatöz hastalığı olup, ilk kez 1895 yılında Colcott-Fox tarafından tanımlanmıştır.1,2 Hastalığın etiyolojisi tam olarak bilinmemektedir. GA’nın lokalize, jeneralize (dissemine), subkutanöz, perfore, papüler ve yama (interstisyel) tip olmak üzere alt grupları vardır.1,3 Yama form GA, daha çok gövde ve ekstremiteleri tutan; papül ve skuamların eşlik etmediği eritemli-viyolase, asemptomatik yamalarla karakterize bir GA alt tipidir.4 Kalsinörin inhibitörleri (takrolimus, pimekrolimus), steroidler, imikimod, dapson ve anti-tümör nekrozis faktör (TNF) ajanlar GA’nın farklı tiplerinde değişen başarı oranlarında kullanılan tedaviler arasında yer almaktadır.5 Pentoksifilin, fosfodiesteraz inhibitörü olup hücre içinde ikincil haberci olan “siklik adenozin monofosfatın (cAMP)” yükselmesine neden olPentoksifilin Tedavisine Yanıt Veren Yama Form Granüloma Anülare Olgusu","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70753530","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}
Pub Date : 2020-01-01DOI: 10.5336/dermato.2020-78570
Z. Balik, A. Balik, Selcen S. Yuksel, N. Karaosmanoglu, H. Ekşioğlu
{"title":"Evaluation of Demographic Features, Clinical Characteristics and Quality of Life in Melasma Patients as Compared to the Control Group","authors":"Z. Balik, A. Balik, Selcen S. Yuksel, N. Karaosmanoglu, H. Ekşioğlu","doi":"10.5336/dermato.2020-78570","DOIUrl":"https://doi.org/10.5336/dermato.2020-78570","url":null,"abstract":"","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"30 1","pages":"81-87"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70756679","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}
Pub Date : 2019-01-01DOI: 10.5336/dermato.2018-63989
A. Türkay, Yuliia Pavlivna Karvatska, O. Denysenko
80 soriasis is a chronic erythematosquamous dermatitis characterized by abnormal keratinocyte hyperproliferation, resulting in thickening of the epidermis and stratum corneum, which affects genetically predisposed individuals. Factors such as family history, stress, trauma, infections, medicines, lifestyle and immune disorders are the well-known predisposing factors and also increased epidermal inflammation, proliferation, angiogenesis, hyperkeratosis, parakeratosis and keratinocytes turn-over are the hallmarks for psoriasis. Psoriasis may present with various manifestations, including generalized pustular psoriasis (GPP) which is generally severe and most commonly associated with systemic symptoms.1 Von Zumbusch pustular psoriasis (VZPP), acute generalized form of GPP is a very severe form Acute Onset of Generalize Pustular Psoriasis in a Patient with Previously Unknown HIV Infection
{"title":"Acute Onset of Generalize Pustular Psoriasis in a Patient with Previously Unknown HIV Infection","authors":"A. Türkay, Yuliia Pavlivna Karvatska, O. Denysenko","doi":"10.5336/dermato.2018-63989","DOIUrl":"https://doi.org/10.5336/dermato.2018-63989","url":null,"abstract":"80 soriasis is a chronic erythematosquamous dermatitis characterized by abnormal keratinocyte hyperproliferation, resulting in thickening of the epidermis and stratum corneum, which affects genetically predisposed individuals. Factors such as family history, stress, trauma, infections, medicines, lifestyle and immune disorders are the well-known predisposing factors and also increased epidermal inflammation, proliferation, angiogenesis, hyperkeratosis, parakeratosis and keratinocytes turn-over are the hallmarks for psoriasis. Psoriasis may present with various manifestations, including generalized pustular psoriasis (GPP) which is generally severe and most commonly associated with systemic symptoms.1 Von Zumbusch pustular psoriasis (VZPP), acute generalized form of GPP is a very severe form Acute Onset of Generalize Pustular Psoriasis in a Patient with Previously Unknown HIV Infection","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70753336","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}
Pub Date : 2019-01-01DOI: 10.5336/dermato.2019-65475
H. Yorulmaz, Dilek Keser, Melek Göçmen
{"title":"Factors Affecting Body Image and Self-Esteem in Leprosy Patients and Comparison to Healthy Individuals","authors":"H. Yorulmaz, Dilek Keser, Melek Göçmen","doi":"10.5336/dermato.2019-65475","DOIUrl":"https://doi.org/10.5336/dermato.2019-65475","url":null,"abstract":"","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70754218","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}
Pub Date : 2019-01-01DOI: 10.5336/dermato.2019-66868
N. Altunışık, S. Şener
ABS TRACT Objective: Hidradenitis suppurativa (HS) is a chronic, recurrent inflammatory skin disease. Our aim of this study is to review the demographic, clinical characteristics, treatment options of the patients who were being followed up with diagnosis of HS in our hospital during the last 9 years and to make a comparison with the data from other countries. Material and Methods: A total of 59 patients with HS diagnosed in our Dermatology Department between 2010-2019 were evaluated retrospectively. Results: Seventeen (28.8%) of 59 patients were female, 42 (71.2%) were male. The mean age at diagnosis was 31.05±1.61 (minimum / maximum: 14-60). Seventeen patients (28.8%) had stage 1, 26 patients (44.1%) had stage 2 and 16 patients (27.1%) had stage 3 disease. Axilla was the most affected area. Topical agents (topical clindamycin, antiseptic solutions) and oral antibiotics (doxycycline, ciprof loxacin, ampicillin-sulbactam, amoxicillin-clavulanic acid) were the most commonly used treatment options. Treatment resistant eight patients were treated with a biological agent adalimumab. Conclusion: In literature, there are few epidemiological studies related to HS in Turkey. The clinical, demographic and therapeutic data of 59 HS cases in our clinic were summarized. However, we believe that multi-center studies conducted with larger number of patients are needed in order to reach more comprehensive data on this subject.
