A clinicopathological and genetic study of sporadic diffuse leukoencephalopathy with spheroids: a report of two cases

Diffuse leukoencephalopathy with spheroids (DLS) is a white matter neurodegenerative disease characterized by progressive cognitive decline and motor symptoms 1–6, and histologically, by axonal swellings (‘spheroids’) and loss of axons and myelin 1–3,5,7–11. It was originally described as a rare, hereditary, autosomal dominant disorder (hereditary DLS: HDLS) 2, but there have been reports on DLS without family history as well (sporadic DLS: SDLS) 6,12–22. In 2012, Rademakers et al. 9 identified 14 different mutations in the colony stimulating factor 1 receptor (CSF1R) gene, which are located in exons 12–22 and affect the tyrosine kinase domain of the protein, in 14 families with HDLS. Interestingly, this gene shares the same signalling pathway as TYROBP (DAP12) and TREM2, whose mutations are implicated in polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL, also known as Nasu-Hakola disease) 23–25. PLOSL shares similar clinicopathological profiles with DLS, such as a progressive neuropsychiatric decline and leukoencephalopathy with spheroids 26,27. In this paper we describe the clinicopathological features of two cases of SDLS. In one of them, genetic analyses of CSF1R, TYROBP and TREM2 were conducted, and no mutations in these genes were identified.

Case 1, a 56-year-old woman presented with forgetfulness and an inability to count. She was hospitalized 8 months after the onset. Her past history included cured uterine cervical cancer at the age of 25. There was no history of bone fractures. She had no relatives with neurological diseases. At presentation, she scored a 24/30 on the mini-mental state examination, and showed left-sided hemispatial agnosia, apraxia, and 'alien hand syndrome' in the left hand. Frontal release signs were positive. There was no weakness in the limbs. Jaw reflex was exaggerated, as were deep tendon reflexes. Extensor plantar reflex was bilaterally positive. The sensation on the left side of the body was ignored when both sides of the body were simultaneously stimulated. Cerebellar functions were normal. Routine haematology was normal. Other tests were noncontributory, including lactate, pyruvate, vitamins, thyroid, Treponema pallidum haemagglutination test, anti-human immunodeficiency virus antibodies, very long chain fatty acid, galactocerebrosidase, arylsulphatase A, and point mutations of the genes for glial fibrillary acidic protein and notch 3. Anti-nuclear antibodies (ANA, centromere type), but not other autoantibodies, were elevated (>¥1280). Cerebrospinal fluid (CSF) was unremarkable, including IgG index, oligoclonal band, polymerase chain reaction (PCR) for JC virus, tau, and 14-3-3 protein. Gadolinium-enhanced magnetic resonance imaging (MRI) disclosed a non-enhanced, highintensity signal in the cerebral white matter on T2-weighted ( Figure 1a) and fluid attenuated inversion recovery (FLAIR) (Figure 1b) images, which descended along the pyramidal tract ( Figure 1c). This signal was high on diffusion weighted image (DWI) and apparent diffusion coefficient (ADC) map. Given the elevated ANA, immunomodulating therapy was attempted, but there was no effect. She gradually deteriorated and eventually became bed-ridden. She died 16 months after the onset. Autopsy limited to the brain was performed.
Case 2, a 35-year-old man presented with mutism. His family gradually noticed that he would not utter or talk. He then began to limp and was hospitalized 3 months after the onset. His past history was unremarkable, with no episodes of bone fractures. One of his uncles and one of his grandmothers died of cerebral haemorrhage; otherwise, his family history was unremarkable. At presentation, he uttered no words and failed to follow commands. There was no weakness in the limbs. Deep tendon reflexes were exaggerated, and extensor plantar reflex was positive on the right side. Sensation and cerebellar functions seemed normal. Gadolinium-enhanced MRI disclosed a non-enhanced, high-intensity signal in the cerebral white matter on T2-weighted ( Figure 1e) and FLAIR (Figure 1f) images, which was high on DWI ( Figure 1g) and low on ADC ( Figure 1h). The pyramidal tract seemed spared. Routine haematology was normal. Very long chain fatty acid, arylsulphatase A, and notch 3 gene were normal. In CSF, protein (50 mg/dl) and myelin basic protein (134 pg/ ml) were elevated; otherwise, the CSF was normal. Given . This signal descends along the pyramidal tract, which is demonstrated on FLAIR in the pontine base (c). Grossly, the autopsied brain of Case 1 (d) shows bilateral, patchy discoloration of the white matter (arrows). The MRI of Case 2 (e-l) shows a high-intensity signal in the cerebral white matter on T2-WI (e) and FLAIR (f). This signal is partially high on DWI (g) and low on ADC (h), which is reminiscent of acute infarction. The follow-up MRI about 1 year after the onset shows persistence of the previously recognized signal, which is still high on DWI (i) and low on ADC (j). In addition, a previously unrecognized abnormal signal is apparent along the pyramidal tract, which is shown on FLAIR in the cerebral peduncle (k) and pontine base (l). MRI, magnetic resonance imaging; T2-WI, T2-weighted image; FLAIR, fluid attenuated inversion recovery; DWI, diffusion weighted image; ADC, apparent diffusion coefficient map. the signal pattern on MRI, that is, high on DWI and low on ADC, a tentative diagnosis of acute infarction was made, but its aetiology remained undetermined. One year after the onset, the patient had prominent bulbar palsy that led to severe dehydration. On the follow-up MRI, the previously recognized signal pattern, that is, high on DWI and low on ADC, was still present (Figure 1i,j), and a previously unrecognized signal became obvious along the pyramidal tract (Figure 1k,l). Brain biopsy was performed 1 year and 3 months after the onset.
