- Research article
- Open Access
Magnetic resonance imaging study in a normal Bengal tiger (Panthera tigris) stifle joint
BMC Veterinary Research volume 11, Article number: 192 (2015)
The purpose of this study was to describe the normal appearance of the bony and soft tissue structures of the stifle joint of a Bengal tiger (Panthera tigris) by low-field magnetic resonance imaging (MRI), and the use of gross anatomical dissections performed as anatomical reference. A cadaver of a mature female was imaged by MRI using specific sequences as the Spin-echo (SE) T1-weighting and Gradient-echo (GE) STIR T2-weighting sequences in sagittal, dorsal and transverse planes, with a magnet of 0.2 Tesla. The bony and articular structures were identified and labelled on anatomical dissections, as well as on the magnetic resonance (MR) images.
MR images showed the bone, articular cartilage, menisci and ligaments of the normal tiger stifle. SE T1-weighted sequence provided excellent resolution of the subchondral bones of the femur, tibia and patella compared with the GE STIR T2-weighted MR images. Articular cartilage and synovial fluid were visualised with high signal intensity in GE STIR T2-weighted sequence, compared with SE T1-weighted sequence where they appeared with intermediate intensity signal. Menisci and ligaments of the stifle joint were visible with low signal intensity in both sequences. The infrapatellar fat pad was hyperintense on SE T1-weighted images and showed low signal intensity on GE STIR T2-weighted images.
MRI provided adequate information of the bony and soft tissues structures of Bengal tiger stifle joints. This information can be used as initial anatomic reference for interpretation of MR stifle images and to assist in the diagnosis of diseases of this region.
In the Felidae family (subfamily pantherinae), six species of tigers belonging to the genus Panthera have been recognized . Since 2010, it has been classified as an endangered species by the International Union for Conservation of Nature and Natural Resources . Many veterinarians and wildlife researchers are involved in large non-domestic feline conservation in zoo and wildlife rehabilitation centers. Conservation task includes anatomical, physiological and clinical works [3–5]. However, studies by means of imaging exploratory techniques have been very sparse and they included radiographic and computed tomography (CT) for anatomical evaluation of the tiger stifle [6, 7], the assessing of a fracture of tibia and fibula , and different head diseases such as a nasopharyngeal myxosarcoma , an extradural hematoma , and a retrobulbar abscess .
In relation to magnetic resonance imaging (MRI), the studies done in this species have been limited to the study of central infarction and haemorrhage  and suspected neurotoxicity , but to date, no detailed MRI anatomic studies of stifle joints in large non-domestic cat have been reported. However, MRI has been used for descriptive anatomic researches of the stifle joints in dog [14–17] and horse , as well as to demonstrate the clinical value of MRI in diagnosing diseases of this region [19–23]. To the author’s knowledge, the lack of MRI stifle studies performed in domestic cats could be due to the small size of the feline stifle joint structures that require the use of high field MRI equipment to obtain high definition images.
The stifle joint is one of the more complexes of the locomotor system and it is particularly interesting because their numerous anatomic structures such as the bones, articular cartilage, menisci and ligaments. Knowledge of feline-specific anatomy is important to avoid over- or misinterpretation of physical examination or imaging findings . Therefore, an accurate interpretation of MRI anatomy of the stifle would be useful in diagnosis of diseases described in feline medicine [25–29]. The aim of this study was to describe the normal anatomy of the stifle joint of a Bengal tiger (Panthera tigris), using gross anatomical dissections, and sagittal, dorsal and transverse MR images.
A cadaver of 6-year-old female Bengal tiger (Panthera tigris) with a weight of 105 kg, born in captivity in Cocodrilos Park Zoo (Gran Canaria, Canary Islands, Spain) that died for natural causes not related to stifle joint disorder was used. The experimental study was conducted with authorization of the Conservation Nature Service (Seprona) of Gran Canaria at the Spanish Ministry of Interior (Protocol 2012) and the control of the Ethical Commission of Veterinary Medicine of the University of Las Palmas de Gran Canaria (agreement MV-2015/05).
