Skip to main content

Clinical and MRI features of sacral insufficiency fractures after radiotherapy in patients with cervical cancer

Abstract

Background

To determine the incidence, clinical and MRI features of sacral insufficiency fracture (SIF) after radiotherapy (RT) in patients with cervical cancer.

Methods

Our study included 167 patients with cervical cancer after radiotherapy that underwent pelvic MRI for follow-up. MRIs included pre-enhanced T1-weighted, coronal fat-Suppressed T2-weighted (FS-T2W) and enhanced T1-weighted imaging. The clinical and MRI dates were reviewed. The gold standard of SIF was based on radiologic findings, clinical data and follow-up at least 12 months.

Results

28 patients (10.8%) with 47 sites were diagnosed with SIFs, including 9 patients with unilateral SIF and 19 patients with bilateral SIFs. The median age was 60 years (range 41–72 years), and 89.3% (25/28) of patients were postmenopausal. 64.3% (18/28) of patients were symptomatic, and 53.6% of patients (15/28) had concomitant pelvic fractures. The median interval time from RT to SIFs was 10 months (range 3–34 months). For the lesion-wise analysis based on all MR images, all lesions were detected by visualizing bone marrow edema patterns, and fracture lines were detected in 64.6% (31/47) of SIFs. No soft-tissue tumors were founded. For each MRI sequence analysis, coronal FS-T2WI detected the most bone marrow edema pattern and fracture line than T1WI or enhanced T1WI.

Conclusion

SIF is a common complication in cervical cancer after radiotherapy, which has some certain clinical and MRI features. Coronal FS-T2WI may be more useful to detect and characterize these fractures than other imaging sequences.

Peer Review reports

Background

Radiotherapy (RT) is one of the main treatment methods for cervical cancer, and the late complications after radiotherapy have drawn more attention, included insufficiency fractures (IFs). IF has been considered as a common RT-induced complication, with the incidences ranged from 20 to 40% for cervical cancer, and the most common occurrence is sacrum, accounting for 75% of all Ifs [1,2,3,4]. The diagnosis of sacrum IF (SIF) after RT was challenging, because of SIF may not always show a fracture line, and SIFs without fracture line could be frequently misinterpreted as bone metastasis, which may result in unnecessary biopsy and aggressive radio-chemotherapy [5,6,7,8,9,10]. Hence, accurate diagnosis of SIF after RT is important and intractable issue in clinical practice.

Recently, the wide use of modern imaging modalities has improved the detection of SIFs, but the diagnostic sensitivity and specificity are still debatable. Bone scintigraphy (BS) is sensitive to detect SIF and the so-called “Honda sign” (H-sign) is well known as a characteristic sign, but this sign is often absent [11, 12]. Computed tomography (CT) has been shown to be specific in depicting fracture lines and osteosclerosis for SIF, but it may have limitations in sensitivity [13, 14].

MRI has been proved to be more sensitive to detect occult IFs than CT or BS, owing to the reveal of reactive bone marrow changes [13,14,15]. Previous literatures and our preliminary studies showed that MRI is extraordinary sensitive for revealing the reactive bone marrow edema associated with post-radiation IF and is useful for detecting soft-tissue mass, which may be valuable for identifying IF from bone metastasis, but MRI findings of insufficiency fractures may not always show a fracture line for SIF, with the disappearance of fracture line, the diagnosis of SIF is challenging [15,16,17,18,19]. Thus, detection of fracture line plays a great role in the diagnosis of SIF.

The coronal fat saturation-T2W (FS-T2W) imaging of sacrum has been recommended to detect fracture line in osteoporotic fracture and sacroiliitis, which shows superior value to other MRI sequences by increasing significant findings detection in 6.8% of patients [20]. To our knowledge, as for the radiation-induced SIF, the superiority of coronal FS-T2W to other MRI sequences in the detection of SIF has not been discussed. Therefore, we carried out this retrospective study to explore the incidence, clinical and MRI features of SIF after radiotherapy in patients with cervical cancer, and compared the ability of coronal FS-T2W imaging with other MRI sequences in the characterization of SIF after RT.

