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Henoch–Schönlein purpura

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382:, serum levels of IgA are high in HSP and there are identical findings on renal biopsy; however, IgA nephropathy has a predilection for young adults while HSP is more predominant among children. Further, IgA nephropathy typically only affects the kidneys while HSP is a systemic disease. HSP involves the skin and connective tissues, scrotum, joints, gastrointestinal tract and kidneys. The genetic basis remains unclear except for involvement of the human leukocyte antigen region of the genome. It is hypothesized to involve autoimmunity triggered by infections. Streptococcus strains and Parainfluenza virus are the most commonly associated pathogens, and in children Human Parvovirus B19 is a frequent viral trigger 391: 378:(C3) are deposited on arterioles, capillaries, and venules (hence it is a type III hypersensitivity reaction). The activation of the alternative complement pathway results in the deposition of IgA aggregates or IgA complexes in target organs (with deposition of C3). This leads to the production of inflammatory mediators, including vascular prostaglandins like prostacyclin, which may play a key role in the development of IgAV and its organ-specific clinical manifestations. As with 46: 256:(IgA); the exact cause for this phenomenon is unknown. In children, it usually resolves within several weeks and requires no treatment apart from symptom control but may relapse in a third of cases and cause irreversible kidney damage in about one in a hundred cases. In adults, the prognosis is different from in children. The average duration of cutaneous lesions is 27.9 months. For many, it tends to be 904: 521: 281: 269: 852:(ESKD) more often than in children. In a UK series of 37 patients, 10 (27%) developed advanced kidney disease. Proteinuria, hypertension at presentation, and pathology features (crescentic changes, interstitial fibrosis and tubular atrophy) predicted progression. About 20% of children that exhibit nephrotic or nephritic features experience long permanent renal impairment. 734:(PReS) classification, include palpable purpura as a mandatory criterion, together with at least one of the following findings: diffuse abdominal pain, predominant IgA deposition (confirmed on skin biopsy), acute arthritis in any joint, and renal involvement (as evidenced by the presence of blood and/or protein in the urine). 939:
in 1799 .In 1920, Eduard Glanzmann(1887-1959), a Swiss pediatrician noted for his contributions in the fields of infectious disease, vitamin therapy and, mostly the field of haematology. He recognised the role of allergy in the pathogenesis of Henoch-Schonlein purpura, hence the understanding of the
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as treatment for HSP. However, if they are given early in the disease episode, the duration of symptoms may be shortened, and abdominal pain can improve significantly. Moreover, the chance of severe kidney problems may be reduced. A systematic review did not find any evidence that steroid treatment
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correlate with the severity of symptoms: those with asymptomatic hematuria may only have focal mesangial proliferation while those with proteinuria may have marked cellular proliferation or even crescent formation. The number of crescentic glomeruli is an important prognostic factor in determining
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Overall prognosis is good in most patients, with one study showing recovery occurring in 94% and 89% of children and adults, respectively (some having needed treatment). In children under ten, the condition recurs in about a third of all cases, usually within the four months of the initial attack.
307:. The purpura typically appear on the legs and buttocks, but may also be seen on the arms, face and trunk. The abdominal pain is colicky in character, and may be accompanied by nausea, vomiting, constipation or diarrhea. There may be blood or mucus in the stools. The joints involved tend to be the 795:
Evidence of worsening kidney damage would normally prompt a kidney biopsy. Treatment may be indicated on the basis of the appearance of the biopsy sample; various treatments may be used, ranging from steroids by mouth to a combination of intravenous
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mechanism of HSP. In 2012, the International Chapel Hill Consensus Conference Nomenclature of Vasculitides renamed HSP IgA vasculitis. Prior to this, the disease was more often known as Henoch–Schönlein purpura rather than the reverse.
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and ulcerations occur. It is uncertain as to whether HSP needs treatment beyond controlling the symptoms. Most people do not receive therapy because of the high spontaneous recovery rate. Experts disagree on whether to routinely use
923:(1793–1864). Johann Schönlein described the condition as an entity in 1837; Eduard Heinrich Henoch in 1868 reported the first case of a patient with colic, bloody diarrhea, painful joints, and a rash. The English physician 532:
using an anti-IgA antibody, the skin is a biopsy of a patient with Henoch–Schönlein purpura. IgA deposits are found in the walls of small superficial capillaries (yellow arrows). The pale wavy green area on top is the
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is found for a patient on RRT, the disease will recur in the graft (transplanted kidney) in about 35% of cases, and in 11%, the graft will fail completely (requiring resumption of the RRT and a further transplant).
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Mills JA, Michel BA, Bloch DA, Calabrese LH, Hunder GG, Arend WP, et al. (August 1990). "The American College of Rheumatology 1990 criteria for the classification of Henoch-Schönlein purpura".
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Gardner-Medwin JM, Dolezalova P, Cummins C, Southwood TR (October 2002). "Incidence of Henoch-Schönlein purpura, Kawasaki disease, and rare vasculitides in children of different ethnic origins".
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may be performed both to establish the diagnosis or to assess the severity of already suspected kidney disease. The main findings on kidney biopsy are increased cells and Ig deposition in the
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agent prevents persistent kidney disease. There is also no evidence that treating children or adults with cyclophosphamide prevents severe kidney disease. Heparin treatment is not justified.
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Murali NS, George R, John GT, Chandi SM, Jacob M, Jeyaseelan L, et al. (June 2002). "Problems of classification of Henoch Schonlein purpura: an Indian perspective".
1091: 2579: 628:. Several diseases have been reported to be associated with HSP, often without a causative link. Only in about 35% of cases can HSP be traced to any of these causes. 350:(generalised swelling due to low protein content of the blood). While abnormalities on urinalysis may continue for a long time, only 1% of all HSP patients develop 299:
are known as the "classic triad" of Henoch–Schönlein purpura. Purpura occur in all cases, joint pains and arthritis in 80%, and abdominal pain in 62%. Some include
327:(blood in the urine), but only a quarter will have this in sufficient quantities to be noticeable without laboratory tests. Problems in other organs, such as the 1581:
Michel BA, Hunder GG, Bloch DA, Calabrese LH (May 1992). "Hypersensitivity vasculitis and Henoch-Schönlein purpura: a comparison between the 2 disorders".
