Thematische Bibliographien / Skin associated / Zeitschriftenartikel
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Zeitschriftenartikel zum Thema „Skin associated“

Autor: Grafiati
Veröffentlicht am 25. Juni 2021
Zuletzt aktualisiert am 5. Februar 2022

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1

Liu, Jesse, und Jesse Veenstra. „COVID-19 Associated Onychomadesis“. SKIN The Journal of Cutaneous Medicine 5, Nr. 3 (17.05.2021): 286–88. http://dx.doi.org/10.25251/skin.5.3.11.

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2

Goldberger, David, Kristin McCloskey, Ryan Surmaitis und Dilan Patel. „Skin necrosis associated with cocaine “skin popping”“. Visual Journal of Emergency Medicine 6 (Januar 2017): 41–42. http://dx.doi.org/10.1016/j.visj.2016.08.007.

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3

Zambito, Jeanette R., Pooja R. Shah, Glynis A. Scott, Andrew Evans und Lisa A. Beck. „CVID-associated Granulomatous Dermatosis Resembling Sarcoidosis“. SKIN The Journal of Cutaneous Medicine 3, Nr. 4 (08.07.2019): 253–57. http://dx.doi.org/10.25251/skin.3.4.4.

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Common variable immunodeficiency (CVID) is a disorder of the adaptive immune system predominantly characterized by hypogammaglobulinemia and variable T-cell abnormalities. Patients classically present with recurrent sinopulmonary infections, but interstitial lung disease, autoimmunity, and lymphoproliferative disorders are also common. Approximately 10% of CVID patients are reported to have noncaseating granulomatous disease that is indistinguishable from sarcoidosis on pathology; it most commonly affects the lungs, lymph nodes, and liver.We present the case of a 75-year-old male with known CVID who presented with granulomatous dermatosis on the trunk and extremities in the setting of progressive cognitive impairment, new-onset cough with ground glass opacities on chest computed tomography in the setting of stable mediastinal lymphadenopathy, and the presence of granulomas on prior bone marrow biopsy, initially suggesting the diagnosis of sarcoidosis. Though clinically and histologically similar, it is important to make the distinction between CVID-associated granulomatous disease and sarcoidosis in order to select appropriate treatment.
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Millichap, J. Gordon. „Lamotrigine-Associated Skin Rash“. Pediatric Neurology Briefs 13, Nr. 8 (01.08.1999): 61. http://dx.doi.org/10.15844/pedneurbriefs-13-8-8.

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5

Lee, Jeong Deuk. „Cold-associated skin disorders“. Journal of the Korean Medical Association 62, Nr. 4 (2019): 193. http://dx.doi.org/10.5124/jkma.2019.62.4.193.

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6

Alessi, Elvio. „HIV-associated skin conditions“. Current Opinion in Infectious Diseases 6, Nr. 5 (Oktober 1993): 668–77. http://dx.doi.org/10.1097/00001432-199310000-00009.

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7

Gray, Mikel, Joyce M. Black, Mona M. Baharestani, Donna Z. Bliss, Janice C. Colwell, Margaret Goldberg, Karen L. Kennedy-Evans, Susan Logan und Catherine R. Ratliff. „Moisture-Associated Skin Damage“. Journal of Wound, Ostomy and Continence Nursing 38, Nr. 3 (2011): 233–41. http://dx.doi.org/10.1097/won.0b013e318215f798.

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8

Blaise, Géraldine, Arjen F. Nikkels, Trihn Hermanns-Lê, Nazli Nikkels-Tassoudji und Gérald E. Piérard. „Corynebacterium-associated skin infections“. International Journal of Dermatology 47, Nr. 9 (September 2008): 884–90. http://dx.doi.org/10.1111/j.1365-4632.2008.03773.x.

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9

McCoy, Christopher M. „Leflunomide-Associated Skin Ulceration“. Annals of Pharmacotherapy 36, Nr. 6 (Juni 2002): 1009–11. http://dx.doi.org/10.1345/aph.1a347.

