[Severe membranoproliferative glomerulonephritis with polyadenopathy associated with hypocomplementemic urticarial vasculitis syndrome]

Presse Med. 2017 May;46(5):547-550. doi: 10.1016/j.lpm.2017.01.020. Epub 2017 May 10.

[Article in French]

Authors

Hubert Gheerbrant¹, Diane Giovannini², Loic Falque³, Fanny Andry⁴, Maxime Lugosi⁴, Alban Deroux⁴

Affiliations

¹ CHU de Grenoble, service de pneumologie, BP 2017, 38043 Grenoble cedex 09, France. Electronic address: [email protected].
² CHU de Grenoble, service d'anatomo-pathologie, BP 2017, 38043 Grenoble cedex 09, France.
³ CHU de Grenoble, service de pneumologie, BP 2017, 38043 Grenoble cedex 09, France.
⁴ CHU de Grenoble, service de médecine interne, BP 2017, 38043 Grenoble cedex 09, France.

PMID: 28502374
DOI: 10.1016/j.lpm.2017.01.020

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Arthralgia / etiology
Autoantibodies / immunology
Autoantigens / immunology
Biopsy
Complement C1q / immunology
Diagnosis, Differential
Female
Glomerulonephritis, Membranoproliferative / etiology*
Glomerulonephritis, Membranoproliferative / immunology
Glomerulonephritis, Membranoproliferative / pathology
Humans
Lupus Erythematosus, Systemic / diagnosis
Lymphadenopathy / diagnostic imaging
Lymphadenopathy / etiology*
Multidetector Computed Tomography
Pancytopenia / etiology
Positron Emission Tomography Computed Tomography
Raynaud Disease / etiology
Syndrome
Urticaria / etiology*
Vasculitis, Leukocytoclastic, Cutaneous / complications*
Vasculitis, Leukocytoclastic, Cutaneous / diagnosis
Vasculitis, Leukocytoclastic, Cutaneous / immunology

Substances

Autoantibodies
Autoantigens
Complement C1q