Skip to main content Accessibility help
×
Hostname: page-component-7479d7b7d-c9gpj Total loading time: 0 Render date: 2024-07-11T12:18:05.708Z Has data issue: false hasContentIssue false

Dictionary

Published online by Cambridge University Press:  03 July 2022

Runjan Chetty
Affiliation:
University of Toronto
Kumarasen Cooper
Affiliation:
University of Pennsylvania
Carol Cheung
Affiliation:
University of Toronto
Srinivas Mandavilli
Affiliation:
Hartford Hospital
Get access
Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2022

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Selected references

Flavell, DJ, Jones, DB, Wright, DH. Identification of tissue histiocytes on paraffin sections by a new monoclonal antibody. J Histochem Cytochem 1987;35:1217–26.Google Scholar

Selected references

Busam, KJ, Jungbluth, AA. Melan-A, a new melanocytic differentiation marker. Adv Anat Pathol 1999;6:182–7.Google Scholar

Selected references

Lele, SM, Graves, K, Gatalica, Z. Immunohistochemical detection of maspin is a useful adjunct in distinguishing radial sclerosing lesion from tubular carcinoma of the breast. Appl Immunohistochem Mol Morphol 2000;8:32–6.Google Scholar

Selected references

Gelsleichter, L, Gown, AM, Zarbo, RJ, et al. P53 and mdm-2 expression in malignant melanoma: An immunocytochemical study of expression of p53, mdm-2, and markers of cell proliferation in primary versus metastatic tumors. Mod Pathol 1995;8:530–5.Google ScholarPubMed
Clay, MR, Martinez, AP, Weiss, SW, et al.MDM2 and CDK4 immunohistochemistry: Should it be used in problematic differentiated lipomatous tumors? Am J Surg Pathol 2016;40:1647–52.Google Scholar

Selected references

Allen, IV, McQuaid, S, McMahon, J, et al. The significance of measles virus antigen and genome distribution in the CNS in SSPE for mechanisms of viral spread and demyelination. J Neuropathol Exp Neurol 1996;55:471–80.Google Scholar

Selected references

Albelda, SM, Muller, WA, Buck, CA, et al. Molecular and cellular properties of PECAM-1 (endoCAM/CD31): A novel vascular cell-cell adhesion molecule. J Cell Biol 1991;114:1059–68.Google Scholar
Kuzu, I, Bicknell, R, Fletcher, CDM, et al. Expression of adhesion molecules on the endothelium of normal tissue vessels and vascular tumors. Lab Invest 1993;69:322–8.Google Scholar

Selected references

Chang, K, Pastan, I. Molecular cloning of mesothelin, a differentiation antigen present on mesothelium, mesotheliomas, and ovarian cancers. Proc Natl Acad Sci USA 1996;93:136–40.Google Scholar
Ordóñez, NG. Value of mesothelin immunostaining in the diagnosis of mesothelioma. Mod Pathol 2003;16:192–7.Google Scholar

Selected references

Jasani, B, Schmid, KW. Significance of metallothionein overexpression in human tumors. Histopathology 1997;31:211–14.Google Scholar
Kagi, JHR. Overview of metallothionein: Metallobiochemistry Part B: metallothionein and related molecules. Meth Enzymol 1993;205:613–26.Google Scholar

Selected references

Busam, KJ, Iversen, K, Copian, KC, et al. Analysis of microphthalmia transcription factor expression in normal tissues and tumors, and comparison of its expression with S-100 protein, gp100, and tyrosinase in desmoplastic malignant melanoma. Am J Surg Pathol 2001;25:197204.Google Scholar

Selected references

Jiricny, J. Eukaryotic mismatch repair: An update. Mutat Res 1998; 409: 107–21.Google Scholar
Lanza, G, Gafa, R, Maestri, I, et al. Immunohistochemical pattern of MLH1/MSH2 expression is related to clinical and pathological features in colorectal adenocarcinomas with microsatellite instability. Mod Pathol 2002; 15: 741–9.Google Scholar