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OBJECTIVE: To report a case of skin ulceration as a result of treatment with leflunomide for rheumatoid arthritis. CASE SUMMARY: A 78-year-old white woman developed bilateral leg ulcers after 6 months of treatment with leflunomide for rheumatoid arthritis. A history of leg ulcers after methotrexate therapy had been documented. Serologic and diagnostic tests did not support an alternate process. Other medications prescribed were oral ethinyl estradiol 0.05 mg/d, felodipine 5 mg/d, and paroxetine 20 mg/d, for which no documented correlation with the skin breakdown could be made. DISCUSSION: This is the first published case describing a possible relationship between the use of the immunosuppressant agent leflunomide and skin ulceration. CONCLUSIONS: Skin breakdown and ulceration is a recognized adverse effect of drugs with immunosuppressant activity such as methotrexate. Leflunomide, a newer agent prescribed in the treatment of rheumatoid arthritis, may now be listed among the drugs in this category associated with this adverse drug effect.
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10

Akgül, Baki, James C. Cooke und Alan Storey. „HPV-associated skin disease“. Journal of Pathology 208, Nr. 2 (2005): 165–75. http://dx.doi.org/10.1002/path.1893.

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11

Fowlie, J., P. D. Stanton und J. R. Anderson. „Heparin-associated skin necrosis.“ Postgraduate Medical Journal 66, Nr. 777 (01.07.1990): 573–75. http://dx.doi.org/10.1136/pgmj.66.777.573.

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12

Dreizen, Samuel, Kenneth B. McCredie, Michael J. Keating, Borje S. Andersson und Jay R. Schachner. „Leukemia-associated skin infiltrates“. Postgraduate Medicine 85, Nr. 2 (Februar 1989): 45–53. http://dx.doi.org/10.1080/00325481.1989.11700567.

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13

Morris-Jones, Rachael, und Stephen Morris-Jones. „Travel-Associated Skin Disease“. Infectious Disease Clinics of North America 26, Nr. 3 (September 2012): 675–89. http://dx.doi.org/10.1016/j.idc.2012.05.010.

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14

Orlowski, Timothy Jay, Hoyt Harris Reynolds und Boni Elizabeth Elewski. „Lichen Planopilaris Associated with Spray-on Sunscreen“. SKIN The Journal of Cutaneous Medicine 4, Nr. 1 (28.01.2020): 62–63. http://dx.doi.org/10.25251/skin.4.1.8.

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This case report further supports a possible association between spray-on sunscreen use and lichen planopilaris (LPP). In order to lead to more accurate diagnosis and treatment, dermatologists should elucidate specific sunscreen use in patients presenting with symptoms consistent with LPP.
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15

Owen, Joshua L., Cory Kosche und Jennifer N. Choi. „Verrucous Keratoses Associated with Checkpoint Inhibitor Immunotherapy“. SKIN The Journal of Cutaneous Medicine 4, Nr. 1 (28.01.2020): 64–67. http://dx.doi.org/10.25251/skin.4.1.9.

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Introduction:Checkpoint inhibitor immunotherapy is associated with numerous adverse events, including eruptive keratoacanthomas and squamous cell carcinomas. However, no cases of immunotherapy-associated verrucous keratoses (VKs) have been reported. VKs are proliferative lesions generally considered benign, although they have been suggested to represent premalignant lesions.Cases:We present the first case series of three patients with immunotherapy-associated VKs. The patients were receiving nivolumab for renal cell carcinoma, combination ipilimumab/nivolumab for non-small cell lung carcinoma, and pembrolizumab for malignant melanoma. The VKs appeared 3-7 months after initiation of immunotherapy. Lesions were treated with shave removal or cryosurgery without recurrence. This report adds to the spectrum of cutaneous squamoproliferative lesions induced by checkpoint inhibitor immunotherapy.
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Collier, Mark, und Debbie Simon. „Protecting vulnerable skin from moisture-associated skin damage“. British Journal of Nursing 25, Nr. 20 (10.11.2016): S26—S32. http://dx.doi.org/10.12968/bjon.2016.25.20.s26.

