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Erschienen in: World Journal of Surgical Oncology 1/2017

Open Access 01.12.2017 | Research

Epidemiological characteristics of primary spinal osseous tumors in Eastern China

Erschienen in: World Journal of Surgical Oncology | Ausgabe 1/2017

Abstract

Background

Primary spinal osseous tumors are rare, yet they represent a difficult treatment paradigm because of the complexities of tumor resection and significant resistance to chemotherapy and radiation therapy. The geographic distribution of primary spinal osseous tumors throughout the world appears to be quite variable, with a very low incidence reported in Asian countries.

Methods

Data on 1209 cases of primary spinal osseous malignant and benign tumor cases diagnosed during the 20-year period of 1995 through 2015 in eastern China were analyzed.

Results

In 780 cases (64.5%), the lesion was benign and in 429 (35.5%) was malignant. The commonest primary malignant tumors were chordoma (9.8% of all cases) followed by plasma cell myeloma (8.5% of all cases). The most common benign tumor was hemangioma (28.1% of all cases) followed by giant cell tumor of bone (15.7% of all cases) and osteoblastoma (4.4% of all cases). The benign tumors affected men in 33.8% of cases and women in 30.7% of cases, the malignant tumors affected men in 23.7% of cases and women in 11.8%. The mean age (mean ± SD) in the benign group was 34.7 ± 19.8 years and in the malignant group was 47.4 ± 16.5 years. Related symptoms were pain (54.4%), radiculopathy (12.9%), cord compression (9.2%), mass (5.7%), pathological fracture (4.7%), deformity (2.1%), and weight loss (1.9%). The anatomical locations included almost every vertebra of the spine. The thoracic spine (38.1%) was the most common location of the tumors, followed by the cervical spine (27.4%) and lumbar spine (18.4%).

Conclusions

Compared with other similar series reported in the literature from the other countries, our results obtained in a developing country were different in some degree. This large series of primary spinal osseous tumors may reflect fairly well their real incidence and provide a sufficiently detailed perspective on epidemiologic studies of primary spinal osseous tumors in eastern China.
Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​s12957-017-1136-1) contains supplementary material, which is available to authorized users.

Background

Primary spinal osseous tumors are uncommon; previous reports showed that spinal osseous tumors were comprising 6 ~ 10% of all bone tumors [15]. Little was known about the etiology of spine osseous tumors. Published case reports focused on spine neoplasm usually had a limited case number, and few reports described epidemiological characteristics of spine osseous tumors. However, it is important to understand the etiology of spinal osseous tumors and information regarding the epidemiology of primary spine osseous tumors.
The present study performed an epidemiological analysis of 1209 consecutive tumors of osseous spine registered in 3 collaborating state bone tumor database (Eastern China) between 1995 and 2015. To our knowledge, the present study is the first report of epidemiological data concerning spinal osseous tumors in Asian population. Our findings showed that epidemiological features of primary spinal osseous tumors in xanthoderm, with respect to relative frequency and distribution of the various histologic types, as well as the clinical data, and compare the results with other epidemiological findings from different geographic locations around the world, which could provide valuable clues for epidemiology of primary spine osseous tumors in Asian.

Methods

Data sources

Data for this study were obtained from Bone Tumors and Nervous System Tumors Biobank of Shanghai (BT&NSTBS), Bone Tumor Sample Databases and Digital Information Platform of Shanghai (BTSD&DIPS), and Shanghai Biobank Network of Common Human Tumor Tissue (SBNCHTT). One thousand two hundred nine cases of spinal osseous tumors registered in abovementioned 3 database between 1995 and 2015 were selected for this study. Data collected for each patient included personal information such as name, age, sex, anatomical site of the tumor, and clinical and histological diagnoses. In the case of recurrent tumors, the histological appearance of the original and the recurrent tumors was compared and was considered as only one case. The diagnoses were re-evaluated according to the criteria suggested for the 2013 WHO histological classification [6].

Statistics

SPSS17.0 software (SPSS Inc., Chicago, IL) was used for statistical analysis of experimental data. Descriptive statistics was performed to calculate the frequency and percentages of variables mentioned before. Age was stratified into various groups at 10-year intervals.

