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Dive into the research topics where Giusto Trevisan is active.

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Featured researches published by Giusto Trevisan.


Cancer | 2001

Dermoscopic criteria for melanoma in situ are similar to those for early invasive melanoma

Maria A. Pizzichetta; Giuseppe Argenziano; Renato Talamini; Domenico Piccolo; Alessandro Gatti; Giusto Trevisan; Gian Mauro Sasso; Andrea Veronesi; Antonino Carbone; H. Peter Soyer

Dermoscopy is a noninvasive technique that increases the diagnostic accuracy of pigmented skin lesions, particularly improving the diagnosis of patients with cutaneous melanoma in situ (CMIS) and early invasive melanoma. To establish reliable and reproducible dermoscopic criteria for the diagnosis of CMIS, the authors conducted a retrospective clinical study of 37 patients with CMIS and 53 patients with invasive cutaneous melanomas (ICM).


Zentralblatt für Bakteriologie, Mikrobiologie, und Hygiene | 1987

Lyme disease in Italy.

Giusto Trevisan; Franco Crovato; Carlo Marcuccio; Donato Fumarola; Carmelo Scarpa

We present the first cases of Lyme disease found in Italy. The diagnosis was based on clinical and laboratory data. The antigen used for indirect immunofluorescence (I.I.F.) was kindly supplied to us by Prof. R. Ackermann (Köln). Reciprocal titer was 64 in five patients, 128 in six, 256 in three and 512 in one. The patients came either from the Eastern Ligurian Coast or the Trieste Karst: these are consequently the first two Italian areas where Lyme disease has been recognized up to the present.


Journal of The European Academy of Dermatology and Venereology | 2001

Intralesional granulocyte‐monocyte colony‐stimulating factor followed by subcutaneous interleukin‐2 in metastatic melanoma: a pilot study in elderly patients

L Ridolfi; R Ridolfi; A Ascari-Raccagni; M Fabbri; S Casadei; Alessandro Gatti; Giusto Trevisan; Mg Righini

Recent data in the literature indicate that antigen‐presenting cells (APC) are inactive in tumour tissue because of local immunosuppression. Tumour‐infiltrating lymphocyte (TIL) signal activation transducing mechanisms are also seriously impaired. Administration of granulocyte macrophage‐colony stimulating factor (GM‐CSF) may lead to APC recovery and interleukin (IL)‐2 may restore local TIL activation. Moreover, IL‐2 increases the systemic lymphocyte population, an event that seems to correlate with a better prognosis.


Journal of The European Academy of Dermatology and Venereology | 1996

Detection of Borrelia burgdorferi in skin biopsies from patients with morphea by polymerase chain reaction

Giusto Trevisan; Giuseppe Stinco; Carla Nobile; Serena Bonin; Giorgio Stanta

Aim We looked for the evidence of Borrelia infection in patients with morphea by serologic means and by polymerase chain reaction (PCR) analysis of skin biopsy samples. Background The possible relationship between Lyme borreliosis and morphea has been suggested by certain clinical, immunological and microbiological findings, but many authors were not be able to demonstrate Borrelia burgdorferi infection in patients with morphea and cast doubts on an etiological role for B. burgdorferi in this skin lesion. Patients and methods Ten patients with morphea, 9 females (range: 8–65 years) and one 44-year-old man were examined. Serological tests for Lyme borreliosis were performed by immunofluorescence assay and flagellin enzyme-linked immunosorbent assay. Skin biopsy specimens were taken from the periphery of morphea lesions for histological examination and PCR. Results Antibodies to B. burgdorferi were detected in 3 patients and B. burgdorferi DNA was demonstrated in 5 patients. Conclusions The amplification of DNA with PCR analysis seems to open new prospects for the detection of Borrelia genome in tissues. In the present study we were able to demonstrate the presence of B. burgdorferi DNA in patients with morphea, even in seronegative patients. These data confirm that PCR is an interesting tool in skin lesion diagnosis and support the hypothesis of an etiological association between B. burgdorferi infection and some cases of morphea.


Journal of Immunotherapy | 2003

Adjuvant immunotherapy with tumor infiltrating lymphocytes and interleukin-2 in patients with resected stage III and IV melanoma.

Laura Ridolfi; Ruggero Ridolfi; Angela Riccobon; Franca De Paola; Massimiliano Petrini; Monica Stefanelli; Emanuela Flamini; Alessandra Ravaioli; Giorgio Maria Verdecchia; Giusto Trevisan; Dino Amadori