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17

Wei, Angela, Sheena Hill und Dennis Vidmar. „Case of Hydroxyurea-Associated Cutaneous Only Polyarteritis Nodosa“. SKIN The Journal of Cutaneous Medicine 5, Nr. 4 (09.07.2021): 410–13. http://dx.doi.org/10.25251/skin.5.4.12.

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Hydroxyurea is a common antineoplastic agent used for the treatment of several cancers and myeloproliferative conditions, such as chronic myelogenous leukemia and polycythemia vera. Long-term use has been associated with several adverse cutaneous reactions, including skin eruptions, skin ulcers, xerosis, and hyperpigmentation, amongst others. We report a patient who presented with tender, indurated, erythematous nodules in his legs and thighs who had been taking hydroxyurea for 8 years to treat polycythemia vera. Biopsy revealed medium-sized arteries with intramural edema and intramural neutrophils and eosinophils. Histopathology and clinical features were highly suggestive of cutaneous polyarteritis nodosa (CPAN). Discontinuation of hydroxyurea resulted in full resolution of his lesions.
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18

Zhang, Jianqin, Fuzhu Liu, Junting Cao und Xiaolin Liu. „Skin Transcriptome Profiles Associated with Skin Color in Chickens“. PLOS ONE 10, Nr. 6 (01.06.2015): e0127301. http://dx.doi.org/10.1371/journal.pone.0127301.

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19

Yosipovitch, Gil, und Alan B. Fleischer. „Itch Associated with Skin Disease“. American Journal of Clinical Dermatology 4, Nr. 9 (2003): 617–22. http://dx.doi.org/10.2165/00128071-200304090-00004.

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20

Rongisch, Robert, Enno Schmidt, Nicolai Deresz, Katharina Deresz, Helmut Schöfer, Knut Schäkel, Thilo Jakob et al. „Travel‐associated infectious skin diseases“. JDDG: Journal der Deutschen Dermatologischen Gesellschaft 18, Nr. 7 (28.04.2020): 730–33. http://dx.doi.org/10.1111/ddg.14094.

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21

Gazyakan, Emre, Christoph Hirche, Holger Engel, Ulrich Kneser und Amir K. Bigdeli. „Skin Burn Associated With Photochemotherapy“. Annals of Plastic Surgery 80, Nr. 4 (April 2018): 344–46. http://dx.doi.org/10.1097/sap.0000000000001333.

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22

Booth, Linda V., Amanda L. Collins, J. A. Lowes und M. Radford. „Skin rash associated withCandida guilliermondii“. Medical and Pediatric Oncology 16, Nr. 4 (1988): 295–96. http://dx.doi.org/10.1002/mpo.2950160417.

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23

Alcázar Lázaro, Victoria, und Antonio Aguilar Martínez. „Skin changes associated to hypothyroidism“. Endocrinología y Nutrición (English Edition) 60, Nr. 6 (Juni 2013): 345–47. http://dx.doi.org/10.1016/j.endoen.2012.08.014.

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24

Rahnama-Moghadam, Sahand, und Hans L. Tillmann. „DILI Associated with Skin Reactions“. Current Hepatology Reports 17, Nr. 3 (12.07.2018): 225–34. http://dx.doi.org/10.1007/s11901-018-0414-x.

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25

Buechler, Connor R., Elena Kurland und Jesse Veenstra. „Extensive Tinea Associated with Tofacitinib Therapy Masquerading as New-Onset SCLE“. SKIN The Journal of Cutaneous Medicine 4, Nr. 5 (26.08.2020): 456–59. http://dx.doi.org/10.25251/skin.4.5.13.

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Rheumatoid arthritis is a chronic autoimmune disorder that often requires treatment with immunomodulatory agents, however, such interventions are not without risk of opportunistic infection. Monitoring for such conditions is critical, whereas recognition and treatment can prove challenging at times, as they may manifest with an atypical presentation or masquerade as another condition entirely. We present here a case of extensive tinea corporis with concomitant tinea capitis masquerading as new-onset connective tissue disorder in a patient being treated for rheumatoid arthritis with the Janus kinase inhibitor tofacitinib.
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26

Ghani, Hira, Stefanie Cubelli, Raphia Rahman und Alexandra Chervonsky. „Molecular Pathogenesis and Complications Associated with Keratosis Follicularis: A Clinical Review“. SKIN The Journal of Cutaneous Medicine 5, Nr. 4 (09.07.2021): 347–52. http://dx.doi.org/10.25251/skin.5.4.2.

