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Morphometry and Frequency of the Pyramidalis Muscle in Adult Humans: A Pyramidalis Muscle’s Anatomical Analysis

Abstract

OBJECTIVES:

To verify the pyramidalis muscle’s frequency (bilaterality, unilaterality, or absence) and morphometry (length of the medial border and width of its origin/base) in a sample of the Brazilian population and the anthropometric influence.

METHODS:

Dissection of 30 cadavers, up to 24h post-mortem.

RESULTS:

The pyramidalis muscle was present bilaterally and unilaterally in 83.33% and 3.33% of the cadavers, respectively, and absent in 13.33%. The muscles on the right and left sides were symmetrical in length but not in width; the pyramidalis muscles of men were longer, while those of the women were wider. We also found that there was greater variation in the dimensions (length and width) of the men’s muscles. Finally, in this sample of the Brazilian population, the pyramidalis muscle’s unilaterality was more prevalent than in other populations, and its complete absence was less prevalent.

CONCLUSIONS:

There were no cases of muscle duplication in one or both sides, as described in some studies. Despite all of its morphometric variation, the pyramidalis muscle maintained its triangular shape with longitudinal fibers in every case. Furthermore, no statistically significant correlation was noted between the muscles’ dimensions and person’s age, height, weight, or gender.

Anatomical Variation; Corpse; Frequency Measurements; Pyramidalis Muscle


INTRODUCTION

The pyramidalis muscle is a small triangular muscle located in the inferior part of the anterior abdominal wall (11. Drake RL, Vogl W, Mitchell AWM. Grays anatomia clínica para estudantes. Rio de Janeiro: Elsevier; 2005.). It originates on the pubis’ anterior-superior surface, upon which it is inserted by the tendinous fibers that in the pubic symphysis region may merge with the suspensory ligament of the penis. The pyramidalis, then, extends upward, narrowing until it reaches its insertion place, the linea alba, midway between the umbilicus and the pubic symphysis. Regarding the stratigraphy, the belly of the pyramidalis muscle is located between the rectus abdominis and rectus sheath. Its morphometry is variable: the length of its medial border usually ranges from 2 to 13.8 cm; the width of its base measures an average of 1.98 cm (22. Van Landuyt K, Hamdi M, Blondeel P, Monstrey S. The pyramidalis muscle free flap. Br J Plast Surg. 2003;56(6):585-92. https://doi.org/10.1016/S0007-1226(03)00211-X.
https://doi.org/10.1016/S0007-1226(03)00...
). There is no relation between the muscle’s length and person’s height (33. Anson BJ, Beaton LE, Mcvay CB. The pyramidalis muscle. Anat Rec. 1938;72(4):405-11. https://doi.org/10.1002/ar.1090720403.
https://doi.org/10.1002/ar.1090720403...
). The pyramidalis muscle’s innervation always comes from the anterior cutaneous branches of the intercostal nerves, but there is considerable variation in the spinal nerves from which this innervation originates, involving Th12, L1, and L2 (44. Tokita K. Anatomical significance of the nerve to the pyramidalis muscle: a morphological study. Anat Sci Int . 2006;81(4):210-24. https://doi.org/10.1111/j.1447-073X.2006.00148.x.
https://doi.org/10.1111/j.1447-073X.2006...
). The pyramidalis muscle does not present pennation: its fibers extend vertically (55. Lovering RM, Anderson LD. Architecture and fiber type of the pyramidalis muscle. Anat Sci Int. 2008;83(4):294-7. https://doi.org/10.1111/j.1447-073X.2007.00226.x.
https://doi.org/10.1111/j.1447-073X.2007...
). It is not a constant muscle since it can be bilateral, unilateral, duplicated in one or both sides (presenting, respectively, three and four bellies), or even absent (66. Kaur H, Singla RK, Brar RS, Singla M. Study Of The Morphometry Of The Pyramidalis Muscle And Its Incidence In The Indian Population. IJAR. 2016;4(2):2207-11. https://doi.org/10.16965/ijar.2016.179.
https://doi.org/10.16965/ijar.2016.179...
). The absence of the pyramidalis muscle is rare, but it has been preponderant in some studies (77. Monkhouse WS, Khalique A. Variations in the composition of the human rectus sheath: a study of the anterior abdominal wall. J Anat. 1986;145:61-6.). Finally, the pyramidalis seems to be more constant in African and South East populations than in white ones (88. Beaton LE, Anson BJ. The pyramidalis muscle: Its occurrence and size in American whites and negroes. Am J Phys Anthropol. 1939;25(2):261-9. https://doi.org/10.1002/ajpa.1330250236.
https://doi.org/10.1002/ajpa.1330250236...
).

