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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.
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Invasive ductal and lobular carcinoma

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Synopsis

Distinguish invasive carcinoma of no special type from invasive lobular carcinoma, integrate morphology with extent and nodal assessment, and plan a concordant multidisciplinary treatment pathway.

  • Invasive breast carcinoma has crossed the basement membrane and can enter lymphatic or blood vessels; “no special type” replaces the older default label invasive ductal carcinoma.
  • Invasive carcinoma of no special type often forms a stellate mass, whereas lobular carcinoma more often infiltrates in single-file strands because loss of cell cohesion can obscure its true extent.
  • Diagnosis needs concordant clinical assessment, age-appropriate bilateral imaging and image-guided core biopsy; record tumour type, grade and ER, PR and HER2 status.

Key red flags

A rapidly enlarging hard mass, skin tethering, peau d’orange, bloody nipple discharge or fixed axillary nodes requires urgent diagnostic breast assessment rather than routine surveillance.

Investigation priorities

01
Image-guided core biopsyFirst step

Confirm invasion and provide sufficient tissue for type, grade and receptor testing.

Management branches

New invasive cancer pathwayBuild a concordant pretreatment map

Core biopsy from a 24 mm lesion confirms grade 2 invasive lobular carcinoma and the patient hopes to conserve the breast.

  1. Confirm that the core sampled the clinical and imaging target; request ER, PR and HER2 together and review grade and any lymphovascular invasion.
  2. Perform pretreatment axillary ultrasound and image-guided sampling of any abnormal node, documenting whether nodal disease is proven or only suspected.
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Sources and review status4 sources · checked 8 Sept 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Apply principles in context and verify current guidance when a decision affects care. Source check completed 8 Sept 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom