Misha Rosenbach
doi : 10.1111/jdv.18511
Jean L. Bolognia
doi : 10.1111/jdv.18643
T. Turk, C. Liu, S. Straube, M. Dytoc, R. Hagtvedt, L. Dennett, A. Abba-Aji, E. Fujiwara
doi : 10.1111/jdv.18478
T. Ju, A. Vander Does, G. Ingrasci, S.A. Norton, G. Yosipovitch
doi : 10.1111/jdv.18408
D.M.W. Balak, L.M. Perez-Chada, L.N. Guo, C Mita, A.W. Armstrong, S.J. Bell, G.C. Gondo, W. Liao, J.F. Merola
doi : 10.1111/jdv.18477
Y.-C. Wang, Y.-H. Lin, S.-H. Ma, Y.-T. Chang, C.-C. Chen
doi : 10.1111/jdv.18407
M. Augustin, L. Misery, L. von Kobyletzski, S. Mealing, M. Redding, C.C. Chuang, R. Massey, M. Cawkwell, G. Bego Le-Bagousse, L. Haddy, R. Rout
doi : 10.1111/jdv.18481
Atopic dermatitis (AD) is a chronic inflammatory disease, driven by type 2 inflammation. The condition manifests as moderate-to-severe disease in approximately 20% of adults with AD across Europe and is associated with a substantial burden on patients, society and healthcare systems. However, systematic assessments capturing the totality of disease burden associated with moderate-to-severe AD are limited; therefore, the overall impacts of the disease may be underestimated.
J. Zoutendijk, S. Koljenovic, M. Wakkee, A.L. Mooyaart, T. Nijsten, R.R. van den Bos
doi : 10.1111/jdv.18346
Lentigo maligna (LM) based on biopsy material might be lentigo maligna melanoma (LMM) after excision.
Y. Luo, Y. Rao, X. Gu, P. Chai, Y. Yang, J. Lin, X. Xu, R. Jia, S. Xu
doi : 10.1111/jdv.18454
Our previous research revealed the relative local aggressiveness of eyelid and periocular squamous cell carcinoma (EPSCC), but its distinct genetic characteristics involved remain unknown.
G.G. Malouf, X. Lu, R. Mouawad, J.-P. Spano, P. Grange, F. Yan, S. Aractingi, X. Su, N. Dupin
doi : 10.1111/jdv.18463
Kaposi sarcoma (KS) is a rare skin tumour caused by herpesvirus 8 infection and characterized by either indolence or an aggressive course necessitating systemic therapies. The genetic basis of this difference remains unknown.
L.G. Campana, P. Quaglino, F. de Terlizzi, M. Mascherini, M. Brizio, R. Spina, G. Bertino, C. Kunte, J. Odili, P. Matteucci, A. MacKenzie Ross, H. Schepler, J.A.P. Clover, E. Kis, InspECT Melanoma and QoL Working Groups
doi : 10.1111/jdv.18456
Electrochemotherapy (ECT) effectively controls skin metastases from cutaneous melanoma.
A. Antúnez-Lay, S. Podlipnik, C. Carrera, M. Potrony, G. Tell-MartÃ, C. Badenas, J.A. Puig-Butille, N. Espinosa, S. Puig, J. Malvehy
doi : 10.1111/jdv.18467
Around 0.5% of cutaneous melanoma (CM) patients will present with synchronous melanomas when first seen. Moreover, 26–40% of patients with multiple primary melanomas present with synchronous lesions.
E.H.A. Stahlie, A.C.J. van Akkooi, E. Plasmeijer
doi : 10.1111/jdv.18479
Currently, the response of cutaneous melanoma metastases (CMM) to treatment with Talimogene Laherparepvec (T-VEC) is evaluated by clinical examination, macroscopic lesion photography and 3-monthly PET-CT scans. When a complete response (CR) is suspected, biopsies are taken for histopathological confirmation.
O. Reiter, N.R. Kurtansky, S.T. Musthaq, S. Dusza, A.C. Halpern, M.A. Marchetti, A.A. Marghoob, A. Scope, V. Rotemberg
doi : 10.1111/jdv.18470
There is little understanding regarding the long-term natural history of melanocytic nevi among adults.