It is believed that the pyramidalis muscle’s function is to strengthen the abdominal wall (99. Dickson MJ. The pyramidalis muscle. J Obstet Gynaecol Res. 1999;19(3):300.) and tense the linea alba. However, its absence does not cause apparent loss of function (22. Van Landuyt K, Hamdi M, Blondeel P, Monstrey S. The pyramidalis muscle free flap. Br J Plast Surg. 2003;56(6):585-92. https://doi.org/10.1016/S0007-1226(03)00211-X.
https://doi.org/10.1016/S0007-1226(03)00...
). Hence, despite the aforementioned extensive description, the pyramidalis muscle’s function is still unclear. Because of that, some authors consider it a vestigial muscle, leftover from the marsupials’ and monotremes’ pouch (1010. Skret-Magierło J, Soja P, Drozdzowska A, Bogaczyk A, Szczerba P, Góra T, et al. Two techniques of pyramidalis muscle dissection in Pfannenstiel incision for cesarean section. Ginekol Pol. 2015;86(7):509-13. https://doi.org/10.17772/gp/57840.
https://doi.org/10.17772/gp/57840...
), evolving into an irregular apparition in more evolved primates, often observed in chimpanzees and gorillas but absent in orangutans (1111. Loth E. Anthropomorphologie des muscles. Bull Mem Soc Anthropol Paris. 1919;10(1):116-33. https://doi.org/10.3406/bmsap.1919.8873.
https://doi.org/10.3406/bmsap.1919.8873...
). There are also anthropological studies suggesting that the pyramidalis has evolved as part of the normal human anatomy, in which case it could be related to the species’ erect posture.

Although its function is not well known, the pyramidalis muscle can be useful in some surgical procedures since its superior insertion may serve as reference for abdominal incisions, for example, Pfannenstiel (1010. Skret-Magierło J, Soja P, Drozdzowska A, Bogaczyk A, Szczerba P, Góra T, et al. Two techniques of pyramidalis muscle dissection in Pfannenstiel incision for cesarean section. Ginekol Pol. 2015;86(7):509-13. https://doi.org/10.17772/gp/57840.
https://doi.org/10.17772/gp/57840...
). Furthermore, given that, as mentioned earlier, its absence does not seem to cause notable dysfunction (22. Van Landuyt K, Hamdi M, Blondeel P, Monstrey S. The pyramidalis muscle free flap. Br J Plast Surg. 2003;56(6):585-92. https://doi.org/10.1016/S0007-1226(03)00211-X.
https://doi.org/10.1016/S0007-1226(03)00...
), it can be used for grafts. Cryopreserved, the pyramidalis muscle can be used as a source of stem cells, which in turn may be used in the treatment of post‐prostatectomy stress urinary incontinence (1212. Sumino Y, Hirata Y, Hanada M, Akita Y, Sato F, Mimata H. Long-term cryopreservation of pyramidalis muscle specimens as a source of striated muscle stem cells for treatment of post-prostatectomy stress urinary incontinence. Prostate. 2011;71(11):1225-30. https://doi.org/10.1002/pros.21338.
https://doi.org/10.1002/pros.21338...
). However, there are still few publications describing the muscle. The most recently published articles have discussed its morphometry in Greece (1313. Natsis K, Piagkou M, Repousi E, Apostolidis S, Kotsiomitis E, Apostolou K, et al. Morphometric variability of pyramidalis muscle and its clinical significance. Surg Radiol Anat. 2016;38(3):285-92. https://doi.org/10.1007/s00276-015-1550-4.
https://doi.org/10.1007/s00276-015-1550-...
), India (1414. Das SS, Saluja S, Vasudeva N. Biometrics of Pyramidalis Muscle and its Clinical Importance. J Clin Diagn Res. 2017;11(2):AC05-AC07. https://doi.org/10.7860/JCDR/2017/24179.9276.
https://doi.org/10.7860/JCDR/2017/24179....
), and North India (66. Kaur H, Singla RK, Brar RS, Singla M. Study Of The Morphometry Of The Pyramidalis Muscle And Its Incidence In The Indian Population. IJAR. 2016;4(2):2207-11. https://doi.org/10.16965/ijar.2016.179.
https://doi.org/10.16965/ijar.2016.179...
).

