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1.
Acta Derm Venereol ; 100(15): adv00249, 2020 Aug 19.
Artículo en Inglés | MEDLINE | ID: mdl-32812055

RESUMEN

Only recently histopathological studies of patients with dermatosis and concomitant SARS-Cov-2 viral infection were published. Seven months into the COVID-19 pandemic, more skin biopsies of COVID-19 positive patients are taking place. We examined the histological features of 30 skin biopsies from two groups of patients: Ten specimens of patients tested positive for COVID-19 with an active systemic infection and associated dermatosis. Twenty specimens were from patients not considered COVID-positive (due to PCR swab negativity or not tested at all) with cutaneous lesions either showing viral infection symptoms (fever, cough, ageusia and severe immunocompromised condition due to HIV infection and malignancies), or presented a high risk of being infected (such as cohabitation with COVID-19 positive parents and siblings with simultaneous chilblains). This study analyses the histological and immunohistochemical (SARS-CoV-2 2019-nCoV nucleocapsid antibody) characteristics of the two groups and identifies 4 histopathological patterns. The histopathological features of the two groups present similar features that may help to identify an ongoing COVID-19 infection even in asymptomatic carriers with dermatosis.


Asunto(s)
Enfermedades Asintomáticas/epidemiología , Técnicas de Laboratorio Clínico/métodos , Infecciones por Coronavirus/diagnóstico , Infecciones por Coronavirus/epidemiología , Neumonía Viral/diagnóstico , Neumonía Viral/epidemiología , Enfermedades de la Piel/patología , Biopsia con Aguja , COVID-19 , Prueba de COVID-19 , Estudios de Cohortes , Comorbilidad , Femenino , Estudios de Seguimiento , Humanos , Inmunohistoquímica , Masculino , Pandemias , Reacción en Cadena de la Polimerasa/métodos , Valores de Referencia , Estudios Retrospectivos , Medición de Riesgo , Índice de Severidad de la Enfermedad , Enfermedades de la Piel/epidemiología , Manejo de Especímenes
2.
BMC Gastroenterol ; 18(1): 1, 2018 Jan 04.
Artículo en Inglés | MEDLINE | ID: mdl-29301491

RESUMEN

BACKGROUND: Pancreatic panniculitis is a rare complication of pancreas disorders occurring in 0.3-3% of patients, most often accompanied by the pancreatic acinar carcinoma. It presents multiple, painful, deep, ill-defined, red-brown, migratory nodules and plaques of hard elastic consistency; often ulcerated and typically located on the lower proximal and distal extremities. The pathogenesis is not fully understood, but it is thought to result from lipolysis and fat necrosis with secondary tissue inflammation induced by pancreatic enzymes. Histopathology shows subcutaneous lobular fat necrosis with anuclear adipocytes (called ghost cells) surrounded by a mixed inflammatory infiltrate. Focal calcification may also be seen. The treatment is directed to the underlying disorder, which may result in regression of skin lesions. CASE PRESENTATION: We present two cases of pancreatic panniculitis with similar clinical, laboratory, and histopathological features associated with different internal malignancy. The first case, after extensive investigations showed the presence of a pancreatic carcinoma with multiple liver metastases and a poor prognosis. The second one instead is the first case in literature where painful subcutaneous nodules of the legs were the early manifestation of a neuroendocrine carcinoma of the adrenal gland. CONCLUSIONS: Although subcutaneous fat necrosis usually occurs late in the course of a malignancy, recognition of the association with pancreatic panniculitis may prevent a long delay in the diagnosis and management of the occult neoplasm. It should be primarily considered when panniculitis is widespread and persistent, and frequent relapses or tendency to ulcerate of the nodules are regarded as red flags.


