Différences entre versions de « Gammapathies monoclonales »

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Neuropathies associated with monoclonal proteins occur in monoclonal gammopathy of undetermined significance, multiple myeloma, Waldenström macroglobulinemia, amyloidosis, and other hematologic malignancies.
 
Neuropathies associated with monoclonal proteins occur in monoclonal gammopathy of undetermined significance, multiple myeloma, Waldenström macroglobulinemia, amyloidosis, and other hematologic malignancies.
 
== Bilan étiologique ==
 
== Bilan étiologique ==
 +
{| class="wikitable"
 +
|-
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! Paramètre || Valeur || Signification
 +
|-
 +
| Hyperthyroïdie||Explication ici||Dosage de la '''TSH'''
 +
|-
 +
| Alcool ("holiday heart")||Explication ici||
 +
|-
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| Péricardite||Explication ici||'''ECG''', '''labo''', '''échocardiographie'''
 +
|-
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| Embolie pulmonaire||Explication ici||Dosage des '''D-dimères''', '''Angio-CT'''
 +
 +
|}
 +
 
== MGUS ==
 
== MGUS ==
 
== Hémopathies malignes ==
 
== Hémopathies malignes ==

Version du 24 mai 2020 à 12:16

Caractéristiques communes

Neuropathies associated with monoclonal proteins occur in monoclonal gammopathy of undetermined significance, multiple myeloma, Waldenström macroglobulinemia, amyloidosis, and other hematologic malignancies.

Bilan étiologique

Paramètre Valeur Signification
Hyperthyroïdie Explication ici Dosage de la TSH
Alcool ("holiday heart") Explication ici
Péricardite Explication ici ECG, labo, échocardiographie
Embolie pulmonaire Explication ici Dosage des D-dimères, Angio-CT

MGUS

Hémopathies malignes

IgG: myélome-plasmocytome

IgM: syndrome lymphoprolifératif (lymphome malin)

  • Leucémie lymphoïde chronique
  • Maladie de Waldenström (lymphome lymphoplasmocytaire)

Amyloïdose

  • Souvent lambda

POEMS

(polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes)

  • Souvent IgG/IgA et lambda
  • POEMS syndrome is characterized by the presence of a monoclonal plasma cell disorder, peripheral neuropathy, and one or more of the following: osteosclerotic myeloma, Castleman disease (angiofollicular lymph node hyperplasia), elevated serum vascular endothelial growth factor, organomegaly, endocrinopathy, edema, typical skin changes, and papilledema.