Reconstruction after Subtotal Sacrectomy for Sacral Ewing’s Sarcoma Using Tibial Allograft Strut Grafting: A Case Report

Case Reports

. 2021 Mar 3;14(1):296-302.


doi: 10.1159/000513117.


eCollection Jan-Apr 2021.

Affiliations

Item in Clipboard

Case Reports

Ryosuke Hirota et al.


Case Rep Oncol.


.

Abstract

We present the case of a 15-year-old girl. Two months after becoming aware of pain, she was diagnosed with a sacral tumor and referred to our department. She was diagnosed with a sacral Ewing’s sarcoma; after chemotherapy, it was determined that the tumor could be resected, so surgical treatment was performed. The sacrum and ilium were partially resected at the lower end of S1, and the lumbar vertebrae and pelvis were fixed with a pedicle screw and two iliac screws on each side of L3, and the sacral resection was reconstructed with a tibial strut allograft. No tumor recurrence or metastasis has been observed 1 year postoperatively. She developed bladder and rectal dysfunction, but she remained independent in activities of daily living and her daily life was not limited. The bone fusion in the reconstructed area confirmed the lack of instrumentation looseness. Surgical treatment for sacral Ewing’s sarcoma was performed to cure the patient. We believe that the tibial allograft contributed to the patient’s ability to walk on her own due to its high mechanical stability. Postoperative bone healing was observed with the same material, suggesting that the tibial allograft is useful for similar procedures.


Keywords:

Ewing’s sarcoma; Reconstruction; Subtotal sacrectomy; Tibial allograft.

Conflict of interest statement

The authors have no conflicts of interest to declare.

Figures


Fig. 1


Fig. 1

Radiograph of the pelvis (A), computed tomography in the coronal plane (B), and magnetic resonance imaging in the coronal plane (C) and in the axial plane (D). A destructive lesion on the right side of the S2 sacrum with no calcification was observed (yellow arrows).


Fig. 2


Fig. 2

Histopathological examination (A) and immunohistochemical analysis (B). Fluorescence in situ hybridization (C, D) showed an ESWR1 split signal in 54% and an FLI1 split signal in 56%.


Fig. 3


Fig. 3

Computed tomography (A) and magnetic resonance imaging of the pelvis (B) after neoadjuvant chemotherapy. Neoadjuvant chemotherapy caused 73% tumor shrinkage. We performed extensive pelvic resection and reconstruction using tibial allograft strut grafting with double posterior rod instrumentation (C–E).


Fig. 4


Fig. 4

Postoperative radiographs (A, B) and computed tomography images (C–E) of the pelvis. There was no osteolysis of the reconstructed area and no implant failure.

References

    1. Fletcher CDM, Bridge JA, Hogendoorn PCW, Mertens F. 4th ed. Lyon: IARC Press; 2013. WHO classification of tumors of soft tissue and bone. WHO classification of Tumours.

    1. Mounessi FS, Lehrich P, Haverkamp U, Willich N, Bölling T, Eich HT. Pelvic Ewing sarcomas. Three-dimensional conformal vs. intensity-modulated radiotherapy. Strahlenther Onkol. 2013 Apr;189((4)):308–14.



      PubMed

    1. Hesla AC, Tsagozis P, Jebsen N, Zaikova O, Bauer H, Brosjö O. Improved prognosis for patients with Ewing sarcoma in the sacrum compared with the innominate bones: the Scandinavian Sarcoma Group Experience. J Bone Joint Surg Am. 2016 Feb;98((3)):199–210.



      PubMed

    1. Puri A, Gulia A, Jambhekar NA, Laskar S. Results of surgical resection in pelvic Ewing’s sarcoma. J Surg Oncol. 2012 Sep;106((4)):417–22.



      PubMed

    1. Chen L, Long C, Liu J, Xing F, Duan X. Characteristics and prognosis of pelvic Ewing sarcoma: a SEER population-based study. PeerJ. 2019;7:e7710.



      PMC



      PubMed

Share on facebook
Facebook
Share on twitter
Twitter
Share on linkedin
LinkedIn
Share on vk
VK
Share on pinterest
Pinterest
Close Menu