Invasive Micropapillary Carcinoma of the Breast: An Update

Yi-Ling Yang, Bing-Bing Liu, Xinmin Zhang

  • 1From the Department of Breast Pathology and Research Laboratory, Key Laboratory of Breast Cancer Prevention and Therapy, Ministry of Education, National Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China (Drs Yang, Liu, and Fu); and the Department of Pathology, Cooper University Hospital, Cooper Medical School of Rowan University, Camden, New Jersey (Dr Zhang). Drs Zhang and Fu jointly supervised the work.

Abstract

Insights

Invasive micropapillary carcinoma (IMPC) is a unique breast cancer subtype. Recent advances in molecular genetics and prognosis-based reclassification improve understanding of its pathogenesis and clinical behavior.

Area of Science:

  • Oncology
  • Pathology
  • Genetics

Background:

  • Invasive micropapillary carcinoma (IMPC) is a distinct breast cancer variant characterized by morule-like clusters lacking fibrovascular cores within empty stromal spaces.
  • Diagnosis relies on morphology and immunohistochemistry, specifically the "inside-out" staining pattern of epithelial membrane antigen and sialyl Lewis X.
  • Distinguishing pure from mixed IMPC and its relationship with mucin-producing carcinomas remain areas of imprecision.

Purpose of the Study:

  • To review current diagnostic and pathogenetic concepts of IMPC.
  • Incorporate recent molecular genetic findings and prognosis-based reclassifications.
  • Provide an updated overview of IMPC of the breast.

Main Methods:

  • Literature review of PubMed and cited references.
  • Synthesis of current knowledge on IMPC diagnosis and pathogenesis.
  • Analysis of recent molecular genetic and prognostic data.

Main Results:

  • IMPCs exhibit distinct molecular genetic profiles, supporting their classification as separate entities.
  • Genomic analyses have not yet identified specific aberrations explaining IMPC's unique morphology or behavior.
  • Prognosis-based reclassification and molecular advances have enhanced understanding of IMPC pathogenesis.

Conclusions:

  • Recent molecular and prognostic reclassification advances have improved understanding of IMPC pathogenesis.
  • Further research is needed to identify molecular alterations driving the "inside-out" growth pattern.
  • Future studies may elucidate mechanisms behind IMPC's unfavorable clinical behavior.

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