Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 16 de 16
Filter
Add more filters











Publication year range
1.
JCI Insight ; 8(2)2023 Jan 24.
Article in English | MEDLINE | ID: mdl-36692020

ABSTRACT

BACKGROUNDAdverse drug reactions are unpredictable immunologic events presenting frequent challenges to clinical management. Systemically administered cholecalciferol (vitamin D3) has immunomodulatory properties. In this randomized, double-blinded, placebo-controlled interventional trial of healthy human adults, we investigated the clinical and molecular immunomodulatory effects of a single high dose of oral vitamin D3 on an experimentally induced chemical rash.METHODSSkin inflammation was induced with topical nitrogen mustard (NM) in 28 participants. Participant-specific inflammatory responses to NM alone were characterized using clinical measures, serum studies, and skin tissue analysis over the next week. All participants underwent repeat NM exposure to the opposite arm and then received placebo or 200,000 IU cholecalciferol intervention. The complete rash reaction was followed by multi-omic analysis, clinical measures, and serum studies over 6 weeks.RESULTSCholecalciferol mitigated acute inflammation in all participants and achieved 6 weeks of durable responses. Integrative analysis of skin and blood identified an unexpected divergence in response severity to NM, corroborated by systemic neutrophilia and significant histopathologic and clinical differences. Multi-omic and pathway analyses revealed a 3-biomarker signature (CCL20, CCL2, CXCL8) unique to exaggerated responders that is suppressed by cholecalciferol and implicates IL-17 signaling involvement.CONCLUSIONHigh-dose systemic cholecalciferol may be an effective treatment for severe reactions to topical chemotherapy. Our findings have broad implications for cholecalciferol as an antiinflammatory intervention against the development of exaggerated immune responses.TRIAL REGISTRATIONclinicaltrials.gov (NCT02968446).FUNDINGNIH and National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS; grants U01AR064144, U01AR071168, P30 AR075049, U54 AR079795, and P30 AR039750 (CWRU)).


Subject(s)
Cholecalciferol , Exanthema , Adult , Humans , Cholecalciferol/pharmacology , Double-Blind Method , Treatment Outcome , Exanthema/chemically induced , Exanthema/drug therapy , Inflammation/drug therapy
3.
Dermatol Surg ; 48(12): 1343-1345, 2022 12 01.
Article in English | MEDLINE | ID: mdl-34935751
6.
Ann Med Surg (Lond) ; 57: 299-302, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32874559

ABSTRACT

INTRODUCTION: Necrotizing neutrophilic dermatoses can clinically resemble necrotizing fasciitis and therefore pose a diagnostic and therapeutic challenge. Given their similar presentations, misdiagnosis and inappropriate or delayed treatments are possible. PRESENTATION OF CASE: We discuss the case of a woman with acute myeloid leukemia who presented with fevers, chills, cough, and a leg wound. She underwent amputation of her lower extremity after she was presumed to have necrotizing fasciitis; however, symptoms persisted. She was ultimately diagnosed with and treated for necrotizing Sweet's syndrome with notable clinical improvement. DISCUSSION: Both, necrotizing neutrophilic dermatoses and necrotizing fasciitis, grossly affect the skin and are associated with rapidly progressing systemic features including fevers, chills, leukocytosis, and elevated inflammatory markers. Recent literature in dermatology addresses these similarities and the appropriate approach to management; however, it is critical that medical and surgical subspecialties have an understanding of necrotizing neutrophilic dermatoses and their clinical presentations, diagnostic approaches, as well as therapeutic interventions. Familiarity with this entity can mitigate the risk of misdiagnosis, morbidity, and mortality. CONCLUSION: With this report, we seek to review the features that are suggestive of and aid in the diagnosis of necrotizing neutrophilic dermatoses to help prevent significant and avoidable morbidity.

8.
Cutis ; 106(6): 309-310, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33471878

ABSTRACT

Recently, several cutaneous manifestations of coronavirus disease 2019 (COVID-19) have been reported. However, there is a paucity of published images. Those that have been published so far tend to fall under distinct morphologic categories. We present a 52-year-old patient with an ill-defined skin eruption that preceded mild gastrointestinal (GI) symptoms and without respiratory symptoms who tested positive for COVID-19. With this case report, we widen the spectrum of the cutaneous manifestations of COVID-19 infection. Consequently, we propose an expansion of the criteria for COVID-19 testing when skin findings are associated with relatively mild GI symptoms.


