open access

Vol 81, No 1 (2022)
Original article
Submitted: 2020-12-08
Accepted: 2021-01-04
Published online: 2021-01-22
Get Citation
Erratum has been published: #1 , #2

Paratenon of the cruciate ligaments of the knee: a macroscopic and histological study of human foetuses

J. H. Kim1, N. Sugai2, D. Suzuki3, G. Murakami4, H. Abe5, J. F. Rodríguez-Vázquez6, M. Yamamoto7
·
Pubmed: 33511626
·
Folia Morphol 2022;81(1):134-143.
Affiliations
  1. Department of Anatomy, Jeonbuk National University Medical School, Jeonju, Korea
  2. Department of Rehabilitation and Physical Therapy, Hitshuji-ga-oka Hospital, Sapporo, Japan
  3. Division of Common Curriculum, Hokkaido Chitose College of Rehabilitation, Chitose, Japan
  4. Division of Internal Medicine, Cupid Clinic, Iwamizawa, Hokkaido, Japan
  5. Emeritus Professor of Akita University School of Medicine, Akita, Japan
  6. Department of Anatomy and Embryology, School of Medicine, Complutense University, Madrid, Spain
  7. Department of Anatomy, Tokyo Dental College, Tokyo, Japan

open access

Vol 81, No 1 (2022)
ORIGINAL ARTICLES
Submitted: 2020-12-08
Accepted: 2021-01-04
Published online: 2021-01-22

Abstract

Background: The paratenon is a sheath-like connective tissue that allows the tendon to move with minimal friction. The careful removal of the paratenon along the cruciate ligaments is a critical step of knee surgery. Thus, orthopaedic surgeons and interventional radiologists consider the paratenon as a basic anatomical tissue along a ligament, not along a tendon.
Materials and methods: We performed macroscopic and histological observations of cruciate ligament-associated paratenons in 43 human foetuses.
Results: This tissue usually had a thick armour-like appearance that was distant from the infrapatellar fat pad. The anterior cruciate ligament, rather than the posterior ligament, was deeply embedded in the paratenon. The paratenon contained abundant arteries and veins and, at and near the crossing between the cruciate ligaments, had a well-developed venous plexus. Notably, there were abundant fused veins in the paratenon venous plexus, and prenatal knee movements (especially rotation) seemed to restrict its blood supply, leading to the development of a large cavity by way of advancing fusion of veins in the degenerating plexus. This unique manner of cavitation likely expanded the joint cavity.
Conclusions: Differences in knee movements in utero seemed to cause differences in the thickness of the paratenon among foetuses. New-borns might have limited knee flexion due to a mass-effect of the thick paratenon around the cruciate ligaments. A slight twisting or rotation at the knee may help to release the knee, because it can break the foetal paratenon and accelerate cavitation.

Abstract

Background: The paratenon is a sheath-like connective tissue that allows the tendon to move with minimal friction. The careful removal of the paratenon along the cruciate ligaments is a critical step of knee surgery. Thus, orthopaedic surgeons and interventional radiologists consider the paratenon as a basic anatomical tissue along a ligament, not along a tendon.
Materials and methods: We performed macroscopic and histological observations of cruciate ligament-associated paratenons in 43 human foetuses.
Results: This tissue usually had a thick armour-like appearance that was distant from the infrapatellar fat pad. The anterior cruciate ligament, rather than the posterior ligament, was deeply embedded in the paratenon. The paratenon contained abundant arteries and veins and, at and near the crossing between the cruciate ligaments, had a well-developed venous plexus. Notably, there were abundant fused veins in the paratenon venous plexus, and prenatal knee movements (especially rotation) seemed to restrict its blood supply, leading to the development of a large cavity by way of advancing fusion of veins in the degenerating plexus. This unique manner of cavitation likely expanded the joint cavity.
Conclusions: Differences in knee movements in utero seemed to cause differences in the thickness of the paratenon among foetuses. New-borns might have limited knee flexion due to a mass-effect of the thick paratenon around the cruciate ligaments. A slight twisting or rotation at the knee may help to release the knee, because it can break the foetal paratenon and accelerate cavitation.

Get Citation

Keywords

paratenon, tendon sheath, cruciate ligament of the knee, histology, human foetus

Erratum (1)
NiezatErratumytułowany
Download
19KB
About this article
Title

Paratenon of the cruciate ligaments of the knee: a macroscopic and histological study of human foetuses

Journal

Folia Morphologica

Issue

Vol 81, No 1 (2022)

Article type

Original article

Pages

134-143

Published online

2021-01-22

Page views

5981

Article views/downloads

1246

DOI

10.5603/FM.a2021.0003

Pubmed

33511626

Bibliographic record

Folia Morphol 2022;81(1):134-143.

