Characterization of primary fibular bone tumors and post-surgical clinical and functional outcomes
Mohamed Ali Bekir1, Coskun Ulucakoy2, Ismail Burak Atalay2, Aras Pervane2, Guray Togral2, Bedii Safak Gungor2
1Department of Orthopaedics and Traumatology, Dr. Nafiz Korez Sincan City Hospital, Ankara, Türkiye
2Department of Orthopaedics and Traumatology, Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital, Ankara, Türkiye
Keywords: Fibula, Malawer, outcome, resection, tumor
Abstract
Objectives: In this study, we present the characterization of tumors located in the fibula, which is a rare site for tumors, and the clinical and functional results of patients with fibular tumors that we operated in our clinic.
Patients and methods: Between February 2008 and December 2018, a total of 104 patients (58 males, 46 females; mean age: 26±18 years; range, 3 to 78 years) who were operated for tumor located in the fibula were retrospectively analyzed. Demographic data, histopathological diagnosis, tumor localization, surgical method and postoperative complications, metastases, follow-up time, and functional results of the patients were recorded. The fibula was divided into three groups as proximal, diaphysis and distal one-third.
Results: The mean follow-up was 56±25.3 (range, 24 to 108) months. Eighty (76.9%), seven (6.7%) and 17 (16.3%) patients were located proximal, diaphysis and distal to the fibula, respectively. The number of patients with malignant tumors located in the fibula was 26 (25%), the tumor was benign in 54 (51.9%) patients and 24 (23%) tumors were borderline. The most common tumor localized to the fibula was osteochondroma with 28 (26.9%) patients. The most common malignant tumors located in the fibula were Ewing sarcoma and osteosarcoma in 11 patients each. The most common surgical method was curettage in 44 (42.3%) patients. Distant organ metastases were present in 18 (17.3%) patients. The Musculoskeleteal Tumor Society score of 17 patients who underwent resection of the proximal fibula were 87%.
Conclusion: Fibula is a rare location for tumors and fibula tumors tend to be located more proximal. Tumors located in the fibula have good functional outcomes after surgery.
Introduction
The fibula is a rare location for tumors, and only 2.5% of all benign and malignant bone tumors are located in the fibula.[1] Diagnosis may be delayed due to knee and ankle pain. The most common presenting complaints are pain, palpable mass, and more rarely, peroneal nerve symptoms.[2]
Treatment of benign tumors located in the fibula is primarily follow-up and conservative. Surgical treatment options are curettage or excision.[2] In malignant and borderline tumors, en-bloc resection is in the foreground. For the proximal fibula, Malawer described two types of en-bloc resection: Type I, marginal resection, includes 2 to 3 cm of the diaphysis of the proximal fibula and resection of the muscles around the fibula, while in Type II, wide extra-compartment resection, proximal fibula, 5 to 6 cm diaphysis, anterior and lateral muscle compartments, anterior tibial artery and peroneal nerve should be resected. In Type I resection, the peroneal nerve is preserved.[3]
In the present study, we aimed to present the characterization of tumors located in the fibula, which is a rare localization area for tumors, and the follow-up results of patients with fibular tumors operated in our clinic.
Patients and Methods
This single-center, retrospective study was conducted at Department of Orthopaedics and Traumatology, Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital between February 2008 and December 2018. A total of 104 patients (58 males, 46 females; mean age: 26±18 years; range, 3 to 78 years) who were operated for tumor located in the fibula were included. Demographic data, histopathological diagnosis, tumor localization, surgical method, postoperative complications, metastases, follow-up time, and functional results of the patients were recorded. Tumors involving the fibula and the tibia, metastases, and tumors with a follow-up period of less than 24 months were excluded from the study. The fibula was divided into three groups as proximal, diaphysis and distal one-third.
