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Cranial ultrasound: and the risk of tunnel vision?

“One man's one eyed perspective”

H.H. Fudenberg

The cranial ultrasound plays an important role in the study of the brain in the newborn and infant, therefore it represents the first choice technique to evaluate many diseases. In addition to the anterior fontanelle which serves as an acoustic window, the posterior fontanelle allows a more detailed study of the posterior fossa and occipital lobes [1, 2]. Ultrasound is an irreplaceable, but not exclusive diagnostic tool; it is relatively simple to use in the majority of birth time points.

The ultrasound method has a high diagnostic value in the evaluation of hemorrhagic lesions, in ventriculomegaly, and in the form of cystic periventricular leukomalacia. Many lesions, however, are at risk of resulting as false positives for non-cystic periventricular leukomalacia. These are linked to the experience of the operator and the resolution of the equipment, as well as to white matter abnormalities. In these cases it is necessary to resort to magnetic resonance and, in particular, the new functional resonance techniques.

Neonatal hypoxic-ischemic encephalopathy, especially in the early stages, may result within normal range or exhibit only a diffuse hyperechoic picture, while more serious injuries may be recognized only later. Failure to visualize the lateral ventricles, the disappearance of the groove impressions and cerebral convolutions may be considered indirect signs of diffuse edema that may, however, be overestimated or underestimated [3].

In congenital infections, ultrasound can easily identify some brain injuries, such as calcifications, germinolytic cysts or ventriculomegaly; while alterations of the posterior intracranial fossa are often underestimated [4], and although ultrasound is possible in disorders of neuronal migration they are inadequately diagnosed (Figure 1). In the case of neonatal meningitis - ultrasound can reveal complications such as ventriculitis, hydrocephalus and intraparenchymal abscesses, which fundamentally impact the choice of therapy.

Figure 1
figure 1

Infant with agyria (complete lissencephaly), the most serious form of abnormal neuronal migration. The coronal sonogram shows the complete absence of convolutions.

Although technological advancements have permitted the production of economical ultrasound equipment with an acceptable level of quality, the gap in image quality and thus diagnostic power between top of the line and economical devices is generally abysmal. Currently, some ultrasound devices allow, under certain conditions, revelation of anatomical details that are almost invisible to the naked eye [5]. However, the use of proper methodology is fundamental, which necessitates the need for both accurate diagnostic and prognostic data, in order to avoid repetitive testing, and negative influences on future diagnostic - therapeutic decisions. It should be emphasized, however, that many ultrasound limitations are actually limitations associated with operator training and experience.

References

  1. van Wezel-Meijler G, Steggerda SJ, Leijser LM: Cranial ultrasonography in neonates: role and limitations. Semin Perinatol. 2010, 34: 28-38. 10.1053/j.semperi.2009.10.002.

    Article  PubMed  Google Scholar 

  2. van Wezel-Meijler G, de Vries LS: Cranial ultrasound - optimizing utility in the NICU. Curr Pediatr Rev. 2014, 10: 16-27. 10.2174/157339631001140408120106.

    Article  Google Scholar 

  3. Plaisier A, Raets MM, Ecury-Goossen GM, Govaert P, Feijen-Roon M, Reiss IK, Smit LS, Lequin MH, Dudink J: Serial cranial ultrasonography or early MRI for detecting preterm brain injury?. Arch Dis Child Fetal Neonatal Ed. 2015, 100: F293-F300. 10.1136/archdischild-2014-306129.

    Article  PubMed  Google Scholar 

  4. Parodi A, Rossi A, Severino M, Morana G, Sannia A, Calevo MG, Malova M, Ramenghi LA: Accuracy of ulttrasound in assessing cerebellar haemorrhages in very low birthweight babies. Arch Dis Child Fetal Neonatal Ed. 2015, 100: F289-92. 10.1136/archdischild-2014-307176.

    Article  PubMed  Google Scholar 

  5. van Wezel-Meijler G, Leijser LM, Wiggers-de Bruïne FT, Steggerda SJ, van der Grond J, Walther FJ: Diffuse hyperechogenicity of basal ganglia and thalami in preterm neonates: a physiologic finding?. Radiology. 2011, 258: 944-50. 10.1148/radiol.10101086.

    Article  PubMed  Google Scholar 

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Correspondence to Alberto Chiara.

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This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Chiara, A., Perrini, S. Cranial ultrasound: and the risk of tunnel vision?. Ital J Pediatr 41 (Suppl 2), A15 (2015). https://doi.org/10.1186/1824-7288-41-S2-A15

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