Scleroderma with type III glomerulonephritis and MPO-ANCA antibodies in the serum

Autor:	Esperanza Avalos-Díaz, Saucedo A, Rafael Herrera-Esparza, Erendira Lopez-Robles, González I, Aguilar Jl
Rok vydání:	2005
Předmět:	CREST Syndrome Pathology medicine.medical_specialty Enzyme-Linked Immunosorbent Assay Dermatology Telangiectases Methylprednisolone Risk Assessment Severity of Illness Index Scleroderma Antibodies Antineutrophil Cytoplasmic Fibrosis Calcinosis medicine Humans cardiovascular diseases Fluorescent Antibody Technique Indirect skin and connective tissue diseases Cyclophosphamide Peroxidase Autoimmune disease Scleroderma Systemic integumentary system business.industry Biopsy Needle Autoantibody Glomerulonephritis IGA Glomerulonephritis Sclerodactyly Middle Aged medicine.disease Immunohistochemistry Treatment Outcome Infectious Diseases embryonic structures Drug Therapy Combination Female medicine.symptom business Follow-Up Studies
Zdroj:	Journal of the European Academy of Dermatology and Venereology. 19:617-620
ISSN:	1468-3083 0926-9959
Popis:	Scleroderma is an autoimmune disease characterized by early inflammatory infiltrates followed by fibrosis in the skin and internal organs. CREST is a relatively benign cutaneous variant of scleroderma that features calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly and telangiectases. Glomerulonephritis is a rare association of CREST. We are reporting a patient with CREST who developed glomerulonephritis and had anticentromere and antineutrophil cytoplasmic autoantibodies (ANCA) in her serum.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b4271e000f35e33773165306de0082c https://doi.org/10.1111/j.1468-3083.2005.01231.x Zobrazit plný text záznamu Plný text