Subject(s)
COVID-19 Testing , COVID-19/diagnosis , Gastrointestinal Diseases/diagnosis , Skin Diseases, Viral/diagnosis , COVID-19/complications , Gastrointestinal Diseases/virology , Humans , Male , Middle Aged , Skin Diseases, Viral/pathology
10.
Melanoma Res ; 28(6): 652-654, 2018 12.
Article in English | MEDLINE | ID: mdl-30211811

ABSTRACT

Advances in the field of molecular genetics have led to the development of multiple tests capable of identifying genetic changes within cutaneous melanoma. Although the majority of these tests are currently used for diagnostic purposes, their potential use as prognostic tools is rapidly emerging. A new 31-gene expression profile test has been developed that promises to accurately predict metastatic risk in patients with early-stage cutaneous melanoma. Although current data are promising, many questions remain in terms of its potential effects in patient care. Thus, before this test is used routinely in clinical practice, we recommend that it first be performed as part of current adjuvant treatment trials as a potential predictive marker or other high-quality studies investigating relevant outcomes resulting from changes in the clinical management of patients on the basis of the gene expression profile test results.


Subject(s)
Gene Expression Profiling/methods , Melanoma/genetics , Skin Neoplasms/genetics , Humans , Melanoma/mortality , Melanoma/pathology , Neoplasm Staging , Prognosis , Skin Neoplasms/mortality , Skin Neoplasms/pathology , Survival Analysis , Melanoma, Cutaneous Malignant
11.
J Drugs Dermatol ; 17(4): 380-382, 2018 Apr 01.
Article in English | MEDLINE | ID: mdl-29601613

ABSTRACT

IMPORTANCE: Surveying identical twins allows us to qualitatively separate genetic and environmental factors that may contribute to acne severity. OBJECTIVE: To study a cohort of identical and fraternal twins to identify environmental factors that may influence acne severity. DESIGN, SETTING, PARTICIPANTS: A survey was administered to 139 identical and fraternal twin multiples (279 subjects) at the Annual Twins Day Festival in Twinsburg, Ohio on August 6-7, 2016. One set of triplets was included. MAIN OUTCOME(S) AND MEASURE(S): Acne incidence, severity, and triggers were analyzed using the N-1 Chi-squared test and paired, 2-tailed t test. RESULTS: The proportion of concordant pairs was significantly higher in identical (64%) vs fraternal (49%) twins (P=0.04). Acne was found to be associated with polycystic ovarian syndrome (PCOS; P=0.045), anxiety (P =0.014), and asthma (P=0.026). Identical twin pairs with acne had a higher BMI (P= 0.020) and exercised significantly less (P=0.001) than those without acne. Analyzing concordant twin pairs, the twin with more severe acne was more likely to report aggravation of acne with cosmetic product use (P=0.002) and sugar intake (P=0.048). CONCLUSIONS AND REVELANCE: This twin study further supports that there may be a genetic phenotypic link, though social and environmental factors may also have an influence in the disease process.

J Drugs Dermatol. 2018;17(4):380-382.

.


Subject(s)
Acne Vulgaris/epidemiology , Acne Vulgaris/genetics , Congresses as Topic , Surveys and Questionnaires , Twins, Dizygotic/genetics , Twins, Monozygotic/genetics , Acne Vulgaris/diagnosis , Adult , Female , Humans , Male , Young Adult
12.
Adv Exp Med Biol ; 996: 3-11, 2017.
Article in English | MEDLINE | ID: mdl-29124686

ABSTRACT

The use of ultraviolet (UV) light, for the treatment of skin conditions, dates back to the early 1900s. It is well known that sunlight can be of therapeutic value, but it can also lead to deleterious effects such as burning and carcinogenesis. Extensive research has expanded our understanding of UV radiation and its effects in human systems and has led to the development of man-made UV sources that are more precise, safer, and more effective for the treatment of wide variety of dermatologic conditions.