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Keratosis follicularis or Darier's disease (DD) is a rare autosomal dominant disorder characterized by the appearance of multiple scaly papules affecting seborrheic areas. It is a multisystem disorder that occurs in the first or second decade of life, and extends beyond cutaneous involvement. It has been reported to be associated with various basal cell carcinoma (BCC) and other skin cancers, nail changes, ocular/mucosal manifestations and neuropsychiatric disorders. Additionally, individuals with DD have a greater risk of being diagnosed with Type 1 Diabetes Mellitus as well as disease-specific risk of heart failure. The goal of this review is to explore the molecular pathogenesis of keratosis follicularis, and to investigate the extent and severity of various complications associated with this condition. Furthermore, dermatologic practice recommendations will be reviewed for the management of DD.
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27

Zulkowski, Karen. „Understanding Moisture-Associated Skin Damage, Medical Adhesive-Related Skin Injuries, and Skin Tears“. Advances in Skin & Wound Care 30, Nr. 8 (August 2017): 372–81. http://dx.doi.org/10.1097/01.asw.0000521048.64537.6e.

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28

Glinos, George D., Irena Pastar, Marjana Tomic-Canic und Rivka C. Stone. „Mislocalization of Adherens Junction- Associated Proteins in a Patient with Darier Disease“. SKIN The Journal of Cutaneous Medicine 2, Nr. 3 (30.04.2018): 184–201. http://dx.doi.org/10.25251/skin.2.3.9.

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Darier disease (DD) is an autosomal dominant keratinizing genodermatosis that manifests clinically with red-brown pruritic papules in a seborrheic distribution often in association with palmoplantar pits and dystrophic nail changes. It is caused by mutation in ATP2A2 which encodes a sarco/endoplasmic reticulum calcium ATPase isoform 2 (SERCA2) pump that regulates calcium flux. Consequent alteration of intracellular calcium homeostasis is thought to impair trafficking of cellular adhesion proteins and to lead to aberrant keratinocyte differentiation, contributing to the characteristic histopathologic features of acantholysis and dyskeratosis in DD, though the precise mechanisms are incompletely understood. Previous studies have identified defective localization of desmosomal attachment proteins in skin biopsies and cultured keratinocytes from DD patients, but reports of effects on adherens junction proteins (including calcium-dependent E-cadherin) are conflicting. Here we describe a case of DD presenting with characteristic clinical and histologic features in which we performed immunofluorescence staining of four adherens junction-associated proteins (E-cadherin, α-catenin, β-catenin, and vinculin). In lesional (acantholytic) DD skin, we identified loss of distinctive bright membranous staining that was present at the periphery of keratinocytes throughout the epidermis in the healthy skin of a matched donor. Perilesional (non-acantholytic) portions of DD skin partially recapitulated the normal phenotype. Our findings support a role for SERCA2 dysfunction in impaired assembly of adherens junctions, which together with defective desmosomes contribute to acantholysis in DD.
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Bowers, Nate, Wasim Haidari, Jennifer Su, Jesus Cardenas-de la Garza, Steve Feldman und Joseph Jorizzo. „Characterization of Clinical Outcomes in Patients with Cutis Marmorata Telangiectatica Congenita“. SKIN The Journal of Cutaneous Medicine 5, Nr. 4 (09.07.2021): 399–402. http://dx.doi.org/10.25251/skin.5.4.9.

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Cutis marmorata telangiectatica congenita (CMTC) is an uncommon, congenital, cutaneous vascular disease with an unknown pathogenesis. Although considered as a benign condition, anomalies such as body asymmetry are frequently associated. Herein we present a series of patient with diagnosis of CMTC with a focus on clinical outcomes. In our series, limb length abnormalities were the most common associate anomaly, occurring in 24% of the subjects, similar to other series with rates of 33% and 27% but higher than the general population (6.7%). Importantly, dermatologist should be aware of the frequently associated anomalies in CMTC, such as leg length discrepancy, which may have serious consequences if not recognized and treated.
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Curcio, Daniel. „Resistant pathogen-associated skin and skin-structure infections: antibiotic options“. Expert Review of Anti-infective Therapy 8, Nr. 9 (September 2010): 1019–36. http://dx.doi.org/10.1586/eri.10.87.