Asunto(s)
Neoplasias de las Glándulas Suprarrenales/diagnóstico , Carcinoma Neuroendocrino/diagnóstico , Carcinoma/diagnóstico , Enfermedades Pancreáticas/etiología , Neoplasias Pancreáticas/diagnóstico , Paniculitis/etiología , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Lipasa/sangre , Masculino , Enfermedades Pancreáticas/enzimología , Enfermedades Pancreáticas/patología , Paniculitis/enzimología , Paniculitis/patología
3.
Ital J Dermatol Venerol ; 156(1): 68-72, 2021 02.
Artículo en Inglés | MEDLINE | ID: mdl-30251808

RESUMEN

BACKGROUND: CD10, CD271 and Nestin, which are proteins associated with tumor-initiating properties and/or progression potential, have not been specifically studied on malignant melanoma (MM) with cutaneous recurrences. METHODS: We evaluated the expression of CD10, CD271 and Nestin in 27 tumor samples from 16 patients. These tumor samples corresponded to 6 primary melanomas which developed 11 ITM and 10 primary melanomas without recurrences at 10-year follow-up from specimens obtained from surgical excisions of patients referred to the Unit of Dermatology, Department of Medical-Surgical and Transplant Physiopathology, University of Milan, between 2006 and 2016. RESULTS: We demonstrated a higher expression of CD271 and Nestin in primary tumors which recurred than control population, Nestin was expressed with significantly higher percentages in primary tumors than recurrences, and CD10 expression was statistically significant correlated with disease-free survival: cases with a lower score recurred lately than cases with higher scores. CONCLUSIONS: Our preliminary results suggested that CD271 and Nestin can be considered early biomarkers for the development of ITM, Nesting can be useful in differentiating primary MM from cutaneous recurrences and CD10 is associated with a rapid disease progression and may be considered a potential prognostic marker.


Asunto(s)
Melanoma , Neoplasias Cutáneas , Adapaleno , Biomarcadores de Tumor , Humanos , Recurrencia Local de Neoplasia , Neprilisina , Proteínas del Tejido Nervioso , Nestina , Pronóstico , Receptores de Factor de Crecimiento Nervioso
4.
Ital J Dermatol Venerol ; 156(5): 606-609, 2021 10.
Artículo en Inglés | MEDLINE | ID: mdl-33070575

RESUMEN

BACKGROUND: Clear cell morphology has been described in several cutaneous neoplasms either as a specific feature of some entities either as a morphological variant in the spectrum, and these two entities are frequently considered together in the differential diagnosis. METHODS: We reviewed our series of cases occurred in our laboratory in order to further quantify the number of cases showing morphological features of tricholemmal differentiation and to investigate other clinical or histological difference. We retrieved 91 cases and, for each of them, all the clinical data regarding age, sex, clinical features, and clinical suspicious were collected, when available. RESULTS: The revision of the specimens concluded with a final diagnosis of tricholemmal carcinoma in 15 cases (17%), all the other cases were thus considered as squamous cell carcinoma with clear cell features. No statistically significant correlations were observed with the demografic or clinicopatholagical parameters such as age, sex or dimensions, but morphological revision highlighted a potentially greater "vertical" growth frequently not matched by a concomitant radial one in tricholemmal carcinoma than in squamous tumors. CONCLUSIONS: The debate upon the diagnostic distinction of these tumors is still ongoing with authors proposing the tricholemmal carcinoma as a variant of a squamous cell carcinoma rather than a distinct entity. Further studies are needed to confirm our data and to evaluate the reproducibility of this feature.


Asunto(s)
Carcinoma de Células Escamosas , Neoplasias Cutáneas , Diagnóstico Diferencial , Humanos , Reproducibilidad de los Resultados , Neoplasias Cutáneas/diagnóstico
5.
Appl Immunohistochem Mol Morphol ; 27(6): 430-435, 2019 07.
Artículo en Inglés | MEDLINE | ID: mdl-30212379

RESUMEN

Spindle or epithelioid melanocytic (Spitz) nevi usually affect children or adolescents and growth in the face or the lower extremities. Histologically, they may show cytoarchitectural atypia and mitotic figures that could represent diagnostic pitfalls with malignant melanoma. Atypical spitzoid tumors (AST) indicate lesions that microscopically show intermediate characteristics between benign nevi and malignant melanoma. Nestin expression has been evaluated in benign nevi and malignant melanoma, but no studies on its role in Spitz lesion have been elaborated so far. Our results indicate that Nestin could allow to discriminate between AST and malignant spiztoid melanoma; the typical dermoscopic pattern is also associated with benign nevi in contrast to the atypical pattern that accumunates AST and malignant spitzoid melanoma.


