Injectable facial fillers: imaging features, complications, and diagnostic pitfalls at MRI and PET CT
Injectable fillers are widely used for facial rejuvenation, correction of disabling volumetric fat loss in HIV-associated facial lipoatrophy, Romberg disease, and post-traumatic facial disfiguring. The purpose of this article is to acquaint the reader with the anatomy of facial fat compartments, as well as with the properties and key imaging features of commonly used facial fillers, filler-related complications, interpretation pitfalls, and dermatologic conditions mimicking filler-related complications. The distribution of facial fillers is characteristic and depends on the anatomy of the superficial fat compartments. Silicone has signature MRI features, calcium hydroxyapatite has characteristic calcifications, whereas other injectable fillers have overlapping imaging features. Most fillers (hyaluronic acid, collagen, and polyalkylimide–polyacrylamide hydrogels) have signal intensity patterns compatible with high water content. On PET-CT, most fillers show physiologic high FDG uptake, which should not be confounded with pathology. Abscess, cellulitis, non-inflammatory nodules, and foreign body granulomas are the most common filler-related complications, and imaging can help in the differential diagnosis. Diffusion weighted imaging helps in detecting a malignant lesion masked by injected facial fillers. Awareness of imaging features of facial fillers and their complications helps to avoid misinterpretation of MRI, and PET-CT scans and facilitates therapeutic decisions in unclear clinical cases.
• Facial fillers are common incidental findings on MRI and PET-CT scans.
• They have a characteristic appearance and typical anatomic distribution
• Although considered as safe, facial filler injections are associated with several complications
• As they may mask malignancy, knowledge of typical imaging features is mandatory.
• MRI is a problem-solving tool for unclear cases.
KeywordsInjectable facial fillers Hyaluronic acid Silicone MRI PET-CT Granuloma
foreign body granulomas
Food and Drug Administration
F18- fluorodeoxy glucose
HIV-associated facial lipoatropy
magnetic resonance imaging
non inflammatory nodule
polyalkylimide - polyacrylamide hydrogels
positron emission tomography CT
superficial musculoaponeurotic system
"We are all of us stars, and we deserve to twinkle". Marilyn Monroe
The number of people undergoing facial filler injections to get a youthful twinkle has strikingly increased in the last decade. In 2015, more than two million individuals in the USA alone underwent hyaluronic acid (HA) injections of which the majority was for facial rejuvenation . Although middle-aged women still constitute the majority, it is not uncommon to see young adults and older people undergo facial filler injections . These injections, touted as safe and simple “lunch-time procedures,” have become an attractive alternative to incision-needing cosmetic surgery such as facelift procedures. Apart from the desire to look young, other indications include the correction of disabling volumetric soft tissue loss in HIV-associated facial lipoatrophy (HIV-LA), Romberg disease, and post-surgical and post-traumatic facial disfiguring [3, 4, 5].
The injection of dermal fillers gives desirable cosmetic outcome by erasing skin rhytides or restoring facial volume loss, or both. The commonly injected sites on the face include the perioral area, periocular region, nasolabial folds, malar fat pad, marionette lines, glabella, and lips. The rising demand for aesthetic procedures has led to the introduction of multiple injectable dermal fillers on the market. The actions by which these fillers produce the desired cosmetic outcome differ from each other and, thus, their complications and imaging features.
A radiologist may be asked to evaluate the complications, extent, and location of a known facial filler injection. The incidentally detected facial filler poses a diagnostic challenge because the patient may forget, deny the history of filler injection, or may not know what type of filler was used . It is a reality of the world market of facial rejuvenation that facial filler injections are not only performed by qualified physicians, but also by many unlicensed practitioners. It is imperative for the radiologist to remain abreast with the commonly used injectable facial fillers, the anatomical context of injection procedures and their complications to avoid misdiagnosis and unnecessary biopsy.
To the best of our knowledge, only very few articles have so far dealt with the imaging features of injectable facial fillers [3, 6, 7, 8, 9, 10, 11]. The purpose of this article is to acquaint the reader with the anatomy of facial fat compartments, as well as with the properties and imaging features of commonly used facial fillers, filler-related complications, interpretation pitfalls, and dermatologic conditions mimicking filler-related complications.
