Background

Chondrosarcoma is a malignant neoplasm in which the tumor cells form a cartilaginous matrix [1]. It is the second most frequent primary malignant tumor of the bone after osteosarcoma [2]. However, the head and neck region has been reported as a rare site of origin for chondrosarcoma, accounting for 1 to 12% of chondrosarcoma cases [3]. Furthermore, chondrosarcoma in the temporomandibular joint (TMJ) area is extremely rare.

Diagnosing chondrosarcoma in the head and neck region is challenging because cartilaginous neoplasms are rare and exhibit various histopathologic patterns, from benign chondroid tumors to malignant undifferentiated neoplasms [4]. According to previous studies, delays in diagnosing TMJ chondrosarcoma have reached 6 to 8 years [5, 6]. Treating chondrosarcoma of the TMJ is also challenging because of the proximity of vital structures and the consequent difficulty of performing an adequate resection. Cranial invasion has been reported previously [5, 6], and chondrosarcoma of the facial skeleton has been reported to have poorer prognosis than that in other regions of the body [7]. The latest therapeutic concepts in TMJ surgery, including resection guide by digital osteotomy templates [8], pre-bent and milled plates [9], 3D-printed patient-specific prostheses [10], and intraoperative navigation [11], can aid in accurate resection and reconstruction.

During the past 20 years, we have encountered multiple cases of destructive cartilaginous neoplasms in the TMJ and neighboring anatomy that were diagnosed by magnetic resonance imaging (MRI) and open biopsy. This article provides a detailed analysis of that case series and a comprehensive literature review of chondrosarcoma involving the TMJ to evaluate diagnostic approaches, management modalities, and final outcomes.

Methods

Subjects

The study sample contains patients with chondrosarcoma arising in the TMJ for which they underwent therapeutic surgery at the Department of Oral and Maxillofacial Surgery at Seoul National University Dental Hospital from April 1, 2000 through October 31, 2021. This study was approved by the Institutional Review Board of Seoul National University Dental Hospital (IRB approval number: ERI21040).

Treatment protocol

In this study, MRI, contrast-enhanced computed tomography (CT), and positron emission tomography-CT (PET-CT) were performed for radiographic examination [12]. Open biopsy was conducted for pathologic confirmation of the diagnosis. For the definite surgery, wide excision and immediate reconstruction were conducted on the same day. Histopathologically, chondrosarcoma is categorized into three subtypes (grades I, II, and III) according to nuclear size, cellularity, and frequency of mitosis [13]. Post-operative radiation therapy was performed for high-grade cases and cases in which the surgical resection margin was involved in pathology. Considering the possibility of primary site recurrence and lung metastasis, contrast-enhanced CT and chest X-ray were recommended at intervals of 3–6 months.

Facial nerve approach

Three surgical approaches to the facial nerve were used according to size and location of the tumor. When the facial nerve was involved in the tumor, segmental resection and nerve graft were performed [14, 15]. When the nerve was retracted to remove the tumor and the tension on the nerve increased, intentional cut and end-to-end repair with epineural suture were used [16]. When the tension did not increase during nerve isolation and retraction, the nerve was preserved without intervention.

Facial nerve function was evaluated using the House-Brackmann (HB) grading scale at least 1 year after the surgical procedure [17]. The HB system assigns patients to categories I to VI based on their degree of facial function. Grade I is normal function, and grade VI is total paralysis.

TMJ reconstruction

The resected condylar and mandibular areas were reconstructed using vascularized costal bone, a condylar prosthesis with a reconstruction plate (Stryker, Kalamazoo, MI, USA), or a ramal condylar implant (Zimmer Biomet, Jacksonville, FL, USA) [18, 19]. To prevent soft tissue depression in the pre-auricular area and to fill the tumor defect, a vascularized serratus anterior or latissimus dorsi free flap was transferred with microvascular anastomosis [20]. Reconstruction of the glenoid fossa depended on the surgical resection margin. When the glenoid fossa was included in the surgical resection margin clinically or pathologically by intraoperative frozen biopsy, the fossa was reconstructed using a fossa implant (Zimmer Biomet, Jacksonville, FL, USA) [19].

Literature search

This study followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [21] (Fig. 1). All case reports about TMJ chondrosarcoma published in English from 1954 to 2021 were collected. The literature search was carried out in PubMed using the keywords “chondrosarcoma” and “temporomandibular joint.” In addition, the reference lists of the retrieved articles were manually cross-checked.

