ARUP Anatomic Pathology Test Menu

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 1 5
Test # Test Name Test Keywords Additional Information
2003860 Hairy Cell Leukemia, DBA.44 by Immunohistochemistry B-Cell Lymphomas Stain and return service only
2003914 HBME-1 (Mesothelial Cell) by Immunohistochemistry Mesothelioma, Thyroid Cancer Stain and return service only
0049090 Heinz Body Stain Unstable Hemoglobinopathies, Hemolytic Anemias
2003941 Helicobacter pylori by Immunohistochemistry Gastric adenocarcinoma, gastric B-cell lymphoma persistent dyspepsia;duodenal ulcer, gastric MALT, early gastric cancer, gastritis Stain and return service only
2003923 Hepatocyte Specific Antigen (HSA) by Immunohistochemistry Hepatocellular Carcinoma Stain and return service only
2007108 Hereditary Paraganglioma-Pheochromocytoma (SDHB) Sequencing and Deletion/Duplication Additional Technical Information
2007167 Hereditary Paraganglioma-Pheochromocytoma (SDHB, SDHC, and SDHD) Sequencing and Deletion/Duplication Panel
2007117 Hereditary Paraganglioma-Pheochromocytoma (SDHC) Sequencing and Deletion/Duplication Additional Technical Information
2007122 Hereditary Paraganglioma-Pheochromocytoma (SDHD) Sequencing and Deletion/Duplication Additional Technical Information
2003932 Herpes Virus 8 by Immunohistochemistry Kaposi Sarcoma, B-Cell Lymphomas, B- and T-Cell Markers Lymphoma, Castleman disease, Primary Effusion Lymphomas, Tumor Markers Stain and return service only
2003935 Melanoma Antibody, HMB45 by Immunohistochemistry Melanoma, Tumor Markers, HMB45 Stain and return service only
0051650 HNPCC/Lynch Syndrome (MLH1) Sequencing and Deletion/Duplication MLH1 FGA, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch
0051654 HNPCC/Lynch Syndrome (MSH2) Sequencing and Deletion/Duplication MSH2 FGA, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch Additional Technical Information
0051656 HNPCC/Lynch Syndrome (MSH6) Sequencing and Deletion/Duplication MSH6 FGA, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch Additional Technical Information
0051737 HNPCC/Lynch Syndrome (PMS2) Sequencing and Deletion/Duplication PMS2 FGA, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch Additional Technical Information
2001728 HNPCC/Lynch Syndrome Deletion/Duplication HNPCC DD, Hereditary Nonpolyposis Colorectal Cancer, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch Syndrome Additional Technical Information
2012175 HRAS Mutation Detection by Pyrosequencing
3000101 HSV Herpes Simplex Virus (HSV) Types I/II by Immunohistochemistry Herpes Simplex Virus (HSV) Stain and return service only
2003920 Human Chorionic Gonadotropin (Beta-hCG) by Immunohistochemistry Trophoblastic, germ cell, lung, melanoma, gastrointestinal, ovarian, testicular cancer Stain and return service only
2003929 Growth Hormone by Immunohistochemistry Acromegaly, Hypopituitarism, Tumor Markers Stain and return service only
2011937 Human Papillomavirus (HPV) 16 and 18 Genotype by PCR, SurePath
0065999 Human Papillomavirus (HPV) DNA Probe, High Risk, Cervical Brush Gynecologic Cancer
2007894 Human Papillomavirus (HPV) Genotypes 16 and 18/45, E6/E7 mRNA by Transcription-Mediated Amplification (TMA)
2002899 Human Papillomavirus (HPV) High Risk In Situ Hybridization, Paraffin Gynecologic Cancer, ISH
2002896 Human Papillomavirus (HPV) Low Risk by In Situ Hybridization, Paraffin Gynecologic Cancer, ISH
0060744 Human Papillomavirus (HPV), High Risk by Hybrid Capture (SurePath) Human Papillomavirus (HPV), Cervical Cancer, Tumor Markers
2008404 Human Papillomavirus (HPV), High Risk by Hybrid Capture, ThinPrep Human Papillomavirus (HPV), Cervical Cancer, Tumor Markers
2011942 Human Papillomavirus (HPV), High Risk by PCR, SurePath
2011947 Human Papillomavirus (HPV), High Risk by PCR, ThinPrep
2011933 Human Papillomavirus (HPV), High Risk with 16 and 18 Genotype by PCR, SurePath
2011940 Human Papillomavirus (HPV), High Risk with 16 and 18 Genotype by PCR, ThinPrep
2007893 Human Papillomavirus (HPV), High Risk, E6/E7 mRNA by Transcription-Mediated Amplification (TMA)
2007890 Human Papillomavirus (HPV), High Risk, E6/E7 mRNA by Transcription-Mediated Amplification (TMA) with Reflex to Genotypes 16 and 18/45
2003938 Human Placental Lactogen (HPL) by Immunohistochemistry Gestational Trophoblastic Disease, Products of Conception Stain and return service only