Methods

Patients

This retrospective study was approved by the institutional review board, and informed consent was not required. We retrospectively analyzed 167 cervical cancer patients received RT between July 2015 and December 2018. Pre-treatment and follow-up pelvic MRI was available for all patients; the median follow-up time was 45 months (range 25–72). The subject inclusion criteria as follows: (1) Pathology-proven cervical cancer, and received RT, (2) Pre-treatment pelvic MR showed no abnormal sign changes in the sacrum, (3) When emerging signal abnormality in sacrum was visualized after RT, one or more pelvic MRI and/or CT examination was performed during their at least 12 months follow-up. Exclusion criteria: (1) had sacrum metastasis, (2) had a history of pelvic trauma.

Finally, 28 patients (age range, 41–72 years; median age, 60 years) were identified as SIFs, whose clinical notes, symptoms and imaging findings were reviewed.

Imaging acquisition

MR imaging

In all 28 subjects, pelvis MRI was performed by using a 1.5 T MR-scanner (Philips Achieva, Philips Healthcare, Best, The Netherlands). MR sequences included an axial T1-weighted spin-echo images (TR/TE, 496 ms/10 ms; matrix, 256 × 256; number of excitations [NEX], 2; echo-train length [ETL],1), an axial T2-weighted spin-echo images (TR/TE, 3500/100 ms; matrix, 512 × 256; NEX, 2; ETL,4) and an coronal fat-saturated T2-weighted images (TR/TE,2400/80 ms; SPAIR TR, 266 ms; matrix, 280 × 306; NEX, 2). Contrast-enhanced axial and sagittal T1-weighted images were also obtained by using a T1-weighted spin-echo sequence. For all scanning sequences, the field of view was 22–26 cm and the section thickness was 5 mm with a 2 mm interscan gap was performed.

Bone scintigraphy

Fifteen patients simultaneously underwent bone scintigraphy (BS) examination, BS studies were performed by using a SPECT/CT scanner (Philips, Netherlands, 4-slice diagnostic CT). The whole-body scan was performed 3 h after intravenous injection of 15~25 mCi 99mTc-MDP.

CT imaging

Eleven patients simultaneously underwent CT examination, imaging included the entire pelvis. CT studies were performed using a several MDCT scanners (64-MDCT scanners, Light Speed Series, GE Healthcare). All studies were performed with 120 kVP and milliampere values ranging from 200 to 300 mA.

Image analysis

All images were analyzed at a diagnostic workstation (Advantage Windows, GE Healthcare, WI). The MRI, CT, and BS studies were analyzed separately in random order by two radiologists (8 and 10 years of experience in musculoskeletal imaging, respectively) in consensus. Radiologists were blinded to the patients’ identity and results of the clinical notes.

All patients underwent MRI and were evaluated for the absence or presence of a SIF and locations (unilateral or bilateral) of fractures. Furthermore, the absence or presence of a reactive bone marrow edema and fracture line in SIF was recorded. A bone marrow edema pattern was classified into three grades as follows [13]: (1) severe, the signal intensity on fat-saturated T2-weighted images was similar to that of spinal fluid or urine in the bladder, (2) moderate, bone marrow edema was visualized > 5 mm around the fracture line or had a diameter of > 10 mm if no fracture line was present and the signal intensity was lower than that of spinal fluid and urine in the bladder, (3) mild, bone marrow edema was visualized only along the fracture line (within 5 mm diameter) but not in the periphery. Fracture line was noted by linear low signal intensity on all MR sequences. The presence of bone marrow edema and fracture lines visualized on T1W, FS-T2W and enhanced T1W images were documented separately. Then, combined all MR images, the presence of bone marrow edema and fracture lines were documented. The presence and location of concomitant fractures in other sites (lumbar, pelvis and proximal femur) were also documented.

Presence of an “H-sign” was documented for 15 patients who had BS examination. “H-sign” is an H-shaped increase in areas of abnormal radiotracer uptake on the sacral body and both alae [11]. The presence of osteosclerosis and fracture line was documented for 11 patients who had CT examination.

SIF reference standard

The conclusive diagnostic criterion was based on radiologic findings, clinical data and follow up at least 12 months. As described in previous studies, the diagnosis of SIF was based on the area of sclerosis without soft-tissue mass or better visualization fracture lines by follow-up CT, as well as areas of regressed bone marrow edema, stationary or fracture lines that were better visualized by MRI follow-up [13,14,15, 17].

Statistical analysis

All the statistical tests were performed using SPSS Statistics 16.0 (SPSS Inc., Chicago, IL, USA) software package. Categorical data are expressed as numbers and frequency (%), and continuous data are expressed as median and range. Pearson chi-square test (or Fisher test) were performed for comparing the differences of detection sensitivity.