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31

Potolidis, Evangelos, Charalampos Mandros, Kalliopi Kotsa, Evdoxia Mitsiou, Dimitris Potolidis und Panagiotis Fanourgiakis. „Dabigatran Associated Leukocytoclastic Vasculitis“. Case Reports in Medicine 2015 (2015): 1–2. http://dx.doi.org/10.1155/2015/616109.

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Common side effects of dabigatran are bleeding, bruising, nausea, diarrhea, and abdomen discomfort. Skin reactions were not often noted (<0.1%). We report a case of 70-year-old male who developed dabigatran related skin reaction resistant to usual therapy. Skin biopsy revealed leukocytoclastic vasculitis.
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Jafri, Zainab, Lydia Shedlofsky, Andrew Newman, Travis Lam und Yebabe Mengesha. „Sweet Presentation of a Bitter Disease: Acute Febrile Neutrophilic Dermatosis Associated with Coccidioidomycoses“. SKIN The Journal of Cutaneous Medicine 5, Nr. 2 (06.03.2021): 174–77. http://dx.doi.org/10.25251/skin.5.2.17.

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Acute Febrile Neutrophilic Dermatosis, also known as Sweet Syndrome, is an uncommon inflammatory disorder. Though the exact etiology is unclear, it has been presented in association with various entities. The majority of cases present following upper respiratory infections or viral gastroenteritis. Other causes include drug-induced reactions, pregnancy-related manifestations, or in association with specific hematologic or solid tumors. Rarely, it has been associated with Coccidioidomycosis, a prevalent fungus endemic to the Southwestern regions of the United States with a literature review revealing only three previous cases of Coccidioidomycosis-associated Sweet Syndrome. Here we report two new cases in individuals residing in Arizona.
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Baumer, Fiona M., und Maureen Sheehan. „Quinidine-associated skin discoloration in KCNT1-associated pediatric epilepsy“. Neurology 89, Nr. 21 (20.11.2017): 2212. http://dx.doi.org/10.1212/wnl.0000000000004674.

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Cymerman, Rachel. „De novo versus nevus-associated melanomas: differences in associations with prognostic indicators and survival“. SKIN The Journal of Cutaneous Medicine 3, Nr. 2 (11.03.2019): 126. http://dx.doi.org/10.25251/skin.3.2.19.

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35

Galimberti, Fabrizio, und Natasha A. Mesinkovska. „Skin findings associated with nutritional deficiencies“. Cleveland Clinic Journal of Medicine 83, Nr. 10 (Oktober 2016): 731–39. http://dx.doi.org/10.3949/ccjm.83a.15061.

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36

Fekete, GyL, und Júlia Edit Fekete. „Tattoo-Associated Skin Reactions — Clinical Cases“. Acta Medica Marisiensis 59, Nr. 3 (01.06.2013): 172–74. http://dx.doi.org/10.2478/amma-2013-0041.

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Abstract Tatooing has been practiced for thousands of years. It has become a common practice for people of Western countries in the last 10-20 years, where approximately 3-5% of the population has at least one tattoo. Various pigmented substances introduced into the skin may cause the occurrence of adverse irritative, immunological, infectious or other reactions of the skin. We present three clinical cases with adverse reactions after tattooing.
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Maharaj, M., und N. Dungwa. „Neonatal tetanus associated with skin infection“. South African Medical Journal 106, Nr. 9 (03.08.2016): 888. http://dx.doi.org/10.7196/samj.2016.v106i9.11139.

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38

Yamamoto, Toshiyuki, Hiroko Ohkubo und Kiyoshi Nishioka. „Skin Manifestations Associated with Rheumatoid Arthritis“. Journal of Dermatology 22, Nr. 5 (Mai 1995): 324–29. http://dx.doi.org/10.1111/j.1346-8138.1995.tb03396.x.