486:, digestive tract hemorrhage (not due to intussussception), hematuria and age less than 20. The presence of three or more of these indicators has an 87% 362:
of the kidney if performed, may predict progression to advanced kidney disease. Adults are more likely than children to develop advanced kidney disease.
319:, but arthritis in the hands and feet is possible; the arthritis is nonerosive and hence causes no permanent deformity. Forty percent have evidence of 631:
The exact cause of HSP is unknown, but most of its features are due to the deposition of abnormal antibodies in the wall of blood vessels, leading to
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the pioneer of neurology who published his classic textbook between 1840 and 1846 and the first to describe Romberg's sign.) and his teacher
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Fauci AS (1987). "269:The Vasculitis Syndromes". In Braunwald E, Isselbacher KJ, Petersdorf RG, Wilson JD, Martin JB, Fauci AS (eds.).
482:(HV). In a series comparing 85 HSP patients with 93 HV patients, five symptoms were found to be indicative of HSP: palpable purpura, 3141: 3136: 2737: 3092: 895:
Cases of HSP may occur anytime throughout the year, but some studies have found that fewer cases occur during the summer months.
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The diagnosis is based on the combination of the symptoms, as very few other diseases cause the same symptoms together.
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count may be raised, and distinguishes it from diseases where low platelets are the cause of the purpura, such as
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of HSP in children is about 20 per 100,000 children per year, making it the most common vasculitis in children.
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has fallen into disuse. Moreover, Willan was the first to describe an exanthematous rash of childhood known as
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López-Mejías R, Castañeda S, Genre F, Remuzgo-Martínez S, Carmona FD, Llorca J, et al. (March 2018).
647:) or decreased removal of abnormal IgA from the circulation. It is suspected that abnormalities in the IgA 3347: 2989: 2792: 888:
are below the age of six, and 90% are under ten. It occurs about twice as often in boys as in girls. The
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and numerous others. Drugs linked to HSP, usually as an idiosyncratic reaction, include the antibiotics
3248: 3020: 2698: 1648: 821: 221:), but this usually goes unnoticed; in a small proportion of cases, the kidney involvement proceeds to 3313: 3050: 2873: 2049:"Henoch-Schönlein purpura in adulthood and childhood: two different expressions of the same syndrome" 1292:"Henoch Schönlein purpura with nephritis in adults: adverse prognostic indicators in a UK population" 651:
molecule may provide an explanation for its abnormal behaviour in both HSP and the related condition
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Blanco R, Martínez-Taboada VM, Rodríguez-Valverde V, García-Fuentes M, González-Gay MA (May 1997).
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of the skin may be performed to distinguish the purpura from other diseases that cause it, such as
358:(high blood pressure) may occur. Protein loss and high blood pressure, as well as the features on 303:
as a fourth criterion; this occurs in 33% of cases, sometimes, but not necessarily always, due to
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Henoch–Schönlein purpura may present with an atypical manifestation, which can be confused with
683:. The majority of the serines and the threonines have elaborate sugar chains, connected through 3258: 3207: 2968: 912: 696: 550: 375: 351: 338:
Of the 40% of patients who develop kidney involvement, almost all have evidence (visible or on
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over a long period of time, rather than self-limiting and there tend to be more complications.
222: 2514: 1051:"Prognostic factors in leukocytoclastic vasculitis: a clinicopathologic study of 160 patients" 3405: 3382: 2227: 2273: 1997:"Interventions for preventing and treating kidney disease in Henoch-Schönlein Purpura (HSP)" 1670:
Jennette JC, Falk RJ, Andrassy K, Bacon PA, Churg J, Gross WL, et al. (February 1994).
3377: 3238: 3220: 3126: 3121: 3105: 3015: 2945: 2802: 2714: 2557: 2101: 1165:"Henoch-Schönlein purpura in children. Report of 100 patients and review of the literature" 936: 931:(1757–1812) had already described the disease in 1802 and 1808, respectively, but the name 558: 394: 2833: 1672:"Nomenclature of systemic vasculitides. Proposal of an international consensus conference" 980:"2012 revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides" 643:; it is uncertain whether the main cause is overproduction (in the digestive tract or the 8: 3415: 3410: 3199: 2463: 1756:"EULAR/PReS endorsed consensus criteria for the classification of childhood vasculitides" 720: 575: 502: 487: 398: 3148: 2105: 978:
Jennette JC, Falk RJ, Bacon PA, Basu N, Cid MC, Ferrario F, et al. (January 2013).
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As of 2017, the optimal way to treat Henoch–Schönlein purpura remains controversial.
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Ozen S, Ruperto N, Dillon MJ, Bagga A, Barron K, Davin JC, et al. (July 2006).
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Multiple standards exist for defining Henoch–Schönlein purpura, including the 1990
691:). This process is thought to stabilise the IgA molecule and make it less prone to 534: 506: 483: 456: 371: 253: 186: 69: 39:
IgA vasculitis, anaphylactoid purpura, purpura rheumatica, Schönlein–Henoch purpura
2207: 3040: 3010: 2894: 2822: 2676: 2629: 2479: 2335: 2114: 1507: 1490: 784: 751: 652: 514: 475:) in the blood vessel wall. However, overall serum complement levels are normal. 468: 379: 178: 174: 19: 2531: 2528: 2248: 1290:
Shrestha S, Sumingan N, Tan J, Alhous H, McWilliam L, Ballardie F (April 2006).
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Henoch–Schönlein purpura is a small-vessel vasculitis in which complexes of
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Sais G, Vidaller A, Jucglà A, Servitje O, Condom E, Peyri J (March 1998).
2681: 2661: 2645: 2509: 2382:"H20: <scp>Henoch–Schönlein</scp> purpura: what's in a name?" 2088:
Watson L, Richardson AR, Holt RC, Jones CA, Beresford MW (January 2012).