Considering this literary scarceness, the inexistence of morphometric data for the muscle in Brazil, and the potential surgical applications of this data, collecting it becomes considerably relevant to verify if, indeed, the pyramidalis muscle could be a good incision reference in the Brazilian population and add to the literature regarding this muscle. Therefore, this study verifies the pyramidalis muscle’s frequency (including unilaterality, bilaterality, absence, and other anatomical variations) in a sample of the Brazilian population and describes its morphometry (length of its medial border and width of its base). The results allowed comparisons between genders and with studies of other populations.

MATERIALS AND METHODS

The study comprised 30 fresh cadavers (11 females and 19 males) of individuals from 32 to 98 years old, provided by the Serviço de Verificação de =bitos da Capital da Universidade de São Paulo (SVOC/USP). Regarding their ethnicity, 27 were white and three were nonwhite. Cadavers that had been submitted to previous incisions in the abdomen’s inferior region, which could alter the pyramidalis muscle’s morphology, were excluded from the study and not computed among the 30. Each approved cadaver was dissected during the medical residents’ dissection class; no procedures were performed outside of these class periods. The dissections were made through surgical incisions and performed according to the following procedures:

  • Median longitudinal incision in the suprapubic and infraumbilical regions and two symmetrical bilateral incisions (Pfannenstiel-like). These three incisions were made through the skin and subcutaneous cellular tissue, forming flaps that preserved the superficial layer of the rectus sheath. Afterward, two parallel longitudinal incisions were made in the lateral borders of the rectus abdominis, going through the anterior layer of the rectus sheath. Finally, one transverse incision was made connecting those longitudinal incisions so that the aponeurosis flap could be folded, exposing both the rectus abdominis and median line and allowing the study of the pyramidalis muscles (if present) (Figure 1).

  • Exposure of the pyramidalis muscles without releasing them from their original place, allowing for photographic recording for posterior measuring (length of the medial border and width of the origin/base) in image processing program ImageJ. During the dissection, there was no removal of the structures from the cadavers (Figure 2).

  • Suture by layers, according to the SVOC/USP routine, after the collection of the data, which was processed and then compared with data from other studies.

The study was approved by the “Plataforma Brasil” (Brazilian Platform), according to the Brazilian Ministry of Health, National Health Council, and National Commission for Research Ethics (CONEP-Comiss�o Nacional de �tica em Pesquisa) (number 2.178.874, 06/07/2017). Therefore, the present study has been performed with the Declaration of Helsinki’s ethical standards. The dissections were made in accordance with the SVOC/USP regulations, which respect the guidelines related to cadaver studies and dissecting. Informed consent, made by the SVOC/USP, was obtained post-mortem by the next of kin.

Figure 1
Dissection methods and measurements. Global vision of the inferior abdominal wall dissected according to this study’s methods, showing a pyramidalis muscle with average dimensions.
Figure 2
Dissection methods and measurements. Zoom window of the same dissection of Figure 1 (cadaver positioned with the head upward and feet downward), showing the right and left pyramidalis muscles (Rpm and Lpm, respectively), right and left rectus abdominis (Rra and Lra, respectively) underneath the pyramidalis, and part of the rectus sheath (Rs), cut and folded, exposing these muscles. The longer arrow indicates the pyramidalis muscle’s medial border, where the length was measured; the shorter arrow indicates its base, where the width was measured.

Regarding statistical analysis, the frequencies and percentages are shown for the categorical variables. For continuous variables, means and standard deviations were calculated. The Shapiro-Wilk W test was performed to test for normality of continuous data. The two-sample t-test and Wilcoxon/Kruskal-Wallis tests were used for comparison of parametric and nonparametric data, respectively. Linear regressions were performed to test association between continuous data. A two-tailed p-value of 0.05 was considered statistically significant. Given the exploratory nature of the study, no adjustment for multiple analyses was performed.

RESULTS

The pyramidalis muscle was present bilaterally in 25 out of the 30 cadavers (83.33%; Figures 3, 4, and 5) and unilaterally (left-sided, Figure 6) in 1 (3.33%) and absent in 4 (13.33%, Figures 7 and 8). Regarding its dimensions, the length of its medial border ranged from 3.12 to 10.67 cm on the left side and 3.50 to 10.76 cm on the right side, and the width of its base ranged from 0.91 to 2.93 cm on the left side and 1.10 to 2.64 cm on the right side (Table 1).

