Case report: double dermal sinus tracts of the cervical and thoracic spine associated with congenital intracranial pathology (hydrocephalus and an interhemispheric cyst) in a newborn patient

被引:0
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作者
Cicutti, Santiago Ezequiel [1 ]
Cuello, Javier [2 ]
Gromadzyn, Guido [1 ]
Mantese, Beatriz Elida [1 ]
机构
[1] Juan P Garrahan Hosp, Neurosurg Dept, Buenos Aires, Argentina
[2] Hosp Prov Petrona V de Cordero San Fernando, Neurosurg Dept, Buenos Aires, Argentina
关键词
Dermal sinus tract; Spinal dysraphisms; Hydrocephalus; Pediatric; Case report; COMPLICATIONS;
D O I
10.1007/s00381-023-05865-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction A dermal sinus tract (DST) is an uncommon type of spinal dysraphisms characterized by a tract lined with stratified squamous epithelium that extends from the subcutaneous tissue to the underlying thecal sac or neural tube. These developmental anomalies can present asymptomatically with cutaneous abnormalities or with devastating complications. Usually, it is presented as a unique lesion, and there are only a few reports that show multiple sinuses, and none of them associated with midline brain malformations. Methods We present the case of a 3-day-old girl with an antenatal diagnosis of hydrocephalus who was diagnosed with double dermal sinus tracts of the cervical and thoracic regions at admission. The patient presented signs of elevated intracranial pressure (ICP), which imposed a challenge in the management of the case. Results Our patient was successfully treated initially with a lumbar puncture in order to discard a cerebrospinal fluid (CSF) infection. With negative CSF cultures, a ventriculoperitoneal shunt (VPS) was placed. Nine days after the VPS surgery and without signs of infection, the DST was excised in a single procedure, without follow-up complications. Conclusion To our knowledge, this is the first description of a patient with multiple midline neural tube defects (NTDs) associated with congenital intracranial pathology. Although there are no guidelines regarding the best treatment for this complex associated pathology, the patient was treated, without follow-up complications.
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页码:1673 / 1677
页数:5
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