Morphological types of the external oblique abdominal muscle aponeurosis: a morphometric and histological justification
DOI:
https://doi.org/10.30978/GS-2026-2-8Keywords:
external oblique aponeurosis, EIT Ambivium, linea semilunaris, Spigelian zone, morphometry, histology, morphotypes, abdominoplastyAbstract
Objective – to investigate the histological and morphometric characteristics of the external oblique aponeurosis in the region associated with the linea semilunaris (the Ambivium zone).
Materials and methods. The study included 34 women aged 22 – 54 years (mean age: 36.2±7.3 years) who underwent abdominoplasty for cosmetic defects of the anterior abdominal wall. During surgery, standardized fragments of the external oblique aponeurosis were obtained from symmetrical regions adjacent to the lateral border of the rectus sheath. Histological, histochemical, and morphometric analyses were performed, including assessment of collagen bundle thickness, width of the endotenonium and peritenonium, parameters of the microcirculatory bed, and the relative areas occupied by collagen, peritenonium, and vessels. Hierarchical cluster analysis and the k-means method were applied to systematize the identified structural variants.
Results. Morphometric analysis revealed substantial variability in the structural organization of the aponeurosis: the proportion of collagen fibers ranged from 61.1% to 91.2%, the proportion of peritenonium from 7.3% to 33.9%, and the compactness coefficient from 0.64 to 0.93. Cluster analysis enabled the identification of three morphotypes: compact (35.3%), transitional (26.5%), and disorganized (38.2%). The compact morphotype was characterized by a high proportion of collagen (89.32±1.52%), minimal content of peritenonium (8.86±1.15%), and the highest compactness coefficient 0.91±0.01. In contrast, the disorganized morphotype demonstrated the lowest proportion of collagen (68.18±4.04%), the highest content of peritenonium (26.87±4.11%), a low compactness coefficient 0.72±0.05, widening of interfascicular spaces, remodeling of the vascular component, and signs of pronounced histostructural reorganization. The transitional morphotype occupied an intermediate position. All intercluster differences were statistically significant (p < 0.001).
Conclusions. Morphometric and cluster analysis of the external oblique aponeurosis revealed substantial structural variability and enabled the identification of three morphotypes–compact, transitional, and disorganized–which differed in the proportions of collagen fibers, peritenonium, vascular component, and compactness parameters. The identified morphological heterogeneity of the aponeurosis reflects different degrees of structural remodeling and may represent one of the factors contributing to variability in the outcomes of surgical correction of the anterior abdominal wall, thereby supporting the rationale for further individualization of surgical strategy.
References
Axer H, von Keyserlingk DG, Prescher A. Collagen fibers in linea alba and rectus sheaths. I. General scheme and morphological aspects. J Surg Res. 2001;96(1):127-134. http://doi.org/10.1006/jsre.2000.6070.
Brown SH, McGill SM. How the inherent stiffness of the in vivo human trunk varies with changing magnitudes of muscular activation. Clin Biomech (Bristol). 2008 Jan;23(1):15-22. http://doi.org/10.1016/j.clinbiomech.2007.08.011. Epub 2007 Oct 1. PMID: 17910898.
Hodges PW, Eriksson AE, Shirley D, Gandevia SC. Intra-abdominal pressure increases stiffness of the lumbar spine. J Biomech. 2005 Sep;38(9):1873-80. http://doi.org/10.1016/j.jbiomech.2004.08.016. PMID: 16023475.
Hodges PW, Moseley GL. Pain and motor control of the lumbopelvic region: effect and possible mechanisms. J Electromyogr Kinesiol. 2003 Aug;13(4):361-70. http://doi.org/10.1016/s1050-6411(03)00042-7. PMID: 12832166.
Hodges PW, Richardson CA. Contraction of the abdominal muscles associated with movement of the lower limb. Phys Ther. 1997 Feb;77(2):132-42; discussion 142-4. http://doi.org/10.1093/ptj/77.2.132. PMID: 9037214.
Huttinger R, Sugumar K, Baltazar-Ford KS. Spigelian hernia. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. Available from: https://www.ncbi.nlm.nih.gov/books/NBK538290/.
Jourdan A, Soucasse A, Scemama U, Gillion JF, Chaumoitre K, Masson C, et al. Abdominal wall morphometric variability based on computed tomography: influence of age, gender, and body mass index. Clin Anat. 2020 Nov;33(8):1110-1119. http://doi.org/10.1002/ca.23548.