{"title":"Hidradenitis Suppurativa: A 9-Year Retrospective Study from Malatya, Turkey","authors":"N. Altunışık, S. Şener","doi":"10.5336/dermato.2019-66868","DOIUrl":"https://doi.org/10.5336/dermato.2019-66868","url":null,"abstract":"ABS TRACT Objective: Hidradenitis suppurativa (HS) is a chronic, recurrent inflammatory skin disease. Our aim of this study is to review the demographic, clinical characteristics, treatment options of the patients who were being followed up with diagnosis of HS in our hospital during the last 9 years and to make a comparison with the data from other countries. Material and Methods: A total of 59 patients with HS diagnosed in our Dermatology Department between 2010-2019 were evaluated retrospectively. Results: Seventeen (28.8%) of 59 patients were female, 42 (71.2%) were male. The mean age at diagnosis was 31.05±1.61 (minimum / maximum: 14-60). Seventeen patients (28.8%) had stage 1, 26 patients (44.1%) had stage 2 and 16 patients (27.1%) had stage 3 disease. Axilla was the most affected area. Topical agents (topical clindamycin, antiseptic solutions) and oral antibiotics (doxycycline, ciprof loxacin, ampicillin-sulbactam, amoxicillin-clavulanic acid) were the most commonly used treatment options. Treatment resistant eight patients were treated with a biological agent adalimumab. Conclusion: In literature, there are few epidemiological studies related to HS in Turkey. The clinical, demographic and therapeutic data of 59 HS cases in our clinic were summarized. However, we believe that multi-center studies conducted with larger number of patients are needed in order to reach more comprehensive data on this subject.","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70754703","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}
Pub Date : 2019-01-01DOI: 10.5336/DERMATO.2017-56793
I. An
{"title":"A Case of Congenital Erythropoetic Porphyria With Common Scar on the Face and Hands: Original Image","authors":"I. An","doi":"10.5336/DERMATO.2017-56793","DOIUrl":"https://doi.org/10.5336/DERMATO.2017-56793","url":null,"abstract":"","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70750539","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}
Pub Date : 2019-01-01DOI: 10.5336/dermato.2017-56862
I. An, I. Ibiloğlu
{"title":"Dermatofibrosarcoma Protuberans","authors":"I. An, I. Ibiloğlu","doi":"10.5336/dermato.2017-56862","DOIUrl":"https://doi.org/10.5336/dermato.2017-56862","url":null,"abstract":"","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70751068","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}
Pub Date : 2019-01-01DOI: 10.5336/DERMATO.2018-61372
Z. Serdar, Ezgi Aktaş Karabay, N. Döner
nevus syndromes (ENSs). ENS is defined as epidermal nevus with multisystem involvement such as central nervous system, skeleton, and in some cases, the gastrointestinal tract.1,2 Presence of keratinocytic nevus and nevus spilus among with other abnormalities has been reported in some epidermal nevus syndromes.1-3 Here a case of 5-year-old girl with keratinocytic epidermal nevus, nevus spilus and hemi-hypertrohpy which is not consistent with any of the reported ENSs, showing a rare coexistence, is presented.
{"title":"Keratinocytic Epidermal Nevus with Nevus Spilus and Underlying Hemihypertrophy","authors":"Z. Serdar, Ezgi Aktaş Karabay, N. Döner","doi":"10.5336/DERMATO.2018-61372","DOIUrl":"https://doi.org/10.5336/DERMATO.2018-61372","url":null,"abstract":"nevus syndromes (ENSs). ENS is defined as epidermal nevus with multisystem involvement such as central nervous system, skeleton, and in some cases, the gastrointestinal tract.1,2 Presence of keratinocytic nevus and nevus spilus among with other abnormalities has been reported in some epidermal nevus syndromes.1-3 Here a case of 5-year-old girl with keratinocytic epidermal nevus, nevus spilus and hemi-hypertrohpy which is not consistent with any of the reported ENSs, showing a rare coexistence, is presented.","PeriodicalId":39132,"journal":{"name":"Turkiye Klinikleri Dermatoloji","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70752302","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}
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