Fig. 1
figure 1

PRISMA flow chart of systematic search on TMJ chondrosarcoma (PRISMA Preferred Reporting Items for Systematic reviews and Meta‑Analyses, TMJ Temporomandibular joint)

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Eligibility criteria and data analysis

All publications reporting cases of chondrosarcoma arising in the TMJ were eligible. The inclusion criterion was conventional chondrosarcoma cases. Other types, including synovial, mesenchymal, and dedifferentiated chondrosarcomas, were excluded. Articles that were not written in English or whose entire text was unavailable were also excluded. Each individual case was thoroughly reviewed to obtain data on demographics, diagnosis, tumor extent, surgical management, adjunctive therapy, and treatment outcomes.

Results

Radiographic findings

The following radiological findings were observed in MRI and CT images: condyle destruction, sclerotic changes in the condyle, displacement of surrounding structures by a mass in the TMJ, calcified foci inside the mass, bulging of the mass with an enhancing rim, and joint space widening (Fig. 2). In this case series, distant metastasis was not found on pre-operative PET-CT in any cases.

Fig. 2
figure 2

Pre-operative images (case 2) a CT (bone window image): an irregularly destructed condyle is observed. The cortical bone of the condyle is severely perforated and bone marrow is also infiltrated. b CT (soft tissue window image): tiny calcified foci are scattered around the margin of and inside the mass. c MRI (T2 weighted image): heterogeneous high signal intensity is observed around the right condyle. d MRI (contrast-enhanced T1 weighted image): heterogeneous enhancement around the right condyle is noted

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Facial nerve recovery

Of the 10 cases in our institution, segmental resection was performed in two because of nerve involvement in the tumor (Table 1 and Fig. 3). In one case, a segment of the frontal branch of the facial nerve was resected, and the great auricular nerve was grafted interpositionally (case 1). In the other, the temporofacial trunk was partially resected and interpositionally grafted with the thoracodorsal nerve from a latissimus dorsi free flap (case 2). In four cases, the facial nerve was intentionally cut due to high tension while retracting it during approach to the mass (Fig. 3). The zygomatic branch (case 3), temporofacial trunk (case 9), and temporofacial and cervicofacial trunks (cases 4 and 5) of the facial nerve were intentionally cut, and neurorrhaphy was conducted. In the other four cases, the facial nerve was preserved because no excessive retraction was required during the tumor approach (Fig. 4). In cases involving segmental resection, the patients experienced moderately severe facial nerve dysfunction (HB grade IV). When an intentional cut was performed, facial nerve dysfunction was moderate-mild (HB grade III) or mild (HB grade II) at more than 1 year after surgery. In the patients who underwent only nerve retraction, nerve dysfunction was mild (HB grade II) or absent (HB grade I).

Table 1 Reconstruction of the TMJ after chondrosarcoma ablation and surgical approaches to the facial nerve in our cases
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Fig. 3
figure 3

Surgical approaches to the facial nerve a (Case 2) Segmentally resected temporofacial trunk (arrowhead) and preserved cervicofacial trunk (arrow). b (Case 2) Retracted buccal branch (arrow) during mass resection. c (Case 2) Nerve graft using 10 cm length of thoracodorsal nerve for temporofacial trunk (arrow). d (Case 4) Temporofacial and cervicofacial trunks before intentional cut. e (Case 4) Intentionally cut temporofacial and cervicofacial trunks. f (Case 4) Temporofacial and cervicofacial trunks after end-to-end nerve repair

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Fig. 4
figure 4

Reconstruction of the mandibular condyle and glenoid fossa and surgical approach to the facial nerve (Case 7) a Facial nerve isolation and retraction during mass resection. b Preserved facial nerve after mass resection and reconstruction with a fossa implant and a metal condyle prosthesis. c Harvesting of the serratus anterior free flap with a vascular pedicle (the serratus branch of the thoracodorsal artery and the vena comitans). d Reconstruction with micro-anastomosed serratus anterior free flap

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Mandibular condyle and glenoid fossa reconstruction

All patients underwent primary mass removal and reconstructive surgery simultaneously. The resected condyle area was reconstructed with a condylar prosthesis with a reconstruction plate or ramal condylar implant except in one patient, whose TMJ was reconstructed with vascularized costal bone (Table 1 and Fig. 5). In six patients, the glenoid fossa was also reconstructed using a fossa implant (Figs. 4 and 5). In case 6, the reconstruction plate fractured 23 months after the primary surgery, and the mandible was reconstructed with a fibular free flap (Fig. 5).

