Hematoma espinal epidural espontáneo asociado a tratamiento anticoagulante con acenocumarol: a propósito de un caso / Spontaneous spinal epidural hematoma in patients treated with acenocumarol. A case study

El hematoma epidural espontáneo es una entidad muy poco frecuente que supone una urgencia neurológica. Su presentación es muy variable, desde un dolor de espalda hasta una tetraplejia, según la gravedad y el nivel de compresión. Se comunica el caso de un paciente cardiópata de 71 años, tratado con acenocumarol, que presentó un hematoma epidural de modo espontáneo. Al inclinarse hacia el suelo, el paciente, que no tenía síntomas, sufrió un dolor brusco cervical seguido de debilidad en los miembros superiores e inferiores. Ante la sospecha clínica de una compresión medular, se decide realizar una resonancia magnética de urgencia, que mostró un hematoma de localización epidural con extensión desde C4 hasta T8. El diagnóstico urgente y el tratamiento de descompresión precoz son fundamentales para reducir al mínimo los daños neurológicos posteriores permanentes. Nivel de Evidencia: IV

Spontaneous spinal epidural hematoma is an uncommon condition and a neurological emergency. The clinical presentation of this type of hematoma is very variable, ranging from a backache up to a quadriplegia, according to the severity and the site of compression. Here, we discuss the clinical case of a 71-year-old patient with heart problems, under previous treatment with acenocumarol, that suffered a spontaneous epidural hematoma. The patient, previously asymptomatic, presented, sudden cervical pain when he bent over, followed by weakness in the lower and the upper limbs. Due to the clinical suspicion, an emergency MRI was performed, showing an epidural hematoma extending from C4 to T8. Early diagnosis and decompressive treatment are mandatory to minimize permanent neurological damage. Level of Evidence: IV

Clival SubduralHematoma after Drainage of Concomitant Intracranial and Spinal Cord Subdural Hematomas ­ Rare Case Report

Concomitant traumatic spinal cord and intracranial subdural hematomas associated with a retroclival hematoma are very uncommon. Their pathophysiology is not totally elucidated, but one hypothesis is the migration of the hematoma from the head to the spine. In the present case report, the authors describe the case of a 51-year-old man presenting with headache, nauseas and back pain after a head trauma who presented with intracranial and spinal cord subdural hematomas. Drainage was performed but, 1 week later, a retroclival subdural hematoma was diagnosed. The present paper discusses the pathophysiology, the clinical presentation, as well as the complications of concomitant traumatic spinal cord and intracranial subdural hematomas associated with a retroclival hematoma, and reviews this condition.

Spontaneous Epidural Hematoma of the Cervical Spine Mimicking a Cerebrovascular Accident: A Case Report

Objective The present study is a case report of a 57-year-old female with controlled hypertension who presented with spontaneous spinal epidural hematoma (SSEH) mimicking a cerebrovascular accident (CVA) and was successfully treated by surgical decompression. Methods A 57-year-old woman with a medical history of hypertension presented with a sudden onset of weakness in the right upper and lower extremities. Weakness of grade 3/5 was noted in her right upper and lower extremities, but there was no motor weakness of the right facial muscles. A magnetic resonance imaging (MRI) exam of the cervical spine revealed an epidural hematoma extending from level C5 to level C7, causing spinal cord compression. Results During surgery, a cervical spinal epidural hematoma (SEH) was evacuated. Postoperatively, the power in both limbs improved to grade 5/5 just after surgery. Conclusions A high degree of suspicion, meticulous history taking, and physical examination have a great importance in these rare conditions because anticoagulant therapy as a routine treatment for ischemic CVA could be life-threatening.

Hematoma espinal epidural espontáneo: reporte de un caso / Spontaneous spinal epidural hematoma: a case report

El hematoma espinal epidural espontáneo es raro en niños, especialmente en lactantes menores de un año. A esta edad, en la literatura inglesa se han reportado solamente cuatro casos. Considerando que en los lactantes los síntomas iniciales no son específicos, el diagnóstico se puede retrasar. Presentamos el primer caso reportado en Chile de un lactante con hematoma espinal epidural espontáneo. Un lactante varón de 11 meses de edad, inicia cuadro de repentino llanto, irritabilidad sostenida, con llanto al movilizar el cuello, agregándose cuatro días después, postura con leve inclinación de cabeza a izquierda, elevación de hombro izquierdo y paresia braquial derecha. Al 13°día desarrolla episodio repentino de distonía lingual, hipertonía de extremidades superiores y ataxia respiratoria. Al 16° día de evolución la RM demuestra una lesión epidural que comprime la médula espinal entre C2 y C5. Se realizó una laminectomía de emergencia extrayéndose el hematoma. Angio-RM y angio-TAC cervical fueron normales. Tres meses después de la cirugía, se mantiene con apoyo de ventilación mecánica y tetraparesia.