Results

Incidence

Of these167 cervical cancer patients after RT, we found 10.8% of the patients (28 patients) diagnosed with SIFs in the follow-up by using MRI.

Patients’ clinical features

The median age was 60 years (range 41–72 years), and 85.7% (24/28) of patients aged ≥55 years. The clinical history, symptom, interval time from RT to MRI, associated fractures and additional imaging examination in 28 patients with SIF were showed in Table 1.

Table 1 The clinical history, RT project, symptom, interval time from RT to MRI, associated fractures and additional imaging examination in 28 patients with radiation-induced SIF detected by MRI

SIFs were frequently occurred in patients with a postmenopausal status, accounting for 89.3% (25/28) of patients. 89.3% (25/28) of patients accepted definitive RT, the median dose was 62 Gy (range 50–110 Gy); 3 patients accepted postoperative RT, the median dose was 56 Gy (range 50 – 100 Gy). The median interval time from RT to SIFs by MRI was 10 months (range 3–34 months), and the great majority of affected patients developed with SIFs within 2 years after RT (92.9%, 26 of 28 patients).

Nine patients (31.0%) developed with unilateral SIFs (Figs. 1 and 2), and nineteen patients (69.0%) with bilateral SIFs (Figs. 3, 4 and 5). In total of 15 patients (53.6%) developed with concomitant fractures, include L5 fractures (14.3%, 4 patients) (Fig. 3), acetabulum fractures (17.8%, 5 patients) (Fig. 3), ilium fractures (21.4%, 6 patients) (Fig. 4) and pubis fractures (14.3%, 4 patients) (Fig. 5).

Fig.1
figure 1

Right SIF in a 58-year-old woman with cervical cancer after radiotherapy. A BS showed right sacrum increased accumulation (arrow). B Axial T1WI showed hypointensity. C Axial T2WI showed moderate hyperintensity. D Coronal FS-T2WI showed severe bone marrow edema and diagonal fracture line (arrow). E Axial enhanced T1WI showed mild contrast enhancement

Fig.2
figure 2

Right SIF in a 65-year-old woman with cervical cancer after radiotherapy. A Axial T1WI showed hypointensity. B Coronal FS-T2WI showed severe bone marrow edema with fracture line (arrow). C, D Axial and sagittal enhanced T1WI showed contrast enhancement. E, F Coronal and axial CT images showed no overt positive finding

Fig.3
figure 3

Bilateral SIFs had coexistent L5, acetabulum fractures in a 68-year-old woman with cervical cancer after radiotherapy. A, B Axial TWI and enhanced T1WI showed right sacrum abnormal signal (arrow). C Coronal FS-T2WI showed abnormal signal in bilateral sacrum, right sacrum showed severe bone marrow edema, and left sacrum showed mild bone marrow edema (arrow). D, E Coronal FS-T2WI showed acetabulum and L5 fractures. F Coronal CT image showed osteosclerosis change in L5 and right sacrum

Fig.4
figure 4

Bilateral SIFs had coexistent bilateral ilium fractures in a 70-year-old woman with cervical cancer after radiotherapy. A, B Axial T1WI and T2WI showed bilateral sacrum low signal (arrow). C Coronal FS-T2WI showed bilateral sacrum and ilium hyperintensity, bilateral sacrum with severe bone marrow edema. D Axial enhanced T1WI showed mild contrast enhancement in bilateral sacrum. E, F. Axial and coronal CT image showed osteosclerosis change

Fig.5
figure 5

Bilateral SIFs had coexistent pubis fracture in a 63-year-old woman with cervical cancer after radiotherapy. A BS showed bilateral sacrum increased accumulation (white arrow) as an “H-sign”, and left pubis increased accumulation (red arrow). B Axial T1WI showed hypointensity. C Coronal FS-T2WI showed severe bone marrow edema. D Axial enhanced T1WI showed contrast enhancement in bilateral sacrum. E Axial enhanced T1WI showed enhancement with fracture line

Eighteen patients (64.3%) had hip pain or low back pain, and ten patients were asymptomatic. 72.2% (13/18) of the symptomatic patients developed with concomitant fractures, but only 20% (2/10) of the asymptomatic patients with concomitant fractures.

MRI findings

A total of 47 lesions were identified as SIFs in 28 patients (9 patients unilateral SIF, 19 patients bilateral SIFs) according to the reference standard. The detection rate of bone marrow edema and fracture line on MRI for the SIFs lesions were showed in Table 2.