Figure 3
Pyramidalis muscle with average dimensions. Left side: length, 7.73 cm; width, 2.33 cm. Right side: length, 7.23 cm; width, 2.64 cm. Note: cadaver positioned with the head upward and feet downward. Right pyramidalis muscle, Rpm; left pyramidalis muscle, Lpm; right rectus abdominis, RRA; left rectus abdominis, Lra; linea alba, La; rectus sheath, Rs.
Figure 4
Short and wide pyramidalis muscle. Left side: length, 3.12 cm; width, 2.26 cm. Right side: length, 3.96 cm; width, 1.97 cm. Note: cadaver positioned with the head upward and feet downward. Right pyramidalis muscle, Rpm; left pyramidalis muscle, Lpm; right rectus abdominis, Rra; left rectus abdominis, Lra; linea alba, La; rectus sheath, Rs.
Figure 5
Long pyramidalis muscle. Left side: length, 10.20 cm; width, 1.93 cm. Right side: length, 9.95 cm; width, 1.49 cm. Note: cadaver positioned with the head upward and feet downward. Right pyramidalis muscle, Rpm; left pyramidalis muscle, Lpm; right rectus abdominis, Rra; left rectus abdominis, Lra; linea alba, La; rectus sheath, Rs.
Figure 6
Unilateral left pyramidalis muscle. The linea alba can be seen as a vertical line by the right side of the muscle. Left side: length, 5.70 cm; width, 2.49 cm. Left pyramidalis muscle, Lpm; right rectus abdominis, Rra; left rectus abdominis, Lra; linea alba, La; rectus sheath, Rs.
Figure 7
A case of absent pyramidalis muscle. Right rectus abdominis, Rra; left rectus abdominis, Lra; linea alba, La; rectus sheath, Rs.
Figure 8
Another case of absent pyramidalis muscle. Right rectus abdominis, Rra; left rectus abdominis, Lra; linea alba, La; rectus sheath, Rs.

Table 1
Incidence and dimensions of the pyramidalis muscle in the dissected cadavers. Description of the cases (separated in male, female, and total), with the incidence of the pyramidalis muscle (absence, unilaterality, and bilaterality) and maximum, minimum, and mean dimensions (length of the medial border and width of its base).

The mean length of the medial border on the left side was 6.64±2.04 cm, and that on the right side was 6.80±2.14 cm. The mean width of both the left and right pyramidalis muscles’ bases was 1.87±0.45 cm (Table 1).

Among the 11 women, we found 1 (9.09%) case of pyramidalis absence and no cases of unilaterality; the pyramidalis was present bilaterally in 10 (90.90%) of them. The length of the muscle’s medial border ranged from 3.12 to 9.50 cm on the left side and 3.96 to 9.00 cm on the right side; the width of the pyramidalis’ base ranged from 1.47 to 2.48 cm on the left side and 1.41 to 2.50 cm on the right side (Table 1).

For women, the mean length of the medial border of the left-sided pyramidalis was 6.38±1.93 cm, and that of the right-sided pyramidalis was 6.42±1.78 cm. The mean width of the left pyramidalis’ base was 1.94±0.30 cm, and that of the right pyramidalis’ base was 1.91±0.35 cm (Table 1).

Among the 19 men, the pyramidalis was absent in 3 (15.78%) of the cadavers and present unilaterally in 1 (5.26%) and bilaterally in 15 (78.94%). The length of the muscle’s medial border ranged from 3.50 to 10.67 cm on the left side and 3.50 to 10.76 cm on the right side; the width of the pyramidalis’ base ranged from 0.91 to 2.93 cm on the left side and 1.10 to 2.64 cm on the right side (Table 1).

For men, the mean length of the medial border of the left-sided pyramidalis was 6.80±2.16 cm, and that of the right-sided pyramidalis was 7.06±2.38 cm. The mean width of the left pyramidalis’ base was 1.83±0.53 cm, and that of the right pyramidalis’ base was 1.85±0.52 cm (Table 1).

The length and width measurements of the pyramidalis muscle, on both right and left sides, showed a normal distribution (Figures 9, 10, 11, and 12).