After her death, the tiger was immediately frozen. Two days later, the animal was defrosted during 48 h to perform the MR imaging study using a 0.2-Tesla magnet (Vet-MR Esaote, Genova, Italy). The animal was positioned in right lateral recumbency on the scanning table with the hindlimbs in semi-extended position. Each stifle joint was subjected to MRI examination. Spin-echo (SE) T1-weighted and Gradient-Echo (GE) STIR T2-weighted MR images were obtained in 2D sagittal, dorsal and tranverse planes. SE T1-weighted sagittal images were acquired with the following settings: echo time (TE) = 26 msec, repetition time (TR) = 760 msec, number of acquisitions (NEX) = 3, 4 mm slice thickness with 4.4 mm spacing between slices, a field of view of 512 × 512 and a matrix of 192 × 136. For GE STIR T2-weighted sagittal images, the TE was 25 msec, TR was 1500 msec, inversion time (TI) was 75 msec, flip angle was 90°, number of acquisitions (NEX) = 2, 4 mm slice thickness with 4.4 mm interslice spacing, a field of view of 256 × 256 and a matrix of 192 × 136 matrix. For SE T1-weighted dorsal images, the TE was 26 msec, TR was 690 msec, number of acquisitions (NEX) = 3, and 4.5 mm slice thickness with 4.9 mm interslice spacing, a field of view of 256 × 256 and a matrix of 256 × 172. For GE STIR T2-weighted dorsal images, the TE was 25 msec, TR was 1680 msec, TI was 75 msec, flip angle was 90°, number of acquisitions (NEX) = 2, 4.5 mm slice thickness with 4.9 mm interslice spacing, a field of view of 256 × 256 and a matrix of 192 × 136. For SE T1-weighted transverse images, the TE was 26 msec, TR was 640 msec, number of acquisitions (NEX) = 3, 4 mm slice thickness with 4.4 mm interslice spacing, a field of view of 512 × 512 and a matrix of 288 × 199. For GE STIR T2-weighted transverse images, the TE was 25 msec, TR was 1600 msec, TI was 75 msec, flip angle was 90°, number of acquisitions (NEX) = 2, 4 mm slice thickness with 4.4 mm interslice spacing, a field of view of 256 × 256 and a matrix of 192 × 136.
At the conclusion of the MR study, gross anatomical dissections of the stifle joint, osseous preparations and textbooks of anatomy [30–33] were used to facilitate an accurate interpretation of the MR images.
The main structures were labelled on gross anatomical dissections and MRI images. Gross anatomical dissections of the tiger stifle joint from different views are presented in Fig. 1. Nine representative MR images in different planes were selected. Therefore, the sagittal MR images are shown in a lateromedial direction from the lateral to the medial femoral condyles (Figs. 2, 3, 4 and 5). The dorsal MR images began at the level of the caudal intercondylar area of the tibia and continued cranially to the transverse ligament of the stifle (Figs. 6, 7 and 8). The transverse MR images are shown in a proximodistal direction from the cruciate ligaments of stifle to the menisci and transverse ligament of the stifle (Figs. 9 and 10).
On the gross anatomical dissections, the femur (including the metaphysis, the trochlea, the lateral and medial condyles and the intercondylar notch), the tibia (with their metaphysis, the lateral and medial condyles, and the intercondylar eminence), the patella and the head of fibula could be identified (Fig. 1). The articular structures of the femorotibial joint such as the lateral meniscus with its meniscofemoral ligament attached proximally to the inner surface of the medial femoral condyle (Fig. 1d-f), as well as the transverse ligament of stifle that connects the menisci cranially (Fig. 1c) were observed. The cruciate ligaments of stifle were also visible, especially in the cranial (Fig. 1c), caudal (Fig. 1d, e) and dorsal views (Fig. 1f). Therefore, the cranial cruciate ligament, coursing from the inner surface of lateral femoral condyle to the central intercondylar area of the tibia was seen. In contrast, the caudal cruciate ligament was observed from the inner surface of medial femoral condyle to the caudal intercondylar area of the tibia. In relation to the lateral and medial collateral ligaments, they were seen from the lateral femoral epicondyle to the head of fibula and tibia, and from the medial femoral epicondyle to the tibia, respectively (Fig. 1a-d).
In addittion, several articular structures of the femoropatellar joint were identified. The patellar ligament that connected the distal tip of the patella to the tibial tuberosity was seen (Fig. 1a, b). The lateral and medial femoropatellar ligaments were extended from the lateral border of the patella to the lateral sesamoid bone of the gastrocnemius muscle (Fig. 1a), and from the medial border of the patella to the medial sesamoid bone of gastrocnemius muscle (Fig. 1b), respectively.
