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Infantile-onset Alexander disease in a child with long-term follow-up by serial magnetic resonance imaging: a case report
© Nishibayashi et al.; licensee BioMed Central Ltd. 2013
Received: 9 April 2013
Accepted: 15 May 2013
Published: 26 July 2013
Alexander disease is a rare disorder resulting from a glial fibrillary acidic protein gene mutation which causes progressive degeneration of white matter. With the usual poor prognosis, there are few case reports with long-term follow-up. We report the five-year clinical course of Alexander disease in one case using serial magnetic resonance imaging.
A 12-month-old Japanese male was referred to the pediatrics department in our hospital because of developmental retardation. Alexander disease was diagnosed by gene examination of the mutation of a glial fibrillary acidic protein. Magnetic resonance imaging findings showed abnormalities in white matter, deep gray matter, and medulla oblongata. Serial magnetic resonance imaging examinations until the age of five were performed and changes in magnetic resonance imaging findings were compared to the progression in clinical symptoms.
Alexander disease is a very rare disease with a variety of clinical phenotypes. Therefore serial magnetic resonance imaging studies for long-term survival infantile cases including our case may be important in the analysis of the pathophysiological mechanism.
Alexander disease is a rare disorder resulting from a glial fibrillary acidic protein (GFAP) gene mutation which causes progressive degeneration in white matter. Most cases are solitary, but hereditary cases have also been reported. Abnormalities predominate in the white matter of both frontal lobes, making magnetic resonance imaging (MRI) useful for diagnosis. In this report, we show the clinical course of Alexander disease in one case using MRI.
A 12-month-old Japanese male was referred to the pediatrics department of our hospital because he was unable to sit independently. At the initial examination, the 12-month-old could hold his head up but could not maintain a sitting posture. Macrocephaly was not noted. He had no history of perinatal abnormalities. Birth weight was 3058g, height 49cm, and head circumference 34.5cm. There was no family history of neurological disorder.
These findings suggested infantile leukodystrophy, and other diseases in the differential diagnosis including Alexander disease, megalencephalic leukoencephalopathy with subcortical cysts (MLC), van der Knaap disease, Canavan disease, Pelizaeus-Merzbacher disease, and metachromatic leukodystrophy. Alexander disease or MLC were strongly suspected, as these types of infantile leukodystrophy involve cyst formation. Alexander disease was diagnosed by gene examination, and Murakami et al. already reported by the mutation of the GFAP gene in this case: the patient had a heterozygous deletion of genomic sequence 1247-1249GGG>GG in exon 8 of the GFAP gene .
Pathological features in Alexander disease include deposits of Rosenthal fibers in astrocytes. Rosenthal fibers contain ubiquitin, heat shock proteins (HSP27) and partially degraded fragments of GFAP. Astrocyte function impairment is considered to cause adverse effects to adjacent structures, such as oligodendroglia and myelin sheath. Some cases result from autosomal recessive inheritance, but the majority is isolated (spontaneous mutations).
MRI is a crucial examination in the diagnosis and observation of Alexander disease. Under the MRI-based diagnostic criteria proposed by van der Knaap , at least four of the five imaging findings below must be present for the diagnosis: 1) white matter abnormalities (swelling, signal change, atrophy, cysts) with frontal preponderance, 2) periventricular rim of high signal intensity on T1-weighted images and low signal intensity on T2-weighted images, 3) abnormalities in the basal ganglia and thalami, 4) brain stem abnormalities, 5) contrast enhancement involving one or more of the following structures: ventricular lining, periventricular rim, white matter of the frontal lobes, optic chiasm, fornix, basal ganglia, thalamus, dentate nucleus, and brain stem. In our study, four of the five criteria proposed by van der Knaap except for a periventricular rim were seen at 1 year of age, and MRI findings at 4 years of age showed all five criteria exactly.
High signal intensity on T2-weighted images are reported to correspond to deposits of Rosenthal fibers or associated demyelination, and because these fibers cause breakdown of the blood–brain barrier, contrast enhancement is seen in sites with significant deposits [3, 4]. Loss of brain tissue also leads to cyst formation. ADC and MR spectroscopy, although not included in van der Knaap’s diagnostic criteria, have been reported to be useful in diagonosing Alexander disease [4, 5]. In our case, elevation of ADC values at the affected areas were recognized (Figure 3d, e), which was thought to correspond with white matter degeneration.
As a result of a nationwide investigation, Yoshida et al.[4, 5] proposed a new classification on the basis of neurological and MR findings: cerebral Alexander disease (type 1), bulbospinal Alexander disease (type 2), and intermediate form (type 3) [6, 7]. According to this classification, our case is classified as cerebral Alexander disease at the onset, and then features of the bulpospinal type become apparent as the disease progresses.
Shiihara et al. reported MRI in a long survival case. Unlike our case, cyst formation was not seen in early MRI like in their case. However, in addition to the abnormalities in the frontal lobes, brainstem lesion and brain atrophy became apparent in the progression of the disease in a follow up period of 15 years. Further studies are needed to clarify the relationship between the initial and serial MRI findings and clinical course after diagnosis.
In our case, the initial MRI and MRI-based serial observations were essential to diagnose and ascertain the image-based progression of clinical symptoms. Initial MRI and MRI-based serial observations were essential to diagnose Alexander disease. Because Alexander disease is a very rare disease with a variety of clinical phenotypes, serial MR studies for long-term survival of infantile cases including our case may be useful for the analysis of the pathophysiological mechanism.
Written informed consent was obtained from the mother of the patient for publication of this manuscript and any accompanying images. A copy of the written consent is available for review by the Edior-in-Chief of this journal.
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