Aquilina K, O'Brien D F, Phillips J P
Department of Neurosurgery, Beaumont Hospital, Dublin, Eire.
Br J Neurosurg. 2004 Oct;18(5):518-23. doi: 10.1080/02688690400012491.
Primary non-Hodgkin's lymphoma of the skull vault is a rare disease. We describe a case occurring in a 72-year-old woman presenting with generalized tonic clonic seizures on a background of a 1-year history of headaches and progressively enlarging scalp masses. Imaging showed diffuse infiltration of the skull vault with multifocal intra- and extracranial soft tissue masses, causing compression and probably infiltration of the cerebral cortex. Further investigation failed to identify any other evidence of systemic lymphoma. Biopsy of one of the scalp masses showed a small to intermediate cell B cell lymphoma. The other nine reported cases of primary skull vault lymphoma are reviewed. The diffuse vault infiltration as well as the multiple intracranial, scalp and temporalis muscle masses renders this case unique.
颅骨原发性非霍奇金淋巴瘤是一种罕见疾病。我们描述了一例发生在一名72岁女性身上的病例,该患者在有1年头痛病史且头皮肿块逐渐增大的背景下出现全身性强直阵挛性发作。影像学检查显示颅骨弥漫性浸润,伴有多灶性颅内和颅外软组织肿块,导致大脑皮质受压并可能受浸润。进一步检查未发现任何其他系统性淋巴瘤的证据。对其中一个头皮肿块进行活检显示为小至中等细胞B细胞淋巴瘤。本文还回顾了其他9例报道的原发性颅骨淋巴瘤病例。颅骨的弥漫性浸润以及多个颅内、头皮和颞肌肿块使该病例具有独特性。