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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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Granulomatous mastitis

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Synopsis

Diagnose granulomatous mastitis only after representative tissue and microbiological exclusion, manage abscesses and symptoms through a multidisciplinary plan, and avoid unsafe corticosteroids when infection remains possible.

  • Granulomatous mastitis is a lobulocentric inflammatory breast disorder that can produce painful masses, sterile or infected abscesses, skin ulceration and draining sinuses.
  • Idiopathic granulomatous mastitis is a diagnosis of exclusion; pregnancy-related history and Corynebacterium association are relevant, but tuberculosis, fungi, foreign body and carcinoma must be considered.
  • Ultrasound maps collections and sinus tracts, while image-guided core biopsy provides architecture needed to show granulomas and exclude invasive malignancy.

Key red flags

Rapid progression, sepsis, necrotic skin or a mass and oedema that remain suspicious for inflammatory cancer requires urgent breast and surgical assessment.

Investigation priorities

01
Targeted ultrasoundFirst step

Map masses, collections, oedema and sinus tracts and select aspiration or core targets.

Management branches

Diagnostic pathwayProve the pattern and exclude causes

A non-lactating patient has recurrent culture-negative breast collections and an irregular inflammatory mass despite two antibiotic courses.

  1. Reassess for sepsis and inflammatory cancer, map collections with ultrasound and obtain mammography appropriate to age and tissue tolerance.
  2. Core the solid inflammatory margin and aspirate fluid, alerting pathology and microbiology to possible granulomatous disease before specimens are processed.
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Sources and review status5 sources · checked 7 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 7 Sept 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom