Definition/General

Introduction:
-Invasive micropapillary carcinoma (IMPC) is a rare and aggressive variant of invasive ductal carcinoma characterized by a distinctive growth pattern of small, hollow, morula-like clusters of tumor cells within clear stromal spaces
-It has a high propensity for lymphovascular invasion and lymph node metastasis.
Origin: It arises from the ductal epithelium.
Classification:
-It is a subtype of invasive ductal carcinoma
-It can be pure or mixed with other types of invasive carcinoma.
Epidemiology:
-It is rare, accounting for less than 2% of all invasive breast cancers
-It typically affects postmenopausal women.

Clinical Features

Presentation: Presents as a palpable, firm, irregular mass.
Symptoms: A painless breast lump is the most common symptom.
Risk Factors: The risk factors are similar to those for other types of breast cancer.
Screening: Mammography shows a spiculated, high-density mass, often with calcifications.

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Gross Description

Appearance:
-A firm, gray-white, infiltrative mass.
Characteristics: The size is variable.
Size Location: Can occur anywhere in the breast.
Multifocality: Can be multifocal.

Microscopic Description

Histological Features:
-The tumor is composed of small, cohesive clusters of cells that lie within clear, empty stromal spaces, mimicking lymphatic vessels
-The cell clusters have a characteristic "inside-out" or reverse polarity, with the apical surface facing the stroma
-There are no true fibrovascular cores.
Cellular Characteristics:
-The cells are typically high-grade, with pleomorphic nuclei and prominent nucleoli
-Mitotic activity is often high.
Architectural Patterns:
-The micropapillary pattern is the key feature
-It is often associated with extensive lymphovascular invasion.
Grading Criteria: These are typically high-grade tumors.

Immunohistochemistry

Positive Markers:
-The tumor cells are positive for cytokeratins and are often ER-positive
-The reverse polarity can be highlighted by staining for EMA, which shows a characteristic "inside-out" pattern.
Negative Markers: HER2 is overexpressed in a subset of cases.
Diagnostic Utility:
-EMA staining can be helpful to demonstrate the reverse polarity
-D2-40 can be used to highlight true lymphatic invasion.
Molecular Subtypes: Most are of the luminal subtype.

Molecular/Genetic

Genetic Mutations: Not well characterized.
Molecular Markers: No specific molecular markers are routinely used for diagnosis.
Prognostic Significance:
-IMPC has a poor prognosis due to its high rate of lymphovascular invasion and lymph node metastasis, even when the tumor is small.
Therapeutic Targets:
-Treatment is similar to that of conventional breast cancer, based on ER and HER2 status.

Differential Diagnosis

Similar Entities:
-Adenocarcinoma with extensive lymphovascular invasion
-Papillary carcinoma.
Distinguishing Features:
-The clear spaces in IMPC are artefactual and are not true lymphatic vessels (they are negative for D2-40)
-Papillary carcinomas have true fibrovascular cores.
Diagnostic Challenges: The main challenge is recognizing the characteristic micropapillary pattern and distinguishing it from extensive lymphovascular invasion.
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]