Ematuria e proteinuria

Author:

Scaramuzzino Fabiola1,Burlo Francesca2,Delcaro Giulia2,Peinkhofer Martina2,Sutera Marco2,Persia Sabrina1,Emma Francesco3

Affiliation:

1. Scuola di Specializzazione in Pediatria, Università “Tor Vergata”, Roma

2. Scuola di Specializzazione in Pediatria, Università di Trieste

3. IRCCS Ospedale Pediatrico “Bambino Gesù”, Roma

Abstract

Proteinuria and haematuria are common findings in children. However, they are indicative of a renal or urinary condition only in a minority of cases. The probability of an underlying disease causing haematuria and /or proteinuria increases when they are associated and in the presence of symptoms that suggest kidney damage, such as oedema, hypertension, or kidney failure. Transient and orthostatic proteinurias are benign conditions that do not require further investigations. Proteinuria should always be investigated when constant or heavy. If patients present with nephrotic syndrome, oedema and hypoalbuminemia, proteinuria is always pathologic. Tubular proteinuria should always be ruled out, in particular in male subjects with persistent proteinuria. Haematuria can be glomerular or non-glomerular and may present as gross haematuria or can only be detected microscopically. Macroscopic haematuria should always be investigated as it may be associated with benign conditions (fever, exertion, dehydration, nutcracker syndrome), but also with several conditions such as glomerular diseases or urolithiasis. The urine colour, the urinary sediment, the morphology of red blood cells, kidney function, the presence of proteinuria and the medical history help in the differential diagnosis. On the other hand, microscopic haematuria should be investigated only when persistent or if there is a positive family history. This paper presents 5 illustrative cases to highlight the above points.

Publisher

Medico e Bambino

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