Hormone receptor-positive breast cancer (luminal A and B)

Exam relevance: in 14 of 197 board exam reports · rank 55

Specialty
Gynaecology · Breast
Images
Histology & cytology 2
Exam relevance
14 of 197 reports · rank 55
Last updated
10/2026 · Dr. Pascal Bafteh
Contents
  1. Images (2)
  2. Definition
  3. Classification
  4. Occurrence & epidemiology
  5. Aetiopathogenesis
  6. Clinical features
  7. Diagnosis
  8. Keep learning in the app
  9. Further reading (selection)
  10. Cross-references

Images (2)

Hormone receptor-positive breast cancer (luminal A and B) – Histology & cytology: Estrogen receptor immunohistochemistry: strong nuclear staining of nearly all tumour cells of a metastatic breast carcinoma (pleura) – hormone receptor positiveHistology & cytology
Estrogen receptor immunohistochemistry: strong nuclear staining of nearly all tumour cells of a metastatic breast carcinoma (pleura) – hormone receptor positiveImage: Yale Rosen from USA (Wikimedia Commons) · CC BY-SA 2.0 · Source
Hormone receptor-positive breast cancer (luminal A and B) – Histology & cytology: Progesterone receptor immunohistochemistry: diffuse strong nuclear staining of the tumour cells of the same metastatic breast carcinoma (pleura)Histology & cytology
Progesterone receptor immunohistochemistry: diffuse strong nuclear staining of the tumour cells of the same metastatic breast carcinoma (pleura)Image: Yale Rosen from USA (Wikimedia Commons) · CC BY-SA 2.0 · Source
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Definition

  • Hormone receptor-positive breast cancer with oestrogen and/or progesterone receptors, corresponding to the luminal A and luminal B molecular subtypes.

Classification

  • Luminal A tumours are grade 1 or 2, oestrogen and progesterone receptor-positive, HER2-negative and have low Ki-67.
  • Luminal B tumours are oestrogen receptor positive, often have a high Ki-67 fraction and may be HER2 positive or negative.

Occurrence & epidemiology

Epidemiology

  • Most breast cancers are luminal A; about 70% are hormone receptor-positive and HER2-negative.
  • Most oestrogen receptor-positive tumours are also progesterone receptor-positive; overall, about 70% of all breast cancers are progesterone receptor-positive.

Aetiopathogenesis

Aetiology and pathogenesis

  • Oestrogen and progesterone receptors are nuclear hormone receptors that promote DNA replication and cell division when their hormones bind, so oestrogen and progesterone can fuel tumour growth.
  • Early menarche, late menopause and older age at first pregnancy increase breast cancer risk.

Clinical features

  • Luminal A and B tumours generally grow more slowly than HER2-enriched and triple-negative (basal-like) tumours.

Diagnosis

  • Breast cancers are usually tested for oestrogen and progesterone receptors and HER2, often also for the Ki-67 protein.
  • Most guidelines regard immunohistochemical staining of 1% or more as oestrogen receptor-positive; ER-low tumours with 1–10% expression (about 2–7% of cases) resemble oestrogen receptor-negative tumours at the molecular level.
  • Ki-67 is found only in dividing cells, and a high proportion of Ki-67-positive tumour cells indicates rapid division.
  • Hormone receptor status can change over time.

Keep learning in the app

In the GynFuchs app you can learn Hormone receptor-positive breast cancer (luminal A and B) with flashcards, exam questions and image tasks (colposcopy, ultrasound, CTG) – free, in your browser or as an app.

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Further reading (selection)

  1. National Cancer Institute: Breast Cancer Biomarkers
  2. MSD Manual Professional: Breast Cancer
  3. Clinical implication of low estrogen receptor (ER-low) expression in breast cancer (Front Endocrinol (Lausanne) 2022, PubMed Central)

Cross-references

Note: Learning content from the GynFuchs app (flashcards, exam questions, image cases) for medical education – not a treatment recommendation and no substitute for diagnosis or treatment decisions in individual cases. Treatment and management are deliberately not covered on this page.