Pogoda Pia, Linhart Wolfgang, Priemel Matthias, Rueger Johannes M, Amling Michael
Department of Trauma, Hand and Reconstructive Surgery, Hamburg University School of Medicine, Martinistrasse 52, 20246 Hamburg, Germany.
Arch Orthop Trauma Surg. 2003 Jun;123(5):247-51. doi: 10.1007/s00402-003-0496-x. Epub 2003 Apr 12.
Aneurysmal bone cysts, first described by Jaffe and Lichtenstein in 1942, are benign lesions that may easily be mistaken for a malignant tumor both radiographically and pathologically. These diagnostic problems are due to their rapid growth, extensive destruction of bone, wide extraosseous tumor masses, and marked cellular exuberance. The differential diagnosis of aneurysmal bone cysts including giant cell tumor, calcified solitary bone cysts, low-grade osteosarcoma, and teleangiectatic osteosarcoma becomes even more complicated when the lesion arises at sites other than the long bones and presents with extensive extraosseous, soft-tissue tumor masses. The latter cases--especially when they occur as sacral or presacral tumors--present challenges with respect to successful treatment, which should combine surgical removal of the entire lesion following oncological criteria to prevent recurrences and osteosynthesis to guarantee the biomechanical stability of the spinal-pelvic junction. Here we report on the clinical case of a female patient with an aneurysmal bone cyst of the sacrum and extensive extraosseous tumor masses. The report includes the diagnostic challenges, the surgical options of sacral and/or presacral tumors, the histopathological findings, and long-term clinical and radiographic surveillance.
The patient was treated by a combination of preoperative adjuvant selective arterial embolization, radical surgical excision through an anterior approach followed by subsequent osteosynthesis and stabilization through a posterior approach.
Clinical and radiographic follow-up for 2 years was uneventful, and the patient is still free of recurrence or any complaints.
The current report documents the diagnostic and surgical challenge of a gigantic aneurysmal bone cyst of the sacrum and its successful management.
动脉瘤样骨囊肿于1942年由贾菲和利希滕斯坦首次描述,是一种良性病变,在影像学和病理学上都很容易被误诊为恶性肿瘤。这些诊断难题归因于其生长迅速、对骨的广泛破坏、广泛的骨外肿瘤肿块以及明显的细胞增生。当病变发生在长骨以外的部位并伴有广泛的骨外软组织肿瘤肿块时,动脉瘤样骨囊肿的鉴别诊断包括巨细胞瘤、钙化性孤立性骨囊肿、低度骨肉瘤和毛细血管扩张性骨肉瘤,会变得更加复杂。后一种情况——尤其是当它们作为骶骨或骶前肿瘤出现时——在成功治疗方面存在挑战,治疗应结合按照肿瘤学标准手术切除整个病变以防止复发,以及进行骨固定以保证脊柱-骨盆交界处的生物力学稳定性。在此,我们报告一例患有骶骨动脉瘤样骨囊肿并伴有广泛骨外肿瘤肿块的女性患者的临床病例。该报告包括诊断挑战、骶骨和/或骶前肿瘤的手术选择、组织病理学发现以及长期临床和影像学监测。
该患者接受了术前辅助选择性动脉栓塞、经前路根治性手术切除,随后经后路进行骨固定和稳定治疗。
2年的临床和影像学随访无异常,患者仍无复发或任何不适。
本报告记录了骶骨巨大动脉瘤样骨囊肿的诊断和手术挑战及其成功治疗。