PubMed Health⌕ Search

PubMed · 7933597

[Polyangiitis overlap syndrome].

Abstract

Polyangiitis overlap (PO) syndrome is a relatively new syndrome proposed by Leavitt and Fauci in 1986 (1). They noticed there are several patients who do not belong to a single disease entity of the already established vasculitis and show systemic manifestations seen in more than two diseases. They called these patients as having PO syndrome. PO syndrome also contained unclassified systemic necrotizing vasculitis in the original paper. Although there are various combinations of vasculitis, the most common type of PO syndrome is the overlap of classical polyarteritis nodosa and Churg-Strauss syndrome. The prognosis of PO syndrome is not so bad. The majority of the patients experienced remissions after the treatment with corticosteroid and cyclophosphamide.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

K Tanimoto. 1994. [Polyangiitis overlap syndrome].. https://pubmed.ncbi.nlm.nih.gov/7933597/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Osler and the Churg-Strauss syndrome.

This paper records a patient of Osler's, who showed many features compatible with the Churg-Strauss syndrome of allergic granulomatous angiitis to be described 50 years later.

Churg-Strauss Syndrome↗

[Churg-Strauss syndrome complicated by polyneuropathy].

Apart from some inherited forms, polyneuropathy is a disorder secondary to systemic diseases. The symptoms of chronic polyneuropathy usually appear some years after the main disease has been diagnosed. However, the acute-subacute form can be the first manifestation of a systemic disease, when its typical clinical features are still absent. The diagnosis of polyneuropathy is based on clinical symptoms and electrophysiologic studies, and it also could be supported by spinal fluid examination and peripheral nerve biopsy. The authors report here a case presenting as Churg-Strauss syndrome complicated with subacute axonal polyneuropathy and eosinophilia characteristic of the disease. Although Churg-Strauss syndrome is rare, it is important to recognise it, because remission depends on immunosuppressive therapy introduced in the early stage.

Churg-Strauss Syndrome↗