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HSP occurs more often in children than in adults, and usually follows an
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Weiss PF, Feinstein JA, Luan X, Burnham JM, Feudtner C (November 2007).
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may occur, but is much less common than in the skin, bowel and kidneys.
1517: 789: 775: 664: 632: 621: 617: 602: 598: 593: 570: 452: 413: 409: 339: 237: 190: 150: 3168: 2397: 1384:"Abnormalities of vascular prostaglandins in Henoch-Schönlein purpura" 996: 979: 346:(protein in the urine), which in one eighth is severe enough to cause 2520: 771: 700: 680: 613: 609: 525: 498: 402: 324: 292: 226: 214: 2381: 98: 2540: 827:
There is no good evidence that treating children who have HSP with
817: 779: 433: 432:(ESR) results; none are specific for Henoch–Schönlein purpura. The 54: 2301:. Landmarks in medicine series. Boca Raton: Parthenon Pub. Group. 1645:"1990 criteria for the classification of Henoch–Schönlein purpura" 1331:
Song Y, Huang X, Yu G, Qiao J, Cheng J, Wu J, et al. (2021).
189:(small, raised areas of bleeding underneath the skin), often with 2604: 945: 813: 672: 640: 588: 580: 478:
On the basis of symptoms, it is possible to distinguish HSP from
288: 273: 206: 2090:"Henoch schonlein purpura--a 5-year review and proposed pathway" 3290: 3276: 2973: 2442: 885: 684: 676: 538: 494: 448: 359: 320: 198: 2322:
Beighton P, Beighton G (1997), Beighton P, Beighton G (eds.),
1092:"Treatment Challenges, Uncertainty Abound with IgA Vasculitis" 2940: 2608: 903: 743: 584: 520: 316: 308: 210: 202: 182: 2587: 1851:
Hetland LE, Susrud KS, Lindahl KH, Bygum A (November 2017).
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Hetland LE, Susrud KS, Lindahl KH, Bygum A (November 2017).
2452: 513:. The changes are indistinguishable from those observed in 417: 332: 312: 280: 170: 122: 107: 84: 78: 1580: 1208:. Vol. 2 (11th ed.). McGraw Hill. p. 1441. 1048: 268: 119: 95: 2087: 1891: 1850: 1669: 1607: 1539: 1382:
Turi S, Belch JJ, Beattie TJ, Forbes CD (February 1986).
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Saulsbury FT (January 2001). "Henoch-Schönlein purpura".
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If there is doubt about the cause of the skin lesions, a
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whether the patient will develop chronic renal disease.
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Recurrence is more common in older children and adults.
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followed by prednisone. Other regimens include steroids/
671:-fixating regions 1 and 2. Of the amino acids, half is 1995:
Hahn D, Hodson EM, Willis NS, Craig JC (August 2015).
1805:"Atypical clinical course of Henoch-Schonlein purpura" 1753: 1710: 1381: 1333:"Pathogenesis of IgA Vasculitis: An Up-To-Date Review" 1994: 1023: 977: 284:
More severe case of HSP on child's foot, leg, and arm
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involvement, there may be a loss of small amounts of
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or equivalent renal replacement therapy (RRT). If a
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More than half also have 812:, and steroids/cyclophosphamide (with or without 774:may be needed for the abdominal and joint pains. 3397: 3059:Transfusion-associated graft-versus-host disease 2321: 1940: 1853:"Henoch-Schönlein Purpura: A Literature Review" 1542:"Henoch-Schönlein Purpura: A Literature Review" 1330: 1239: 1237: 1235: 1233: 1231: 1229: 1227: 1225: 1158: 1156: 1154: 1115: 2042: 2040: 1846: 1844: 1842: 1840: 1285: 1283: 944:is also the first to recognise the underlying 915:(1820–1910), a German pediatrician (nephew of 3297:Eosinophilic granulomatosis with polyangiitis 3184: 2573: 1941:Hahn D, Hodson EM, Craig JC (February 2023). 1454:Journal of the American Society of Nephrology 1885: 1704: 1447: 1222: 1151: 848:In adults, kidney involvement progresses to 2081: 2037: 2001:The Cochrane Database of Systematic Reviews 1990: 1988: 1986: 1947:The Cochrane Database of Systematic Reviews 1837: 1663: 1636: 1601: 1574: 1280: 1111: 1109: 1107: 1105: 1042: 1024:Rapini RP, Bolognia JL, Jorizzo JL (2007). 3191: 3177: 2580: 2566: 2192:"Epidemiology of Henoch-Schönlein purpura" 1443: 1441: 1439: 1437: 1435: 1433: 1431: 1429: 1427: 1116:Kraft DM, Mckee D, Scott C (August 1998). 