Tokoro K, Nakajima F, Yamataki A
Department of Neurosurgery, Odawara Municipal Hospital, Kanagawa, Japan.
Neurosurgery. 1988 Mar;22(3):595-8. doi: 10.1227/00006123-198803000-00029.
Osteogenesis imperfecta with infantile chronic subdural hematoma is extremely rare and has not been previously described in the literature. Our patient was a baby girl suffering from osteogenesis imperfecta tarda (Type I) who had an acute subdural hematoma at birth and who developed a progressive chronic subdural hematoma with local protrusion of the overlying skull. She was treated surgically with a good result. This rare complication is due to weakness of an insufficiently calcified skull, which is peculiar to this disorder of bone and connective tissue development.
成骨不全合并婴儿慢性硬膜下血肿极为罕见,此前文献中未有描述。我们的患者是一名患有迟发型成骨不全(I型)的女婴,出生时即有急性硬膜下血肿,并逐渐发展为慢性硬膜下血肿,伴有颅骨局部隆起。她接受了手术治疗,效果良好。这种罕见的并发症是由于颅骨钙化不足导致的颅骨薄弱,这是这种骨与结缔组织发育障碍所特有的。