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OMICS Journal of Radiology - A typical Depiction of Renal Nephrocalcinosis Reflecting the Superiority of Ultrasound to Computed Tomography
ISSN:2167-7964

OMICS Journal of Radiology
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  • Image Article   
  • OMICS J Radiol 2022, Vol 11(2): 369
  • DOI: 10.4172/2167-7964.1000369

A typical Depiction of Renal Nephrocalcinosis Reflecting the Superiority of Ultrasound to Computed Tomography

Amsiguine Najwa*, Iraqi Housaini Zaynab, Halfi Mohamed Ismail, Lrhorfi Najlae, Chat Latifa and Allali Nasik
Department of Pediatric Radiology, Hospital Ibn Sina, Faculty of Medicine, Rabat, Morocco
*Corresponding Author: Amsiguine Najwa, Department of Pediatric Radiology, Hospital Ibn Sina, Faculty of Medicine, Rabat, Morocco, Email: thealmanac101@gmail.com

Received: 23-Jan-2022 / Manuscript No. roa-22-55845 / Editor assigned: 03-Mar-2022 / PreQC No. roa-22-55845(PQ) / Reviewed: 17-Mar-2022 / QC No. roa-22- 55845 / Revised: 22-Mar-2022 / Manuscript No. roa-22-55845(R) / Published Date: 29-Mar-2022 DOI: 10.4172/2167-7964.1000369

Abstract

Nephrocalcinosis is defined by calcium phosphate or calcium oxalate deposits in the kidney parenchyma, particularly in tubular epithelial cells and interstitial tissue. It should be differentiated from nephrolithiasis where calcium salts deposits are located in the kidney and urinary tract. We report a case of a 5 years old child with history of hypoparathyroidism of recent discovery , and the clear upper hand that ultrasound had in the assessment of medullary nephrocalcinosis in patients with metabolic disorders.

Keywords

Nephrocalcinosis; Ultrasound; Children; Imaging modalities

Image Article

A renal calcifying disorder generally includes two entities: nephrocalcinosis and nephrolithiasis. In addition to their difference in location, nephrolithiasis may occur in healthy individuals while nephrocalcinosis suggests an underlying genetic or metabolicendocrine disorder, such as hypoparathyroidism often detected as an incidental finding as reflected in our case, nephrocalcinosis may be classified according to the radiological type: medullary, cortical or diffuse. [1]

Unlike nephrolithiasis, nephrocalcinosis is asymptomatic, and may progress to renal insufficiency. Early diagnosis is important because therapeutic interventions may stabilize, slow or, rarely, reverse disease.

Therefore surveillance in high-risk patients is a crucial component of management. Diagnostic imaging for nephrocalcinosis includes radiographs, computed tomography (CT), and ultrasonography (US). Radiographs are insensitive due to poor delineation of renal anatomy and confounding by bowel gas. CT offers superior contrast resolution and definition of anatomic structures and is the gold standard for nephrolithiasis ultrasound however offers a higher sensitivity in term of early diagnosis of mild and moderate nephrocalcinosis compared to the CT [2] (Figures 1 and 2).

radiology-Transversal

Figure 1: Transversal US image of the left kidney showing clear hyper echoic lesions on the medulla.

radiology-enhanced

Figure 2: Coronal non enhanced CT image of the left kidney revealing lithiasis on the superior region of the kidney in addition to diffuse mild hyper density spread across the medulla.

References

  1. Monet-Didailler C, Chateil JF, Allard L, Godron-Dubrasquet A, Harambat J (2021) Nephrocalcinosis in children. Nephrol Ther. 17: 58-66.
  2. Indexed at, Google Scholar, Crossref

  3. Boyce AM, Shawker TH, Hill SC, Choyke PL, Hill MC, et al. (2013) Ultrasound is superior to computed tomography for assessment of medullary nephrocalcinosis in hypoparathyroidism. J Clin Endocrinol Metab 98: 989-994.
  4. Indexed at, Google Scholar, Crossref

Citation: Najwa A, Zaynab IH, Ismail HM, Najlae L, Latifa C, et al. (2022) A typical Depiction of Renal Nephrocalcinosis Reflecting the Superiority of Ultrasound to Computed Tomography. OMICS J Radiol 11: 368. DOI: 10.4172/2167-7964.1000369

Copyright: © 2022 Najwa A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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