Livros e Capítulos de Livros - LIM/56

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A coleção de Livros e Capítulos de Livros reúne capítulos e resumos de obras produzidas por autores do sistema FMUSP-HC que inclui a Faculdade de Medicina da Universidade de São Paulo (FMUSP), o Hospital das Clínicas da FMUSP e demais institutos associados.

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  • bookPart 0 Citação(ões) na Scopus
    Dermatological Manifestations
    (2023) CURY-MARTINS, J.; SANCHES, J. A.
    Cutaneous involvement by amyloidosis is characterized by extracellular deposition of amyloid protein within the skin and appendages and can occur as a skin-limited disorder (localized cutaneous amyloidosis—LCA) or as a manifestation of systemic amyloidosis (SA). LCA can be divided into primary LCA—macular, lichen and nodular amyloidosis; or secondary LCA. The main subtypes of SA with cutaneous involvement include immunoglobulin light chain (AL) amyloidosis, secondary (AA) amyloidosis, dialysis-related amyloidosis, and heredofamilial amyloidosis. Skin involvement is present, for example, in approximately 40% of patients with AL amyloidosis, and might provide an early clue to the existence of an underlying plasma-cell dyscrasia. © The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG 2023.
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    Apresentação
    (2019) FESTA NETO, Cyro; CUCé, Luiz Carlos; REIS, Vitor Manoel Silva dos
  • bookPart
    Erros inatos da imunidade
    (2023) DUARTE, Alberto José da Silva; VASCONCELOS, Dewton de Moraes; SANTOS, Andréia Rangel; SUMITA, Nairo Massakazu; CARNEIRO-SAMPAIO, Magda
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    Introdução à patologia clínica aplicada à pediatria
    (2023) ANDRIOLO, Adagmar; SLHESSARENKO, Natasha; SUMITA, Nairo Massakazu; DUARTE, Alberto José da Silva
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  • bookPart
    Apresentação
    (2023) CARNEIRO-SAMPAIO, Magda; SILVA, Clovis Artur Almeida da; GOMES, Filumena Maria da Silva; SLHESSARENKO, Natasha; SUMITA, Nairo Massakazu; DUARTE, Alberto José da Silva
  • bookPart 0 Citação(ões) na Scopus
    Tinea capitis
    (2021) ROMITI, R.; ANZAI, A.
  • bookPart 0 Citação(ões) na Scopus
    Nail disorders in diabetics
    (2018) CERVANTES, J.; LAMAS, A. P.; LENCASTRE, A.; Sá, D. C. de; TOSTI, A.
  • bookPart 0 Citação(ões) na Scopus
    Zika virus in Brazil
    (2021) NASCIMENTO, A.; DUARTE, A. J. S.; SANABANI, S. S.
    Zika virus (ZIKV) is a newly emerging arbovirus belonging to the family Flaviviridae and is transmitted to humans by Aedes species mosquitoes. In March 2015, certain regions in the northeast of Brazil were hit particularly hard by an outbreak of rash illness and mild and self-limiting febrile disease; soon, the etiological agent was identified as ZIKV infection. The virus has since spread and touched nearly every corner of the country. Shortly after the initiation of the epidemic, some reports have suggested that ZIKV infection can cause serious sequelae such as microcephaly in newborns of mothers infected with the virus during pregnancy, other congenital abnormalities, fetal death, as well as neurologic complications such as Guillain-Barré syndrome. It is anticipated that ZIKV will continue to spread, particularly in tropical and subtropical regions. The purposes of this chapter are to cover various aspects such as the historical background and current knowledge related to ZIKV infection in Brazil. © 2021 Elsevier Inc. All rights reserved.
  • bookPart 0 Citação(ões) na Scopus
    Elastosis perforans serpiginosa
    (2016) SAMORANO, L.; PIMENTEL, E. R. De Almeida; NICO, M. M. S.
    Elastosis perforans serpiginosa is an uncommon and chronic dermatosis characterized by transepidermal elimination of abnormal elastic fibers originating in the dermis. Diagnosis is based on clinical and histopathologic aspects. Treatment has included various modalities and cryotherapy is one of the effective options. Favored method includes the use of open spray timed spot freeze technique and one to two sessions are usually enough to treat some grouped papules. © Springer-Verlag London 2016. All rights reserved.
  • bookPart 0 Citação(ões) na Scopus
    Pemphigus Foliaceus and Endemic Forms
    (2015) JAMES, K. A.; AOKI, V.; DIAZ, L. A.
    Autoimmune bullous diseases are a heterogeneous group of diseases also in terms of epidemiological characteristics. Recent high-quality epidemiological studies have provided valuable new knowledge in this area. It has become clear that the incidence of bullous pemphigoid in Central Europe has at least doubled over the last decade and that incidences of the different autoimmune diseases vary considerably between geographical regions. The increased mortality risk as well as the association with neurological diseases in patients with bullous pemphigoid has been highlighted in several studies, raising the intriguing question about the link between the neurological and skin diseases in affected patients. © Springer-Verlag Berlin Heidelberg 2015.
  • bookPart 0 Citação(ões) na Scopus
    Pemphigus foliaceus, var. Herpetiformis and Sulphonamide
    (2015) AOKI, V.; MIYAMOTO, D.
    A 43-year-old woman presented a 2-year history of tender blisters and erythematous and crusted excoriations on the face, trunk and proximal extremities. During her first examination in 1995, erosions and yellow crusts on her face, thorax, upper torso and proximal limbs were present, without mucosal involvement. Laboratory profile confirmed the diagnosis of pemphigus foliaceus, as follows: histopathological analysis exhibited subcorneal abscess with mild spongiosis and scanty acantholytic cells; neutrophilic and linfohystiocitic perivascular infiltrate was present in the superficial dermis; direct immunofluorescence showed intercellular IgG deposits within the entire epidermis; indirect immunofluorescence revealed circulating IgG antibodies (titer=1:1,280) and positive ELISA index (99, recombinant desmoglein 1). Treatment with systemic corticosteroid (prednisone 1 mg/kg/day) was initiated. Clinical remission was achieved after 2 months, followed by gradual corticosteroid tapering. The patient presented reactivation when receiving prednisone 10 mg/day, with vesicles with a herpetiform arrangement on erythematous plaques on her legs, with intense pruritus (Fig. 13.1). © Springer International Publishing Switzerland 2015.
  • bookPart
    Vasculites cutâneas na infância
    (2022) YENDO, Tatiana Mina
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    Hipercromias
    (2022) GORDILHO, Juliana Olivieri; MEDEIROS, Marcella Palhano; MIYAMOTO, Denise
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    Erupções paravirais
    (2022) YENDO, Tatiana Mina; SANTI, Claudia Giuli
  • bookPart
    Hipocromias e acromias
    (2022) MEDEIROS, Marcella Palhano; GORDILHO, Juliana Olivieri; MIYAMOTO, Denise
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    Manifestações cutâneas de doenças infecciosas congênitas
    (2022) YENDO, Tatiana Mina; MACHADO, Maria Cecilia da Matta Rivitti
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    Anomalias vasculares
    (2022) SAMORANO, Luciana de Paula; ROTTER, Anita
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    Dermatoses do recém-nascido
    (2022) BESSA, Vanessa Rolim; SAMORANO, Luciana de Paula; OLIVEIRA, Zilda Najjar Prado de
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    Afecções fisiológicas da pele do recém-nascido
    (2022) BESSA, Vanessa Rolim; SAMORANO, Luciana de Paula; OLIVEIRA, Zilda Najjar Prado de