Ryan M Svoboda
Pennsylvania State University
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SKIN The Journal of Cutaneous Medicine | 2018
Rachel S. Mirsky; Giselle Prado; Ryan M Svoboda; Darrell S. Rigel
There has been recent extensive controversy concerning potential environmental and health hazards of oxybenzone (also known as benzophenone-3 and Eusolex 4360). Although there has been widespread related media attention, there is little definitive scientific research supporting the associated concerns.xa0Given these controversies, it is critical that dermatologists have a clear understanding of the underlying issues related to oxybenzone in order to effectively counsel their patients. The purpose of this article is to provide dermatologists with a framework for presenting this issue to patients. Within, we address questions such as:xa01) Is oxybenzone the reason for coral bleaching? 2) Is there data to suggest that oxybenzone is harmful to humans? 3) Why is oxybenzone used in the majority of US sunscreens? and 4) Are there other potential problems with oxybenzone restrictions that could lead to more skin cancer in the future? After a careful review of the evidence, we conclude that, in our opinion, there is little definitive scientific research supporting the associated concerns and that before this evidence exists, given the benefits of oxybenzone-containing sunscreens in skin cancer prevention, this ban is premature.xa0 Banning an ingredient commonly used in most sunscreens may lead to confusion among consumers and have the untoward outcome of less sunscreen being used overall.
SKIN The Journal of Cutaneous Medicine | 2018
Ryan M Svoboda; Joshua D Zuckerman; Darrell S. Rigel
Background. The topical adhesive, 2-octyl cyanoacrylate, has been used as an alternative to sutures for closure of skin in a variety of surgical procedures. While potential benefits exist, reports of allergic contact dermatitis and exothermic reactions have been a barrier to widespread adoption by dermatologic surgeons. Objective. To describe our experience using a novel formulation of 2-octyl cyanoacrylate for skin closure after surgical excision of cutaneous lesions. Methods. We describe the results of 9 office-based dermatologic excisions in 8 patients utilizing a novel formulation of 2-octyl cyanoacrylate for skin closure. At two weeks of follow-up, all incisions were examined for cosmetic result and signs of infection as per the office’s standard of care. Results. At follow-up, there were no signs of infection. One wound demonstrated mild tissue hypertrophy, while another showed very minimal skin separation (< 1mm) that did not require reintervention. No incidences of contact dermatitis, application discomfort, or burns were noted. Patient satisfaction was high. Conclusion. A novel formulation of 2-octyl cyanoacrylate topical adhesive demonstrates feasibility as a potential alternative to the use of sutures for skin closure following dermatologic excisions. Larger studies are imperative to fully describe the outcomes associated with use of this new preparation.
Journal of The American Academy of Dermatology | 2018
Ryan M Svoboda; Manish Gharia; John Shell; William D. Gregory
REFERENCES 1. Vinay K, Bishnoi A, Parsad D, Saikia UN, Sendhil Kumaran M. Dermatoscopic evaluation and histopathological correlation of acquired dermal macular hyperpigmentation. Int J Dermatol. 2017;56:1395-1399. 2. Ebihara T, Nakayama H. Pigmented contact dermatitis. Clin Dermatol. 1997;15:593-599. 3. Debroy Kidambi A, Dobson K, Holmes S, et al. Frontal fibrosing alopecia in men: an association with facial moisturizers and sunscreens. Br J Dermatol. 2017;177:260-261. 4. Fernandez-Crehuet P, Rodrigues-Barata AR, Vano-Galvan S, et al. Trichoscopic features of frontal fibrosing alopecia: results in 249 patients. J Am Acad Dermatol. 2015;72:357-359. 5. Moreno-Arrones OM, Saceda-Corralo D, Fonda-Pascual P, et al. Frontal fibrosing alopecia: clinical and prognostic classification. J Eur Acad Dermatol Venereol. 2017;31:1739-1745. 6. Sharma VK, Gupta V, Pahadiya P, Vedi KK, Arava S, Ramam M. Dermoscopy and patch testing in patients with lichen planus pigmentosus on face: a cross-sectional observational study in fifty Indian patients. Indian J Dermatol Venereol Leprol. 2017;83: 656-662. 7. Ma SA, Imadojemu S, Beer K, Seykora JT. Inflammatory features of frontal fibrosing alopecia. J Cutan Pathol. 2017; 44:672-676. 8. Ramot Y, Mastrofrancesco A, Camera E, Desreumaux P, Paus R, Picardo M. The role of PPAR -mediated signalling in skin biology and pathology: new targets and opportunities for clinical dermatology. Exp Dermatol. 2015;24:245-251. 9. Schneider MR, Schmidt-Ullrich R, Paus R. The hair follicle as a dynamic miniorgan. Curr Biol. 2009;19:R132-R142. 10. Lin J, Valdebran M, Bergfeld W, Conic RZ, Piliang M, Atanaskova Mesinkovska N. Hypopigmentation in frontal fibrosing alopecia. J Am Acad Dermatol. 2017;76:1184-1186. 11. Pirmez R, Duque-Estrada B, Donati A, et al. Clinical and dermoscopic features of lichen planus pigmentosus in 37 patients with frontal fibrosing alopecia. Br J Dermatol. 2016; 175:1387-1390. 12. Romiti R, Biancardi Gavioli CF, Anzai A, et al. Clinical and Histopathological findings of frontal fibrosing alopecia-associated lichen planus pigmentosus. Skin Appendage Disord. 2017;3:59-63.
