Improvement in Nerve Size on Ultrasound After IV IG in a Multifactorial Chronic Inflammatory Neuropathy
Himanshu Verma1, Laura Danielson3, Saif Bawaneh4, Mittal Prajapati2
1neurology, Creighton University School of Medicine, 2Creighton University School of Medicine, 3CHI Health, 4creighton university
Objective:

Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an immune-mediated, acquired polyneuropathy affecting spinal nerve roots and peripheral nerves, typically progressive or relapsing-remitting. Diagnosis can be challenging due to strict criteria and confounding comorbidities, especially with the growing range of CIDP variants and CIDP-like neuropathies. This case highlights a patient with chronic inflammatory neuropathy and multiple comorbidities that likely contributed to her condition.

Background:

A 52-year-old woman with history of type-1 diabetes, hypothyroidism, hemolytic anemia and breast cancer (treated with carboplatin, paclitaxel and pembrolizumab) presented to the neuromuscular clinic in mid-2023 with difficulty walking and leg pain for 4 months, bilateral foot numbness since 2020, and foot drop starting in mid-2022.

Nerve conduction studies (NCS) and electromyogram (EMG) demonstrated a chronic, generalized, moderately severe axonal > demyelinating sensorimotor peripheral polyneuropathy. Due to demyelinating features on EMG, a neuromuscular ultrasound (NMUS) was conducted, revealing marked multifocal enlargement of the median and ulnar nerves, and brachial plexus trunks at both entrapment and non-entrapment sites.

Lumbar puncture showed profound albuminocytologic dissociation. IVIG was initiated, resulting in clinical improvement with patient being discharged on maintenance IVIG every 3 weeks. Unfortunately, her diabetes and hypothyroidism became uncontrolled for several months post-hospitalization. She subsequently tested borderline positive for Caspr-1 antibodies, raising concerns for an alternative diagnosis of autoimmune nodo-paranodopathy. However, sural nerve biopsy showed diffuse loss of large and small myelinated axons with C5b-9 expression in endoneurial microvasculature, with no signs of vasculitis or active demyelination. A follow-up NMUS in March 2024 evaluated the response to IVIG, demonstrated reduced or normalized nerve size at some sites, despite clinical and electrophysiologic decline.

Design/Methods:
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Results:
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Conclusions:

Ultrasound showing reduced or normalized nerve size has been reported in response to successful CIDP treatment. This case illustrates an ultrasound response to IVIG treatment in a chronic inflammatory neuropathy, despite confounding comorbidities limiting clinical improvement.

10.1212/WNL.0000000000212469
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