Hypersensitivity vasculitis

Hypersensitivity vasculitis

Infobox_Disease
Name = PAGENAME


Caption =
DiseasesDB = 7423
ICD10 = ICD10|M|31|0|m|30
ICD9 = ICD9|446.2
ICDO =
OMIM =
MedlinePlus =
eMedicineSubj = med
eMedicineTopic = 2930
MeshID = D018366

Hypersensitivity vasculitis (or hypersensitivity angiitis or leukocytoclastic vasculitis) is a small vessel vasculitis, [DorlandsDict|eight/000114508|hypersensitivity vasculitis] usually due to a hypersensitivity reaction.

Causes

It is usually due to a known drug (such as cefoperazonecite journal |author=Islek I, Baris S, Katranci AO, Ariturk E, Gurses N |title=Hypersensitivity vasculitis induced by cefoperazone/sulbactam |journal=Ann. Clin. Microbiol. Antimicrob. |volume=2 |issue= |pages=1 |year=2003 |month=January |pmid=12556245 |pmc=149382 |doi= |url=http://www.ann-clinmicrob.com/content/2//1] or nicoumalonecite journal |author=Susano R, Garcia A, Altadill A, Ferro J |title=Hypersensitivity vasculitis related to nicoumalone |journal=BMJ |volume=306 |issue=6883 |pages=973 |year=1993 |month=April |pmid=8490477 |pmc=1677426 |doi= |url=] ), auto-antigens or infectious agents such as bacteria. Immune complexes lodge in the vessel wall, attracting polymorphonuclear leukocytes who in turn release tissue-degrading substances leading to an inflammatory process.

Clinical Presentation

Palpable, normally painful, petechiae or purpura (skin vasculitis). The lesions normally arise in crops, with common localizations being the forearms and legs. Necrosis of skin tissue can yield lesions with black or brown centres. This disorder may affect the skin only, but sometimes affect nerves, the kidneys, joints and the heart. Renal involvement is common.

Investigations

The primary goal is to identify the causing agent, be it a drug or a microbe. Questioning is important, as is a thorough physical examination, chest X-ray, ESR and biochemical organ tests. Skin biopsy of the lesions reveal inflammation of the small vessels, termed leukocytoclastic vasculitis, which is most prominent in postcapillary venules. Tests for hepatitis virus, antinuclear antibodies, rheumatoid factor and cryoglobulins might be indicated.

Diagnostic Criteria

An important differential is Henoch-Schönlein purpura. cite journal |author=Michel BA, Hunder GG, Bloch DA, Calabrese LH |title=Hypersensitivity vasculitis and Henoch-Schönlein purpura: a comparison between the 2 disorders |journal=J. Rheumatol. |volume=19 |issue=5 |pages=721–8 |year=1992 |pmid=1613701 |doi=]

At least 3 out of 5 criteria yields a sensitivity of 71% and a specificity of 84%:

* Age > 16.
* Use of possible triggering drug in relation to symptoms.
* Palpable painful purpura (the three P's).
* Maculopapular rash.
* Skin biopsy showing neutrophil infiltration around vessel.

Treatment

The most important part of the treatment is to eliminate the cause of the vasculitis, if at all possible. Antihistamines prove helpful to some patients. If the vasculitis is damaging organ systems such as the kidneys, immunosuppressive agents are indicated.

ee also

* Vasculitis
* Goodpasture's syndrome

References


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