Skin and Nerve Neovascularization in POEMS Syndrome: Insights From a Small Cohort.


Journal

Journal of neuropathology and experimental neurology
ISSN: 1554-6578
Titre abrégé: J Neuropathol Exp Neurol
Pays: England
ID NLM: 2985192R

Informations de publication

Date de publication:
01 05 2020
Historique:
received: 07 01 2020
revised: 04 02 2020
entrez: 17 4 2020
pubmed: 17 4 2020
medline: 15 12 2020
Statut: ppublish

Résumé

Polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes (POEMS) syndrome is a rare systemic disorder linked to plasma cell dyscrasia and is related to elevation of vascular endothelial growth factor (VEGF). Diagnosis is still challenging and pathophysiology unclear. Because VEGF drives neovascularization, we investigated skin and nerve vascularization in 6 patients with POEMS syndrome compared with 5 control groups of polyneuropathies and healthy subjects (n = 104) from the University Hospital of Limoges between 2009 and 2018. We evaluated loss of small and large fibers in these patients. Skin and nerve vascularization were quantified manually on immunofluorescence using vessel staining (anti-α-SMA antibody). Dermal vascularization was significantly higher in POEMS syndrome than in other groups, but unrelated to loss of small fibers and VEGF. Perineurial vascularization was higher in POEMS syndrome than in healthy controls, and was related to loss of large fibers and VEGF level. Our study highlights the existence of neovascularization in skin of patients with this rare disorder. These data suggest that skin neovascularization could be an additional biomarker to help in the diagnosis and understanding of POEMS syndrome. Moreover, nerve neovascularization, driven by VEGF overexpression, may play a role in the pathophysiology of large fiber loss in this condition.

Identifiants

pubmed: 32296845
pii: 5819361
doi: 10.1093/jnen/nlaa021
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

542-550

Informations de copyright

© 2020 American Association of Neuropathologists, Inc. All rights reserved.

Auteurs

Camille Guibert (C)

Department of Pathology, Limoges, France.

Laurence Richard (L)

Department of Neurology, National Referral Center for 'Rare Peripheral Neuropathies', Limoges, France.
EA 6309, Schools of Medicine and Pharmacy, University of Limoges, France, Limoges, France.

Stéphanie Durand (S)

Dupuytren University Hospital, Limoges, France; Bioinformatics Team, BISCEM Platform.
EA 7500, Faculty of Sciences and Technology, Limoges, France.

Fanny Maquin (F)

Department of Neurology, National Referral Center for 'Rare Peripheral Neuropathies', Limoges, France.

Claire Demiot (C)

EA 6309, Schools of Medicine and Pharmacy, University of Limoges, France, Limoges, France.

Jean-Michel Vallat (JM)

Department of Neurology, National Referral Center for 'Rare Peripheral Neuropathies', Limoges, France.

Arnaud Jaccard (A)

Department of Hematology, National Reference Center of Light-Chain Systemic Amyloidosis, Dupuytren University Hospital, Limoges, France.

Laurent Magy (L)

Department of Neurology, National Referral Center for 'Rare Peripheral Neuropathies', Limoges, France.
EA 6309, Schools of Medicine and Pharmacy, University of Limoges, France, Limoges, France.

Mathilde Duchesne (M)

Department of Pathology, Limoges, France.
Department of Neurology, National Referral Center for 'Rare Peripheral Neuropathies', Limoges, France.
EA 6309, Schools of Medicine and Pharmacy, University of Limoges, France, Limoges, France.

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