Adoptive immunotherapy with tumor infiltrating lymphocytes (TIL) and interleukin (IL)-2 is reasonably effective in the treatment of patients with advanced melanoma. However, theoretically it should be of greater benefit as adjuvant therapy, especially in high-risk stages (resected stages III and IV). In a preliminary study, 25 patients (aged 23–72 years) with stage III–IV melanoma who underwent resection of metachronous metastases were reinfused with TIL cultivated and expanded in vitro with IL-2 from surgically removed metastases. IL-2 (starting dose 12 × 106 IU/m2) was co-administered as a continuous infusion according to Wests scheme. A total of 8/22 (36.3%) evaluable patients were disease-free (DF) at a median follow-up of 5 years. DF survival (DFS) and overall survival (OS) rates were 44% and 37%, respectively, at 2 years, and 52% and 45% at 3 years. The CNS was the only site of disease recurrence in 57% of patients who relapsed. DF patients received a higher median dose of IL-2 than those who progressed (total dose 110 × 106 versus 86 × 106 IU/m2, respectively). The progressive reduction in IL-2 dosage allowed all patients to complete treatment without permanent grade 4 toxicity. Analysis of tumor immunosuppression factors in lymphocytes inside the tumor (TCR ζ and ε chains, p56lck, FAS, and FAS-ligand) confirmed that the immunologic potential of TIL, depressed at the time of metastasectomy, was significantly restored after in vitro culture with IL-2. Adoptive immunotherapy with TIL and IL-2 could improve DFS and OS, although further work is required to determine its role in the treatment of patients with high-risk melanoma.


Apmis | 1989

Characterization of the first tick isolate of Borrelia burgdorferi from Italy

Marina Cinco; Elena Banfi; Giusto Trevisan; Gerold Stanek

We report on the first isolation of a spirochetal organism from Ixodes ricinus ticks of the Trieste area (Northern Italy) which was identified as Borrelia burgdorferi by its reactivity with specific monoclonal antibodies directed against the OSPA and flagella proteins.


Journal of The European Academy of Dermatology and Venereology | 2002

MOLECULAR ANALYSES OF SENTINEL LYMPH NODES: AN OPEN QUESTION

Serena Bonin; Benedetta Niccolini; R Calacione; B Gambardella; O Geatti; Giorgio Stanta; Giusto Trevisan

Aims To detect micrometastases in the sentinel lymph nodes (SLN) of melanoma patients the authors analysed 52 lymph nodes (47 SLNs and five non‐sentinel) and 17 corresponding primary skin melanomas using reverse transcriptase–polymerase chain reaction assays in paraffin‐embedded tissues to detect the mRNAs of tyrosinase, MAGE1, MAGE3, MIA, MART‐1 and mRNA coding for telomerase catalytic component.


Acta Dermato-venereologica | 2004

Detection of spirochaetal DNA simultaneously in skin biopsies, peripheral blood and urine from patients with erythema migrans

Paolo Pauluzzi; Serena Bonin; Maria Angeles Gonzalez Inchaurraga; Giorgio Stanta; Giusto Trevisan

Lyme borreliosis is an emerging zoonosis transmitted by infected hard-bodied ticks. The disease is multisystemic. In the initial stage its typical manifestation is the erythema migrans, a cutaneous lesion that occurs in up to 90% of patients. In order to investigate the presence of the specific agent, Borrelia burgdorferi, in the early stages of the disease, DNA from skin biopsies, urine and peripheral blood of 30 patients with clinically documented erythema migrans and without apparent systemic involvement was analysed by polymerase chain reaction. Borrelia DNA in both blood and skin biopsies was detected in 23 patients, while in 9 patients it was discovered in urine and skin biopsies. These results demonstrate that Borrelia DNA is detectable systemically also in patients with early Lyme borreliosis and strongly suggest a possible dissemination of the causative agents even when only a local infection is assumed.


Experimental and Molecular Pathology | 2010

Evidence of multiple infectious agents in mycosis fungoides lesions

Serena Bonin; Stanislava Miertusova Tothova; Renzo Barbazza; Davide Brunetti; Giorgio Stanta; Giusto Trevisan

The etiology of mycosis fungoides (MF) remains to be determined. Several studies have proposed a viral etiology with controversial results. In this case-control study we investigated the presence of Epstein-Barr virus (EBV) and the debated presence of Human T-cell lymphotrophic virus I (HTLV-I) sequences, by polymerase chain reaction on nucleic acid extracts from formalin-fixed paraffin-embedded skin biopsies. Moreover, by a multivariate approach we analyzed in the same case-control study also the contribution of two previously examined pathogens: Hepatitis C virus (HCV) and Borrelia burgdorferi (Bb). Significant differences in the frequency of infectious agents in cases and controls were detected for Bb, HTLV-I and EBV. In MF patients we found the concurrent presence of two or three of these pathogen sequences in 21 out of 83 cases, but only in 1 out of 83 healthy controls. Our results suggest that the persistence of multiple infectious agents may cause a long-term antigenic stimulation contributing to the malignant transformation of T lymphocytes, especially when associated with HTLV-I like sequences. However, these infectious agents do not seem to have effects on disease progression.


Journal of The European Academy of Dermatology and Venereology | 1998

Efficacy of cyclosporine plus etretinate in the treatment of erythrodermic psoriasis (three case reports)

F. Kokelj; Carmela Plozzer; Pierpaolo Torsello; Giusto Trevisan

Association of different treatments are often used in erythrodermic psoriasis in order to increase the effectiveness and decrease the incidence of side effects due to single drugs.

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Maria A. Pizzichetta

Seconda Università degli Studi di Napoli

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Andrea Veronesi

European Institute of Oncology

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