Results 21 to 30 of about 20,564 (250)

CASE OF THE LATE DIAGNOSIS OF POEMS-SYNDROME

Klinicist, 2014
POEMS-syndrome (P — polyneuropathy, O — organomegaly, E — endocrinopathy, M — M-protein, S — skin) in 64-year old patient isdescribed in the article.
P. N. Barlamov, M. E. Golubeva, E. R. Vasiliev, S. V. Meres, V. V. Shchekotov   +4 more
doaj   +3 more sources

Adenopathy and extensive skin patch overlying plasmacytoma syndrome—the clue to early diagnosis of polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes: A case series and literature review

SAGE Open Medical Case Reports, 2022
Importance: Adenopathy and extensive skin patch overlying plasmacytoma syndrome is a paraneoplastic syndrome characterized by a cutaneous vascular patch overlying a plasmacytoma and systemic manifestations.
Elizabeth Guevara Sanchez, César Ramos, Kayadri Ratnarajah, Francisco P Bravo, Manuel A Del Solar, Michelle Le, Elena Netchiporouk   +6 more
doaj   +1 more source

Treatment for POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes) syndrome.

Cochrane Database of Systematic Reviews, 2012
POEMS (polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes) syndrome is a rare cause of demyelinating and axonal mixed neuropathy with monoclonal plasma cell proliferative disorder and multiorgan involvement. The pathogenesis of POEMS syndrome is not well understood, but overproduction of vascular endothelial growth factor (VEGF),
S. Kuwabara, A. Dispenzieri, K. Arimura, S. Misawa, C. Nakaseko   +4 more
semanticscholar   +4 more sources

Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis/Renal Failure, and Organomegaly (TAFRO) Syndrome with Bilateral Adrenal Hemorrhage in Two Caucasian Patients

The American journal of case reports, 2020
Case series Patients: Male, 19-year-old • Female, 31-year-old Final Diagnosis: TAFRO syndrome Symptoms: Fever • splenomegaly • lymphadenopathies Medication: — Clinical Procedure: — Specialty: Hematology Objective: Unusual clinical course Background ...
Grégoire Ducoux, Arthur Guerber, C. Durel, B. Asli, Jehane Fadlallah, A. Hot   +5 more
semanticscholar   +1 more source

Chronic adult T-cell Leukemia in a young male after blood transfusion as a newborn [PDF]

, 2016
Human T-cell Lymphotropic virus type 1 (HTLV-1) is the etiological agent of Adult T-cell Leukemia/Lymphoma (ATLL) and HTLV-1 Associated Myelopathy/Tropical Spastic Paraparesis (HTM/TSP).
Altube, Alejandra, Berini, Carolina Andrea, Biglione, Mirna Marcela, Cabral Lorenzo, María Cecilia, Colucci, Magalí, Cánepa, Camila, Deves, Alberto, Halperin, Nora Silvia, Hermine, Olivier, Rojas, Francisca, Ruggieri, Matias   +10 more
core   +2 more sources

Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes (POEMS) Syndrome With IgG Kappa/IgG Lambda Biclonal Gammopathy: A Rare Presentation of a Rare Disease

Cureus, 2020
Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome is a low prevalence multisystemic paraneoplastic disease.
Leonardo Mejia Buritica, Vanessa Santiago-Pacheco, Oliver Perilla, Dayana Quintero   +3 more
semanticscholar   +1 more source

Hemophagocytic lymphohistiocytosis in an infant with multiple triggers!!

Asian Journal of Transfusion Science, 2018
Hemophagocytic lymphohistiocytosis (HLH) is a disorder of immune dysregulation secondary to a massive unregulated cytokine storm and its downstream consequences.
Sataroopa Mishra, Amitabh Singh, Lavleen Singh, Anirban Mandal, Rahul Jain   +4 more
doaj   +1 more source

POEMS neuropathy: optimising diagnosis and management [PDF]

, 2018
POEMS syndrome is a rare and disabling autoinflammatory condition characterised by a typical peripheral neuropathy and the presence of a monoclonal plasma cell disorder.
Carr, AS, D'Sa, S, Foldes, D, Keddie, S, Lunn, MPT, Reilly, MM   +5 more
core   +1 more source

Gaucher Disease and Myelofibrosis: A Combined Disease or a Misdiagnosis? [PDF]

, 2018
Background: Gaucher disease (GD) and primary myelofibrosis (PMF) share similar clinical and laboratory features, such as cytopenia, hepatosplenomegaly, and marrow fibrosis, often resulting in a misdiagnosis.
Cardarelli, L, Foà, R, Giona, F, Mariani, S, Palumbo, G, Santopietro, M   +5 more
core   +1 more source

Safe discontinuation of nilotinib in a patient with chronic myeloid leukemia: a case report [PDF]

, 2014
Case presentation. We report the case of a 64-year-old Caucasian man diagnosed with chronic-phase chronic myeloid leukemia in April 2005. After 4 years of treatment with imatinib, he became intolerant to the drug and was switched to nilotinib.
CAOCCI, GIOVANNI, Greco M, LA NASA, GIORGIO   +2 more
core   +2 more sources