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Ⅰ.はじめに
Maffucci症候群とは先天性,非遺伝性の,中胚葉性形成不全症であり,内軟骨腫症および多発性血管腫を合併する稀れな症候群である.
諸外国で,せいぜい150例程度の報告があったと思われるが,本邦での神経内科または脳神経外科関係の雑誌への報告は未だなく,整形外科,皮膚科からのものが主で,頭蓋内病巣が少ない事が,この一因かとも思われる.われわれは,頭蓋内軟骨腫を伴うMaffucci症候群を経験したので,文献考察を加えて報告したい.
A rare case of Maffucci's syndrome with intracranial chondroma was reported and the literature reviewed. A 16-year-old female high-school student was reffered to our service with 2 month history of diplopia and headache. She had been noticed to have multiple subcutaneous blueish nodules in the lower extremities and multiple bony deformities in the four extremities since 6 months old. A biopsy of a skin lesion revealed cavernous hemangioma with calcified thrombi. Another biopsy from the deformed right femur showed it to he enchondroma.
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