Statistical analysis
Statistical analysis was performed using the IBM SPSS version 22.0 software (IBM Corp., Armonk, NY, USA). Continuous variables were expressed in mean ± standard deviation (SD) or median (min-max), while categorical variables were expressed in number and frequency. Descriptive analyses were presented using percentile and quantitative values.
Results
The mean follow-up was 56±25.3 (range, 24 to 108) months. Eighty (76.9%), seven (6.7%), and 17 (16.3%) patients were located proximal, diaphysis and distal to the fibula, respectively (Table I). While the number of patients with malignant tumors located in the fibula was 26 (25%), the tumor was benign in 54 (51.9%) patients and 24 (23%) tumors were borderline (Table II). The most common tumor localized to the fibula was osteochondroma with 28 (26.9%) patients. This was followed by giant cell tumors with 15 (14.4%) patients. The most common malignant tumors located in the fibula were Ewing sarcoma and osteosarcoma in 11 patients each. Considering the frequency of tumors by fibula location, they were proximal, diaphysis and distal osteochondroma (31%), Ewing sarcoma (42%), and giant cell tumor (29%), respectively (Table III).
Curettage was the most common surgical method for tumors located in the fibula in 44 (42%) patients. These were followed by total excision (28%), resection (23%) and amputation (5%), respectively (Table I). Resection was performed in 17 (21%) of 80 patients with tumors located proximal to the fibula. While 12 of them (70%) were Malawer Type I, five of them were Malawer Type II (Table IV). Distant organ metastases were present in 18 (17.3%) patients. The most common metastasis was to the lung in 10 (55.5%) patients. Of the 26 malignant tumors, 61% were older than 21 years of age. Peroneal nerve palsy was observed in five (6%) patients located proximal to the fibula.
An 18-year-old male patient was consulted to our clinic with the complaint of knee pain in his left knee lasting for four months. A cystic lesion was detected in the head of the fibula in the direct X-ray of the patient (Figure 1a, b). En-bloc resection (Figure 2a, b) was performed in the patient whose Tru-cut biopsy revealed an aneurysmal bone cyst. The result of the mass sent to pathology (Figure 3a, b) was compatible with aneurysmal bone cyst. No neurological deficit was detected in the postoperative patient.
Discussion
The literature indicates that tumors located in the fibula are frequently located proximal.[4,5] Gümüştaş et al.[6] in their epidemiological study on tumors located in the fibula, the most common sites were proximal fibula (61%), distal fibula (27%), and diaphysis (11%). Similarly, in the study of Arikan et al.,[4] the most common localizations were proximal (67%), distal (25%) and diaphysis (8%). In our study, similar to the literature, the most common location was the proximal fibula (76.9%). This was followed by distal (16.3%) and diaphysis (6.7%), respectively.
Although tumors located in the fibula are rarely encountered, the rate of malignant tumors in the literature on the malignancy rate reaches 50%.[1] In a study including 52 patients, Guo et al.[7] reported that 15.4% of all tumors located in the fibula were malignant. In the study of Arikan et al.[4] including 264 patients, this rate was 20.8%. In our study, 24% of 104 tumors localized to the fibula were malignant and 23% were borderline. We believe that the reason for the high rates of malignant and borderline in our study is that patients with suspected malignancy are referred to us more, as we are a reference oncology hospital. In addition, as another reason, we included only the patients we operated on. Many benign tumors such as non-ossifying fibroma were excluded from the study, since they were followed conservatively.
Abdel et al.[8] had a mean age of 24.3±9.6 (range, 2 to 64) years in patients who operated for a tumor located in the fibula and followed for an average of 88 months. In the study of Guo et al.,[7] the mean age of 52 patients followed for 31 months was 26.5±5.2 (range, 4 to 72) years. Gümüştaş et al.[6] had a mean age of 25.6±17.6 years in their study, and they found that increasing patient age may be a potential risk factor for the development of malignant fibular tumor. Similarly, Arikan et al.[4] reported that fibular tumors were more common under 21 years of age and that most fibular tumors under 21 years of age were benign. In this study, the mean age of 104 patients we followed for an average of 56±25.3 months was 26±18 years, and 61% of 26 malignant tumors were older than 21 years.
