L. Alos
University of Barcelona
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Publication
Featured researches published by L. Alos.
British Journal of Dermatology | 2014
Ivette Alarcon; Cristina Carrera; Josep Palou; L. Alos; J. Malvehy; Susana Puig
The number needed to treat (NNT) ratio is an effective method for measuring accuracy in melanoma detection. Dermoscopy reduces the number of false positives and subsequently unnecessary excisions. In vivo reflectance confocal microscopy (RCM) is a noninvasive technique that allows examination of the skin with cellular resolution.
Journal of The European Academy of Dermatology and Venereology | 2015
Louise Lovatto; Cristina Carrera; Gabriel Salerni; L. Alos; Josep Malvehy; Susana Puig
Digital follow‐up is a useful method for the detection of melanoma in atypical mole syndrome patients. The combination of digital follow‐up (DFU) and reflectance confocal microscopy (RCM) could be useful to increase the accuracy in the classification of equivocal lesions in atypical mole syndrome patients.
British Journal of Dermatology | 2014
F.C. Pozzobon; Joan-Anton Puig-Butille; Tatiana González-Álvarez; Cristina Carrera; Paula Aguilera; L. Alos; Celia Badenas; James M. Grichnik; J. Malvehy; Susana Puig
The identification of BRAF mutations in melanoma led to the development and implementation of new and effective therapies. Few clinical and histological features have been associated with this mutational status.
British Journal of Dermatology | 2015
Danielle Shitara; Gemma Tell-Marti; Celia Badenas; M.M.S.S. Enokihara; L. Alos; A.B. Larque; Nilceo Schwery Michalany; Joan-Anton Puig-Butille; Cristina Carrera; Josep Malvehy; Susana Puig; Ediléia Bagatin
The origin of melanoma has always been a debated subject, as well as the role of adjacent melanocytic naevi. Epidemiological and histopathological studies point to melanomas arising either de novo or from a naevus.
International Journal of Cancer | 2015
Simone Ribero; John R. Davies; Celia Requena; Cristina Carrera; Daniel Glass; Ramón Rull; Sergi Vidal-Sicart; Antonio Vilalta; L. Alos; Virtudes Soriano; Pietro Quaglino; V. Traves; Julia Newton-Bishop; Eduardo Nagore; Josep Malvehy; Susana Puig; Veronique Bataille
A high number of nevi is the most significant phenotypic risk factor for melanoma and is in part genetically determined. The number of nevi decreases from middle age onward but this senescence can be delayed in patients with melanoma. We investigated the effects of nevus number count on sentinel node status and melanoma survival in a large cohort of melanoma cases. Out of 2,184 melanoma cases, 684 (31.3%) had a high nevus count (>50). High nevus counts were associated with favorable prognostic factors such as lower Breslow thickness, less ulceration and lower mitotic rate, despite adjustment for age. Nevus count was not predictive of sentinel node status. The crude 5‐ and 10‐year melanoma‐specific survival rate was higher in melanomas cases with a high nevus count compared to those with a low nevus count (91.2 vs. 86.4% and 87.2 vs. 79%, respectively). The difference in survival remained significant after adjusting for all known melanoma prognostic factors (hazard ratio [HR] = 0.43, confidence interval [CI] = 0.21–0.89). The favorable prognostic value of a high nevus count was also seen within the positive sentinel node subgroup of patients (HR = 0.22, CI = 0.08–0.60). High nevus count is associated with a better melanoma survival, even in the subgroup of patients with positive sentinel lymph node. This suggests a different biological behavior of melanoma tumors in patients with an excess of nevi.
European Journal of Cancer | 2015
Eduardo Nagore; Susana Puig; Caroline Robert; Philippe Saiag; Elena Gallego; Enrique Herrera-Acosta; José Aguilera; Josep Malvehy; Cristina Carrera; Andrea Cavalcanti; Ramón Rull; Antonio Vilalta-Solsona; Emilie Lannoy; Céline Boutros; Naima Benannoune; Gorana Tomasic; Philippe Aegerte; Sergi Vidal-Sicart; Josep Palou; L. Alos; Celia Requena; V. Traves; Ángel Pla; Isidro Bolumar; Virtudes Soriano; Carlos Guillén; Enrique Herrera-Ceballos
INTRODUCTION In patients with primary cutaneous melanoma, there is generally a delay between excisional biopsy of the primary tumour and sentinel-node biopsy. The objective of this study is to analyse the prognostic implications of this delay. PATIENTS AND METHOD This was an observational, retrospective, cohort study in four tertiary referral hospitals. A total of 1963 patients were included. The factor of interest was the interval between the date of the excisional biopsy of the primary melanoma and the date of the sentinel-node biopsy (delay time) in the prognosis. The primary outcome was melanoma-specific survival and disease-free survival. RESULTS A delay time of 40 days or less (hazard ratio (HR), 1.7; confidence interval (CI), 1.2-2.5) increased Breslow thickness (Breslow ⩾ 2 mm, HR, > 3.7; CI, 1.4-10.7), ulceration (HR, 1.6; CI, 1.1-2.3), sentinel-node metastasis (HR, 2.9; CI, 1.9-4.2), and primary melanoma localised in the head or neck were independently associated with worse melanoma-specific survival (all P < 0.03). The stratified analysis showed that the effect of delay time was at the expense of the patients with a negative sentinel-node biopsy and without regression. CONCLUSION Early sentinel-node biopsy is associated with worse survival in patients with cutaneous melanoma.
