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Dive into the research topics where Laura Moneghini is active.

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Featured researches published by Laura Moneghini.


Human Pathology | 1995

bcl-2 oncoprotein in colorectal hyperplastic polyps, adenomas, and adenocarcinomas

Silvano Bosari; Laura Moneghini; Daniela Graziani; Arthur K.C. Lee; John J. Murray; Guido Coggi; Giuseppe Viale

The bcl-2 gene is an oncogene that inhibits programmed cell death (apoptosis). We investigated by immunocytochemistry bcl-2 expression in normal colonic mucosa, hyperplastic polyps, adenomas, and adenocarcinomas of the large bowel. The purpose of the investigation was twofold; to assess the possible role of bcl-2 in colorectal tumorigenesis and to evaluate its clinical significance. The cases studied included 24 hyperplastic polyps, 49 adenomas, and 205 colorectal carcinomas. In both normal mucosa and hyperplastic polyps bcl-2 immunoreactivity was detected only in the proliferative cells of the colonic crypts. Conversely, bcl-2 immunoreactivity was noted in all adenomas irrespective of the degree of dysplastic change; it was diffuse in 84% of adenomas and focal in the remaining cases. In colorectal carcinomas bcl-2 expression was undetectable in 50% and focal (less than 50% immunostained neoplastic cells) in 38% of tumors. The remaining 12% of the carcinomas displayed diffuse (more than 50% immunostained neoplastic cells) bcl-2 immunoreactivity. In colorectal carcinomas bcl-2 expression was not correlated with relevant clinicopathologic parameters, including disease stage, tumor location and growth fraction, DNA ploidy, and p53 protein accumulation, and had no prognostic significance by univariate or multivariate analysis. These results suggest that bcl-2 oncoprotein may play a role in colorectal tumorigenesis, probably in the early phases of the adenoma-carcinoma sequence. bcl-2 expression in established tumors has no prognostic significance.


Journal of Dermatology | 1997

Giant Basal Cell Carcinomas: Report of Four Cases and Considerations

Roberto Betti; Elena Inselvini; Laura Moneghini; Carlo Crosti

Four cases of giant basal cell carcinoma (BCC) are reported and the problems of giant BCCs are briefly discussed. In particular, we consider the relationship between the size of the tumor and its clinical behaviour. The importance of the site location in tumor development, the histologic subtypes involved, the associated findings, and problems of treatment are also discussed.


Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology | 2009

Low-grade myofibroblastic sarcoma of the oral cavity

Frederica Demarosi; Alessandro Bay; Laura Moneghini; Antonio Carrassi

Two cases of low-grade myofibroblastic sarcoma (LGMS) are presented: one of lateral tongue, the other of lower buccal vestibule. LGMS represents a distinct atypical myofibroblastic tumor that occurs in several sites, primarily within the head and neck regions. A painless, enlarging mass is the most common clinical presentation, but a definitive diagnosis requires both histopathological and immunohistochemical analyses. Histologically, LGMS commonly presents as a cellular lesion composed of spindle-shaped tumor cells arranged primarily in fascicles with a diffusely infiltrative pattern. Immunohistochemically, LGMS shows positive staining for at least one myogenic marker, such as desmin, and muscle actin.


European Journal of Dermatology | 2013

Basosquamous cell carcinoma: a survey of 76 patients and a comparative analysis of basal cell carcinomas and squamous cell carcinomas

Roberto Betti; Carlo Crosti; Simona Ghiozzi; Amilcare Cerri; Laura Moneghini; S. Menni

BACKGROUND Basosquamous carcinoma (BSC) is a rare epithelial tumor with a still confusing terminology. Since 2005 a more comprehensive and broader classification has existed. AIM To retrospectively review our cases of BSC according to the new WHO definition and to re-evaluate their clinical and demographic characteristics and the margin involvement after traditional surgical excision. The data were compared with the same results obtained by basal cell carcinomas (BCCs) and squamous cell carcinomas (SCCs). PATIENTS AND METHODS Histologically confirmed carcinomas observed in our Department during a sixteen-year period (1994-2011) were studied. Surgical excision was evaluated following the international guidelines. Histopathologic subtypes of BSC were classified in accordance with accepted criteria. RESULTS Seventy-six patients had a BSC, 305 a SCC, 3,643 a BCC. There were significant differences among the median age of BSCs, the total BCCs and Non-Aggressive BCCs (74.7, 68.8 and 68.3 years respectively; p<0.05). BSC was more significantly located on head-neck region than Non-Aggressive BCC (p<0.04), and less on trunk than Mixed Histology BCC (p<0.01) and Non-Aggressive BCC (p<0.005). BSC has higher prevalence of positive margins after excision than total (p<0.03) and Non-Aggressive BCC (p<0.001). CONCLUSION Basosquamous carcinoma fits to a tumor type with a different behavior pattern from non-aggressive basal cell carcinoma and more similar to squamous cell carcinoma or aggressive variants of basal cell carcinoma. Its infiltrative growth and the stromal reaction patterns give enough evidence to support the notion of considering basosquamous carcinoma as a relatively aggressive tumor.