Results

The histological types of the spinal osseous tumors are listed in Table 1 and Fig. 1. Of these, 64.5% (780 cases) were benign and 35.5% (429 cases) were malignant, The most common histological type of benign tumors was hemangioma accounting for 28.1% of all tumors (340 cases), followed by giant cell tumor (15.7%; 190 cases), osteoblastoma (4.4%; 53 cases), aneurysmal bone cyst (2.9%; 35 cases), eosinophilic granuloma (3.9%; 47 cases), osteochondroma (3.8%; 46 cases), solitary bone cyst (2.1%; 25 cases), osteoid osteoma (1.4%; 17 cases), fibroma (1.3%; 16 cases), lipoma (0.6%; 7 cases), and fibrous dysplasia (0.3%; 4 cases). Of malignant tumors, chordoma was the most common malignant tumor (9.8% of all tumors, 119 cases), followed by plasma cell myeloma multiple myeloma (8.5%,103 cases), chondrosarcoma (5.2%, 63 cases), malignant lymphoma (4.5%; 54 cases), malignant neurilemmoma (2.5%; 30 cases), primitive neural ectodermal tumor (PNET)\Ewing’s sarcoma (1.4%; 17 cases), malignant fibrous histiocytoma (1.3%; 16 cases), osteosarcoma (1.1%; 13 cases), and other sarcomas such as angiosarcoma, fibrosarcoma, liposarcoma, and leiomyosarcoma (less than 1%).
Table 1
Frequency, age, and gender distribution of primary spine osseous tumors
Type of tumor
Number (%)
Male
Female
Male vs female
Age range (years)
Mean ± SD (age)
No.
%a
No.
%a
No.
%a
Male
Female
Total
Benign tumors
780
64.5
409
33.8
371
30.7
52.4 vs 47.6%
9–79
33.7 ± 19.2
35.9 ± 20.6
34.7 ± 19.8
Hemangioma
340
28.1
174
14.4
166
13.7
51.2 vs 48.8%
12–79
47.1 ± 14.3
51.5 ± 12.9
49.2 ± 13.7
Giant cell tumor
190
15.7
91
7.5
99
8.2
47.9 vs 52.1%
15–66
34.5 ± 11.0
32.9 ± 12.1
33.6 ± 11.5
Eosinophililc granuloma
47
3.9
36
3.0
11
0.9
76.6 vs 23.4%
10–56
23.7 ± 14.3
29 ± 17.6
23.7 ± 14.7
Osteoblastoma
53
4.4
28
2.3
25
2.1
52.8 vs 47.2%
9–54
32.6 ± 10.5
26.5 ± 15.0
28.7 ± 13.2
Fibroma
16
1.3
10
0.8
6
0.5
62.5 vs 37.5%
26–76
41.6 ± 18.2
50.5 ± 15.0
44.9 ± 17.1
Osteoid osteoma
17
1.4
8
0.7
9
0.7
47.1 vs 52.9%
16–67
31.2 ± 22.3
39.0 ± 16.8
34.6 ± 19.8
Osteochondroma
46
3.8
28
2.3
18
1.5
60.9 vs 39.1%
13–64
34.0 ± 16.6
38.7 ± 20.8
36.1 ± 18.4
Solitary bone cyst
25
2.1
8
0.7
17
1.4
32.0 vs 68.0%
15–64
29.5 ± 15.2
48.8 ± 11.9
41.1 ± 16.2
Lipoma
7
0.6
5
0.4
2
0.2
71.4 vs 28.6%
23–63
41.8 ± 16.5
31.0 ± 11.3
38.7 ± 15.2
Aneurysmal bone cyst
35
2.9
19
1.6
16
1.3
54.3 vs 45.7%
10–62
25 ± 12.5
36.4 ± 15.3
30.4 ± 14.8
Fibrous dysplasia
4
0.3
2
0.2
2
0.2
50.0 vs 50.0%
25–32
29.5 ± 3.5
27 ± 2.8
28.3 ± 3.0
Malignant tumors
429
35.5
286
23.7
143
11.8
66.7 vs 33.3%
8–81
48.3 ± 16.7
46.3 ± 16.3
47.4 ± 16.5
PNET/ Ewing’s sarcoma
17
1.4
9
0.7
8
0.7
52.9 vs 47.1%
11–46
26 ± 13.3
25.8 ± 7.9
25.9 ± 10.9
Chordoma
119
9.8
79
6.5
40
3.3
66.4 vs 33.6%
27–81
56.6 ± 15.0
53.3 ± 13.3
55.5 ± 14.1
Malignant fibrous histiocytoma
16
1.3
11
0.9
5
0.4
68.8 vs 31.2%
29–67
51 ± 14.5
50.7 ± 1.9
50.9 ± 11.3
Liposarcoma
1
0.0
1
0.0
0
0.0
NA
44
44
NA
44
Osteosarcoma
13
1.1
5
0.4
8
0.7
38.5 vs 61.5%
14–60
40.2 ± 21.0
25.8 ± 11.7
33.6 ± 18.2
Angiosarcoma
10
0.8
7
0.6
3
0.2
70.0 vs 30.0%
36–73
54.3 ± 11.3
45.0 ± 7.8
51.5 ± 10.9
Malignant neurilemmoma
30
2.5
15
1.2
15
1.2
50.0 vs 50.0%
8–71
40.4 ± 16.3
50.3 ± 12.1
45.3 ± 15.0
Plasma cell myeloma
103
8.5
75
6.2
28
2.3
72.8 vs 27.2%
10–76
49.8 ± 15.3
57.2 ± 12.6
52.0 ± 14.8
Malignant lymphoma
54
4.5
30
2.5
24
2.0
55.6 vs 44.4%
10–77
47.2 ± 21.0
46.5 ± 18.7
46.9 ± 19.6
Leiomyosarcoma
1
0.0
1
0.0
0
0.0
NA
55
55
NA
55
Chondrosarcoma
63
5.2
52
4.3
11
0.9
82.5 vs 17.5%
20–68
46.1 ± 14.5
37.3 ± 14.8
44.0 ± 14.7
Fibrosarcoma
2
0.2
1
0.0
1
0.0
50.0 vs 50.0%
30–61
61
30
45.5 ± 21.9
Total
1209
100
695
57.5
514
42.5
57.5 vs 42.5%
8–81
39.1 ± 16.9
39.6 ± 16.7
39.3 ± 16.8
NA not applicable
a% in all tumors
