Guidelines For Acquiring a Diagnosis
- Completion of a thorough patient history
- Careful skin examination and biopsy of lesions
- Acquisition of labs including CBC, peripheral smear, serum chemistry
- Testing for markers of systemic disease including CD2 and CD25, C-kit mutation D816V, serum
tryptase levels.
- Exam of liver and spleen for hepatosplenomegaly
- Any other exam relevant to individual symptoms (endoscopy, colonoscopy, etc)
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