On the MR images (Figs. 2, 3, 4, 5, 6, 7, 8, 9 and 10), anatomic details of Bengal tiger stifle joints were compared with the anatomical dissections and evaluated according to the signal intensity of the different bony components and soft-tissues structures. Several structures of femorotibial joint were clearly visible with low-field MRI. Therefore, on SE T1-weighted sequences, the signal intensity of the cortical and subchondral bone of the femur and tibia was lower compared with the high signal intensity of the trabecular bone. However, on GE STIR T2-weighted MR images, the trabecular bone appeared with low signal intensity, as well as by observing the area of negligible signal corresponding to the cortical and subchondral bone of those bones. The articular cartilage of the femur and tibia was visualised with intermediate signal intensity in SE T1-weighted sequences, compared with GE STIR T2-weighted sequences where they showed high intensity signal. In both sequences, the signal of the articular cartilage was differentiated from trabecular bone by a dark line that corresponded to the subchondral bone (Figs. 2, 5, 6, 7 and 8). Articular capsule, menisci and ligaments were also seen with low signal intensity in both sequences. The synovial fluid could be identified in the articular cavity with intermediate signal intensity on the T1-weighted MR images. However, this fluid showed high signal intensity in GE STIR T2-weighted sequences.
The lateral and medial menisci were easily identified between the femoral condyles and the tibia as two triangular formations. These structures had low signal intensity in the sagittal (Figs. 2 and 5) and dorsal (Figs. 6, 7 and 8) planes, but they were not clearly observed in the transverse plane (Fig. 10). The meniscofemoral ligament was visible on the sagittal (Figs. 3 and 4), dorsal (Figs. 6 and 7) and transverse (Fig. 9) planes with low signal intensity. The cruciate ligaments were not completely distinguished in all three planes because of their oblique orientation and appeared with low signal intensity (Figs. 3, 4, 7 and 9). The lateral and medial collateral ligaments were well defined on the dorsal (Figs. 6, 7 and 8) and transverse (Figs. 9 and 10) planes as linear low signal intensity bands. These structures were difficult to differentiate to the cortical bone because of their similar signal intensity.
Several structures of femoropatellar joint were also seen with MRI. The patella was well visualized on SE T1-weighted sequences compared with GE STIR T2-weighted MR images, especially on the sagittal (Figs. 3 and 4) and transverse (Fig. 9) planes. On SE T1-weighted images, the patella showed intermediate signal intensity due to the trabecular bone, although the cortical bone appeared with low intensity signal on SE T1-weighted images. However, on GE STIR T2-weighted images, the cortical and trabecular bone of the patella had lower signal intensity. The patellar ligament (Figs. 3, 9 and 10) and the lateral and medial femoropatellar ligaments (Figs. 9 and 10) were well defined (Figs. 9 and 10) and appeared with low signal intensity in both sequences. The infrapatellar fat pad had high signal intensity on SE T1-weighted images and low signal intensity on GE STIR T2-weighted sequences.
Exploration and clinical evaluation of the bony and soft tissue structures of the stifle joint of Bengal tiger is laborious because of their anatomical complexity that makes difficult to diagnose morphological changes only by means of physical examination. In feline medicine, the patient has an excellent prognosis for return to normal stifle function with all but the most severe knee injuries. Thorough physical and radiographic evaluation of the stifle predicts successful management of stifle injury .
Diagnostic imaging techniques such as radiography, ultrasonography, CT and MRI have been used to evaluate the bony and soft-tissue structures of the stifle joint . In some cases, radiography may be sufficient to make a diagnosis when the clinical signs and physical examination give full information of the disorder [8, 34]; however, if radiographic assessment is inconclusive, more advanced imaging techniques are necessary . Ultrasonography is considered helpful to evaluate menisci, ligaments and tendons, although the animal’s size can limit their visualization . In contrast, CT has shown to be particularly beneficial for evaluating stifle osseous structures [7, 36], whereas the use of other modalities of this technique as CT arthrography may identify abnormalities of the cruciate ligaments, but is of questionable value for assessing the menisci . However, MR imaging is highly recommended for visualization of the normal stifle joint [14–18] and become the preferred imaging method for the evaluation of diseases in the articular cartilage, menisci and ligaments of synovial joints [19–23].