In a study performed in Mayo Clinic, the most common benign tumor located in the proximal fibula was osteochondromas (38%).[8] The most common benign tumors in the diaphyseal and distal involvement were osteoid osteoma and aneurysmal bone cyst, respectively.[6] In the study of Abdel et al.,[9] the most common malignant tumor located in the proximal fibula was osteosarcoma, while in the study of Arikan et al.,[4] the most common malignant tumors were chondrosarcoma (29.1%), Ewing sarcoma (27.3%) and osteosarcoma (27.3%). Similarly, in the study of Guo et al.,[7] the most common benign tumor located in the proximal fibula was osteochondroma, and malignant tumor osteosarcoma. Atalay et al.[10] reported the results of proximal fibula tumors, and the most common malignant tumor was osteosarcoma. Similarly, in this study, the most common tumor was osteochondroma (26.9%), while the most common malignant tumors were Ewing sarcoma and osteosarcoma (10%) with 11 patients each.
Function after surgery for proximal fibular tumors varies depending on the resection performed and the tumor type. The Musculoskeleteal Tumor Society scores of benign and malignant proximal fibular tumors treated surgically are available in the literature. Dieckmann et al.[11] reported the mean MSTS scores of 90 to 97% for 57 patients who were operated for benign and malignant proximal fibular tumors. Similarly, Inatani et al.[12] reported that, in a smaller number of patients (n=12), the mean MSTS score was 96% (range, 70 and 100%) in those whose peroneal nerve could not be resected, and 65% (range, 60 and 100%) in those who were resected. 70) has been reported. Kundu et al.[13] on the other hand, in the study in which they presented the results of 46 patients, they reported MSTS as 88%. Similarly, in this study, the MSTS score of 17 patients who underwent post-tumor resection in the proximal fibula was 87% (range, 70 and 100%). The most common complication after proximal fibula resection is peroneal nerve palsy and instability in the knee. Peroneal nerve palsy is seen at a rate of 3 to 57% in the literature. 3,14 Guo et al.[7] reported peroneal nerve palsy as 13.5% in 52 patients they operated. A total of 7.7% of these persisted as permanent peroneal nerve palsy. Guo et al.[7] did not report knee instability in any of the patients they operated. While knee instability was not encountered in this study, peroneal nerve palsy was seen in nine (11%) patients located proximal to the fibula. Of these, five patients (patients who underwent Malaver type II resection) continued as permanent peroneal nerve palsy.
To the best of our knowledge, only two studies have analyzed fibular tumors as a whole so far.[4,6] In these studies, the epidemiology was emphasized. The strength of our study is that it is the first study to analyze fibular tumors as a whole and to share the oncology experience (clinical and functional outcome) of a single center with this large number of patients. However, the lack of homogeneous groups due to its retrospective nature and considering all tumors together are the main limitations.
In conclusion, the fibula is a rare location for tumors and fibula tumors tend to be located more proximal. Tumors located in the fibula have good functional outcomes after surgery.
Citation: Bekir MA, Ulucakoy C, Atalay IB, Pervane A, Togral G, Gungor BS. Characterization of primary fibular bone tumors and post-surgical clinical and functional outcomes. Jt Dis Relat Surg 2022;33(2):419-425.
The study protocol was approved by the Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital Ethics Committee (number 2021-06/1151). The study was conducted in accordance with the principles of the Declaration of Helsinki.
A written informed consent was obtained from each patient.
Data Sharing Statement: The data that support the findings of this study are available from the corresponding author upon reasonable request.
Writer: M.A.B., C.U., I.B.A.; Data analysis: A.P.; Critical review: G.T., B.S.G.
The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.
The authors received no financial support for the research and/or authorship of this article.
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