Abstract
Introduction
Knowledge of the vascular anatomy is critical to performing safe gluteal surgery. To date, only the course of the main blood vessels within the muscles has been outlined. These findings are based on MRI and CTA images that do not conform to a topographically standardized and normalized probability distribution.
Objectives
The aim of this study was to develop a three-dimensional mapping of the gluteal zones of high vascular density in relation to anatomical landmarks.
Materials and Methods
This single-center retrospective cohort analysis comprised all consecutive patients who underwent cone-beam computed tomography (CBCT) scans between January 2016 and October 2021. The location of blood vessels in the gluteal region was allometrically normalized in relation to anatomical landmarks. Moreover, the caliber and area of the blood vessels were assessed.
Results
CBCT scans of 32 patients with an average age of 64 ± 12 years (range 34–87 years) were included. Fifty-three percent were female. The median [IQR] caliber of the intramuscular gluteal vessels was 1.47 [1.15–1.88] mm, significantly greater than that of the subcutaneous vessels 1.09 [0.72–1.44] mm (p < 0.001). Vascular density was higher intramuscularly, as 4.5% of the area of the muscle was occupied by blood vessels, as opposed to 0.3% in the adipose tissue.
Conclusion
The analysis of the CBCT scans showed a higher vascular density and larger vessels intramuscularly. We, therefore, recommend the injection of autologous fat merely to the subcutaneous plane.
Level of Evidence II
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Most Important Information
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Our study pioneers the measurement of the diameter of all gluteal vessels and presents a three-dimensional allometrically standardized representation of the topographical gluteal anatomy.
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Intramuscular vessels had a significantly larger caliber than subcutaneous vessels (p < 0.001).
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The largest arteries were located intramuscularly, either at the level of or just above the greater sciatic foramen or at the uppermost level of the pubic symphysis.
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Our results provide validation for the recommendations of the British Association of Aesthetic Plastic Surgeons (BAAPS), which advise limiting injections to the subcutaneous layer.
Introduction
Knowledge of microvascular anatomy is crucial for conducting safe reconstructive surgery [1, 2]. The occurrence of life-threatening fat embolisms is still a matter of great concern [3, 4], despite efforts to deepen the knowledge of gluteal microvascular anatomy.
Two prior in vivo studies, using 40 CTA [2] and 8 MRI venographies [5], provided valuable information on the trajectory and diameter of the superior and inferior gluteal arteries (SGA and IGA), presenting a two-dimensional mapping of gluteal vessels. However, there remains a notable knowledge gap regarding the caliber and distribution of all gluteal vessels in an allometrically standardized three-dimensional representation. Moreover, their methodological approach is less robust than the one we propose, as these studies do not provide a comprehensive portrayal of the probabilities associated with various vascular courses. We also pioneer at measuring the diameter and recording the location of subcutaneous gluteal vessels.
In order to reduce the incidence of fatal and nonfatal pulmonary fat embolisms, the American Society of Plastic Surgeons (ASPS) [6, 7] and several authors recommend limiting the fat transfer to the subcutaneous plane [6, 8, 9], where fewer and smaller vessels are located [6, 8, 9]. However, a systematic review found it did not reduce the complication rate significantly in comparison to the injection into the intramuscular and subcutaneous planes (p = 0.059) [10].
This study aimed to evaluate gluteal vessel location and create a standardized three-dimensional, easily reproducible system for representing areas of greater vascular density. This system was designed in relation to palpable bone landmarks in order to guide plastic surgeons during the procedure.
Material and Methods
Study Sample
This retrospective study was approved by the Ethics Committee of the University of Tübingen (Project No. 276/2020BO2). Informed consent was waived.
We evaluated all consecutive pelvic CBCT examinations from January 2016 to October 2021, excluding patients with peripheral artery disease, scans with significant artifacts, unclear vascular delineation, or missing anatomical landmarks (specifically, the posterior superior iliac spine (PSIS)). We assessed patient age, gender, anthropometrics (height, weight, and BMI), CBCT indication, and secondary diagnoses for patients aged 18 or older.
