Delgado Ruben, Bahmad Hisham F, Bhatia Vinay, Kantrowitz Allen B, Vincentelli Cristina
Mount Sinai Medical Center, The Arkadi M. Rywlin M.D. Department of Pathology and Laboratory Medicine, Miami Beach, FL, USA.
Mount Sinai Medical Center, Department of Diagnostic Radiology, Miami Beach, FL, USA.
Autops Case Rep. 2021 Oct 29;11:e2021332. doi: 10.4322/acr.2021.332. eCollection 2021.
Predominantly intraosseous meningiomas are rare entities that include true primary intraosseous meningiomas (PIM), as well as meningiomas that may show extensive bone involvement, such as meningiomas. Different hypotheses have been proposed to decipher the origin of PIMs, such as ectopic arachnoid cap cell entrapment during birth or after trauma. Surgical resection is the treatment of choice of such lesions.
We present a case of a 65-year-old man with an enlarging mass in the parieto-occipital region that grew slowly and progressively over 13 years, following head trauma during a motor vehicle accident. One year prior to presentation, he started experiencing daily holocranial headaches and blurry vision. CT and MRI studies revealed a permeative midline calvarial lesion measuring 14 cm in greatest dimension with extensive periosteal reaction, extension into the subcutaneous soft tissues, subjacent dural thickening and intracranial extension with invasion of the superior sagittal sinus. The favored pre-operative clinical diagnosis was osteosarcoma. The abnormal calvarium was excised and histopathological examination confirmed the diagnosis of a predominantly intraosseous calvarial meningioma, WHO grade I.
The present case highlights the importance of histopathologic diagnosis in guiding therapeutic decisions and reiterates the necessity of considering PIM or meningiomas with extensive intraosseous component in the differential diagnosis of calvarial masses, even when imaging suggests a neoplasm with aggressive behavior, such as osteosarcoma.
主要位于骨内的脑膜瘤是罕见的实体肿瘤,包括真正的原发性骨内脑膜瘤(PIM)以及可能表现出广泛骨受累的脑膜瘤。已经提出了不同的假说来解释PIM的起源,例如出生时或外伤后异位蛛网膜帽细胞的陷入。手术切除是这类病变的首选治疗方法。
我们报告一例65岁男性,在机动车事故中头部受伤后,顶枕部有一肿块逐渐增大,在13年中缓慢且渐进性生长。在就诊前一年,他开始每天出现全颅头痛和视力模糊。CT和MRI检查显示一个弥漫性的中线颅骨病变,最大直径为14cm,伴有广泛的骨膜反应,延伸至皮下软组织,下方硬脑膜增厚,并向颅内延伸侵犯上矢状窦。术前最可能的临床诊断是骨肉瘤。切除异常颅骨,组织病理学检查确诊为主要位于骨内的颅骨脑膜瘤,WHO I级。
本病例强调了组织病理学诊断在指导治疗决策中的重要性,并重申在颅骨肿块的鉴别诊断中,即使影像学提示为具有侵袭性的肿瘤,如骨肉瘤,也有必要考虑PIM或具有广泛骨内成分的脑膜瘤。