N. Macagno, L. Mastorino, M. Rubatto, G. Avallone, M. Merli, A. Agostini, P. Fava, S. Ribero, P. Quaglino
doi : 10.1111/jdv.18469
Primary cutaneous lymphomas (PCL) are rare diseases, but the indolent course makes their prevalence high. Although there are many treatment options, no hierarchy is recommended.
K. Reich, K.B. Gordon, B. Strober, R.G. Langley, M. Miller, Y.-W. Yang, Y.-K. Shen, Y. You, Y. Zhu, P. Foley, A. Blauvelt
doi : 10.1111/jdv.18474
Psoriasis is a chronic immune-mediated inflammatory skin disease that often leads to a diminished quality of life. Goals of treating patients with psoriasis have shifted with more focus on achieving near or complete clearance of the skin. Guselkumab, a fully human monoclonal antibody targeting interleukin-23, is effective in treating moderate-to-severe psoriasis.
C. Li, X. Li, J. Lin, Y. Cui, H. Shang
doi : 10.1111/jdv.18459
Epidemiological studies have suggested psoriasis was associated with an increased risk of Parkinson's disease (PD). However, whether psoriasis has an effect on PD progression is not explored yet.
Z. Ali, A. Egeberg, J.P. Thyssen, C.S. Ulrik, S.F. Thomsen
doi : 10.1111/jdv.18415
Atopic dermatitis (AD) and asthma often co-occur in the same patient, and healthcare utilization is related to disease severity of these diseases.
J.C. Ho, H.J. Wen, C.W. Sun, S.F. Tsai, P.H. Su, C.L. Chang, H.L. Sun, S.L. Wang, C.H. Lee
doi : 10.1111/jdv.18425
Nickel, the fifth most common element on Earth, is the leading inducer of contact allergies in humans, with potent immunological effects. Nickel-induced contact allergies predominantly affect females. Maternal exposure to nickel has been associated with several developmental abnormalities. However, how a maternal nickel exposure affects the development of atopic diathesis and immune abnormalities in children has never been addressed.
A. Lasek, N. Bellon, S. Mallet, E. Puzenat, A.C. Bursztejn, C. Abasq, J. Mazereeuw-Hautier, C. Chiaverini, T. Hubiche, N. Raison Peyron, A. Du Thanh, S. Barbarot, H. Aubert, Z. Reguiai, C. Droitcourt, C. Fievet, A. Bellissen, M. Bachelerie, A. Nosbaum, A. Leymarie, P. Armingaud, M. Masson Regnault, E. Mahé, Research Group of the Société Française de Dermatologie Pédiatrique (GR SFDP), Research Group of eczéma atopique (GREAT)
doi : 10.1111/jdv.18450
Dupilumab is the first biotherapy available for the treatment of moderate-to-severe childhood atopic dermatitis (AD).
K. Piontek, T. Ittermann, U. Wiesmann, A. Arnold, H.J. Grabe, H. Völzke, C. Apfelbacher
doi : 10.1111/jdv.18480
Childhood maltreatment (CM) is related to poor physical and mental health outcomes in adults. Knowledge on the impact of CM on skin diseases is limited, and no study has previously addressed the association of CM with atopic dermatitis (AD) in adult age.
A. Weill, V. Descamps, F. Chasset, T. Mahévas, I. Bourgault-Villada, P. Wolkenstein, S. Chollet-Martin, S. Ingen-Housz-Oro, S. Grootenboer-Mignot
doi : 10.1111/jdv.18259
Erythema multiforme (EM) is a muco-cutaneous inflammatory disease mainly triggered by herpes simplex virus (HSV) recurrences. Association of EM and circulating auto-antibodies against plakins (anti-PLK-Abs [EM-PLK+]) has been reported. However, little is known about this subset of EM.
A. Bangalore Kumar, J.S. Lehman, E.F. Johnson, H.M. Cantwell, J.C. Sartori Valinotti, O. Sokumbi, M.D.P. Davis, D.A. Wetter
doi : 10.1111/jdv.18203
Reactive granulomatous dermatitis (RGD) is an umbrella term used to describe interstitial granulomatous dermatitis (IGD), palisaded neutrophilic and granulomatous dermatitis (PNGD), and interstitial granulomatous drug eruption (IGDR).