In veterinary medicine, different magnetic fields scanners have been used to the study of the stifle joint. Some works used a high field magnet that provided excellent resolution of the anatomic structures of the equine stifle joint . In the present study, the images were obtained using a low-field MRI magnet that showed adequate visualization of the normal structures of the tiger stifle joint. Similar results have been observed in dogs using low field intensity protocol [14–16, 18]. The main limitations of low-field MR imaging result from a lower signal-to-noise ratio, poor spatial resolution and motion artefacts are compensated by increasing the section thickness; the reduction in-plane resolution; the increase of the number of acquisitions and consecutively the acquisition time; and decreasing the bandwidth. In addition, with recent improvements, as a better homogeneity of magnets, better technology of the receiver coils and specialized pulse sequences have renewed interest in low-field MRI .
In our study, the SE T1-weighted and the GE STIR T2-weighted sequences were selected. Similar sequences have been used in other studies of the normal stifle in the dog [15, 16]. In contrast, Baird et al.  and Holcombe et al.  used only the SE T1 weighted sequence in the canine and the equine stifle studies, respectively. Recently, other authors have used the fast spin echo T2-weighted sequence to analyse the effects of stifle flexion angle in the evaluation of the normal canine cranial cruciate ligament .
SE T1-weighted and GE STIR T2-weighted MR images provided excellent detail of bone, soft-tissues, and synovial fluid of tiger stifle joint. However, SE T1-weighted sequences gave a better definition of the anatomic structures of the femorotibial and femoropatellar joints compared to GE STIR T2-weighted sequences.
As in other works done in dogs [15, 16] and horses , all the Bengal tiger stifle joint structures were showed in sagittal, dorsal and transverse MRI planes. However, in studies performed in normal canine stifle joint  that only use the sagittal and dorsal MRI planes, specific structures such as the femoropatellar ligaments were not visible.
In the present study, the articular cartilage of the femur and tibia, the cruciate and the meniscofemoral ligaments were visualized in the three anatomic planes. However, the articular cartilage was not clearly defined because the presence of synovial fluid that showed similar intensity signal. Menisci were visualized in all three planes, especially in the sagittal and dorsal planes due to a better identification of their shape. Gross anatomical dissections and MRI examinations revealed meniscal mineralization in the medial meniscus. Meniscal ossicles had been reported previously in tigers, lions, leopards, and jaguars [6, 7]. In tigers, medial meniscal ossification appears to be a normal anatomical variation that progressively develops following birth, and may serve as a model for the phylogenetic (developmental) theory of etiology . In addition, the lateral and medial collateral ligaments were visualized in the dorsal and transverse planes. Other structures of femopatellar joint such as the patellar ligament and infrapatellar fat pad were both visualized in the sagittal and transverse planes, whereas the lateral and medial patellofemoral ligaments were visualized in the transverse planes. Similar observations of the anatomical structures of the stifle joint in all the three planes have been described in dogs [14–16] and horses .
The gross anatomical dissections used in this study contributed to a correct morphologic and topographic evaluation of the bony and soft tissue structures of the Bengal tiger stifle joint, and were a helpful tool for the identification of the MR images.
The use of MRI in captive tiger is currently limited because of its expense, availability, and the logistical problems of acquiring MR images in these animals, but its use in wildlife is justified in captive species because of the amount of diagnostic information obtained with little risk to the animal’s evaluated [12, 13]. This study used only one animal due to the difficulty to access to these species in Gran Canary Island. In the future would be interesting perform additional studies with higher number of animals to better evaluate all the anatomical structures of the stifle joint using high field MRI, as well as to establish a protocol for diagnosis of diseases of this area.
In the present study, MRI has provided some clinically relevant anatomical details of the bony and soft tissues structures of Bengal tiger stifle joint.
Magnetic resonance imaging
Wilson DE, Reeder DM. Subfamilia pantherinae mammal species of the world. A taxonomic and geographic reference. 3rd ed. Baltimore, Maryland: The Johns Hopkins University Press; 2005.
Chundawat RS, Khan JA, Mallon DP. "Panthera tigris tigris" Red List of Threatened Species. Version 2014.3. International Union for Conservation of Nature 2011.
Cagnini DQ, Salgado BS, Linardi JL, Grandi F, Rocha RM, Rocha NS, et al. Ocular melanoma and mammary mucinous carcinoma in an African Lion. BMC Vet Res. 2012;8:176–80.