Of the benign tumors, 20.5% were situated in the cervical spine, 26.1% in the thoracic spine, 12.0% in the lumbar spine, and 5.4% in the sacral spine. Of the malignant tumors, 6.9% were situated in the cervical spine, 12.0% in the thoracic spine, 6.3% in the lumbar spine, and 10.7% in the sacral spine. Of all tumors, 27.4% were situated in the cervical spine, 38.1% in the thoracic spine, 18.4% in the lumbar spine, and 16.1% in the sacral spine (Table 2).
Table 2
Distribution of spine osseous tumors by location
Type of tumor
Cervical spine
Thoracic spine
Lumbar spine
Sacral spine
Totals
No.
%
No.
%
No.
%
No.
%
No.
%
Benign tumors
257
20.5
328
26.1
151
12.0
68
5.4
804(780)a
64.0
Hemangioma
104
8.3
149
11.7
86
6.8
11
0.9
350(340)a
27.9
Giant cell tumor
44
3.5
87
6.9
23
1.8
36
2.9
190
15.1
Eosinophililc granuoma
20
1.6
22
1.6
5
0.4
0
0.0
47
3.7
Osteoblastoma
17
1.4
30
2.4
5
0.4
1
0.0
53
4.2
Fibroma
17
1.4
5
0.4
5
0.4
3
0.2
30(16)
2.4
Osteoid osteoma
12
1.0
2
0.2
3
0.2
0
0.0
17
1.4
Osteochondroma
21
1.7
12
1.0
11
0.9
2
0.2
46
3.7
Solitary bone cyst
8
0.6
2
0.2
5
0.4
10
0.8
25
2.0
Lipoma
5
0.4
1
0.0
0
0.0
1
0.0
7
0.6
Aneurysmal bone cyst
9
0.7
16
1.3
6
0.5
4
0.3
35
2.8
Fibrous dysplasia
0
0.0
2
0.2
2
0.2
0
0.0
4
0.3
Malignant tumors
87
6.9
151
12.0
80
6.3
134
10.7
452(429) a
36.0
PNET/Ewing’s sarcoma
1
0.0
4
0.3
9
0.7
3
0.2
17
1.4
Chordoma
29
2.3
5
0.4
5
0.4
80
6.4
119
9.5
Malignant fibrous histiocytoma
0
0.0
8
0.6
3
0.2
5
0.4
16
1.3
Liposarcoma
0
0.0
0
0.0
0
0.0
1
0.0
1
0.0
Osteosarcoma
2
0.2
6
0.6
0
0.0
5
0.4
13
1.0
Angiosarcoma
1
0.0
12
1.0
4
0.3
0
0.0
17(10)
1.4
Malignant neurilemmoma
4
0.3
4
0.3
12
1.0
12
1.0
32(30) a
2.5
Plasma cell myeloma
27
2.1
50
4.0
26
2.1
9
0.7
112(103)
8.9
Leiomyosarcoma
0
0.0
0
0.0
0
0.0
1
0.0
1
0.0
Malignant lymphoma
9
0.7
26
2.1
18
1.4
6
0.5
59(54)a
4.7
Chondrosarcoma
14
1.1
36
2.9
2
0.2
11
0.9
63
5.0
Fibrosarcoma
0
0.0
0
0.0
1
0.0
1
0.0
2
0.2
Total
344
27.4
479
38.1
231
18.4
202
16.1
1256(1209) a
100
aMore than two anatomical position involved in the same patient
In our series, most tumors with different histological types showed a similar distribution in males and females, although chordoma (119 cases, M:F = 2:1), plasma cell myeloma (103 cases, M:F = 2.7:1), chondrosarcoma (63 cases, M:F = 4.7:1), and eosinophilic granuoma (47 cases, M:F = 3.3:1) affected more frequently males than females (Table 3). From a total of 1209 bone tumors, the mean age (mean ± SD) was 39.3 ± 16.8 years (range, 8–81 years), 57.5% (695 cases) of the tumors occurred in males and 42.5% (514cases) in females, with a mean age (mean ± SD) of 39.1 ± 16.9 and 39.6 ± 16.7 years. The mean age (mean ± SD) of benign tumors group was 34.7 ± 19.8 years (range, 9–79 years). Of 780 benign tumors, 409 cases (33.8% of all cases) occurred in males and 371 cases (30.7% of all cases) in females (M:F = 1.1:1), with a mean age (mean ± SD) of 33.7 ± 19.2 and 35.9 ± 20.6 years. The mean age (mean ± SD) of malignant tumors group was 47.4 ± 16.5 years (range, 8–81 years). Of 429 malignant tumors, 286 cases (23.7% of all cases) occurred in males and 143 cases (11.8% of all cases) in females, with a mean age (mean ± SD) of 48.3 ± 16.7 and 46.3 ± 16.3 years. The most commonly affected age group for benign tumors was the 31- to 40-year-old group (14.3%; 173 cases), followed by the 51- to 60-year-old group (11.4%; 138 cases), and by the 41- to 50-year-old group (11.2%; 136 cases). The most common age group affected by malignant bone tumors was the 41- to 50-year-old group (7.9%; 95cases), followed by the 61- to 70-year-old group (6.8%; 82 cases). A similar frequency was observed in the 31- to 40-year-old group (6.7%; 81cases) and the 51- to 60-year-old group (6.5%; 79 cases).
Table 3
Age distribution of patients with primary spine osseous tumors (years)