Most often injectable facial fillers are detected incidentally on cross-sectional imaging studies. Therefore, radiologists need to be familiar with the imaging features of injectable fillers in order not to confound these with true pathology or vice-versa in order not to miss true pathology obscured by filler injections.
Patients with suspected filler-related complications are most often evaluated clinically and treated accordingly . Therefore, the reported use of cross-sectional imaging in this clinical setting is limited. Nevertheless, dermatologic conditions (cutaneous lymphoma, sarcoidosis, dermatomyositis) may present clinically with non-specific features and imaging can help in differentiating these entities from filler-related complications. The imaging requirements for the evaluation of the facial skin and subcutaneous tissues including facial fillers vary according to the practicing centre. Depending on the availability, radiologists use MRI or high-frequency ultrasound to assess the location and volume of the injected facial fillers and to evaluate filler-related complications. At our institute, MRI is the preferred modality due to its excellent soft tissue discrimination capability, large field of view, and ability to provide anatomic, quantitative, and functional information. MRI has an excellent ability to detect soft tissue inflammation, abscess, and also foreign material in the soft tissues . It is preferred over ultrasound for the localisation of dislodged fillers because it provides anatomical reference .
At our institution, the MR examination protocol for facial fillers and dermatologic conditions includes high-resolution thin-slice (512 × 512 matrix for a field of view of 16-20 cm, 1-3 mm slices) acquisitions on a 1.5 or 3 Tesla MRI magnet with surface coils and parallel imaging techniques. We acquire the following sequences: T1 W (axial), T2 W ± fat saturation or a STIR sequence (axial and coronal), diffusion weighted sequences with ADC maps (axial), and post gadolinium injection T1 W with fat saturation. If the injected filler is not known, a “silicone only” sequence with simultaneous water and fat saturation (axial) before gadolinium injection should equally be obtained. A “silicone-only” sequence is designed to suppress all tissues except silicone. It is a combination of inversion recovery–turbo spin echo (IR-TSE) with a TI chosen to suppress fat signal (TI = 230 ms) and a spectrally selective pre-pulse, which suppresses water . Although widely used to image patients with silicone breast implants, the sequence is rarely obtained in other parts of the body. For the detection of injected silicone in the face, the sequence parameters at 3 T MRI that are used in our institution are as follows: TR = 7.8 ms, TE = 3.69 ms, TI = 230 ms, flip angle = 20 deg., voxel size = 1.5 × 1.5 × 6.0 mm, one average, six concatenations. We equally recommend inclusion of a DWI sequence in the protocol for two reasons. First, DWI helps in detecting a malignant lesion masked by injected facial fillers . Second, DWI discriminates between a frank abscess and inflammation and, thus, helps in avoiding futile attempts of percutaneous aspiration .
High-frequency ultrasound is a safe, cost-effective, and widely available modality for the evaluation of facial fillers. Various studies have documented its ability to localise commonly used facial fillers. Ultrasound has also been useful to detect filler-related complications, such as abscesses or granulomas localised in the superficial fat spaces. In cases with suspected deep spread of infection, MRI or contrast-enhanced CT (in the emergency setting) is, however, necessary. Operator dependability and poor reproducibility remain major shortcomings of ultrasound in the evaluation of facial fillers [16, 17, 18, 19].
CT does not offer advantages over MRI. However, it can identify calcifications, which are a hallmark of certain fillers and filler-related complications (see below). To reduce the radiation exposure, cone beam CT (CBCT) can be used as an alternative to CT to identify calcifications. However, CBCT does not allow assessment of soft tissues. Therefore, contrast-enhanced CT is preferred whenever infectious complications are suspected.
