Anatomical Description of the Structures That Cause Tibialis Posterior Tendon Dysfunction

Tibialis posterior tendon (TPT) dysfunction is defined as a clinical pathology of the foot. It occurs as a sudden and progressive loss of strength due to TPT tendinopathy as a result of causes such as vascular and acute trauma or overuse. This retrospective study aimed to identify the anatomical aspects that can cause TPT dysfunction. The association between the control group and the patient group with stage 1 TPT dysfunction was assessed. The variables evaluated for this purpose were medial malleolus type, presence and type of accessory navicular tubercle, TPT width (TPTW), TPT thickness (TPTT), retromalleolar groove width (RGW), retromalleolar groove depth (RGD), retromalleolar groove angle (RGA), anterior posterior malleolar length (APML), posterior malleolar length (PML), and total posterior malleolar length (TPML). The RGA and TPML differences between the control and patient groups were determined to be statistically significant. In our opinion, identifying the risk factors for TPT dysfunction will aid in planning the therapeutic procedure.

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Publication Details

Journal
Cureus
Published
2025-03-07
DOI
https://doi.org/10.7759/cureus.80196
Primary Topic
Foot and Ankle Surgery
Type
article
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article

Anatomical Description of the Structures That Cause Tibialis Posterior Tendon Dysfunction

Halil Gökkuş, Tacettin Ayanoğlu, Emre Arikan, Abdullah Ray et al.
Cureus
Foot and Ankle Surgery
article

Anatomical Description of the Structures That Cause Tibialis Posterior Tendon Dysfunction

Halil Gökkuş, Tacettin Ayanoğlu, Emre Arikan, Abdullah Ray, Gamze Taskin Senol
article en

Abstract

Tibialis posterior tendon (TPT) dysfunction is defined as a clinical pathology of the foot. It occurs as a sudden and progressive loss of strength due to TPT tendinopathy as a result of causes such as vascular and acute trauma or overuse. This retrospective study aimed to identify the anatomical aspects that can cause TPT dysfunction. The association between the control group and the patient group with stage 1 TPT dysfunction was assessed. The variables evaluated for this purpose were medial malleolus type, presence and type of accessory navicular tubercle, TPT width (TPTW), TPT thickness (TPTT), retromalleolar groove width (RGW), retromalleolar groove depth (RGD), retromalleolar groove angle (RGA), anterior posterior malleolar length (APML), posterior malleolar length (PML), and total posterior malleolar length (TPML). The RGA and TPML differences between the control and patient groups were determined to be statistically significant. In our opinion, identifying the risk factors for TPT dysfunction will aid in planning the therapeutic procedure.

CureusVol. 17(3)
S.B.Ü. Bursa Yüksek İhtisas Eğitim ve Araştırma Hastanesi (TR), Bolu Abant İzzet Baysal University (TR)
Openalex Percentile: Top 95%
Foot and Ankle Surgery
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