Disease | Clinical Findings | In Vivo Dx (Imaging) | In Vitro Dx (Laboratory Medicine) | In Vitro Dx (Pathology) | References |
---|---|---|---|---|---|
Cancer | |||||
Prostate | DRE, osseous lesion | Transrectal ultrasound, MRI, PET | PSA, acid phosphatase | ||
Colorectal | Occult blood, ileus | CT, MRI, PET | CEA, CA 19–9, blood count | Histopathology, MSI assessment | [42] |
Pancreatic | Jaundice | MRI | CA 19–9, bilirubin, GGT | Histopathology | [43] |
Breast | Clinical examination | CT | CA 15–3 | Histopathology, ER and PR status, HER2neu | [44] |
Brain | Neurologic deficit | CT, MRI | S100β | [45] | |
Lung | CEA, SCC, NSE, CYFRA 21–1 | [46] | |||
Plasmocytoma | Spontaneous fractures | Whole-body MRI | Blood count, serum electrophoresis, IEF | ||
Cardiovascular | |||||
Chest pain | Triple-rule-out ECG-gated CT | TnI/TnT, NT-proBNP, BNP, D-dimer | [49] | ||
Dyspnea | Thorax | NT-proBNP, BNP, differential blood count, creatinine, GFR, CRP, PCT | [50] | ||
Neurological | |||||
Stroke | Hemiparesis | CT angiography, MRI | GFAP, S100β | [51] | |
Meningitis | Neurologic deficit, meningitis sign (eg, Kernig sign) | CSF cell count, albumin, IgG, IgA, IgM, glucose, lactate, bacteria, CRP, PCT, sepsis parameter, bacterial culture | [52] | ||
Multiple sclerosis | Specific neurologic deficit | CSF cell count, albumin, IgG, IgA, IgM, glucose, CRP, oligoclonal bands | [53] | ||
Encephalitis | |||||
Inflammation | |||||
Sepsis | Focus search | CRP, PCT, cytokine profiles IL-6, IL-8, differential blood count, blood culture | [54] | ||
Rheumatoid arthritis | Bone imaging | CRP, sedimentation rate | |||
Endocrinology | |||||
Addison or Conn syndrome | Hypertension/hypotension, cardiovascular symptoms, stress | MRI, selective adrenal venous sampling | Adrenal hormones, orthostasis test, salt exposure test | ||
Hypophysitis | Headache, altered vision, diabetes insipidus, signs of adrenal insufficiency | CT, MRI | Adrenal hormones, TSH, CRH, CRP, drugs and therapeutic medications | [59] | |
Multiple endocrine neoplasia syndromes | Mutation status: MEN, Ret, VHL1 | ||||
Diabetes | Polyuria, polydipsia, fatigue, weight change, CKD, retinopathy | Glucose, HbA1c, C-peptide, urine-Stix, blood gases and blood pH, lactate, ADH, copeptin, GADD45 antibodies, islet cell antibodies, IA-2 antibodies, insulin | |||
Hypothyroidism | Fatigue, weight gain, low activity, depression, blood pressure, HR | Thyroid ultrasound | TSH, FT4, FT3, Tg, TRAK and TPO antibodies | [62] | |
Congenital adrenal hyperplasia | Virilization, salt loss | Ultrasound | Cortisol, aldosterone, electrolytes | Karyotyping, mutation status: 21-OHase, 17a-OHase | [63] |