Results 21 to 30 of about 1,068 (155)

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

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   +1 more source

Recurrence of membranoproliferative glomerulonephritis post transplant – Is this mere recurrence of pattern or recurrence of disease?

Saudi Journal of Kidney Diseases and Transplantation, 2019
Recurrence of membranoproliferative glomerulonephritis (MPGN) is seen in 1965% cases of postrenal transplant resulting in graft loss in up to 35-50% of cases.
Umesh Lingaraj, Shivanagouda Ramanagouda Patil, Kishan Aralapuram, Shivaprasad Sasivehalli Mallappa, Sreedhara Chikkanayakanahalli Gurusiddaiah, Mahesha Vankalakunti   +5 more
doaj   +1 more source

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

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   +1 more source

ESCLEREDEMA DE BUSCHKE – A propósito de um caso clínico

Galicia Clínica, 2017
RESUMO: O Escleredema de Buschke (EB) é uma doença rara do tecido conjuntivo, de etiologia desconhecida, caracterizada por espessamento e endurecimento da pele, geralmente localizado nas regiões proximais e posteriores do tronco e pescoço.
Jorge Henriques, Paulo Almeida, Ana Araújo, Susana Cavadas   +3 more
doaj   +1 more source

Clinical observation of monoclonal fibrillary glomerulonephritis

Вестник медицинского института «Реавиз»: Реабилитация, врач и здоровье
Monoclonal gammopathy of renal significance is a condition caused by the proliferation of a clone of B-lymphocytes or plasma cells that does not reach the criteria required for the initiation of treatment for oncohematological indications, but is ...
T. A. Garkusha, F. V. Alyab'ev, T. A. Vdovik   +2 more
doaj   +1 more source

Nefropatía no amiloidea por depósito de inmunoglobulinas monoclonales A propósito de un caso de enfermedad idiopática por depósito de cadenas ligeras

Biomédica: revista del Instituto Nacional de Salud, 2009
La nefropatía de las gammapatías monoclonales es debida, principalmente, al depósito de cadenas ligeras. Las enfermedades renales paraproteinémicas son lesiones asociadas con depósitos de inmunoglobulinas intactas o fragmentos de inmunoglobulinas ...
Jorge de Jesús Cantillo, Rocío del Pilar López, Rafael Enrique Andrade   +2 more
doaj   +1 more source

Bone Marrow Pathology in Cold Agglutinin‐Mediated Autoimmune Hemolytic Anemia: A Study of 56 Cases

European Journal of Haematology, EarlyView.
ABSTRACT Cold agglutinin disease (CAD) is a rare form of autoimmune hemolytic anemia (AIHA). CAD occurs in the context of a small clonal B‐cell lymphoproliferation restricted to blood and/or bone marrow (BM), without overt or extramedullary lymphoma. The WHO‐HAEM5 introduced a description of the CAD‐associated lymphoproliferative disorder (CAD‐LPD) in ...
Anne‐Marie L. Becking, Sophie J. Bernelot Moens, Marie José Kersten, Femke V. M. Mulder, Steven T. Pals, Lianne Koens, Josephine M. I. Vos   +6 more
wiley   +1 more source

Mieloma múltiple de novo post-trasplante renal manifestado inicialmente con disfunción del injerto. Reporte de 3 casos y revisión de la literatura

Biomédica: revista del Instituto Nacional de Salud, 2016
El compromiso renal por cadenas ligeras es frecuente en el contexto de las gammapatías monoclonales, afectando los glomérulos o los túbulos renales y siendo el mieloma múltiple la causa más común; puede desarrollarse posterior a un trasplante renal por ...
John Fredy Nieto, Monica Zuluaga, Lina Maria Serna, Arbey Aristizábal, Catalina Ocampo, Kenny Mauricio Galvez, Adriana Alejandra Flórez, Gustavo Zuluaga   +7 more
doaj   +1 more source

Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): A Comprehensive Review of Types, Pathophysiology, and Treatment Approaches

Brain and Behavior, Volume 16, Issue 5, May 2026.
Chronic inflammatory demyelinating polyneuropathy is an autoimmune disorder causing demyelination, leading to distal weakness, sensory loss, and autonomic dysfunction. Immune activation triggers macrophage‐mediated myelin damage and conduction failure.
Ayesha Khan, Arsal Khan, Kuldeep Dalpat Rai, Anzel Saeed, Harsh Kumar, Aneesh Kumar Sangtiani, Tehreem Fatima, Muhammad Tanveer Alam, Faiza Rajput, Sakshi Chawla, Hussain Haider Shah, Humaira Kalam   +11 more
wiley   +1 more source

Low Dose Pegylated Interferon Alpha as a First‐Line Treatment for Necrobiotic Xanthogranuloma

JEADV Clinical Practice, Volume 5, Issue 1, Page 215-218, March 2026.
ABSTRACT Necrobiotic xanthogranuloma (NXG) is a rare, progressive granulomatous disorder frequently associated with monoclonal gammopathy, particularly monoclonal gammopathy of undetermined significance (MGUS). It typically presents with indurated to ulcerative yellowish plaques or nodules, often with ocular involvement.
Ishana Dixit, Charmaine Vanessa S. Chamberlin, Pablo Fernandez‐Peñas   +2 more
wiley   +1 more source