Phyllodes tumor
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]
Synonyms and keywords: Cystosarcoma phyllodes;
Overview
Phyllodes tumor (also known as cystosarcoma phyllodes), is a typically large, fast-growing mass that arises from the periductal stromal cells of the breast. Phyllodes tumors account for less than 1% of all breast neoplasms.
Historical Perspective
- Phyllodes tumor was first discovered by Johannes Muller, a German physician in 1838.
Classification
- Phyllodes tumor may be classified according to histological grade into 3 subtypes:
- Benign
- Borderline
- Malignant
Pathophysiology
- The pathogenesis of phyllodes tumor is characterized by the overgrowth of stromal cells.
- Phyllodes tumor arises from the periductal stromal cells of the breast, which are normally involved in the supportive function of the parenchymal tissue.
- Genes involved in the development of phyllodes tumor, include:
- p53 gene
- EGFR gene
- IGF1R gene
- On gross pathology, characteristic findings of phyllodes tumor, include:
- Cleft/leaf-like structures
- Friable mass
- Well-defined margins
- On microscopic histopathological analysis,characteristic findings of phyllodes tumor, include:
- Large slit-like spaces
- Cellular myxoid stroma
- Infiltrative border
- Stromal overgrowth
Causes
- There are no established causes for phyllodes tumor.
Differentiating Phyllodes Tumor from Other Diseases
- Phyllodes tumor must be differentiated from other diseases that cause a breast mass, such as:
- Juvenile fibroadenoma
- Breast abscess
- Adenocarcinoma
- Mastitis
Epidemiology and Demographics
- The prevalence of phyllodes tumor is approximately 0.05 per 100,000 individuals worldwide.
- Approximately 6% of all phyllodes tumors are malignant.
- Phyllodes tumor accounts for less than 0.3-1% of all breast neoplasms
Age
- Patients of all age groups may develop phyllodes tumor.
- However, phyllodes tumor is more commonly reported in adult women between 40 and 60 years.
Gender
- Females are more commonly affected with phyllodes tumor than males.
Race
- There is no racial predilection for phyllodes tumor.
Risk Factors
- Common risk factors in the development of phyllodes tumor, include:
Natural History, Complications and Prognosis
- The majority of patients with phyllodes tumor remain asymptomatic for years.
- The most important early clinical feature is a rapid growing palpable mass.
- If left untreated, the minority of patients with phyllodes tumor may progress to develop metastases.
- Complications of phyllodes tumor are usually related to surgery (mastectomy).
- Common complications, include:
- Infection
- Seroma formation
- Local or distant recurrence
- Prognosis is generally poor, and the 5 year survival rate of patients with phyllodes tumor is approximately
Diagnosis
Diagnostic Criteria
- The diagnosis of phyllodes tumor is made with biopsy.
Symptoms
- Phyllodes tumor is usually asymptomatic.
- There are no remarkable symptoms of phyllodes tumor.
Physical Examination
- Patients with phyllodes tumor usually appear [general appearance].
- Breast physical examination may be remarkable for:
- Breast mass, with the following characteristics:
- Firm
- Mobile
- Well-circumscribed
- Non-tender
Laboratory Findings
- There are no specific laboratory findings associated with phyllodes tumor.
Imaging Findings
- [Imaging study 1] is the imaging modality of choice for phyllodes tumor.
- On [imaging study 1], findings of phyllodes tumor include:
Treatment
Medical Therapy
- There is no medical therapy for phyllodes tumor.
Surgery
- Surgery is the mainstay of therapy for phyllodes tumor.
- Wide local excision is the most common approach to the treatment of phyllodes tumor.
Prevention
- Effective measures for the primary prevention of phyllodes tumor include periodical self-breast examination, and routine mammography.
- Once diagnosed and successfully treated, patients with phyllodes tumor are followed-up periodically.
- Follow-up testing, includes: ultrasound examination.