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R Gianotti

Publications and source records attributed to R Gianotti.

At least 19 recordsLinked to original sources
PubMed1992

Morphometric study of primary cutaneous germinal center cell lymphomas.

BACKGROUND: Primary cutaneous germinal center cell lymphomas (PCGCCL) are B-cell neoplasias; most are mixed cell type, composed of small and large cleaved cells and large noncleaved cells (centrocytes and centroblasts). Because of the significant pleomorphism of the cells, which ranged in size from small elements with indented nuclei to larger ones with multilobulated vesiculous nuclei, histopathologic examination of PCGCCL of mixed cell type has the worst degree of histologic interobserver reproducibility. METHODS: In this study, the authors determined whether the light microscopic morphologic classification criteria applied in quantifying cleaved and noncleaved cells in these lymphomas are substantiated by morphometric analysis and have good reproducibility in differentiating the various cell subsets. They used an image analyzer (IBAS 2000, Zeiss Kontron, Munich, Germany) to study 17 centroblastic/centrocytic and centroblastic follicular and/or diffuse primary cutaneous lymphomas. RESULTS: The data obtained showed morphometric differences between the follicular and diffuse patterns of neoplastic cells. In follicular neoplasms, the cells tend to be smaller, more cleaved, and more monomorphic than those observed in the diffuse forms. In all the follicular and diffuse cases, the authors observed a unimodal population with a wide peak composed of cells with intermediate morphometric features that cannot be labeled properly. CONCLUSIONS: These data underline the considerable overlap of nuclear parameters of lymphocytes between the subtypes of cells in cutaneous mixed small and large cell lymphoma, making the Kiel classification and Working Formulation unsuitable for this kind of neoplasia and supporting revision of classification criteria in cutaneous germinal center cell lymphomas.

Adult↗
PubMed1991

Primary cutaneous pleomorphic T-cell lymphoma expressing CD30 antigen.

Pleomorphic peripheral T-cell lymphomas (PPTL) arising primarily in the skin are uncommon. The observation of pleomorphic T-cell lymphoma composed of 100% CD30+ cells is rare. We report the case of a woman in whom such a tumor manifested itself with a single cutaneous lesion. It was composed of medium to large cells expressing markers of helper/inducer T-lymphocytes, as well as activation (CD30) and proliferation antigens (Ki-67), but not the CD25 activation antigen. The lesion was excised and the patient is alive and disease free 2 years after the diagnosis. This case confirms previous reports about the favorable course of some cutaneous pleomorphic lymphomas, and shows that the activation antigen expression and proliferation antigen (Ki-67) expression do not seem to worsen the prognosis.

Antigens, CD↗
PubMed1990

Papular xanthoma in children.

Papular xanthoma is a normolipemic xanthomatosis that mainly affects adults. We describe the clinical, histologic, ultrastructural, and immunologic findings in 10 children with this disease. Papular xanthoma in children has the same clinical and histopathologic features as in adults, but it appears to be self-healing within 1 to 5 years.

Age Factors↗
PubMed1990

[Eosinophilic cellulitis (Wells' syndrome)].

The Authors report a case of eosinophilic cellulitis (Wells' syndrome). The patient was a 61 year old woman, diabetic, with a cardio-respiratory insufficiency and a maniaco-depressive psycosis. She presented, on the upper arms and trunk, a cutaneous eruption of erythematous-urticarial plaques, that histopathologically were characterized by a dermic leukocyte population, with a prevalence of eosinophils, distributed in the perivascular site. Laboratory tests revealed eosinophilia and circulating immune complexes. The etiopathogenesis of the disease is discussed as is the possible role of immune complexes in eosinophilic cellulitis.

Cellulitis↗
PubMed1990

[Normolipemic plane xanthomas and IgG-k multiple myeloma. Description of a clinical case].

The Authors describe the case of a woman affected by generalized plane xanthoma and IgG multiple myeloma with k type immunoglobulins. The association between the two affections is well known. The antilipoprotein activity of the paraprotein has been proved in some cases, associated or not to hyperlipemia. The pathogenetic mechanism of plane xanthoma formation is described briefly. The possible occurrence of plane xanthoma with multiple myeloma is stressed, along with the possible association with other systemic diseases.

Aged↗
PubMed1990

[Atenolol-induced psoriasiform dermatitis].

We report the case of a patient who presented a psoriasiform dermatitis after 8 months of atenolol therapy. Regression of the lesions was obtained after suspension of therapy. To our knowledge, few reports of psoriasiform dermatitis induced by atenolol are present in the literature. The Authors briefly discuss the pathogenesis of this drug induced disease.

