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Noon Conference
Benjamin Fife
6 Feb 2018
© 2016 Virginia Mason Medical Center 2
Objectives
Meningioma
• Review differential for headache
• Discuss clinical presentation
• Discuss diagnostics & WHO grading
• Review illness script
© 2016 Virginia Mason Medical Center
Secondary headaches in patients >50
3
Condition Presentation
Giant cell (temporal)
arteritis
Temporal pain
Constitutional symptoms (fever, fatigue, etc.)
Trigeminal neuralgia Brief, unilateral, stabbing pain
Involves jaw, lips, gums
Chronic subdural
hematoma
Light headedness, cognitive impairment, apathy
Occasionally seizures
Herpes zoster &
postherpetic neuralgia
Unilateral, dermatomal, can be prodromal
Pain persistent >4mths after rash
Brain tumor Progressive, worse in morning
Seizures, cognitive dysfunction, focal weakness
Differential Diagnosis
© 2016 Virginia Mason Medical Center
Danger Signs with Headaches
Systemic symptoms or condition
Neurologic symptoms or abnormal signs
Onset is new
Other associated conditions or features
Previous headache history with headache
progression
4
© 2016 Virginia Mason Medical Center
Meningioma: Clinical Presentation
HEENT: headache
visual field defects
unilateral vision loss
weakness of EOM
papilledema
loss of hearing or smell
Neuro: seizures – 30%
apathy, inattention
extremity weakness/numbness
5
© 2016 Virginia Mason Medical Center
Characterizing Meningiomas
WHO Grade I –
Benign
Everything else
WHO Grade II –
Atypical
≥4 mitoses per 10 high-powered fields
brain invasion, or
three or more of the following:
• increased cellularity
• small cells with a high nuclear-to-cytoplasmic ratio,
• prominent nucleoli,
• Uninterrupted, sheet-like growth, or
• foci of spontaneous or geographic necrosis
WHO Grade III -
Malignant
≥20 mitoses per 10 high-powered fields and/or
malignant characteristics
6
© 2016 Virginia Mason Medical Center
Meningiomas - Imaging
7
WHO Grade I -
Benign
Smooth contour
Homogeneous enhancement
Dural tail
Calcification
WHO Grade II –
Atypical
Large or disproportionate amount of associated edema
Intra-tumoral cystic change
Extensive bone involvement
Brain or leptomeningeal invasion
Low apparent diffusion coefficient
Elevated cerebral blood volume
WHO Grade III -
Malignant
© 2016 Virginia Mason Medical Center
• Imaging comparison
• typical vs atypical
• meningioma vs other
space occupying lesion
•
•
8
Meningiomas -
Imaging
1 2
3
© 2016 Virginia Mason Medical Center
Meningiomas - Imaging
9
1
1 2
© 2016 Virginia Mason Medical Center 10
Meningioma Dural Metastases
Pathophysiology Pluripotent mesenchymal progenitor cells
Seeding through blood (arterial/venous
plexus), lymphatics, from skull mets
Epidemiology
Most common primary CNS tumor
Median age: 65
Women > Men
History of radiation, NF2, breast cancer
Breast, prostate, lung cancer
Systemic malignancy: 10-30%
20% have unknown primary tumor
Time course Slow growing, present later in life Generally faster growing
Clinical
presentation
Headache, mental status change,
confusion, focal deficits, seizures
Headache, fatigue, confusion, focal
deficits
Diagnostics
Contrast enhanced MRI
Biopsy
Contrast enhanced MRI
Biopsy
Unknown primary: CXR, Chest CT, PET
Therapeutics
Small (<2cm) – Active surveillance
Large (>2cm) or symptomatic – resection
Atypical/Malignant – resection + radiation
Untreated: prognosis is 1-2 months
Stable extracranial  resection +
radiation
Illness Scripts
© 2016 Virginia Mason Medical Center
Vital signs of increased ICP are:
A)Low HR, high RR, high BP
B)High HR, low RR, low BP
C)Low HR, low RR, high BP
D)High HR, high RR, low BP
11
© 2016 Virginia Mason Medical Center
What are vital signs of increased ICP?
