Acute nephritis
Revisado por pares por Dr Laurence KnottÚltima actualización por Dr Colin Tidy, MRCGPLast updated 21 Mar 2022
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Profesionales Médicos
Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find the Glomerulonefritis article more useful, or one of our other artículos de salud.
En este artículo:
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What is nephritis?
Nephritis essentially means inflammation of the kidney. Nephritis may involve the glomerulus, tubule, or the interstitial renal tissue.
When inflammation involves the glomeruli it is called glomerulonefritis.
When kidney disease involves structures in the kidney outside the glomerulus, it is broadly referred to as tubulo-interstitial disease. This disease generally involves the tubules and/or the interstitium of the kidney and spares the glomeruli.
When inflammation affects the area of the kidney between the nephrons (the renal interstitium) it is known as interstitial nephritis, or sometimes tubulo-interstitial nephritis.
Renal disease can present in a number of different ways, including as:
Nephritic syndrome (nephritis).
Renal pain and dysuria.
Glomerulonefritis can present with different clinical syndromes. These include nephrotic and nephritic syndrome. Glomerulonephritis accounts for about 10% of cases of acute kidney injury in adults, mainly related to rapidly progressive glomerulonephritis resulting from granulomatous polyangiitis (GPA, Wegener granulomatosis), microscopic polyangiitis (MPA), and anti-glomerular basement membrane (GBM) disease.1 Glomerulonephritis is discussed in more detail in the separate Glomerulonefritis article.
Nefritis intersticial can be acute or chronic. Acute interstitial nephritis is commonly due to a drug hypersensitivity reaction and presents as sudden-onset acute kidney injury.2 Acute interstitial nephritis is estimated to account for 15-20% of cases of lesión renal aguda.3
Granulomatous interstitial nephritis (GIN) is rare, detected in 0.5-0.9% of all renal biopsies.4
So, nephritis and nephrosis are responses to renal disease or injury. There are a number of underlying disease processes that can lead to both nephritic and nephrotic syndromes.5 See also separate articles:
Acute nephritic syndrome
Volver al contenidoAcute nephritic syndrome is often the most serious and potentially devastating form of the various renal syndromes.
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Características clínicas
Volver al contenidoThe key clinical features of acute nephritic syndrome are:
Disminución de la producción de orina.
Fluid retention and oedema (including periorbital, edema periférico y edema pulmonar).
Proteinuria (usually <3.5 g/day).
Hipertensión.
Uraemic symptoms (including anorexia, pruritus, lethargy, nausea).
Deteriorating renal function.
Acute nephritis causes (aetiology)
Volver al contenidoPost-infection with nephritogenic strains of Group A beta-haemolytic streptococcus (typically occurs in children).
Any of the other causes of glomerulonephritis:
Other bacterial infections - eg, typhoid, secondary syphilis, meticillin-resistant Staphylococcus aureus (MRSA) infection, pneumococcal pneumonia, endocarditis infecciosa.
Viral infections - eg, hepatitis B, paperas, sarampión, infectious mononucleosis, varicella, Coxsackievirus.
Parasitic infections - eg, malaria, toxoplasmosis.
Multisystem systemic diseases - eg, lupus eritematoso sistémico (LES), vasculitis, Púrpura de Henoch-Schönlein, Síndrome de Goodpasture, granulomatosis con poliangeítis.
Primary glomerular diseases - eg, Berger's disease (IgA nephropathy), membranoproliferative glomerulonephritis.
Diphtheria-pertussis-tetanus vaccine.
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Manejo
Volver al contenidoIn primary care
Take a history - ask about onset of nephritis symptoms and uraemic symptoms; look for a clue to an underlying cause - eg, recent streptococcal infection, other infection, multisystem disease.
Measure blood pressure.
Assess for peripheral, periorbital and pulmonary oedema.
Perform urine dipstick for protein and blood.
If acute nephritic syndrome is suspected, patients should be referred to secondary care. Acute admission may be required.
In secondary care
Investigations are focused on assessing severity of renal injury and looking for the underlying cause - discussed in detail in the separate Glomerulonefritis article.
Management depends on the underlying cause of acute nephritis and is also discussed in the same article.
Nephritis prognosis
Volver al contenidoThis depends on the underlying cause of nephritis. The prognosis for nephritic syndrome caused by acute post-streptococcal glomerulonephritis in children is generally excellent.
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Lecturas adicionales y referencias
- KDIGO Clinical Practice Guideline for Glomerulonephritis; International Society of Nephrology (2021).
- Pesce F, Stea ED, Rossini M, et al; Glomerulonephritis in AKI: From Pathogenesis to Therapeutic Intervention. Front Med (Lausanne). 2021 Mar 2;7:582272. doi: 10.3389/fmed.2020.582272. eCollection 2020.
- Moledina DG, Perazella MA; Drug-Induced Acute Interstitial Nephritis. Clin J Am Soc Nephrol. 2017 Dec 7;12(12):2046-2049. doi: 10.2215/CJN.07630717. Epub 2017 Sep 11.
- Raghavan R, Eknoyan G; Acute interstitial nephritis - a reappraisal and update. Clin Nephrol. 2014 Sep;82(3):149-62. doi: 10.5414/cn108386.
- Shah S, Carter-Monroe N, Atta MG; Granulomatous interstitial nephritis. Clin Kidney J. 2015 Oct;8(5):516-23. doi: 10.1093/ckj/sfv053. Epub 2015 Jul 5.
- Moledina DG, Parikh CR; Differentiating Acute Interstitial Nephritis from Acute Tubular Injury: A Challenge for Clinicians. Nephron. 2019;143(3):211-216. doi: 10.1159/000501207. Epub 2019 Jun 14.
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About the authorView full bio

Dr Colin Tidy, MRCGP
Médico General, Autor Médico
MBBS, MRCGP, MRCP (Paediatrics), DCH
Dr Colin Tidy is an NHS Doctor, based in Oxfordshire.
About the reviewerView full bio

Dr Laurence Knott
Médico General, Autor Médico
BSc (Hons) Biochemistry, MBBS
Dr Laurence Knott qualified in 1973 and has had extensive experience as a General Practitioner.
Historial del artículo
La información en esta página está escrita y revisada por pares por clínicos calificados.
Next review due: 20 Mar 2027
21 Mar 2022 | Última versión

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