Fig. 5
figure 5

Reconstruction of the mandibular condyle and glenoid fossa, post-operative panoramic radiographs a (Case 1) The condyle was reconstructed with vascularized costal bone. b (Case 2) The condyle was reconstructed with a condylar prosthesis with a reconstruction plate. c (Case 3) The condyle was reconstructed with a condylar prosthesis with a reconstruction plate. d (Case 4) The condyle was reconstructed with a condylar prosthesis with a reconstruction plate and the glenoid fossa was reconstructed with a fossa implant. e (Case 5) The condyle was reconstructed with a condylar prosthesis with a reconstruction plate and the glenoid fossa was reconstructed with a fossa implant. f (Case 6) The condyle was reconstructed with a condylar prosthesis with a reconstruction plate. g (Case 6) The reconstruction plate fractured 23 months after the primary surgery and the condylar and mandibular areas were reconstructed with a vascularized fibular free flap. h (Case 7) The condyle was reconstructed with a metal condyle prosthesis and the glenoid fossa was reconstructed with a fossa implant. i (Case 8) The condyle was reconstructed with a metal condyle prosthesis and the glenoid fossa was reconstructed with a fossa implant. j (Case 9) The condyle was reconstructed with a metal condyle prosthesis and the glenoid fossa was reconstructed with a fossa implant. k (Case 10) The condyle was reconstructed with a condylar prosthesis with a reconstruction plate and the glenoid fossa was reconstructed with a fossa implant

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Histopathologic findings

Microscopic examination of sections stained with hematoxylin–eosin showed atypical chondrocytes exhibiting increased cellularity, pleomorphism, multinucleation, and mitoses. Chondrosarcomas demonstrate proliferation of tumor cells within the chondroid matrix with focal calcification, as seen in Fig. 6. On stained slides, we identified surgical resection margins by measuring distances from the tumor borders in the anterior, posterior, superior, inferior, medial, and lateral directions. When tumor cells were observed in the margins in more than one direction, the sample was judged to have positive margins. Immunohistochemical examination was carried out with antibodies against vimentin, S-100 protein, and Ki-67. All cases were positive for vimentin and showed diffuse positive expression of S-100 protein. Ki-67 was expressed in more than 25% of grade III, 10–20% of grade II, and less than 5% of grade I patients (Fig. 6).

Fig. 6
figure 6

Histopathologic images a H&E staining, × 100 (case 7, grade II). The lesion showed proliferation of tumor cells within the chondroid matrix with focal calcification. b H&E staining, × 200 (case 7, grade II) Atypical chondrocytes presented with increased cellularity, pleomorphism, multinucleation, and mitoses. c S-100 protein, × 100 (case 3, grade II) immunohistochemistry showed diffuse positive expression of S-100 protein. d Ki-67, × 200 (case 4, grade II) immunohistochemistry showed 15–20% positive expression of Ki-67

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Post-operative courses

Seven patients received post-operative radiation therapy (Table 2) and experienced complications such as pain, trismus, facial nerve weakness, headache and amblyacousia, for which they underwent rehabilitation treatment such as physical therapy through the department of rehabilitation medicine. The mouth openings for most cases were greater than 25 mm. However, the mouth openings for cases 1 and 7 were 18 mm and 22 mm, respectively. In case 5, the patient’s mouth opening was sufficient to allow dental implant surgery under local anesthesia about 21 months after the primary operation. In case 1, grafted costal bone in the ramus area was partially removed due to an infection at 2 months post-operatively. No other post-operative infections occurred. All patients were alive at last follow-up, and no recurrences in the condyle or glenoid fossa had occurred. In case 6, lung metastasis occurred 16 months after the mass resection surgery. After partial lobectomy, the patient is undergoing periodic follow-up.