Imaging-relevant anatomy of facial fat compartments
Traditionally, surgeons performing facial rejuvenation injections and cosmetic surgeries divided the facial fat into the superficial and deep fat layers separated by the superficial musculoaponeurotic system (SMAS). The SMAS is a three-dimensional fibrous network that connects the periosteum, the muscles of facial expression, the platysma, and the fascia of the parotid gland with the dermis . The superficial fat layer (located superficial to the SMAS) was long considered a single confluent mass, and treatments were designed to lift and reposition the fat pad as one single unit . Similarly, practitioners injected facial fillers in arbitrarily defined facial compartments . More recently, Gosai et al. were the first to classify the superficial facial fat into medial and lateral compartments (units) based on their relationship with the underlying muscles of facial expression on MRI . Rohrich and Pessa demonstrated the actual anatomical divisions of the facial fat by injecting methylene blue dye into cadaveric facial specimen . Subsequent studies by Rohrich et al. and other groups validated the anatomical division of the facial fat and also identified additional distinct compartments [24, 25, 26, 27, 28]. In 2012, Girrloff et al. quantified various facial fat compartments on CT scans after injecting iodinated contrast in a cadaveric facial specimen .
Facial fat in these compartments age differently (hypotrophic versus hypertrophic changes or ptosis). For example, ageing causes hypertrophic ptotic changes in the nasolabial fat and middle cheek fat, and hypotrophic involution in the lateral temporal cheek fat and deep medial cheek fat, respectively. In patients with HIV-LA, substantial volumetric changes of the superficial fat compartments (nasolabial, medial and middle superficial cheek fat) occur, whereas deep facial fat units appear to be less affected . Therefore, qualitative assessment of these compartments plays an important role in facial rejuvenation methods and, in particular, in deciding which fat compartments should be volumised [32, 33]. Knowledge of facial fat compartments may also help in understanding facial filler distribution and migration.
Because of its high soft tissue resolution, MRI is excellently suited to depict the facial fat units. Their relative position with respect to the SMAS, orbit and facial skeleton allows correct identification of individual compartments (Fig. 3). Nevertheless, the tiny fibrous septae that separate these compartments, as well as the supporting ligaments of the face cannot be seen on routine high-resolution MR images obtained with standard coils.
Types of facial fillers and normal imaging features
The Food and Drug Administration (FDA) of the USA considers injectable facial fillers as medical devices used to improve appearance and without health benefit . The classifications of injectable facial fillers vary according to their properties such as nature of the filler, time interval for its biodegradation, and whether it is composed of one or more materials [35, 36]. The filler can be autologous, biological, or synthetic. Autologous fillers consist of the patient’s own body fat. Biological fillers consist of either collagen of bovine, porcine, or human origin or hyaluronic acid (HA) of bacterial origin. Synthetic fillers include paraffin, silicone, calcium hydroxyapatite (CHA), polymethylmethacrylate (PMMA) microspheres, polyacrylamide hydrogel, hydroxyethyl/ethyl methacrylate, and poly-L-lactic acid (PLLA) . Based on biodegradation features, fillers can be classified as rapidly resorbable (<12 months), slowly resorbable (<24 months), and permanent. Rapidly resorbable fillers include HA, collagen and autologous fat. Slowly resorbable fillers include PLLA, CHA and dextran, whereas permanent fillers include liquid silicone and PMMA . Silicone is the most widely used non-resorbable synthetic substance for medical purposes. Of the three forms of silicone, only the liquid silicone is used as facial filler while the elastomer and gel are used in breast implants [37, 38]. The FDA and the European Community (EC) do not recommend all commercially available products. While some products may be FDA approved, they are not EC approved and vice-versa [39, 40]. Besides, some products have a limited approval, which limits their use to the specified areas in the face.
Autologous fat fillers
Calcium hydroxyapatite (CHA) fillers
CHA (Radiesse) comprises spherical microparticles of bone-like composition suspended in an aqueous sodium carboxymethyl cellulose gel. Marionette lines and nasolabial folds have been successfully corrected with CHA. The filler has a tendency to nodule formation and foreign-body reaction, which discourages its use for lip augmentation. The microparticles disintegrate over time, and the volumising effect may last for 1 to 2 years [9, 45]. However, the persisting soft tissue volume gain even after complete filler resorption implies in vivo de novo collagen formation [46, 47].
CHA is hyperattenuating (HU 280-700) on CT and presents with well-defined linear streaks or rounded masses (Fig. 5). CT filler density diminishes after 12 months as the microspheres get absorbed, and eventually the filler may disappear after 24 months [9, 46]. On MRI, CHA fillers have low to intermediate signal intensity on T1 W and T2 W images. They show mild post-contrast enhancement due to vascularisation of the calcified matrix [9, 48]. On FDG PET-CT, CHA appears strongly FDG-avid, which, if detected incidentally, warrants correlation with patient history and morphological imaging to avoid misdiagnosis .