Figure 9
Analysis with the Shapiro–Wilk W test to show the normal distribution of the measurements (cm) of the pyramidalis muscles’ length at the medial border of the left side. W=0.975129; p-value=0.7578. Note: Ho=the data is from the normal distribution. Small p-values reject Ho.
Figure 10
Analysis with the Shapiro–Wilk W test to show the normal distribution of the measurements (cm) of the pyramidalis muscles’ length at the medial border of the right side. W=0.959641; p-value=0.4074. Note: Ho=the data is from the normal distribution. Small p-values reject Ho.
Figure 11
Analysis with the Shapiro–Wilk W test to show the normal distribution of the measurements (cm) of the pyramidalis muscles’ width at the base of the left side. W=0.964588; p-value=0.4898. Note: Ho=the data is from the normal distribution. Small p-values reject Ho.
Figure 12
Analysis with the Shapiro–Wilk W test to show the normal distribution of the measurements (cm) of the pyramidalis muscles’ width at the base of the right side. W=0.961571; p-value=0.4466. Note: Ho=the data is from the normal distribution. Small p-values reject Ho.

Through linear regression, we found that the pyramidalis muscle’s length was symmetrical (RSquare: 0.79; p<.0001) but the width at its base was not (RSquare: 0.10; p=0.1102). In other words, if the pyramidalis muscle is long or short on one side, the contralateral muscle tends to have the same length. However, conversely, whether the pyramidalis muscle is wide or narrow on one side, nothing can be predicted about the other side’s width (Figures 13 and 14). It must be emphasized that despite the statistical length symmetry, there were exceptional cases with considerable length asymmetry. For example, in one case, the medial border of the pyramidalis measured 6.47 cm on the left side and 10.76 cm on the right side (Figure 7).

Figure 13
Linear regression showing symmetry between the right and left sides of the pyramidalis muscle’s length (cm) at its medial border. Linear fit given as follows: left length (cm)=0.7878651+0.8658011*right length (cm); F ratio=90.6430; p-value<0.0001.
Figure 14
Linear regression showing asymmetry between the right and left sides of the pyramidalis muscle’s width (cm) at its base. Linear fit given as follows: left base (cm)=1.2503428+0.3213754*right base (cm). F ratio=2.7603; p-value=0.1102.

In the present study, we can also see that the range of the dimensions (length and width) of the pyramidalis muscle was bigger in men.

The mean length of the muscle was bigger in men than in women: the mean length on the left side was 6.80±2.16 cm in men and 6.38±1.93 cm in women, that on the right side was 7.06±2.38 cm in men and 6.42±1.78 cm in women, and the combined mean length (considering the right and left sides altogether) was 6.92±2.23 cm in men and 6.40±1.81 cm in women (Table 1).

Women had wider pyramidalis muscles: the mean width of the left pyramidalis’ base was 1.94±0.30 cm in women and 1.83±0.53 cm in men, that of the right pyramidalis’ base was 1.91±0.35 cm in women and 1.85±0.52 cm in men, and the combined mean width was 1.92±0.31 cm in women and 1.84±0.52 cm in men (Table 1).

Statistically, however, this difference regarding length and width in genders was not significant (p=0.5982 and p=0.6373, respectively) (Figures 15 and 16).

Figure 15
Correlation analysis between gender and the pyramidalis muscle’s mean length (cm) at its medial border. Females, F; males, M. Sample test, normal approximation: S=120; Z=-0.52697; p-value=0.5982.
Figure 16
Correlation analysis between gender and the pyramidalis muscle’s mean width (cm) at its base. Females, F; males, M. Sample test, normal approximation: S=139; Z=0.47150; p-value=0.6373.

Linear regression was also used to analyze correlation between mean length and height, mean width and height, mean length and weight, mean width and weight, mean length and age, and mean width and age. None of these analyses showed any correlation (Table 2).

Table 2
Analysis of the anthropometric influence (height, weight, and age) upon the pyramidalis muscles’ dimensions (mean length of the medial border and mean width of its base).

DISCUSSION

Comparing our data with studies on other populations, the Brazilian population had an average incidence of the pyramidalis muscle (Table 3). In Table 3, we can see a considerable range of incidences, from 72% in the Indian population up to 99% in the Chinese; in this study, the Brazilian population’s sample presented an incidence of 83.33%.

