Results 61 to 70 of about 1,421,260 (161)

Gastrointestinal Involvement In Poems Syndrome: A Novel Clinical Manifestation

open access: yes, 2005
POEMS syndrome ( polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) is characterised by a rare multisystem disorder of unknown pathogenesis.
A Shorbagi   +14 more
core   +1 more source

Rethinking Common Diagnoses: Idiopathic Multicentric Castleman Disease Presenting as TAFRO Syndrome: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Idiopathic multicentric Castleman disease (TAFRO subtype) can mimic common differentials. High suspicion is required for chronic systemic symptoms and generalized lymphadenopathy. As fine‐needle aspiration is often non‐diagnostic, early excisional biopsy is important.
Divita Rohatgi   +3 more
wiley   +1 more source

When Liver Disease Misleads the Diagnosis: Two Cases of TAFRO Syndrome With Porto‐Sinusoidal Vascular Disease

open access: yeseJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Background TAFRO syndrome is a rare inflammatory disorder whose hepatic manifestations may mimic decompensated cirrhosis. Cases: We report two women with TAFRO syndrome associated with portal‐sinusoidal vascular disorder (PSVD), a rare cause of non‐cirrhotic portal hypertension. In both cases, liver biopsy excluded cirrhosis and confirmed PSVD.
Laura Dassy   +12 more
wiley   +1 more source

Longitudinal bioimpedance assessments to evaluate hydration in POEMS syndrome [PDF]

open access: yes, 2016
Polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes (POEMS) syndrome is a rare paraneoplastic disorder associated with an underlying plasma cell dyscrasia and multiorgan failure.
Morris, Lauren   +5 more
core   +3 more sources

Characterization of patients with medically unexplained intolerance to enteral feeding treated with home parenteral nutrition: A descriptive cohort study

open access: yesJournal of Parenteral and Enteral Nutrition, Volume 50, Issue 7, Page 1024-1030, October 2026.
Abstract Background and Aims Dutch intestinal failure centers are increasingly confronted with patients started on total parenteral nutrition because of reported intolerance to enteral feeding without meeting clinical criteria for intestinal failure.
J. W. Korzilius   +11 more
wiley   +1 more source

Association of co-existing vitamin B6 and B12 deficiency with polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes (POEMS) syndrome: a case report

open access: yesBMC Neurology
Background Both vitamin B6 deficiency and vitamin B12 deficiency can present with symptoms that appear like polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes (POEMS) syndrome, with painful peripheral neuropathy and sensorimotor ...
Stephan Hu   +3 more
doaj   +1 more source

POEMS- A Diagnostic Odyssey

open access: yesOnline Journal of Health & Allied Sciences, 2021
POEMS syndrome is a rare multisystem paraneoplastic disease that manifests with a spectrum of symptoms namely peripheral neuropathy (P), organomegaly (O), endocrinopathy (E) monoclonal plasma-cells proliferative disorder (M) and skin changes (S).
Cynthia Amrutha Sukumar   +3 more
doaj  

Nerve Ultrasound Features of Peripheral Nervous System Lymphoma and Non‐Systemic Vasculitic Neuropathy

open access: yesEuropean Journal of Neurology, Volume 33, Issue 10, October 2026.
Nerve ultrasound distinguishes peripheral nervous system lymphoma (PNSL) from non‐systemic vasculitic neuropathy (NSVN). PNSL shows severe focal, persistent enlargement on the initially affected side with frequent cranial/root involvement; NSVN presents milder, variable, and contralateral‐predominant enlargement, especially in newly involved nerves ...
Huihong Tian   +7 more
wiley   +1 more source

Gastroparesis Phenotyping: Current Methods and Emerging Opportunities With Magnetic Resonance Imaging

open access: yesNeurogastroenterology &Motility, Volume 38, Issue 10, October 2026.
Anatomical and dynamic MRI performed before and after ingestion of a natural test meal provide complementary assessments of gastric accommodation, emptying, and regional wall kinematics. This integrated, noninvasive examination supports mechanistic phenotyping of gastric motor dysfunction in gastroparesis. ABSTRACT Background Gastroparesis is a complex
Xiaokai Wang   +2 more
wiley   +1 more source

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