Table 2 Summary of TMJ chondrosarcoma cases in the literature and our series
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Literature review

The 34 articles reporting on 37 cases on chondrosarcoma of the TMJ published between 1976 and 2021 are summarized in Table 2 [5,6,7, 22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46, 48,49,50,51,52]. Of the 37 cases, facial nerve preservation was reported in 14, and the facial nerve was sacrificed in 3 cases. Glenoid fossa reconstruction was reported in 13 cases, and glenoid fossa reconstruction was completed for 3 patients. Among the 47 total cases, including our cases, the tumor grade was specified in 43. Among them, 28 cases (65.1%) were reported to be grade I, 2 (4.7%) were grade I–II, 10 (23.3%) were grade II, 1 (2.3%) was grade II–III, and 2 (4.7%) were grade III. All the patients underwent surgical therapy. Of the 47 patients, 19 underwent post-operative radiation therapy. Among the 42 cases in which recurrence was specified, it occurred in 4 (9.5%). Of the 4 cases with recurrence, 3 recurred within 1 year, and the other recurred after 10 years. Among those 4 patients, 1 died of the recurred disease, and the other 3 survived. Distant metastasis to the lung occurred in 1 patient who remained alive after partial lobectomy.

Discussion

Chondrosarcoma arising in the TMJ area is extremely rare. Among the 10 patients in our series, 2 were male and 8 were female (Table 2). This female predominance is consistent with previous studies [46, 47, 53]. The mean age of the patients in our study was 48.3 (16–64) years. This was not different from recent studies, in which the reported mean ages were 46.7 years [46] and 46.5 years [47, 53].

The major radiological features of chondrosarcoma arising in the TMJ were consistent with previous studies [35, 39, 45,46,47, 53]. MRI is recommended for preoperative planning because it provides detailed information about the anatomic limits and the most accurate assessment of the extent of the lesion [34, 36]. Contrast-enhanced CT is also recommended. In our cases and the cases from the literature, CT and MRI demonstrated bony destruction and tumor spread, which aided in the differential diagnosis and enabled creation of an adequate treatment plan [24, 45]. Image findings such as outward growth from the condyle, various patterns of internal enhancement, and markedly hyperintense T2 signal areas were noted [12]. In our cases, an active lesion in the TMJ with no metastatic bone lesion was observed on PET-CT.

Biopsy was performed for diagnosis and pre-operative confirmation of chondrosarcoma. Biopsy of chondrosarcoma is not recommended by some authors because of the risk of anaplastic transformation and diffusion during manipulation of the mass [54, 55]. Moreover, fine needle aspiration biopsy does not always provide a reliable diagnosis [6, 24, 36, 53]. Nonetheless, incisional biopsy is the best option for distinguishing among osteogenic sarcoma, pleomorphic adenoma, and chondroma [35]. Other authors recommend open biopsy as a definite means to achieve final diagnosis [45]. In our cases, aspiration biopsy and core needle biopsy were ineffective. In case 5, aspiration biopsy failed, and the result of a subsequent core needle biopsy under local anesthesia performed 4 years later was a hyperplastic cartilage chip. However, an incisional biopsy under general anesthesia diagnosed chondrosarcoma 1 month after the previous biopsy. In case 7, the result of a core needle biopsy under local anesthesia was fibromuscular tissue with no diagnostic abnormalities. However, the result of an open biopsy performed 2 months later under general anesthesia was chondrosarcoma. Core needle biopsy has been recognized as a dependable diagnostic technique for musculoskeletal tumors, exhibiting minimal associated complications [56, 57]. However, core needle biopsy was not conducted in previous cases of TMJ chondrosarcoma and yielded unsatisfactory results in cases 5 and 7 among our patients. Incorporation of ultrasound [58], CT [59], or computer-assisted navigation [60] alongside core needle biopsy might enhance its diagnostic capabilities for TMJ diseases.

Surgical management is the standard primary treatment for chondrosarcoma [61,62,63,64,65,66]. Wide local resection was performed in all our cases. No significant cervical lymphadenopathy was observed in any cases. Selective neck dissection was performed only in case 1. No metastasis to regional lymph nodes was observed in the biopsy. This is consistent with previous studies, which concluded that neck node dissection is usually unnecessary because of the low incidence of regional lymph node metastasis [3, 65]. In our cases, the treatment protocol did not include neck dissection unless suspicious cervical lymph nodes were found. After successful tumor resection, facial appearance is an important outcome in the head and neck area. A vascularized free flap was used for reconstruction in our cases. In the literature, local flaps such as a temporal muscle flap [5, 35] or microvascular free flaps such as a fibular free flap [39, 46] have been used depending on the defect size and location. A serratus anterior free flap for relatively small defects and a latissimus dorsi free flap for relatively large defects were used in our cases. Costal bone was also harvested with the serratus anterior muscle for reconstruction of the mandibular condyle and ramus (case 1) or the zygomatic process of the maxilla (case 3).

