Clinical course of extrarenal symptoms in henoch schonlein purpura. Gastrointestinal involvement in henochschonlein purpura. Background 1st described in 1801 by william heberden, a physician in london, who wrote about a case of a 5 year old boy with hematuria, abdominal pain, joint pains and skin rash. Hsp presents with purple spots on the skin purpura, arthralgia, digestive problems, and kidney injury.
Henoch schonlein purpura causes skin rash, pain in the abdomen, and joint inflammation. Schonleinhenoch purpura is a leukocytoclastic vasculitis, most common in. Dec 10, 2018 henoch schonlein purpura hsp, also called immunoglobulin a vasculitis igav, is a vascular disease that primarily affects small blood vessels. Its incidence is low in childhood with the exception of henoch schonlein purpura hsp and. It gets its name from two german doctors, johann schonlein and eduard henoch, who.
Chartapisak w, opastirakul s, hodson em, willis ns, craig jc. Risk of long term renal impairment and duration of follow up recommended for henochschonlein purpura with normal or minimal urinary findings. Schonleinhenoch purpura, anaphylactoid purpura rhumatoid purpura diagnosis diagnosis of hsp is established when at least 2 of the following 4 criteria are present. Henochschonlein purpura hsp is the most common form of vasculitis in children. Introduction cassio lynm, ma in jama, february 15, 2012 vol 307, no.
Cinthia claros arispe 1,a, haldrin antonio bejarano forqueras 1,b. Henochschonlein purpura allergy and clinical immunology. The prognosis for patients with henochschonlein purpura is generally excellent. Schonleinhenoch purpura in pediatric patients, a case purpose. Henoch schonlein purpura hsp is a shortterm inflammation of certain blood vessels vasculitis thought to be triggered by a malfunction of the immune system. Henochschonlein purpura hsp, also known as iga vasculitis, is a disease of the skin, mucous membranes, and sometimes other organs that most commonly affects children. Hsp is the most common vasculitis in childhood with an incidence of 1020 cases per 100,000 in children under 17 years with a peak incidence of 70 cases per 100,000 in the 46 year age group 1, 2. The inflammation causes blood vessels in the skin, intestines. Hemorrhagic bullous lesions in henochschonlein purpura.
Jul 26, 2017 henochschonlein purpura hsp is a disease that causes small blood vessels to become inflamed and leak blood. Should children with henochschonlein purpura and abdominal pain be treated with steroids. A randomized, doubleblind, placebocontrolled trial. Henochschonlein purpura causes skin rash, pain in the abdomen, and joint inflammation. Early prednisone therapy in henoch schonlein purpura. This smallvessel vasculitis is mediated by immunoglobulin a igacontaining immune complexes and is characterized by nonthrombocytopenic purpura, abdominal pain, arthralgias, and renal disease. Frequently, hsp leads to abdominal pain and intestinal bleeding, renal involvement and joint pain. The prognosis for patients with henoch schonlein purpura is generally excellent.
Henochschonlein purpura hsp, also called immunoglobulin a vasculitis igav, is a vascular disease that primarily affects small blood vessels. In the skin, the disease causes palpable purpura small, raised areas of bleeding underneath the skin, often with joint pain and abdominal pain. Therapy for children with henochschonlein purpura nephritis. Nov 25, 2015 background henochschonlein purpura hsp or anaphylactoid purpura. Henochschonlein purpura hsp is a rare inflammatory disease of the small blood vessels capillaries and is usually a selflimited disease.
The treatment of henochschonlein purpura is directed toward the most significant area of involvement. Henochschonlein purpura hsp is a vasculitis inflammation of blood vessels that affects small blood vessels mainly in the skin, intestines, and kidneys. Henoch schonlein purpura is an idiopathic, iga associated, systemic smallvessel vasculitis characterized by the clinical tetrad of palpable purpura, arthralgias, renal dysfunction, and abdominal. Henochschonlein purpura is an idiopathic, iga associated, systemic smallvessel vasculitis characterized by the clinical tetrad of palpable purpura, arthralgias, renal dysfunction, and abdominal. The disease is characterized by abnormal deposits of immunoglobulin a an antibody in the blood vessels, leading to their inflammation vasculitis. Purpura henoch schonlein penyakit ini ditandai oleh lesi kulit spesifik berupa purpura nontrombositopenik, artritis, nyeri perut dan perdarahan saluran cerna, serta dapat pula disertai nefritis. It is the most common form of childhood vascular inflammation vasculitis and results in inflammatory changes in the small blood vessels.
Symptom, treatment and advice from community members. Henochschonlein purpura is an iga vasculitis characterized by a tetrad of palpable purpura. Schonleinhenoch purpura is the most common infantile vasculitis and is mostly clinically diagnosed. Eularprintopres criteria for henochschonlein purpura, childhood polyarteritis nodosa, childhood wegener granulomatosis and childhood takayasu arteritis. Gastrointestinal manifestations of henoch schonlein purpura. Henochschonlein purpura american academy of pediatrics. The treatment of henoch schonlein purpura is directed toward the most significant area of involvement. Henoch schonlein purpura hsp is an immunemediated vasculitis. Henochschonlein purpura hsp is a shortterm inflammation of certain blood vessels vasculitis thought to be triggered by a malfunction of the immune system. Clinical course of extrarenal symptoms in henochschonlein purpura. In the skin, the disease causes palpable purpura small, raised areas of bleeding. Diagnostic and management of henoch schonlein purpura. Precedidas por una infecciondel tracto respiratorio superiorpatologia mediada por elsistema inmuneinducida por factoresambientales.
Henochschonlein purpura, nephritis, therapy, children introduction henochschonlein purpura hsp is an immunologically mediated disease associating purpura plus urticaria, characteristically affecting lower limbs, buttocks, and elbows. Pdf on aug 24, 2010, chetan mukhtyar and others published henochschonlein purpura find, read and cite all the research you need on researchgate. Symptoms can begin in children, most commonly between the ages of 4 and 7 years, soon after an upper respiratory tract infection or a streptococcal pharyngitis sore throat infection. Risk of long term renal impairment and duration of follow up recommended for henoch schonlein purpura with normal or minimal urinary findings. The disease is characterized by abnormal deposits of immunoglobulin a an antibody in the blood vessels, leading to. Henochschonlein purpura, leucocitoclastic vasculitis. The source of information was medical records and a data gathering guide containing the studied variables was used. The cause of this malfunction is unknown, but hsp tends to develop after an upper respiratory tract infection or a bout of hay fever. A retrospective descriptive study of patients with scholeinhenoch purpura diagnosis was conducted for 4 years.
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