Table 2 The detection rate of bone marrow edema and fracture line on MRI for the SIFs lesions (n=47)

For the lesion-wise analysis based on all MR images. All SIFs showed reactive bone marrow with hypointensity on pre-enhanced T1WI, hyperintensity on SPAIR-T2WI. According to the grading criterion, severe bone marrow edema patterns were found to be most frequently associated with SIFs (82.9%, 39/47), followed by moderate bone marrow edema (12.8%, 6/47), only two SIFs showed mild bone marrow edema. Fracture lines were also frequently founded in SIFs (Figs. 1, 2 and 4), accounting for 64.6% (31/47) of lesions, which was visualized as a linear low signal structure on either T1-weighted, SPAIR-T2 weighted and enhanced T1-weighted images. No soft-tissue tumor was founded in SIFs.

For individual MRI sequence analysis, coronal FS-T2WI detected more bone marrow edema pattern and fracture lines than pre-enhanced T1WI or enhanced T1WI (Table 2). The bone marrow edema pattern detection rates of coronal FS-T2WI was significantly higher than enhanced T1WI (100% vs 87.2% [41/47], P = 0.011), higher than pre-enhanced T1WI but without statistic difference (100% vs 95.7% [45/47], P = 0.153). Furthermore, the fracture lines detection rates of coronal FS-T2WI was significantly higher than pre-enhanced T1WI (60.4% [29/47] vs 36.2% [17/47], P=0.013), higher than enhanced T1WI but without statistic difference (60.4% [29/47] vs 51.1% [24/47], P=0.298).

Additional BS and CT findings

15 patients with SIFs (5 patients, unilateral SIFs; 10 patients, bilateral SIFs) simultaneously underwent WBS, 8 patients (53.3%) showed the typical “H-sign” (Fig. 5). 11 patients simultaneously underwent CT (4 patients, unilateral SIFs; 7 patients, bilateral SIFs). Of the 18 SIFs, 15 lesions were involved osteosclerosis change (Figs. 3 and 4), fracture lines were showed in only 5 lesions, and other three lesions were invisible on CT (Fig. 2).

Discussion

In the present study, we found that postradiotherapy SIF was a relatively common occurrence for patients with cervical cancer, and patients have some certain clinical characteristics, such as older ages with postmenopausal status, developed with SIFs within 2 years after RT, involved bilateral sacrum, concomitant fractures. MRI, especially coronal FS-T2W imaging was useful to detect and character SIFs.

The sacrum is the initial site of fracture and then lead to increased stress on other sites of the pelvis. The actual incidence of RT-induced SIFs is unclear, the incidence in our study was 10.8%, which was similar with previous studies [21,22,23,24]. In our study, almost 53.6% of patients had concomitant fractures, suggested that identification of SIFs should arouse clinical suspicion of fractures in other sites. However, SIFs are most frequently associated with pubis fractures, with a reported coincidence of 78% [24]. We found that only 14.3% patients had coexistent pubis fractures, it was lower than that of the presences of fracture in L5 (14.3%), acetabulum (17.8%), ilium (21.4%).

The clinical presentation of SIF is vague and non-specific. We observed almost two-thirds of SIFs were clinically symptomatic, the incidence was higher than a study reported about one third [21]. First, this may be most likely explainable by the fact that 53.6% of patients with concomitant fractures were included, and 72.2% of the symptomatic patients developed with concomitant fractures. Multiple site fractures may be contributed to some patients with pain [9]. Second, 82.9% of SIFs presented severe bone marrow edema patterns in present study, which was the same as Blomlie et al. [25] revealed, larger lesions (> 1 cm2) on MRI tended to be more likely painful.

Older patients with postmenopausal status after RT are more susceptible to the development of IF [1, 2, 9]. We found that SIFs frequently occurred in postmenopausal patients, and the median age was 60 years. Based on our results, most of affected patients developed with SIFs within 2 years, and the median interval time from RT to SIFs was 10 months, which is almost similar with previous studies with a median interval time between 8 and 14 months [1, 6, 21]. Supporting a previous study demonstrated that 88.9% of patients with RT-induced SIFs were bilateral [19], we observed over two-third of SIFs have arosen bilaterally.