Diogo R, Pastor F, De Paz F, Potau JM, Bello-Hellegouarch G, Ferrero EM, et al. The head and neck muscles of the serval and tiger: homologies, evolution, and proposal of a mammalian and a veterinary muscle ontology. Anat Rec. 2012;295:2157–78.
Maas M, Keet DF, Nielen M. Hematologic and serum chemistry reference intervals for free-ranging lions (Panthera leo). Res Vet Sci. 2013;95:266–8.
Ganey TM, Ogden JA, Abou-Madi N, Colville B, Zdyziarski JM, Olsen JH. Meniscal ossification. II. The normal pattern in the tiger knee. Skeletal Radiol. 1994;23:173–9.
Walker M, Phalan D, Jensen J, Johnson J, Drew M, Samii V, et al. Meniscal ossicles in large non-domestic cat. Vet Radiol Ultrasound. 2002;43:249–54.
Ghosh GL, Paul JC, Biswas A, Nandi SK, Biswas BK. Synthetic material used for repair of tibia and fibula fracture in a tiger. Zoo Print J. 2003;18:1027–8.
Shilton CM, Thompson MS, Meisner R, Lock B, Lindsay WA. Nasopharyngeal myxosarcoma in a Bengal tiger (Panthera tigris). J Zoo Wildl Med. 2002;33:371–7.
Ketz-Riley CJ, Galloway DS, Hoover JP, Rochat MC, Bahr RJ, Ritchey JW, et al. Paresis secondary to an extradural hematoma in a Sumatran tiger (Panthera tigris sumatrae). J Zoo Wildl Med. 2004;35:208–15.
Dziallas P, Becker A, Bösing B, Zimmering T, Böer M, Mischke R, et al. Computed tomography diagnostic of a retrobulbar abscess in a white tiger. Tierarztl Prax. 2012;40:59–63.
Snow TM, Litster AL, Gregory RJW, Hanger JJ. Big cat scan: Magnetic resonance imaging of the tiger. Australas Radiol. 2004;48:93–5.
Zeira O, Briola C, Konar M, Dumas MP, Wrzosek MA, Papa V. Suspected neurotoxicity due to Clostridium perfringens type B in a tiger (Panthera tigris). J Zoo Wildl Med. 2012;43:666–9.
Baird DK, Hathlock JT, Rumph PF, Kincaid SA, Visco DM. Low-field magnetic resonance imaging of the canine stifle joint: normal anatomy. Vet Radiol Ultrasound. 1998;39:87–97.
Soler M, Murciano J, Latorre R, Belda E, Rodríguez MJ, Agut A. Ultrasonographic, computed tomographic and magnetic resonance imaging anatomy of the normal canine stifle joint. Vet J. 2007;174:351–61.
Pujol E, Van Bree H, Cauzinille L, Poncet C, Gielen I, Bouvy B. Anatomic study of the canine stifle using low-field magnetic resonance imaging (MRI) and MRI arthrography. Vet Surg. 2011;40:395–401.
Podadera J, Gavin P, Saveraid T, Hall E, Chau J, Makara M. Effects of stifle flexion angle and scan plane on visibility of the normal canine cranial cruciate ligament using low-field magnetic resonance imaging. Vet Radiol Ultrasound. 2014; doi:10.1111/vru.12142.
Holcombe SJ, Bertone AL, Biller DS, Haider V. Magnetic resonance imaging of the equine stifle. Vet Radiol Ultrasound. 1995;36:119–25.
Blond L, Thrall DE, Roe SC, Chailleux N, Robertson ID. Diagnostic accuracy of magnetic resonance imaging for meniscal tears in dogs affected with naturally occuring cranial cruciate ligament rupture. Vet Radiol Ultrasound. 2008;49:425–31.
Harper TA, Jones JC, Saunders GK, Daniel GB, Leroith T, Rossmeissl E. Sensitivity of low-field T2 images for detecting the presence and severity of histopathologic meniscal lesions in dogs. Vet Radiol Ultrasound. 2011;52:428–35.
Böttcher P, Armbrust L, Blond L, Brühschwein A, Gavin PR, Gielen I, et al. Effects of observer on the diagnostic accuracy of low-field MRI for detecting canine meniscal tears. Vet Radiol Ultrasound. 2012;53:628–35.
