Zobrazeno 1 - 10
of 101
pro vyhledávání: '"M Giangiacomi"'
Publikováno v:
Dermatologic therapy. 29(5)
Granuloma faciale (GF) is a rare chronic inflammatory dermatosis of unknown etiology, characterized by leukocitoclastic vasculitis usually occurring on the face. We report a case of 60-years-old man with 3 year history of multiple actinic keratoses (
Publikováno v:
Digestive and Liver Disease. 48:e195-e196
Publikováno v:
British Journal of Dermatology. 146:877-881
We report a 22-year-old woman who developed systemic lupus erythematosus (SLE) immediately after an Epstein-Barr virus (EBV)-induced mononucleosis infection. The link between these two conditions has long been suspected. The close temporal relationsh
Autor:
G, Ganzetti, A, Campanati, O, Simonetti, K, Giuliodori, M, Giangiacomi, G, Lemme, A, Offidani
Publikováno v:
Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia. 150(4)
Toxic epidermal necrolysis (TEN), also known as Lyell syndrome, is a potential life-threatening muco-cutaneous disease with important systemic implications. It affects the skin and mucous membranes, with involvement of more than 30% of body surface a
Publikováno v:
Dermatology. 195:289-292
Lymphoblastic lymphoma (LBL) is a neoplasm of lymphoid precursors presenting usually as acute leukemia with bone marrow and peripheral blood involvement. Primary cutaneous involvement of LBL with a pre-B phenotype has to be considered an extremely un
Publikováno v:
Digestive and Liver Disease. 46:S69-S70
Publikováno v:
British Journal of Dermatology. 143:675-677
Autor:
Oriana Simonetti, M. Giangiacomi, A. M. Offidani, Maria Luisa Bernardini, Bossi G, C. Simoncini
Publikováno v:
British Journal of Dermatology. 143:675-677
Publikováno v:
Annals of the Rheumatic Diseases. 74:1221.3-1222
Background Pigmented Villonodular synovitis (PVNS) is a rare disease in children. The treatment of choice is the synovectomy, which nevertheless often results in joint function impairement, especially in pediatric subjects in which more frequently it
Publikováno v:
Lupus. 12(1)
We report on a case of 40-year-old female with systemic lupus erythematosus (SLE) who developed a severe bullous eruption on sun-exposed areas. The bullous manifestation was associated with a flare of lupus serologies, whereas the previous manifestat