Although SIFs are rarely life-threatening, they should be deserved special attention because they can influence the quality of life [26]. Only 20–38% of SIF could be identified on plain films [27,28,29]. Recently, modern imaging modalities during follow-up have been applied in the detection and characterization of SIFs. Both BS and CT have some limitations, BS is one of the most sensitive imaging modalities for detecting SIF, but the “H-sign” is often absent [11]. In our study, only 53.3% (8/15) of patients who had additional BS showed the typical “H-sign”. CT is useful to detect fracture lines, which has been shown to be less sensitive to detect SIFs than MRI, with a recorded sensitivity between 60 and 75% [13, 14].

MRI is an alternative technique due to its high soft-tissue contrast, multiplanar imaging, and avoidance of ionizing radiation. MRI is one of the most sensitive imaging techniques to detect RT-induced IF by visualizing the bone marrow edema. Cabarrus et al. [13], showed that the overall sensitivity of MRI was significantly higher than CT (100 vs 74.6%), although the sensitivity for detecting fracture lines was similar (93.3% for MRI vs 89.7% for CT). We found all SIFs showed bone marrow edema, and fracture lines were visualized in 64.6% of lesions. Furthermore, MRI is also helpful to differentiate SIF from the bone metastasis, because MRI is very useful to identify the soft-tissue component, the absence of focal or discrete soft-tissue mass around fracture sites is an important sign for distinguishing SIF from malignancy [15,16,17,18,19]. In present study, no soft-tissue tumor was detected in fracture sites.

The FS-T2W imaging is especially sensitive for visualizing early bone marrow edema, and FS-T2W imaging is recommended to be included in suspected fracture cases [30]. Gupta et al. [30] demonstrated that coronal STIR sequence had additional value to the L-spine MRI by increasing significant findings detection in 6.8% of patients, including SIF or sacroiliitis [20]. The advantage of our study was that both coronal FS T2-weighted and gadolinium-enhanced T1-weighted imaging were performed for all patients. We found coronal FS-T2WI was more sensitive to detect both bone marrow edema and fracture lines than that of T1WI or enhanced T1WI. In addition, this study revealed that T1WI detected the least fracture lines because of bone marrow edema pattern was also hypointensity, and enhanced T1WI detected least bone marrow edema due to some SIFs with no or mild enhancement, which may be difficult to identify.

There were several limitations to our study. First, our study was retrospectively performed in a single-institution. Second, the follow-up period was inconsistent (range, 25–72 months), which might have resulted in underestimation of the true prevalence of SIF. Third, only a small number of patients undergone simultaneous BS or CT examinations, we were unable to compare the diagnostic ability of MRI with BS or CT. Fourth, none of the IF lesion was diagnosis based on histopathology, as a pathologic diagnosis was generally impractical and actually unnecessary.

Conclusion

SIF is a common complication for patients with cervical cancer after radiotherapy, which has some certain clinical and MRI features. MRI, especially coronal FS-T2WI may be more useful to detect and characterize these fractures than other imaging sequences. Knowing well these features help to prevent confusion with metastatic disease and inappropriate treatment.

Availability of data and materials

The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.

Abbreviations

RT:

Radiotherapy

IF:

Insufficiency fracture

SIF:

Sacral insufficiency fracture

MRI:

Magnetic resonance imaging

CT:

Computed tomography

BS:

Bone scintigraphy

FS-T2W:

Fat-suppressed T2-weighted

References

  1. Uezono H, Tsujino K, Moriki K, Nagano F, Ota Y, Sasaki R, Soejima T. Pelvic insufficiency fracture after definitive radiotherapy for uterine cervical cancer: retrospective analysis of risk factors. J Radiat Res. 2013;54(6):1102–9.

    Article  Google Scholar 

  2. Tokumaru S, Toita T, Oguchi M, Ohno T, Kato S, Niibe Y, et al. Insufficiency fractures after pelvic radiation therapy for uterine cervical cancer: an analysis of subjects in a prospective multi-institutional trial, and cooperative study of the Japan Radiation Oncology Group (JAROG) and Japanese Radiation Oncology Study Group (JROSG). Int J Radiat Oncol Biol Phys. 2012;84(2):e195-200.

    Article  Google Scholar 

  3. Razavian N, Laucis A, Sun Y, Spratt DE, Owen D, Schonewolf C, et al. Radiation-induced insufficiency fractures after pelvic irradiation for gynecologic malignancies: a systematic review. Int J Radiat Oncol Biol Phys. 2020;108(3):620–34.