Hyaluronic acid (HA) fillers
HA is a naturally occurring polysaccharide in healthy soft tissue, which binds the collagen and elastic fibres to provide intercellular stability. The naturally occurring HA has a very short half-life. Pre-processing and cross-linking prolong the half-life of HA before its use as filler [43, 49]. Depending on cross-linking HA fillers can be divided into cohesive (monophasic) or non-cohesive (biphasic) gels. The cohesive gel disperses diffusely to fill the small gaps between collagen and elastin bundles, whereas the non-cohesive gel deposits in puddles [44, 50]. The injected HA combines with natural HA in the soft tissue, binds water due to its hygroscopic nature and also induces new collagen formation. Thus, a volume is created, which may last for a few months to 1 year [51, 52, 53]. HA fillers are the most widely used fillers for their safety, easy reversibility, and minimal side effects.
MRI with T2 W and contrast-enhanced T1 W sequences can accurately assess the volumetric and temporal changes of subdermal HA filler injection [3, 54]. Because of its high water content, HA filler appears strongly hyperintense on T2 W and STIR sequences and hypointense on T1 W sequences. Injected HA typically shows well-defined serpiginous margins at imaging (Fig. 5). Minor post contrast enhancement is seen in the initial 6 months of injection, which represents increased vascularisation of injected tissue. This minor enhancement and the signal intensity on T2 W images gradually decrease during the first year after injection . The volume gain after HA filler injection is maximal in the first month and remains more or less stable for the next 12 months. Using 3D fat-saturated T2 W sequences, HA was found in anatomical regions situated much deeper than the compartment of the initial injection . The hydrophilic nature of HA and the diffusion permeability of the fibrous septae between the facial fat compartments are thought to be responsible for this finding . As HA binds water in vivo and as the filler also induces in vivo procollagen formation (which has high water content), MRI actually depicts a mixture of all three substances (injected HA, bound water, and de novo formed procollagen) and differentiation between these three components is not possible with MRI . On CT, HA fillers appear as areas of soft tissue attenuation. On PET-CT, they are occasionally FDG-avid .
Poly-l-lactic acid (PLLA)
PLLA (Sculptra), a biodegradable synthetic polymer suspended in sodium carboxymethylcellulose and mannitol has been used for the treatment of HIV-LA and the correction of rhytides . It induces subclinical inflammation with collagen formation and fibrosis . It has a gradual onset of action and results last for a few years . PLLA appears hypointense on T2 W images and shows soft tissue attenuation on CT [6, 10, 47]. On FDG PET CT, there is increased uptake due to the filler-induced subclinical inflammation .
Polyalkylimide and polyacrylamide hydrogels (PAAG)
PAAG (Bio-Alcamid = polyalkylimide and Aquamid = polyacrylamide) are non-biodegradable injectable hydrogel polymers. Aquamid comprises 2.5-4.5% crosslinked polyacrylamide hydrogel and 97.5-95.5% purified water [35, 59]. PAAG induces accumulation of fibroblasts and macrophages, and formation of a fibrous capsule . Correcting nasolabial fold, facial contouring, rhytides, and facial lipoatrophy by PAAG injection is approved in many countries. Delayed reactions like infection, granuloma and migration have been reported . All abscesses reported in a study occurred after polyalkylimide gel . In analogy to other fillers containing large amounts of water, PAAG fillers appear hyperintense on T2 W and hypointense on T1 W sequences [2, 61] and reveal no post-contrast enhancement. On CT, PAAG appears as a well-defined area of fluid attenuation.
Silicone oil filler
Silicone is a permanent filler, which restores volume and induces new collagen formation. The pure silicone oil is considered inert, minimally antigenic, non-carcinogenic, and a poor medium for bacterial growth . Its use as a tissue filler became controversial due to the reported high rate of complications. Many authors attribute the silicone injection-related complications to the poor injection technique, use of industrial silicone and large volume injections [62, 63]. The off-label use of FDA/CE approved silicone products as facial fillers with microdroplet techniques is reported to have minimal side effects [62, 63]. Illicit silicone oil, however, continues to be in use as facial filler in many parts of the world despite complications.
