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110 citation(s) found for "Mangold, A R".

Melanoma mimicking Rosai‐Dorfman disease
Xie, Daniel Y., Costello, Collin M. , Liang, Helen J. , Thomas, Brett G., DiCaudo, David J. , Mangold, Aaron R. , Mangold, A R , Liang, Helen J. , Costello, Collin M

Mayo Clinic

Journal of Cutaneous Pathology | February 5, 2018 | Volume: 45 | Issue: 5 | Pages: 355-359

10.1111/cup.13121 | PMID 29405342 Get It

Despite well‐defined clinical and histopathological features of melanoma, atypical presentations mimicking other skin disorders can result in a delayed diagnosis or misdiagnosis and subsequent inappropriate treatment. Rosai‐Dorfman disease (RDD) is a rare histiocytic disorder with unique clinical and histopathological features. We report a case of melanoma treated with cryotherapy that mimicked RDD both clinically and histopathologically. We compare this RDD‐like melanoma to classic RDD, outlining the importance of clinicopathological correlation prior to treatment, as well as the potential pitfalls in diagnosis after cryotherapy of pigmented lesions.
Registered nurse intent to promote physical activity for hospitalised liver transplant recipients
Pearson, Jocelyn A. , Mangold, Kara , Montez, Morgan, Smith, Diane, Tyler, Brenda, Smith, Diane M, Tyler, Brenda J, Kosiorek, Heidi

Mayo Clinic

Journal of Nursing Management | December 26, 2017 | Volume: 26 | Issue: 4 | Pages: 442-448

10.1111/jonm.12561 | PMID 29277974 Get It

Educational and practice gaps in the management of volar melanocytic lesions
Costello, Collin M. , Ghanavatian, Shirin, Temkit, M’hamed , Buras, Matthew , DiCaudo, David J. , Swanson, David C. , Mangold, Aaron R. , Mangold, A R , Buras, Matthew R , Costello, Collin M

Mayo Clinic

Journal of the European Academy of Dermatology and Venereology | November 25, 2017 | Volume: 32 | Issue: 9 | Pages: 1450-1455

10.1111/jdv.14712 | PMID 29178552 Get It

AbstractBackgroundThe benign and malignant patterns of acral melanocytic naevi (AMN) and acral melanomas (AM) have been defined in a series of retrospective studies. A three‐step algorithm was developed to determine when to biopsy acral melanocytic lesions. This algorithm has only been applied to a Japanese population.ObjectivesOur study aimed to review the current management strategy of acral melanocytic lesions and to investigate the utility of the three‐step algorithm in a predominately Caucasian cohort.MethodsA retrospective search of the pathology and image databases at Mayo Clinic was performed between the years 2006 and 2016. Only cases located on a volar surface with dermoscopic images were included. Two dermatologists reviewed all dermoscopic images and assigned a global dermoscopic pattern. Clinical and follow‐up data were gathered by chart review. All lesions with known diameter and pathological diagnosis were used for the three‐step algorithm.ResultsRegular fibrillar and ridge patterns were more likely to be biopsied (P = 0.01). The majority of AMN (58.1%) and AM (60%) biopsied were due to physician‐deemed concerning dermoscopic patterns. 39.2% of these cases were parallel furrow, lattice‐like or regular fibrillar. When patients were asked to follow‐up within a 3‐ to 6‐month period, only 16.7% of the patients returned within that interval. The three‐step algorithm would have correctly identified four of five AM for biopsy, missing a 6 mm, multicomponent, invasive melanoma.ConclusionWe found one major educational gap in the recognition of low‐risk lesions with high rates of biopsy of the fibrillary pattern. Recognizing low‐risk dermoscopic patterns could reduce the rate of biopsy of AMN by 23.3%. We identified two major practice gaps, poor patient compliance with follow‐up and the potential insensitivity of the three‐step algorithm to small multicomponent acral melanocytic lesions.
Dermoscopic Findings of Irritant “Poral” Reactions to Cobalt During Patch Testing
Yang, Yul W. , Costello, Collin M. , Mangold, Aaron R. , Mangold, A R , Costello, Collin M

