Home   Chapter Home   Jobs   Conferences   Fellowships   Books

 

 

Advertisement

 

Stains

Cytokeratin 20 (CK20, K20)

 

Authors: Kara Hamilton, M.S., Nat Pernick, M.D., PathologyOutlines.com, Inc.

Revised: 2 March 2012, last major update - June 2009

Copyright: (c) 2002-2010, PathologyOutlines.com, Inc.

 

Definition

=========================================================================

● Epithelial marker (MW 46 kDa), with restricted expression compared to CK7 (OMIM 608218)

 

Uses

=========================================================================

General patterns (specificity varies)

(1) CK7+/CK20+ in carcinomas of bile duct (extrahepatic/gallbladder, often, Pathol Res Pract 2003;199:65), lung-mucinous bronchioloalveolar (AJCP 2004;122:421), pancreas (Cancer 2006;106:693 but see Archives 2000;124:1196)

-Urothelium (often, Archives 2001;125:921, Hum Path 2002;33:1136)

-Also primary mucinous tumors of ovary (74%), upper GI tract (78%), endocervix (88%, AJSP 2006;30:1130)

 

(2) CK7+/CK20- in carcinomas of bile duct (intrahepatic, Pathol Res Pract 2003;199:65), breast (Ann Diagn Pathol 1999;3:350), endocervical and endometrial adenocarcinoma (Int J Gynecol Pathol 2002;21:4), esophagus (distal, AJSP 2002;26:1213), lung (not mucinous bronchioloalveolar, BMC Cancer 2006;6:31), salivary gland (Pathol Int 2005;55:386), thyroid (Appl Immunohistochem Mol Morphol 2000;8:189)

-Also mesothelioma (Cancer 2001;92:2727)

 

(3) CK7-/CK20+ in carcinoma of colon (particularly early stage, Hum Path 2005;36:275)

-CK20 is less sensitive for poorly differentiated colonic carcinoma (Chin J Physiol 2006;49:298)

-Primary mucinous tumors of lower GI tract (79%, AJSP 2006;30:1130) and primary bladder adenocarcinomas (29%, AJSP 2001;25:1380)

 

(4) CK7-/CK20- in carcinomas of adrenal cortex and prostate (Mod Path 2000;13:962, free full text)

 

(5) To distinguish primary lung carcinoma (CK7+/CK20-) from metastatic colonic carcinoma to lung (CK7-/CK20+, BMC Cancer 2006;6:31)

 

(6) To help distinguish colon carcinoma (80% are CK20+) and poorly differentiated prostatic carcinoma (90% are CK20-) at biopsy (Archives 2007;131:599)

 

(7) To distinguish Merkel cell carcinoma (CK20+, dot like, TTF1-) and metastatic small cell carcinoma of lung (CK20-, TTF1+, Am J Dermatopathol 2006;28:99)

 

(8) To distinguish anal carcinoma (CK7+/CK20-) from downward growth of colorectal carcinoma (CK7-/CK20+, Archives 2001;125:1074)

 

(9) May confirm Barrett’s mucosa, which has strong diffuse CK7+ surface and crypt epithelium, strong CK20+ surface and superficial crypt staining

-Interpretation is affected by fixative (Hum Path 2005;36:58, but see Mod Path 2002;15:611-free full text)

-Pattern may help distinguish short segment Barrett’s from cardiac intestinal metaplasia (World J Gastroenterol 2005;11:6360)

 

(10) To distinguish Rathke cleft cysts and pituitary gland pars intermedia (CK8+, CK20+) from craniopharyngioma (CK8-, CK20-, Archives 2002;126:1174)

 

(11) To distinguish adenocarcinoma of distal esophagus (CK7+/CK19+: 90%, CK7+/CK20-: 74%) from proximal stomach (CK7+/CK19+: 44%, CK7+/CK20-: 24%, AJSP 2002;26:1213)

 

(12) To detect occult nodal tumor cells in colorectal adenocarcinoma (Hum Path 2006;37:1259, Br J Cancer 2006;95:218)

 

(13) RT-PCR to detect tumor cells of breast and colorectal carcinoma in blood (J Mol Diagn 2006;8:105)

 

(14) RT-PCR assessment in peritoneal wash may predict recurrence in gastric carcinoma (Oncol Rep 2007;17:667)

 

Urothelial carcinoma:

(a) CK20+ p53+ CD44- favors urothelial carcinoma in situ vs. reactive urothelium (AJSP 2001;25:1074)

(b) CIS shows CK20 staining of deep urothelial cells compared with surface cells only in non-neoplastic lesions (Appl Immunohistochem Mol Morphol 2006;14:260)

(c) CK20+ in voided urine by RT-PCR is sensitive and specific for bladder carcinoma (Clin Biochem 2004;37:803, J Egypt Natl Canc Inst 2006;18:82, but see J Urol 2003;169:86)

