Literature DB >> 11493407

Zonal dermal separation: a distinctive histopathological lesion associated with hyperelastosis cutis in a Quarter Horse.

S H Brounts1, A M Rashmir-Raven, S S Black.   

Abstract

This case report describes a distinctive deep cutaneous lesion in a 1-year-old Quarter Horse filly with hyperelastosis cutis. The horse had a typical clinical presentation of hyperelastic skin associated with a 6-month history of cutaneous wounds that developed following minor cutaneous trauma. Punch biopsies of skin from the affected horse were thinner than similar biopsies from an age- and breed-matched control. Significant microscopic lesions were not seen in cutaneous punch biopsies stained with haematoxylin and eosin and Masson's trichrome stains, but the ultrastructure of the dermis from the affected horse was characterized by variation in collagen fibre diameter and loose packing of collagen fibres within bundles. The horse was euthanized and necropsied, and full-thickness sections of skin were collected and examined microscopically. Affected skin was of normal thickness; however, the deep dermis contained a distinctive horizontal linear zone in which separation of collagen bundles resulted in the formation of large empty cleft-like spaces between the upper and lower regions of the deep dermis. We suggest the term 'zonal dermal separation' for this microscopic lesion. Incisional full-thickness skin biopsies should be taken in suspected cases of equine hyperelastosis cutis because punch biopsies may not obtain enough deep dermis to adequately represent pathological change in the skin of horses with this disorder.

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Year:  2001        PMID: 11493407     DOI: 10.1046/j.0959-4493.2001.00256.x

Source DB:  PubMed          Journal:  Vet Dermatol        ISSN: 0959-4493            Impact factor:   1.589


  3 in total

1.  Mutation in cyclophilin B that causes hyperelastosis cutis in American Quarter Horse does not affect peptidylprolyl cis-trans isomerase activity but shows altered cyclophilin B-protein interactions and affects collagen folding.

Authors:  Yoshihiro Ishikawa; Janice A Vranka; Sergei P Boudko; Elena Pokidysheva; Kazunori Mizuno; Keith Zientek; Douglas R Keene; Ann M Rashmir-Raven; Kazuhiro Nagata; Nena J Winand; Hans Peter Bächinger
Journal:  J Biol Chem       Date:  2012-05-03       Impact factor: 5.157

2.  Skin malformations in a neonatal foal tested homozygous positive for Warmblood Fragile Foal Syndrome.

Authors:  Chloé Monthoux; Simone de Brot; Michelle Jackson; Ulrich Bleul; Jasmin Walter
Journal:  BMC Vet Res       Date:  2015-01-31       Impact factor: 2.741

3.  Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States.

Authors:  Simone Reiter; Barbara Wallner; Gottfried Brem; Elisabeth Haring; Ludwig Hoelzle; Monika Stefaniuk-Szmukier; Bogusława Długosz; Katarzyna Piórkowska; Katarzyna Ropka-Molik; Julia Malvick; Maria Cecilia T Penedo; Rebecca R Bellone
Journal:  Genes (Basel)       Date:  2020-12-18       Impact factor: 4.096

  3 in total

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