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Case Conference. K. Myra Lalas PGY 3. CC: “walking funny”. History of Present Illness. 2 days PTA, started walking funny (like a drunk person), loses balance when standing, has been worsening When he talks, his mouth turns to the L side, once yesterday, twice today No seizures No LOC
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Case Conference K. Myra Lalas PGY 3
History of Present Illness • 2 days PTA, started walking funny (like a drunk person), loses balance when standing, has been worsening • When he talks, his mouth turns to the L side, once yesterday, twice today • No seizures • No LOC • No fevers
HPI • No staring spells • (+) frontal headache this morning • No vomiting • Last week, (+) belly pain and NBNB emesis for 6 days • No diarrhea • No rash
HPI • No incontinence • Able to move neck • No head trauma • No known sick conracts • Mom takes anti-anxiety meds (no missing meds.) • No sick contacts
Went to CA 4 months ago. • Usually “hyper” but has been more calm the past 2 days
Past Medical History • Dental surgery at 3 yo • Surgery for trigger thumb at 2 yo • No seizures • No asthma
Birth History • FT via NSVD; no complications Immunization History • Up to date
Developmental History • Walked before 12 mns of age • In SPED; has an IEP- 1st grade but failing his classes
Family Medical History • Mom has anxiety d/o. • No seizures • No mental retardation • No schizophrenia • No malignancies
Personal/ Social History • Lives with mom • No pets or smokers at home
Physical Exam VS Temp 99.8 HR 88 RR 20 BP 100/60 100%RA Gen awake, alert, oriented x 3, speech slurred mildly HEENT PERRLA, EOMI, (+) vertical and horizontal nystagmus, clear OP, no LAD CHEST CTA b/l HEART N S1/S2, no murmurs ABD soft, (+) BS, no HSM EXT FEP, CRT < 2 secs
Neuro Exam • Cranial nerves: I grossly intact II PERRLA, visual field testing normal III, IV, VI EOMI; (+) vertical and horizontal nystagmus V intact VII depressed RNLF with smile, weak eye closure and eye wrinkling on the R
Neuro Exam VIII grossly intact IX, X no gag XI able to shrug shoulders XII no tongue fasciculation, tongue midline
Neuro Exam Motors 5/5 Sensory no deficits Reflexes 1+, L toes upgoing Cerebellar ataxic gait, R dysmetria
Acute Ataxia • Brain Tumor • Drug Ingestion • Encephalitis (Brainstem) • Genetic Disorders • Dominant recurrent ataxia • Episodic ataxia • Hartnup Disease • MSUD • Pyruvate dehydrogenase deficiency
Acute Ataxia • Migraine • Basilar • BPPV • Postinfectious- immune • Acute postinfectious cerebellitis • Miller Fisher Syndrome • MS • Neuroblastoma • Pseudoataxia (epileptic)
Acute Ataxia • Trauma • Hematoma • Postconcussion • Vertebrobasilar occlusion • Vascular Disorders Cerebellar hemorrhage Kawasaki disease
Where is the lesion? • Ataxia • R facial palsy • Upgoing toes on the L • R dysmetria
What labs will you order? • MRI • CBC • Lyme titers • ESR/ CRP • Urine toxicology
MRI • Axial mass in the R posterior brainstem, R middle cerebellar peduncle with surrounding vasogenic edema compressing the 4th ventricle with 2 separate areas of cystic changes
CNS tumors in Childhood • Primary malignant CNS tumors are the second most common childhood malignancies (after hematologic malignancies.) • Most common pediatric solid organ tumor
Signs and Symptoms • Headache • Nausea and vomiting • Abnormal gait or coordination • Papilledema • Seizures • Squint • Change in behavior or school performance • Macrocephaly • Cranial nerve palsies
Signs and Symptoms • Lethargy • Abnormal eye movements • Hemiplegia • Weight loss • Unspecified visual or eye abnormalities • Altered level of consciousness
Diagnosis • MRI *Compared to CT, it provides more detailed images of parenchymal lesions *More sensitive in detecting lesions within the posterior fossa, subarachnoid spaces, and leptomeninges • CT Scan
Diagnosis • Fluorodeoxyglucose PET imaging or 11C-methionine PET may indicate foci of higher grade within a predominantly low-grade tumor. • 11C-methionine PET may also be able to differentiate astrocytic from oligodendroglial tumors. • Histology
Brainstem Gliomas • Occur in the brain stem, which is the area between the aqueduct of Sylvius and the fourth ventricle. • Originate from glial cells or their stem cell precursors and include astrocytoma, oligodendroglioma, and ependymoma.
Brainstem gliomas are divided into 3 distinct anatomic locations—diffuse intrinsic pontine,1tectal, and cervicomedullary.
Anatomic location determines the pathophysiological manifestation of the tumor. • With tectal lesions- hydrocephalus may occur as a result of fourth ventricular compression. • With pontine and cervicomedullary lesions, cranial nerve or long tract signs are observed commonly.
WHO Grading • Histopathologically, brainstem gliomas can range from WHO Grade 1 to 4. Based on nuclear atypia, vascular proliferation, mitoses, necrosis • Grade 1 - juvenile pilocytic astrocytoma • Grade 2 - diffuse astrocytoma • Grade 3 - anaplastic astrocytoma • Grade 4 - glioblastoma multiforme.
A low grade glioma or astrocytoma may show only a low density area (dark area) whereas high grade gliomas (Glioblastoma) usually show more contrast enhancement (white on the outside) and necrosis in the middle (looks black on the MRI,)
Treatment • Low-grade astrocytomas, which include Grade 1 (juvenile pilocytic astrocytomas) and Grade 2 (diffuse astrocytomas) astrocytomas Complete surgical resection. If additional treatment is required, radiation therapy is usually used for the older children and chemotherapy is used for the younger children.
Treatment High-grade astrocytomas include Grade 3 (anaplastic astrocytomas) and Grade 4 (glioblastoma multiforme) astrocytomas Surgery, radiation therapy, and chemotherapy are usually recommended.
References • Fenichel, G. Clinical Pediatric Neurology. 1997: WB Saunders Company, USA. • Rowland, LP et al. Merrit’s Neurology. 2010: Lippincott and Williams, USA. • www.uptodate.com • www.emedicine.com • www.aan.com • www.mskcc.org