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  1. Article ; Online: Segmental lichen aureus: an uncommon presentation.

    Torraca, Pedro de Freitas Silva / Murback, Nathalia Dias Negrão / Wiziack, Nayara de Castro / Freitas, Tânia Christina Marchesi de / França, Greicy Mara

    Anais brasileiros de dermatologia

    2017  Volume 92, Issue 5, Page(s) 704–706

    Abstract: Pigmented purpuric dermatoses are chronic vascular inflammatory conditions characterized by the presence of pigmented macules. Among its different presentations, lichen aureus is distinguished by the lichenoid conformation of its plaques and the ... ...

    Abstract Pigmented purpuric dermatoses are chronic vascular inflammatory conditions characterized by the presence of pigmented macules. Among its different presentations, lichen aureus is distinguished by the lichenoid conformation of its plaques and the predilection for lower limb involvement. Its segmented form is rare and difficult to control, especially in cases of symptomatic lesions. We report a rare case of segmental lichen aureus with six years of evolution associated with light itching. We also discuss the main therapeutic approaches to control the disease.
    MeSH term(s) Betamethasone/therapeutic use ; Female ; Glucocorticoids/therapeutic use ; Humans ; Lichenoid Eruptions/pathology ; Lichenoid Eruptions/therapy ; Methoxsalen/therapeutic use ; Middle Aged ; Photosensitizing Agents/therapeutic use ; Sunlight
    Chemical Substances Glucocorticoids ; Photosensitizing Agents ; Betamethasone (9842X06Q6M) ; Methoxsalen (U4VJ29L7BQ)
    Language English
    Publishing date 2017-11-21
    Publishing country Spain
    Document type Case Reports
    ZDB-ID 433655-0
    ISSN 1806-4841 ; 0365-0596
    ISSN (online) 1806-4841
    ISSN 0365-0596
    DOI 10.1590/abd1806-4841.20174781
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 359: Show issues Location:
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    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)
    Zs.MO 344: Show issues

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  2. Article ; Online: Henoch-Schönlein purpura with c-ANCA antibody in an adult.

    Torraca, Pedro de Freitas Silva / Castro, Bruna Corrêa de / Hans, Günter

    Anais brasileiros de dermatologia

    2016  Volume 91, Issue 5, Page(s) 667–669

    Abstract: The Henoch-Schönlein purpura is the vasculitis associated with deposits of immunoglobulin A in small vessels. Its association with cytoplasmic antineutrophil cytoplasmic antibodies is possible, but rare. This vasculitis is uncommon in adults and the main ...

    Abstract The Henoch-Schönlein purpura is the vasculitis associated with deposits of immunoglobulin A in small vessels. Its association with cytoplasmic antineutrophil cytoplasmic antibodies is possible, but rare. This vasculitis is uncommon in adults and the main clinic manifestations are purpuric lesions in lower limbs with gastrointestinal symptoms and renal involvement. The present work describes a rare case of Henoch-Schönlein purpura in an adult with cytoplasmic antineutrophil cytoplasmic antibodies.
    MeSH term(s) Antibodies, Antineutrophil Cytoplasmic/analysis ; Fluorescent Antibody Technique, Direct ; Humans ; Male ; Purpura, Schoenlein-Henoch/diagnosis ; Young Adult
    Chemical Substances Antibodies, Antineutrophil Cytoplasmic
    Language English
    Publishing date 2016-10-25
    Publishing country Spain
    Document type Case Reports
    ZDB-ID 433655-0
    ISSN 1806-4841 ; 0365-0596
    ISSN (online) 1806-4841
    ISSN 0365-0596
    DOI 10.1590/abd1806-4841.20164181
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Cutaneous metastases in a patient with no previous diagnosis of cancer: diagnostic challenge.

    Torraca, Pedro de Freitas Silva / Castro, Bruna Corrêa de / Hans, Günter / Lima, Alexandre Moretti de

    Anais brasileiros de dermatologia

    2017  Volume 92, Issue 5 Suppl 1, Page(s) 47–49

    Abstract: On rare occasions, skin lesions are the first local of metastatic manifestation of internal malignancies. In case of no previous diagnosis of these tumors, the approach of suspicious skin lesions becomes a challenge, especially in differentiating ... ...

