EMPD Report

A territory wide follow-up of primary and secondary extramammary Paget disease of two decades – effects of local disease on survival

A territory wide follow-up of primary and secondary extramammary Paget disease of two decades – effects of local disease on survival

Extramammary Paget disease (EMPD) is an uncommon malignant cutaneous neoplasm that are divided into primary and secondary forms. In this multicenter study, histologically proven cases of primary and secondary EMPD were reviewed for clinical outcomes with subgroup analysis for secondary EMPD.Secondary EMPD is associated with poorer outcomes. Margin involvement is strong and independent indicator of shorter OS and DSS, including secondary EMPD. Resectability is a strong predictor of favorable outcome and excision with clear margins should be attempted when surgically feasible.

Maladie de Paget extramammaire, primitive et multisiège chez un homme de 77 ans

Maladie de Paget extramammaire, primitive et multisiège chez un homme de 77 ans

Un homme de 77 ans a consulté pour des plaques érythémateuses et squameuses sur les régions génitale, sus-pubienne et sous les aisselles, diagnostiquées initialement comme eczéma ou infection fongique, mais ne répondant pas aux traitements. Les biopsies ont révélé des signes de maladie de Paget extramammaire, confirmée par des examens complémentaires ne montrant aucune tumeur interne. Une exérèse locale large a été effectuée avec succès, sans récidive en 4 ans. La maladie de Paget extramammaire, souvent confondue avec d'autres affections cutanées, nécessite un diagnostic précis pour un traitement efficace.

Simultaneous Occurrence of Two Ectopic Extramammary Paget Disease Lesions: A Case Report

Simultaneous Occurrence of Two Ectopic Extramammary Paget Disease Lesions: A Case Report

Paget disease of the breast is a malignant tumor that occurs primarily on the skin of the nipple, whereas extramammary Paget disease occurs on the skin in regions other than the breast, such as the pubis, perianal area, and axilla. Paget disease can also arise outside these areas; this is referred to as ectopic extramammary Paget disease. In this study, we present a case of a Japanese woman in her 70s who experienced simultaneous occurrence of two ectopic extramammary Paget disease lesions on the skin of the anterior chest and left buttock. Both lesions, exceeding 5 cm in diameter, were surgically excised, and the histopathological examination led to a diagnosis of ectopic extramammary Paget disease without invasion. To the best of our knowledge, this is the third reported case of multiple simultaneous ectopic extramammary Paget disease. Clinically, diagnosis of a patient with ectopic extramammary Paget disease is challenging because of its unusual location; however, the disease may be considered a differential diagnosis for Bowen disease.

Genetic Alterations and Prognosis in Extramammary Paget’s Disease

Genetic Alterations and Prognosis in Extramammary Paget’s Disease

Extramammary Paget’s Disease (EMPD) is a relatively rare skin cancer that typically appears in genital area. As a result, little is known about the association between genetic changes and prognosis for people diagnosed with this condition. This study was conducted in Japan using a national database. This database included people who had undergone comprehensive genomic profiling tests to examine genetic changes in their cancer. We aimed to explore the relationship between specific genetic changes and the prognosis of EMPD cases. To do this, we analyzed 167 cases from the database, focusing on 127 people for whom survival data was available. Our main goal was to see how genetic alterations might impact patient survival. In our cohort, a gene called ‘CDKN2A’ was most frequently altered (56%), and we found that changes to CDKN2A (such as loss) was linked to poorer prognosis. Similarly, cases with changes to a gene called ‘BRCA2’ were also associated with a poorer prognosis. We further noted that earlier testing for genetic changes could lead to better treatment planning and outcomes. In conclusion, identifying CDKN2A genetic changes in EMPD may be related to poor prognosis. These novel findings may help doctors create more personalized treatment plans for people with EMPD. Understanding these genetic factors also opens new research opportunities in EMPD.

Navigating the Maze: Insights from a Case Series of Vulval Extramammary Paget’s Disease

Navigating the Maze: Insights from a Case Series of Vulval Extramammary Paget’s Disease

Extramammary Paget’s remains a rare neoplastic condition, which although shares the name with Paget’s disease of the breast, is a distinct entity. The condition predominantly affects the epidermis of the vulval skin of postmenopausal women. In this case series, we present the cases of two geriatric patients who were diagnosed with this rare condition and the different treatment options available in managing the disease. Despite its rarity, understanding of this neoplastic condition is vital due to its potential for misdiagnosis and its impact on patient quality of life.