Type of tumor
0–10
11–20
21–30
31–40
41–50
51–60
61–70
71–80
81–90
Total no. (%)
No. (%)
No. (%)
No. (%)
No. (%)
No. (%)
No. (%)
No. (%)
No. (%)
No. (%)
Benign tumors
14(1.2%)
102(8.4%)
122(10.1%)
173(14.3%)
136(11.2%)
138(11.4%)
76(6.3%)
19(1.6%)
0(0.0%)
780(64.5%)
Hemangioma
1(0.0%)
14(1.2%)
18(1.5%)
62(5.1%)
78(6.5%)
96(7.9%)
53(4.4%)
18(1.5%)
0(0.0%)
340(28.1%)
Giant cell tumor
0(0.0%)
27(2.2%)
50(4.1%)
62(5.1%)
32(2.6%)
11(0.9%)
8(0.7%)
0(0.0%)
0(0.0%)
190(15.7%)
Eosinophililc granuloma
3(0.2%)
23(1.9%)
9(0.7%)
5(0.4%)
2(0.2%)
5(0.4%)
0(0.0%)
0(0.0%)
0(0.0%)
47(3.9%)
Osteoblastoma
6(0.5%)
11(0.9%)
14(1.2%)
11(0.9%)
5(0.4%)
6(0.5%)
0(0.0%)
0(0.0%)
0(0.0%)
53(4.4%)
Fibroma
0(0.0%)
0(0.0%)
4(0.3%)
4(0.3%)
2(0.2%)
2(0.2%)
3(0.2%)
1(0.0%)
0(0.0%)
16(1.3%)
Osteoid osteoma
0(0.0%)
5(0.4%)
3(0.2%)
2(0.2%)
2(0.2%)
3(0.2%)
2(0.2%)
0(0.0%)
0(0.0%)
17(1.4%)
Osteochondroma
2(0.2%)
12(1.0%)
8(0.7%)
9(0.7%)
5(0.4%)
5(0.4%)
5(0.4%)
0(0.0%)
0(0.0%)
46(3.8%)
Solitary bone cyst
0(0.0%)
2(0.2%)
3(0.2%)
5(0.4%)
6(0.5%)
6(0.5%)
3(0.2%)
0(0.0%)
0(0.0%)
25(2.1%)
Lipoma
0(0.0%)
0(0.0%)
2(0.2%)
3(0.2%)
1(0.0%)
1(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
7(0.6%)
Aneurysmal bone cyst
2(0.2%)
8(0.7%)
9(0.7%)
8(0.7%)
3(0.2%)
3(0.2%)
2(0.2%)
0(0.0%)
0(0.0%)
35(2.9%)
Fibrous dysplasia
0(0.0%)
0(0.0%)
2(0.2%)
2(0.2%)
0(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
4(0.3%)
Malignant tumors
5(0.4%)
17(1.4%)
36(3.0%)
81(6.7%)
95(7.9%)
79(6.5%)
82(6.8%)
32(2.6%)
2(0.2%)
429(35.5%)
PNET/Ewing’s sarcoma
0(0.0%)
5(0.4%)
7(0.6%)
3(0.2%)
2(0.2%)
0(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
17(1.4%)
Chordoma
0(0.0%)
0(0.0%)
3(0.2%)
17(1.4%)
27(2.2%)
23(1.9%)
32(2.6%)
15(1.2%)
2(0.2%)
119(9.8%)
Malignant fibrous histiocytoma
0(0.0%)
0(0.0%)
2(0.2%)
0(0.0%)
5(0.4%)
6(0.5%)
3(0.2%)
0(0.0%)
0(0.0%)
16(1.3%)
Liposarcoma
0(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
1(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
1(0.0%)
Osteosarcoma
0(0.0%)
6(0.5%)
2(0.2%)
0(0.0%)
3(0.2%)
2(0.2%)
0(0.0%)
0(0.0%)
0(0.0%)
13(1.1%)
Angiosarcoma
0(0.0%)
0(0.0%)
0(0.0%)
2(0.2%)
3(0.2%)
3(0.2%)
1(0.0%)
1(0.0%)
0(0.0%)
10(0.8%)
Malignant neurilemmoma
1(0.0%)
1(0.0%)
1(0.0%)
9(0.7%)
8(0.7%)
5(0.4%)
4(0.3%)
1(0.0%)
0(0.0%)
30(2.5%)
Plasma cell myeloma
2(0.2%)
0(0.0%)
3(0.2%)
17(1.4%)
26(2.2%)
22(1.8%)
24(2.0%)
9(0.7%)
0(0.0%)
103(8.5%)
Leiomyosarcoma
0(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
1(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
1(0.0%)
Malignant lymphoma
2(0.2%)
3(0.2%)
6(0.5%)
9(0.7%)
12(1.0%)
8(0.7%)
8(0.7%)
6(0.5%)
0(0.0%)
54(4.5%)
Chondrosarcoma
0(0.0%)
2(0.2%)
11(0.9%)
24(2.0%)
8(0.7%)
9(0.7%)
9(0.7%)
0(0.0%)
0(0.0%)
63(5.2%)
Fibrosarcoma
0(0.0%)
0(0.0%)
1(0.0%)
0(0.0%)
0(0.0%)
0(0.0%)
1(0.0%)
0(0.0%)
0(0.0%)
2(0.2%)
Total
19(1.6%)
119(9.8%)
158(13.1%)
254(21.0%)
231(19.1%)
217(17.9%)
158(13.1%)
51(4.2%)
2(0.2%)
1209(100%)
As the most common presenting symptom, pain was found in 54.4% (658/1209) of patients, affecting 35.0% (273/780) of the benign and 89.7% (385/429) of the malignant tumors. Mass (swelling) was seen in 4.0% (31/780) of benign tumors and 8.9% (38/429) of malignant tumors. One hundred fifty-six patients (12.9%) had the symptoms of radiculopathy. Of all cases, 9.2% (111/1209) of patients had signs of subtotal or complete cord compression. The cord compression symptoms included motor weakness (8.2%, 99/1209), sphincter dysfunction (0.7%, 8/1209), and paraplegia (0.3%, 4/1209). Pathological fracture was found in 4.7% (57/1209) of patients. Other symptoms included deformity (2.1%, 25/1209) and weight loss (1.9%, 23/1209) (Table 4).
Table 4
First presenting features when diagnosed with primary spine osseous tumors
 
