窦鑫 刘小燕 张利华

[Abstract]：Chondrosarcoma of temporal bone is a primary malignant bone tumor composed of chondrocytes and cartilage matrix. It is common for middle-aged and old people around 50 years old. We report CT and MRI appearances of a 64 year old man with chondrosarcoma of temporal bone that was proven by postoperative pathological examination. This article describes the imaging features of the tumor， which may help to know its characteristic of T2WI high signal， DWI low signal， ADC high signal.We further discuss disease characteristics， pathological characteristics， types， imaging features， differential diagnosis， treatment and prognosis， conclusion .

[Key words] Temporal bone Chondrosarcoma Pathology Imaging Prognosis

【中圖分类号】R4 【文献标识码】A 【文章编号】1673-9026（2021）11-02

1.Introduction

Chondrosarcomas are malignant tumors that occur in chondrocytes. Most of them were found in long bones， pelvis and scapula， and in the head and neck， accounting for 5% ～ 12%[1]. The primary chondrosarcomas of the skull base account for about 1.5‰[2] of all skull base tumors. However， the primary chondrosarcomas of the temporal bone are very rare.It has been suggested that chondrosarcomas arise from fetal cartilage remains or multipotent mesenchymal cells are involved in tumorigenesis[3]. This article reports the imaging features of a case of well-differentiated chondrosarcoma of the temporal bone， and literature review， in order to deepen the understanding of this disease.

2. Case presentation

A 64-year-old man， right ear intermittent discharge， deafness， tinnitus history 10 years， no special treatment， the main cause of intermittent headache， dizziness 20 days in hospital. Physical examination： old abscess in the right external auditory canal， occasionally a small amount of purulent leakage.

After the hospital examination，the CT findings of the temporal bone showed that the right temporal bone and the large wing of the sphenoid bone were corroded like worms. The lesion is adjacent to the temporal lobe and extends downward to the medial pterygoid muscle.The lesion involved the right inner ear， middle ear， external auditory meatus and temporomandibular joint （Fig. 1）. The MRI findings of the right temporal brain were 3.4 * 6.1 * 6.1 cm in size， T1WI low signal intensity， T2WI mixed high signal intensity， FLAIR equal/slightly high signal intensity， DWI low signal intensity， ADC high signal intensity， and enhanced scan shows significant enhancement. The lesion grew to the right infratemporal fossa and penetrated deep into the medial pterygoid muscle with destruction of bone （Fig. 2）. The final diagnosis was eosinophilic granuloma of the right temporal region. Surgical findings： part of the right temporal bone was completely eroded by the lesion， part of the lesion was exposed and yellow in color. The lesion was excised in several parts， showing that the blood supply of the lesion was abundant， the petrous bone is partly eroded and a small portion of the lesion penetrates the dura and grows into the subdural space. It was found that the anterior part of the lesion was located in the infratemporal fossa， and the posterior part grew into the extradural part of the middle fossa. Postoperative follow-up： no recurrence or metastasis was observed for two years. Pathological findings： it appears as grey-red nodular broken tissue with grey-white cut surface and total volume of 7cm* 4cm * 3cm. Microscopically， a large number of chondrocytes with slightly heterogeneous nuclei are seen. Immunohistochemical： S-100（+）， D2-40（+）， R132H（+）. Pathological diagnosis： well-differentiated chondrosarcoma of right temporal bone.

3.Discussion

3.1 General characteristics

Chondrosarcomas are most common in the 40 to 70 years old[4]， and some literature reports have reported that they often occur in the 50 years old or so[5]， and usually occur in sphenoid fissure， occipital fissure， sphenoid scale fissure， pore fissure near oblique fissure and so on[6]， the temporal bone is rare. Chondrosarcomas of the temporal bone generally grow slowly， and may not show any symptoms when the tumor mass is small in the early stage. When the tumor mass increases to a certain extent， it presents local mass swelling and corresponding structural and functional disorders [7-8]， the length and wide range of lesions usually make it difficult to determine the exact primary site of the tumor. It is easy to grow into adjacent tissues， so it is easy to recur， but with less metastasis. There are no reports of distant metastasis from chondrosarcoma of the temporal bone.

3.2 Pathological characteristics

Chondrosarcomas were pale translucent rotten cartilage-like， light yellow fish flesh-like， gray-red nodules， lobulated masses， medium soft texture， the cut surface was mostly gray-white. Microscopically， the tumor is lobulated， with sheets of chondroid cells varying in size and shape， with mild atypia， and calcification and ossification of the stroma. Immunohistochemistry showed that both cytoplasm and nucleus of tumor cells expressed S-100， cytoplasm expressed D2-40 and Isocitrate dehydrogenase 1.

