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Dive into the research topics where Horacio Cabo is active.

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Featured researches published by Horacio Cabo.


Archives of Dermatology | 2008

Dermoscopic Evaluation of Amelanotic and Hypomelanotic Melanoma

Scott W. Menzies; Juergen Kreusch; Karen Byth; Maria A. Pizzichetta; Ashfaq A. Marghoob; Ralph P. Braun; Josep Malvehy; Susana Puig; Giuseppe Argenziano; Iris Zalaudek; Harold S. Rabinovitz; Margaret Oliviero; Horacio Cabo; Verena Ahlgrimm-Siess; Michelle Avramidis; Pascale Guitera; H. Peter Soyer; Giovanni Ghigliotti; Masaru Tanaka; Ana Perusquia; Gianluca Pagnanelli; Riccardo Bono; Luc Thomas; Giovanni Pellacani; David Langford; Domenico Piccolo; Karin Terstappen; Ignazio Stanganelli; Alex Llambrich; Robert H. Johr

OBJECTIVE To determine the predictive dermoscopic features of amelanotic and hypomelanotic melanoma. DESIGN A total of 105 melanomas (median Breslow thickness, 0.76 mm), 170 benign melanocytic lesions, and 222 nonmelanocytic lesions lacking significant pigment (amelanotic, partially pigmented, and light colored) were imaged using glass-plate dermoscopy devices and scored for 99 dermoscopic features. Diagnostic models were derived from and tested on independent randomly selected lesions. SETTING Predominantly hospital-based clinics from 5 continents. MAIN OUTCOME MEASURES Sensitivity, specificity, and odds ratios for individual features and models for the diagnosis of melanoma and malignancy. RESULTS The most significant negative predictors of melanoma were having multiple (>3) milialike cysts (odds ratio, 0.09; 95% confidence interval, 0.01-0.64), comma vessels with a regular distribution (0.10; 0.01-0.70), comma vessels as the predominant vessel type (0.16; 0.05-0.52), symmetrical pigmentation pattern (0.18; 0.09-0.39), irregular blue-gray globules (0.20; 0.05-0.87), and multiple blue-gray globules (0.28; 0.10-0.81). The most significant positive predictors were having a blue-white veil (odds ratio,13; 95% confidence interval, 3.9-40.0), scarlike depigmentation (4.4; 2.4-8.0), multiple blue-gray dots (3.5; 1.9-6.4), irregularly shaped depigmentation (3.3; 2.0-5.3), irregular brown dots/globules (3.2; 1.8-5.6), 5 to 6 colors (3.2; 1.6-6.3), and predominant central vessels (3.1; 1.6-6.0). A simple model distinguishing melanomas from all nonmelanomas had a sensitivity of 70% and a specificity of 56% in the test set. A model distinguishing all malignant lesions from benign lesions had a sensitivity of 96% and a specificity of 37%. Conclusion Although the diagnostic accuracy of dermoscopy for melanoma lacking significant pigment is inferior to that of more pigmented lesions, features distinguishing the former from benign lesions can be visualized on dermoscopic evaluation.


Dermatology | 2008

Entodermoscopy: A New Tool for Diagnosing Skin Infections and Infestations

Iris Zalaudek; Jason Giacomel; Horacio Cabo; Alessandro Stefani; Gerardo Ferrara; Rainer Hofmann-Wellenhof; J. Malvehy; Susana Puig; Wilhelm Stolz; Giuseppe Argenziano

Background: There is upcoming evidence that dermoscopy facilitates the in vivo diagnosis of skin infections and infestations. As such, dermoscopy connects the research fields of dermatologists and entomologists, opening a new research field of ‘entodermoscopy’. Objective: To provide an overview on the current applications of entodermoscopy. Methods: Systematic review of the English- and German-language literature by searches of Medline, Medscape and abstracts of the 1st World Congress of the International Dermoscopy Society. Results: Dermoscopic patterns have been described for viral warts, molluscum contagiosum, scabies, pediculosis, tinea nigra, tungiasis, cutaneous larva migrans, ticks and reactions to spider leg spines. Besides the diagnostic role of dermoscopy, there is increasing evidence that it can also assist in the monitoring of treatment efficacy for some of these conditions. Conclusion: Although most of the current available literature is based on single observations and small case studies rather than controlled trials, an increasing interest in this field can be observed.


