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Dive into the research topics where Alberto Woscoff is active.

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Featured researches published by Alberto Woscoff.


International Journal of Dermatology | 2000

Prevalence of cutaneous manifestations in 200 patients with eating disorders

Roberto Glorio; Miguel Allevato; Ana B. de Pablo; Mario Abbruzzese; Luz Carmona; Mario Savarin; M Ibarra; Corina I. M Busso; Ana Mordoh; Carolina Llopis; Roxana Haas; Mabel Bello; Alberto Woscoff

Background Eating disorders are increasing and show a variety of symptoms. They mainly include anorexia nervosa (AN), bulimia nervosa (BN), and eating disorders not specified (EDNOS). They predominate in females and represent an important danger, especially in teenagers. In serious cases, they may be life‐threatening.


Journal of The American Academy of Dermatology | 1999

Nevoid keratosis of the nipple

Mariana Xifra; César Lagodín; Dolores Wright; Mario Abbruzzese; Alberto Woscoff

A patient with nevoid keratosis of the nipple is described. The clinical features, histology, therapy, and prognosis are discussed.


International Journal of Dermatology | 1999

Lichenoid secondary syphilis

Sergio Carbia; César Lagodín; Mario Abbruzzese; Luis Sevinsky; Ricardo Casco; José Casas; Alberto Woscoff

Argentina Case 1 A married, heterosexual, promiscuous, 29‐year‐old white man had experienced an asymptomatic eruption on the trunk and left palm for the last 3 months. After 2 months, the trunk involvement disappeared, but 2 weeks later lip and tongue lesions developed. No history of genital ulcer was found.


Clinical Immunology | 2003

Up-regulated expression of MICA and proinflammatory cytokines in skin biopsies from patients with seborrhoeic dermatitis

Luciana Molinero; Mijal Gruber; Juliana Leoni; Alberto Woscoff; Norberto W. Zwirner

Seborrhoeic dermatitis is a disease of unknown etiopathogenesis that affects 5% of the population. In this study, we investigated expression of mRNA for IL-1 alpha, IL-6, IL-4, IFN-gamma, and the stress-inducible MICA molecule in skin biopsies from 12 patients with moderate to severe seborrhoeic dermatitis and 2 healthy volunteers by RT-PCR and hybridization with specific probes. Eight patients expressed INF-gamma, 2 expressed IL-6, 8 expressed IL-1 alpha, and 2 expressed IL-4 (1 with moderate disease). Eight patients expressed inflammatory cytokines (IL-1 alpha, IL-6, and/or IFN-gamma) in healthy skin. Higher cytokine mRNA in damaged vs healthy skin was also observed, suggesting the existence of an inflammation that predisposes healthy skin to develop overt disease. Up-regulated expression of MICA mRNA was observed in 8 patients. Although the pathogenesis of seborrhoeic dermatitis remains to be elucidated, expression of cytotoxicity-activating ligands (MICA), recruitment of NK cells, and a local pro-inflammatory microenvironment may facilitate the development of tissue injury.


Journal of The European Academy of Dermatology and Venereology | 2002

Mycosis fungoides presenting with extensive pyoderma gangrenosum-like ulcers

Sergio Carbia; Adrian Hochman; Myriam Chain; Ignacio Dei-Cas; César Lagodín; Alberto Devés; Alberto Woscoff

Mycosis fungoides (MF) may present with atypical clinical manifestations. Usually it mimics various chronic dermatoses, with the appearance of ulcers during the tumour stage. Infrequently, cutaneous ulcers are the main or initial sign of lymphoma. We report the case of a man who presented multiple skin lesions that clinically appeared to be pyoderma gangrenosum (PG). However, histological and immunohistochemical examination revealed MF. This case illustrates that PG‐like ulcers may be atypical cutaneous manifestations of MF and exceptionally the presenting sign of this disease.


Anais Brasileiros De Dermatologia | 2010

Haga su diagnóstico

Olga Gabriela Pérez; Rodolfo Righetti; Alberto Woscoff; Hugo Amante

A 30-year-old woman developed a slowly progressive reddish-violet multinodular rubbery lesion, measuring 20 x 10 cm in diameter, on the upper outer quadrant of her right breast four years after the surgical excision of a dermatofibrosarcoma protuberans (DFSP) in the same area. The diagnosis of DFSP was confirmed histologically and by positive immunomarkers at immunohistochemistry. A complete excision was performed and after a 2-year follow-up no recurrence was observed. It should be emphasized that DFSP of the breast is a rare occurrence.


International Journal of Dermatology | 2008

Lymphogranuloma venereum: tertiary stage

Luis Sevinsky; Alberto Lambierto; Ricardo Casco; Alberto Woscoff

From the Division of Dermatology, University Hospital, University of Buenos Aires Medical School; and the Sanatorio Otamendi, Buenos Aires, Argentina A 64-year-old, heterosexual white man presented with a 3-year history of lymphedema of the scrotum and penis, purulent discharge from fistulas, and abscess of the perineal and perianal area. The patient had an indolent progression of the disease without systemic manifestations. Twelve years before, the right testis had been totally excised because of an abscess of unknown etiology. Histopathologic examination revealed a chronic nonspecific inflammatory orchitis with abscess formation. The patient and his wife denied a history of sexually transmitted diseases.


Journal of The American Academy of Dermatology | 2004

Cutaneous true histiocytic malignancy: True histiocytic lymphoma

Myriam Chain; Ignacio Dei-Cas; Sergio Carbia; Mariana Xifra; Dolores Wright; Roberto Glorio; Alberto Devés; Alberto Woscoff

True histiocytic malignancies (THM) are controversial disorders that are being re-evaluated with modern cellular and molecular biology techniques. True histiocytic lymphoma (THL) is a low-incidence, poor-prognosis THM. It mainly affects the skin, gastrointestinal tract, and bone tissues. Occasionally, skin lesions are the presenting clinical features. A patient with initially cutaneous THL is described. This and other reported cases confirm that THM are a nosologic entity by themselves.


Anais Brasileiros De Dermatologia | 2003

Pitiríase rósea purpúrica: relato de caso e revisão da literatura

Sergio Carbia; Myriam Chain; Ignacio Dei-Cas; Adrian Hochman; César Lagodín; Alberto Devés; Alberto Woscoff

Purpuric pityriasis rosea is an unusual disease with ten published cases in the American and European literature. The main feature is an hemorrhagic or purpuric eruption with or without scaling. A case is reported of a 25-year-old man with skin lesions affecting the scapular region. The review emphasizes the differential diagnosis of purpuric cutaneous diseases. According to LILACS and MEDLINE, no similar case has been reported in the Latin-American literature.


Archives of Dermatology | 1980

Giant pilar tumor of the scalp.

José Casas; Alberto Woscoff

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Roberto Glorio

University of Buenos Aires

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Sergio Carbia

University of Buenos Aires

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Horacio Cabo

University of Buenos Aires

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León Jaimovich

University of Buenos Aires

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César Lagodín

University of Buenos Aires

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Ignacio Dei-Cas

University of Buenos Aires

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Alberto Devés

University of Buenos Aires

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Luis Sevinsky

University of Buenos Aires

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Adrian Hochman

University of Buenos Aires

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José Casas

University of Buenos Aires

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