Limbic encephalitis

Limbic encephalitis
The limbic system within the brain.
Classification and external resources
Specialty neurology
ICD-10 G04.81
ICD-9-CM 323.81
DiseasesDB 30707
MeSH D020363

Limbic encephalitis is a form of encephalitis, a disease characterised by inflammation of the brain.[1] Limbic encephalitis is caused by autoimmunity: an abnormal state where the body produces antibodies against itself. Some cases are associated with cancer and some are not.[1] Although the disease is known as "limbic" encephalitis, it is seldom limited to the limbic system and post-mortem studies usually show involvement of other parts of the brain.[2][3][4] The disease was first described by Brierley and others in 1960 as a series of three cases. The link to cancer was first noted in 1968[3] and confirmed by later investigators.[5]

The majority of cases of limbic encephalitis are associated with a tumour (diagnosed or undiagnosed). In cases caused by tumour, cure is only achieved when the tumour is removed completely (this is not always possible). Limbic encephalitis is classified according to the auto-antibody that causes the disease.The most common types are:

Since 1999 following a report of case of a 15-year-old teenager of Indian descent from South Africa, subacutely developed memory loss subsequent to herpes simplex type 1 encephalitis[6] similar cases of non paraneoplastic LE its association with auto-antibody and response to steroid has been described.[7][8] Limbic encephalitis associated with voltage‐gated potassium channel antibodies (VGKC‐Abs)[9] may frequently be non‐paraneoplastic.[10] A recent study of 15 cases of limbic encephalitis found raised VGKC‐Abs associated with non‐paraneoplastic disorders and remission following immunosuppressive treatment.[11]

Classification

Symptoms and signs

Symptoms develop over days or weeks. The subacute development of short-term memory deficits is considered the hallmark of this disease,[1] but this symptom is often overlooked, because it is overshadowed by other more obvious symptoms such as headache, irritability, sleep disturbance, delusions, hallucinations, agitation, seizures and psychosis, or because the other symptoms mean the patient has to be sedated, and it is not possible to test memory in a sedated patient.

Diagnosis

The diagnosis of limbic encephalitis is extremely difficult and it is usual for the diagnosis to be delayed for weeks. The key diagnostic test (detection of specific auto-antibodies in cerebrospinal fluid) is not routinely offered by most immunology laboratories. Some of the rarer auto-antibodies (e.g., NMDAR) have no commercially available assay and can only be measured by a very small number of research laboratories worldwide, further delaying diagnosis by weeks or months. Most patients with limbic encephalitis are initially diagnosed with herpes simplex encephalitis, because the two syndromes cannot be distinguished clinically.[1] HHV-6 (human herpes virus 6) encephalitis is also clinically indistinguishable from limbic encephalitis.[1]

There are two sets of diagnostic criteria used. The oldest are those proposed by Gultekin et al. in 2000.[12]

Gultekin criteria
EITHER, Pathological demonstration of limbic encephalitis
OR, All four of:
  • Short-term memory loss, seizures, or psychiatric symptoms suggestive of limbic system involvement
  • <4 years between onset of neurological symptoms and cancer diagnosis
  • Exclusion of metastases, infection, metabolic and nutritional deficits, stroke and side-effects of therapy that may cause limbic encephalopathy
  • At least one of
    • CSF with inflammatory findings
    • Hyperintensity of the temporal lobes bilaterally on MRI FLAIR or T2
    • EEG with epilepsy or slow activity involving the temporal lobes focally

A revised set of criteria were proposed by Graus and Saiz in 2005.[13]

Graus and Saiz criteria
All four of
  • Subacute onset (<12 weeks) of seizures, short-term memory loss, confusion, and psychiatric symptoms
  • Neuropathologic or radiologic evidence (MRI, SPECT, PET) of involvement of the limbic system
  • Exclusion of other possible aetiologies of limbic dysfunction
  • Demonstration of a cancer within 5 years of the diagnosis of neurologic symptoms, or the development of classic symptoms of limbic dysfunction in association with a well-characterized paraneoplastic antibody (Hu, Ma2, CV2, amphiphysin, Ri)

The main distinction between the two sets of criteria is whether or not the detection of a paraneoplastic antibody is needed for diagnosis.

Antibodies against intracellular neuronal antigens

The main antibodies within this group are those against Hu, Ma2, CV2, amphiphysin and Ri. The syndrome of anti-Ma2 encephalitis may be clinically mistaken for Whipple's disease.[14]

Antibodies against cell membrane antigens

The main antibodies within this group are those against anti-N-methyl-D-aspartate receptors (NMDAR) and the voltage-gated potassium channel-complex (VGKC-complex). Anti-NMDAR encephalitis is strongly associated with benign tumours of the ovary (usually teratomas or dermoid cysts). Anti-VGKC-complex encephalitis is most often not associated with tumours.

