Results 1 to 10 of about 1,366 (167)

Scleromyxedema: clinical diagnosis and autopsy findings [PDF]

Anais Brasileiros de Dermatologia, 2016
Scleromyxedema is a rare chronic cutaneous mucinosis of unknown etiology. It is characterized by papular eruption and scleroderma with microscopic evidence of mucin deposition, fibroblast proliferation, and fibrosis.
Ana Carolina Bulhões Sala, Paulo Rowilson Cunha, Clóvis Antônio Lopes Pinto, Célia Antônia Xavier de Moraes Alves, Ingrid Barreto Paiva, Ana Paula Vieira Araujo   +5 more
doaj   +4 more sources

Clinical Determinants of Urinary Podocyte Biomarkers and Their Feasibility in Paraprotein-Related Kidney Disease [PDF]

Diagnostics
Background/Objectives: Kidney injury is a frequent complication of multiple myeloma (MM) and monoclonal gammopathies. Podocyte stress markers, such as urinary nephrin and podocin, have been studied in other renal diseases but their utility in paraprotein-
Oliver Helk, Ludwig Wagner, Gürkan Sengölge, Thomas Reiter, Daniela Gerges, Hermine Agis, Wolfgang Winnicki   +6 more
doaj   +2 more sources

Xantoma plano difuso normolipêmico idiopático com hiperesplenismo Diffuse plane idiopathic normolipemic xanthoma with hiperesplenism [PDF]

Anais Brasileiros de Dermatologia, 2010
O xantoma plano difuso normolipêmico é doença rara, do grupo das histiocitoses, caracterizada pelo aparecimento de placas amareladas ou amarelo-alaranjadas, distribuídas simetricamente na pele e geralmente acompanhadas por xantelasma.
Danielle Machado da Silva, Jorge João Chacha, Nayara de Castro Wiziack, Luiz Carlos Takita, Fernando Kenzo Hayashi   +4 more
doaj   +2 more sources

Diffuse plane xanthomatosis associated with monoclonal gammopathy Xantomatose plana difusa associada a gamopatia monoclonal [PDF]

Anais Brasileiros de Dermatologia, 2011
Diffuse plane normolipemic xanthomatosis (DPNX) is a rare, non-inherited disease that is often associated with systemic diseases, mainly malignant hematological (especially multiple myeloma) or lymph proliferative disorders.
Aristóteles Rosmaninho, Iolanda Fernandes, Arlindo Guimas, Isabel Amorim, Manuela Selores   +4 more
doaj   +2 more sources

Xantogranuloma necrobiótico solitário sem paraproteinemia Necrobiotic xanthogranuloma without paraproteinemia

Anais Brasileiros de Dermatologia, 2008
O xantogranuloma necrobiótico é doença crônica granulomatosa e xantomatosa, caracterizada por pápulas e placas infiltradas, eritematosas e amareladas, preferencialmente localizadas na região periorbital.
Danielle Mazziero Macedo, Sérgio Henrique Hirata, Nílceo S. Michalany, Mílvia Maria Simões, Silva Enokihara, Mauro Y. Enokihara   +5 more
doaj   +3 more sources

Impact of single versus multiple infection on serum protein fractions in cats. [PDF]

Vet Res Commun
Serum protein electrophoresis (SPE) is a widely used diagnostic tool for identifying acute and chronic inflammation, as well as immunodeficiencies. However, the impact of co-infections on SPE patterns in cats remains poorly understood.
Marteles D, Lebrero ME, Fernández A, Ortín A, González A, Morell C, Villanueva MJ, Schäfer I, Quílez P, Verde M, Gómez A, Villanueva-Saz S.   +11 more
europepmc   +3 more sources

Systemic amyloidosis: an aggressive evolution in a patient with relapsing polychondritis and monoclonal gammopathy of undetermined significance (MGUS) undergoing peritoneal dialysis [PDF]

Autopsy and Case Reports
Herein, we report the case of primary amyloidosis with multi-organ involvement in a female patient in her 50s. The patient had a history of relapsing polychondritis, chronic kidney disease, and monoclonal gammopathy of undetermined significance (MGUS ...
Thiago Cavalcanti Matos, William George Giusti Fischer, Rosa Maria Rodrigues Pereira, Andre Silva Franco   +3 more
doaj   +2 more sources

Caracterización del mieloma múltiple y de su componente monoclonal durante 14 años en Las Tunas [PDF]

Revista Electrónica Dr. Zoilo E. Marinello Vidaurreta, 2015
El mieloma múltiple es una neoplasia de células plasmáticas que representa el 10% de las enfermedades hematológicas malignas. La mayoría de los pacientes presentan síntomas, signos y trastornos de laboratorio sugestivos de enfermedad activa, incluyendo ...
Olga Lina Pupo Rodríguez, María M. Bello Rodríguez, Rogelio Pérez Rivero, Mario C. Vázquez Carmenate   +3 more
doaj   +2 more sources

Dysproteinemia-Associated Kidney Disease: A Single-Center Observational Study [PDF]

Revista Portuguesa de Nefrologia e Hipertensão, 2022
Introduction: Dysproteinemia is associated with kidney damage and treatment of underlying conditions is crucial to minimize kidney damage. The aim of this study was to describe and analyze the characteristics and outcome of the patients diagnosed with ...
João Bernardo, João Oliveira, Filipe Marques, Joana Gameiro, Cristina Outerelo, Estela Nogueira, Sofia Jorge, José António Lopes   +7 more
doaj   +1 more source

Macroglobulinemia de Waldenström: primer caso con confirmación molecular en Honduras [PDF]

Revista Médica Hondureña, 2021
Antecedentes: La Macroglobulinemia de Waldens tröm (MW) es un desorden proliferativo en el cual está presente un Linfoma Linfoplasmocitoide (LLP) en la médula ósea y asociado a una gammapatía monoclonal IgM.
Flora Duarte, Rafael Mojica, Eda Sofía Cálix, Carlos José Fajardo, Abigail Artica, Danilo Alvarado   +5 more
doaj   +1 more source