Total no. of case
Pain
Mass (swelling)
Radiculopathy
Motor weakness
Sphincter dysfunction
Paraplegia
Pathological fracture
Deformity
Weight loss
Benign tumors
780
273(35.0%)
31(4.0%)
72(9.2%)
45(5.8%)
0
0
23(2.9%)
4(0.5%)
7(0.9%)
Hemangioma
340
18
2
1
0
0
0
0
0
1
Giant cell tumor
190
169
11
65
43
0
0
21
3
2
Eosinophililc granuloma
47
35
17
4
1
0
0
0
0
1
Osteoblastoma
53
2
0
0
0
0
0
0
0
0
Fibroma
16
4
0
0
0
0
0
0
0
0
Osteoid osteoma
17
3
0
0
0
0
0
0
0
1
Osteochondroma
46
13
0
0
0
0
0
0
0
1
Solitary bone cyst
25
2
1
0
0
0
0
0
0
0
Lipoma
7
0
0
0
0
0
0
0
0
0
Aneurysmal bone cyst
35
25
0
1
1
0
0
1
0
1
Fibrous dysplasia
4
2
0
1
0
0
0
1
1
0
Malignant tumors
429
385(89.7%)
38(8.9%)
84(19.9%)
54(12.6%)
8(1.9%)
4(0.9%)
34(7.9%)
21(4.9%)
16(3.7%)
PNET/Ewing’s sarcoma
17
16
1
0
0
0
0
1
0
0
Chordoma
119
101
15
43
35
7
2
12
6
3
Malignant
fibrous histiocytoma
16
13
10
0
0
0
0
1
0
0
Liposarcoma
1
1
0
1
0
0
0
1
0
0
Osteosarcoma
13
13
2
 