Tissue harvested from the postauricular area is cultured to produce fibroblasts cell lines. These fibroblasts are injected intradermally to correct dermal depressions and rhytides. Autologuous fibroblasts increase thickness and density of dermal collagen. They have a low incidence of hypersensitivity [35, 44].
Paraffin was perhaps the first substance to be used as facial filler and caused severe granulomatous reactions and “paraffinoma formation” . CT features of “paraffinoma” include calcific rounded foci and soft tissue density nodules with a calcific rim .
Role of imaging for filler detection and characterisation
The detection of injected facial fillers is straightforward with cross-sectional imaging provided radiologists are aware of the typical injection sites (Figs. 1, 2, 3, 4, 5, and 6) and of MRI/CT features. Earlier published studies have demonstrated the ability of MRI in locating all complicated and non-complicated facial fillers in 100% of patients [2, 8, 10]. According to these studies, MRI could detect injected fillers as small as 2 mm in diameter , and also those filler-related abscesses and granulomas missed on clinical examination .
Regarding filler characterisation, Tal et al. have claimed that they could accurately differentiate between the individual types of injected fillers on the basis of their signature MRI features . The existing literature and experience at our institution do not support their assertions. As discussed in the previous section, most facial fillers (HA, collagen, and PAAG) have a similar appearance on MRI due to their high water content [3, 6, 10]. In our experience, only silicone fillers have a characteristic MRI appearance on the “silicone only” sequence. The “silicone only” sequence is, however, prone to artefacts from non-homogenous fat and water saturation, especially in the presence of dental implants. Therefore, experience and caution are required for its interpretation.
CHA shows characteristic linear or clumps of calcifications on CT , whereas all other filler types do not show calcifications unless the injected filler causes foreign body reaction. Foreign body granulomas (FBGs) induced by liquid silicone or paraffin have typical eggshell, rounded, or nodular calcifications [7, 11].
Complications of facial filler injections and role of imaging
Notwithstanding the much-touted minimally invasive nature of facial filler injection procedures and safety claims of filler manufacturers, all types of injectable facial fillers can cause short-term and long-term complications [38, 40, 66, 67].
Occasionally, severe and acute complications like local soft tissue necrosis, blindness, and cerebral infarct may occur due to vascular occlusion [72, 73]. A retrospective study reported acute blindness with glabella and nasolabial fold injection of autologous fat in seven patients, HA in four patients and collagen in one patient, respectively .
Long-term complications are related to the injected filler itself and delayed host response. These complications include FBG, delayed manifestations of infection including abscess formation, migration of filler, disfiguring nodules and scarring, tissue necrosis and ulcer, and persistent discoloration [40, 66].
Most complications like erythema, bruising and hypersensitivity do not require radiological evaluation. Non-erythematous nodules formed soon after injection are caused by the uneven distribution of the filler and are likely to resolve spontaneously. Even the nodules caused by inflammation/infection may resolve spontaneously . In one study involving PLLA injection in HIV-LA, patients showed small palpable, painless nodules in 44% cases. Most of these nodules resolved spontaneously .
Non-inflammatory nodule (NIN) and foreign body granuloma (FBG)
FBG and a NIN differ on imaging and histopathology . Differentiation between the two conditions is important as it influences patient management . A FBG is a non-allergic chronic granulomatous reaction that appears months to years after filler injection and grows very slowly. FBG can be multiple and recurring. On histology, FBG has wide spaces between the foreign body particles, abundant macrophages, fibroblasts and giant cells. It shows finger-like projections in adjacent tissues. Although all types of injectable fillers cause FBG formation, FBG is most often seen after long-standing silicone oil injection (“siliconoma”, especially with nonmedical grade silicone), whereas fillers such as HA have a low FBG incidence. FBG shows three histological types: cystic, lipomatous, and sclerotic. Discussion on the histological FBG types is, however, beyond the scope of this article [39, 40, 76].
