DIVISION OF NEUROPATHOLOGY

UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE
DEPARTMENT OF PATHOLOGY

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Division of Neuropathology
University of Pittsburgh
School of Medicine
Room A506 PUH
200 Lothrop Street
Pittsburgh, PA 15213
Tel: 412-647-9417

NEUROPATHOLOGY TRAINING MANUAL

Educational Objectives
Non-Glial Tumors of the CNS

  1. Know how to recognize histologic patterns of meningiomas with prognostic significance, as well as those patterns that present potential diagnostic confusion with other tumors.
  2. Know how to discuss the current Mayo criteria for meningioma grading, and its major differences from earlier grading schemes
  3. Know the role of immunohistochemistry and electron microscopy in the work-up of pituitary adenomas.
  4. Know how to recognize the major phenotypes of CNS lymphoma and lymphoproliferative disorders, the populations at risk, viral associations, and the role of ancillary studies
  5. Know the anatomical, pathologic, and prognostic characteristics of chordoma vs. chondrosarcoma.
  6. Know how to discuss the differential diagnosis of sellar/suprasellar, pineal region, and intraventricular mass lesions.
  7. Know how to discuss the differential diagnosis for spinal tumors in the extradural, intradural extramedullary, and intramedullary compartments.
  8. Know how to distinguish between schwannomas and neurofibromas, and recognize pathologic patterns with potential clinical impact, as well as those patterns that present potential diagnostic confusion with more aggressive entities.
  9. Know how to discuss the differential diagnosis and work-up of malignant peripheral nerve sheath tumor, and name the clinical setting where CNS leiomyosarcoma enters the differential.
  10. Know the common primary sites for tumors metastatic to the brain, understand the role of immunohistochemistry in the work up of metastatic lesions, and be aware of less common metastases of younger patients such as alveolar soft part sarcoma and choriocarcinoma
  11. Know the genetics, CNS, skin, ophthalmic, visceral and osseus manifestations of neurofibromatosis types 1 & 2, tuberous sclerosis, Cowden’s , Gorlin’s, hereditary polyposis, Li Fraumeni, MEN1, 2a, and 2b.
Path Department