Journal of Dermatology | 2003

Basal cell carcinomas of the areola-nipple complex: case reports and review of the literature.

Roberto Betti; Patrizia Martino; Laura Moneghini; Raffaelle Vergani; Elena Tolomio; Carlo Crosti

Two white men 57 and 39 years old, and a 47‐year‐old white woman were seen with slowly developing papulo‐nodular lesions of the areola‐nipple complex. None of the patients presented with regional lymphadenopathy, history of trauma, or relevant sun‐exposure. After excison of the mass, the histologic diagnosis of basal cell carcinoma was made. At two years of follow‐up, no recurrence was evident. The low incidence of basal cell carcinoma in this particular site allows us to consider the areola‐nipple complex location as unusual. Moreover, literature reports do not suggest that these BCCs have an increased potential for malignancy. The treatment options depend on the extension of the tumor and on the possible involvement of the areola‐nipple complex and mammary tissue.


Journal of Oncology | 2009

Biomolecular Markers in Cancer of the Tongue

Daris Ferrari; Carla Codecà; Jessica Fiore; Laura Moneghini; Silvano Bosari; Paolo Foa

The incidence of tongue cancer is increasing worldwide, and its aggressiveness remains high regardless of treatment. Genetic changes and the expression of abnormal proteins have been frequently reported in the case of head and neck cancers, but the little information that has been published concerning tongue tumours is often contradictory. This review will concentrate on the immunohistochemical expression of biomolecular markers and their relationships with clinical behaviour and prognosis. Most of these proteins are associated with nodal stage, tumour progression and metastases, but there is still controversy concerning their impact on disease-free and overall survival, and treatment response. More extensive clinical studies are needed to identify the patterns of molecular alterations and the most reliable predictors in order to develop tailored anti-tumour strategies based on the targeting of hypoxia markers, vascular and lymphangiogenic factors, epidermal growth factor receptors, intracytoplasmatic signalling and apoptosis.


Journal of The American Academy of Dermatology | 1998

Symmetrical, papular, eruptive auricular collagenomas

Roberto Betti; Elena Inselvini; Claudia Pazzini; Laura Moneghini; Carlo Crosti

Collagenomas are connective tissue nevi of the skin consisting of excessive deposition of collagen in the dermis. We describe a patient with acquired eruptive collagenomas located on both ears. Histologically, thickening of the dermis, caused by collagen deposition was present.


Oral Diseases | 2010

Detection of survivin mRNA in healthy oral mucosa, oral leucoplakia and oral cancer.

Giovanni Lodi; R. Franchini; Cristina Bez; Andrea Sardella; Laura Moneghini; C Pellegrini; Silvano Bosari; Maddalena Manfredi; P. Vescovi; Antonio Carrassi

BACKGROUND Survivin is involved in modulation of cell death and cell division processes. Survivin expression in normal adult tissues has not been fully understood, although it is markedly lower than in cancer, where it is over-expressed. OBJECTIVE To investigate survivin expression in normal, potentially malignant and cancerous oral mucosa. METHODS We measured survivin mRNA levels by real-time RT-PCR in specimens of oral mucosa (15 from normal mucosa, 17 from potentially malignant lesions, 17 from neoplasms). Scores were compared using Kruskal-Wallis test and post hoc according to Conover. Chi-squared test was used for dichotomous data. RESULTS The median relative levels of survivin mRNA resulted six for normal mucosa, eight for potentially malignant lesions, 13 for cancers: differences among these three groups were statistically significant, as between cancer and potentially malignant lesions. Expression in normal mucosa and potentially lesions group showed no significant difference. Low, but not marginal expression of survivin in normal mucosa is a new finding, and it could be explained with the higher sensibility of our methods. CONCLUSIONS Survivin expression in oral potentially malignant lesions might indicate a progressive deregulation of expression paralleling oncogenesis, particularly during the first stages of process, suggesting a putative predictive role for survivin.


Journal of The European Academy of Dermatology and Venereology | 2012

Margin involvement and clinical pattern of basal cell carcinoma with mixed histology

Roberto Betti; Giovanni Radaelli; Carlo Crosti; S. Ghiozzi; Laura Moneghini; S. Menni

Background  Mixed basal cell carcinoma (BCC) has not been sufficiently and specifically studied.


Journal of The European Academy of Dermatology and Venereology | 2014

Observational study on the mitotic rate and other prognostic factors in cutaneous primary melanoma arising from naevi and from melanoma de novo

Roberto Betti; R. Santambrogio; Amilcare Cerri; Raffaella Vergani; Laura Moneghini; S. Menni

Melanomas can arise from naevi or appear de novo. The frequency or the effect of their origin on prognosis is still debated. Mitotic rate (MR) and ulceration of melanomas have been proposed as further new prognostic indexes.

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Carlo Crosti

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

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