SciELO - Scientific Electronic Library Online

 
vol.38 número3Fístula Colecistobulbar Associada a Síndrome de Bouveret e Obstrução IlealPara Além da Mielite Transversa: A Importância da Neurorradiologia no Diagnóstico do Enfarte Medular índice de autoresíndice de assuntosPesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Journal

Artigo

Indicadores

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Acta Radiológica Portuguesa

versão impressa ISSN 2183-1351versão On-line ISSN 2976-0763

Acta Radiol Port vol.38 no.3 Lisboa set. 2026  Epub 31-Dez-2026

https://doi.org/10.25748/arp.42089 

Imagens de Interesse

Male Adult Breast Hamartoma

Hamartoma Mamário num Homem Adulto

1Hospital Garcia de Orta, Serviço de Radiologia, Almada, Portugal


Abstract

A 43-year-old man presented with a slowly growing periareolar lump. Mammography and ultrasound showed a well-defined encapsulated oval mass with intermixed fat and fibroglandular tissue, creating the classic “breast-within-a-breast” appearance. Male breast hamartoma is exceedingly rare-fewer than ten cases reported-but its hallmark imaging allows confident diagnosis without biopsy. The lesion was categorised BI-RADS 2, and annual clinical follow-up was recommended. This case highlights the value of recognising this benign entity and sparing unnecessary intervention.

Keywords: Hamartoma; Breast neoplasms; Male; Mammography; Ultrasonography; Mammary.

Resumo

Homem de 43 anos com nódulo periareolar direito de crescimento lento. Realizou mamografia e ecografia, que revelaram uma massa oval encapsulada, com mistura de gordura e tecido fibroglandular, configurando o clássico “breast-within-a-breast”. O hamartoma mamário é raro no sexo masculino - menos de uma dezena de casos descritos -, mas quando apresenta aspeto típico dispensa biópsia. A lesão foi classificada como BI-RADS 2 e recomendou-se vigilância clínica anual. O caso sublinha a importância de reconhecer esta entidade benigna e evitar procedimentos invasivos.

Palavras-chave: Hamartoma; Neoplasia da mama; Homem; Mamografia; Ecografia; Mama.

Images in Case

A 43-year-old man reported a painless enlarging right periareolar lump noticed two years earlier. Physical examination showed a well-circumscribed, mobile, subareolar mass; skin and nipple were normal and no axillary lymph-nodes were palpable.

Bilateral mammography demonstrated an oval, sharply marginated lesion measuring 25 × 8 mm in the right retro-areolar region (Fig. 1). Its interior displayed an admixture of radiolucent fat and radiodense fibroglandular tissue, producing the characteristic “breast-within-a-breast” pattern; a faint delimiting rim was suggested around the mass. The left breast was fatty (BI-RADS 1).

Figure 1: Bilateral craniocaudal and mediolateral-oblique mammograms. In the right breast, an oval periareolar mass (arrow) is circumscribed by a faint capsule; the mixture of radiolucent fat and radiodense fibroglandular tissue produces the characteristic “breast-within-a-breast” appearance. 

Ultrasound confirmed an encapsulated, oval, heterogeneous lesion parallel to the skin (Fig. 2A). Intermingled hyperechoic (fibroglandular) and hypoechoic (fatty) foci were seen, bound by an echogenic rim; Doppler showed no internal vascularity. A measurement view (Fig. 2B) documented a maximum length of 25 mm and underscored the lesion’s smooth capsule and mixed fibroglandular-fat composition.

Figure 2: Ultrasound images of the right breast hamartoma. (A) Radial view: an encapsulated oval lesion (arrow) with heterogeneous echotexture-intermixed hyperechoic fibroglandular tissue and hypoechoic fat-lying parallel to the skin, without posterior shadowing or internal Doppler flow. (B) Long-axis measurement view confirms a maximal length of 25 mm (arrow) and better delineates the smooth echogenic capsule and the mixed fibroglandular-fat composition. 

The imaging constellation matched textbook criteria for hamartoma, so the lesion was categorised BI-RADS 2 (benign); biopsy was deemed unnecessary. Annual clinical review was advised, reserving repeat imaging for growth or new symptoms.

Discussion

Breast hamartoma corresponds to a disorganised but benign aggregation of mammary fat and fibroglandular tissue within a pseudocapsule. Although it represents up to 1 % of benign breast tumours in women, it is exceedingly rare in men, with fewer than ten well-documented cases published to date.1 The male breast typically contains little glandular tissue, which explains both the rarity of hamartoma and the striking visual contrast between fat and fibroglandular tissue when it does occur.

The triad of (1) oval or round morphology, (2) thin capsule and (3) heterogeneous internal fat-fibroglandular pattern appears in more than 90 % of hamartomas on mammography.2 Ultrasound mirrors this architecture, showing an encapsulated, parallel, heterogeneous, avascular mass. When all features are present-and no suspicious calcifications, angular margins or skin changes coexist-the BI-RADS lexicon allows a benign (category 2) assessment, obviating biopsy.3 Our patient fulfilled every criterion, and the long symptom duration without change further reinforced benignity.

Most solid male breast masses require tissue diagnosis because male breast cancer may appear deceptively benign; a classic hamartoma is an exception. Benign mimics include pseudoangiomatous stromal hyperplasia (PASH; circumscribed solid mass or focal asymmetry without internal fat), myofibroblastoma (well-circumscribed homogeneous solid mass in men, no fat), hemangioma (circumscribed mass with internal vascular channels/flow or phleboliths), and intraductal papilloma (retroareolar intraductal nodule with duct ectasia and Doppler flow). Other differentials in men comprise nodular gynaecomastia (ill-defined, flame-shaped subareolar proliferation, purely fibroglandular, non-encapsulated), lipoma (entirely fat-density with a thin capsule and homogeneous echogenicity), and carcinoma (irregular/spiculated margins, desmoplastic reaction, or suspicious microcalcifications/skin-nipple changes). Recognising the “breast-within-a-breast” sign and the mixed fat-fibroglandular composition is therefore crucial, as it supports a benign BI-RADS 2 assessment and may avert unnecessary biopsy when present.3

Although malignant transformation within a hamartoma is exceptionally rare, isolated reports justify continued surveillance.1 We recommend yearly clinical examination, reserving imaging for interval enlargement or new clinical findings-an approach aligned with published experience in both sexes.2

References

1. Li M, Lin G, You W, et al. Hamartoma of the breast in a man: a rare case report. Medicine (Baltimore). 2019;98:e18372. [ Links ]

2. Yadav P. Imaging spectrum of breast hamartoma on mammography, ultrasound and MRI. J Clin Diagn Res. 2019;13:TE01-TE03. [ Links ]

3. Mannix J, Duke H, Almajnooni A, Ongkeko M. Imaging the male breast: gynecomastia, male breast cancer, and beyond. RadioGraphics. 2024;44:e230181. [ Links ]

Ethical Disclosures

Financing Support: This work has not received any contribution, grant or scholarship.

Received: June 23, 2025; Accepted: September 14, 2025

Address Eduardo Fernandes, Serviço de Radiologia, Hospital Garcia de Orta, Av. Torrado da Silva, 2805-267 Almada, e-mail: edu.aspf@gmail.com

Conflicts of interest: The authors have no conflicts of interest to declare.

Confidentiality of data: The authors declare that they have followed the protocols of their work center on the publication of data from patients.

Protection of human and animal subjects: The authors declare that the procedures followed were in accordance with the regulations of the relevant clinical research ethics committee and with those of the Code of Ethics of the World Medical Association (Declaration of Helsinki).

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License