Table 3
Pyramidalis muscle’s incidence in different populations (based on Kaur et al. (66. Kaur H, Singla RK, Brar RS, Singla M. Study Of The Morphometry Of The Pyramidalis Muscle And Its Incidence In The Indian Population. IJAR. 2016;4(2):2207-11. https://doi.org/10.16965/ijar.2016.179.
https://doi.org/10.16965/ijar.2016.179...
)).

In this sample of the Brazilian population, the unilaterality of the pyramidalis was less prevalent than in other populations, and its absence was more prevalent. Both Brazilian men and women presented wider pyramidalis than other populations (Table 4).

Table 4
Pyramidalis muscle’s incidence of unilaterality, bilaterality, and absence and mean length and width per gender in different populations (based on Das et al. (1414. Das SS, Saluja S, Vasudeva N. Biometrics of Pyramidalis Muscle and its Clinical Importance. J Clin Diagn Res. 2017;11(2):AC05-AC07. https://doi.org/10.7860/JCDR/2017/24179.9276.
https://doi.org/10.7860/JCDR/2017/24179....
)).

Despite all statistical data and descriptions collated, the pyramidalis muscle’s great variability on morphometry and frequency (Figures 17 and 18), found in this and other studies, makes it hard to predict what will be found when incising a person’s abdomen.

Figure 17
Anatomical variations. Asymmetrical pyramidalis muscle. Left side: length, 6.47 cm; width, 1.53 cm. Right side: length, 10.76 cm; width, 1.24 cm.
Figure 18
Anatomical variations. Contralateral pyramidalis muscles widely separated from each other at the base. Left side: length, 5.34 cm; width, 1.76 cm. Right side: length, 5.34 cm; width, 1.68 cm.

In this study, we found that the pyramidalis muscle’s dimensions have no statistical correlations to age, gender, height, or weight (at least in this sample of the Brazilian population). Therefore, considering the clinical applications of our findings, it seems to be a poor reference for incisions because of its inconsistency.

In contrast, the pyramidalis proved to be a very prevalent muscle, present in more than 70% of the people in populations from other studies and 83.33% of the corpses from this study (Table 3). This increases its viability as a graft since, in spite of its high prevalence, its absence does not seem to cause any dysfunction. Therefore, supposedly, it can be removed and used for grafts with no collateral effects. Moreover, the mean length and width of the pyramidalis muscle in this study provide an estimate of the size of the lesions that can be treated with the pyramidalis muscles’ grafts in the Brazilian population.

Furthermore, clearly, the high prevalence of the muscle in the Brazilian population may enable its use as a source of stem cells although this possibility is still being studied.

Finally, we can say that the pyramidalis muscle is still a great mystery for science: the variability in its frequency and morphometry (in this and other studies) and indifference of its absence perpetuate the uncertainties about its functions. Its phylogenetic origin has not yet been truly elucidated, which makes it difficult to ascertain its future development: while some studies say that the pyramidalis muscle is a vestigial muscle (thus tending to disappear in the future), others argue that its presence is related to the erect posture (thus tending to become more prevalent).

CONCLUSION

In this sample of the Brazilian population, the pyramidalis muscle was present bilaterally in 83.33% of the cadavers and unilaterally in 3.33% and absent in 13.33%. There were no cases of duplication of the muscle in one or both sides, as described in some studies.

In some cases, there was great asymmetry in both length and width. However, statistically, it was found that there was length symmetry between the left and right pyramidalis muscles, but no width symmetry. Despite all of its morphometric variation, the pyramidalis muscle maintained its triangular shape with longitudinal fibers in every case.