Independent Risk Factors for Postoperative Recurrence of Patients with Primary Extramammary Paget’s Disease: A Retrospective Analysis

Independent Risk Factors for Postoperative Recurrence of Patients with Primary Extramammary Paget’s Disease: A Retrospective Analysis

Primary extramammary Paget’s disease (EMPD) is a rare type of intraepithelial adenocarcinoma that shares histological features with Paget's disease but affects areas rich in apocrine glands outside the breast. It predominantly manifests in regions like the vulva, perianal, scrotum, and penile areas, with symptoms such as pruritus, erythema, and occasionally nodules or exudation. Unlike mammary Paget’s disease, primary EMPD affects both sexes, with a higher prevalence in Asian men and white women. The disease is rare, with an incidence of approximately 0.4-0.6 per million person-years in Europe and China. Despite its slow growth and nonspecific symptoms, primary EMPD carries significant morbidity due to high recurrence rates following surgical resection, prompting studies to identify prognostic factors like ill-defined tumor borders, exudation, and nodules.

A recent retrospective study from the First Affiliated Hospital of Chongqing Medical University aimed to analyze factors influencing postoperative recurrence of primary EMPD. The study enrolled 40 Chinese patients diagnosed between 2009 and 2019, predominantly male (77.5%), with a median age of 75.52 years. Clinical characteristics such as ill-defined tumor borders, presence of exudation, and nodules on the lesions were identified as significant risk factors for recurrence in multivariate analysis. Despite advancements in surgical techniques like wide local excision and Mohs micrographic surgery, the study highlighted challenges in early diagnosis due to misdiagnosis and delayed treatment, often mistaken for common dermatological conditions. The findings underscored the importance of vigilant clinical assessment and the need for tailored surgical approaches to improve outcomes in primary EMPD. This study contributes insights into managing primary EMPD by identifying specific clinical features associated with recurrence risk. Further research with larger cohorts and longer follow-up periods is necessary to validate these findings and refine treatment strategies for this challenging disease.

National incidence and survival of extramammary Paget disease 2013–2020 in England: reporting a total of 740 cases

National incidence and survival of extramammary Paget disease 2013–2020 in England: reporting a total of 740 cases

Extramammary Paget disease (EMPD) is a rare cancer primarily affecting genital and perianal areas, first described in 1889. Diagnosis can be delayed due to its subtle symptoms, but it's crucial as it often signals underlying malignancies, most commonly urothelial or anorectal. Recent epidemiological data from England suggest a fluctuating annual incidence around 0.17 per 100,000 person-years, with a noticeable decrease during the COVID-19 pandemic, highlighting its impact on diagnostic and healthcare services.

Clinicopathological Correlation and Recurrence Outcome of Adnexal Involvement on Primary Extramammary Paget’s Disease (EMPD)

Clinicopathological Correlation and Recurrence Outcome of Adnexal Involvement on Primary Extramammary Paget’s Disease (EMPD)

Primary extramammary Paget's disease (EMPD) is a rare type of cancer that appears as well-defined red plaques, often misdiagnosed due to its similarity to other skin conditions. This study aimed to evaluate the clinicopathological correlation of primary EMPD with adnexal features by analyzing 43 confirmed cases in patients aged 45-95. Expert dermatopathologists, blinded to initial diagnoses, conducted thorough histopathological evaluations. Statistical analyses included Pearson’s Chi-square, Mann-Whitney U, Spearman’s Correlations, Kaplan-Meier, log-rank tests, and Cox regression to assess correlations and recurrence predictions.

The results showed significant associations between adnexal involvement and the site of lesions, as well as between adnexal depth and EMPD subtypes. Smaller, non-invasive EMPD lesions were associated with longer recurrence-free periods, while the primary EMPD subtype was the only independent predictor for recurrence time. The study concludes that adnexal proliferation is crucial for both clinicopathological correlations and recurrence predictions, highlighting its importance in the diagnosis and prognosis of primary EMPD.