Asunto(s)
Dermis/patología , Melanoma/metabolismo , Nestina/metabolismo , Nevo de Células Epitelioides y Fusiformes/metabolismo , Neoplasias Cutáneas/metabolismo , Adolescente , Adulto , Niño , Preescolar , Diagnóstico Diferencial , Femenino , Regulación Neoplásica de la Expresión Génica , Humanos , Inmunohistoquímica , Lactante , Masculino , Melanoma/diagnóstico , Persona de Mediana Edad , Nestina/genética , Nevo de Células Epitelioides y Fusiformes/diagnóstico , Neoplasias Cutáneas/diagnóstico , Adulto Joven
6.
Int J STD AIDS ; 29(14): 1454-1456, 2018 12.
Artículo en Inglés | MEDLINE | ID: mdl-30170530

RESUMEN

We report a case of secondary syphilis mimicking lupus vulgaris in an HIV-infected patient. A 21-year-old Brazilian man presented with a two-month history of asymptomatic cutaneous lesions accompanied by fever and fatigue. Dermatological evaluation revealed an erythematous, crusted, large plaque on the neck with the 'apple jelly' sign on diascopy and two smaller scaly elements on the trunk and left palm. Bacteriological examinations for bacteria and mycobacteria gave negative results. Histology revealed psoriasiform epidermal hyperplasia and dermal lymphoplasmacytic infiltrate. Serology for syphilis was positive, and immunohistochemistry confirmed the presence of Treponema pallidum in lesional skin. A diagnosis of secondary syphilis was made, and the patient was successfully treated with benzathine penicillin G. Cutaneous manifestations of secondary syphilis are protean and skin tuberculosis may be considered in the differential diagnosis, especially in HIV-infected patients. In the current case, clinical examination, and particularly, 'apple jelly' sign positivity, was suggestive of lupus vulgaris, but only typical histopathology and immunohistochemistry led to the correct diagnosis of secondary syphilis.


Asunto(s)
Antibacterianos/uso terapéutico , Infecciones por VIH/tratamiento farmacológico , Lupus Vulgar/diagnóstico , Penicilina G Benzatina/administración & dosificación , Sífilis/tratamiento farmacológico , Treponema pallidum/aislamiento & purificación , Bisexualidad , Diagnóstico Diferencial , Humanos , Inyecciones Intramusculares , Masculino , Penicilina G Benzatina/uso terapéutico , Sífilis/diagnóstico , Sífilis/patología , Resultado del Tratamiento , Treponema pallidum/inmunología , Adulto Joven
8.
Eur J Dermatol ; 27(6): 609-614, 2017 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-29160213

RESUMEN

BACKGROUND: Cutaneous metastases represent 2% of all skin tumours. Their recognition can be challenging, as they may present with different clinical features, with consequent frequent delay and failure in diagnosis. OBJECTIVES: To review our series of cutaneous metastatic lesions, analyse their frequency according to patient gender, histotype, localization of the primary tumour, and site of cutaneous metastasis, and correlate this data with clinicopathological parameters. MATERIALS & METHODS: We conducted a retrospective review of all cases of cutaneous metastases from visceral neoplasms diagnosed in our dermatopathology department from July 2003 to February 2017. We registered clinical, histological, and immunohistochemical data. Additional immunohistochemical staining panels were elaborated to confirm or identify the origin of the primary tumour, or at least to specify the histological subtype. RESULTS: We identified 45 histological diagnoses of cutaneous and mucocutaneous metastases. The primary tumour that was most likely to metastasize to the skin was breast cancer. Most cases of breast (89%) and lung cancer (86%) metastasized to the trunk. Of the lesions, 57.5% were nodules and 32.5% were plaques, more frequently multiple (64.4%). In 58% of cases, a metastasis was clinically suspected. Histological examination most frequently revealed an adenocarcinoma, sometimes suggestive of the site of origin. CONCLUSIONS: Cutaneous metastases should be primarily considered when discrete firm painless nodules emerge rapidly. Clinicians should carefully consider infiltrated lesions of the chest in women since scleroderma and erysipelas-like presentation can be a clue for undiagnosed breast cancer.