NINs are single lumps that usually appear 1 to 2 months after a technically erroneous superficial facial filler injection. They occur more often after injections of non-resorbable than resorbable fillers. In patients with HIV-LA, NINs can be seen years after PLLA injection. NINs are usually evenly sized, appear harder and whiter than granulomas, and remain stable. On histology, they show a dense cluster of foreign material, few macrophages, occasional giant cells, and a fibrous pseudo-capsule [39, 40, 76].
According to Kadouch et al. , clinico-radiologic agreement was substantial for fillers without complications and non-inflammatory nodules (85%), moderate for abscesses (60%), fair for low-grade inflammation (32%), and slight for migration (9%). The patient population in the study of Kadouch et al. comprised patients with filler injections either for cosmetic reasons or treatment of HIV-LA . In our practice, regular use of MRI makes decision-altering contributions to the evaluation of filler-related complications and in patients with both head-neck cancer and fillers. Thus, the utility of MRI for the assessment of filler-related complications might differ in a different set of patients and, also, according to the clinical expertise. Nevertheless, the high cost of MRI warrants its judicious use [10, 79].
According to the literature, FBG is usually treated with intralesional corticosteroid injection, systemic steroid therapy and, occasionally, surgical excision. NIN requires surgical excision and does not respond to intralesional or systemic steroid therapy.
Migration of fillers and overfilling
Filler migration is a common indication for evaluation with MRI. Poor injection technique has been thought to cause filler migration. Although migration is not typical of any particular filler, permanent fillers (typically silicone) are more likely to migrate due to their longer presence in the body. They may migrate through lymphatic or haematogenous routes and may mimic a malignant pathology of distant organs or granulomatous skin conditions [62, 66, 80]. Authors have showed that MRI was able to detect migrated facial fillers even in the absence of clinical suspicion and denial of a history of filler injection [2, 11].
Overfilling due to excessive filler injection can cause serious patient dissatisfaction. The incidence of overfilling varies from 0.8 to 8% of cases. It may appear as a focal lump or diffuse facial asymmetry. Overfilling due to HA injection can be reversed to some extent by injection of hyaluronidase. Needle aspiration and surgical excision may also be required .
Scarring and lymph node enlargement
Severe chronic inflammatory thickening of the soft tissues may cause significant disfiguring and subsequent scarring. These reactions are common with permanent fillers, especially silicone. CT/MRI may show a thick band-like subcutaneous deposition of silicone associated with diffuse soft tissue swelling and post-contrast enhancement (figure 6) [6, 62, 66]. Mild enlargement of lymph nodes associated with facial fillers is non-specific. The enlarged lymph nodes in case of complicated silicone implants may or may not show silicone contents on imaging [2, 6, 8].
Pitfalls in image interpretations
Uncomplicated facial fillers, FBG, non-granulomatous inflammation and abscess associated with facial fillers may show increased uptake on FDG PET-CT/MRI. This uptake is attributed to increased glycolysis in activated inflammatory cells, mainly macrophages . The increased FDG uptake by facial fillers may pose a diagnostic challenge in head and neck cancer and melanoma patients by mimicking a new primary or recurrence, especially if the injection is performed between two follow up scans and the history is denied or simply forgotten. Careful correlation with morphological imaging and the anatomical context of FDG uptake may help in avoiding unnecessary biopsy.
Although FDG CT/MRI is not an imaging modality of choice for the detection of filler-related complications, it is increasingly used for the detection of a source of infection and inflammation, sarcoidosis, and large vessel vasculitis. The increased cost of treating multi-drug resistant infections in immune-compromised patients, diabetics, and elderly patients justifies the use of expensive PET-CT. FDG PET-CT is very sensitive but lacks the specificity to differentiate aseptic inflammation from septic infection [55, 81, 82].
Injectable fillers are widely used for facial rejuvenation and treatment of post-traumatic disfigurement, HIV-LA and other causes of facial volume loss. This review provides a comprehensive approach to the anatomy of facial fat compartments and summarises key imaging features of commonly used fillers and filler-related complications. Awareness of imaging features of facial fillers and their complications helps to avoid misinterpretation of MRI and PET-CT scans and facilitates therapeutic decisions in unclear clinical cases.
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