TY - JOUR
T1 - Extramammary Paget's Disease
T2 - A Review of the Literature Part II: Treatment and Prognosis
AU - Morris, Caroline R.
AU - Hurst, Eva A.
N1 - Publisher Copyright:
© 2019 by the American Society for Dermatologic Surgery, Inc. Published by Wolters Kluwer Health, Inc. All rights reserved.
PY - 2020/3/1
Y1 - 2020/3/1
N2 - BACKGROUNDExtramammary Paget's disease (EMPD) is a rare malignancy with unclear pathophysiology that occurs predominantly on apocrine-rich skin. Surgery is the treatment of choice; however, procedures tend to be extensive and associated with a high rate of recurrence.OBJECTIVETo review the current literature on EMPD regarding treatment and prognosis.MATERIALS AND METHODSLiterature review using PubMed search for articles related to EMPD.RESULTSExtramammary Paget's disease classically presents as a slowly growing red plaque, which often mimics an inflammatory condition leading to significant delay in diagnosis. Diagnosis requires histopathologic examination and is often supported by immunohistochemical analysis. Once a diagnosis of EMPD is made, the patient must be risk-stratified and evaluated for an underlying malignancy.CONCLUSIONStandard of treatment is surgery, with data suggesting that Mohs micrographic surgery may have superior clinical outcomes and lower recurrence rates. Alternatives such as photodynamic therapy and topicals have been explored and may be appropriate in certain situations. Patients with EMPD generally have a good prognosis with a 5-year overall survival rate of 75% to 95%.
AB - BACKGROUNDExtramammary Paget's disease (EMPD) is a rare malignancy with unclear pathophysiology that occurs predominantly on apocrine-rich skin. Surgery is the treatment of choice; however, procedures tend to be extensive and associated with a high rate of recurrence.OBJECTIVETo review the current literature on EMPD regarding treatment and prognosis.MATERIALS AND METHODSLiterature review using PubMed search for articles related to EMPD.RESULTSExtramammary Paget's disease classically presents as a slowly growing red plaque, which often mimics an inflammatory condition leading to significant delay in diagnosis. Diagnosis requires histopathologic examination and is often supported by immunohistochemical analysis. Once a diagnosis of EMPD is made, the patient must be risk-stratified and evaluated for an underlying malignancy.CONCLUSIONStandard of treatment is surgery, with data suggesting that Mohs micrographic surgery may have superior clinical outcomes and lower recurrence rates. Alternatives such as photodynamic therapy and topicals have been explored and may be appropriate in certain situations. Patients with EMPD generally have a good prognosis with a 5-year overall survival rate of 75% to 95%.
UR - http://www.scopus.com/inward/record.url?scp=85081945354&partnerID=8YFLogxK
U2 - 10.1097/DSS.0000000000002240
DO - 10.1097/DSS.0000000000002240
M3 - Review article
C2 - 31688232
AN - SCOPUS:85081945354
SN - 1076-0512
VL - 46
SP - 305
EP - 311
JO - Dermatologic Surgery
JF - Dermatologic Surgery
IS - 3
ER -