Tantbirojn Patou, Sanpavat Anapat, Bunyaratavej Krishnapundha, Desudchit Tayard, Shuangshoti Shanop
Department of Pathology. Faculty of Medicine, King Chulalongkorn Memorial Hospital, Rama IV Rd, Bangkok 10330, Thailand.
J Med Assoc Thai. 2005 Dec;88(12):1962-5.
Desmoplastic infantile ganglioglioma (DIG) is an uncommon neuroepithelial tumor associated with epilepsy, mostly occurring in the first 2 years of life. Most DIGs carry good prognosis after complete resection, even when a primitive cellular element is present. However a few examples of DIG with histologic anaplasia have recently been reported, and one demonstrated an unusual aggressive behavior. The authors describe herein a DIG with high Ki-67 proliferation index (30%) in a 10-month-old male infant with epilepsy, but with an excellent prognosis after total tumor resection.
促纤维增生性婴儿型节细胞胶质瘤(DIG)是一种与癫痫相关的罕见神经上皮肿瘤,多发生于生命的头两年。大多数DIG在完全切除后预后良好,即使存在原始细胞成分。然而,最近有报道称少数DIG具有组织学间变,其中一例表现出异常侵袭性。本文作者描述了一名10个月大患癫痫的男婴,其DIG的Ki-67增殖指数较高(30%),但肿瘤全切后预后良好。