3.3 Types

Histologically， it can be divided into three subtypes： well-differentiated chondrosarcoma， myxoid chondrosarcoma and mesenchymal chondrosarcoma， of which the most common is well-differentiated chondrosarcoma.

Well-differentiated chondrosarcoma consists mainly of a large number of chondrocytes， common calcification and ossification. Myxoid chondrosarcoma： because the tumor cell stroma is mainly for maid named. Mesenchymal chondrosarcoma： because the tumor is composed of short fusiform mesenchymal cells and highly differentiated chondrocytes [9] .

3.4 Image characteristics

CT findings： slightly low or isodensity irregular soft tissue mass with clear margin. Some of them showed calcification. Some of them were considered to be the important pathologic and imaging features of chondrosarcoma. Most of the lesions involved the skull base sutures or bone fracture joint. The surrounding bone had no sclerotic edge， and the edge was irregular. Non-uniform enhancement on the enhanced scan. The DSA examination showed no obvious blood supply artery.

MRI findings： compared with the adjacent gray matter， T1WI showed low signal intensity， T2WI showed uneven high signal intensity， FLAIR showed equal or slightly high signal intensity， DWI showed low signal intensity， ADC showed high signal intensity， the average ADC value was about 2.1 x 10-3 mm2/ s， enhanced and delayed enhancement， TIC curve increased obviously.Some of the tumors showed rosette-like or separate enhancement due to the rich blood vessels in the periphery and septa. MRS： NAA peak was absent/very low， and the ratio of Cho peak to Cr peak is less than 1[10]

Histopathologic basis： high signal intensity of T2 indicates that the tumor is composed of chondrocytes and cartilage matrix with long T2 relaxation time[11]. The high ADC values were presumed to be related to the presence of a large amount of mucus and cartilage matrix in the tumor， and the low density of tumor cells and the unrestricted movement of water molecules[10]. Delayed enhancement may be related to the presence of a large amount of mucin matrix within the tumor and the role of mucin in the absorption of contrast media [12].

3.5 Differential diagnosis of eosinophilic granuloma

Eosinophilic granuloma is a benign bone tumor-like lesion with reticuloendothelial cell proliferation. It accounts for about 60% of Langerhans histiocytes [13]. From the board， frontal bone is more common， temporal bone is rare. Eosinophilic granuloma of the temporal bone occurs at the age of 1～4 years. The ratio of males to females is approximately 2：1[14]. It is composed mainly of Langerhans cells and is infiltrated with numerous eosinophils， lymphocytes， plasma cells， and neurophils. Immunohistochemistry CD1a （+）， S-100 （+）

CT findings： the appearance of irregular perforation-like bone destruction， complete destruction of the inner and outer plates leading to oblique sign or bilateral sign [15] ， the destruction scope of the outer plate is larger than that of the inner plate， the edge of the destruction area is clear and not smooth， and slightly higher soft tissue filling can be seen， the soft tissue shadow was more than skull destruction when the lesion broke through skull inner and outer plate， and it was dumbbell shape when protruded to both sides.

MRI findings： isointense on T1WI， moderately hyperintense on T2WI， high/slightly hyperintense on Flair， medium/slightly hyperintense on DWI， mild to moderate inhomogeneous enhancement on enhanced scan， intracranial growth of the lesion， invasion and compression of the dura mater and brain tissue， meningeal tail sign seen on enhanced scan [16]. Eosinophilic granulomas are very different from chondrosarcomas by their general features and imaging findings.

3.6 Treatment and prognosis

As with other chondrosarcomas of the temporal bone， chondrosarcomas are not sensitive to radiotherapy and chemotherapy [4] . Therefore， surgical resection of the tumor is the main treatment. Because of its invasive growth to adjacent tissues， it is difficult to remove completely and has a high recurrence rate. In recent years， some foreign literature suggests that postoperative radiotherapy and chemotherapy can improve the local control rate [17-18] . The prognosis of the patients was related to the degree of differentiation of the tumor， and the prognosis was better in those with high differentiation; 15% of the chondrosarcomas had distant metastasis， but no distant metastasis of the chondrosarcomas of the temporal bone was reported[6]. For the first two years， physical examination， chest x-ray and pathological changes were carried out every 6-12 months， then annually. Local recurrences occur and extensive excision may be continued if resectable[19].

4.Conclusion

If HRCT showed multi-bone worm erosion in skull base， dot-like and flake calcification were found in different areas， and heterogeneous hyperintense lesions were found on T2WI， and the enhancement was obviously enhanced. The ADC value was about （1.96 ± 0.1） x 10-3mm2/ s [10]， the ratio of Cho Peak to CR peak is less than 1， so the possibility of highly differentiated chondrosarcoma should be considered.

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作者简介： First author： 窦鑫 E-mail： 2223169080@qq.com

Corresponding author： 张利华 副主任医师 E-mail： hpzlhfsk@126.com