0
0
0
0
0
0
Angiosarcoma
10
9
1
1
0
0
0
0
0
0
Malignant neurilemmoma
30
28
0
28
15
1
0
0
0
0
Plasma cell myeloma
103
92
0
7
2
2
2
19
15
13
Leiomyosarcoma
54
51
7
3
1
0
0
0
0
0
Malignant lymphoma
1
1
0
0
0
0
0
0
0
0
Chondrosarcoma
63
58
0
0
0
0
0
0
0
0
Fibrosarcoma
2
2
2
1
1
0
0
0
0
0
Total
1209
658(54.4%)
69(5.7%)
156(12.9%)
99(8.2%)
8(0.7%)
4(0.3%)
57(4.7%)
25(2.1%)
23(1.9%)
In our series, 398 cases with malignant tumors and 187 cases with benign tumors undergone surgery. Two hundred seventy-one cases with malignancies received chemotherapy. Thirty-four cases with malignant tumors were given radiotherapy. And other treatments were performed to 6 malignant cases and 35 benign cases respectively (Additional file 1: Table S1).

Discussion

Primary bone tumors of the spine are representing only less than 10% of all bone neoplasms. Available reports on the epidemiologic features of primary osseous spine tumors were mostly among Americans and Europeans [711]. To our knowledge, the present report represents epidemiologic features based the largest series of spinal osseous tumors from Asian. However, there are some differences of epidemiological characteristics in our study and previous reports (Table 5) [8, 10]. In Kelley’s series [10], 23.02% tumors were benign and 76.98% tumors were malignant, plasma cell myeloma was the most common primary malignant tumor, accounting for 26%, followed by chordoma (22.22%) and osteosarcoma (9.52%). Osteoblastoma (5.56%) was the most common benign tumor, followed osteoclastoma (0.79%) and aneurysmal bone cyst (0.79%). In our series, benign tumors comprised 64.5% of primary tumors. The most frequent benign was hemangioma (28.1%), followed by giant cell tumor (15.7%) and osteoblastoma (4.4%). The most frequent malignant was chordoma (9.8%), followed by plasma cell myeloma (8.5%) and chondrosarcoma (5.2%). These findings were not consistent with results from previous studies based in Caucasian, which would be influenced by geographical and racial variations in different reports.
Table 5
World literature of population-based studies on the epidemiology of primary spine osseous tumor
 