Histology was evaluated with haematoxylin and eosin (HE), Klüver-Barrera (KB), HE-periodic acid-Schiff stain (HE-PAS), luxol fast blue (LFB)-PAS and/or Bodian stains using formalin-fixed, paraffin-processed sections. Also, immunostains were performed using the following antibodies: Genetic analyses of CSF1R, TYROBP and TREM2 were conducted in Case 1, according to the methods described in previous papers [9,[23][24][25]29]. Briefly, genomic DNA was extracted using Gentra Puregene Blood Kit (Qiagen) from the frozen block of the frontal lobe, and the whole exons of each gene were amplified by polymerase chain reaction (PCR). Direct sequence analyses were applied to the PCR-amplified DNA.
In Case 1, the brain weighed 1320 g and showed discolouration and attenuation of the deep white matter, particularly in the frontal lobe (Figure 1d). Histology showed the following white matter changes: marked rarefaction and vacuolation; many spheroids (Figure 2a,b); marked loss of axons ( Figure 2b) and myelin ( Figure 2c); dysmorphism of the spheroids (Figure 2a); marked astrocytosis, including bizarre reactive astrocytes (Figure 2d); and scattered macrophages. These changes descended along the pyramidal tract (Figure 2e). In the cortex, ballooned neurones were noted sporadically (Figure 2f). The U-fibres were well preserved (Figure 2c). The basal ganglia and the cerebellum were unremarkable. By immunohistochemis-try, the spheroids were immunoreactive for p-NF ( Figure 2g) and APP (Figure 2h).
The biopsy material of Case 2 consisted of white matter. As in Case 1, the histology showed the following: many spheroids ( Figure 2i); loss of axons ( Figure 2k) and myelin ( Figure 2j); dysmorphism of the spheroids (Figure 2i); marked astrocytosis, including bizarre reactive astrocytes ( Figure 2i); and scattered macrophages. A few microcalcifications were seen. By immunohistochemistry, the spheroids were immunoreactive for p-NF ( Figure 2k) and APP (Figure 2l).
In both cases, there were neither vascular or neoplastic changes nor abnormal structures immunoreactive for amyloid beta, phosphorylated tau, phosphorylated alpha-synuclein or TDP-43.
The leukoencephalopathies involving axons are grouped under the umbrella term 'neuroaxonal dystrophy (NAD)' [27]. NAD is divided into three categories: physiological NAD, secondary NAD and primary NAD [27]. Physiological NAD is due to ageing, and is seen in the gracile and cuneate nuclei. The present cases are pathologically different from physiological NAD in the neuroanatomical distribution and severity of the lesions. Secondary NAD stems from various conditions, such as Parkinson's disease, motor neurone diseases or neuronal storage diseases. In the present cases, secondary NAD was excluded by the clinical work-up and the pathological assessment. Primary NAD corresponds to neurodegeneration involving axons, such as infantile neuroaxonal dystrophy, neurodegeneration with brain iron accumulation type I, or PLOSL. These are hereditary, and tend to have a more systemic manifestation and an earlier onset than do the present cases. Among these, PLOSL in particular needs to be differentiated from the present cases; however, the present cases lack bone symptoms, and in Case 1, the genetic analyses of TYROBP and TREM2 excluded PLOSL. Taken together with the pathological findings, the present cases can be diagnosed as DLS, one of primary NAD.
The neuroradiology of DLS includes increased signal intensity in the subcortical white matter and the pyramidal tract on T2-weighted or FLAIR MRI [6, 13,21,30] with or without gadolinium enhancement [8,30]. Recently, a few studies have shown that white matter lesions of DLS can be  high on DWI and low on ADC [13,15,30], potentially mimicking acute infarction. For example, Mateen et al. [13] reported a 24-year-old woman of SDLS with a 7-month course of dysarthria and gait impairment. Brain MRI showed T2 signal abnormality in periventricular and subcortical regions with extension into the right internal capsule and cerebral peduncle. Several areas were high on DWI and low on ADC, which led to a diagnosis of acute infarction; but this signal persisted even after 19 weeks. Brain biopsy was performed, and a diagnosis of DLS was established. This case and the present Case 2 are exactly comparable to each other, suggesting that the signal pattern on MRI in DLS can lead to a misdiagnosis of acute infarction.
In 2012 Rademakers et al. [9] identified 14 different mutations of CSF1R, which are located in exons 12-22 affecting the tyrosine kinase domain of the protein, in 14 families with HDLS. Kinoshita et al. [29] identified another novel mutation of CSF1R, a heterozygous c.2345 G>A (p.782 Arg>His) in exon 18, in a Japanese family with HDLS. In the present study, we performed a direct sequence analysis of CSF1R, TYROBP and TREM2 in Case 1, a case of SDLS. This case was considered as pathologically proven DLS with no apparent family history of neuropsychiatric disorders, and did not carry any mutations in the coding regions and exon-intron boundaries of CSF1R, TYROBP or TREM2. Therefore, this case might be a phenocopy of HDLS; however, the possibility that rare mutations in one of these genes or unidentified genes responsible for HDLS are operative in this patient cannot totally be excluded. DLS, encompassing HDLS and SDLS, needs to be taken as a disease spectrum with a heterogeneous genetic background.