Cranial ultrasonography in infantile encephalitic beriberi: A useful first-line imaging tool for screening and diagnosis in suspected cases

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Abstract

BACKGROUND AND PURPOSE: Brain imaging is central to the diagnosis of infantile encephalitic beriberi. Because cranial sonography findings have not been described in infantile encephalitic beriberi, our aim was to investigate its role in the diagnosis of this condition. MATERIALS AND METHODS: We performed a retrospective review of head sonography of infants (admitted between November 1, 2014, and March 31, 2015) who presented with encephalopathy. Cranial ultrasonography scans were studied for the alteration of echogenicity of the basal ganglia. RESULTS: Of the 145 consecutive infants who presented with encephalopathy, 58 had thiamine-responsive encephalopathy (infantile encephalitic beriberi) and 87 had encephalopathy due to other causes. Forty-eight of 145 infants with encephalopathy showed hyperechoic basal ganglia. A hyperechoic appearance of the basal ganglia on cranial ultrasonography was found to have a sensitivity of 71% (41/58) and a specificity of 92% (80/87) in diagnosing infantile encephalitic beriberi. The sensitivity of cranial sonography increased with age. It was a maximum of 93% (14/15) in the 5 months and older age group. Specificity was a maximum of 100% (18/18) in infants older than 5 months of age. Sensitivity was maximum in Wernicke encephalopathy at 90% (18/20) and least in the acidotic form at 43% (10/23). Follow-up showed gradual normalization of the hyperechoic appearance of the basal ganglia during 8 weeks in 26/41 (63%), with mild atrophy of the basal ganglia in 6/41 (15%) CONCLUSIONS: Hyperechogenicity of the basal ganglia on cranial ultrasonography is a sensitive finding for the diagnosis of infantile encephalitic beriberi in infants who present with Wernicke encephalopathy.

Figures

  • FIG 1. Breakdown of infants with encephalopathy. “Hyperechoic BG” indicates cUS finding of increased echogenicity of the bilateral basal ganglia. “Normal” indicates cUS showing normal brain parenchyma and basal ganglia echogenicity. “Other findings” indicates cUS abnormalities other than hyperechoic basal ganglia-like hydrocephalus or a mass lesion.
  • FIG 2. A 3-month-old girl with encephalopathy, reflux, and ptosis due to IEBB. A, Coronal plane cUS shows a bilaterally symmetric hyperechoic putamen (arrows). B, Follow-up cUS (after thiamine supplementation) in the coronal plane 6 weeks later shows very minimal hyperechogenicity in the putamen (arrows). Hyperechogenicity has regressed compared with the initial cUS (A).
  • FIG 3. A 3-month-old girl with encephalopathy, reflux, and ptosis due to IEBB. A, Sagittal plane cUS shows a hyperechoic putamen (arrows). B, Coronal plane cUS shows a bilaterally symmetric hyperechoic caudate nucleus (downward arrows) and putamen (upward arrows).
  • FIG 4. A 4-month-old boy with encephalopathy, moaning, and seizures diagnosed as IEBB. A, Sagittal plane cUS shows a curvilinear hyperechoic structure representing the caudate nucleus (arrows). B, Coronal plane cUS shows a bilateral symmetric hyperechoic caudate head (arrows).
  • FIG 5. A 3-month-old boywith encephalopathy, ptosis, moaning, and reflux due to IEBB. Coronal plane cUS shows bilaterally symmetric hyperechoic putamen (downward arrows) and mildly hyperechoic thalami (upward arrows).

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APA

Wani, N. A., Qureshi, U. A., Ahmad, K., & Choh, N. A. (2016). Cranial ultrasonography in infantile encephalitic beriberi: A useful first-line imaging tool for screening and diagnosis in suspected cases. American Journal of Neuroradiology, 37(8), 1535–1540. https://doi.org/10.3174/ajnr.A4756

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