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OKADA, N., K. MORIYA, K. NISHIDA, Y. KITANO, T. KOBAYASHI, H. NISHIMURA, M. AOYAMA und K. YOSHIKAWA. „Skin pigmentation associated with minocycline therapy“. British Journal of Dermatology 121, Nr. 2 (August 1989): 247–54. http://dx.doi.org/10.1111/j.1365-2133.1989.tb01807.x.

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40

MARTIN, ANN G., und SUSANA LEAL–KHOURI. „PHYSIOLOGIC SKIN CHANGES ASSOCIATED WITH PREGNANCY“. International Journal of Dermatology 31, Nr. 6 (Juni 1992): 375–78. http://dx.doi.org/10.1111/j.1365-4362.1992.tb02662.x.

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41

Daoud, Mazen S., John A. Lust, Robert A. Kyle und Mark R. Pittelkow. „Monoclonal gammopathies and associated skin disorders“. Journal of the American Academy of Dermatology 40, Nr. 4 (April 1999): 507–35. http://dx.doi.org/10.1016/s0190-9622(99)70434-2.

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42

Shumrick, Kevin A., und Brett Coldiron. „Genetic Syndromes Associated With Skin Cancer“. Otolaryngologic Clinics of North America 26, Nr. 1 (Februar 1993): 117–37. http://dx.doi.org/10.1016/s0030-6665(20)30869-0.

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43

Murad, A., und P. Lenane. „Exertional dyspnoea associated with skin lesions“. Emergency Medicine Journal 32, Nr. 2 (05.05.2014): 148. http://dx.doi.org/10.1136/emermed-2014-203869.

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44

Foti, Caterina, Nicoletta Cassano, Michele De Mari, Margherita Sorino und Gino A. Vena. „Bullous skin eruption associated with entacapone“. International Journal of Dermatology 43, Nr. 6 (Juni 2004): 471–72. http://dx.doi.org/10.1111/j.1365-4632.2004.02081.x.

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Stuhec, Matej. „Oxcarbamazepine Associated With Serious Skin Reaction“. Journal of Clinical Psychopharmacology 34, Nr. 3 (Juni 2014): e2-e3. http://dx.doi.org/10.1097/jcp.0000000000000086.

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Gul, Murat, Mehmet Kaynar, Tamer Sekmenli, Ilhan Ciftci und Serdar Goktas. „Epinephrine Injection Associated Scrotal Skin Necrosis“. Case Reports in Urology 2015 (2015): 1–3. http://dx.doi.org/10.1155/2015/187831.

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Male circumcision is among the most frequent surgical interventions throughout history. Although considered as a minor intervention, it may have complications ranging from insignificant to catastrophic. These complications can be attributed to the surgical procedure and anesthesia. In this report we present two cases of scrotal skin necrosis after lidocaine with epinephrine injection using subcutaneous ring block technique prior to circumcision.
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Amin, Asim, und Earle F. Burgess. „Skin manifestations associated with kidney cancer“. Seminars in Oncology 43, Nr. 3 (Juni 2016): 408–12. http://dx.doi.org/10.1053/j.seminoncol.2016.02.016.

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48

Bodey, Gerald P., Maha Boktour, Steven Mays, Madeleine Duvic, Dimitrios Kontoyiannis, Ray Hachem und Issam Raad. „Skin lesions associated with Fusarium infection“. Journal of the American Academy of Dermatology 47, Nr. 5 (November 2002): 659–66. http://dx.doi.org/10.1067/mjd.2002.123489.

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49

Samit, A., und K. Kent. „Complications associated with skin graft vestibuloplasty“. Plastic and Reconstructive Surgery 75, Nr. 2 (Februar 1985): 288. http://dx.doi.org/10.1097/00006534-198502000-00054.

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Ross, J. Barrie. „Goodpasture's Syndrome Associated With Skin Involvement“. Archives of Dermatology 121, Nr. 11 (01.11.1985): 1442. http://dx.doi.org/10.1001/archderm.1985.01660110090022.

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