Results 11 to 20 of about 1,385 (185)
Hospitalisations With Cryoglobulin-Related Diseases in Spain Over 25 Years. [PDF]
Liver IntABSTRACT Background The epidemiology of cryoglobulinemia in Spain has likely changed following the widespread adoption of direct‐acting antivirals (DAAs) since 2015 for the treatment of hepatitis C virus (HCV) infection, the principal cause of mixed cryoglobulinemia (MC).
Martín-Portugués M +9 more
europepmc +2 more sources
Aspirin Versus LMWH for Thromboprophylaxis Following Hip or Knee Arthroplasty-Clinical Implications and Budget Impact. [PDF]
Pharmacol Res PerspectPRISMA flow diagram for a systematic review of RCTs that compared aspirin versus LMWH for thromboprophylaxis following hip or knee arthroplasty. ABSTRACT Venous thromboembolism (VTE) remains a significant concern for patients undergoing hip or knee arthroplasty, with a need to balance effective thromboprophylaxis and bleeding risk.
Javor E +7 more
europepmc +2 more sources
Spectacular skin nodules: Cutaneous necrobiotic xanthogranuloma without paraproteinemia
Indian Journal of Dermatology, 2012 Necrobiotic xanthogranuloma (NXG) is a very rare, progressive variant of non-Langerhans cell histiocytosis. It is known to be associated with multisystem involvement and paraproteinemias.
Shimoni Kadakia +3 more
doaj +1 more source
Skin Signs of Systemic Disease [PDF]
, 1976 The subject of this Mcguire Lecture series, the skin, is a relatively enormous organ vulnerable to an enormous variety of external and internal insults. Its total visibility is both a blessing and a curse.
Scoggins, Robert B.
core +2 more sources
Heavy-chain deposition disease associated with multiple myeloma: a case report [PDF]
Kosin Medical JournalHeavy-chain deposition disease (HCDD) is a rare disorder characterized by the deposition of monoclonal immunoglobulin. Due to the disease's rarity and diagnostic challenges, its prognosis is generally poor.
Young Rong Lee +5 more
doaj +1 more source
Scleromyxedema without paraproteinemia
International Journal of Dermatology, 2014 AbstractBackgroundScleromyxedema is a rare generalized form of lichen myxedematosus, a chronic cutaneous mucinosis of unknown etiology usually associated with a monoclonal gammopathy and underlying systemic disorders. It is characterized by the presence of lichenoid papules and diffuse indurations of the skin.
Abarzúa, Alvaro A. +3 more
openaire +3 more sources
A Case of Multiple Myeloma Diagnosed by Skin Lesions [PDF]
, 2010 Multiple myeloma, being a malignant proliferation of plasma cells in the bone marrow, has clinical spectrum varying from monoclonal gammopathy with unknown significance to plasma cell leukemia.
Aylin Okçu Heper +3 more
core +1 more source
Escleromixedema associado a miocardiopatia Scleromyxedema with associated cardiomyopathy
Anais Brasileiros de Dermatologia, 2004 Relato de um caso de escleromixedema com lesões cutâneas associadas a miopatia, disfunção esofageana e paraproteinemia. Durante a evolução, a paciente apresentou sintomas de insuficiência cardíaca congestiva (ICC) que foram relacionados à miocardiopatia,
Gladys Aires Martins +2 more
doaj +1 more source
Hematology, Transfusion and Cell Therapy, 2021 Relato de caso: Paciente, sexo feminino, 43 anos, sem comorbidades, admitida na clínica cirúrgica do Hospital Jean Bitar (HJB) devido quadro de massa abdominal hipogástrica.
BLSA Lima +9 more
doaj +1 more source
Necrobiotic xanthogranuloma associated with smoldering multiple myeloma: satisfactory response to cyclophosphamide, dexamethasone, and thalidomide [PDF]
Anais Brasileiros de Dermatologia, 2019 : Necrobiotic xanthogranuloma is a rare chronic condition, belonging to the group C non-Langerhans cell histiocytoses, which is relevant due to the possibility of extracutaneous involvement and association with systemic diseases, particularly hematologic
Renan Bernardes de Mello +1 more
doaj +1 more source