British Journal of Dermatology | 2015
Tatiana González-Álvarez; Cristina Carrera; Antoni Bennàssar; Antonio Vilalta; Ramón Rull; L. Alos; Josep Palou; Sergi Vidal-Sicart; J. Malvehy; Susana Puig
Histological features such as Breslow thickness, ulceration and mitosis are the main criteria to guide sentinel lymph node biopsy (SLNB) in melanoma. Dermoscopy may add complementary information to these criteria.
Journal of The European Academy of Dermatology and Venereology | 2014
Cristina Carrera; Antoni Bennàssar; P. Ishioka; Stéphane Dalle; Antonio Vilalta; I. Fuertes; L. Alos; L. Thomas; Susana Puig; J. Malvehy
Desmoplastic malignant melanoma (DMM) is a rare and usually misdiagnosed type of melanoma. Delayed detection at complicated anatomical locations can lead to the necessity of alternative therapies.
Dermatology | 2013
M. Armengot-Carbo; A. Abrego; T. Gonzalez; Ivette Alarcon; L. Alos; Cristina Carrera; J. Malvehy; Susana Puig
Inverted follicular keratosis (IFK) is a rare benign tumor which usually appears as a firm papule on the face. The diagnosis is generally made by histopathology because the clinical appearance is difficult to differentiate from other lesions. Dermoscopic features of IFK have not been established to date. Herein we describe the dermoscopic findings of 4 cases of IFK. Radial peripheral hairpin vessels surrounded by a whitish halo arranged around a central white-yellowish amorphous area were observed in 3 cases, and glomerular vessels were present in the central area of one of them. The fourth case also presented a central white amorphous area but showed arborizing vessels. Reflectance confocal microscopy (available in 1 case) revealed a broadened honeycomb pattern, epidermal projections and hairpin and glomerular vessels. To our knowledge this is the first case series describing the dermoscopic features of inverted follicular keratosis and the first confocal microscopy description of this entity.
Journal of Virological Methods | 2011
Cristina Gil; M. Teresa Garcia; Felipe García; José M. Miró; Fernando Agüero; L. Alos; Laura Zamora; Alicia Capón; Josep Costa; Tomás Pumarola; José M. Gatell
Lymphoid tissue is the main reservoir of HIV-1 in infected individuals. In this study the COBAS® TaqMan® HIV-1 test was evaluated for use with the High Pure System (HPS), for quantifying HIV-1 RNA in infected cells and lymphoid tissue specimens. Serial dilutions of 8E5-LAV1 infected T-cells into SUP-T1 cells and 44 tonsil specimens were examined. Some modifications of the test were required, such as the removal of residual DNA and the HIV-1 RNA output copies were adjusted to the sample input and expressed as HIV-1 RNA copies/μg of total RNA. The Roche COBAS® TaqMan HIV-1® (HPS) test proved to be a robust, sensitive, specific and reproducible method for quantifying HIV-1 RNA in infected cells and lymphoid tissue. Linearity and reproducibility were observed in serial dilutions of 8E5-LAV1 infected T-cells (R²>0.86). High reproducibility was found in clinical tonsil specimens (Wilcoxon test p > 0.05). rDNase I treatment was essential to avoid false positives caused by residual HIV-1 DNA, mainly in tonsil specimens obtained from infected patients receiving effective antiretroviral treatment. Probit analysis determined the limit of detection as 22HIV-1 RNA copies/μg of total RNA. The Roche COBAS® TaqMan® HIV-1 (HPS) test thereby proved to be a helpful tool for measuring the HIV-1 viral load in infected cells and lymphoid tissue reservoirs.