Among the post-operative complications, facial nerve weakness was thought to be due to segmental resection or an intentional nerve cut when those approaches were used or due to irritation during the operation. Facial nerve function gradually recovered through rehabilitation treatment such as physical therapy. With respect to post-operative facial nerve function, the HB grades were closest to normal in cases in which the nerve was not transected (Table 1). Patients were able to close their eyes completely in all cases except those involving segmental resection. Prognosis was better in cases involving an intentional cut than in those involving segmental resection, and prognosis was also better when one of the five branches of the facial nerve was transected than when the temporofacial or cervicofacial trunk was transected. Although a conservative approach to the facial nerve yielded better recovery of nerve function, a radical approach might be required to completely resect the mass and prevent recurrence.

Because the patient in case 1 was only 19 years old, the mandibular condyle was reconstructed with vascularized costal bone instead of an artificial prosthesis. However, ankylosis of the TMJ occurred during follow up. Mouth opening improved after gap arthroplasty. Although a costochondral graft is a viable option with growth potential, recurrent ankylosis has been reported as a major problem [67, 68]. After ablative surgery, joint ankylosis has been reported when a vascularized fibular free flap is used to reconstruct the mandibular condyle [69]. When autogenous bone is being considered for condyle reconstruction, the possibility of ankylosis should be considered. In the present study, condyles were reconstructed using a condylar prosthesis with no fossa reconstruction in 3 cases (cases 2, 3, and 6). In other studies involving metal condylar replacement alone, the condyle eroded into the glenoid fossa [70] or penetrated the middle cranial fossa [71]. However, Marx et al. reported long-term stability of a metal condyle replacement without alloplastic replacement of the glenoid fossa [18]. The condylar prostheses in the present study were maintained without severe complications. Because the forces imposed on the glenoid fossa by the condylar prosthesis can be reduced in ablative surgery cases, the condylar prostheses seemed to function in place. In case 6, the reconstruction plate fractured 23 months after the primary surgery [72] and was reconstructed with a vascularized fibular free flap. This might have occurred because the boundary of resection in that case was the widest of the 10 cases, leading to a mechanically unfavorable situation.

Chemotherapy was not performed in our cases because the consulting opinion from the department of hemato-oncology was that it would offer no benefit because chondrosarcomas are poorly responsive to chemotherapy. In the literature, chemotherapy was reported to have a limited role in chondrosarcoma treatment, but it can be used as an adjuvant therapy in cases with aggressive behavior, rapid local recurrence, or high-grade chondrosarcoma [3, 33]. Obtaining adequate resection margins with chondrosarcoma arising in the TMJ is challenging because of the proximity to vital structures. Therefore, post-operative radiation therapy was performed in the 7 of our 10 cases that involved surgical resection margin or high-grade chondrosarcoma on pathology. Radiation therapy is recommended post-operatively only for high-grade or incompletely resected chondrosarcomas [73,74,75,76,77]. A treatment protocol involving radical surgery with radiotherapy resulted in a better prognosis in a recent study [65]. In the present cases series, post-operative radiation therapy was also thought to be beneficial because no local recurrence occurred in the 7 applicable patients. However, complications such as trismus, fibrosis, oral mucositis, and xerostomia were observed in those patients. Therefore, radiotherapy should be strictly applied for limited indications.

After the definitive surgeries, periodic follow-up with chest X-ray and enhanced CT is important. In case 6, which involved grade III chondrosarcoma, lung metastasis was found on a chest X-ray 16 months after surgery. Additional imaging with chest CT and PET-CT revealed a right lower lobe mass and no other distant metastases. The patient underwent partial lobectomy and is now undergoing periodic follow-up. Strict observation is ongoing because the recurrence and metastasis occurred after a long period of follow-up [65]. No other distant metastases and no local recurrences were observed. Because of the possibility of primary site recurrence and lung metastasis, it is recommended that enhanced head and neck CTs and chest X-rays be obtained at intervals of 3–6 months.