Selected references

Edwards, C, Oates, J. OV 632 and MOC 31 in the diagnosis of mesothelioma and adenocarcinoma: An assessment of their use in formalin fixed and paraffin wax embedded material. J Clin Pathol 1995;48:626–30.Google Scholar

Selected references

Bedeir, A, Krasinskas, AM. Molecular diagnostics of colorectal cancer. Arch Pathol Lab Med 2011;135(5):578–87.Google Scholar
Bellizzi, AM, Frankel, WL. Colorectal cancer due to deficiency in DNA mismatch repair function: A review. Adv Anat Pathol 2009;16(6):405–17.Google Scholar
Garg, K, Leitao, MM Jr, Kauff, ND, et al. Selection of endometrial carcinomas for DNA mismatch repair protein immunohistochemistry using patient age and tumor morphology enhances detection of mismatch repair abnormalities. Am J Surg Pathol 2009;33(6):925–33.CrossRefGoogle ScholarPubMed
Hall, G, Clarkson, A, Shi, A, et al. Immunohistochemistry for PMS2 and MSH6 can replace a four antibody panel for mismatch repair deficiency screening in colorectal adenocarcinoma. Pathology 2010;42(5):409–13.CrossRefGoogle ScholarPubMed
Klarskov, L, Holck, S, Bernstein, I, et al. Challenges in the identification of MSH6-associated colorectal cancer: Rectal location, less typical histology, and a subset with retained mismatch repair function. Am J Surg Pathol 2011;35(9):1391–9.Google Scholar
Radu, OM, Nikiforova, MN, Farkas, LM, et al. Challenging cases encountered in colorectal cancer screening for Lynch syndrome reveal novel findings: Nucleolar MSH6 staining and impact of prior chemoradiation therapy. Hum Pathol 2011;42(9):1247–58.Google Scholar
Shia, JR, Tang, LH, Vakiani, E, et al. Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: A 2-antibody panel may be as predictive as a 4-antibody panel. Am J Surg Pathol 2009;33(11):1639–45.Google Scholar

Selected references

Adsay, NV, Merati, K, Basturk, O, et al. Pathologically and biologically distinct types of epithelium in intraductal papillary mucinous neoplasms: Delineation of an “intestinal” pathway of carcinogenesis in the pancreas. Am J Surg Pathol 2004;28(7): 839–48.CrossRefGoogle ScholarPubMed
Chu, PG., Schwarz, RE, Lau, SK, et al. Immunohistochemical staining in the diagnosis of pancreatobiliary and ampulla of Vater adenocarcinoma: Application of CDX2, CK17, MUC1, and MUC2. Am J Surg Pathol 2005;29(3): 359–67.CrossRefGoogle ScholarPubMed
Kuan, SF, Montag, AG, Hart, J, et al. Differential expression of mucin genes in mammary and extramammary Paget’s disease. Am J Surg Pathol 2001;25(12): 1469–77.Google Scholar
Lau, SK, Weiss, LM, Chu, PG. Differential expression of MUC1, MUC2, and MUC5AC in carcinomas of various sites. Am J Clin Pathol 2004;122(1): 61–9.Google Scholar
McIntire, MG, Soucy, G, Vaughan, TL, et al. MUC2 is a highly specific marker of goblet cell metaplasia in the distal esophagus and gastroesophageal junction. Am J Surg Pathol 2011;35(7): 1007–13.CrossRefGoogle ScholarPubMed
Rousseau, K, Byrne, C, Kim, YS, et al. The complete genomic organization of the human MUC6 and MUC2 mucin genes. Genomics 2004;83(5): 936–9.CrossRefGoogle ScholarPubMed