Image Acquisition of Cone-Beam CT scans
A robotic digital subtraction angiography system (Artis Zeego Q, VE 40 A, Siemens, Forchheim, Germany) was used for diagnostic angiography and endovascular procedures. A local anesthetic was applied and a 19-G needle was inserted into the common femoral artery, followed by a 4-Fr sheath (Terumo, Belgium). Next, 30 mL of 80% diluted contrast medium (Ultravist 370, Bayer Schering, Germany) was injected into a 4-Fr pigtail catheter in the infrarenal area for aortography (2 frames/s) at 15 mL/s rate.
Then, pelvis CBCT images were acquired with patients holding their breath and arms above their heads to reduce streak artifacts. A 50% diluted contrast medium (Ultravist 300) was administered at 8 mL/s for 10s, with a 6-second rotation time and a 60°/s detector speed. The settings were 90 kVp, 48 cm field of view, and a 512 × 512 voxel matrix.
CBCT data were transferred to a workstation (syngo XWP, Siemens Healthineers); afterward, CT-like axial images with a 0.5 mm voxel size were automatically reconstructed. Planes were predefined to have a 10mm thickness.
Anatomic Boundaries and Image Assessment
Lumbar spine anatomy is a reliable predictor of the human stature [11, 12], particularly the anterior height of the fifth lumbar vertebra [12]. To standardize the gluteal evaluation, we defined the region of interest’s height as the distance between PSIS and the upper pubic symphysis border, allocating four equidistant horizontal planes (z1, z2, z3, z4) (Fig. 1).
Our coordinate system employed a vertical axis (z) crossing the anterocaudal corner of the fifth vertebral body, an anteroposterior axis (y) intersecting the midpoint between PSIS (dividing planes into left and right), and a transverse axis (x) forming a 90° angle with the other axes and partitioning planes into anterior and posterior sections.
Standardization of the coordinates was based on predefined distances (Fig. 1):
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Xs denotes the distance between PSIS and the midline, accounting for pelvic dimorphism, as females have wider pelvises [13] and greater sacrum breadths than males (p = 0.008) [14].
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Ys signifies the distance between the midline point between PSIS and the lower anterior corner of the fifth vertebral body, as lumbar vertebral anterior-posterior diameters are reliable predictors of stature [11, 15] and exhibit no sexual dimorphism (p > 0.05) [16].
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Zs represents the anterior height of the fifth lumbar vertebra and was employed to estimate pelvic height when the symphysis was not depicted in CBCT scans, due to its correlation with human stature [12].
Negative x values indicate the left patient side and positive x values the right side. Additionally, the maximal thickness of muscle and fat layers were recorded in each plane.
ImageJ, a software by the National Institutes of Health and the Laboratory for Optical and Computational Instrumentation (University of Wisconsin), was used to measure vessel calibers.
Statistical Analysis
We used mean and standard deviation for normally distributed quantitative data and median with interquartile range for asymmetric data. SPSS version 28 (SPSS Inc, Chicago, Illinois, USA) was used to conduct the statistical tests. We assumed that the depth of the vessels (represented as distance to the centre of the coordinate axes) is linear based on preliminary descriptive results. To account for repeated measures within individuals and clusters, mixed models were used to assess the vascular diameter (dependent variable) and right/left side, planes, locations (intramuscular versus subcutaneous), depth, and gender (Table 4). Random intercept models with fixed effects were estimated using the restricted maximum likelihood (REML) with scaled identity error covariance. Because of the skewed distribution of the vascular diameters, these measurements were log transformed. Significance was set at P ≤ 0.05.
Results
Demographic Data
Between January 2016 and October 2021, 46 patients underwent a CBCT examination of the pelvis performed at a single institution. Thirty-two of these patients met the inclusion criteria (Fig. 2). Approximately half of the patients was female and 91% of patients were 50 years of age or older (Table 1). Five patients (16%) were obese, and seven (22%) were overweight. The weight of two patients was unknown.
