Neurol. praxi. 2023;24(1):60-64 | DOI: 10.36290/neu.2023.012

Autoimmune disease with positivity of anti­‑CASPR2 antibodies - a case report

MUDr. Lubomír Jurák, Ph.D.^{1, 2, 3}, MUDr. Zuzana Eichlová⁴, MUDr. Eva Řeháčková⁴, MUDr. Martin Jíra⁴, MUDr. David Krýsl, Ph.D.⁵, MUDr. Martin Elišák, Ph.D.⁵, prof. MUDr. Petr Suchomel, Ph.D.¹

¹ Neurochirurgické oddělení, Krajská nemocnice Liberec, a. s., Liberec

² Neurochirurgická klinika LF UP a FN Olomouc

³ Fakulta zdravotnických studií, Technická univerzita v Liberci

⁴ Neurologické oddělení, Krajská nemocnice Liberec, a. s., Liberec

⁵ Neurologická klinika 2. LF UK a FN Motol, Praha

Autoimmune disease associated with anti-CASPR2 antibodies is a relatively rare neurological illness characterized by the presence of anti-CASPR2 antibodies in serum and/or CSF. It manifests with a variety of symptoms - from the central nervous system (cognitive impairment, epilepsy and cerebellar symptoms), from the peripheral nervous system (peripheral nerve hyperexcitability and neuropathic pain), and from the autonomic nervous system (autonomic dysfunction, insomnia and weight loss).

Case report: The 61-year-old patient was admitted to the intensive care unit of our neurological department with myoclonic abdominal muscle twitching with intermittent generalization and right upper limb myoclonus, associated with behavioral change, cognitive deterioration, intermittent disorientation and aggression, bulbar syndrome, dysarthria, and dysautonomia (hypersalivation, bronchial hypersecretion, and circulatory instability). Due to progressive hypercapnia and loss of consciousness, the patient had to be intubated and connected to artificial pulmonary ventilation. EMG investigation demonstrated axonal motor polyneuropathy of both upper and lower limbs. Several unspecific gliotic lesions located in the white matter adjacent to the left cerebral ventricle were described on the brain MRI. Significant anti-CASPR2 antibody positivity was found both in serum and cerebrospinal fluid. Treatment with i.v. methylprednisolone and intravenous immunoglobulins was applied. With this treatment, the patient's neurological status gradually improved to the ability of verticalization. However, his cachectization, which was already present on admission, progressed despite the maximal effort in nutrition therapy. Also, repeated episodes of respiratory insufficiency resulting in transitory impairment of consciousness occurred. One such episode resulted in cardiac arrest followed by successful cardiopulmonary resuscitation. However, myoclonic jerks reappeared afterward and the patient's overall condition worsened. At this stage, it was decided not to further escalate and extend the treatment. Palliative treatment was commenced. The patient died during the following episode of respiratory failure. Comment: This case report of a patient with autoimmune disease associated with anti-CASPR2 antibodies highlights its multiple and often disease-unspecific clinical symptoms on the one hand, and on the other, its severe and ultimately fatal clinical course despite the initial effect of immunotherapy. Early diagnosis and early and aggressive immunomodulatory treatment are crucial in patients with this disorder.

Keywords: CASPR2 antibodies, autoimmune disease, limbic encephalitis, immunosuppressive therapy, plasmapheresis.

Accepted: February 28, 2023; Published: March 3, 2023  Show citation