Difference between revisions of "Fuchs dystrophy"

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*Decreased endothelial density.<ref name=pmid19236704>{{Cite journal  | last1 = Klintworth | first1 = GK. | title = Corneal dystrophies. | journal = Orphanet J Rare Dis | volume = 4 | issue =  | pages = 7 | month =  | year = 2009 | doi = 10.1186/1750-1172-4-7 | PMID = 19236704 }}</ref>
*Decreased endothelial density.<ref name=pmid19236704>{{Cite journal  | last1 = Klintworth | first1 = GK. | title = Corneal dystrophies. | journal = Orphanet J Rare Dis | volume = 4 | issue =  | pages = 7 | month =  | year = 2009 | doi = 10.1186/1750-1172-4-7 | PMID = 19236704 }}</ref>
*Thickening of ''Descemet's membrane''.<ref>URL: [http://www.mrcophth.com/pathology/fuchendothelialdystrophy.html http://www.mrcophth.com/pathology/fuchendothelialdystrophy.html]. Accessed on: 27 August 2015.</ref>
*Thickening of ''Descemet's membrane''.<ref>URL: [http://www.mrcophth.com/pathology/fuchendothelialdystrophy.html http://www.mrcophth.com/pathology/fuchendothelialdystrophy.html]. Accessed on: 27 August 2015.</ref>
**Older normal individuals: 16 +/- 2 micrometres.<ref name=pmid20163865/>
**Fuchs dystrophy: 34 +/- 11 micrometres.<ref name=pmid20163865>{{Cite journal  | last1 = Shousha | first1 = MA. | last2 = Perez | first2 = VL. | last3 = Wang | first3 = J. | last4 = Ide | first4 = T. | last5 = Jiao | first5 = S. | last6 = Chen | first6 = Q. | last7 = Chang | first7 = V. | last8 = Buchser | first8 = N. | last9 = Dubovy | first9 = SR. | title = Use of ultra-high-resolution optical coherence tomography to detect in vivo characteristics of Descemet's membrane in Fuchs' dystrophy. | journal = Ophthalmology | volume = 117 | issue = 6 | pages = 1220-7 | month = Jun | year = 2010 | doi = 10.1016/j.ophtha.2009.10.027 | PMID = 20163865 }}</ref>


===Images===
===Images===

Revision as of 16:50, 27 August 2015

Fuchs dystrophy, also Fuchs endothelial dystrophy, is a rare pathology of the eye that may be seen in Descemet's membrane specimens.

General

  • Uncommon.

Microscopic

Features:[1]

  • Guttae accumulations.
    • Collagenous material from the basement membrane.
  • Decreased endothelial density.[2]
  • Thickening of Descemet's membrane.[3]
    • Older normal individuals: 16 +/- 2 micrometres.[4]
    • Fuchs dystrophy: 34 +/- 11 micrometres.[4]

Images

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Descemet’s Membrane, Right Eye, Excision:
- Thickened Descemet’s membrane with marked decrease of endothelial cells and gutta consistent with Fuch's dystrophy.

See also

References

  1. McLaren, JW.; Bachman, LA.; Kane, KM.; Patel, SV. (Feb 2014). "Objective assessment of the corneal endothelium in Fuchs' endothelial dystrophy.". Invest Ophthalmol Vis Sci 55 (2): 1184-90. doi:10.1167/iovs.13-13041. PMID 24508788.
  2. 2.0 2.1 Klintworth, GK. (2009). "Corneal dystrophies.". Orphanet J Rare Dis 4: 7. doi:10.1186/1750-1172-4-7. PMID 19236704.
  3. URL: http://www.mrcophth.com/pathology/fuchendothelialdystrophy.html. Accessed on: 27 August 2015.
  4. 4.0 4.1 Shousha, MA.; Perez, VL.; Wang, J.; Ide, T.; Jiao, S.; Chen, Q.; Chang, V.; Buchser, N. et al. (Jun 2010). "Use of ultra-high-resolution optical coherence tomography to detect in vivo characteristics of Descemet's membrane in Fuchs' dystrophy.". Ophthalmology 117 (6): 1220-7. doi:10.1016/j.ophtha.2009.10.027. PMID 20163865.