Anatomical Data
Evaluation of the maximal thickness of the gluteal musculature and subcutaneous fatty tissue showed a moderate and weak positive and significant correlation with BMI, but neither with age nor with gender (Table 2).
The largest arteries were located intramuscularly at the level of or directly above the greater sciatic foramen (plane z3) and at the upper level of the pubic symphysis and femoral head (plane z1) and subcutaneously in the most caudal plane (plane z1) (Table 3, Fig. 1). The median (IQR) of all gluteal vessels was 1.43 [1.10–1.84] mm (Table 3).
This analysis showed a positive and significant correlation between the area of muscle and adipose tissue occupied by vessels (p < 0.001). The vascular density is higher intramuscularly, as 4.5% [3.0–6.4%] of the area of the muscle is occupied by blood vessels (p < 0.001), as opposed to 0.3% [0.0–1.1%] in the adipose tissue (p < 0.001).
Mixed model analysis of fixed effects revealed that plane, tissue type, and patient side are significant predictors of the vascular caliber (all p < 0.001), while gender was not significant (p = 0.054). Likewise, depth of the vessel was a significant predictor of the caliber (p < 0.001). As represented in Tables 3 and 4, planes 1 and 3 had the largest vessels, while plane 2 is not significantly different from the reference group (plane 4). Intramuscular vessels had a significantly larger diameter than subcutaneous vessels (difference in median = 0.38 mm, p < 0.001). The gender-based disparity in vessel caliber was found to be statistically insignificant, with females exhibiting marginally thinner vessels compared to males (p = 0.054) (Table 4). Interestingly, the right buttock displayed larger vessels (p < 0.001) and a greater muscular area (p = 0.011) than the left side. Both sides exhibited outliers and a skewed distribution in vascular caliber.
Discussion
The present study pioneers the measurement of the diameter of all gluteal vessels and presents a three-dimensional allometrically standardized representation of the topographical anatomy of the gluteal vessels in relation to bone landmarks. This map is tailored for applications in plastic surgery.
Our findings reveal a scarcity of subcutaneous blood vessels (Fig. 2) and smaller vessel sizes (Table 3). While a systematic review indicated no significant decrease in complication rates with subcutaneous-only injections compared to intramuscular and subcutaneous (p = 0.059) [10], fat embolism was reported in only one article [10]. To date, only survey results have been published [17], which carry an inherent bias.
Several studies explored the gluteal anatomy to improve the safety of gluteal augmentation. A “danger triangle,” amid PSIS, greater trochanter, and ischial tuberosity, housing major gluteal vessels and the sciatic nerve has been described in the literature [8]. However, some assert that the subcutaneous plane is the only safe area for fat grafting [7, 18]. Our results demonstrate an even distribution of the intramuscular vessels and scarcer subcutaneous vessels. Lateral subcutaneous vessels were not visible due to the limited CBCT scan field of view (Fig. 3).
Accidental injection of fat into or near injured veins is a well-documented mechanism of fat embolism [8, 19,20,21]. CBCT scans depicted gluteal arterial anatomy. However, vessels typically travel together [22] and, in normovolemic patients, the diameter of the femoral vein and artery are similar [23]. Level 5 evidence advises intraoperative ultrasound for subcutaneous fat injection to reduce embolism risk [7, 19, 24], as it lacks large veins. Vein size may predict pulmonary fat embolism risk more than injected fat amount [25, 26]. Further research is required to correlate vein cannulation likelihood with higher intramuscular vascular density.
The gluteal region displays a tissue-dependent vascularity. Unlike gluteal augmentation, breast lipofilling is overwhelmingly done in the subcutaneous plane. A similar vascular distribution in the breast would explain why breast lipofilling lacks analogous risks and should discourage from lipofilling into the pectoralis muscle.