Journal of The American Academy of Dermatology | 2018
Rebeca W. Teplitz; Alex M. Glazer; Ryan M Svoboda; Darrell S. Rigel
Among the 3 central dermatopathologists All diagnosesy 0.91 0.86-0.95 92 KC 0.91 0.83-0.97 95 BCC 0.96 0.92-0.99 97 BCC, aggressivez 0.57 0.45-0.70 83 BCC, all subtypes 0.78 0.72-0.84 80 SCC 0.90 0.82-0.96 95 SCC, invasive 0.79 0.67-0.88 92 SCC, in situ 0.52 0.29-0.72 92 AK 0.77 0.63-0.90 94 Between local pathologists and central dermatopathologists All diagnosesx 0.83 0.76-0.90 90 KC 0.78 0.66-0.90 93 BCC 0.93 0.87-0.99 97 SCC 0.83 0.73-0.93 94 SCC, invasive 0.82 0.70-0.94 95 SCC, in situ 0.48 0.20-0.75 94 AK 0.56 0.34-0.78 93 Between dermatopathologist 1 and local pathologists All diagnosesk 0.79 0.77-0.82 86 KC 0.83 0.80-0.87 93 BCC 0.92 0.90-0.95 96 SCC 0.78 0.73-0.83 94 SCC, invasive 0.75 0.68-0.81 95 AK 0.59 0.52-0.66 91 Intrarater (test-retest) reliability of dermatopathologist 1 All diagnoses{ 0.83 0.76-0.90 89 KC 0.91 0.83-0.98 96 BCC 0.92 0.86-0.98 96 SCC 0.92 0.84-1.0 97 AK 0.56 0.36-0.77 91
Journal of The American Academy of Dermatology | 2018
Ryan M Svoboda; Giselle Prado; Rachel S. Mirsky; Darrell S. Rigel
8. Duffin KC, Yeung H, Takeshita J, et al. Patient satisfaction with treatments for moderate-to-severe plaque psoriasis in clinical practice. Br J Dermatol. 2014;170(3):672-680. 9. Weinstein GD, Koo JY, Krueger GG, et al. Tazarotene cream in the treatment of psoriasis: two multicenter, double-blind, randomized, vehicle-controlled studies of the safety and efficacy of tazarotene creams 0.05% and 0.1% applied once daily for 12 weeks. J Am Acad Dermatol. 2003;48(5):760-767. 10. Gupta SK, Singh KK, Lalit M. Comparative therapeutic evaluation of different topicals and narrow band ultraviolet B therapy combined with systemic methotrexate in the treatment of palmoplantar psoriasis. Indian J Dermatol. 2011 Mar; 56(2):165-170.
SKIN The Journal of Cutaneous Medicine | 2017
Ryan M Svoboda; Abigail I Franco; Darrell S. Rigel
• Only biopsy-positive lesions were included in the data analysis • There were few advanced lesions • EIS potentially has a lower incidence of false negative results than other common diagnostic adjuncts in the detection of melanoma • There appears to be a moderate positive correlation between increasing EIS score and advancing tumor stage • A subset of 265 lesions from the EIS pivotal trial (2,416 total lesions from 22 sites in 7 countries) was analyzed, representing all biopsy-proven melanoma specimens in the sample • Prior to biopsy, each lesion was characterized by: • Clinical ABCD rule • ABCD rule of dermoscopy (cutoff >4.75 for +ve score) • 7-point checklist (cutoff ≥3 for +ve score) • Weighted 7-point checklist (cutoff ≥3 for +ve score) • EIS (cutoff ≥4 for +ve score)
Journal of The American Academy of Dermatology | 2012
Ryan M Svoboda; Timothy J. Hansen; Joslyn S. Kirby
A68-year-oldwhitemanpresentedwith a 2-month history of a pruritic rash at the base of his scrotum. The patient had used topical ketoconazole 2% cream twice daily for 2 weeks with no effect. His medical, family, and social histories were noncontributory. The physical examination revealed a pink plaque with focal areas of brown-gray discoloration andmild scale on the inferior portion of the scrotum (Fig 3). A shave biopsy specimen was obtained (Fig 4).
Journal of The American Academy of Dermatology | 2012
Ryan M Svoboda; Donald R. Mackay; Michael Jude Welsch; Bryan E. Anderson
SKIN The Journal of Cutaneous Medicine | 2018
Alex M. Glazer; Aaron S. Farberg; Ryan M Svoboda; Darrell S. Rigel
SKIN The Journal of Cutaneous Medicine | 2018
Ryan M Svoboda; Clay J. Cockerell; Roger I Ceilley; Darrell S. Rigel
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New York Institute of Technology College of Osteopathic Medicine
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