Widmer WR, Buckwalter KA, Braunstein EM, Hill MA, O’Connor BL, Visco DM. Radiographic and magnetic resonance imaging of the stifle joint in experimental osteoarthritis of dogs. Vet Radiol Ultrasound. 1994;35:371–84.
Galindo-Zamora V, Dziallas P, Ludwig DC, Nolte I, Wefstaedt P. Diagnostic accuracy of a short-duration 3 Tesla magnetic resonance protocol for diagnosing stifle joint lesions in dogs with non-traumatic cranial cruciate ligament rupture. BMC Vet Res. 2013;9:40–8.
Grierson J. Hips, elbows and stifles: common joint diseases in the cat. J Feline Med Surg. 2012;14:23–30.
McLaughlin RM. Surgical diseases of the feline stifle joint. Vet Clin North Am Small Anim Pract. 2002;32:963–82.
Umphlet RC. Feline stifle disease. Vet Clin North Am Small Anim Pract. 1993;23:897–913.
Harasen GL. Feline cranial cruciate rupture: 17 cases and a review of the literature. Vet Comp Orthop Traumatol. 2005;18:254–7.
Mahoney P. Musculoskeletal imaging in the cat. J Feline Med Surg. 2012;14:13–22.
Das S, Thorne R, Langley-Hobbs SJ, Perry KL, Burton NJ, Mosley JR. Patellar ligament rupture in the cat: repair methods and patient outcomes in seven cases. J Feline Med Surg. 2014; doi:10.1177/1098612X14544345.
Sandoval J. Articulación de la rodilla. In: José Sandoval Juárez, editor. Tratado de Anatomía Veterinaria. Tomo II. Aparato Locomotor. Madrid; 1998. p. 209–12.
Nomina Anatomica Veterinaria. In: Arthrologia. 5th ed. Hannover, Columbia-Missouri, Gent, Sapporo: World Association of Veterinary Anatomists; 2005. p. 36–7.
Schaller O, Constantinescu GM. Arthrologia. In: Illustrated Veterinary Anatomical Nomenclature. 2nd ed. Sttutgart: Enke Verlag; 2007. p. 92–3.
Latorre R, Gil F, Climent S, López O, Henry R, Ayala M, et al. Rodilla, pierna y pie. In: Atlas en color sobre abordajes quirúrgicos a huesos y articulaciones en el perro y el gato. Miembros toracico y pelviano. Buenos Aires: Inter-Médica; 2008. p. 189–209.
Freire M, Brown J, Robertson ID, Pease AP, Hash J, Hunter S, et al. Meniscal mineralization in domestic cats. Vet Surg. 2010;39:545–52.
Marino DC, Loughin CA. Diagnostic imaging of the canine stifle: a review. Vet Surg. 2010;39:284–95.
Rahal SC, Fillipi MG, Mamprim MJ, Oliveira HS, Teixeira CR, Teixeira RHF, et al. Meniscal mineralisation in little spotted cats. BMC Vet Res. 2013;9:50–5.
Samii VF, Dyce J, Pozzi A, Drost WT, Mattoon JS, Green EM, et al. Computed tomographic arthrography of the stifle for detection of cranial and caudal cruciate ligament and meniscal tears in dogs. Vet Radiol Ultrasound. 2009;50:144–50.
Tavernier T, Cotton A. High–versus low-field MR imaging. Radiol Clin N Am. 2005;43:673–81.
MR images acquisition and gross anatomical dissections were financed by funds of the Department of Morphology of Las Palmas de Gran Canaria University (Spain).
The authors declare that they have no competing interests.
AA: conceived the study, participated in the obtention of the gross anatomical dissections, the anatomical recognition of the structures and drafted the manuscript; ME and AArt: participated in the obtention of the MR images; JRJ and JMV: contributed to the study design and participated in the anatomical recognition of the structures; DB and DM participated in the obtention of the gross anatomical dissections. All authors read and approved the final manuscript.
About this article
Cite this article
Arencibia, A., Encinoso, M., Jáber, J.R. et al. Magnetic resonance imaging study in a normal Bengal tiger (Panthera tigris) stifle joint. BMC Vet Res 11, 192 (2015) doi:10.1186/s12917-015-0532-4
- Magnetic resonance imaging
- Stifle joint