Gajaria Pooja Kamlesh, Shenoy Asha Sharad, Chaudhari Jayashri Popat, Goel Naina Atul
Department of Pathology, Seth G S Medical College, KEM Hospital, Mumbai, Maharashtra, India.
Asian J Neurosurg. 2020 Dec 21;15(4):997-1002. doi: 10.4103/ajns.AJNS_184_20. eCollection 2020 Oct-Dec.
Solitary plasmacytoma of the dura without systemic involvement are extremely rare lesions, with <15 cases reported in the literature. Among these, ours is the second case to show the presence of amyloid. Fifty-year-old male had presented with headache, sudden onset right-sided weakness, and vomiting. Magnetic resonance imaging revealed an extra-axial mass in the left fronto-parietal region measuring 10 cm × 8.7 cm × 3.9 cm, suggestive of meningioma. The left fronto-parietal craniotomy was performed and multiple tissue bits aggregating to 10 cm × 8.5 cm × 2 cm along with thinned out membrane-like bit of calvarium was sent for pathologic examination. H and E stained sections showed sheets of plasmacytoid cells along with amyloid, which showed apple-green birefringence on Congo red staining. On immunohistochemistry, tumor cells were positive for CD38, CD138, showed kappa light chain restriction and were negative for CD45, CD34. Hence, it was diagnosed as a plasma cell neoplasm. Further work-up with whole-body positron-emission tomography scan revealed no systemic involvement. Dural-based lesions can mimic meningioma radiographically as well as intraoperatively. Histopathological examination unveils the diagnosis, to guide appropriate therapeutic regimens.
无全身受累的硬脑膜孤立性浆细胞瘤是极为罕见的病变,文献报道的病例不足15例。其中,我们的病例是第二例显示存在淀粉样变的。一名50岁男性,表现为头痛、突发右侧肢体无力和呕吐。磁共振成像显示左额顶叶区有一个轴外肿块,大小为10 cm×8.7 cm×3.9 cm,提示为脑膜瘤。行左额顶开颅手术,将多个聚集在一起大小为10 cm×8.5 cm×2 cm的组织块以及变薄的颅骨膜样组织送去做病理检查。苏木精-伊红染色切片显示成片的浆细胞样细胞以及淀粉样变,刚果红染色显示苹果绿双折射。免疫组化显示,肿瘤细胞CD38、CD138阳性,κ轻链受限,CD45、CD34阴性。因此,诊断为浆细胞肿瘤。全身正电子发射断层扫描进一步检查显示无全身受累。基于硬脑膜的病变在影像学和手术中均可类似脑膜瘤。组织病理学检查可明确诊断,以指导合适的治疗方案。