(d) In papillary urothelial neoplasms, CK20+ is associated with increasing tumor grade and stage in pTa and pT1 patients (Mod Path 2000;13:1315, free full text)

 

Positive stains - normal

=========================================================================

● Colon, Merkel cells, small intestine (AJSP 2004;28:1352), stomach

● Urothelium (umbrella cells, AJSP 2001;25:1074)

● Uterus

 

Positive stains – not carcinoma

=========================================================================

Bladder intestinal metaplasia (Mod Path 2006;19:1395)

Fibroepithelioma of Pinkus (Am J Dermatopathol 2007;29:7)

● GI carcinoid (25%)

● Hydatidiform mole (complete-100%, partial-50%, Gynecol Oncol 2002;87:34)

● Renal oncocytoma (dot-like pattern, J Histochem Cytochem 2001;49:919)

 

Positive stains - carcinoma

=========================================================================

● Ampullary (variable-AJSP 2005;29:359)

● Anal (variable-Br J Dermatol 2000;142:243, Cancer 2001;92:2045)

Appendiceal epithelial neoplasms (benign and malignant, 100%, Hum Path 2005;36:1217)

Biliary papillary tumors (benign and malignant, Hepatology 2006;44:1333)

Colon (references above)

● Gastric (18-31%, Appl Immunohistochem Mol Morphol 2006;14:303, reduced if high levels of microsatellite instability, AJSP 2004;28:712)

Hepatocellular (20% positive, Hum Path 2005;36:1226)

● Hepatoid adenocarcinoma (AJSP 2003;27:1302)

● Lung mucinous bronchioloalveolar (Hum Path 2002;33:915)

Merkel cell (dot like, references above)

Ovarian (Mod Path 2006;19:1421)

Paget’s disease (secondary only-Br J Dermatol 2000;142:243)

● Pancreatic ductal (Cancer 2006;106:693)

● Prostatic (variable)

● Sinonasal adenocarcinoma (50%, Archives 2007;131:530)

● Small cell of major salivary glands (AJSP 2004;28:762), urothelial (references above)

Vulvar Paget’s disease secondary to anorectal or urothelial carcinoma but not primary (Hum Path 2002;33:545)

 

Negative stains

=========================================================================

● Anal glands (Archives 2001;125:1074)

● Inverted urothelial papilloma (Hum Path 2004;35:1499)

 

Micro images

=========================================================================

 

anal glands are CK20- (fig 1C) but rectal adenocarcinoma is CK20+ (fig 2-)

 

Barrett’s-non classic staining pattern

 

cervical adenocarcinoma-intestinal type is CK20 neg (fig 1E)

 

colonic adenocarcinoma #1 (well differentiated)#2 (poorly differentiated)#3-metastatic#4-primary (fig G) and metastatic to lung (fig H)

 

colonic medullary carcinoma (fig 4)

 

craniopharyngioma is CK20- (fig 1C), Rathke cleft cyst is CK20+ (fig 2C), pituitary gland pars intermedia is CK20+ (fig 3C)

 

gastric epithelium (normal)

 

gastric carcinoma-poorly differentiated (fig 4a)

 

lung-nonmucinous bronchioloalveolar carcinoma is CK20 neg

 

lung-mucinous bronchioloalveolar carcinoma is CK20+

 

Merkel cell carcinoma #1#2#3-FNA

 

pancreatic ductal carcinoma is CK20 neg (fig 1f)

 

prostatic adenocarcinoma #1;  #2 with positive staining of verumontanum

  

sinonasal adenocarcinoma-intestinal type (fig 4B)

 

testicular mucinous cystadenoma is CK20+ (fig 3a) but ovarian tumor is CK20-(fig 5a)

 

urothelium (normal)

 

urothelial papilloma (fig 2C)

 

urothelial papillary neoplasm of LMP (fig 3C)

 

urothelial CIS is diffusely CK20+ (fig B)

 

urothelial carcinoma #1-high grade#2-papillary-high grade (fig 5C)#3-papillary-low grade (fig 4C)#4-CK20+ primary and nodal metastasis#5 (CK20 neg, uncommon)

 

Contributed by Leica Microsystems, Biosystems Division - colon (normal)-Cytokeratin 20 (PW31) with intense cytoplasmic staining

 

End of Stains > Cytokeratin 20 (CK20, K20)

 

 

This information is intended for physicians and related personnel, who understand that medical information is often imperfect, and must also be interpreted in the context of a patient's clinical data using reasonable medical judgment.  This website should not be used as a substitute for the advice of a licensed physician.

 

All information on this website is protected by Copyright, (c) 2001-2009, PathologyOutlines.com, Inc.  Information from third parties may also be protected by copyright.  Please contact us at copyrightPathOut@gmail.com with any questions.