1019: 1017: 1015: 635:. These antibodies are of the subclass IgA 459:; on microscopy, the appearances are of a 44: 2189: 2123: 2113: 2064: 2020: 1966: 1917: 1868: 1820: 1796: 1779: 1687: 1557: 1516: 1506: 1465: 1407: 1358: 1348: 1307: 1243: 1180: 1162: 1066: 995: 971: 737: 1983: 1448:Rai A, Nast C, Adler S (December 1999). 1203: 1102: 902: 519: 389: 279: 267: 248:) and is characterized by deposition of 3198: 3093:Allergic bronchopulmonary aspergillosis 2271: 1424: 1089: 1012: 420:levels (in kidney involvement), raised 3398: 726:More recent classifications, the 2006 545:HSP can develop after infections with 3431:Vascular-related cutaneous conditions 3172: 2915:Post-streptococcal glomerulonephritis 2561: 1802: 1713:Clinical and Experimental Dermatology 843: 263: 2330:, London: Springer, pp. 62–63, 2196:Cleveland Clinic Journal of Medicine 1450:"Henoch-Schönlein purpura nephritis" 1206:Harrison's Book of Internal Medicine 1118:"Henoch-Schönlein purpura: a review" 2296: 655:. One of the characteristics of IgA 442:thrombotic thrombocytopenic purpura 438:idiopathic thrombocytopenic purpura 401:of a patient with Henoch–Schönlein 323:involvement, mainly in the form of 13: 3343:Acute hemorrhagic edema of infancy 1643:American College of Rheumatology. 927:(1710–1801) and the dermatologist 760:acute hemorrhagic edema of infancy 728:European League Against Rheumatism 528:of human skin prepared for direct 424:levels (in about 50%), and raised 365: 185:. In the skin, the disease causes 53:Typical purpura on lower legs and 14: 3442: 3358:Cutaneous small-vessel vasculitis 3322:Cutaneous small-vessel vasculitis 3132:Autoimmune polyendocrine syndrome 2416: 959:Cutaneous small-vessel vasculitis 882:upper respiratory tract infection 710: 537:, the bottom fibrous area is the 3283:Granulomatosis with polyangiitis 2769:Hemolytic disease of the newborn 1760:Annals of the Rheumatic Diseases 1725:10.1046/j.1365-2230.2002.01063.x 1388:Archives of Disease in Childhood 1258:10.1097/00002281-200101000-00006 1182:10.1097/00005792-199911000-00005 717:American College of Rheumatology 551:β-haemolytic, Lancefield group A 68: 3353:Bullous small vessel vasculitis 2951:Subacute bacterial endocarditis 2813:Immune thrombocytopenic purpura 2374: 2357: 2315: 2290: 2265: 2241: 2183: 1934: 1747: 1533: 1482: 1375: 1324: 1246:Current Opinion in Rheumatology 875: 2386:British Journal of Dermatology 2328:The Person Behind the Syndrome 2013:10.1002/14651858.CD005128.pub3 1959:10.1002/14651858.CD005128.pub4 1197: 1163:Saulsbury FT (November 1999). 863:In ESKD, some eventually need 732:Pediatric Rheumatology Society 675:, while the others are mainly 430:erythrocyte sedimentation rate 225:. HSP is often preceded by an 1: 3031:Postorgasmic illness syndrome 2208:10.3949/ccjm.69.suppl_2.sii87 2161:10.1016/S0140-6736(02)11279-7 964: 824:(IVIG) is occasionally used. 667:-long "hinge region" between 3088:Hypersensitivity pneumonitis 2336:10.1007/978-1-4471-0925-9_31 2299:Dates in infectious diseases 2115:10.1371/journal.pone.0029512 1508:10.1016/j.autrev.2017.11.024 834: 765: 748:systemic lupus erythematosus 699:(GalNAc), followed by other 695:. The first sugar is always 505:, where blood is filtered), 385: 331:(brain and spinal cord) and 7: 3348:Cryoglobulinemic vasculitis 3154:Systemic autoimmune disease 2990:Allergic contact dermatitis 2910:Hypersensitivity vasculitis 2793:Autoimmune hemolytic anemia 1583:The Journal of Rheumatology 952: 940:allergic component in HSP. 911:The disease is named after 663:) is the presence of an 18 480:hypersensitivity vasculitis 461:hypersensitivity vasculitis 301:gastrointestinal hemorrhage 181:that most commonly affects 10: 3447: 3249:Thromboangiitis obliterans 2660:common allergies include: 2249:"Schönlein-Henoch purpura" 1857:Acta Dermato-Venereologica 1546:Acta Dermato-Venereologica 1090:Collins TR (August 2016). 1068:10.1001/archderm.134.3.309 898: 822:Intravenous immunoglobulin 616:, anti-inflammatory agent 17: 3426:Ailments of unknown cause 3370: 3335: 3314:Type III hypersensitivity 3312: 3266: 3257: 3229: 3206: 3114: 3080: 3071: 3049: 3003: 2982: 2963: 2933: 2887: 2872: 2831: 2783: 2776: 2762: 2732: 2707: 2622: 2599: 2500: 2424: 1811:(Review. Case Reports.). 