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Case Reports
. 2024 Dec;45(12):5933-5937.
doi: 10.1007/s10072-024-07747-7. Epub 2024 Sep 3.

Charcot-Marie-Tooth type 2CC misdiagnosed as Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Isabella Di Sarno  1 , Stefano Tozza  2 , Filippo Maria Santorelli  3 , Emanuele Cassano  1 , Gemma Natale  3 , Raffaele Dubbioso  1 , Lucia Ruggiero  1 , Alessandra Tessa  3 , Rosa Iodice  1 , Maria Nolano  1 , Fiore Manganelli  1
Affiliations
Case Reports

Charcot-Marie-Tooth type 2CC misdiagnosed as Chronic Inflammatory Demyelinating Polyradiculoneuropathy

Isabella Di Sarno et al. Neurol Sci. 2024 Dec.

Abstract

Background and aims: Charcot-Marie-Tooth (CMT) is a heterogeneous group of genetic neuropathies and is typically characterized by distal muscle weakness, sensory loss, pes cavus and areflexia. Herein we describe a case of CMT2CC presenting with proximal muscle weakness and equivocal electrophysiological features, that was misdiagnosed as chronic inflammatory demyelinating polyneuropathy (CIDP).

Case report: A 30-year-old woman complained of proximal muscle weakness with difficulty climbing stairs. Neurological examination showed weakness in lower limb (LL) muscles, that was marked proximally and mild distally, and absence of deep tendon reflexes in the ankles. Nerve conduction studies (NCS) showed sensory-motor neuropathy with non-uniform NC velocity and a partial conduction block (CBs) in peroneal nerve and tibial nerves. Thus, a diagnosis of CIDP was entertained and the patient underwent ineffective treatment with intravenous immunoglobulins. At electrophysiological revaluation CB in peroneal nerve was undetectable as also distal CMAP had decreased whereas the CBs persisted in tibial nerves. Hypothesizing a hereditary neuropathy, we examined the proband's son, who presented mild weakness of distal and proximal muscles at lower limbs. Neurophysiological investigation showed findings consistent with an intermediate-axonal electrophysiological pattern. A targeted-NGS including 136 CMT genes showed the heterozygous frameshift mutation (c.3057dupG; p.K1020fs*43) in the NEFH gene, coding for the neurofilament heavy chain and causing CMT2CC.

Interpretation: Diagnosis of a genetic neuropathy may be challenging when clinical features are atypical and/or electrophysiological features are misleading. The most common misdiagnosis is CIDP. Our report suggests that also CMT2CC patients with proximal muscle weakness and equivocal electrophysiological features might be misdiagnosed as CIDP.

Keywords: CIDP; CMT2CC; Charcot-Marie-tooth; Conduction block; NEFH.

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Conflict of interest statement

Declarations Ethical statement The study was conducted in accordance with the Declaration of Helsinki. Ethical review and approval were waived for this study due to of the retrospective nature of the study and all the procedures being performed were part of the routine care. Conflicting interests The authors declare that there are no competing interests.

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