Katsaros I, Papapanou M, Kontogeorgi E, Tsakotos G, Filippou D, Papaconstantinou D, Paspala A, Chatzimavroudis G, Kykalos S, Schizas D. Spigelian hernias in the adult population: a systematic review of the literature. Langenbecks Arch Surg. 2024 Jul 29;409(1):230. http://doi.org/10.1007/s00423-024-03427-4. PMID: 39073648.
Korenkov M, Beckers A, Koebke J, Lefering R, Tiling T, Troidl H. Biomechanical and morphological types of the linea alba and its possible role in the pathogenesis of midline incisional hernia. Eur J Surg. 2001;167(12):909-14. http://doi.org/10.1080/110241501753361596.
Larson DW, Farley DR. Spigelian hernias: repair and outcome for 81 patients. World J Surg. 2002;26(10):1277-1281. http://doi.org/10.1007/s00268-002-6605-0.
Levillain A, Orhant M, Turquier F, Hoc T. Contribution of collagen and elastin fibers to the mechanical behavior of an abdominal connective tissue. J Mech Behav Biomed Mater. 2016;61:308-317. http://doi.org/10.1016/j.jmbbm.2016.04.006.
Lockwood T. High-lateral-tension abdominoplasty with superficial fascial system suspension. Plast Reconstr Surg. 1995 Sep;96(3):603-15. http://doi.org/10.1097/00006534-199509000-00012. PMID: 7638284.
Matarasso A, Matarasso DM, Matarasso EJ. Abdominoplasty: classic principles and technique. Clin Plast Surg. 2014 Oct;41(4):655-72. http://doi.org/10.1016/j.cps.2014.07.005. PMID: 25283453.
Nahas FX. An aesthetic classification of the abdomen based on the myoaponeurotic layer. Plast Reconstr Surg. 2001;108(6):1787-1795. doi: 10.1097/00006534-200111000-00043.
Nessel R, Lesch C, Vollmer M, Kallinowsk F. Biomechanical principles of a permanently durable abdominal wall reconstruction: current status and potential future development. Mini-invasive Surgery. 2023;7(1):21. http://doi.org/10.20517/2574-1225.2023.21.
Ramirez OM, Ruas E, Dellon AL. «Components separation» method for closure of abdominal-wall defects: an anatomic and clinical study. Plast Reconstr Surg. 1990 Sep;86(3):519-26. http://doi.org/10.1097/00006534-199009000-00023.
Richardson CA, Hodges PW, Hides JA. Therapeutic Exercise for Lumbopelvic Stabilization. 2nd ed. Churchill Livingstone; 2004.
Saldanha OR, Federico R, Daher PF, Malheiros AA, Carneiro PRG, Azevedo SFD, Saldanha Filho OR, Saldanha CB. Lipoabdominoplasty. Plast Reconstr Surg. 2009 Sep;124(3):934-942. http://doi.org/10.1097/PRS.0b013e3181b037e3. PMID: 19730314.
Schleip R, Findley TW, Chaitow L, Huijing PA. Fascia: The Tensional Network of the Human Body. Elsevier; 2012.
Shestak KC, Rios L, Pollock TA, Aly A. Evidenced-based approach to abdominoplasty update. Aesthetic Surg J. 2019;39(6):628-642. http://doi.org/10.1093/asj/sjy215.
Skandalakis JE, Colborn GL, Weidman TA, Foster RS, Kingsnorth AN. Skandalakis’ surgical anatomy: the embryologic and anatomic basis of modern surgery. Athens: Paschalidis Medical Publications; 2004.
Standring S, ed. Gray’s Anatomy: The Anatomical Basis of Clinical Practice. 42nd ed. London: Elsevier; 2021.
Urquhart DM, Hodges PW, Allen TJ, Story IH. Abdominal muscle recruitment during a range of voluntary exercises. J Orthop Res. 2005;23(2):463-470. http://doi.org/10.1016/j.math.2004.08.011.
Vierstraete M, Pereira Rodriguez JA, Renard Y, Muysoms F. EIT Ambivium, Linea Semilunaris, and Fulcrum Abdominalis. J Abdom Wall Surg. 2023 Dec 22;2:12217. http://doi.org/10.3389/jaws.2023.12217. PMID: 38312427; PMCID: PMC10831682.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Authors

This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License.