1809:Canadian Family Physician 1350:10.3389/fimmu.2021.771619 1122:American Family Physician 886:Half of affected patients 509:, and the development of 140: 60: 52: 43: 35: 30: 3302:Microscopic polyangiitis 2905:Henoch–Schönlein purpura 2720:Eosinophilic esophagitis 2365:Schönlein-Henoch purpura 2272:Hellman N (2008-09-23). 2202:(Suppl 2): SII87–SII89. 2053:Arthritis and Rheumatism 1676:Arthritis and Rheumatism 1610:Arthritis and Rheumatism 984:Arthritis and Rheumatism 850:end-stage kidney disease 756:dermatitis herpetiformis 723:than those of the CHCC. 252:containing the antibody 159:Henoch–Schönlein purpura 31:Henoch–Schönlein purpura 18:Not to be confused with 3021:Hashimoto's thyroiditis 2808:Guillain–Barré syndrome 1803:Lawee D (August 2008). 1772:10.1136/ard.2005.046300 1337:Frontiers in Immunology 1055:Archives of Dermatology 933:Heberden–Willan disease 917:Moritz Heinrich Romberg 3122:Autoimmune adrenalitis 2392:(S1): 193. July 2022. 2066:10.1002/art.1780400513 1910:10.1542/peds.2007-0667 1689:10.1002/art.1780370206 1622:10.1002/art.1780330809 921:Johann Lukas Schönlein 913:Eduard Heinrich Henoch 908: 907:Johann Lukas Schönlein 738:Differential diagnosis 697:N-acetyl-galactosamine 542: 405: 376:complement component 3 352:chronic kidney disease 329:central nervous system 285: 277: 223:chronic kidney disease 177:, and sometimes other 169:, is a disease of the 2190:Saulsbury FT (2002). 1870:10.2340/00015555-2733 1559:10.2340/00015555-2733 1467:10.1681/ASN.V10122637 906: 524:Microphotograph of a 523: 467:demonstrates IgA and 393: 283: 271: 3378:Goodpasture syndrome 3239:Polyarteritis nodosa 3221:Giant cell arteritis 3216:Takayasu's arteritis 3127:Autoimmune hepatitis 3106:Transplant rejection 3016:Giant cell arteritis 2946:Rheumatoid arthritis 2803:Goodpasture syndrome 2715:Autoimmune urticaria 2297:Lee HS, ed. (2002). 2278:Renal Fellow Network 1495:Autoimmunity Reviews 1400:10.1136/adc.61.2.173 1309:10.1093/qjmed/hcl034 1028:. St. Louis: Mosby. 937:erythema infectiosum 559:herpes simplex virus 526:histological section 490:for predicting HSP. 3421:Autoimmune diseases 3200:Systemic vasculitis 2593:autoimmune diseases 2324:"GLANZMANN, Eduard" 2274:"Maladie de Berger" 2155:(9341): 1197–1202. 2106:2012PLoSO...729512W 576:Helicobacter pylori 397:showing IgA in the 258:relapsing–remitting 3383:Sneddon's syndrome 3036:Reactive arthritis 3026:Multiple sclerosis 2920:Reactive arthritis 2818:Pemphigus vulgaris 2798:Bullous pemphigoid 2699:Penicillin allergy 2635:Allergic urticaria 2501:External resources 2253:www.whonamedit.com 1096:The Rheumatologist 909: 844:Kidney involvement 798:methylprednisolone 543: 530:immunofluorescence 471:(a protein of the 465:immunofluorescence 426:C-reactive protein 412:may show elevated 406: 348:nephrotic syndrome 286: 278: 264:Signs and symptoms 236:HSP is a systemic 3391: 3390: 3366: 3365: 3166: 3165: 3162: 3161: 3067: 3066: 2959: 2958: 2868: 2867: 2864: 2863: 2856:Pernicious anemia 2851:Myasthenia gravis 2728: 2727: 2651:Atopic dermatitis 2640:Allergic rhinitis 2555: 2554: 2398:10.1111/bjd.21511 2345:978-1-4471-0925-9 2308:978-1-84214-150-2 1863:(10): 1160–1166. 1552:(10): 1160–1166. 1460:(12): 2637–2644. 1215:978-0-07-079454-2 1128:(2): 405–8, 411. 1035:978-1-4160-2999-1 997:10.1002/art.37715 869:kidney transplant 744:papular urticaria 507:white blood cells 473:complement system 165:), also known as 156: 155: 25:Medical condition 3438: 3264: 3263: 3244:Kawasaki disease 3193: 3186: 3179: 3170: 3169: 3149:Sjögren syndrome 3078: 3077: 2980: 2979: 2885: 2884: 2781: 2780: 2760: 2759: 2620: 2619: 2589:Hypersensitivity 2582: 2575: 2568: 2559: 2558: 2422: 2421: 2410: 2409: 2378: 2372: 2361: 2355: 2354: 2353: 2352: 2319: 2313: 2312: 2294: 2288: 2287: 2285: 2284: 2269: 2263: 2262: 2260: 2259: 2245: 2239: 2238: 2236: 2235: 2226:. Archived from 2187: 2181: 2180: 2144: 2138: 2137: 2127: 2117: 2085: 2079: 2078: 2068: 2044: 2035: 2034: 2024: 1992: 1981: 1980: 1970: 1938: 1932: 1931: 1921: 1904:(5): 1079–1087. 1889: 1883: 1882: 1872: 1848: 1835: 1834: 1824: 1815:(8): 1117–1120. 1800: 1794: 1793: 1783: 1751: 1745: 1744: 1708: 1702: 1701: 1691: 1667: 1661: 1660: 1658: 1656: 1647:. Archived from 1640: 1634: 1633: 1616:(8): 1114–1121. 