Unusual case of extramammary Paget disease of the oral mucosa: A case report and literature review

Unusual case of extramammary Paget disease of the oral mucosa: A case report and literature review

Paget disease is an intraepithelial neoplastic proliferation, commonly occurring in the breast and apocrine-rich areas, often associated with an underlying internal malignancy. Extramammary Paget disease (EMPD) of the oral cavity is exceedingly rare, with only eight reported cases, four of which were associated with an underlying internal malignancy. Here, we report a case of oral EMPD involving the buccal mucosa and gingiva of an 81-year-old male with no known underlying internal malignancy. The Paget cells were positive for CK7, CK20, CAM5.2, and androgen receptor, but negative for SOX10 and p63. The immunophenotype, association with internal malignancies, and treatment approaches for oral EMPD are reviewed.

Preoperative mapping biopsies with local excision in the treatment of Extramammary Paget Disease

Preoperative mapping biopsies with local excision in the treatment of Extramammary Paget Disease

Surgical excision of extramammary Paget disease (EMPD) is associated with a high local recurrence rate. This study found that PMB before local excision significantly reduced the risk of recurrence when treating EMPD. Further studies are necessary to compare the recurrence rates of PMB, Mohs micrographic surgery and WLE for EMPD.

Extramammary Paget Disease of Oral Mucosa: Case Report with Literature Review

Extramammary Paget Disease of Oral Mucosa: Case Report with Literature Review

Extramammary Paget disease (EPMD) of the oral mucosa is an unusual and extremely rare condition, with fewer than ten cases documented. Here, we report a case of EMPD extensively involving oral mucosa and underlying salivary ducts in a 72-year-old male and review published clinical, histologic, immunophenotypic, and prognostic features of this rare entity.

Topical Imiquimod in Primary Cutaneous Extramammary Paget’s Disease: A Systematic Review

Topical Imiquimod in Primary Cutaneous Extramammary Paget’s Disease: A Systematic Review

The main treatment for extramammary Paget’s disease (EMPD) is still surgery, but this neoplasm usually spreads beyond the clinical surroundings of the lesion, and achieving histopathologically free margins can be challenging and requires mutilating surgery. Moreover, the recurrence rate of the disease is high, reflecting its multifocal nature. Topical immunotherapy could be an alternative treatment for EMPD. The aim of this systematic review was to assess the effectiveness of topical imiquimod in the clinical response of EMPD patients and to describe the management of topical imiquimod in EMPD. Learning about non-surgical treatments such as topical imiquimod can help clinicians manage EMPD and find a balance between disease resolution and treatment morbidity.

Prognostic Factors of Extramammary Paget’s Disease: A Retrospective Study at a Medical Center in Taiwan

Prognostic Factors of Extramammary Paget’s Disease: A Retrospective Study at a Medical Center in Taiwan

Extramammary Paget's disease (EMPD) is a rare, slow growing intra-epidermal malignant neoplasm that arises in areas rich in apocrine glands. Several common sites of occurrence have been reported, including the vulva, perianal region, perineum, and scrotum. Most relevant studies rely on small data bases. Our objective was to evaluate prognostic factors of EMPD patients at a single medical center in Taiwan.

Treatment of Extramammary Paget Disease and the Role of Reflectance Confocal Microscopy: A Prospective Study

Treatment of Extramammary Paget Disease and the Role of Reflectance Confocal Microscopy: A Prospective Study

Extramammary Paget disease (EMPD) poses treatment challenges. Invasive and non-invasive treatment modalities exist with variable success reported. Reflectance confocal microscopy (RCM) is emerging as an adjuvant diagnostic tool.

EMPD is challenging and lesion demarcation is of the utmost importance. Using a staged surgical excision approach, the mean margins needed were 1.8 cm, less than previously reported. Non-surgical modalities including RT, imiquimod or PDT can be considered if surgery is not pursued. RCM is a valuable non-invasive imaging modality for the management of EMPD.