Subject(s)
Lasers/history , Photochemotherapy/history , Skin Diseases/history , Ultraviolet Rays/history , Ultraviolet Therapy/history , Animals , Equipment Design , History, 19th Century , History, 20th Century , History, 21st Century , Humans , Lasers/adverse effects , Patient Safety , Photochemotherapy/adverse effects , Photochemotherapy/instrumentation , Radiation Dosage , Radiation Exposure/history , Risk Factors , Skin Diseases/drug therapy , Skin Diseases/radiotherapy , Treatment Outcome , Ultraviolet Rays/adverse effects , Ultraviolet Therapy/adverse effects , Ultraviolet Therapy/instrumentation
13.
Adv Exp Med Biol ; 996: 89-104, 2017.
Article in English | MEDLINE | ID: mdl-29124693

ABSTRACT

The effects of ultraviolet radiation on human skin have been studied for years, and both its harmful and therapeutic effects are well known. Exposure to UV light can lead to sunburn, immunosuppression, skin aging, and carcinogenesis, and photoprotection is strongly advocated. However, when used under controlled conditions, UV radiation can also be helpful in the diagnosis and treatment of many skin conditions.


Subject(s)
Dermatology/methods , Lasers , Skin Diseases/radiotherapy , Skin/radiation effects , Ultraviolet Rays , Ultraviolet Therapy , Humans , Laser Therapy/adverse effects , Laser Therapy/instrumentation , Laser Therapy/methods , Lasers/adverse effects , Risk Factors , Skin/metabolism , Skin/pathology , Skin Diseases/diagnosis , Skin Diseases/metabolism , Treatment Outcome , Ultraviolet Rays/adverse effects , Ultraviolet Therapy/adverse effects , Ultraviolet Therapy/instrumentation , Ultraviolet Therapy/methods
14.
Article in English | MEDLINE | ID: mdl-28438926

ABSTRACT

In an effort to increase the efficacy of topical medications for treating onychomycosis, several new nail penetration enhancers were recently developed. In this study, the ability of 10% (wt/wt) miconazole nitrate combined with a penetration enhancer formulation to permeate the nail is demonstrated by the use of a selection of in vitro nail penetration assays. These assays included the bovine hoof, TurChub zone of inhibition, and infected-nail models.


Subject(s)
Antifungal Agents/pharmacokinetics , Miconazole/pharmacokinetics , Nails/microbiology , Onychomycosis/drug therapy , Administration, Topical , Animals , Antifungal Agents/administration & dosage , Antifungal Agents/therapeutic use , Cattle , Hoof and Claw/microbiology , Humans , Miconazole/administration & dosage , Miconazole/therapeutic use , Onychomycosis/microbiology
15.
J Pediatr Surg ; 52(1): 56-59, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27863823

ABSTRACT

BACKGROUND: Very pre-term infants (VP) at <32 weeks post menstrual age PMA have a high incidence of bronchopulmonary dysplasia BPD. BPD places them at risk for pulmonary-related perioperative complications from general endotracheal anesthesia GE during elective inguinal hernia repair. METHODS: A retrospective cohort study was done to compare pulmonary-related perioperative risks between VP patients undergoing non-emergent inguinal hernia repair prior to NICU discharge under GE (n=58) vs regional anesthesia RA (n=37). RESULTS: Median PMA (RA 26 vs GE 27 weeks), operative weight (RA 2.2 vs GE 2.27 kg), % with BPD, medical and surgical comorbidities, number of concurrent procedures are similar between groups, except for sac laparoscopy (0% RA vs 36% GE). Procedural anesthesia time was 40 minutes for RA vs 69 minutes for GE, (p < 0.001). GE (17%) vs RA (0%) remained intubated post op (p<0.001). Oral feeding was fully tolerated in RA (97%) vs GE (72%, p=0.002) by 48h after surgery. The statistical differences hold after regression analysis controlling for sac laparoscopy and procedure time. No difference in intraoperative or postoperative hernia complications is found. CONCLUSION: RA is safe. RA is associated with early resumption of full feed, avoidance of prolonged mechanical intubation. We recommend a randomized controlled trial comparing the safety and efficacy of GE vs RA in VP infants undergoing elective NICU inguinal hernia repair. LEVEL OF EVIDENCE: II Retrospective study.


Subject(s)
Anesthesia, Conduction , Anesthesia, General , Hernia, Inguinal/surgery , Anesthesia, Conduction/adverse effects , Anesthesia, General/adverse effects , Bronchopulmonary Dysplasia/complications , Elective Surgical Procedures , Female , Humans , Infant , Infant, Extremely Premature , Infant, Newborn , Intraoperative Complications , Male , Postoperative Complications , Retrospective Studies , Risk Factors
SELECTION OF CITATIONS
SEARCH DETAIL