Karamanakos Petros N, Jaaskelainen Juha E, Alafuzoff Irina, Pirinen Elina, Vanninen Ritva, Silvennoinen Sanna, Sankilampi Ulla, Immonen Arto
Department of Neurosurgery, Kuopio University Hospital, Kuopio, Finland.
J Neurosurg Pediatr. 2010 Mar;5(3):277-82. doi: 10.3171/2009.10.PEDS09453.
Giant cell tumors (GCTs) of the bone are rare, usually benign but locally aggressive neoplasms that primarily occur in the epiphyses of long bones. They seldom develop in the cranium; when they do, they involve principally the sphenoid and temporal bones. These tumors usually affect young adults, and few reports in children have been published. Primary malignant GCTs of the skull are even more uncommon. The 3 published cases all involved adults over 40 years of age. Herein, the authors present a case of a highly aggressive primary malignant GCT of the posterior fossa in a 5-week old preterm infant. One month after the gross-total resection of the tumor found in the bone, the infant's condition rapidly deteriorated and she died. Magnetic resonance imaging and postmortem examination revealed a tumor larger than it had been before the operation, with expansion toward the brain. To the best of the authors' knowledge, this is the youngest patient reported with a primary malignant GCT of the skull, and actually the first case in a pediatric patient. In addition, the extremely high growth rate of the tumor in the postoperative period renders this case the most aggressive primary malignant GCT of the cranium described so far.
骨巨细胞瘤(GCTs)较为罕见,通常为良性但具有局部侵袭性的肿瘤,主要发生于长骨的骨骺。它们很少在颅骨中发生;一旦发生,主要累及蝶骨和颞骨。这些肿瘤通常影响年轻人,关于儿童病例的报道很少。颅骨原发性恶性GCTs更为罕见。已发表的3例病例均为40岁以上的成年人。在此,作者报告1例5周大的早产婴儿后颅窝高度侵袭性原发性恶性GCTs病例。在对骨内发现的肿瘤进行全切除术后1个月,婴儿病情迅速恶化并死亡。磁共振成像和尸检显示肿瘤比手术前更大,并向脑内扩展。据作者所知,这是报道的最年轻的颅骨原发性恶性GCTs患者,实际上也是儿科患者中的首例。此外,肿瘤在术后极高的生长速度使该病例成为迄今为止所描述的最具侵袭性的颅骨原发性恶性GCTs。