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Published on: October 7, 2021
A pediatric case of critical illness polyneuropathy: clinical and pathological findings
Tatsuyuki Ohto1, Nobuaki Iwasaki, Norio Ohkoshi
1Department of Pediatrics, Institute of Clinical Medicine, University of Tsukuba, 1-1-1 Tennohdai, Tsukuba, Ibaraki 305-8575, Japan. tohto@md.tsukuba.ac.jp
Insights
Critical illness polyneuropathy (CIP) is a rare condition in children. This case study details a 13-year-old boy with CIP, highlighting his peripheral nerve pathology during the chronic stage.
Area of Science:
- Neurology
- Pediatrics
- Intensive Care Medicine
Background:
- Critical illness polyneuropathy (CIP) is a sensorimotor neuropathy typically seen in adult ICU patients.
- Cases of CIP in children are rare, often associated with sepsis and multiple organ dysfunction.
Observation:
- A 13-year-old Japanese boy developed tetraplegia during encephalopathy recovery.
- Neurological examination revealed absent deep tendon reflexes.
- Standard diagnostic tests including MRI and CSF analysis were normal.
Findings:
- Nerve conduction studies showed undetectable motor and sensory velocities in lower limbs.
- Sural nerve biopsy revealed significant loss of large myelinated fibers, thin myelin sheaths, and small fiber clusters.
- Pathology indicated primary axonal degeneration with evidence of regeneration.
Implications:
- This report provides the first neuropathological description of chronic-stage CIP in a pediatric patient.
- Understanding these changes is crucial for diagnosing and managing CIP in children.
- Further research is needed to elucidate the long-term outcomes and treatment strategies for pediatric CIP.
Abstract:
Critical illness polyneuropathy (CIP) is a sensorimotor polyneuropathy recognized in adult intensive care patients with sepsis and multiple organ dysfunction and only a few cases have been reported in children. Here we report a 13-year-old Japanese boy with CIP that developed during the course of encephalopathy. Two months after the onset of encephalopathy, he developed tetraplegia although consciousness had already recovered. Deep tendon reflex was absent. MRI of the brain and spinal cord was normal and no abnormality in the cerebrospinal fluid was detected. Motor and sensory nerve conduction velocities of the lower limbs and somatosensory evoked potential could not be detected. The motor activity subsequently showed gradual recovery, although standing and walking could not be achieved. Sural nerve biopsy performed 3 years after the onset showed severe reduction of the number of myelinated large-diameter fibers, thin myelin in almost all fibers and cluster formation of myelinated small-diameter fibers, indicating primary axonal degeneration with regeneration. We report here for the first time the neuropathological changes in peripheral nerves during the chronic stage of CIP in children.
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