Journal of The American Academy of Dermatology | 2012

Accuracy in melanoma detection: A 10-year multicenter survey

Giuseppe Argenziano; Lorenzo Cerroni; Iris Zalaudek; Stefania Staibano; Rainer Hofmann-Wellenhof; Nicola Arpaia; Renato Marchiori Bakos; B. Balme; Jadran Bandic; Roberto Bandelloni; Alexandra Maria Giovanna Brunasso; Horacio Cabo; David A. Calcara; Blanca Carlos-Ortega; Ana Carolina Carvalho; Gabriel Casas; Huiting Dong; Gerardo Ferrara; Raffaele Filotico; Guillermo Gómez; Allan C. Halpern; Gennaro Ilardi; Akira Ishiko; Gulsen Kandiloglu; Hiroshi Kawasaki; Ken Kobayashi; Hiroshi Koga; Ivanka Kovalyshyn; David Langford; Xin Liu

BACKGROUND Early excision is the only strategy to reduce melanoma mortality, but unnecessary excision of benign lesions increases morbidity and healthcare costs. OBJECTIVE To assess accuracy in melanoma detection based on number-needed-to-excise (NNE) values over a 10-year period. METHODS Information was retrieved on all histopathologically confirmed cutaneous melanomas or melanocytic nevi that were excised between 1998 and 2007 at participating clinics. NNE values were calculated by dividing the total number of excised lesions by the number of melanomas. Analyses included changes in NNE over time, differences in NNE between specialized clinical settings (SCS) versus non-specialized clinical settings (NSCS), and patient factors influencing NNE. RESULTS The participating clinics contributed a total of 300,215 cases, including 17,172 melanomas and 283,043 melanocytic nevi. The overall NNE values achieved in SCS and NSCS in the 10-year period were 8.7 and 29.4, respectively. The NNE improved over time in SCS (from 12.8 to 6.8), but appeared unchanged in NSCS. Most of the effect on NNE in SCS was due to a greater number of excised melanomas. Higher NNE values were observed in patients younger than 40 years and for lesions located on the trunk. LIMITATIONS No data concerning the use of dermatoscopy and digital monitoring procedures were collected from the participating centers. CONCLUSION Over the 10-year study period, accuracy in melanoma detection improved only in specialized clinics maybe because of a larger use of new diagnostic techniques such as dermatoscopy.


Archives of Dermatology | 2011

Dermoscopy of pigmented lesions of the mucosa and the mucocutaneous junction: results of a multicenter study by the International Dermoscopy Society (IDS).

Andreas Blum; Olga Simionescu; Giuseppe Argenziano; Ralph P. Braun; Horacio Cabo; Astrid Eichhorn; Herbert Kirchesch; Josep Malvehy; Ashfaq A. Marghoob; Susana Puig; Fezal Ozdemir; Wilhelm Stolz; Isabelle Tromme; Ulrike Weigert; Ingrid H. Wolf; Iris Zalaudek; Harald Kittler