Asunto(s)
Neoplasias Cutáneas/secundario , Adenocarcinoma , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Biomarcadores de Tumor/análisis , Neoplasias de la Mama/patología , Femenino , Humanos , Inmunohistoquímica , Neoplasias Intestinales/patología , Neoplasias Pulmonares/patología , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Factores Sexuales , Neoplasias Cutáneas/epidemiología , Neoplasias Cutáneas/patología , Neoplasias Gástricas/patología , Adulto Joven
9.
An Bras Dermatol ; 90(3 Suppl 1): 200-2, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26312716

RESUMEN

We present the rare case of a 47-year-old patient, suffering from cheilitis granulomatosa and lupus erythematosus discoid: this association is really exceptional because only once reported in English literature. In addition, the treatment of cheilitis granulomatosa is a challenge for the dermatologist: the gold standard, represented by steroids, is in fact designed as a short-time option. Our report confirms the good efficacy of methotrexate as a steroid-sparing agent.


Asunto(s)
Fármacos Dermatológicos/uso terapéutico , Lupus Eritematoso Discoide/tratamiento farmacológico , Síndrome de Melkersson-Rosenthal/tratamiento farmacológico , Metotrexato/uso terapéutico , Biopsia , Dermis/patología , Humanos , Labio/patología , Lupus Eritematoso Discoide/patología , Masculino , Síndrome de Melkersson-Rosenthal/patología , Persona de Mediana Edad , Resultado del Tratamiento
10.
An Bras Dermatol ; 90(4): 577-9, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26375231

RESUMEN

Atypical fibroxanthoma is an uncommon mesenchymal tumor that manifests clinically as a reddish papule or nodule in sun-exposed areas of the body. The clinical presentation is not specific and histology and immunohistochemistry are both necessary for a correct diagnosis. Surgery is the gold standard of therapy. Recurrence and metastasis should be excluded with a follow-up at 6 months, since this tumor should nowadays be considered a medium-grade neoplasm, rather than low-grade as previously believed. We report the case of two friends who came to our hospital during the same period, complaining of very similar lesions. After biopsy and immunohistochemical examination, a diagnosis of atypical fibroxanthoma in both cases was formulated.


Asunto(s)
Pabellón Auricular/patología , Neoplasias del Oído/patología , Fibroma/patología , Neoplasias Cutáneas/patología , Xantomatosis/patología , Anciano , Biopsia , Diagnóstico Diferencial , Amigos , Humanos , Inmunohistoquímica , Masculino
12.
An. bras. dermatol ; 90(3,supl.1): 200-202, May-June 2015. ilus
Artículo en Inglés | LILACS | ID: lil-755732

RESUMEN

Abstract

We present the rare case of a 47-year-old patient, suffering from cheilitis granulomatosa and lupus erythematosus discoid: this association is really exceptional because only once reported in English literature. In addition, the treatment of cheilitis granulomatosa is a challenge for the dermatologist: the gold standard, represented by steroids, is in fact designed as a short-time option. Our report confi rms the good efficacy of methotrexate as a steroid-sparing agent.

.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Fármacos Dermatológicos/uso terapéutico , Lupus Eritematoso Discoide/tratamiento farmacológico , Síndrome de Melkersson-Rosenthal/tratamiento farmacológico , Metotrexato/uso terapéutico , Biopsia , Dermis/patología , Labio/patología , Lupus Eritematoso Discoide/patología , Síndrome de Melkersson-Rosenthal/patología , Resultado del Tratamiento
13.
An. bras. dermatol ; 90(4): 577-579, July-Aug. 2015. ilus
Artículo en Inglés | LILACS | ID: lil-759206

RESUMEN

AbstractAtypical fibroxanthoma is an uncommon mesenchymal tumor that manifests clinically as a reddish papule or nodule in sun-exposed areas of the body. The clinical presentation is not specific and histology and immunohistochemistry are both necessary for a correct diagnosis. Surgery is the gold standard of therapy. Recurrence and metastasis should be excluded with a follow-up at 6 months, since this tumor should nowadays be considered a medium-grade neoplasm, rather than low-grade as previously believed. We report the case of two friends who came to our hospital during the same period, complaining of very similar lesions. After biopsy and immunohistochemical examination, a diagnosis of atypical fibroxanthoma in both cases was formulated.


Asunto(s)
Anciano , Humanos , Masculino , Pabellón Auricular/patología , Neoplasias del Oído/patología , Fibroma/patología , Neoplasias Cutáneas/patología , Xantomatosis/patología , Biopsia , Diagnóstico Diferencial , Amigos , Inmunohistoquímica
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