Patients with NMDAR encephalitis are frequently young women who present with fever, headache and fatigue. This is often misdiagnosed as influenza, but progresses to severe behavioural and personality disturbance, delusions, paranoia and hallucinations.[15] Patients may therefore initially be admitted to a psychiatric ward for acute psychosis or schizophrenia. The disease then progresses to catatonia, seizures and loss of consciousness. The next stage is hypoventilation (inadequate breathing) requiring intubation, orofacial dyskinesia and autonomic instability (dramatic fluctuations in blood pressure, temperature and heart rate).[16]

Investigation

Cerebrospinal fluid (CSF)

Examination of cerebrospinal fluid (CSF) shows elevated numbers of lymphocytes (but usually < 100 cells/µl); elevated CSF protein (but usually <1.5 g/l), normal glucose, elevated IgG index and oligoclonal bands. Patients with antibodies to voltage-gated potassium channels may have a completely normal CSF examination.[17][18][19]

Neuroimaging

MRI brain is the mainstay of initial investigation pointing to limbic lobe pathology revealing increased T2 signal involving one or both temporal lobes in most cases.[20][12]

Serial MRI in LE starts as an acute disease with uni- or bilateral swollen temporomesial structures that are hyperintense on fluid attenuation inversion recovery and T2-weighted sequences. Swelling and hyperintensity may persist over months to years, but in most cases progressive temporomesial atrophy develops.[21]

PET CT scan: Not an essential investigation but can help in suspected cases with MRI negative for early diagnosis.[22]

Neuro-electrophysiology

EEG: Mostly nonspecific slowing and epileptiform activity arising from temporal lobes.[12]

Treatment

Limbic encephalitis is a rare condition with no randomised-controlled trials to guide treatment. Treatments that have been tried include intravenous immunoglobulin, plasmapheresis, corticosteroids, cyclophosphamide and rituximab.[1]

If an associated tumour is found, then recovery is not possible until the tumour is removed. Unfortunately, this is not always possible, especially if the tumour is malignant and advanced.

History

Clinical Features Pathology Year Syndromes
Subacute onset of episodic memory impairment, disorientation and agitation, commonly associated with seizures, hallucinations, sleep disturbance Medial temporal lobe inflammation 1960 Subacute encephalitis of later adult life mainly affecting the limbic areas[2]
1968 Limbic Encephalitis association with Carcinoma[23][2]
2008 Paraneoplastic LE with Lung Carcinoma, thymoma,[24]
2002 Non Paraneoplastic LE[6]

