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Peripheral nervous system manifestations of Shiga toxin-producing E. coli-induced haemolytic uremic syndrome in children

The Neurological involvement is the most common extra-renal complication of Shiga toxin-producing E. coli-hemolytic uremic syndrome (HUS) or typical HUS. On brain magnetic resonance examination, main neurological signs encompass acute lesions of the basal ganglia and the white matter, which could us...

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Published in:Italian journal of pediatrics 2021-09, Vol.47 (1), p.181-181, Article 181
Main Authors: Santangelo, Luisa, Netti, Giuseppe Stefano, Torres, Diletta Domenica, Piscopo, Giovanni, Carbone, Vincenza, Losito, Luciana, Milella, Leonardo, Lasorella, Maria Luigia, Conti, Pasquale, Gagliardi, Delio, Chironna, Maria, Spadaccino, Federica, Bresin, Elena, Trabacca, Antonio, Ranieri, Elena, Giordano, Mario
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cited_by cdi_FETCH-LOGICAL-c563t-c476c28f7e379fcdf5d5cfe303b3b730886fa22ea63b222a27877899fc12ff03
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container_title Italian journal of pediatrics
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creator Santangelo, Luisa
Netti, Giuseppe Stefano
Torres, Diletta Domenica
Piscopo, Giovanni
Carbone, Vincenza
Losito, Luciana
Milella, Leonardo
Lasorella, Maria Luigia
Conti, Pasquale
Gagliardi, Delio
Chironna, Maria
Spadaccino, Federica
Bresin, Elena
Trabacca, Antonio
Ranieri, Elena
Giordano, Mario
description The Neurological involvement is the most common extra-renal complication of Shiga toxin-producing E. coli-hemolytic uremic syndrome (HUS) or typical HUS. On brain magnetic resonance examination, main neurological signs encompass acute lesions of the basal ganglia and the white matter, which could usually regress after Eculizumab infusion. In contrast, peripheral nervous system (PNS) manifestations in typical HUS are very rare and, when occurring, they require a careful management of neurological sequelae and an intensive multidisciplinary neuro-rehabilitation program. Here, we present two pediatric cases of severe and complicated typical HUS with PNS manifestations who required therapeutic treatment and an intensive multidisciplinary neuro-rehabilitation program. In both cases, PNS manifestations were followed by the recovery from typical HUS-related severe central neurological damage and manifested mainly with marked bilateral motor deficit and hyporeflexia/areflexia in the lower limbs. The peripheral polyneuropathy was treated with immunosuppressive therapy (methylprednisolone boluses, i.v. immunoglobulins, plasma exchange), followed by a prolonged intensive neuro-rehabilitation program. After 8 months of rehabilitation, both patients gained complete functional recovery. PNS manifestations during typical HUS are a rare event and potentially leading to severe disability. A timely clinical assessment is mandatory to set up a prompt therapeutic and rehabilitation program and to obtain a complete clinical and functional recovery.
doi_str_mv 10.1186/s13052-021-01133-1
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ispartof Italian journal of pediatrics, 2021-09, Vol.47 (1), p.181-181, Article 181
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source Publicly Available Content Database; PubMed Central
subjects Anemia
Anti-Inflammatory Agents - therapeutic use
Basal ganglia
Blood pressure
Case Report
Child
Child, Preschool
Coma
Creatinine
Diarrhea
E coli
Eculizumab
Electroencephalography
Enterohemorrhagic Escherichia Coli
Escherichia coli Infections
Female
Hemolytic uremic syndrome
Hemolytic-Uremic Syndrome - complications
Hemolytic-Uremic Syndrome - therapy
Humans
Hypokalemia
Hypoxia
Immunoglobulins
Immunoglobulins, Intravenous - therapeutic use
Immunosuppressive agents
Infectious diseases
Laboratories
Methylprednisolone
Methylprednisolone - therapeutic use
Nephrology
Nervous system
Neurological complications
Neurological Rehabilitation
Neurorehabilitation
Neutrophils
Patients
Pediatrics
Peripheral nervous system
Plasma Exchange
Polyneuropathies - etiology
Polyneuropathies - therapy
Polyneuropathy
Potassium
Recovery of function
Rehabilitation
Renal replacement therapy
Shiga toxin
Shiga-Toxigenic Escherichia coli
Streptococcus infections
Substantia alba
Thrombocytopenia
Ventilators
Visual impairment
title Peripheral nervous system manifestations of Shiga toxin-producing E. coli-induced haemolytic uremic syndrome in children
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