Only two other in vivo studies investigated the gluteal vascular anatomy. Vigato et al. [2] reported mean calibers of the largest SGA and IGA perforators (1.3 ± 0.4 mm and 1.2 ± 0.4 mm, correspondingly), aligning with our findings (gluteal vessels' median caliber: 1.43 [1.10–1.84]). Vigato et al. [2] plotted vessel data using the lumbosacral joint to greater trochanter distance as reference, without standardizing the height of the pelvis according to body size or the depth of the vessels in relation to the skin surface. Body mass index has a positive and statistically significant correlation with muscle and subcutaneous fat layer thickness (Table 2). Lower BMI patients might face heightened risks from unintended deep injections if the stated correlation is not taken into consideration.
Our results present medians and interquartile ranges due to skewed data, which may explain why the average diameter of the larger perforators is similar to the median caliber of all gluteal vessels. While the mentioned study investigated the location and number of other gluteal vessels (perforators of lumbar, lateral circumflex, internal pudendal, and profunda femoris arteries), their diameter within the intramuscular and subcutaneous course was not assessed. In our study, both tissue type and vascular depth proved to be reliable predictors of vascular diameter. However, we argue that tissue type supersedes the influence of depth, given that depth is contingent upon tissue type, while the inverse relationship does not hold true. Moreover, our adjusted model revealed that the disparities in vascular diameters across both tissue types were more pronounced than those associated with varying depths.
Turin et al. [5] reported SGV tributary diameters ranging from 1.5 to 2.5 mm on MRI venography, with subsequent branching into smaller veins (< 2 mm) within the muscle. In contrast, our research revealed intramuscular perforators often exceeding 2 mm in diameter. Notably, the aforementioned study did not specify the measurement positions, although vein diameter can decrease by up to 27% in the jackknife and 15% in lateral decubitus positions [5]. Adipose tissue’s incompressibility [27] implies that position changes are unlikely to affect subcutaneous vessel locations.
Both studies lack depth information relative to skin, limiting their practical value for surgeons. Areas with higher vascular density were the superior lateral region of the gluteus maximus muscle (SGA perforators) and the horizontal level of the greater trochanter and ischiadic tuberosity (IGA perforators) [2]. Our findings furnish empirical support for the guidelines of the British Association of Aesthetic Plastic Surgeons (BAAPS), which recommend limiting injections to the subcutaneous plane.
Females, older individuals, and those with smaller stature exhibit lower skeletal muscle mass [28]. Conversely, overweight elderly individuals exhibit resistance to muscle anabolic processes [29]. We found a positive correlation between muscle thickness and BMI (r = 0.563, p < 0.001) (Table 2). However, BMI's correlation with fat volume has limited significance, as it does not consider body composition, age, and gender. The intramuscular vessel area increases with gluteal muscle thickness (rho = 0.537, p < 0.001).
The calibers of lower limb arteries, with the exception of the arteria dorsalis pedis, did not exhibit any gender-specific differences [30]. Our study extends this finding to include gluteal arteries. Furthermore, the observed 5.4% difference in mean vascular diameter between sides aligns closely with the range of normal anatomical variations reported, which falls between 6 and 8% [30]. This variation may be attributed to the typical anatomical dominance of one limb side.
To our knowledge, this is the first plastic surgery study based on allometric normalization. We refrained from identifying the source artery, as its relevance to surgeons is negligible. CBCT demonstrated superior image quality than 3D-CTA [31, 32], high spatial resolution [32,33,34,35], strong blood vessel contrast [32], and lower radiation than MDCT [33]. CBCT is used for patients with inconclusive results on pre-interventional CTA and selective angiography to identify vessels for targeted embolization [32, 36]. The vessel-tracking software has a 92% sensitivity in detecting prostatic arteries [36, 37], surpassing selective angiography and/or CTA in diagnostic confidence [32].