1605: 1599: 1598: 1578: 1572: 1571: 1561: 1537: 1531: 1530: 1520: 1510: 1486: 1480: 1479: 1469: 1445: 1422: 1421: 1411: 1379: 1373: 1372: 1362: 1352: 1328: 1322: 1321: 1311: 1287: 1278: 1277: 1241: 1220: 1219: 1201: 1195: 1194: 1184: 1160: 1149: 1148: 1146: 1145: 1136:. Archived from 1113: 1100: 1099: 1087: 1081: 1080: 1070: 1046: 1040: 1039: 1021: 1010: 1009: 999: 975: 925:William Heberden 855:The findings on 802:cyclophosphamide 778:is warranted if 484:abdominal angina 457:cryoglobulinemia 372:immunoglobulin A 254:immunoglobulin A 250:immune complexes 231:throat infection 187:palpable purpura 175:mucous membranes 132: 131: 128: 127: 124: 121: 118: 113: 112: 109: 106: 103: 100: 97: 94: 90: 89: 86: 83: 80: 77: 74: 48: 28: 27: 3446: 3445: 3441: 3440: 3439: 3437: 3436: 3435: 3396: 3395: 3392: 3387: 3362: 3331: 3308: 3253: 3225: 3202: 3197: 3167: 3158: 3110: 3073: 3063: 3045: 3041:Type 1 diabetes 3011:Coeliac disease 2999: 2971: 2955: 2929: 2895:Arthus reaction 2876: 2860: 2846:Graves' disease 2827: 2823:Rheumatic fever 2772: 2740: 2724: 2703: 2630:Allergic asthma 2611: 2595: 2586: 2556: 2551: 2550: 2496: 2495: 2450: 2433: 2419: 2414: 2413: 2380: 2379: 2375: 2362: 2358: 2350: 2348: 2346: 2320: 2316: 2309: 2295: 2291: 2282: 2280: 2270: 2266: 2257: 2255: 2247: 2246: 2242: 2233: 2231: 2188: 2184: 2145: 2141: 2086: 2082: 2045: 2038: 2007:(8): CD005128. 1993: 1984: 1953:(2): CD005128. 1939: 1935: 1890: 1886: 1849: 1838: 1801: 1797: 1752: 1748: 1709: 1705: 1668: 1664: 1654: 1652: 1651:on 27 July 2011 1641: 1637: 1606: 1602: 1579: 1575: 1538: 1534: 1487: 1483: 1446: 1425: 1380: 1376: 1329: 1325: 1288: 1281: 1242: 1223: 1216: 1202: 1198: 1161: 1152: 1143: 1141: 1114: 1103: 1088: 1084: 1047: 1043: 1036: 1022: 1013: 976: 972: 967: 955: 901: 878: 846: 837: 785:corticosteroids 768: 752:meningococcemia 740: 713: 689:O-glycosylation 658: 653:IgA nephropathy 650: 638: 515:IgA nephropathy 388: 380:IgA nephropathy 368: 366:Pathophysiology 305:intussusception 266: 136: 115: 91: 71: 67: 26: 23: 20:IgA nephropathy 12: 11: 5: 3444: 3434: 3433: 3428: 3423: 3418: 3413: 3408: 3389: 3388: 3386: 3385: 3380: 3374: 3372: 3368: 3367: 3364: 3363: 3361: 3360: 3355: 3350: 3345: 3339: 3337: 3333: 3332: 3330: 3329: 3327:IgA vasculitis 3324: 3318: 3316: 3310: 3309: 3307: 3306: 3305: 3304: 3299: 3287: 3286: 3285: 3272: 3270: 3261: 3255: 3254: 3252: 3251: 3246: 3241: 3235: 3233: 3227: 3226: 3224: 3223: 3218: 3212: 3210: 3204: 3203: 3196: 3195: 3188: 3181: 3173: 3164: 3163: 3160: 3159: 3157: 3156: 3151: 3146: 3145: 3144: 3139: 3129: 3124: 3118: 3116: 3112: 3111: 3109: 3108: 3103: 3097: 3096: 3095: 3084: 3082: 3075: 3069: 3068: 3065: 3064: 3062: 3061: 3055: 3053: 3047: 3046: 3044: 3043: 3038: 3033: 3028: 3023: 3018: 3013: 3007: 3005: 3001: 3000: 2998: 2997: 2992: 2986: 2984: 2977: 2961: 2960: 2957: 2956: 2954: 2953: 2948: 2943: 2937: 2935: 2931: 2930: 2928: 2927: 2925:Serum sickness 2922: 2917: 2912: 2907: 2902: 2897: 2891: 2889: 2882: 2879:Immune complex 2870: 2869: 2866: 2865: 2862: 2861: 2859: 2858: 2853: 2848: 2842: 2840: 2829: 2828: 2826: 2825: 2820: 2815: 2810: 2805: 2800: 2795: 2789: 2787: 2778: 2774: 2773: 2771: 2766: 2764: 2757: 2756: 2755: 2754: 2753: 2748: 2730: 2729: 2726: 2725: 2723: 2722: 2717: 2711: 2709: 2705: 2704: 2702: 2701: 2696: 2695: 2694: 2689: 2684: 2679: 2674: 2669: 2664: 2653: 2648: 2643: 2637: 2632: 2626: 2624: 2617: 2597: 2596: 2585: 2584: 2577: 2570: 2562: 2553: 2552: 2549: 2548: 2537: 2517: 2505: 2504: 2502: 2498: 2497: 2494: 2493: 2482: 2471: 2456: 2434: 2429: 2428: 2426: 2425:Classification 2418: 2417:External links 2415: 2412: 2411: 2373: 2356: 2344: 2314: 2307: 2289: 2264: 2240: 2182: 2139: 2080: 2059:(5): 859–864. 2036: 1982: 1933: 1884: 1836: 1795: 1766:(7): 936–941. 1746: 1719:(4): 260–263. 1703: 1682:(2): 187–192. 1662: 1635: 1600: 1589:(5): 721–728. 1573: 1532: 1501:(3): 301–315. 1481: 1423: 1394:(2): 173–177. 1374: 1323: 1302:(4): 253–265. 1279: 1221: 1214: 1196: 1175:(6): 395–409. 1150: 1101: 1082: 1061:(3): 309–315. 1041: 1034: 1011: 969: 968: 966: 963: 962: 961: 954: 951: 900: 897: 877: 874: 845: 842: 836: 833: 767: 764: 739: 736: 712: 711:Classification 709: 656: 648: 636: 607:ACE inhibitors 567:Coxsackievirus 563:parvovirus B19 493:Biopsy of the 395:Immunostaining 387: 384: 367: 364: 297:abdominal pain 265: 262: 195:abdominal pain 167:IgA vasculitis 154: 153: 144: 138: 137: 135: 134: 64: 62: 58: 57: 50: 49: 41: 40: 37: 33: 32: 24: 9: 6: 4: 3: 2: 3443: 3432: 3429: 3427: 3424: 3422: 3419: 3417: 3414: 3412: 3409: 3407: 3404: 3403: 3401: 3394: 3384: 3381: 3379: 3376: 3375: 3373: 3369: 3359: 3356: 3354: 3351: 3349: 3346: 3344: 3341: 3340: 3338: 3334: 3328: 3325: 3323: 3320: 3319: 3317: 3315: 