    Article  Google Scholar 

  4. Sapienza LG, Salcedo MP, Ning MS, Jhingran A, Klopp AH, Calsavara VF, et al. Pelvic insufficiency fractures after external beam radiation therapy for gynecologic cancers: a meta-analysis and meta-regression of 3929 patients. Int J Radiat Oncol Biol Phys. 2020;106(3):475–84.

    Article  Google Scholar 

  5. Ikushima H, Osaki K, Furutani S, Yamashita K, Kishida Y, Kudoh T, Nishitani H. Pelvic bone complications following radiation therapy of gynecologic malignancies: clinical evaluation of radiation-induced pelvic insufficiency fractures. Gynecol Oncol. 2006;103(3):1100–4.

    Article  Google Scholar 

  6. Ogino I, Okamoto N, Ono Y, Kitamura T, Nakayama H. Pelvic insufficiency fractures in postmenopausal woman with advanced cervical cancer treated by radiotherapy. Radiother Oncol. 2003;68(1):61–7.

    Article  Google Scholar 

  7. Kwon JW, Huh SJ, Yoon YC, Choi SH, Jung JY, Oh D, Choe BK. Pelvic bone complications after radiation therapy of uterine cervical cancer: evaluation with MRI. AJR Am J Roentgenol. 2008;191(4):987–94.

    Article  Google Scholar 

  8. Park SH, Kim JC, Lee JE, Park IK. Pelvic insufficiency fracture after radiotherapy in patients with cervical cancer in the era of PET/CT. Radiat Oncol J. 2011;29(4):269–76.

    Article  Google Scholar 

  9. Oh D, Huh SJ, Nam H, Park W, Han Y, Lim DH, et al. Pelvic insufficiency fracture after pelvic radiotherapy for cervical cancer: analysis of risk factors. Int J Radiat Oncol Biol Phys. 2008;70(4):1183–8.

    Article  Google Scholar 

  10. Bazire L, Xu H, Foy JP, Amessis M, Malhaire C, Cao K, et al. Pelvic insufficiency fracture (PIF) incidence in patients treated with intensity-modulated radiation therapy (IMRT) for gynaecological or anal cancer: single-institution experience and review of the literature. Br J Radiol. 2017;90(1073):20160885.

    Article  Google Scholar 

  11. Fujii M, Abe K, Hayashi K, Kosuda S, Yano F, Watanabe S, et al. Honda sign and variants in patients suspected of having a sacral insufficiency fracture. Clin Nucl Med. 2005;30(3):165–9.

    Article  Google Scholar 

  12. Zhang L, He Q, Jiang M, Zhang B, Zhong X, Zhang R. Diagnosis of insufficiency fracture after radiotherapy in patients with cervical cancer: contribution of technetium Tc 99m-labeled methylene diphosphonate single-photon emission computed tomography/computed tomography. Int J Gynecol Cancer. 2018;28(7):1369–76.

    Article  Google Scholar 

  13. Cabarrus MC, Ambekar A, Lu Y, Link TM. MRI and CT of insufficiency fractures of the pelvis and the proximal femur. AJR Am J Roentgenol. 2008;191(4):995–1001.

    Article  Google Scholar 

  14. Henes FO, Nuchtern JV, Groth M, Habermann CR, Regier M, Rueger JM, et al. Comparison of diagnostic accuracy of magnetic resonance imaging and multidetector computed tomography in the detection of pelvic fractures. Eur J Radiol. 2012;81(9):2337–42.

    Article  CAS  Google Scholar 

  15. Zhong X, Li J, Zhang L, Lu B, Yin J, Chen Z, et al. Characterization of insufficiency fracture and bone metastasis after radiotherapy in patients with cervical cancer detected by bone scan: role of magnetic resonance imaging. Front Oncol. 2019;9:183.

    Article  Google Scholar 

  16. Lapina O, Tiskevicius S. Sacral insufficiency fracture after pelvic radiotherapy: a diagnostic challenge for a radiologist. Medicina. 2014;50(4):249–54.

    Article  Google Scholar 

  17. Zhong X, Dong TF, Tan Y, Li JS, Mai H, Wu SX, et al. Pelvic insufficiency fracture or bone metastasis after radiotherapy for cervical cancer? The added value of DWI for characterization. Eur Radiol. 2020;30(3):1885–18952.

    Article  Google Scholar 

  18. White JH, Hague C, Nicolaou S, Gee R, Marchinkow LO, Munk PL. Imaging of sacral fractures. Clin Radiol. 2003;58(12):914–21.