The retention of fat graft volume is influenced by physiological, anatomical, technical, and patient-specific factors. Regarding physiological aspects, graft survival depends on the diffusion of nutrients and oxygen [38]. Consequently, it is reasonable to infer that the success of a fat graft is higher in well-vascularized tissues, such as muscle, in comparison to adipose tissue. However, there is currently no supporting evidence suggesting that the success of a fat graft is equivalent to that of a skin graft, indicating that grafting into muscle is not necessarily superior to grafting into adipose tissue. A study on subcutaneous fat transfer outcomes demonstrated a 12-month postoperative absorption rate of 18.2%, aligning with previous studies on intramuscular fat injection, which showed absorption rates ranging between 20 and 36% [4]. Regarding anatomical factors, fat graft requires a uniform distribution to prevent the formation of fat cysts. Therefore, a larger recipient volume allows for the transplantation of a greater amount of fat graft. Larger volume gains, when fat is injected into the muscle may simply be attributed to the fact that the recipient volume of muscle and subcutaneous fat is greater that subcutaneous fat alone. Furthermore, the graft survival and the subsequent volume gain are notably influenced by factors such as patients' age [39] and smoking habits [40]. Finally, the tumescent solution [41], the time between harvesting and infiltration [42], the isolation of fat cells and stem cells from the lipoaspirate [43] as well as the negative pressure during aspiration influence graft survival and volume gain [44]. Based on current evidence, the risks of fat graft to the gluteus muscle outweigh the benefits. Since the recipient’s volume increases after every successful fat graft, the achievable volume gain increases from one procedure to another. Safe large volume augmentations can be achieved by optimizing every factor that influences graft survival, with the option to repeat the procedure at the patient's discretion.
Study limitations include an older study population than that of gluteal augmentation [4, 10, 45, 46], due to ethical concerns that apply to all vascular research studies. Although the male percentage was higher than in the reported 1.8% male patients [10], gender-based vascular caliber differences were statistically insignificant (p = 0.054).
The CBCT scans were performed in supine position. Even though the IGV and SGV calibers diminish in the gluteal fat grafting positions (“jackknife” [8], prone [4, 10], lateral decubitus [47]) when compared to the prone position [5]. We reason that arteries are unsusceptible to the diameter variation that occurs with different positions, because they are not influenced by blood pooling. To date, there has been no evidence of the existence of non-concomitant veins of the gluteal region.
Conclusion
This article explores the gluteal arterial anatomy in relation to anatomical landmarks. Our findings show larger, more numerous intramuscular vessels than subcutaneous ones. We, therefore, support the recommendation of injecting autologous fat merely to the subcutaneous plane. Additionally, vessel-occupied tissue area correlates positively with the buttock area. Our results help improve the knowledge of gluteal microvascular anatomy, reducing fat embolism rates.
References
Woo SJ, Koo HT, Park SO, Suami H, Chang H (2021) Evolution of anatomical studies on the arterial, venous, and lymphatic system in plastic surgery. Archiv Plast Surg 49(6):773–781. https://doi.org/10.1055/s-0042-1758636
