Your browser doesn't support javascript.
7 year old male with 2 months of progressive left sidedweakness
Pediatrics ; 147(3):956-957, 2021.
Artigo em Inglês | EMBASE | ID: covidwho-1177797
ABSTRACT

Introduction:

Gliomas are the most common primary CNS tumors making up 50-60% of brain tumors inchildren. Prognosis for gliomas depends on histologic grade and location of tumor. Impingement on normalbrain tissue or increase in intracranial pressure is caused by either obstruction of CSF flow or by direct masseffect. Symptoms can include lethargy, headache and vomiting. Signs of slow growing CNS tumors can includeirritability, poor school performance and loss of developing milestones. Most arise with no known underlyingrisk factor or disorder. Case Presentation 7-year-old male with no significant past medical history presented with left sided weakness that began 8 weeks prior to admission. Initially mother noticed the patient to have anasymmetric smile. Patient was seen by PCP and was referred to ophthalmology and neurology at that time. 4weeks later, he was noted to have left arm weakness and difficulty writing with his left hand. A week later hebegan having weakness in his left leg and was noticed to have increased instability. Patient was reevaluated byPCP who instructed him to complete a 5-day course of steroids and follow-up with neurology. On the day of admission he was seen by an outpatient neurologist using telemedicine due to COVID outbreak. It was notedthe patient had left sided paralysis, a dilated left pupil, weakness of the left arm and leg with elevation. Afterseeing the physical exam findings through a webcam, the neurologist suggested for the patient to have urgentevaluation in the emergency department. CT brain with contrast revealed a heterogenous, complex mass inthe region of the right hypothalamus. MRI brain showed mass that involved the right and left cerebralhemisphere, with infiltration of the left optic tract. A brain biopsy was performed by neurosurgery andpathology was GFAP positive confirming astrocytoma in the brainstem.

Discussion:

About 25% ofastrocytomas are aggressive or high grade. Brainstem gliomas make up 10-20% of CNS tumors in children lessthan 15 years old. Diffuse midline gliomas are infiltrative tumors, usually with astrocytic morphology and arelocated in the pons, thalamus or spinal cord. Most cases have high grade features and are histologicallyconsistent with Grade 4. Treatment includes surgery, radiotherapy and chemotherapy. For high grade tumorssurgery can be performed as well as radiotherapy and chemotherapy. But without reasonable resectionchemotherapy is palliative. Brainstem gliomas cannot be removed, and therefore have a poor outcome.

Conclusion:

Despite lack of in person evaluation, this case highlights the importance of prompt recognitionand action when performing history and physical exams even in this new era of telemedicine. In the setting ofthe COVID-19 pandemic, the use of telemedicine proved to be prominent in the diagnosis of this patient.

Texto completo: Disponível Coleções: Bases de dados de organismos internacionais Base de dados: EMBASE Idioma: Inglês Revista: Pediatrics Ano de publicação: 2021 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS


Texto completo: Disponível Coleções: Bases de dados de organismos internacionais Base de dados: EMBASE Idioma: Inglês Revista: Pediatrics Ano de publicação: 2021 Tipo de documento: Artigo