Meet Inspiring Speakers and Experts at our 3000+ Global Conference Series Events with over 1000+ Conferences, 1000+ Symposiums
and 1000+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business.

Explore and learn more about Conference Series : World's leading Event Organizer

Back

Akanksha Gupta

Akanksha Gupta

Hartford Hospital, USA

Title: GATA3 expression in primary cutaneous mucinous carcinoma

Biography

Biography: Akanksha Gupta

Abstract

Introduction: Primary cutaneous mucinous carcinoma (PCMC) is a rare adnexal tumor of sweat gland origin with an indolent course. The primary challenge in diagnosis is distinguishing PCMC from metastatic mucinous breast carcinoma (MMBC)-an important distinction because of the poorer prognosis with metastatic disease, requiring aggressive management. GATA3 binding protein is a transcription factor known to be a sensitive marker for breast and urothelial carcinomas. Most primary and metastatic breast carcinomas express GATA3, making it useful in evaluating metastatic disease. GATA3 expression has also been demonstrated in various epithelial skin tumors but it has not been specifically studied in a cohort of PCMC.

Case Series: We evaluated the potential of GATA3 as a distinguishing marker between PCMC and MMBC by applying it in four consecutive cases of PCMC diagnosed at our institution. All patients were females, making mammary metastasis a relevant diagnostic consideration. All cases were CK7 (+)/CK20 (-), CDX2 (-) and expressed mammaglobin, ER and PR. Based on morphology and immunophenotype alone, the cases were practically indistinguishable from MMBC, except that they showed p63 (+) myoepithelial cells, suggestive of a primary cutaneous process. For each case, the diagnosis of PCMC was eventually made after possible extracutaneous primaries had been excluded by extensive systemic workup.

Result: All PCMC cases showed strong nuclear GATA3 expression.

Conclusion: GATA3 immunohistochemistry is not useful in contrasting PCMC from MMBC. In differentiating these histologic mimics, additional markers and thorough systemic workup are necessary to establish primary cutaneous derivation.