Kishaba Kazutaka, Hokama Yohei, Kuninaka Tomomi, Miyahira Hirofumi, Tomita Mariko, Wada Naoki, Yogi Akira, Hamasaki Tadashi
Neurosurgery, University of the Ryukyus Hospital, Ginowan, JPN.
Diagnostic Pathology, University of the Ryukyus Hospital, Ginowan, JPN.
Cureus. 2025 Jul 7;17(7):e87472. doi: 10.7759/cureus.87472. eCollection 2025 Jul.
Primary lymphoma of the cranial vault is extremely rare and often mimics other cranial bone tumors on imaging. We report a 75-year-old female with a scalp mass and occasional headache. MRI revealed a lesion centered in the cranial vault, extending both intra- and extracranially. The initial diagnosis was intraosseous meningioma, but the lesion rapidly decreased in size over a few weeks without any treatment. Biopsy revealed histology consistent with non-Hodgkin lymphoma. Further classification suggested marginal zone B-cell lymphoma, a rare entity arising in the cranial vault. We managed the patient with imaging follow-up and found no recurrence for six months. The present case supports the notion that indolent lymphomas arising in the cranial bone share regression potential seen in other tissues. Accurate diagnosis requires histopathological confirmation even when lesions regress spontaneously. A watch-and-wait approach may be reasonable for selected cases, with careful monitoring for progression or transformation.
颅骨原发性淋巴瘤极为罕见,在影像学上常与其他颅骨肿瘤相似。我们报告一例75岁女性,有头皮肿块并偶尔头痛。磁共振成像(MRI)显示一个以颅骨为中心的病变,向颅内和颅外扩展。最初诊断为骨内脑膜瘤,但未经任何治疗,该病变在几周内迅速缩小。活检显示组织学与非霍奇金淋巴瘤一致。进一步分类提示为边缘区B细胞淋巴瘤,这是一种在颅骨中出现的罕见类型。我们对该患者进行影像学随访,发现六个月内无复发。本病例支持这样一种观点,即起源于颅骨的惰性淋巴瘤具有在其他组织中所见的消退潜力。即使病变自发消退,准确诊断仍需组织病理学证实。对于某些选定的病例,观察等待的方法可能是合理的,同时要密切监测病情进展或转变。