This study
Simon P. Kelley
S. Boriani
Author’s country
China
UK
Italy
Year of publication
2016
2007
1995
Period of study
1995–2015 (20 years)
1958–2000 (42 years)
1946–1992 (46 years)
No. of cases
1209
127
366
Gender
Male: 695 Female:514
Male: 66 Female:61
Not reported
Predominant presenting symptom
Pain
Pain
Not reported
Percentage of benign tumors
64.5%
22.8%
56.8%
Percentage of malignant tumors
35.5%
77.2%
43.2%
Most common type of benign tumors
Hemangioma
Osteoblastoma (7/127)
Eosinophilic granuloma
Most common type of malignant tumors
Chordoma
Plasma cell myeloma
Plasma cell myeloma
Most common segment of spine affected
Thoracic spine (479/1256)a
Thoracic spine (48/127)
Lumbar spine (181/366)
Mean age at presentation (range)
39.3 ± 16.8 (range 8–81 years)
42 (range 7–76 years)
Not reported
aMore than two anatomical position involved in the same patient
As the most frequent benign primary spine osseous tumor in present study, hemangioma was accounting for approximately one third of all primary tumors. During the past 20 years (1995–2015), 340 (28.1% of all cases) cases of spinal hemangioma were diagnosed, and 350 vertebrae were involved. This incidence of spinal hemangioma was significantly higher than that in other country [12], which suggested different epidemiologic features of spinal hemangioma in Asians. Giant cell tumor (GCT) of bone was considered a benign osteolytic tumor with variable aggressiveness and accounted for approximately 5% of all bone tumors [4, 13, 14]. In our study, GCTs accounted for 15.7% of spine osseous lesions, this incidence was markedly higher than that reported in other studies [1519]. Almost of GCTs occurred in the second to fourth decades, with a slight female predilection (M:F = 1:1.1) in the present series. The female predilection of GCT is supported by the earlier reports [17, 2022]. Furthermore, GCTs also showed predilection for the thoracic vertebra of spine in our study, which is not in accordance with other reports [19, 23]. Osteoblastoma was the third most common benign tumor in our study, with a relative frequency of 4.4% which was higher compared with the previous report [24]. In Herman M. Kroon’s and Richard A. Mcleod’s reports [25, 26], osteoblastoma obviously affected more males than females (64:34 and 87:36 respectively). In our study, we only observed a slight male predilection (M:F = 1:1.1). The most involved location was the thoracic spine, which is consistent with those reported from Europe and America [27, 28].
Chordoma was the most common malignant tumor which occurred more in males than in females in the present study. We found a significant predilection for males (M:F = 79:40), in agreement with reports by S Boriani (M:F = 37:15) [29], Silvia Stacchiotti (M:F = 91:47) [30], and Johannm Bjornsson (M:F = 27:13) [31]. It is worth noting that female preponderance (17:22) of chordoma was reported in Sweden [32]. In our series, chordomas were typically seen in adults and elderly, tended to occur in the sacrum (9.5%, 119 cases), which is consistent with the previous reports. In the present study, plasma cell myeloma accounted for 8.5% (103 cases) of all cases, representing the second most frequent primary malignant osseous tumor of spine, and often occurring in thoracic spine (4.0%, 50 vertebrae were involved). All plasma cell myeloma cases were found in the 4th–7th decade of life with a male predominance (M:F = 2.7:1). Previous studies reported that chondrosarcoma accounted for 3–12% of all spine primary tumors [3336]. In S Boriani’s report, the lumbar spine was the most frequently involved location (15/22, 68%) [33]. However, in the present study, thoracic spine was the most common location involved with chondrosarcoma (2.9%, 36 cases), and only 2 cases were observed in the lumbar spine. Most patients commonly encountered chondrosarcoma after the age of 20, with a great male predilection (M:F = 4.7:1).
Surgery is the first choice for the pain and neurological symptoms caused by spine tumors. Surgery can completely or partly alleviate tumor compression to the spinal cord, establish a tumor-free solid spine and relieve pain. In primary malignant tumors of the spine, total/partial laminectomy, total/partial vertebral body resection, and piecemeal resection and curettage, in addition to the surgical procedures described above, can be used. Chemotherapy and radiotherapy after surgery were used to reduce the risk of the cancer relapse or shrinks some malignant tumor such Ewing’s sarcoma that cannot be completely removed with surgery. Many benign silent (no symptom) tumors such as hemangioma were found in health checkup, and most of them did not receive any treatment. Although the WHO defines GCT as a benign osteolytic neoplasm, GCT displays the characteristics of both malignant and benign tumors and actually represents a benign tumor with the potential of malignancy [3739]. In our series, most cases of GCT undergone total spondylectomy, vertebrectomy, piecemeal resection or curettage. Some cases of GCT received other therapy such as bisphosphonate treatment after surgery.

