Heroin-associated spongiform leukoencephalopathy

By Liu S, Tanoura T

CASE SUMMARY

A 29-year-old man presented with a three-week history of slurred speech, poor coordination, and imbalance while walking. He did not have a family history of neurodegenerative disorders or autoimmune conditions. On physical exam, he was alert and oriented to person, place, time, and situation. He displayed dysarthric speech and ataxic gait, and he scored 4/5 in upper and lower extremity strength testing. Cerebrospinal fluid studies revealed normal protein, cell count, and glucose levels. Syphilis, HIV, West Nile, HSV, JC virus, CMV, and arbovirus serologies returned negative. Likewise, the patient tested negative for ANA and rheumatoid factor antibodies. Urine toxicology was positive for opiates. Upon further questioning, the patient admitted to smoking heroin vapor. Over six days of hospitalization, his physical exam findings were stable, and the patient was discharged to a rehabilitation facility.

IMAGING FINDINGS

On MRI, FLAIR sequence showed bilateral and symmetrical hyperintensities in the posterior limb of the internal capsule, occipital lobe white matter, and splenium of the corpus callosum (Figure 1). Additional symmetrical FLAIR hyperintensities involved the cerebellar white matter extending to the middle cerebellar peduncles (Figure 2). On T1 sequences, these lesions were hypointense and did not enhance following contrast administration. On diffusion weighted imaging (DWI), the lesions displayed increased signal (Figure 3), and corresponding apparent diffusion coefficient (ADC) sequence findings were consistent with diffusion restriction.

DIAGNOSIS

Heroin-associated spongiform leukoencephalopathy (HASL).

DISCUSSION

Heroin-associated spongiform leukoencephalopathy was initially described in 1982 in the Netherlands among 47 patients who inhaled heated heroin vapor, and the resulting clinical and radiological manifestations reflect spongiform degeneration of the white matter.1 The coalescence of vacuoles formed between myelin lamellae in the oligodendroglia results in a pattern termed “vacuolating myelinopathy” when seen under electron microscopy.2,3 Although the etiology of HASL is unknown, it is postulated that heating of heroin releases pathogenic contaminants, likely a lipophilic impurity given the high lipid content of myelin. These histopathological changes have not been described after intravenous use of heroin.2,3

Ataxia and dysarthria are common presenting signs; however three clinical stages of the disease have been described. The initial stage is characterized by cerebellar ataxia, soft speech, and motor restlessness.4 Patients may remain within the first stage or progress onto the second and third stages. Approximately half of patients develop an intermediate form of illness and exhibit worsening cerebellar signs, hyperactive reflexes, spastic paraparesis, myoclonus, and chorea.4 One-quarter of patients enter the third stage of illness marked by akinetic mutism, hypotonic areflexic paresis, central pyrexia, and eventual death.4 The natural history of HASL is variable, with survivors exhibiting mild to marked improvement.

White matter changes on MRI T2-weighted sequences are highly specific for toxicity from heroin vapor inhalation. Supratentorial disease is characterized by bilateral white matter hyperintensities with occipital and parietal lobe predominance.2 The posterior limb of the internal capsule is involved while the anterior limb is spared.2 Abnormal signal also shows predilection for the splenium of the corpus callosum.3 Characteristically, gray matter structures including the cortex, basal ganglia, and thalami remain uninvolved.5 Posterior fossa disease manifests as bilateral and symmetrical cerebellar white matter hyperintensities with extension into the cerebellar peduncles.2,3,5 The involvement of brainstem structures is also well-documented, and increased T2 signal may affect the corticospinal, solitary, and central tegmental tracts.2,3

Increased DWI signal is common; however associated ADC findings are variable and likely reflect a dynamic disease process. In the acute setting, increased DWI signal with concomitant low ADC signal reflects diffusion restriction that is postulated to correlate with vacuolization and fluid entrapment between myelin lamellae.6 Subsequently, the extracellular space becomes enlarged as the number of oligodendroglia and neuronal axons decrease, causing increased water diffusion and giving rise to high DWI signal without low ADC signal.7,8

Clinical management for HASL is based on supportive care. In case reports, treatment with coenzyme Q has been associated with reversal of clinical and radiological findings.9 Enhanced cognition has been observed after treatment with methylphenidate.10 To date, however, no randomized clinical trials have tested the efficacy of these interventions.

Conclusion

The inhalation of impurities in heroin vapor is responsible for a vacuolating myelinopathy termed heroin-associated spongiform leukoencephalopathy. Findings on MRI T2-weighted sequences are nearly pathognomonic and are characterized by bilateral and symmetrical white matter hyperintensities with a predilection for the occipital and parietal lobes, splenium of the corpus callosum, and posterior limb of the internal capsule with sparing of the anterior limb. Infratentorial involvement is characterized by T2 hyperintensity in the cerebellar white matter and peduncles. Three distinct stages of illness are recognized, with ataxia and dysarthria being common initial presenting signs. The clinical course is variable, and no definitive treatment has been identified.

References

  1. Wolters EC, Stam FC, Lousberg RJ, et al. Leucoencephalopathy after inhaling “heroin” pyrolysate. The Lancet. 1982;320:1233-1237.
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  6. Bega DS, McDaniel LM, Jhaveri MD, Lee VH. Diffusion weighted imaging in heroin-associated spongiform leukoencephalopathy. Neurocritical Care. 2009;10:352-354.
  7. Offiah C, Hall E. Heroin-induced leukoencephalopathy: characterization using MRI, diffusion-weighted imaging, and MR spectroscopy. Clinical Radiology. 2008;63:146-152.
  8. Bartlett E, Mikulis DJ. Chasing “chasing the dragon” with MRI: leukoencephalopathy in drug abuse. The British Journal of Radiology. 2005;78:997-1004.
  9. Gacouin A, Lavoue S, Signouret T, et al. Reversible spongiform leucoencephalopathy after inhalation of heated heroin. Intensive Care Medicine. 2003;29:1012-1015.
  10. 10. Rao M, Wilson Z. Chasing the dragon. Current Psychiatry. 2010;9:77.
Liu S, Tanoura T. (Nov 02, 2016). Heroin-associated spongiform leukoencephalopathy. Appl Radiol. 2016; 45(11):50-52.
Prepared by Dr. Liu while a Radiology Resident and Dr. Tanoura while a Neuroradiologist at Harbor-UCLA Medical Center, Torrance, CA.
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