OBJECTIVE To better characterize the dermoscopic patterns of mucosal lesions in relation to the histopathologic characteristics. DESIGN Retrospective and observational study. SETTING Fourteen referral pigmented lesion clinics in 10 countries. PATIENTS A total of 140 pigmented mucosal lesions (126 benign lesions, 11 melanomas, 2 Bowen disease lesions, and 1 metastasis) from 92 females (66%) and 48 males (34%) were collected from October 2007 through November 2008. MAIN OUTCOME MEASURES Scoring the dermoscopic patterns (dots, globules, or clods, circles, lines, or structureless) and colors (brown, black, blue, gray, red, purple, and white) and correlation with the histopathologic characteristics. RESULTS Based on univariate analysis and 2 diagnostic models, the presence of structureless zones inside the lesions with blue, gray, or white color (the first model) had a 100% sensitivity for melanoma and 92.9% sensitivity for any malignant lesion, and 82.2% and 83.3% specificity for benign lesions in the group with melanoma lesions and the group with malignant lesions, respectively. Based on the colors (blue, gray, or white) only (the second model), the sensitivity for the group with melanoma was 100% and for the group with any malignant lesion was 92.9%, and the specificity was 64.3% and 65.1%, respectively. Patients with malignant lesions were significantly older than patients with benign lesions (mean [SD] ages, 60.1 [22.8] years vs 43.2 [17.3] years, respectively). CONCLUSION The combination of blue, gray, or white color with structureless zones are the strongest indicators when differentiating between benign and malignant mucosal lesions in dermoscopy.


British Journal of Dermatology | 2006

Three-point checklist of dermoscopy: an open internet study

Iris Zalaudek; Giuseppe Argenziano; H.P. Soyer; Rosamaria Corona; Francesco Sera; Andreas Blum; Ralph Braun; Horacio Cabo; G. Ferrara; Alfred W. Kopf; David Langford; Scott W. Menzies; Giovanni Pellacani; Ketty Peris; Stefania Seidenari

Background  In a pilot study, the three‐point checklist of dermoscopy has been shown to represent a valid and reproducible tool with high sensitivity for the diagnosis of skin cancer in the hands of a small group of nonexperts.


Dermatology | 2007

Dermoscopy Key Points: Recommendations from the International Dermoscopy Society

Jonathan Bowling; Giuseppe Argenziano; A Azenha; J Bandic; R Bergman; Andreas Blum; Horacio Cabo; A Di Stephani; James M. Grichnik; Allan C. Halpern; R Hofman-Wellenhof; Robert H. Johr; Harald Kittler; Alfred W. Kopf; Jürgen Kreusch; David Langford; J. Malvehy; Ashfaq A. Marghoob; Scott W. Menzies; Fezal Ozdemir; Ketty Peris; D Piccolo; Maria A. Pizzichetta; D Polsky; Susana Puig; Harold S. Rabinovitz; Pietro Rubegni; Toshiaki Saida; Massimiliano Scalvenzi; Stefania Seidenari

J. Bowling G. Argenziano A. Azenha J. Bandic R. Bergman A. Blum H. Cabo A. Di Stephani J. Grichnik A. Halpern R. Hofman-Wellenhof R. Johr H. Kittler A. Kopf J. Kreusch D. Langford J. Malvehy A. Marghoob S. Menzies F. Ozdemir K. Peris D. Piccolo M.A. Pizzichetta D. Polsky S. Puig H. Rabinovitz P. Rubegni T. Saida M. Scalvenzi S. Seidenari H.P. Soyer M. Tanaka I. Zalaudek R.P. Braun


JAMA Dermatology | 2013

Dermoscopic evaluation of nodular melanoma

Scott W. Menzies; Fergal J. Moloney; Karen Byth; Michelle Avramidis; Giuseppe Argenziano; Iris Zalaudek; Ralph P. Braun; Josep Malvehy; Susana Puig; Harold S. Rabinovitz; Margaret Oliviero; Horacio Cabo; Riccardo Bono; Maria A. Pizzichetta; Magdalena Claeson; Daniel C Gaffney; H. Peter Soyer; Ignazio Stanganelli; Richard A. Scolyer; Pascale Guitera; John W. Kelly; Olivia McCurdy; Alex Llambrich; Ashfaq A. Marghoob; Pedro Zaballos; Herbert Kirchesch; Domenico Piccolo; Jonathan Bowling; Luc Thomas; Karin Terstappen