Spontaneous spinal epidural hematoma is rare in children, especially in infants less than one year old. Only four cases in this age range have been reported in the english literature Because of non-specific presenting symptoms in infants, the diagnosis may be delayed. We report the first case of spontaneous spinal epidural hematoma in Chile. An eleven month-old boy initially presented with sudden weeping, irritability and crying in response to neck mobilization. Four days later he developed head lateralization and upper right limb motor weakness. On the 13th day he had a sudden episode of lingual dystonia, upper limb hypertonia and respiratory ataxia. MRI showed epidural mass compressing the spinal cord at C2 to C5 level. At 16th day of evolution an emergency laminectomy and evacuation of hematoma was done. Cervical Angio-MRI and Angio-CT scan were normal. Three months after surgery, he is still tetraparetic and requires ventilatory support.

Chronic spontaneous cervicothoracic epidural hematoma in an 8-month-old infant

Spontaneous spinal epidural hematoma is an uncommon cause of cord compression in children, especially in infants. An 8-month-old infant was admitted to our hospital for a 40-day history of paraparesis in the lower extremities. This rapidly progressed to paraparesis with an inability to move the lower extremities. MRI of the cervicothoracic spine revealed an epidural mass with compression of the spinal cord. The infant underwent C7-T3 total laminectomies. The pathology and postoperative MRI confirmed spinal epidural hematoma from a vascular malformation. We present the case to highlight the significance of recognizing this chronic spontaneous spinal epidural hematoma and discuss the diagnosis, treatment options and prognosis

Spontaneous spinal epidural haematoma

Spinal epidural haematomas [SHE] is a potentially reversible cause of spinal cord and nerve root compression, may be acute or chronic; usually its occurrence may be associated with coagulation dysfunction from medications and disease states. Patients usually present with sudden onset of neurological dysfunction. The prompt diagnosis and treatment of this relatively rare condition, when attained rapidly requires surgical decompression and can result in satisfactory neurological recovery. In the period from 2001 - 2007, 7 patients were diagnosed as spontaneous SEH and managed by urgent spinal cord decompression, age from 12-44 years. Urgent magnetic resonance imaging [MRI] was done for all patients followed by urgent decompression according to the affected levels. Spontaneous spinal epidural haematomas are a rare spinal problem and need immediate diagnosis. Imaging study, mainly MRI according to the sensory level is the key for diagnosis and immediate surgical intervention is the cornerstone to get a good result

Hematoma extradural espinhal espontâneo: relato de caso / Spontaneous spinal epidural hematoma: case report

O hematoma extradural espinhal espontâneo é considerado raro. Tem sido associado com hipertensão arterial e coagulopatias. O exame de escolha para diagnóstico é a ressonância nuclear magnética.O tratamento de escolha é drenagem cirúrgica do hematoma. O prognóstico está relacionado com a etiologia, intervalo entre icto e diagnóstico e o grau de déficits neurológicos. Os autores relatam um caso de hematoma extradural espinhal espontâneo, localizado na região torácica, com quadro de choque medular, sendo submetido a tratamento cirúrgico, que evoluiu para óbito.

The spontaneous spinal extradural hematoma is rare. It has been associated with arterial hypertension and coagulopaties. Magnetic resonance is the first choice for neuroimaging diagnosis. The surgical drainage of the hematoma is the best treatment. Prognosis is related to etiology, interval between ictus and diagnosis and degree of neurological deficits. The authors report a case of spontaneous spinal extradural hematoma, located in thoracic region, with medullar shock syndrome, that was submitted tosurgical treatment but died for non neurological complications.

[Spontaneous spinal hematoma]

The spontaneous spinal hematoma is a rare and serious pathology. Through four observations colliged in the service of neurosurgery of the CHU of Casablanca, over one 10 years period, the authors point out the topographic, etiology aspects and the principles of treatment. Four types are distinguished according to the localization compared to the dura mater; the epidural hematoma, sub-dural hematoma, the sub-arachoidienne haemorrhage, and intra-medullarly hematoma. The etiologies are dominated by three principal causes with knowing; disorders of coagulation, arteriovenous malformations and the haemorrhage of tumoral origin. The assumption of responsibility starts with the correction of possible disorders of the coagulation generally followed by surgical evacuation