M. Szczepanek, A. Frątczak, K. Polak, A. Lis-Święty
doi : 10.1111/jdv.18483
Infrared thermography (IRT) is a useful method to detect activity/inflammation in localized scleroderma (LoS); however, inactive skin lesions with a severe degree of dermal and subcutaneous atrophy may show false-positive results. Narrow-band reflectance spectrophotometry (NBRS) is an objective, non-invasive technique of measuring erythema and hyperpigmentation severity, yet has not been extensively studied in LoS.
S. Utz, V.G.A. Suter, S. Cazzaniga, L. Borradori, L. Feldmeyer
doi : 10.1111/jdv.18457
Topical tacrolimus has been shown to be beneficial in the treatment of oral lichen planus (OLP). However, long-term effects and its optimal application protocol with gradual reduction have not been studied. Accordingly, we analysed the clinical response of OLP to tacrolimus in our daily clinical practice with a focus on the optimal long-term therapeutic scheme.
M.V. Quaresma, L.S. Azevedo, N.V. Pereira, M.G. Saldanha, E. David-Neto, M.N. Sotto
doi : 10.1111/jdv.18430
Renal transplant recipients (RTRs) are at increased risk of developing skin cancer; however, the role of immunosuppression is not yet fully understood. In this study, we evaluated the immunohistochemical changes in the skin of RTRs under three different immunosuppression regimens: mTOR inhibitors (mTORi), sirolimus or everolimus, mycophenolic acid (MPA) precursors such as mycophenolate sodium or mofetil, or azathioprine (AZA).
F. Bardazzi, F. Filippi, M.A. Chessa, M. Iommi, C. Loi, A. Campanati, G. Rizzetto, C. Tagliati, L. Atzori, S. Muratori, G. Genovese, P. Gisondi, D. Schena, R. Balestri, G. Rech, C. Feliciani, C. Lasagni, L. Bigi, C. De Simone, G. Di Zenzo, F. Moro, A. Borghi, V. Di Lernia, G. D'Arrigo, G. Tripepi, M. Gori, A. Pitino
doi : 10.1111/jdv.18441
Bullous pemphigoid is the most common autoimmune bullous dermatosis. In recent years several studies have tried to identify the main factors of the disease related with an increased risk of death. The aim of this multicenter Italian study was to assess the risk score of death considering epidemiologic, clinical, immunological, and therapeutic factors in a cohort of patients affected by bullous pemphigoid and try to identify the cumulative survival up to 120 months.
S. Lehrer, P.H. Rheinstein
doi : 10.1111/jdv.18413
Analyses of the hereditary propensity to dermatophytosis have revealed several proven genetic relationships. They include CARD9 deficiency, HLA-DR4 and HLA-DR8 type and genes encoding interleukin-22, defensin 2 and 4, and genetic defects in dectin-1, which increased the prevalence of dermatophytosis in families and were involved in the inheritance of susceptibility in their members.
V.G. Frings, L. Jopp, M. Srivastava, D. Presser, M. Goebeler, M. Schmidt
doi : 10.1111/jdv.18465
The pathogenetic factors generating the innate immune signal necessary for T-cell activation, initiation and chronification of Hidradenitis suppurativa (HS, also known as Acne inversa) are still poorly understood. Emerging evidence suggests that a defective keratinocyte function critically contributes to HS disease development and progression.
B.M. Clanner-Engelshofen, L.M. Ständer, T. Steegmüller, T. Kämmerer, L.H. Frommherz, P.-C. Stadler, A. Gürtler, M. Reinholz
doi : 10.1111/jdv.18468
Demodex spp. mites are the most complex resident of the human skin microbiome. Although they are considered commensals, they can be pathophysiologically relevant in inflammatory skin diseases like rosacea. Until now, there is no culture system available for these mites except for using live vertebrate hosts.