IMPORTANCE Nodular melanoma (NM) is a rapidly progressing potentially lethal skin tumor for which early diagnosis is critical. OBJECTIVE To determine the dermoscopy features of NM. DESIGN Eighty-three cases of NM, 134 of invasive non-NM, 115 of nodular benign melanocytic tumors, and 135 of nodular nonmelanocytic tumors were scored for dermoscopy features using modified and previously described methods. Lesions were separated into amelanotic/hypomelanotic or pigmented to assess outcomes. SETTING Predominantly hospital-based clinics from 5 continents. MAIN OUTCOME MEASURES Sensitivity, specificity, and odds ratios for features/models for the diagnosis of melanoma. RESULTS Nodular melanoma occurred more frequently as amelanotic/hypomelanotic (37.3%) than did invasive non-NM (7.5%). Pigmented NM had a more frequent (compared with invasive non-NM; in descending order of odds ratio) symmetrical pigmentation pattern (5.8% vs 0.8%), large-diameter vessels, areas of homogeneous blue pigmentation, symmetrical shape, predominant peripheral vessels, blue-white veil, pink color, black color, and milky red/pink areas. Pigmented NM less frequently displayed an atypical broadened network, pigment network or pseudonetwork, multiple blue-gray dots, scarlike depigmentation, irregularly distributed and sized brown dots and globules, tan color, irregularly shaped depigmentation, and irregularly distributed and sized dots and globules of any color. The most important positive correlating features of pigmented NM vs nodular nonmelanoma were peripheral black dots/globules, multiple brown dots, irregular black dots/globules, blue-white veil, homogeneous blue pigmentation, 5 to 6 colors, and black color. A model to classify a lesion as melanocytic gave a high sensitivity (>98.0%) for both nodular pigmented and nonnodular pigmented melanoma but a lower sensitivity for amelanotic/hypomelanotic NM (84%). A method for diagnosing amelanotic/hypomelanotic malignant lesions (including basal cell carcinoma) gave a 93% sensitivity and 70% specificity for NM. CONCLUSIONS AND RELEVANCE When a progressively growing, symmetrically patterned melanocytic nodule is identified, NM needs to be excluded.


Journal of The American Academy of Dermatology | 2012

Total body skin examination for skin cancer screening in patients with focused symptoms

Giuseppe Argenziano; Iris Zalaudek; Rainer Hofmann-Wellenhof; Renato Marchiori Bakos; Wilma Bergman; Andreas Blum; Paolo Broganelli; Horacio Cabo; Filomena Caltagirone; Caterina Catricalà; Maurizio Coppini; Lucas Dewes; Maria Grazia Francia; Alessandro Garrone; Bengü Gerçeker Türk; Giovanni Ghigliotti; Jason Giacomel; Jean-Yves Gourhant; Gerald Hlavin; Nicole A. Kukutsch; Dario Lipari; Gennaro Melchionda; Fezal Ozdemir; Giovanni Pellacani; Riccardo Pellicano; Susana Puig; Massimiliano Scalvenzi; Ana Maria Sortino-Rachou; Anna Virgili; Harald Kittler

BACKGROUND The value of total body skin examination (TBSE) for skin cancer screening is controversial. OBJECTIVE We sought to determine whether TBSE could be helpful in patients with focused skin symptoms who would not otherwise have undergone TBSE. METHODS In a prospective, multicenter, cross-sectional study consecutive adult patients were recruited during a period of 18 months. Physicians first inspected problem areas and uncovered areas and then performed TBSE. Equivocal lesions detected in both steps were excised or biopsied. Primary outcomes were the absolute and relative risks of missing skin cancer and the number of patients needed to examine to detect melanoma or another malignancy. A secondary outcome was the proportion of false-positive results obtained by TBSE. RESULTS We examined 14,381 patients and detected 40 (0.3%) patients with melanoma and 299 (2.1%) with at least one nonmelanoma skin cancer by TBSE. In 195 (1.3%) patients equivocal lesions found by TBSE turned out to be benign. We calculated that 47 patients need to be examined by TBSE to find one skin malignancy and 400 patients to detect one melanoma. The risk of missing one malignancy if not performing TBSE was 2.17% (95% confidence interval 1.25-3.74). Factors significantly increasing the chance to find a skin cancer were age, male gender, previous nonmelanoma skin cancer, fair skin type, skin tumor as the reason for consultation, and presence of an equivocal lesion on problem/uncovered areas. LIMITATIONS The impact of TBSE on skin cancer mortality was not evaluated. CONCLUSIONS TBSE improves skin cancer detection in patients with focused skin symptoms and shows a low rate of false-positive results.