    Article  CAS  Google Scholar 

  19. Blomlie V, Lien HH, Iversen T, Winderen M, Tvera K. Radiation-induced insufficiency fractures of the sacrum: evaluation with MR imaging. Radiology. 1993;188(1):241–4.

    Article  CAS  Google Scholar 

  20. Kim YY, Chung BM, Kim WT. Lumbar spine MRI versus non-lumbar imaging modalities in the diagnosis of sacral insufficiency fracture: a retrospective observational study. BMC Musculoskelet Disord. 2018;19(1):257.

    Article  Google Scholar 

  21. Bostel T, Nicolay NH, Welzel T, Bruckner T, Mattke M, Akbaba S, et al. Sacral insufficiency fractures after high-dose carbon-ion based radiotherapy of sacral chordomas. Radiat Oncol. 2018;13(1):154.

    Article  Google Scholar 

  22. Mammone JF, Schweitzer ME. MRI of occult sacral insufficiency fractures following radiotherapy. Skeletal Radiol. 1995;24(2):101–4.

    Article  CAS  Google Scholar 

  23. Featherstone T. Magnetic resonance imaging in the diagnosis of sacral stress fracture. Br J Sports Med. 1999;33(4):276–7.

    Article  CAS  Google Scholar 

  24. Aretxabala I, Fraiz E, Perez-Ruiz F, Rios G, Calabozo M, Alonso-Ruiz A. Sacral insufficiency fractures. High association with pubic rami fractures. Clin Rheumatol. 2000;19(5):399–401.

    Article  CAS  Google Scholar 

  25. Blomlie V, Rofstad EK, Talle K, Sundfor K, Winderen M, Lien HH. Incidence of radiation-induced insufficiency fractures of the female pelvis: evaluation with MR imaging. AJR Am J Roentgenol. 1996;167(5):1205–10.

    Article  CAS  Google Scholar 

  26. Henry AP, Lachmann E, Tunkel RS, Nagler W. Pelvic insufficiency fractures after irradiation: diagnosis, management, and rehabilitation. Arch Phys Med Rehabil. 1996;77(4):414–6.

    Article  CAS  Google Scholar 

  27. Gotis-Graham I, McGuigan L, Diamond T, Portek I, Quinn R, Sturgess A, Tulloch R. Sacral insufficiency fractures in the elderly. J Bone Joint Surg Br. 1994;76(6):882–6.

    Article  CAS  Google Scholar 

  28. Finiels H, Finiels PJ, Jacquot JM, Strubel D. Fractures of the sacrum caused by bone insufficiency. Meta-analysis of 508 cases. Presse Med. 1997;26(33):1568–73.

    CAS  PubMed  Google Scholar 

  29. Blake SP, Connors AM. Sacral insufficiency fracture. Br J Radiol. 2004;77(922):891–6.

    Article  CAS  Google Scholar 

  30. Gupta R, Mittal P, Mittal A, Mittal K, Gupta S, Kaur R. Additional merit of coronal STIR imaging for MR imaging of lumbar spine. J Craniovertebr Junction Spine. 2015;6(1):12–5.

    Article  Google Scholar 

Download references

Acknowledgements

The authors thank Elixigen Corporation (http://www.elixigen.com) for editorial assistance.

Funding

We would like to thank the Guangdong Medical Research Foundation (A2020263), National Natural Science Foundation of China (Grant No. 8210071052) and Guangdong Basic and Applied Basic Research Foundation (2019A1515010845) for the funding to carry out this project. The funding bodies were not involved in the study design, data collection, analysis, interpretation, writing or revisions of this manuscript.

Author information

Authors and Affiliations

Authors

Contributions

JSL and XZ conceived and designed this study. LQZ, BGL and LH conducted the study and collected important background data. TFD and HM analyzed the medical images. ZX and LQZ drafted the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Jiansheng Li.

Ethics declarations

Ethics approval and consent to participate

The Institutional Review Board of Affiliated Cancer Hospital & Institute of Guangzhou Medical University approved this retrospective study and waived the requirement for written informed consent due to its retrospective nature.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhong, X., Zhang, L., Dong, T. et al. Clinical and MRI features of sacral insufficiency fractures after radiotherapy in patients with cervical cancer. BMC Women's Health 22, 166 (2022). https://doi.org/10.1186/s12905-022-01758-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12905-022-01758-2

Keywords