REFERENCES

  • 1
    Drake RL, Vogl W, Mitchell AWM. Grays anatomia clínica para estudantes. Rio de Janeiro: Elsevier; 2005.
  • 2
    Van Landuyt K, Hamdi M, Blondeel P, Monstrey S. The pyramidalis muscle free flap. Br J Plast Surg. 2003;56(6):585-92. https://doi.org/10.1016/S0007-1226(03)00211-X
    » https://doi.org/10.1016/S0007-1226(03)00211-X
  • 3
    Anson BJ, Beaton LE, Mcvay CB. The pyramidalis muscle. Anat Rec. 1938;72(4):405-11. https://doi.org/10.1002/ar.1090720403
    » https://doi.org/10.1002/ar.1090720403
  • 4
    Tokita K. Anatomical significance of the nerve to the pyramidalis muscle: a morphological study. Anat Sci Int . 2006;81(4):210-24. https://doi.org/10.1111/j.1447-073X.2006.00148.x
    » https://doi.org/10.1111/j.1447-073X.2006.00148.x
  • 5
    Lovering RM, Anderson LD. Architecture and fiber type of the pyramidalis muscle. Anat Sci Int. 2008;83(4):294-7. https://doi.org/10.1111/j.1447-073X.2007.00226.x
    » https://doi.org/10.1111/j.1447-073X.2007.00226.x
  • 6
    Kaur H, Singla RK, Brar RS, Singla M. Study Of The Morphometry Of The Pyramidalis Muscle And Its Incidence In The Indian Population. IJAR. 2016;4(2):2207-11. https://doi.org/10.16965/ijar.2016.179
    » https://doi.org/10.16965/ijar.2016.179
  • 7
    Monkhouse WS, Khalique A. Variations in the composition of the human rectus sheath: a study of the anterior abdominal wall. J Anat. 1986;145:61-6.
  • 8
    Beaton LE, Anson BJ. The pyramidalis muscle: Its occurrence and size in American whites and negroes. Am J Phys Anthropol. 1939;25(2):261-9. https://doi.org/10.1002/ajpa.1330250236
    » https://doi.org/10.1002/ajpa.1330250236
  • 9
    Dickson MJ. The pyramidalis muscle. J Obstet Gynaecol Res. 1999;19(3):300.
  • 10
    Skret-Magierło J, Soja P, Drozdzowska A, Bogaczyk A, Szczerba P, Góra T, et al. Two techniques of pyramidalis muscle dissection in Pfannenstiel incision for cesarean section. Ginekol Pol. 2015;86(7):509-13. https://doi.org/10.17772/gp/57840
    » https://doi.org/10.17772/gp/57840
  • 11
    Loth E. Anthropomorphologie des muscles. Bull Mem Soc Anthropol Paris. 1919;10(1):116-33. https://doi.org/10.3406/bmsap.1919.8873
    » https://doi.org/10.3406/bmsap.1919.8873
  • 12
    Sumino Y, Hirata Y, Hanada M, Akita Y, Sato F, Mimata H. Long-term cryopreservation of pyramidalis muscle specimens as a source of striated muscle stem cells for treatment of post-prostatectomy stress urinary incontinence. Prostate. 2011;71(11):1225-30. https://doi.org/10.1002/pros.21338
    » https://doi.org/10.1002/pros.21338
  • 13
    Natsis K, Piagkou M, Repousi E, Apostolidis S, Kotsiomitis E, Apostolou K, et al. Morphometric variability of pyramidalis muscle and its clinical significance. Surg Radiol Anat. 2016;38(3):285-92. https://doi.org/10.1007/s00276-015-1550-4
    » https://doi.org/10.1007/s00276-015-1550-4
  • 14
    Das SS, Saluja S, Vasudeva N. Biometrics of Pyramidalis Muscle and its Clinical Importance. J Clin Diagn Res. 2017;11(2):AC05-AC07. https://doi.org/10.7860/JCDR/2017/24179.9276
    » https://doi.org/10.7860/JCDR/2017/24179.9276
  • 15
    Vallois HV. Valeur et signification du muscle pyramidal de l’abdomen. Arch Anat Histol Embryol. 1926;5:497-525.
  • 16
    Le Double AF. Traité des Variations du Système Musculaire de l’Homme et de Leur Signification au Point de vue de l’Anthropologie, Zoologique. Vol 2. 1897. Publisher: Scheicher Frères. Paris.
  • 17
    Mori M. Statistics on the musculature of the Japanese. Okajimas Folia Anat Jpn. 1964;40:195-300. https://doi.org/10.2535/ofaj1936.40.3_195
    » https://doi.org/10.2535/ofaj1936.40.3_195
  • 18
    Wagenseil F. Muskelbefunde bei Chinesen. Verh Ges Phys Anthrop. Anthropol Anz, Stuttgart. 1927;2:42-50.
  • 19
    Didia B, Oghenemavwe E, Christian I. Variation and incidence of agenesis of the pyramidalis muscles in Nigerian males. J Exp Clin Anat. 2009;8(1). https://doi.org/10.4314/jeca.v8i1.48031
    » https://doi.org/10.4314/jeca.v8i1.48031

Publication Dates

  • Publication in this collection
    10 July 2020
  • Date of issue
    2020

History

  • Received
    4 Jan 2020
  • Accepted
    19 Feb 2020
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