3311: 3303: 3300: 3298: 3295: 3294: 3293: 3292: 3288: 3284: 3281: 3280: 3279: 3278: 3274: 3273: 3271: 3269: 3265: 3262: 3260: 3256: 3250: 3247: 3245: 3242: 3240: 3237: 3236: 3234: 3232: 3231:Medium vessel 3228: 3222: 3219: 3217: 3214: 3213: 3211: 3209: 3205: 3201: 3194: 3189: 3187: 3182: 3180: 3175: 3174: 3171: 3155: 3152: 3150: 3147: 3143: 3140: 3138: 3135: 3134: 3133: 3130: 3128: 3125: 3123: 3120: 3119: 3117: 3113: 3107: 3104: 3101: 3100:Latex allergy 3098: 3094: 3091: 3090: 3089: 3086: 3085: 3083: 3079: 3076: 3070: 3060: 3057: 3056: 3054: 3052: 3048: 3042: 3039: 3037: 3034: 3032: 3029: 3027: 3024: 3022: 3019: 3017: 3014: 3012: 3009: 3008: 3006: 3002: 2996: 2993: 2991: 2988: 2987: 2985: 2981: 2978: 2975: 2970: 2969:cell-mediated 2966: 2962: 2952: 2949: 2947: 2944: 2942: 2939: 2938: 2936: 2932: 2926: 2923: 2921: 2918: 2916: 2913: 2911: 2908: 2906: 2903: 2901: 2900:Farmer's lung 2898: 2896: 2893: 2892: 2890: 2886: 2883: 2880: 2875: 2871: 2857: 2854: 2852: 2849: 2847: 2844: 2843: 2841: 2839: 2835: 2830: 2824: 2821: 2819: 2816: 2814: 2811: 2809: 2806: 2804: 2801: 2799: 2796: 2794: 2791: 2790: 2788: 2786: 2782: 2779: 2775: 2770: 2767: 2765: 2761: 2758: 2752: 2749: 2747: 2744: 2743: 2742: 2741: 2739: 2735: 2731: 2721: 2718: 2716: 2713: 2712: 2710: 2706: 2700: 2697: 2693: 2690: 2688: 2685: 2683: 2680: 2678: 2675: 2673: 2670: 2668: 2665: 2663: 2659: 2658: 2657: 2654: 2652: 2649: 2647: 2644: 2641: 2638: 2636: 2633: 2631: 2628: 2627: 2625: 2621: 2618: 2615: 2610: 2606: 2602: 2598: 2594: 2590: 2583: 2578: 2576: 2571: 2569: 2564: 2563: 2560: 2547: 2543: 2542: 2538: 2536: 2533: 2530: 2527: 2523: 2522: 2518: 2516: 2512: 2511: 2507: 2506: 2503: 2499: 2492: 2488: 2487: 2483: 2481: 2477: 2476: 2472: 2470: 2466: 2465: 2461: 2457: 2454: 2449: 2445: 2444: 2440: 2436: 2435: 2432: 2427: 2423: 2407: 2403: 2399: 2395: 2391: 2387: 2383: 2377: 2371: 2370:Who Named It? 2367: 2366: 2360: 2347: 2341: 2337: 2333: 2329: 2325: 2318: 2310: 2304: 2300: 2293: 2279: 2275: 2268: 2254: 2250: 2244: 2230:on 2020-03-27 2229: 2225: 2221: 2217: 2213: 2209: 2205: 2201: 2197: 2193: 2186: 2178: 2174: 2170: 2166: 2162: 2158: 2154: 2150: 2143: 2135: 2131: 2126: 2121: 2116: 2111: 2107: 2103: 2100:(1): e29512. 2099: 2095: 2091: 2084: 2076: 2072: 2067: 2062: 2058: 2054: 2050: 2043: 2041: 2032: 2028: 2023: 2018: 2014: 2010: 2006: 2002: 1998: 1991: 1989: 1987: 1978: 1974: 1969: 1964: 1960: 1956: 1952: 1948: 1944: 1937: 1929: 1925: 1920: 1915: 1911: 1907: 1903: 1899: 1895: 1888: 1880: 1876: 1871: 1866: 1862: 1858: 1854: 1847: 1845: 1843: 1841: 1832: 1828: 1823: 1818: 1814: 1810: 1806: 1799: 1791: 1787: 1782: 1777: 1773: 1769: 1765: 1761: 1757: 1750: 1742: 1738: 1734: 1730: 1726: 1722: 1718: 1714: 1707: 1699: 1695: 1690: 1685: 1681: 1677: 1673: 1666: 1650: 1646: 1639: 1631: 1627: 1623: 1619: 1615: 1611: 1604: 1596: 1592: 1588: 1584: 1577: 1569: 1565: 1560: 1555: 1551: 1547: 1543: 1536: 1528: 1524: 1519: 1514: 1509: 1504: 1500: 1496: 1492: 1485: 1477: 1473: 1468: 1463: 1459: 1455: 1451: 1444: 1442: 1440: 1438: 1436: 1434: 1432: 1430: 1428: 1419: 1415: 1410: 1405: 1401: 1397: 1393: 1389: 1385: 1378: 1370: 1366: 1361: 1356: 1351: 1346: 1342: 1338: 1334: 1327: 1319: 1315: 1310: 1305: 1301: 1297: 1293: 1286: 1284: 1275: 1271: 1267: 1263: 1259: 1255: 1251: 1247: 1240: 1238: 1236: 1234: 1232: 1230: 1228: 1226: 1217: 1211: 1207: 1200: 1192: 1188: 1183: 1178: 1174: 1170: 1166: 1159: 1157: 1155: 1140:on 2011-06-06 1139: 1135: 1131: 1127: 1123: 1119: 1112: 1110: 1108: 1106: 1097: 1093: 1086: 1078: 1074: 1069: 1064: 1060: 1056: 1052: 1045: 1037: 1031: 1027: 1020: 1018: 1016: 1007: 1003: 998: 993: 989: 985: 981: 974: 970: 960: 957: 956: 950: 947: 943: 942:William Osler 938: 934: 930: 929:Robert Willan 926: 922: 918: 914: 905: 896: 893: 891: 887: 883: 873: 870: 866: 861: 858: 853: 851: 841: 832: 830: 825: 823: 819: 815: 811: 807: 803: 799: 793: 791: 786: 781: 777: 773: 763: 761: 757: 753: 749: 745: 735: 733: 729: 724: 722: 718: 708: 706: 702: 698: 694: 690: 686: 682: 678: 674: 670: 666: 662: 654: 646: 642: 634: 629: 627: 626:streptokinase 623: 620:, as well as 619: 615: 611: 608: 604: 600: 596: 595: 590: 586: 582: 578: 577: 572: 568: 564: 560: 556: 552: 548: 540: 536: 531: 527: 522: 518: 516: 512: 508: 504: 501:(part of the 500: 496: 491: 489: 485: 481: 476: 474: 470: 466: 462: 458: 454: 450: 445: 443: 439: 435: 431: 427: 423: 419: 415: 411: 404: 400: 396: 392: 383: 381: 