A)Low HR, high RR, high BP
B)High HR, low RR, low BP
C)Low HR, low RR, high BP
D)High HR, high RR, low BP
12
© 2016 Virginia Mason Medical Center 13

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Meningioma

  • 2. © 2016 Virginia Mason Medical Center 2 Objectives Meningioma • Review differential for headache • Discuss clinical presentation • Discuss diagnostics & WHO grading • Review illness script
  • 3. © 2016 Virginia Mason Medical Center Secondary headaches in patients >50 3 Condition Presentation Giant cell (temporal) arteritis Temporal pain Constitutional symptoms (fever, fatigue, etc.) Trigeminal neuralgia Brief, unilateral, stabbing pain Involves jaw, lips, gums Chronic subdural hematoma Light headedness, cognitive impairment, apathy Occasionally seizures Herpes zoster & postherpetic neuralgia Unilateral, dermatomal, can be prodromal Pain persistent >4mths after rash Brain tumor Progressive, worse in morning Seizures, cognitive dysfunction, focal weakness Differential Diagnosis
  • 4. © 2016 Virginia Mason Medical Center Danger Signs with Headaches Systemic symptoms or condition Neurologic symptoms or abnormal signs Onset is new Other associated conditions or features Previous headache history with headache progression 4
  • 5. © 2016 Virginia Mason Medical Center Meningioma: Clinical Presentation HEENT: headache visual field defects unilateral vision loss weakness of EOM papilledema loss of hearing or smell Neuro: seizures – 30% apathy, inattention extremity weakness/numbness 5
  • 6. © 2016 Virginia Mason Medical Center Characterizing Meningiomas WHO Grade I – Benign Everything else WHO Grade II – Atypical ≥4 mitoses per 10 high-powered fields brain invasion, or three or more of the following: • increased cellularity • small cells with a high nuclear-to-cytoplasmic ratio, • prominent nucleoli, • Uninterrupted, sheet-like growth, or • foci of spontaneous or geographic necrosis WHO Grade III - Malignant ≥20 mitoses per 10 high-powered fields and/or malignant characteristics 6
  • 7. © 2016 Virginia Mason Medical Center Meningiomas - Imaging 7 WHO Grade I - Benign Smooth contour Homogeneous enhancement Dural tail Calcification WHO Grade II – Atypical Large or disproportionate amount of associated edema Intra-tumoral cystic change Extensive bone involvement Brain or leptomeningeal invasion Low apparent diffusion coefficient Elevated cerebral blood volume WHO Grade III - Malignant
  • 8. © 2016 Virginia Mason Medical Center • Imaging comparison • typical vs atypical • meningioma vs other space occupying lesion • • 8 Meningiomas - Imaging 1 2 3
  • 9. © 2016 Virginia Mason Medical Center Meningiomas - Imaging 9 1 1 2
  • 10. © 2016 Virginia Mason Medical Center 10 Meningioma Dural Metastases Pathophysiology Pluripotent mesenchymal progenitor cells Seeding through blood (arterial/venous plexus), lymphatics, from skull mets Epidemiology Most common primary CNS tumor Median age: 65 Women > Men History of radiation, NF2, breast cancer Breast, prostate, lung cancer Systemic malignancy: 10-30% 20% have unknown primary tumor Time course Slow growing, present later in life Generally faster growing Clinical presentation Headache, mental status change, confusion, focal deficits, seizures Headache, fatigue, confusion, focal deficits Diagnostics Contrast enhanced MRI Biopsy Contrast enhanced MRI Biopsy Unknown primary: CXR, Chest CT, PET Therapeutics Small (<2cm) – Active surveillance Large (>2cm) or symptomatic – resection Atypical/Malignant – resection + radiation Untreated: prognosis is 1-2 months Stable extracranial  resection + radiation Illness Scripts
  • 11. © 2016 Virginia Mason Medical Center Vital signs of increased ICP are: A)Low HR, high RR, high BP B)High HR, low RR, low BP C)Low HR, low RR, high BP D)High HR, high RR, low BP 11
  • 12. © 2016 Virginia Mason Medical Center What are vital signs of increased ICP? A)Low HR, high RR, high BP B)High HR, low RR, low BP C)Low HR, low RR, high BP D)High HR, high RR, low BP 12
  • 13. © 2016 Virginia Mason Medical Center 13

Editor's Notes

  1. Noon Conference Best Practices 1. Choose a case! Don’t worry about whether it’s too simple or “not interesting” – part of the goal of conference is to get learning out of any case we see. Talk with the chiefs if you’re uncertain. 