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1 Faculty: Case Number: HBPatient Name: - Diagnosis Peripheral Blood: Bone Marrow: Comment -Immunophenotyping of bone marrow aspirate by flow cytometry (report HF- -Bone marrow aspirate was sent for cytogenetics, FISH panel for Tumor Summary Specimen: Peripheral blood smear Bone marrow aspiration Bone marrow aspirate clot Bone marrow core (trephine) biopsy Bone marrow core touch preparation (imprint) Procedure: Bone marrow Aspiration site: R posterior iliac crest Biopsy site: R posterior iliac crest Histologic type: Immunophenotyping Immunohistochemistry: Performed Flow cytometry: Performed, see separate report (HF-xx-_) Not performed Cytogenetic studies: Performed, see separate report Not performed Specimen Source 1. Bone marrow aspirate and clot 2. Bone marrow core biopsy, decal, touch prep 3. Peripheral blood smear Bone marrow procedure was performed by IR Clinical Information . - ) shows 2 Gross Description [by Surg Path] Microscopic Description CBC Results with cell differential to be inserted here Date/time: PERIPHERAL BLOOD: Erythrocytes: White cells: Granulocytes: Lymphocytes: Monocytes: Platelets: Case Number: HB- - Bone marrow Differential (%) Myeloblasts: Promyelocytes: Myelocytes: Metas: Bands & PMN's: Eos: Baso: Monos: Lymphs: Plasma cells: Erythroids: M:E ratio Cellularity: Megakaryopoiesis: Erythropoiesis: Iron Content (aspirate): Granulopoiesis: Lymphocytes: Plasma Cells: Biopsy and clot section: 3 Iron content (biopsy and clot section): Intradepartmental Consultation -This case was reviewed with a consensus at the University of Texas-Houston Medical School Hematopathology QA Conference on xx/xx/xxxx. Non Clinical Documentation CPT:88305 x 2, 88313 x 2, 88311, 85097, 85060 The positive controls and internal negative controls for the special stains have been reviewed, and appropriate staining is confirmed by the pathologist whose signature appears above. Some of the immunohistochemical tests in this panel were developed and their performance characteristics determined by Memorial Hermann Southwest Hospital Laboratory. They have not been cleared or approved by the U. S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. These tests are used for clinical purposes. They should not be regarded as investigational or for research. This laboratory is regulated under the Clinical Laboratory Improvement Amendments of the 1988 (CLIA) as qualified to perform high complexity clinical testing. Teaching Physician Statement "I have personally reviewed the resident's preliminary interpretation and all specimen preparations and have personally issued this report".