Selected references

Doyle, LA, Möller, E, Dal Cin, P, et al. MUC4 is a highly sensitive and specific marker for low-grade fibromyxoid sarcoma. Am J Surg Pathol 2011;35:733–41.CrossRefGoogle ScholarPubMed
Doyle, LA, Wang, WL, Dal Cin, P, et al. MUC4 is a sensitive and extremely useful marker for sclerosing epithelioid fibrosarcoma: Association with FUS gene rearrangement. Am J Surg Pathol 2012;36:1444–51.Google Scholar
Matsuyama, A, Jotatsu, M, Uchihashi, K, et al. MUC4 expression in meningiomas: Under-recognized immunophenotype particularly in meningothelial and angiomatous subtypes. Histopathology 2019;74:276–83.Google Scholar

Selected references

Brown, IS, Whiteman, DC, Lauwers, GY. Foveolar type dysplasia in Barrett esophagus. Mod Pathol 2010;23(6):834–43.Google Scholar
Handra-Luca, A, Lamas, G, Bertrand, J-C, et al. MUC1, MUC2, MUC4, and MUC5AC expression in salivary gland mucoepidermoid carcinoma: Diagnostic and prognostic implications. Am J Surg Pathol 2005;29(7):881–9.Google Scholar
Kuan, SF, Montag, AG, Hart, J, et al. Differential expression of mucin genes in mammary and extramammary Paget’s disease. Am J Surg Pathol 2001;25(12):1469–77.Google Scholar
Lau, SK, Weiss, LM, Chu, PG. Differential expression of MUC1, MUC2, and MUC5AC in carcinomas of various sites. Am J Clin Pathol 2004;122(1):61–9.Google Scholar
O’Connell, FP, Wang, HH, Odze, RD. Utility of immunohistochemistry in distinguishing primary adenocarcinomas from metastatic breast carcinomas in the gastrointestinal tract. Arch Pathol Lab Med 2005;129(3):338–47.Google Scholar
Pinto-de-Sousa, J, David, L, Reis, CA, et al. Mucins MUC1, MUC2, MUC5AC and MUC6 expression in the evaluation of differentiation and clinico-biological behaviour of gastric carcinoma. Virchows Arch 2002. 440(3):304–10.CrossRefGoogle ScholarPubMed

Selected references

Adsay, V, Jang, K-T, Roa, JC, et al. Intracholecystic papillary-tubular neoplasms (ICPN) of the gallbladder (neoplastic polyps, adenomas, and papillary neoplasms that are ≥1.0 cm): Clinicopathologic and immunohistochemical analysis of 123 cases. Am J Surg Pathol 2012;36:1279–301.Google Scholar
Bartman, AE, Buisine, MP, Aubert, JP, et al. The MUC6 secretory mucin gene is expressed in a wide variety of epithelial tissues. J Pathol 1999;186:398405.Google Scholar
Chu, PG, Chung, L, Weiss, LM, et al. Determining the site of origin of mucinous adenocarcinoma: An immunohistochemical study of 175 cases. Am J Surg Pathol 2011;35:1830–6.Google Scholar
Khor, TS, Alfaro, EE, Ooi, EMM, et al. Divergent expression of MUC5AC, MUC6, MUC2, CD10, and CDX-2 in dysplasia and intramucosal adenocarcinomas with intestinal and foveolar morphology: Is this evidence of distinct gastric and intestinal pathways to carcinogenesis in Barrett esophagus? Am J Surg Pathol 2012;36:331–42.CrossRefGoogle ScholarPubMed
Kosmahl, M, Wagner, J, Peters, K, et al. Serous cystic neoplasms of the pancreas: An immunohistochemical analysis revealing alpha-inhibin, neuron-specific enolase, and MUC6 as new markers. Am J Surg Pathol 2004 28:339–46.CrossRefGoogle ScholarPubMed