Conclusions

Our study results represent data on the epidemiology of spinal osseous tumors in a large population of patients. We think that these data may reflect the epidemiological features of spine osseous tumors in Eastern China. For geographical and racial variations, the incidence of these neoplasms in a developing country is partly different from that found in other countries. There were several limitations in this study. As medical imaging technology have improved greatly during the study time span, the diagnosis sensitivity of primary spinal osseous tumors should lead to different prevalence in different time. Although the prognosis of spinal osseous tumors and longitudinal changes could not be fully assessed due to the nature of a retrospective study, we hope our work could provide useful epidemiological information as these data may have important implications for public health programs.

Acknowledgements

Not applicable.

Funding

The study was funded by the Bone Tumors and Nervous System Tumors Biobank Project of Shanghai (12DZ2295103), Bone Tumor Sample Databases and Digital Information Platform Project of Shanghai (08DZ2292800), and Shanghai Biobank Network of Common Human Tumor Tissue (12DZ2295100).

Availability of data and materials

The manuscript does not refer to any new software, application, or tool. The authors do not wish to share data analyzed in this manuscript as no such consent was provided by the patients treated and no approval of the Bioethics Committee was obtained.

Authors’ contributions

ZZ wrote the manuscript. ZZ and XW performed data analysis. ZW and WH collected and evaluated information of cases. JX conceived of the study and participated in its designation. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.
Not applicable.
All procedures performed in studies involving human participants were in accordance with the ethical standards of the Clinical Research Ethics Committee of Second Military Medical University and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Human data were obtained with informed consent, and this study was approved by the Clinical Research Ethics Committee of the Second Military Medical University.

Publisher’s Note

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Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
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Metadaten
Titel
Epidemiological characteristics of primary spinal osseous tumors in Eastern China
Publikationsdatum
01.12.2017
Erschienen in
World Journal of Surgical Oncology / Ausgabe 1/2017
Elektronische ISSN: 1477-7819
DOI
https://doi.org/10.1186/s12957-017-1136-1

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Karpaltunnelsyndrom BDC Leitlinien Webinare
CME: 2 Punkte

Das Karpaltunnelsyndrom ist die häufigste Kompressionsneuropathie peripherer Nerven. Obwohl die Anamnese mit dem nächtlichen Einschlafen der Hand (Brachialgia parästhetica nocturna) sehr typisch ist, ist eine klinisch-neurologische Untersuchung und Elektroneurografie in manchen Fällen auch eine Neurosonografie erforderlich. Im Anfangsstadium sind konservative Maßnahmen (Handgelenksschiene, Ergotherapie) empfehlenswert. Bei nicht Ansprechen der konservativen Therapie oder Auftreten von neurologischen Ausfällen ist eine Dekompression des N. medianus am Karpaltunnel indiziert.

Prof. Dr. med. Gregor Antoniadis
Berufsverband der Deutschen Chirurgie e.V.

S2e-Leitlinie „Distale Radiusfraktur“

Radiusfraktur BDC Leitlinien Webinare
CME: 2 Punkte

Das Webinar beschäftigt sich mit Fragen und Antworten zu Diagnostik und Klassifikation sowie Möglichkeiten des Ausschlusses von Zusatzverletzungen. Die Referenten erläutern, welche Frakturen konservativ behandelt werden können und wie. Das Webinar beantwortet die Frage nach aktuellen operativen Therapiekonzepten: Welcher Zugang, welches Osteosynthesematerial? Auf was muss bei der Nachbehandlung der distalen Radiusfraktur geachtet werden?

PD Dr. med. Oliver Pieske
Dr. med. Benjamin Meyknecht
Berufsverband der Deutschen Chirurgie e.V.

S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“

Appendizitis BDC Leitlinien Webinare
CME: 2 Punkte

Inhalte des Webinars zur S1-Leitlinie „Empfehlungen zur Therapie der akuten Appendizitis bei Erwachsenen“ sind die Darstellung des Projektes und des Erstellungswegs zur S1-Leitlinie, die Erläuterung der klinischen Relevanz der Klassifikation EAES 2015, die wissenschaftliche Begründung der wichtigsten Empfehlungen und die Darstellung stadiengerechter Therapieoptionen.

Dr. med. Mihailo Andric
Berufsverband der Deutschen Chirurgie e.V.