2. Condense the meat of the case in a way that will be accessible to you when you present (print H&P, write down labs/vitals/imaging, think about how you want to structure the way you give the residents information) 3. Choose BRIEF teaching points from the case. In particular, at least for the first part of the year we’d like to focus on the concept of illness scripts – if you’re going to make a PowerPoint, one of your slides should be comparing the illness scripts for your case’s diagnosis with the top 1-2 other differential diagnoses. Helpful to highlight similarities and differences. Key teaching points to address: * How did this case fit the illness script? How did this case not fit? * Is there an interesting and relevant piece of media (EKG, imaging, rash photo, etc) that could be shown? * What was surprising to you about this case (presentation, workup, management)? * What were some of the cognitive biases that occurred during the management of this case, and/or where are some places with risk of bias? * Is there a MKSAP question related to this case that could help solidify this script/concept? Common pitfalls to avoid * Avoid choosing a PowerPoint template that is difficult to read. * Choose either a light background with dark/colored text, or a dark background with light text. * Your text should be legible from the back of the room—dark colored text and a dark background is hard to see. * Avoid gradient backgrounds as it might be hard to get a uniform text color to be visible. * When in doubt just use the Virginia Mason template. Avoid overcrowding your slides. * Font size should generally be AT LEAST 20-pt or greater, preferably 24-pt or greater. * If you are having to use smaller fonts you are putting too much text on your slides. While it is ok to use smaller font sizes for tables or lists in which you will highlight the key components for the audience, you should not be using them to deliver most information. * Focus on the 3-5 key points per slide. * Remember, your audience cannot both listen to you talk and read a long slide at the same time—they must do one or the other. You don’t need to write EVERYTHING you want to say on your slides, just give yourself a few words as a cue to what you want to say and emphasize the main points. Avoid a broad overview of a large topic. * Remember, you only have 5-7 minutes to consolidate key learnings from the case * Please try to avoid having more than 5-8 slides – we’re more likely to retain information from a narrow talk than a super broad one. For example, rather than having 12 individual slides on the epidemiology, pathophysiology, clinical presentation, treatment, etc, the broad strokes of those topics could be effectively presented in the context of comparing illness scripts and relating them to your specific case. * Do NOT reproduce an UpToDate (or other review) article on a topic in slide form—selectively choose key points that relate to YOUR case. You should read and review the topic for your own learning, but your job is to extract the points you think are most helpful and relevant, not to regurgitate the whole article. * Leave a lecture of a broad topics to our attending presenters who have a half hour to cover more general information Remember, the goal of these presentations is to synthesize and extract key learnings from a specific case, NOT to provide a full overview of a topic. Focus on the few key points you want the audience to take away from the case.
  2. Our patient: >50 (62yo) “pressure” not stabbing/throbbing woke him up at night associated with neurologic symptoms
  3. Danger signs of headaches S = (eg, fever, weight loss, cancer, pregnancy, immunocompromised state, including HIV) N = (eg, confusion, impaired alertness or consciousness, papilledema, focal neurologic symptoms or signs, meningismus, or seizures) O = (particularly for age >50 years) or sudden (eg, "thunderclap") O = (eg, head trauma, illicit drug use, or toxic exposure; headache awakens from sleep, is worse with Valsalva maneuvers, or is precipitated by cough, exertion) P = or change in attack frequency, severity, or clinical features
  4. Asymptomatic – incidental or autopsy Visual field defects - parasellar meningiomas Progressive unilateral visual loss (which may be mistaken for optic neuritis) - optic nerve sheath meningiomas Mild weakness of extraocular movements - cavernous sinus meningiomas Hearing or smell – cerebellopontine angle Mental status – subfrontal/sphenoid ridge ~Optic atrophy in one eye and papilledema in the other, the so-called Foster-Kennedy syndrome, can be produced by parasellar or subfrontal meningiomas
  5. Grade I – 70%, 80-85%, most infratentorial Grade II – 30% Grade III - <1%
  6. 1. (MRI w/ gad) Dural tail sign, homogenous 2. (CT) Atypical - in general involve bone 20-40% of the time (right parasaggital hy[erdense) 3. (CT) Malignant – parafalcine, entering genu of corpus callosum showing hypervascularity
  7. 2. Heterogenous mass, patchy enhancement, L posterior fossa, edema and broad dural attachment metastatic undifferentiated carcinoma arising from breast
  8. Meningioma: 30% of all primary CNS tumors One sample: 5,000 adults (mean 65yo), 2.5% had meningioma Most commonly asymptomatic! Small ones, incidental and doesn’t always mean the cause of a HA Dural Metastases -
  9. Answer: C Name of this triad? Cushings triad (reflex/response)
  10. Answer: C Brainstem compression? Name of this triad? Cushings triad (reflex/response)
  11. Sen Spec Likli P Likli A BP >=160 37-58 93-94 7.3 0.6 RR