Vigato E, De Antoni E, Tiengo C, Porzionato A, Tortorella C, Governa M et al (2018) Radiological anatomy of the perforators of the gluteal region: the “radiosome” based anatomy. Microsurgery 38(1):76–84. https://doi.org/10.1002/micr.30214
Chopan M, White JA, Sayadi LR, Buchanan PJ, Katz AJ (2019) Autogenous fat grafting to the breast and gluteal regions: safety profile including risks and complications. Plast Reconstr Surg 143(6):1625–1632. https://doi.org/10.1097/PRS.0000000000005617
Cansancao AL, Condé-Green A, David JA, Vidigal RA (2019) Subcutaneous-only gluteal fat grafting: a prospective study of the long-term results with ultrasound analysis. Plast Reconstr Surg 143(2):447–451. https://doi.org/10.1097/PRS.0000000000005203
Turin SY, Fracol M, Keller E, Markl M, Collins J, Krochmal D et al (2020) Gluteal vein anatomy: location, caliber, impact of patient positioning, and implications for fat grafting. Aesthet Surg J 40(6):642–649. https://doi.org/10.1093/asj/sjz260
Ordenana C, Dallapozza E, Said S, Zins JE (2020) Objectifying the risk of vascular complications in gluteal augmentation with fat grafting: a latex casted cadaveric study. Aesthet Surg J 40(4):402–409. https://doi.org/10.1093/asj/sjz237
Tillo O, Nassab R, Pacifico MD (2023) The British Association of Aesthetic Plastic Surgeons (BAAPS) gluteal fat grafting safety review and recommendations. Aesthet Surg J 43(6):675–682. https://doi.org/10.1093/asj/sjac316
Villanueva NL, Del Vecchio DA, Afrooz PN, Carboy JA, Rohrich RJ (2018) Staying safe during gluteal fat transplantation. Plast Reconstr Surg 141(1):79–86. https://doi.org/10.1097/PRS.0000000000003934
Wall S, Delvecchio D, Teitelbaum S, Villanueva NL, Dayan E, Durand P et al (2019) Subcutaneous migration: a dynamic anatomical study of gluteal fat grafting. Plast Reconstr Surg 143(5):1343–1351. https://doi.org/10.1097/PRS.0000000000005521
Condé-Green A, Kotamarti V, Nini KT, Wey PD, Ahuja NK, Granick MS, et al. (2016) Fat grafting for gluteal augmentation: a systematic review of the literature and meta-analysis. Plast Reconstr Surg 138(3):437e–446e. https://doi.org/10.1097/PRS.0000000000002435
Klein A, Nagel K, Gührs J, Poodendaen C, Püschel K, Morlock MM et al (2015) On the relationship between stature and anthropometric measurements of lumbar vertebrae. Sci Justice 55(6):383–387. https://doi.org/10.1016/j.scijus.2015.05.004
Zhang K, Chang YF, Fan F, Deng ZH (2015) Estimation of stature from radiologic anthropometry of the lumbar vertebral dimensions in Chinese. Leg Med 17(6):483–488. https://doi.org/10.1016/j.legalmed.2015.10.004
Fischer B, Mitteroecker P (2017) Allometry and sexual dimorphism in the human pelvis. Anat Rec 300(4):698–705. https://doi.org/10.1002/ar.23549
Saluja S, Tigga SR, Das SS, Thakur A (2023) Determination of sexual dimorphism of the human sacrum based on receiver operating characteristic curve analysis of morphometric parameters. Cureus 15(5):e38629. https://doi.org/10.7759/cureus.38629
Waduud MA, Sucharitkul PPJ, Drozd M, Gupta A, Hammond C, Ashbridge Scott DJ (2019) Validation of two-dimensional vertebral body parameters in estimating patient height in elderly patients. Br J Radiol 92(1104):20190342. https://doi.org/10.1259/bjr.20190342
Gocmen-Mas N, Karabekir H, Ertekin T, Edizer M, Canan Y, Duyar I (2010) Evaluation of lumbar vertebral body and disc: a stereological morphometric study. Int J Morphol 28(3):841–847