377: 373: 363: 361: 357: 353: 349: 345: 341: 336: 334: 330: 326: 322: 318: 314: 310: 306: 302: 298: 294: 290: 282: 275: 270: 261: 259: 255: 251: 247: 246:blood vessels 243: 239: 234: 232: 228: 224: 220: 216: 212: 208: 204: 200: 196: 192: 188: 184: 180: 176: 172: 168: 164: 160: 152: 148: 145: 143: 139: 130: 66: 65: 63: 61:Pronunciation 59: 56: 51: 47: 42: 38: 34: 29: 21: 16: 3406:Rheumatology 3393: 3326: 3289: 3275: 3268:Pauci-immune 3259:Small vessel 3208:Large vessel 2995:Mantoux test 2904: 2656:Food allergy 2539: 2519: 2508: 2484: 2473: 2458: 2437: 2389: 2385: 2376: 2363: 2359: 2349:, retrieved 2327: 2317: 2298: 2292: 2281:. Retrieved 2277: 2267: 2256:. Retrieved 2252: 2243: 2232:. Retrieved 2228:the original 2199: 2195: 2185: 2152: 2148: 2142: 2097: 2093: 2083: 2056: 2052: 2004: 2000: 1950: 1946: 1936: 1901: 1897: 1887: 1860: 1856: 1812: 1808: 1798: 1763: 1759: 1749: 1716: 1712: 1706: 1679: 1675: 1665: 1653:. Retrieved 1649:the original 1638: 1613: 1609: 1603: 1586: 1582: 1576: 1549: 1545: 1535: 1498: 1494: 1484: 1457: 1453: 1391: 1387: 1377: 1340: 1336: 1326: 1299: 1295: 1252:(1): 35–40. 1249: 1245: 1205: 1199: 1172: 1168: 1142:. Retrieved 1138:the original 1125: 1121: 1095: 1085: 1058: 1054: 1044: 1025: 987: 983: 973: 932: 910: 894: 879: 876:Epidemiology 865:hemodialysis 862: 857:renal biopsy 854: 847: 838: 829:antiplatelet 826: 810:azathioprine 806:dipyridamole 794: 769: 741: 730:(EULAR) and 725: 714: 630: 592: 574: 547:streptococci 544: 492: 477: 446: 407: 369: 356:Hypertension 337: 287: 276:on lower leg 242:inflammation 235: 229:, such as a 166: 162: 158: 157: 147:Rheumatology 15: 2646:Anaphylaxis 2642:(Hay fever) 2510:MedlinePlus 1655:15 December 1518:10481/51942 1026:Dermatology 990:(1): 1–11. 800:(steroid), 705:sialic acid 693:proteolysis 645:bone marrow 555:hepatitis B 488:sensitivity 410:Blood tests 344:proteinuria 219:proteinuria 36:Other names 3416:Nephrology 3411:Pediatrics 3400:Categories 3115:Autoimmune 3004:Autoimmune 2934:Autoimmune 2777:Autoimmune 2708:Autoimmune 2486:DiseasesDB 2351:2024-04-29 2283:2024-04-30 2258:2024-04-29 2234:2012-08-26 1898:Pediatrics 1859:(Review). 1343:: 771619. 1144:2007-12-15 965:References 790:prednisone 780:skin death 776:Wound care 772:Analgesics 701:galactoses 669:complement 665:amino acid 633:vasculitis 622:ranitidine 618:diclofenac 603:cefuroxime 599:vancomycin 594:Mycoplasma 571:adenovirus 503:glomerulus 453:vasculitis 414:creatinine 399:glomerulus 374:(IgA) and 340:urinalysis 238:vasculitis 191:joint pain 151:Immunology 3336:Ungrouped 2785:Cytotoxic 2532:emerg/845 2529:emerg/767 2521:eMedicine 2406:0007-0963 890:incidence 835:Prognosis 766:Treatment 721:sensitive 681:threonine 614:captopril 610:enalapril 535:epidermis 511:crescents 499:mesangium 428:(CRP) or 403:nephritis 386:Diagnosis 325:hematuria 293:arthritis 227:infection 215:hematuria 142:Specialty 3074:multiple 3072:Unknown/ 2874:Type III 2838:receptor 2687:Tree nut 2541:Orphanet 2535:ped/3020 2526:derm/177 2455:D69.010) 2216:12086273 2177:25018798 2169:12401245 2134:22235302 2094:PLOS ONE 2031:26258874 1977:36853224 1928:17974746 1879:28654132 1831:18697972 1790:16322081 1741:45849349 1733:12139664 1568:28654132 1527:29353097 1476:10589705 1369:34858429 1318:16565522 1274:32647673 1266:11148713 1191:10575422 1169:Medicine 1006:23045170 953:See also 946:allergic 818:warfarin 641:polymers 434:platelet 272:Typical 183:children 55:buttocks 3081:Foreign 2983:Foreign 2974:T cells 2965:Type IV 2888:Foreign 2763:Foreign 2734:Type II 2677:Seafood 2623:Foreign 2605:allergy 2480:D011695 2224:4714914 2125:3250434 2102:Bibcode 2075:9153547 2022:9588174 1968:9972777 1919:3525094 1822:2515239 1781:1798210 1698:8129773 1630:2202310 1595:1613701 1418:2420289 1409:1777583 1360:8630619 1134:9713395 1077:9521029 899:History 814:heparin 758:, and 687:atoms ( 673:proline 589:rubella 581:measles 455:due to 289:Purpura 274:purpura 209:in the 207:protein 197:. 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Index

IgA nephropathy

buttocks
/ˈhɛnəkˈʃɜːnln,ˈʃn-/
Specialty
Rheumatology
Immunology
skin
mucous membranes
organs
children
palpable purpura
joint pain
abdominal pain
kidney
blood
protein
urine
hematuria
proteinuria
chronic kidney disease
infection
throat infection
vasculitis
inflammation
blood vessels
immune complexes
immunoglobulin A
relapsing–remitting

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