Histopathologically, chondrosarcoma of the TMJ appears similar to chondrosarcoma of the head and neck or of other regions of the body [33, 46]. In our study, microscopic examination of sections stained with hematoxylin–eosin showed atypical chondrocytes exhibiting increased cellularity, pleomorphism, multinucleation and mitoses. Chondrosarcomas demonstrate proliferation of tumor cells within the chondroid matrix with focal calcification, as seen in Fig. 6. Chondrosarcoma is categorized into three subtypes (grades I, II, and III) according to nuclear size, cellularity, and frequency of mitosis [13]. Low-grade (grade I) chondrosarcoma has occasional binucleated cells and can show atypical cells, which can also be binucleated. Intermediate-grade (grade II) chondrosarcoma presents with a higher cellular population than grade I, with greater degree of nuclear atypia, hyperchromasia and nuclear size. The mitotic rate is low. High-grade (grade III) chondrosarcoma has significant areas of marked pleomorphism; large cells with nuclei that are more hyperchromatic, denser, and larger in size than those in grade II chondrosarcoma; occasional giant cells; and abundant necrosis. The mitotic rate is higher than in grade II chondrosarcoma [13].

The clinical behavior of chondrosarcoma is linked to its histopathologic grade [7]. The 5-year survival rates for grades I, II, and III chondrosarcomas were 90%, 81%, and 43% respectively. The 10-year survival rates were more variable, at 83%, 64%, and 29%, respectively. Metastasis was not observed in grade I chondrosarcoma, but it did occur in 10% of grade II chondrosarcomas and 71% of grade III chondrosarcomas [13]. The most common cause of death in chondrosarcoma is recurrence, not metastasis [33].

In a recent cohort study, the recurrence rate of chondrosarcoma in all parts of the body was 19%, and the recurrence rate of chondrosarcoma in the head and neck was 5% [78]. In the extremities, 45.7%, 34.3%, and 20%, of chondrosarcomas were grades I, II, and III, respectively. By grade, the recurrence rates of chondrosarcoma of the extremities were 11% (grade I), 12% (grade II), and 17% (grade III). In chondrosarcoma of the TMJ, the recurrence rate is lower than in chondrosarcomas of other areas of the body because most cases are low-grade, and relatively few cases with long-term follow-up have been reported. No definitive relationship has been found between histopathologic grade and local recurrence because such recurrence depends primarily on the adequacy of surgical therapy rather than tumor grade [47]. The most important factor in prognosis is surgical resectability [46, 66].

In our cases, immunohistochemical examination was carried out with antibodies against vimentin, S-100 protein, and Ki-67, for which most patients were positive (Fig. 6). Prior to this study, only 7 case reports of TMJ chondrosarcoma included immunostaining [7, 33, 34, 36, 43, 53, 79]. Excluding 1 case [53] that was included in the present study (case 5), S-100 was expressed in 5–35% of chondrocytes [7, 33, 36], and Ki-67 was expressed in 5–50% [33, 36, 43]. Immunohistochemical examination in the present study showed high expression of vimentin in all cases, and diffuse expression of S-100. Ki-67 was expressed in fewer than 5% of grade I chondrosarcomas, 10–20% of grade II chondrosarcomas, and more than 25% of grade III chondrosarcomas. This result was consistent with those in previous studies. Future immunohistochemical investigations of chondrosarcoma are necessary to achieve more accurate diagnoses.

This study is subject to limitations caused by the rarity of TMJ chondrosarcoma, which results in an insufficient number of cases for a robust statistical analysis. Among the 43 cases in which tumor grade was specified, a mere 3 cases were classified as high grade. Recurrence was reported in only 4 cases. Furthermore, the scarcity of cases with long-term follow-up necessitates caution in interpretation. Among the 47 cases included in this analysis, 41 had specified follow-up periods. Of these, only 15 cases were followed for more than 5 years. Notably, 1 case experienced recurrence 10 years post-surgery, although only 4 cases were observed for more than 10 years. Consequently, it is imperative to exercise caution when interpreting the findings of this study.

Conclusions

To diagnose chondrosarcoma arising in the TMJ, it is recommended to conduct a radiographic assessment comprising MRI, contrast-enhanced CT, and PET-CT, followed by confirmation through histopathological analysis via open biopsy. In terms of treatment, a wide surgical resection is necessary while taking care to the preserve the facial nerve. A conservative approach to the facial nerve is advantageous for optimal recovery outcomes. Nevertheless, a radical approach can be imperative to achieve complete mass excision. Reliable reconstructive surgery can be accomplished using a metal condyle prosthesis in conjunction with a vascularized free flap. If the tumor involves the glenoid fossa of the temporal bone or the temporomandibular joint disc, reconstruction of the glenoid fossa with a fossa implant is necessary. However, in an oncological context, glenoid fossa reconstruction is deemed unnecessary if those structures are unaffected by the tumor. Post-operative radiation therapy is required in cases involving surgical resection margin or when dealing with high-grade chondrosarcoma.