Journal of The European Academy of Dermatology and Venereology | 2012

Dermoscopy of scalp tumours: a multi-centre study conducted by the international dermoscopy society

Ignazio Stanganelli; Giuseppe Argenziano; Francesco Sera; Andreas Blum; Fezal Ozdemir; Isil Kilinc Karaarslan; Domenico Piccolo; Ketty Peris; Herbert Kirchesch; Riccardo Bono; Maria A. Pizzichetta; S. Gasparini; Ralph P. Braun; Osvaldo Correia; Luc Thomas; Pedro Zaballos; Susana Puig; Josep Malvehy; Massimiliano Scalvenzi; Harold S. Rabinovitz; A Bergamo; Giovanni Pellacani; Caterina Longo; M Pavlovic; Cliff Rosendahl; Rainer Hofmann-Wellenhof; Horacio Cabo; Ashfaq A. Marghoob; David Langford; Stefano Astorino

Background  Little is known about the dermoscopic features of scalp tumours.


JAMA Dermatology | 2014

Recurrent Melanocytic Nevi and Melanomas in Dermoscopy: Results of a Multicenter Study of the International Dermoscopy Society

Andreas Blum; Rainer Hofmann-Wellenhof; Ashfaq A. Marghoob; Giuseppe Argenziano; Horacio Cabo; Cristina Carrera; Bianca Costa Soares de Sá; Eric Ehrsam; Roger González; Josep Malvehy; Ausilia Maria Manganoni; Susana Puig; Olga Simionescu; Masaru Tanaka; Luc Thomas; Isabelle Tromme; Iris Zalaudek; Harald Kittler

IMPORTANCE Differentiating recurrent nevi from recurrent melanoma is challenging. OBJECTIVE To determine dermoscopic features to differentiate recurrent nevi from melanomas. DESIGN, SETTING, AND PARTICIPANTS Retrospective observational study of 15 pigmented lesion clinics from 12 countries; 98 recurrent nevi (61.3%) and 62 recurrent melanomas (38.8%) were collected from January to December 2011. MAIN OUTCOMES AND MEASURES Scoring the dermoscopic features, patterns, and colors in correlation with the histopathologic findings. RESULTS In univariate analysis, radial lines, symmetry, and centrifugal growth pattern were significantly more common dermoscopically in recurrent nevi; in contrast, circles, especially if on the head and neck area, eccentric hyperpigmentation at the periphery, a chaotic and noncontinuous growth pattern, and pigmentation beyond the scars edge were significantly more common in recurrent melanomas. Patients with recurrent melanomas were significantly older than patients with recurrent nevi (mean [SD] age, 63.1 [17.5] years vs 30.2 [12.4] years) (P<.001), and there was a significantly longer time interval between the first procedure and the second treatment (median time interval, 25 vs 8 months) (P<.001). In a multivariate analysis, pigmentation beyond the scars edge (P=.002), age (P<.001), and anatomic site (P=.002) were significantly and independently associated with the diagnosis of recurrent melanoma in dermoscopy. CONCLUSIONS AND RELEVANCE Dermoscopically, pigmentation beyond the scars edge is the strongest clue for melanoma. Dermoscopy is helpful in evaluating recurrent lesions, but final interpretation requires taking into account the patient age, anatomic site, time to recurrence, growth pattern, and, if available, the histopathologic findings of the first excision.

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Giuseppe Argenziano

Seconda Università degli Studi di Napoli

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Susana Puig

University of Barcelona

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Iris Zalaudek

Medical University of Graz

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Ashfaq A. Marghoob

Memorial Sloan Kettering Cancer Center

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Rosario Peralta

University of Buenos Aires

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Andreas Blum

University of Tübingen

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Alberto Woscoff

University of Buenos Aires

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