Mofid MM, Teitelbaum S, Suissa D, Ramirez-Montañana A, Astarita DC, Mendieta C et al (2017) Report on mortality from gluteal fat grafting: recommendations from the ASERF task force. Aesthet Surg J 37(7):796–806. https://doi.org/10.1093/asj/sjx004
Del Vecchio DA, Rohrich RJ (2020) A changing paradigm: the Brazilian butt lift is neither Brazilian nor a lift-why it needs to be called safe subcutaneous buttock augmentation. Plast Reconstr Surg 145(1):281–283. https://doi.org/10.1097/PRS.0000000000006369
Del Vecchio D, Kenkel JM (2022) Practice advisory on gluteal fat grafting. Aesthet Surg J 42(9):1019–1029. https://doi.org/10.1093/asj/sjac082
Alvarez-Alvarez FA, González-Gutiérrez HO, Ploneda-Valencia CF (2019) Safe gluteal fat graft avoiding a vascular or nervous injury: an anatomical study in cadavers. Aesthet Surg J 39(2):174–184. https://doi.org/10.1093/asj/sjy237
Chia CT, Theodorou SJ, Dayan E, Tabbal G, Del Vecchio D (2018) “Brazilian butt lift” under local anesthesia: a novel technique addressing safety concerns. Plast Reconstr Surg 142(6):1468–1475. https://doi.org/10.1097/PRS.0000000000005067
Meng BL, Pang A, Li M (2013) Principle of relative positioning of structures in the human body. Neural Regen Res 8(9):853–856. https://doi.org/10.3969/j.issn.1673-5374.2013.09.010
Ma Z, Gai J, Sun Y, Bai Y, Cai H, Wu L et al (2021) Measuring the ratio of femoral vein diameter to femoral artery diameter by ultrasound to estimate volume status. BMC Cardiovasc Disord 21(1):506. https://doi.org/10.1186/s12872-021-02309-7
Cansancao AL, Condé-Green A, Vidigal RA, Rodriguez RL, D’Amico RA (2018) Real-time ultrasound-assisted gluteal fat grafting. Plast Reconstr Surg 142(2):372–376. https://doi.org/10.1097/PRS.0000000000004602
Astarita DC, Scheinin LA, Sathyavagiswaran L (2015) Fat transfer and fatal macroembolization. J Forensic Sci 60(2):509–510. https://doi.org/10.1111/1556-4029.12549
Pane TA (2019) Experience with high-volume buttock fat transfer: a report of 137 cases. Aesthet Surg J 39(5):526–532. https://doi.org/10.1093/asj/sjy191
Comley K, Fleck NA (2010) A micromechanical model for the Young’s modulus of adipose tissue. Int J Solids Struct 47(21):2982–2990. https://doi.org/10.1016/j.ijsolstr.2010.07.001
Janssen I, Heymsfield SB, Wang Z, Ross R (2000) Skeletal muscle mass and distribution in 468 men and women aged 18–88 yr. J Appl Physiol (Bethesda, Md. : 1985) 89(1):81–88. https://doi.org/10.1152/jappl.2000.89.1.81
Morgan PT, Smeuninx B, Breen L (2020) Exploring the impact of obesity on skeletal muscle function in older age. Front Nutr 7:569904. https://doi.org/10.3389/fnut.2020.569904
Kubarewicz KJ, Ustymowicz A, Czyzewska D, Kaminski MJ, Sledziewski R, Krejza J (2020) Normal tolerance limits for side-to-side differences in diameters of major lower limbs arteries of 228 healthy subjects. Adv Med Sci 65(1):30–38. https://doi.org/10.1016/j.advms.2019.10.001
Hashimoto Y, Matsushige T, Ogawa T et al (2020) Impact of cone-beam computed tomography angiography on visualization of Sylvian veins. World Neurosurg 143:e206–e214. https://doi.org/10.1016/j.wneu.2020.07.118
Grosse U, Syha R, Ketelsen D, Hoffmann R, Partovi S, Mehra T et al (2018) Cone beam computed tomography improves the detection of injured vessels and involved vascular territories in patients with bleeding of uncertain origin. Br J Radiol 91(1088):20170562. https://doi.org/10.1259/bjr.20170562
Posadzy M, Desimpel J, Vanhoenacker F (2018) Cone beam CT of the musculoskeletal system: clinical applications. Insights Imaging 9(1):35–45. https://doi.org/10.1007/s13244-017-0582-1
