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Identifying Palmar Skin Surface Landmark for Locating A2 Pulley during Cadaveric Dissection of the Hand
The A2 and A4 pulleys are fibro-osseous structures that support the flexor tendon function. Injury to these pulleys can result in bowstringing and limited tendon excursion. Thus, having an understanding of the skin surface landmark of the A2 pulley is crucial to safeguard it during hand surgery. MET...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368382/ https://www.ncbi.nlm.nih.gov/pubmed/37496981 http://dx.doi.org/10.1097/GOX.0000000000005138 |
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author | Alowais, Fahad Abdullah Alnaeem, Hassan |
author_facet | Alowais, Fahad Abdullah Alnaeem, Hassan |
author_sort | Alowais, Fahad Abdullah |
collection | PubMed |
description | The A2 and A4 pulleys are fibro-osseous structures that support the flexor tendon function. Injury to these pulleys can result in bowstringing and limited tendon excursion. Thus, having an understanding of the skin surface landmark of the A2 pulley is crucial to safeguard it during hand surgery. METHODS: We performed cadaveric dissection of 62 hands. For 248 fingers, the measurement of distance A, which is half the distance between the palmar digital crease and proximal interphalangeal crease reflected in the palm, and distance B, which is the distance between the A2 pulley’s starting point and the palmar digital crease, were taken by a caliber. Statistical analysis was performed using the paired sample t test to determine whether there was a significant difference between distances A and B. RESULTS: Our study revealed that there was no significant difference (p>0.05) between the measured starting point of the A2 pulley and its proposed surface landmark for the index, middle, and small fingers. Conversely, the ring finger showed a statistically significant difference of 1 mm more proximal. CONCLUSIONS: By measuring the distance between the palmar digital crease and proximal interphalangeal crease and reflecting it proximally in the palms, one can anticipate the location of the A2 pulley’s starting point for each digit, except for the ring finger. The ring finger’s starting point is 1 mm more proximal than the other digits. Knowing the starting point of the A2 pulley will help hand surgeons limit incisions and avoid accidental injury during hand surgery. |
format | Online Article Text |
id | pubmed-10368382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-103683822023-07-26 Identifying Palmar Skin Surface Landmark for Locating A2 Pulley during Cadaveric Dissection of the Hand Alowais, Fahad Abdullah Alnaeem, Hassan Plast Reconstr Surg Glob Open Hand The A2 and A4 pulleys are fibro-osseous structures that support the flexor tendon function. Injury to these pulleys can result in bowstringing and limited tendon excursion. Thus, having an understanding of the skin surface landmark of the A2 pulley is crucial to safeguard it during hand surgery. METHODS: We performed cadaveric dissection of 62 hands. For 248 fingers, the measurement of distance A, which is half the distance between the palmar digital crease and proximal interphalangeal crease reflected in the palm, and distance B, which is the distance between the A2 pulley’s starting point and the palmar digital crease, were taken by a caliber. Statistical analysis was performed using the paired sample t test to determine whether there was a significant difference between distances A and B. RESULTS: Our study revealed that there was no significant difference (p>0.05) between the measured starting point of the A2 pulley and its proposed surface landmark for the index, middle, and small fingers. Conversely, the ring finger showed a statistically significant difference of 1 mm more proximal. CONCLUSIONS: By measuring the distance between the palmar digital crease and proximal interphalangeal crease and reflecting it proximally in the palms, one can anticipate the location of the A2 pulley’s starting point for each digit, except for the ring finger. The ring finger’s starting point is 1 mm more proximal than the other digits. Knowing the starting point of the A2 pulley will help hand surgeons limit incisions and avoid accidental injury during hand surgery. Lippincott Williams & Wilkins 2023-07-25 /pmc/articles/PMC10368382/ /pubmed/37496981 http://dx.doi.org/10.1097/GOX.0000000000005138 Text en Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Hand Alowais, Fahad Abdullah Alnaeem, Hassan Identifying Palmar Skin Surface Landmark for Locating A2 Pulley during Cadaveric Dissection of the Hand |
title | Identifying Palmar Skin Surface Landmark for Locating A2 Pulley during Cadaveric Dissection of the Hand |
title_full | Identifying Palmar Skin Surface Landmark for Locating A2 Pulley during Cadaveric Dissection of the Hand |
title_fullStr | Identifying Palmar Skin Surface Landmark for Locating A2 Pulley during Cadaveric Dissection of the Hand |
title_full_unstemmed | Identifying Palmar Skin Surface Landmark for Locating A2 Pulley during Cadaveric Dissection of the Hand |
title_short | Identifying Palmar Skin Surface Landmark for Locating A2 Pulley during Cadaveric Dissection of the Hand |
title_sort | identifying palmar skin surface landmark for locating a2 pulley during cadaveric dissection of the hand |
topic | Hand |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368382/ https://www.ncbi.nlm.nih.gov/pubmed/37496981 http://dx.doi.org/10.1097/GOX.0000000000005138 |
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