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    Sarcoidosis Medical Slides

    Generate publication-quality sarcoidosis lecture slides in 30 seconds. AI-powered content structured for clinical education.

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    Why teach Sarcoidosis?

    Sarcoidosis has a global incidence of 1-35 per 100,000, with highest rates in African Americans (35.5/100,000) and Northern Europeans. The disease is characterized by non-caseating granulomas in virtually any organ, with pulmonary involvement in >90% of cases. The 2020 ERS clinical practice guidelines provide evidence-based treatment recommendations, though management remains guided largely by expert opinion due to limited randomized controlled trial data.

    Sample Lecture Slides

    What AI generates for Sarcoidosis

    Enter “Sarcoidosis” and SlideCraft generates a complete lecture deck with slides like these.

    01Scadding Chest Radiograph Staging: Stages 0-IV and Prognostic Implications
    02Non-Caseating Granuloma: Histopathology, Differential Diagnosis, and Exclusions
    03Extrapulmonary Manifestations: Cardiac, Neurologic, Hepatic, and Cutaneous Sarcoidosis
    04Treatment Indications: When to Treat vs Observe, and First-Line Corticosteroid Protocol
    05Steroid-Sparing Agents: Methotrexate, Azathioprine, Mycophenolate, and Anti-TNF Therapy
    06Cardiac Sarcoidosis: Screening, Diagnosis (PET/MRI), and Device/Immunosuppression Decisions
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    Sarcoidosis Presentation FAQ

    How should Scadding staging and prognosis be presented in sarcoidosis slides?

    Present the five stages with spontaneous remission rates: Stage 0 (normal CXR, extrapulmonary only), Stage I (bilateral hilar lymphadenopathy — 60-80% spontaneous remission), Stage II (BHL + pulmonary infiltrates — 50-60% remission), Stage III (pulmonary infiltrates without BHL — 30% remission), Stage IV (pulmonary fibrosis — 0% remission). Emphasize that staging is prognostic, not sequential — patients do not necessarily progress through stages.

    What cardiac sarcoidosis screening criteria should be included?

    Present the HRS 2014 expert consensus recommendations: screen all patients with unexplained AV block (especially age <60), ventricular tachycardia, or new-onset cardiomyopathy. Screening tools: ECG, echocardiography, and if abnormal → cardiac MRI (late gadolinium enhancement) or FDG-PET (focal uptake after 12-18 hour fast to suppress physiologic myocardial uptake). The 2014 JMHW criteria vs HRS criteria — HRS has higher sensitivity by incorporating advanced imaging.

    How should treatment decisions be framed for sarcoidosis?

    Present clear indications for treatment: organ-threatening disease (cardiac, neurologic, sight-threatening ocular, severe hypercalcemia), progressive pulmonary impairment (FVC decline >10% or DLCO decline >15%), disabling symptoms. First-line: prednisone 20-40 mg/day tapered over 6-12 months. Early steroid-sparing for: anticipated >6 months therapy, relapse on taper, significant steroid side effects. Reference methotrexate as preferred steroid-sparing agent (10-15 mg/week) per 2020 ERS guidelines.

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