M.A.S. Henning, R. Reguant, I.F. Jørgensen, R.K. Andersen, K.S. Ibler, O.B. Pedersen, G.B.E. Jemec, S. Brunak
doi : 10.1111/jdv.18351
Research on hyperhidrosis comorbidities has documented the co-occurrence of diseases but has not provided information about temporal disease associations.
T. Okamoto, M. Kawai, Y. Ogawa, S. Shimada, T. Kawamura
doi : 10.1111/jdv.18354
PASI score is globally used to assess disease activity of psoriasis. However, it is relatively complicated and time-consuming, and the score will vary due to the inconsistent subjectivity between dermatologists. Therefore, an AI system capable of assessing psoriasis severity will be useful.
S. Krammer, Y. Li, N. Jakob, A.S. Boehm, H. Wolff, P. Tang, T. Lasser, L.E. French, D. Hartmann
doi : 10.1111/jdv.18460
Artificial intelligence (AI) techniques are promising in early diagnosis of skin diseases. However, a precondition for their success is the access to large-scaled annotated data. Until now, obtaining this data has only been feasible with very high personnel and financial resources.
L. Amruthalingam, P. Gottfrois, A. Gonzalez Jimenez, B. Gökduman, M. Kunz, T. Koller, DERMANATOMY Consortium, M. Pouly, A.A. Navarini
doi : 10.1111/jdv.18476
The exact location of skin lesions is key in clinical dermatology. On one hand, it supports differential diagnosis (DD) since most skin conditions have specific predilection sites. On the other hand, location matters for dermatosurgical interventions. In practice, lesion evaluation is not well standardized and anatomical descriptions vary or lack altogether. Automated determination of anatomical location could benefit both situations.
J. Lu, Y. Liu, Y. Sun
doi : 10.1111/jdv.18379
N. A. Alelq, M. E. Kubieniec, L. E French, J. C. Prinz
doi : 10.1111/jdv.18388
J. Franceschi, A.S. Darrigade, P. Sanchez-Pena, V. Legrain-Lifermann, B. Milpied
doi : 10.1111/jdv.18389
A. Bhandari, Shilpa, S. Gupta, S. Dogra, T. Narang
doi : 10.1111/jdv.18390
V. Piccolo, A. Bassi, C. Mazzatenta, T. Russo, G. Argenziano, M. Cutrone, Markus ES Danielsson Darlington, R. Grimalt
doi : 10.1111/jdv.18392
F. Falcinelli, A. Lamberti, C. Cota, P. Rubegni, E. Cinotti
doi : 10.1111/jdv.18398
F. Drago, G. Ciccarese, A. Guadagno, A. Parodi
doi : 10.1111/jdv.18418
A. Baba, Y. Maki, T. Kanekura, H. Tsubouchi
doi : 10.1111/jdv.18420
P. Burgos-Blasco, M. González-Cañete, A. Melian-Olivera, D. Vega-Diez, I. Aldanondo-Fernandez de la Mora, B. Perez-Garcia, D. De Perosanz-Lobo
doi : 10.1111/jdv.18434
R. Sommer, L. Westphal, U. Mrowietz, S. Gerdes, M. Augustin
doi : 10.1111/jdv.18396
D. Wu, B.S. Daniel, A.J.X. Lai, N. Wong, D.K.A. Lim, D.F. Murrell, B.X.H. Lim, J.S. Mehta, C.H.L. Lim
doi : 10.1111/jdv.18397
J.R. Terrell, L. Qi, H. Wu, J. Joo, M.A. Fung, A.R. Vaughn, M. Kiuru
doi : 10.1111/jdv.18399