Selected references

Falini, B, Fizzotti, M, Pucciarini, A, et al. A monoclonal antibody (MUM1p) detects expression of the MUM1/IRF4 protein in a subset of germinal center B cells, plasma cells, and activated T cells. Blood 2000; 95(6):2084–92.Google Scholar
Gualco, G, Weiss, LM, Bacchi, CE. MUM1/IRF4: A review. Appl Immunohistochem Mol Morphol 2010; 18:301–10.CrossRefGoogle ScholarPubMed
Klein, U, Casola, S, Cattoretti, G, et al. Transcription factor IRF4 controls plasma cell differentiation and class-switch recombination. Nat Immunol 2006;7:773–82.CrossRefGoogle ScholarPubMed
Shaffer, AL, Emre, NC, Lamy, L, et al. IRF4 addiction in multiple myeloma. Nature 2008;454:226–31.Google Scholar

Selected references

Azumi, N, Ben-Erza, J, Battifora, H. Immunophenotypic diagnosis of leiomyosarcomas and rhabdomyosarcomas with monoclonal antibodies to muscle specific actin and desmin in formalin-fixed tissue. Mod Pathol 1988;1:469–74.Google ScholarPubMed

Selected references

Carabias, E, Palenque, E, Serrano, R, et al. Evaluation of an immunohistochemical test with polyclonal antibodies raised against mycobacteria used in formalin-fixed tissue compared with mycobacterial specific culture. APMIS 1998;106:385–8.CrossRefGoogle ScholarPubMed

Selected references

Clark, HB, Minesky, JJ, Agrawal, D, et al. Myelin basic protein and P2 protein are not immunohistochemical markers for Schwann cell neoplasms: A comparative study using antisera to S100, P2, and myelin basic proteins. Am J Pathol 1985;121:96101.Google Scholar

Selected references

Mason, DY, Taylor, CR. The distribution of muramidase (lysozyme) in human tissues. J Clin Pathol 1975;28:124–32.CrossRefGoogle ScholarPubMed
Pinkus, GS, Pinkus, JL. Myeloperoxidase: A specific marker for myeloid cells in paraffin sections. Mod Pathol 1991;4:733–41.Google Scholar

Selected references

Cessna, MH, Zhou, H, Perkins, SL, et al. Are myogenin and myoD1 expression specific for rhabdomyosarcoma? A study of 150 cases, with emphasis on spindle cell mimics. Am J Surg Pathol 2001;25:1150–7.CrossRefGoogle ScholarPubMed
Wesche, WA, Fletcher, CDM, Dias, E, et al. Immunohistochemistry of MyoD1 in adult pleomorphic soft tissue sarcomas. Am J Surg Pathol 1995;19:261–9.CrossRefGoogle ScholarPubMed

Selected references

Cessna, M, Zhou, H, Perkins, S, et al. Are myogenin and MyoD1 expression specific for rhabdomyosarcoma? A study of 150 cases, with emphasis on spindle cell mimics. Am J Surg Pathol 2020;99:7579. doi:10.1016/j.humpath.2020.03.006.Google Scholar
Flope, AL. MyoD1 and myogenin expression in human neoplasia: A review and update. Adv Anat Pathol 2002;9:198203.Google Scholar
Olson, NJ, Fritchie, KJ, Torres-Mora, J, et al. MyoD1 expression in fibroepithelial stromal polyps. Hum Pathol 2020;99:7579. doi: 10.1016/j.humpath.2020.03.006. Epub 2020 Mar 23.Google Scholar

Selected references

Kunishige, M, Mitsui, T, Akaike, M, et al. Localisation and amount of myoglobin and myoglobin mRNA in ragged-red fiber of patients with mitochondrial encephalomyopathy. Muscle Nerve 1996;19:175–82.3.0.CO;2-B>CrossRefGoogle ScholarPubMed
Zhang, JM, Piddick, L. Cytoskeleton immunohistochemical study of early ischemic myocardium. Forensic Sci Int 1996;80:229–38.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×