Keywords

paratenon
tendon sheath
cruciate ligament of the knee
histology
human foetus

Authors

J. H. Kim
N. Sugai
D. Suzuki
G. Murakami
H. Abe
J. F. Rodríguez-Vázquez
M. Yamamoto

References (21)
  1. Benjamin M, Kaiser E, Milz S. Structure-function relationships in tendons: a review. J Anat. 2008; 212(3): 211–228.
  2. Broughton NS, Wright J, Menelaus MB. Range of knee motion in normal neonates. J Pediatr Orthop. 1993; 13(2): 263–264.
  3. Chahla J, Moatshe G, Cinque ME, et al. Arthroscopic anatomic single-bundle anterior cruciate ligament reconstruction using bone-patellar tendon-bone autograft: pearls for an accurate reconstruction. Arthrosc Tech. 2017; 6(4): e1159–e1167.
  4. Clark CR, Ogden JA. Development of the menisci of the human knee joint. Morphological changes and their potential role in childhood meniscal injury. J Bone Joint Surg Am. 1983; 65(4): 538–547.
  5. Gray DJ, Gardner E. Prenatal development of the human knee and superior tibiofibular joints. Am J Anat. 1950; 86(2): 235–287.
  6. Higginbottom J, Bagnall KM, Harris PF, et al. Ultrasound monitoring of fetal movements. A method for assessing fetal development? . Lancet. 1976; 307(7962): 719–721.
  7. Humphrey T. Some correlations between the appearance of human fetal reflexes and the development of the nervous system. Progr Brain Res. 1964: 93–135.
  8. Huisman ES, Andersson G, Scott A, et al. Regional molecular and cellular differences in the female rabbit Achilles tendon complex: potential implications for understanding responses to loading. J Anat. 2014; 224(5): 538–547.
  9. Isogai S, Murakami G, Wada T, et al. Which morphologies of synovial folds result from degeneration and/or aging of the radiohumeral joint: an anatomic study with cadavers and embryos. J Shoulder Elbow Surg. 2001; 10(2): 169–181.
  10. Katz K, Naor N, Merlob P, et al. Rotational deformities of the tibia and foot in preterm infants. J Pediatr Orthop. 1990; 10(4): 483–485.
  11. Katz K, Mashiach R, Bar On A, et al. Normal range of fetal knee movements. J Pediatr Orthop. 1999; 19(6): 739–741.
  12. Khan KM, Maffulli N, Coleman BD, et al. Patellar tendinopathy: some aspects of basic science and clinical management. Br J Sports Med. 1998; 32(4): 346–355.
  13. Kitamura K, Hayashi S, Jin ZWu, et al. Fetal cervical zygapophysial joint with special reference to the associated synovial tissue: a histological study using near-term human fetuses. Anat Cell Biol. 2021; 54(1): 65–73.
  14. Lalam RK, Winn N, Cassar-Pullicino VN. Interventional articular and para-articular knee procedures. Br J Radiol. 2016; 89(1059): 20150413.
  15. Mérida-Velasco J, Sánchez-Montesinos I, Espín-Ferra J, et al. Development of the human knee joint ligaments. Anat Rec. 1997; 248(2): 259–268, doi: 10.1002/(sici)1097-0185(199706)248:2<259::aid-ar13>3.0.co;2-o.
  16. McDermott L. Development of the human knee joint. Arch Surg. 1943; 46(5): 705.
  17. Movat HZ, More RH. The nature and origin of fibrinoid. Am J Clin Pathol. 1957; 28(4): 331–353.
  18. Shaw HM, Vázquez OT, McGonagle D, et al. Development of the human Achilles tendon enthesis organ. J Anat. 2008; 213(6): 718–724.
  19. Stecco C, Corradin M, Macchi V, et al. Plantar fascia anatomy and its relationship with Achilles tendon and paratenon. J Anat. 2013; 223(6): 665–676.
  20. Takayama T, Hirano-Kawamoto Ai, Yamamoto M, et al. Macrophage infiltration into thyroid follicles: an immunohistochemical study using donated elderly cadavers. Okajimas Folia Anat Jpn. 2016; 93(3): 73–80.
  21. Uchiyama Y, Oomiya A, Murakami G. Fluctuations in follicular structures of rat thyroid glands during 24 hours: fine structural and morphometric studies. Am J Anat. 1986; 175(1): 23–33.

Regulations

Important: This website uses cookies. More >>

The cookies allow us to identify your computer and find out details about your last visit. They remembering whether you've visited the site before, so that you remain logged in - or to help us work out how many new website visitors we get each month. Most internet browsers accept cookies automatically, but you can change the settings of your browser to erase cookies or prevent automatic acceptance if you prefer.

By VM Media Group sp. z o.o., Grupa Via Medica, Świętokrzyska 73, 80–180 Gdańsk, Poland

tel.: +48 58 320 94 94, faks: +48 58 320 94 60, e-mail: viamedica@viamedica.pl