Paget´s disease of the male breast: An unusual case in a young man and literature review
•Paget's disease of the breast is rare, comprising about 1–4% of all breast cancers. Male breast cancer is also uncommon, representing less than 1% of all breast cancer. Thus, male mammary Paget´s disease is extremely rare.•We present a postoperative diagnosis of an exceptional case of mammary...
Gespeichert in:
| Veröffentlicht in: | Current problems in cancer. Case reports Jg. 1; S. 100019 |
|---|---|
| Hauptverfasser: | , , , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
Elsevier Inc
01.12.2020
Elsevier |
| Schlagworte: | |
| ISSN: | 2666-6219, 2666-6219 |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| Zusammenfassung: | •Paget's disease of the breast is rare, comprising about 1–4% of all breast cancers. Male breast cancer is also uncommon, representing less than 1% of all breast cancer. Thus, male mammary Paget´s disease is extremely rare.•We present a postoperative diagnosis of an exceptional case of mammary Paget´s disease in man who complained of bilateral gynecomastia and mild eczematous changes in the nipple. Our case describes the youngest man diagnosed with Paget´s disease in the literature.•The detailed presentation of this case and the literature review allow us to achieve a high degree of suspicion of Paget´s disease. Clinical recognition of this entity allows an early diagnosis with a favorable prognosis.
Mammary Paget's disease (PD) is characterized by eczematous changes of the nipple-areolar complex and is usually associated with an underlying breast cancer (BC). PD of the breast is rare, comprising about 1–4% of all BC. Male BC is also uncommon, representing less than 1% of all BC. Thus, male mammary PD is extremely rare. We report the case of mammary PD associated with an underlying BC in situ in a 41-year-old young man who complained of bilateral gynecomastia and mild eczematous signs in the nipple.
[Display omitted] |
|---|---|
| ISSN: | 2666-6219 2666-6219 |
| DOI: | 10.1016/j.cpccr.2020.100019 |