Atenolol↗
PubMed1990

[Hidradenoma of the external acoustic meatus: ceruminoma].

Benign tumour originating from the ceruminous glands of the external auditory meatus are quite rare and present similar histological features to sweat gland tumours elsewhere. The paper reports the case of a nodule in the external auditory meatus diagnosed as a myoepitheliomatous-type hidradenoma . Three histological forms of benign ceruminous gland tumours are recognised: the myoepitheliomatous, cribriform and mixed salivary type. Currently, the term hidradenoma of the external ear is preferred.

Adenoma, Sweat Gland↗
PubMed1989

Clonal immunoglobulin gene rearrangements and normal T-cell receptor, bcl-2, and c-myc genes in primary cutaneous B-cell lymphomas.

Fourteen cases of primary cutaneous B-cell lymphomas were investigated at the immunohistochemical and molecular level to further characterize this newly defined entity. Neoplastic cells from all cases, phenotyped with a panel of monoclonal antibodies, were positive for HLA-DR, for the B-cell markers CD19, CD22, but not CD23 (except one case), and negative for the T-cell marker CD2. Monoclonal immunoglobulin light chains were demonstrated in six cases. The reactivity with the Ki-67 monoclonal antibody indicated that the neoplastic cells are proliferating. In five biopsies the presence of dendritic cells infiltrating the neoplastic areas was revealed using the monoclonal antibody Kim4b. By Southern blot analysis, clonal rearrangement of the immunoglobulin heavy chain gene (involving one or both alleles) was shown in 12 of 14 cases and of the light chain genes in 13 cases. The bcl-2 oncogene, normally involved in nodal follicular lymphomas, was in germ-line configuration. The c-myc and the beta and gamma chain genes of the T-cell receptor were also in the germ-line configuration. None of the cases presented Epstein-Barr virus sequences. These data indicate that primary cutaneous lymphomas of B-cell origin share morphological and phenotypic similarities with the nodal B-cell lymphomas of follicular histotype, are proliferating, and express in 45% of cases clear monoclonal immunoglobulin light chain; the molecular analysis confirms the B-cell derivation and the monoclonal nature of this neoplasia; it also shows that neither bcl-2 nor c-myc oncogenes are involved and that no inappropriate rearrangements of the T-cell receptor genes are found in this lymphoma.

Adult↗
PubMed1989

Primary anaplastic large cell lymphoma of the skin.

Anaplastic large cell lymphoma is a subtype of nodal and extranodal lymphoproliferative disorder characterized by peculiar histopathological features and the positivity of lymphoid proliferating cells for Ki-1/Ber-H2 monoclonal antibody. A case, misdiagnosed as cutaneous metastasis and treated by surgery, in a woman with a history of previous neoplasms, is reported. In spite of the histopathological malignancy of the tumor, the patient is alive and free from recurrent or metastatic disease after 3 years of follow-up.

Aged↗
PubMed1988

Reticulohistiocytoma of the dorsum.

To clarify the nature of reticulohistiocytoma of the dorsum, 19 cases, including three of the seven original cases described by Crosti, were evaluated clinically, histologically, and immunologically. In seven cases gene rearrangement analysis was also performed. Results indicate that reticulohistiocytoma of the dorsum must be considered a primary cutaneous B cell lymphoma of follicular center cell origin. This localized skin disease has a very slowly progressive course, with many patients showing no systemic involvement even after prolonged follow-up.

Adult↗
PubMed1988

Cutaneous manifestations of tetrachlorodibenzo-p-dioxin in children and adolescents. Follow-up 10 years after the Seveso, Italy, accident.

After an accident in a chemical plant in Seveso, Italy, on July 10, 1976, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) spread over a populated area. The event was exceptional because children were also affected and because the contamination took place not only through direct exposure but also through inhalation and the ingestion of contaminated foods, especially fruits and vegetables. This paper illustrates the early dermatologic lesions, the late acneic (chloracne) lesions, and their evolution during a 10-year period. Peculiar cutaneous findings, histologic data, and a comparison with previously reported similar accidents are also included.

Accidents, Occupational↗
PubMed1988

Unusual cutaneous histiocytosis expressing an intermediate immunophenotype between Langerhans' cells and dermal macrophages.

Cutaneous histiocytosis was discovered in a 40-year-old man with a slow-growing nodule located on his right arm. Histologic findings showed an epidermotropic infiltrate of histiocytes with folded, irregular nuclei. Immunologically, the cells presented an intermediate phenotype between Langerhans' cells and dermal macrophages. After surgical removal of the lesion, neither a relapse nor visceral involvement was observed during two years of follow-up.

Adult↗