An analysis of PLAG1 and HMGA2 rearrangements in salivary duct carcinoma and examination of the role of precursor lesions. Issue 2 (6th June 2013)
- Record Type:
- Journal Article
- Title:
- An analysis of PLAG1 and HMGA2 rearrangements in salivary duct carcinoma and examination of the role of precursor lesions. Issue 2 (6th June 2013)
- Main Title:
- An analysis of PLAG1 and HMGA2 rearrangements in salivary duct carcinoma and examination of the role of precursor lesions
- Authors:
- Bahrami, Armita
Perez‐Ordonez, Bayardo
Dalton, James D
Weinreb, Ilan - Abstract:
- <abstract abstract-type="main" id="his12152-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="his12152-sec-0001" sec-type="section"> <title>Aims</title> <p>Salivary duct carcinoma (SDC) often arises in pleomorphic adenoma (PA). Putative precursors, including low‐grade cribriform cystadenocarcinoma (LGCCC) and ductal carcinoma <italic>in‐situ</italic> (DCIS), are more controversial. Rearrangement of <italic>PLAG1</italic> or <italic>HMGA2</italic> is seen in 50–70% of PAs, but this has not been investigated in SDC. Using a large collection of SDCs from a single institution, we aimed to study these genes by fluorescence in‐situ hybridization (FISH), and to correlate the presence of precursor lesions/intraductal proliferations with gene alterations.</p> </sec> <sec id="his12152-sec-0002" sec-type="section"> <title>Methods and results</title> <p>Forty‐four SDCs were stained for smooth muscle actin, CK14, and p63, and examined with <italic>PLAG1</italic> and <italic>HMGA2</italic> FISH. Eight cases were SDC ex‐PA; ten had a hyalinized nodule (HN), which is suspicious for PA; six arose in association with LGCCC; and twenty were '<italic>de‐novo</italic>' SDCs. Ten cases had <italic>PLAG1</italic> rearrangement/amplification (22.7%) and eight had <italic>HMGA2</italic> (18.2%) rearrangement/amplification. The positive cases were four SDC ex‐PAs, eight SDCs with an HN, and five '<italic>de‐novo</italic>' SDCs. Twenty‐three SDC ex‐PAs were present in total<abstract abstract-type="main" id="his12152-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="his12152-sec-0001" sec-type="section"> <title>Aims</title> <p>Salivary duct carcinoma (SDC) often arises in pleomorphic adenoma (PA). Putative precursors, including low‐grade cribriform cystadenocarcinoma (LGCCC) and ductal carcinoma <italic>in‐situ</italic> (DCIS), are more controversial. Rearrangement of <italic>PLAG1</italic> or <italic>HMGA2</italic> is seen in 50–70% of PAs, but this has not been investigated in SDC. Using a large collection of SDCs from a single institution, we aimed to study these genes by fluorescence in‐situ hybridization (FISH), and to correlate the presence of precursor lesions/intraductal proliferations with gene alterations.</p> </sec> <sec id="his12152-sec-0002" sec-type="section"> <title>Methods and results</title> <p>Forty‐four SDCs were stained for smooth muscle actin, CK14, and p63, and examined with <italic>PLAG1</italic> and <italic>HMGA2</italic> FISH. Eight cases were SDC ex‐PA; ten had a hyalinized nodule (HN), which is suspicious for PA; six arose in association with LGCCC; and twenty were '<italic>de‐novo</italic>' SDCs. Ten cases had <italic>PLAG1</italic> rearrangement/amplification (22.7%) and eight had <italic>HMGA2</italic> (18.2%) rearrangement/amplification. The positive cases were four SDC ex‐PAs, eight SDCs with an HN, and five '<italic>de‐novo</italic>' SDCs. Twenty‐three SDC ex‐PAs were present in total (52.3%). All six SDC ex‐LGCCCs were FISH‐negative. Myoepithelial staining surrounded all LGCCCs, and demonstrated DCIS in 17 cases. Eleven DCIS lesions were in SDC ex‐PAs or FISH‐positive '<italic>de‐novo</italic>' SDCs. These cases represent 'cancerization' of ducts. Only six FISH‐negative '<italic>de‐novo</italic>' SDCs showed DCIS.</p> </sec> <sec id="his12152-sec-0003" sec-type="section"> <title>Conclusions</title> <p>A large proportion of SDCs arise in PAs (with or without residual evidence of a PA). A small proportion of SDCs arise in LGCCCs. Cases showing DCIS often represent cancerization.</p> </sec> </abstract> … (more)
- Is Part Of:
- Histopathology. Volume 63:Issue 2(2013)
- Journal:
- Histopathology
- Issue:
- Volume 63:Issue 2(2013)
- Issue Display:
- Volume 63, Issue 2 (2013)
- Year:
- 2013
- Volume:
- 63
- Issue:
- 2
- Issue Sort Value:
- 2013-0063-0002-0000
- Page Start:
- 250
- Page End:
- 262
- Publication Date:
- 2013-06-06
- Subjects:
- Histology, Pathological -- Periodicals
611.018 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=his ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2559 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/his.12152 ↗
- Languages:
- English
- ISSNs:
- 0309-0167
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4316.027000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3311.xml