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成骨不全伴 Arnold-Chiari 畸形 I 型。

Osteopetrosis with Arnold Chiari malformation type I.

机构信息

Radiodiagnosis, All India Institute of Medical Sciences Bhubaneswar, Bhubaneswar, Odisha, India.

Department of pediatrics, All India Institute of Medical Sciences Bhubaneswar, Bhubaneswar, Orissa, India.

出版信息

BMJ Case Rep. 2023 Aug 16;16(8):e254559. doi: 10.1136/bcr-2023-254559.

Abstract

Osteopetrosis is a rare genetic disorder resulting in increased bone density and decreased bone remodelling. Bone expansion results in the crowding of neural foramina causing cranial nerve compression. Here, we describe a female infant in her mid infancy presented with no eye contact since birth, and abdominal distension for 2 months. On CT evaluation, sclerotic bones with bilateral optic canal narrowing were present. A crowded posterior fossa with Arnold Chiari type I malformation was seen on MRI evaluation, suggesting a rare association of osteopetrosis with Arnold Chiari's malformation.

摘要

石骨症是一种罕见的遗传性疾病,导致骨密度增加和骨重建减少。骨扩张导致神经孔拥挤,从而导致颅神经受压。在这里,我们描述了一名处于中期婴儿期的女性婴儿,她从出生起就没有眼神交流,并且腹部肿胀了 2 个月。CT 评估显示,双侧视神经管狭窄的硬化性骨。MRI 评估显示后颅窝拥挤,存在 Arnold-Chiari Ⅰ型畸形,提示石骨症与 Arnold-Chiari 畸形罕见相关。

相似文献

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Osteopetrosis with Arnold Chiari malformation type I.成骨不全伴 Arnold-Chiari 畸形 I 型。
BMJ Case Rep. 2023 Aug 16;16(8):e254559. doi: 10.1136/bcr-2023-254559.
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Clinicoradiological findings of benign osteopetrosis: report of two new cases.良性骨硬化症的临床放射学表现:两例新病例报告。
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Osteopetrosis.骨质石化症
Orphanet J Rare Dis. 2009 Feb 20;4:5. doi: 10.1186/1750-1172-4-5.
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Osteopetrorickets: case report.骨质石化性佝偻病:病例报告
Eur J Pediatr. 2000 Aug;159(8):579-81. doi: 10.1007/s004310000485.

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