Hypopigmentation as a diagnostic clue in primary extramammary Paget disease: Case report and short literature review

Hypopigmentation as a diagnostic clue in primary extramammary Paget disease: Case report and short literature review

Primary extramammary Paget disease (EMPD) is a rare malignant tumour occurring in apocrine gland-bearing areas, such as the genitals (mean age at diagnosis 60–70 years).1 Clinically, EMPD exhibits well-circumscribed, erythematous and scaly patches or plaques often mimicking inflammatory skin disorders, but occasional pigmentary changes such as hypo- or hyperpigmentation are reported.

Extramammary Paget Disease: a Therapeutic Challenge, for a Rare Entity

Extramammary Paget Disease: a Therapeutic Challenge, for a Rare Entity

Extramammary Paget disease (EMPD) is a rare entity which is more frequently localized at the vulva, though it only accounts for 1–2% of vulvar neoplasms. It is a primary cutaneous adenocarcinoma whose cell of origin is still a matter of controversy: it can either arise from apocrine/eccrine glands or from stem cells. The diagnosis demands a biopsy and entails a histopathological analysis by which cells show similar characteristics as breast Paget disease.

Treatment approach can entail surgery, radiotherapy, photodynamic therapy, systemic chemotherapy, and topical chemotherapy. For metastatic disease, many different chemotherapy regimens have been explored and even targeted therapy can play an important role in this disease. Since almost 30–40% of patients overexpress HER-2, trastuzumab and anti-HER-2 therapies can be employed in this setting.

Due to its low incidence, there is almost no specific evidence on therapeutic interventions for this disease. Thus, there is a neat unmet need for molecular characterization of EMPD and diagnostic tools that allow clinicians to guide treatment both in the early and in the advanced disease settings. In this review, we aim to summarize available evidence about diagnosis and treatment of EMPD, both localized and metastatic, and to provide a comprehensive analysis that may help clinicians for therapeutic decisions.

Mohs surgery for female genital Paget's disease: a prospective observational trial

Mohs surgery for female genital Paget's disease: a prospective observational trial

This study aimed to compare surgical and oncologic outcomes of margin-controlled surgery vs traditional surgical excision for genital extramammary Paget's disease (EMPD) in females.

A clinicopathological analysis of forkhead box A1 (FOXA1) and estrogen receptor alpha expression in extramammary Paget’s disease

A clinicopathological analysis of forkhead box A1 (FOXA1) and estrogen receptor alpha expression in extramammary Paget’s disease

Extramammary Paget’s disease (EMPD) is a neoplastic skin disease of unknown etiology. EMPD is frequently associated with forkhead box A1 (FOXA1) expression, which correlates with the expression of estrogen receptor alpha (ER). FOXA1 regulates the transcriptional activity of ER and may function cooperatively in the tumorigenesis of breast cancer. In the present study, we confirmed that EMPD was frequently associated with FOXA1 expression. However, ER expression varied between patients and did not always coincide with FOXA1 expression. No clear relationship was observed between ER expression, the intensity of ER staining, or EMPD metastasis and prognosis. However, the results indicate that hormone-dependent cancer therapy may be effective in patients with ER-positive EMPD.

Incidental finding of extramammary Paget's disease during active surveillance for early-stage prostate cancer in a prostate biopsy

Incidental finding of extramammary Paget's disease during active surveillance for early-stage prostate cancer in a prostate biopsy

Skin tissue contamination within transcutaneous visceral organ biopsies is seldom found. We encountered a rare case of extramammary Paget's disease incidentally diagnosed by prostate biopsy during active surveillance for prostate cancer. Although the perianal region is a common site of extramammary Paget's disease, early-stage extramammary Paget's disease is often asymptomatic. Thus, during a transcutaneous biopsy, it is important to consider the appearance of the skin and the pathological features of migrating skin tissue.

Extramammary Paget Disease: a Therapeutic Challenge, for a Rare Entity

Extramammary Paget Disease: a Therapeutic Challenge, for a Rare Entity

Extramammary Paget disease (EMPD) is a rare entity which is more frequently localized at the vulva, though it only accounts for 1–2% of vulvar neoplasms. It is a primary cutaneous adenocarcinoma whose cell of origin is still a matter of controversy: it can either arise from apocrine/eccrine glands or from stem cells. The diagnosis demands a biopsy and entails a histopathological analysis by which cells show similar characteristics as breast Paget disease.