Results 121 to 130 of about 20,564 (250)
Polyneuropathy, organomegaly, endocrinopathy, M protein, skin changes: not always a POEMS syndrome.
Haematologica, 2006 POEMS or Crow-Fukase syndrome is a rare plasma cell disease with multiorgan involvement, whose acronym refers to the presence of Polyneuropathy, Organomegaly, Endocrinopathy, M protein, Skin changes. The etiology of POEMS is still unknown, but increasing evidence points to a possible role of Vascular Endothelial Growth Factor (VEGF).
BRIANI, CHIARA +5 more
openaire +2 more sources
MGM Journal of Medical SciencesBackground: Hemophagocytic lymphohistiocytosis (HLH) is a severe hyperinflammatory disorder marked by intense yet ineffective immune activation, resulting in hemophagocytosis, systemic inflammation, and multi-organ dysfunction.
Lipsa Priyadarshini +5 more
doaj +1 more source
Myelomatous Pleural Effusion [PDF]
Multiple myeloma (MM) is a common hematologic malignancy. Pleural effusion is a rare presenting feature of multiple myeloma which carries a poor prognosis.
شیردل, عباس +3 more
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Molecular Genetics and Metabolism ReportsAcid sphingomyelinase deficiency (ASMD) is a lysosomal storage disease with multisystem complications including neurodegeneration, hepatosplenomegaly, interstitial lung disease (ILD), bone marrow disease, and growth failure.
Drew B. Sinha +7 more
doaj +1 more source
Atypical B12 Deficiency with Nonresolving Paraesthesia
Case Reports in Oncological Medicine, 2013 Vitamin B12 deficiency can present with various hematological, gastrointestinal and neurological manifestations. We report a case of elderly female who presented with neuropathy and vitamin B12 deficiency where the final work-up revealed polyneuropathy ...
S. Haider +3 more
doaj +1 more source
Recurrent Transient Ischemic Attacks in a Patient with POEMS Syndrome
Case Reports in Neurological Medicine, 2014 A 47-year-old female with a prior history of POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) syndrome was admitted with transient ischemic attacks complicated by dysarthria and right-sided hemiparesis.
A. Akyol +4 more
doaj +1 more source
Tacrolimus, a forgotten agent in kidney transplant leukopenia [PDF]
, 2013 Leukopenia in kidney transplant patients is frequent, it causes potentially life-threatening complications, but it is often poorly characterized. Opportunistic infections, immunologic disturbances and drug-related toxicity are principal causes of single ...
Aguiar, P. +12 more
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ZAP-70 Expression in B-Chronic Lymphocytic Leukemia in Sudanese Patients
Sudan Journal of Medical Sciences, 2018 Background: Chronic lymphocytic leukemia is the most common form of leukemia in adults. The prognostic impact of ZAP-70 in CLL has been reported in several studies.
Enaam Abdel-Rhman Abdel-Gader +6 more
doaj +1 more source
Mucopoly saccharidosis type maroteaux-lamy, a case report [PDF]
Journal of Mazandaran University of Medical Sciences, 2007 Mucopolysaccharidosis type maroteaux-lamy is a very rare hereditary disease. The disease is marked by the deficiency of the lysosomal enzyme N-Acetyl galactosamine--4-sulfate sulfatase (arylsulfatase B).
A.R. Alaee +3 more
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POEMS Syndrome: Two Case Reports
Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2015 Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome is an uncommon condition related to a paraneoplastic syndrome secondary to an underlying plasma cell disorder.
Turgay Demir +3 more
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