Literature DB >> 35791242

A rare case of bilateral granular corneal dystrophy with keratoconus and primary angle closure glaucoma.

Rama Rajagopal1, Nivisha Bandodkar1, Deepa Mukundan1.   

Abstract

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Year:  2022        PMID: 35791242      PMCID: PMC9426182          DOI: 10.4103/ijo.IJO_2991_21

Source DB:  PubMed          Journal:  Indian J Ophthalmol        ISSN: 0301-4738            Impact factor:   2.969


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A 41-year-old female presented with clinical features of bilateral granular corneal dystrophy (GCD) [Fig. 1a, b], keratoconus on Pentacam [Fig. 2a–d], and primary angle closure glaucoma. GCD with keratoconus is rarely reported.[1234] Although no evidence-based analysis has linked this association, many theories have been proposed, including abnormal synthetic activity of keratocytes and degeneration of defective basal epithelial cells, speculated to occur in both.[2] While GCD is clinically obvious, this case emphasizes the need to identify associated factors in effective planning and management. Documenting keratometry in GCD patients may aid in early diagnosis.
Figure 1

(a) Right eye: Slit section image showing stromal deposits in GCD. (b) Left eye: Diffuse slit-lamp image showing granular deposits in the central cornea. GCD = granular corneal dystrophy

Figure 2

(a, b) Pentacam image of the right and left eyes showing thinnest pachymetry corresponding with area of steepening and highest point of elevation. (c, d) Pentacam image of the right and left eyes showing Belin/Ambrósio enhanced ectasia display

(a) Right eye: Slit section image showing stromal deposits in GCD. (b) Left eye: Diffuse slit-lamp image showing granular deposits in the central cornea. GCD = granular corneal dystrophy (a, b) Pentacam image of the right and left eyes showing thinnest pachymetry corresponding with area of steepening and highest point of elevation. (c, d) Pentacam image of the right and left eyes showing Belin/Ambrósio enhanced ectasia display

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.
  4 in total

1.  Association of keratoconus and Avellino corneal dystrophy.

Authors:  S Igarashi; Y Makita; T Hikichi; F Mori; K Hanada; A Yoshida
Journal:  Br J Ophthalmol       Date:  2003-03       Impact factor: 4.638

2.  Familial case of keratoconus with corneal granular dystrophy.

Authors:  M Mitsui; T Sakimoto; M Sawa; M Katami
Journal:  Jpn J Ophthalmol       Date:  1998 Sep-Oct       Impact factor: 2.447

3.  Keratoconus and granular dystrophy.

Authors:  Clare M Wilson; Penny J D'Ath; Dipak N Parmar; Evripidis Sykakis
Journal:  BMJ Case Rep       Date:  2014-08-25

4.  Association of keratoconus with granular corneal dystrophy.

Authors:  R B Vajpayee; G R Snibson; H R Taylor
Journal:  Aust N Z J Ophthalmol       Date:  1996-11
  4 in total

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