References

  1. 1 2 3 4 5 6 Tüzün E, Dalmau J (2007). "Limbic encephalitis and variants: classification, diagnosis and treatment". The Neurologist. 13 (5).
  2. 1 2 3 Brierley JB, Corsellis JA, Hierons R, et al. (1960). "Subacute encephalitis of later adult life. Mainly affecting the limbic areas". Brain. 83 (3): 357–368. doi:10.1093/brain/83.3.357.
  3. 1 2 Corsellis JA, Goldberg GJ, Norton AR (1968). ""Limbic encephalitis" and its association with carcinoma". Brain. 91 (3): 481–496. PMID 5723018. doi:10.1093/brain/91.3.481.
  4. ↑ Bakheit AM, Kennedy PG, Behan PO (1990). "Paraneoplastic limbic encephalitis: clinico-pathological correlations". J Neurol Neurosurg Psychiatry. 53 (12): 1084–1088. doi:10.1136/jnnp.53.12.1084.
  5. ↑ Henson RA, Hoffman HL, Urich H (1965). "Encephalomyelitis with carcinoma". Brain. 88 (3): 449–464. doi:10.1093/brain/88.3.449.
  6. 1 2 Mori, Masahiro; Kuwabara, Satoshi; Yoshiyama, Mitsuharu; Kanesaka, Toshihide; Ogata, Tsuyoshi; Hattori, Takamichi (2002-09-15). "Successful immune treatment for non-paraneoplastic limbic encephalitis". Journal of the Neurological Sciences. 201 (1–2): 85–88. ISSN 0022-510X. PMID 12163199. doi:10.1016/s0022-510x(02)00188-0.
  7. ↑ Watanabe, Yasuhiro; Shimizu, Yasutaka; Ooi, Shinji; Tanaka, Keiko; Inuzuka, Takashi; Nakashima, Kenji (2003-05-01). "Steroid-responsive limbic encephalitis". Internal Medicine. 42 (5): 428–432. ISSN 0918-2918. PMID 12793715. doi:10.2169/internalmedicine.42.428.
  8. ↑ Lang, Pierre Olivier; Sellal, François (2008-05-01). "[Non-paraneoplastic limbic encephalitis revealed by anterograde amnesia]". Presse Médicale. 37 (5 Pt 1): 775–782. ISSN 0755-4982. PMID 18261871. doi:10.1016/j.lpm.2007.11.013.
  9. ↑ Buckley, C.; Oger, J.; Clover, L.; Tüzün, E.; Carpenter, K.; Jackson, M.; Vincent, A. (2001-07-01). "Potassium channel antibodies in two patients with reversible limbic encephalitis". Annals of Neurology. 50 (1): 73–78. ISSN 0364-5134. PMID 11456313. doi:10.1002/ana.1097.
  10. ↑ Schott, J. M.; Harkness, K.; Barnes, J.; della Rocchetta, A. Incisa; Vincent, A.; Rossor, M. N. (2003-04-12). "Amnesia, cerebral atrophy, and autoimmunity". Lancet. 361 (9365): 1266. ISSN 0140-6736. PMID 12699955. doi:10.1016/s0140-6736(03)12983-2.
  11. ↑ Pozo-Rosich, Patricia; Clover, Linda; Saiz, Albert; Vincent, Angela; Graus, Francesc (2003-10-01). "Voltage-gated potassium channel antibodies in limbic encephalitis". Annals of Neurology. 54 (4): 530–533. ISSN 0364-5134. PMID 14520669. doi:10.1002/ana.10713.
  12. 1 2 3 Gultekin SH, Rosenfeld MR, Voltz R, et al. (2000). "Paraneoplastic limbic encephalitis: neurological symptoms, immunological findings and tumour association in 50 patients". Brain. 123 (7): 1481–1494. PMID 10869059. doi:10.1093/brain/123.7.1481.
  13. ↑ Graus F, Saiz A (2005). "Limbic encephalitis: a probably under-recognized syndrome". Neurologia. 20: 24–30.
  14. ↑ Castle J, Sakonju A, Dalmau J, et al. (2006). "Anti-Ma2-associated encephalitis with normal FDG-PET: a case of pseudo-Whipple's disease". Nat Clin Pract Neurol. 2 (10): 566–572. doi:10.1038/ncpneuro0287.
  15. ↑ Koide R, Shimizu T, Koike K, et al. (2007). "EFA6A-like antibodies in paraneoplastic encephalitis associated with immature ovarian teratoma: a case report". J Neurooncol. 81: 71–74. doi:10.1007/s11060-006-9200-7.
  16. ↑ Dalmau J, Tuzun E, Wu HY, et al. (2007). "Paraneoplastic anti-N-methyl-D-aspartate receptor encephalitis associated with ovarian teratoma". Ann Neurol. 61 (1): 25–36. PMC 2430743 Freely accessible. PMID 17262855. doi:10.1002/ana.21050.
  17. ↑ Buckley C, Oger J, Clover L, et al. (2001). "Potassium channel antibodies in two patients with reversible limbic encephalitis". Ann Neurol. 50: 73–78. PMID 11456313. doi:10.1002/ana.1097.
  18. ↑ Vincent A, Buckley C, Schott JM, et al. (2004). "Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis". Brain. 127 (3): 701–712. PMID 14960497. doi:10.1093/brain/awh077.
  19. ↑ Thieben MJ, Lennon VA, Boeve BF, et al. (2004). "Potentially reversible auto-immune limbic encephalitis with neuronal potassium channel antibody". Neurology. 62 (7): 1177–1182. doi:10.1212/01.WNL.0000122648.19196.02.
  20. ↑ Nicholas, D (2003). "Clinical, Magnetic Resonance Imaging, and Electroencephalographic Findings in Paraneoplastic Limbic Encephalitis". Mayo Clinic Proceedings. 78 (11): 1363–1368. PMID 14601695. doi:10.4065/78.11.1363.
  21. ↑ Horst, Urbach (2006). "Serial MRI of limbic encephalitis". Neuroradiology. 48 (6): 380–386. PMID 16586118. doi:10.1007/s00234-006-0069-0.
  22. ↑ Cózar Santiago, Maria Del Puig; Sanchez Jurado, Raul; Sanz Llorens, Rut; Aguilar Barrios, Jose Enrique; Ferrer Rebolleda, Jose (2016-02-01). "Limbic Encephalitis Diagnosed With 18F-FDG PET/CT". Clinical Nuclear Medicine. 41 (2): e101–103. ISSN 1536-0229. PMID 26571448. doi:10.1097/RLU.0000000000001076.
  23. ↑ Corsellis, JA (1968). "Limbic encephalitis" and its association with carcinoma". Brain. 91 (3): 481–96. PMID 5723018. doi:10.1093/brain/91.3.481.
  24. ↑ Dalmau, Josep; Gleichman, Amy J.; Hughes, Ethan G.; Rossi, Jeffrey E.; Peng, Xiaoyu; Lai, Meizan; Dessain, Scott K.; Rosenfeld, Myrna R.; Balice-Gordon, Rita (2008-12-01). "Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies". The Lancet. Neurology. 7 (12): 1091–1098. ISSN 1474-4422. PMC 2607118 Freely accessible. PMID 18851928. doi:10.1016/S1474-4422(08)70224-2.
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