    Abstract On rare occasions, skin lesions are the first local of metastatic manifestation of internal malignancies. In case of no previous diagnosis of these tumors, the approach of suspicious skin lesions becomes a challenge, especially in differentiating cutaneous metastases and adnexal primary neoplasms. Currently, besides epidemiologic, dermoscopic and histopathologic aspects, the evaluation also integrates immunohistochemical exams and cell markers such as p40 and p63, highly specific for skin metastases. This article describes the case of cutaneous metastases as the sole obvious sign of breast cancer in a previously asymptomatic woman. The diagnosis was made by the finding of neoplastic cells in the dermis and immunohistochemistry compatible with ductal carcinoma.
    MeSH term(s) Aged, 80 and over ; Breast Neoplasms/pathology ; Carcinoma, Ductal, Breast/secondary ; Diagnosis, Differential ; Female ; Humans ; Immunohistochemistry ; Neoplasms, Adnexal and Skin Appendage/pathology ; Skin/pathology ; Skin Neoplasms/secondary
    Language English
    Publishing date 2017-06-02
    Publishing country Spain
    Document type Case Reports
    ZDB-ID 433655-0
    ISSN 1806-4841 ; 0365-0596
    ISSN (online) 1806-4841
    ISSN 0365-0596
    DOI 10.1590/abd1806-4841.20175870
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 359: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
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  4. Article ; Online: Response of chromoblastomycosis to voriconazole.

    Lima, Alexandre Moretti de / Sacht, Gabriely Lessa / Paula, Lauren Zogbi Pereira de / Aseka, Gabriela Kimie / Goetz, Hermann Soares / Gheller, Maicon Felippe / Torraca, Pedro de Freitas Silva

    Anais brasileiros de dermatologia

    2016  Volume 91, Issue 5, Page(s) 679–681

    Abstract: Chromoblastomycosis is a chronic fungal infection of the epidermis, dermis and subcutaneous tissue, in which the most common etiologic agent in Brazil is Fonsecaea pedrosoi. In more advanced cases we found many difficulties in their treatment, and ... ...

    Abstract Chromoblastomycosis is a chronic fungal infection of the epidermis, dermis and subcutaneous tissue, in which the most common etiologic agent in Brazil is Fonsecaea pedrosoi. In more advanced cases we found many difficulties in their treatment, and therefore, we report a case of extensive and severe chromoblastomycosis, with therapeutical failure of first choice treatments, but good response to voriconazole.
    MeSH term(s) Antifungal Agents/therapeutic use ; Chromoblastomycosis/drug therapy ; Humans ; Male ; Middle Aged ; Treatment Outcome ; Voriconazole/therapeutic use
    Chemical Substances Antifungal Agents ; Voriconazole (JFU09I87TR)
    Language English
    Publishing date 2016-10-25
    Publishing country Spain
    Document type Case Reports
    ZDB-ID 433655-0
    ISSN 1806-4841 ; 0365-0596
    ISSN (online) 1806-4841
    ISSN 0365-0596
    DOI 10.1590/abd1806-4841.20165142
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 359: Show issues Location:
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  5. Article ; Online: Granulomatosis with polyangiitis, a new nomenclature for Wegener's Granulomatosis--Case report.

    Lima, Alexandre Moretti de / Torraca, Pedro de Freitas Silva / Rocha, Sheila Pereira da / Santiago, Carmelia Matos Reis / Ferraz, Fabio Humberto Ribeiro Paes

    Anais brasileiros de dermatologia

    2015  Volume 90, Issue 3 Suppl 1, Page(s) 101–103

    Abstract: The granulomatosis with polyangiitis, initially known as Wegener's granulomatosis, is a small and medium vessels vasculitis. It's classic form presents a triad: necrotizing granuloma of respiratory tract, necrotizing cutaneous vasculitis and ... ...

    Abstract The granulomatosis with polyangiitis, initially known as Wegener's granulomatosis, is a small and medium vessels vasculitis. It's classic form presents a triad: necrotizing granuloma of respiratory tract, necrotizing cutaneous vasculitis and glomerulonephritis. This vasculitis has cytoplasmic antineutrophil antibodies as signal. This work illustrates a case, of multisystemic rare disease, in which the segment and treatment were considered satisfactory for symptoms remission.
    MeSH term(s) Adolescent ; Adrenal Cortex Hormones/administration & dosage ; Facial Dermatoses/drug therapy ; Facial Dermatoses/pathology ; Female ; Granulomatosis with Polyangiitis/drug therapy ; Granulomatosis with Polyangiitis/pathology ; Humans ; Leg Dermatoses/drug therapy ; Leg Dermatoses/pathology ; Necrosis/pathology ; Skin Ulcer/drug therapy ; Skin Ulcer/pathology ; Terminology as Topic
    Chemical Substances Adrenal Cortex Hormones
    Language English
    Publishing date 2015-07-29
    Publishing country Spain
    Document type Case Reports ; Journal Article
    ZDB-ID 433655-0
    ISSN 1806-4841 ; 0365-0596
    ISSN (online) 1806-4841
    ISSN 0365-0596
    DOI 10.1590/abd1806-4841.20153455
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Kategorien

    In stock of ZB MED Cologne/Königswinter

    Zs.A 359: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
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    ab Jg. 2022: Lesesaal (EG)
    Zs.MO 344: Show issues

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