Literature DB >> 30672510

Comment on: Bilateral combined central retinal artery and vein occlusion in a 3-year-old child with nephrotic syndrome.

Anamika Dwivedi1, Sujata Lakhtakia1.   

Abstract

Entities:  

Mesh:

Year:  2019        PMID: 30672510      PMCID: PMC6376831          DOI: 10.4103/ijo.IJO_1633_18

Source DB:  PubMed          Journal:  Indian J Ophthalmol        ISSN: 0301-4738            Impact factor:   1.848


× No keyword cloud information.
Dear Sir, We read the article ‘Bilateral combined central retinal artery and vein occlusion in a 3-year-old child with nephrotic syndrome’ by Sinha et al.[1] with deep interest and would like to congratulate the team for an excellent documentation of fundus, fundus fluorescein angiography (FFA) and optical coherence tomography (OCT) in a 3-year-old child. However, we wish to point out certain points which we thought were important for diagnosis. The fundus picture shows areas of retinal opacification in the posterior pole which are well demarcated and bounded by arterioles and not diffuse as seen in central retinal artery occlusion (CRAO). These areas appear to be discrete with clear demarcation between affected retina and the contiguous retinal vessels, suggestive of Purtscher flecken.[2] This sparing of perivascular retina from whitening is obviously evident in extramacular areas of retinal whitening in fundus photographs. A cherry red spot can be seen in Purtscher's retinopathy when the retinal whitening surrounds the fovea and does not necessarily confirm the diagnosis of CRAO. Retinal haemorrhages which are characteristically seen in all four quadrants in central retinal vein occlusion (CRVO) are very few and seen isolated in this case and this is common in Purtscher's retinopathy. We could not find any evidence of delayed filling in the FFA pictures presented and as mentioned in the article, though we understand the technical difficulties involved in a 3-year-old child. Authors have reported arteriolar attenuation at 3 weeks but there seems to be no evidence of arteriolar attenuation in the fundus images of BE presented alongside the spectral domain optical coherence tomography (SDOCT) images.[1] In view of the above-mentioned characteristics, the diagnosis of Purtscher's-like retinopathy is more appropriate instead of combined CRAO and CRVO. There are reports in the literature describing Purtscher's-like retinopathy in children with nephrotic syndrome with similar severity.[345]

Declaration

The manuscript has been read and approved by all the authors and each author believes that manuscript represent honest work.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.
  5 in total

1.  Purtscher-like retinopathy in nephrotic syndrome associated with mild chronic renal failure.

Authors:  D Zwolińska; A Medyńska; A Galar; A Turno
Journal:  Pediatr Nephrol       Date:  2000-11       Impact factor: 3.714

Review 2.  Systematic review of Purtscher's and Purtscher-like retinopathies.

Authors:  A I M Miguel; F Henriques; L F R Azevedo; A J R Loureiro; D A L Maberley
Journal:  Eye (Lond)       Date:  2012-11-23       Impact factor: 3.775

3.  Purtscher-like Retinopathy in Septicemic Disseminated Intravascular Coagulation Associated with Nephrotic Syndrome.

Authors:  Francesco Viola; Diego Vezzola; Edoardo Villani; Chiara Mapelli; Giulio Barteselli; Roberto Ratiglia
Journal:  Eur J Ophthalmol       Date:  2013 Jul-Aug       Impact factor: 2.597

4.  Purtscher-like retinopathy: A rare ocular finding in nephrotic syndrome.

Authors:  Anamika Dwivedi; Deepak Dwivedi; Charudutt Chalisgaonkar; Sujata Lakhtakia
Journal:  Oman J Ophthalmol       Date:  2018 Jan-Apr

5.  Bilateral combined central retinal artery and vein occlusion in a 3-year-old child with nephrotic syndrome.

Authors:  Shivani Sinha; Adoor T K Rau; Rachna V Kumar; Chaitra Jayadev; Anand Vinekar
Journal:  Indian J Ophthalmol       Date:  2018-10       Impact factor: 1.848

  5 in total
  1 in total

1.  Bilateral branch retinal artery occlusion in a child with nephrotic syndrome.

Authors:  Srikanta Kumar Padhy; Tapas Ranjan Padhi; Utpal Bhusal; Krushna Gopal Panda
Journal:  BMJ Case Rep       Date:  2020-05-07
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.