Definition/General

Introduction:
-Papillomatosis, also known as multiple intraductal papillomas, is a benign proliferative breast lesion characterized by the presence of five or more distinct papillomas within a localized segment of the breast.
Origin: They arise from the ductal epithelium of the terminal duct-lobular units.
Classification:
-It is classified as a benign proliferative breast lesion
-It is distinguished from a solitary papilloma by its multiplicity.
Epidemiology: It is less common than solitary papillomas and tends to occur in younger women.

Clinical Features

Presentation:
-It is often asymptomatic and found as an incidental finding
-It can present with nipple discharge or a palpable mass.
Symptoms: Nipple discharge is less common than with solitary papillomas.
Risk Factors: There are no well-established risk factors.
Screening: Mammography may show a cluster of masses or calcifications.

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Gross Description

Appearance:
-Multiple small, friable, polypoid masses within dilated ducts.
Characteristics: The size of individual papillomas is usually small.
Size Location: Typically located in the peripheral ducts.
Multifocality: Defined by its multiplicity.

Microscopic Description

Histological Features:
-The lesion consists of multiple intraductal papillomas, each with a fibrovascular core lined by a double layer of epithelial and myoepithelial cells.
Cellular Characteristics:
-The cells are bland, without atypia.
Architectural Patterns:
-Multiple, distinct papillary lesions are the key feature.
Grading Criteria:
-This is a benign lesion
-Atypia can be present (atypical papillomatosis).

Immunohistochemistry

Positive Markers: The myoepithelial cell layer is highlighted by myoepithelial markers such as p63 and calponin.
Negative Markers: Not typically required for diagnosis.
Diagnostic Utility: IHC for myoepithelial markers is useful to confirm the benign nature of the lesion.
Molecular Subtypes: Molecular subtyping is not relevant for this benign condition.

Molecular/Genetic

Genetic Mutations: Not well characterized.
Molecular Markers: No specific molecular markers are routinely used for diagnosis.
Prognostic Significance: Papillomatosis is associated with a higher risk of subsequent breast cancer than a solitary papilloma.
Therapeutic Targets: Surgical excision is often recommended to exclude associated atypia or carcinoma.

Differential Diagnosis

Similar Entities:
-Papillary DCIS
-Florid usual ductal hyperplasia.
Distinguishing Features:
-Papillary DCIS lacks a myoepithelial layer in the papillae
-Florid UDH has a different architecture and cytology.
Diagnostic Challenges: The main challenge is to assess for atypia and to distinguish from papillary DCIS.
Rare Variants: There are no specific rare variants.

Sample Pathology Report

Template Format

Sample Pathology Report

Complete Report: This is an example of how the final pathology report should be structured for this condition.

Specimen Information

[specimen type], measuring [size] cm in greatest dimension

Diagnosis

[diagnosis name]

Classification

Classification: [classification system] [grade/type]

Histological Features

Shows [architectural pattern] with [nuclear features] and [mitotic activity]

Size and Extent

Size: [X] cm, extent: [local/regional/metastatic]

Margins

Margins are [involved/uninvolved] with closest margin [X] mm

Lymphovascular Invasion

Lymphovascular invasion: [present/absent]

Lymph Node Status

Lymph nodes: [X] positive out of [X] examined

Special Studies

IHC: [marker]: [result]

Molecular: [test]: [result]

[other study]: [result]

Final Diagnosis

Final diagnosis: [complete diagnosis]