Mayo Clinic

Dermatitis® | October 22, 2017 | Volume: 28 | Issue: 6 | Pages: 367-367

10.1097/der.0000000000000322 | PMID 29059096 Get It

Frequent loss of inositol polyphosphate‐5‐phosphatase in oropharyngeal squamous cell carcinoma
Patel, Amisha , Mangold, Aaron R. , Costello, Collin M. , Nagel, Thomas H. , Hayden, Richard E. , Sekulić, Aleksandar , Smith, Maxwell L. , Mangold, A R , Costello, Collin M

Mayo Clinic

Journal of the European Academy of Dermatology and Venereology | July 11, 2017 | Volume: 32 | Issue: 1 | Pages: No page available

10.1111/jdv.14462 | PMID 28696004 Get It

Chronic interstitial granulomatous dermatitis in coccidioidomycosis
Mangold, Aaron R. , DiCaudo, David J. , Blair, Janis E. , Sekulić, Aleksandar , Mangold, A R

Mayo Clinic

British Journal of Dermatology | November 17, 2015 | Volume: 174 | Issue: 4 | Pages: 881-884

10.1111/bjd.14295 | PMID 26574343 Get It

Good syndrome and lichen planus: case and review
Macdonald, James B. , Mangold, Aaron R. , Connolly, S. M., Mangold, A R

Mayo Clinic

Journal of the European Academy of Dermatology and Venereology | March 4, 2014 | Volume: 28 | Issue: 12 | Pages: 1828-1830

10.1111/jdv.12378 | PMID 24588858 Get It

Prognostic value of culprit site neutrophils in acute coronary syndrome
Distelmaier, Klaus, Winter, Max‐Paul , Dragschitz, F., Redwan, Bassam , Mangold, Andreas , Gleiß, Andreas , Perkmann, Thomas , Maurer, Gerald , Adlbrecht, Christopher , Lang, Iréne

Mayo Clinic

European Journal of Clinical Investigation | December 19, 2013 | Volume: 44 | Issue: 3 | Pages: 257-265

10.1111/eci.12228 | PMID 24720533 Get It

AbstractBackgroundRecent data suggest that acute coronary syndromes (ACS) and acute myocardial infarction (AMI) are characterized by an inflammatory subset of thrombosis. We have previously described the accumulation of neutrophils at the coronary culprit lesion site. In this work, we assessed the prognostic value of culprit site (CS) neutrophil accumulation on long‐term mortality in patients with AMI.Materials and methodsIn this prospective study, 417 AMI patients were enrolled after thrombectomy during primary percutaneous coronary intervention. The optimal cut‐off for CS neutrophil accumulation for predicting 4‐year all‐cause mortality was calculated using time‐dependent receiver operator characteristic curve analyses.ResultsThe median follow‐up time was 39 months interquartile range (IQR 21·4–54·6 months) corresponding to 1217 patient years of follow‐up. The cut‐off for CS neutrophil accumulation (difference between culprit neutrophil counts and systemic neutrophil counts) was 0·25 Giga/l. CS neutrophil accumulation occurred in 195 patients (47%) and was independently associated with mortality (hazard ratio 1·88 (95%CI 1·02–3·41, P = 0·043)). In patients with CS neutrophil accumulation, 1‐year mortality (10·8% vs. 7·2%) and 4‐year mortality (19·8% vs. 10·4%) were markedly increased compared with patients without local neutrophil accumulation. Concordance index for CS neutrophil accumulation and mortality was 0·64 (95% CI 0·51–0·77; P = 0·035). Patients with CS neutrophil accumulation had significantly more often nonobstructive lesions compared with patients without neutrophil accumulation (32·6% vs. 22·4%; P = 0·024).Conclusions Neutrophil accumulation at the coronary culprit lesion site is a strong and independent predictor of mortality in patients with ACS/AMI.
Regulatory and Reimbursement Innovation
Lindor, Rachel A. , Allocco, Scott J., Cheatham, Lee, Cortese, Denis A., Hall, Ralph F., Mangold, William J., Pizziconi, Vincent , Poste, George, Quinn, Bruce, Roth, Mollie, Saks, Michael J. , Wassman, E. Robert , Woosley, Raymond L. , Marchant, Gary E. , Lindor, Rachel A

Mayo Clinic

Science Translational Medicine | March 13, 2013 | Volume: 5 | Issue: 176 | Pages: No page available

10.1126/scitranslmed.3005437 | PMID 23486776 Get It

Coverage with evidence development and parallel review for molecular diagnostics aid regulation and reimbursement.