Srilatha Parampalli Srinivas, Rao Lakshmi
Associate Professor, Department of Pathology, Kasturba Medical College, Manipal, Karnataka, India.
Consultant, Department of Pathology, Armed Forces Hospital, Muscat, Oman.
J Clin Diagn Res. 2017 Sep;11(9):ED09-ED11. doi: 10.7860/JCDR/2017/30786.10551. Epub 2017 Sep 1.
Primary Intraosseous Paraganglioma (PGL) of sacrum is highly uncommon. Few of the spinal PGL reported were mostly intradural mass. Paraganglionic tissue is usually not present in the bone. So far, only seven cases of primary intraosseous sacral PGL have been reported in the literature. There are no dependable prognostic histological features to differentiate benign from malignant PGL. The only unequivocal criterion for malignancy is metastasis to an organ where paraganglionic tissue is normally not present. However, an aggressive nature can be identified histologically by loss of architecture, decreased or absent sustentacular cells and Ki-67 index of >3%. We report a case of an elderly male who was admitted with complaints of swelling in the lower back with associated radiating pain and difficulty in sitting of two months duration. A diagnosis of sacral chordoma was made on Magnetic Resonance Imaging (MRI). No other mass was detected elsewhere in his body. The patient underwent surgical excision followed by radiotherapy. On histopathology and immunohistochemistry, a diagnosis of locally aggressive primary intraosseous PGL of sacrum was rendered. Hence, when evaluating a lytic sacral mass, PGL has to be considered as a differential diagnosis.
骶骨原发性骨内副神经节瘤(PGL)极为罕见。已报道的脊柱PGL中,少数大多为硬膜内肿块。副神经节组织通常不存在于骨骼中。迄今为止,文献中仅报道了7例原发性骨内骶骨PGL。尚无可靠的预后组织学特征来区分良性与恶性PGL。恶性的唯一明确标准是转移至副神经节组织通常不存在的器官。然而,组织学上可通过结构丧失、支持细胞减少或缺失以及Ki-67指数>3%来确定其侵袭性。我们报告一例老年男性,因下背部肿胀伴放射性疼痛及坐位困难两个月入院。磁共振成像(MRI)诊断为骶骨脊索瘤。在其身体其他部位未检测到其他肿块。患者接受了手术切除及放疗。经组织病理学和免疫组织化学检查,诊断为骶骨局部侵袭性原发性骨内PGL。因此,在评估溶骨性骶骨肿块时,PGL必须作为鉴别诊断考虑。