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同一节段广泛的脊髓血管瘤合并皮肤痣:围产期截瘫的罕见病例

Extensive Spinal Hemangioma Associated With Cutaneous Nevus in the Same Metamere: An Unusual Case of Paraplegia in the Peripartum Period.

作者信息

Flores Reyes Rogelio D

机构信息

Neurosurgery, Mexican Social Security Institute, Veracruz, MEX.

出版信息

Cureus. 2024 Feb 22;16(2):e54673. doi: 10.7759/cureus.54673. eCollection 2024 Feb.

Abstract

Cavernous hemangiomas occur most commonly in the cerebral hemispheres but can involve any part of the neuroaxis, including the spine. Very rare cases of spinal angiomas are associated with a skin lesion in the same metameric segment. This condition, known as segmental neurovascular syndrome or Cobb syndrome, was first described in 1915. We report a rare case of segmental neurovascular syndrome with extensive cervical and thoracic lumbar involvement expressed as peripartum spinal cord compression syndrome. A 37-year-old female with a cutaneous nevus from the C7 dermatome to the L3 dermatome experienced pelvic limb paralysis 48 hours after giving birth to a healthy newborn by cesarean section. Magnetic resonance imaging (MRI) revealed an enhancing extensive epidural mass from C7 to T7 and subsequently from T10 to L3. Histopathology confirmed a spinal cavernous hemangioma. Although rare, segmental neurovascular syndrome must be considered in patients with cutaneous angioma and radiculopathy or myelopathy. Early diagnosis can lead to curative surgical treatment and more favorable outcomes.

摘要

海绵状血管瘤最常发生于大脑半球,但可累及神经轴的任何部位,包括脊柱。非常罕见的脊柱血管瘤病例与同一节段的皮肤病变相关。这种情况,称为节段性神经血管综合征或科布综合征,于1915年首次被描述。我们报告一例罕见的节段性神经血管综合征,累及广泛的颈段和胸腰段,表现为围产期脊髓压迫综合征。一名37岁女性,从C7皮节到L3皮节有皮肤痣,在剖宫产分娩一名健康新生儿48小时后出现盆腔肢体麻痹。磁共振成像(MRI)显示从C7到T7以及随后从T10到L3有一个强化的广泛硬膜外肿块。组织病理学证实为脊柱海绵状血管瘤。尽管罕见,但对于患有皮肤血管瘤和神经根病或脊髓病的患者,必须考虑节段性神经血管综合征。早期诊断可导致治愈性手术治疗并获得更有利的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ab4/10960251/f1bcbee94ec0/cureus-0016-00000054673-i01.jpg

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