Floridi C, Radaelli A, Abi-Jaoudeh N, Grass M, De Lin M, Chiaradia M et al (2014) C-arm cone-beam computed tomography in interventional oncology: technical aspects and clinical applications. Radiologia Medica 119(7):521–532. https://doi.org/10.1007/s11547-014-0429-5
Tacher V, Radaelli A, Lin M, Geschwind JF (2015) How I do it: cone-beam CT during transarterial chemoembolization for liver cancer. Radiology 274(2):320–334. https://doi.org/10.1148/radiol.14131925
Cadour F, Tradi F, Habert P, Scemama U, Vidal V, Jacquier A et al (2020) Prostatic artery embolization using three-dimensional cone-beam computed tomography. Diagn Interv Imaging 101(11):721–725. https://doi.org/10.1016/j.diii.2020.05.002
Chiaradia M, Radaelli A, Campeggi A, Bouanane M, De La Taille A, Kobeiter H (2015) Automatic three-dimensional detection of prostatic arteries using cone-beam CT during prostatic arterial embolization. J Vasc Interv Radiol 26(3):413–417. https://doi.org/10.1016/j.jvir.2014.11.009
Khouri RK, Khouri RER, Lujan-Hernandez JR, Khouri KR, Lancerotto L, Orgill DP (2014) Diffusion and perfusion: the keys to fat grafting. Plast Reconstr Surg Glob Open 2(9):e220. https://doi.org/10.1097/GOX.0000000000000183
Chung NN, Ransom RC, Blackshear CP, Irizarry DM, Yen D, Momeni A, Lee GK et al (2019) Fat grafting into younger recipients improves volume retention in an animal model. Plast Reconstr Surg 143(4):1067–1075. https://doi.org/10.1097/PRS.0000000000005483
Özalp B, Çakmakoğlu Ç (2017) The effect of smoking on facial fat grafting surgery. J Craniofac Surg 28(2):449–453. https://doi.org/10.1097/SCS.0000000000003356
Sirinoglu H, Yesiloglu N, Kaya Ö, Ercan F, Filinte G (2017) Effects of tumescent solution on fat survival. Facial Plast Surg 33(3):339–346. https://doi.org/10.1055/s-0037-1602164
Lee HJ, Kim EK (2014) Effects of long-term cryopreservation on fat grafts: an experimental study. Archiv Aesthet Plast Surg 20(2):70–74. https://doi.org/10.14730/aaps.2014.20.2.70
Shukla L, Yuan Y, Shayan R, Greening DW, Karnezis T (2020) Fat therapeutics: the clinical capacity of adipose-derived stem cells and exosomes for human disease and tissue regeneration. Front Pharmacol 11:158. https://doi.org/10.3389/fphar.2020.00158
Travnickova M, Pajorova J, Zarubova J, Krocilova N, Molitor M, Bacakova L (2020) The influence of negative pressure and of the harvesting site on the characteristics of human adipose tissue-derived stromal cells from lipoaspirates. Stem Cells Int 2020:1016231. https://doi.org/10.1155/2020/1016231
Kalaaji A, Dreyer S, Vadseth L, Maric I, Jönsson V, Haukebøe TH (2019) Gluteal augmentation with fat: retrospective safety study and literature review. Aesthet Surg J 39(3):292–305. https://doi.org/10.1093/asj/sjy153
Rosique RG, Rosique MJF (2018) Augmentation gluteoplasty: a Brazilian perspective. Plast Reconstr Surg 142(4):910–919. https://doi.org/10.1097/PRS.0000000000004809
Swanson E (2016) Prospective controlled study of buttock fat transfer using ultrasound and photographic measurements. Plast Reconstr Surg Glob Open 4(5):e697. https://doi.org/10.1097/GOX.0000000000000700
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We thank Sofia Palma for the illustrations, which enriched our article greatly.
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Seabra Robalo Gomes Jorge, A.C., Feng, YS., Santos Stahl, A. et al. Danger Zones of the Gluteal Anatomy: Improving the Safety Profile of the Gluteal Fat Grafting. Aesth Plast Surg 48, 1597–1605 (2024). https://doi.org/10.1007/s00266-023-03824-y
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DOI: https://doi.org/10.1007/s00266-023-03824-y