N. da Silva, M. Augustin, C. Hilbring, C.C. von Stülpnagel, R. Sommer
doi : 10.1111/jdv.18400
K. Kosaka, Y. Endo, S. Toki, A. Oka, A. Uehara, O. Ishikawa, H. Koga, N. Ishii, S.-i. Motegi
doi : 10.1111/jdv.18401
N. Theodosakis, J. Yoon, K. Young, E. Getachew, A. Mostaghimi, Y. Semenov
doi : 10.1111/jdv.18402
J.P. Pham, K. Glasenhardt, A. Garg, J.W. Frew
doi : 10.1111/jdv.18403
A. Pulido-Perez, M. Bergon-Sendin, L. Barchino-Ortiz, R. Suarez-Fernandez, P. Muñoz, E. Bouza, Skin&Sepsis Group
doi : 10.1111/jdv.18404
K. Oya, Y. Nakamura, K. Iwamoto, T. Kimura, H. Negoro, H. Nishiyama, Y. Fujisawa
doi : 10.1111/jdv.18406
J. Gherardini, K.E. Rivas, J. Chéret, N. Strbo, R. Paus
doi : 10.1111/jdv.18423
M. Alpalhão, J.V. Frade, D. Sousa, J. PatrocÃnio, P.M. Garrido, C. Correia, C. Brazão, D. Mancha, M.J. Borrego, P. Filipe
doi : 10.1111/jdv.18424
F. Abeck, J. Kött, I. Wiesenhütter, T. Hiebenthal, I. Hansen, S.W. Schneider, J. von Büren
doi : 10.1111/jdv.18426
L. Mastorino, V.L. Cantafio Duò, C. Vecco, F. Gelato, S. Giordano, G. Roccuzzo, G. Cavaliere, G. Avallone, M. Ortoncelli, S. Ribero, P. Quaglino
doi : 10.1111/jdv.18427
S. Chavez-Alvarez, M. Herz-Ruelas, M. Gomez-Flores, M.G. Sanchez-Muñoz, J. Ocampo-Candiani
doi : 10.1111/jdv.18428
Y. Sun, T.-T. Yang, T.H. Huang, Y.-C. Su, C.-C.E. Lan, S.Y. Lin
doi : 10.1111/jdv.18431
G. Peng, S. Tsukamoto, R. Kishi, M. Tominaga, K. Takamori, K. Okumura, H. Ogawa, S. Ikeda, F. Niyonsaba
doi : 10.1111/jdv.18433
D. Rigopoulos, N. Rompoti, A. Tsiogka, S.R. Lipner
doi : 10.1111/jdv.18435
M. Sławińska, M. Sokołowska-Wojdyło, M. Sobjanek, W. Biernat, R.J. Nowicki, R. Happle
doi : 10.1111/jdv.18438
Y. Lim, S.-J. Kang, B.K. Cho, H.J. Kim, J.-H. Mun, M.R. Roh, N. Gulati, H.J. Yang, J.H. Moon, C.H. Won, C.-G. Park
doi : 10.1111/jdv.18443
E. Mahé, K. Ezzedine, C. Thenie, S. Merhand, C. Taïeb
doi : 10.1111/jdv.18444
M. Kabbani, G. Mboyo Mpita, Farida Benhadou
doi : 10.1111/jdv.18445
D.O. Croitoru, J.D. Lu, S.C. Ling, P. Wales, R. Levy
doi : 10.1111/jdv.18446
S.L. Geng, T. Gong, C. Ji, H.H. Su
doi : 10.1111/jdv.18447
K. Bridgewater, A. Levene, A. Lun, D. Keith
doi : 10.1111/jdv.18448
S. Wada, T. Komori, C.S. de Jesus, T. Nomura, T. Komura, S. Yonekura, R. Shibuya, E. Adachi, Y. Sakurai, M. Ishikawa, S. Usui, N. Kambe, K. Kabashima
doi : 10.1111/jdv.18449
A. Wilson, T.L. Cowan, D. Marucci, D.F. Murrell
doi : 10.1111/jdv.18451
G. Cortonesi, P. Rubegni, L. Tognetti, C. Habougit, J. Planello, J.L. Perrot, E. Cinotti
doi : 10.1111/jdv.18452
J. Pünchera, D. Salomon, O.N. Tshikung, M. Becker, L. Toutous-Trellu
doi : 10.1111/jdv.18455
S. Zahid, A. Saussine, A. Calugareanu, M. Jachiet, M.-D. Vignon-Pennamen, M. Rybojad, M. Bagot, J.-D. Bouaziz, T. Mahévas
doi : 10.1111/jdv.18482
آیا می خواهید مدیلیب را به صفحه اصلی خود اضافه کنید؟