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LPL Expert Panel 2 Test -
Reviews histopathology of 9–15 blocks to diagnose cancer, causing swelling or pain
Synonym LPL Panel 2 Test
Test Code CHIS250064
Test Type Histopathology
Pre-Test Condition No special
Report Availability 3–5 D(s)
# Test(s) 1
Test details Sample Report
LPL Expert Panel 2 Test Sample Report Cowin-PathLab
Synonym LPL Panel 2 Test
Test Code CHIS250064
Test Category Cancer
Pre-Test Condition No special
Medical History Share & see Updates
Report Availability 3–5 D(s)
Specimen/Sample Refer Updates
Stability @21-26 deg. C 7 D(s)
Stability @ 2-8 deg. C Not refrigerated
Stability @ Frozen Not frozen
# Test(s) 1
Processing Method Histopathology
Overview: LPL Expert Panel 2 Test
Introduction: The LPL Expert Panel 2 Test reviews histopathology of 9-15 blocks to diagnose cancer, causing swelling or pain. Following 2023 CAP guidelines, it uses histopathology for high specificity, supporting cancer screening. This test is critical for guiding diagnosis, treatment planning, and improving outcomes in histopathology for patients with suspected complex malignancies.
Other Names: LPL Panel 2 Assay, Cancer Histopathology Review (9-15 Blocks).
FDA Status: Laboratory-developed test (LDT), meeting histopathology standards for diagnostic accuracy.
Historical Milestone: Expert histopathology panels expanded in the 1990s with cancer diagnostics. Multi-block reviews improved in the 2000s, enhancing diagnostic precision.
Purpose: Reviews histopathology of 9-15 blocks to diagnose cancer, guides treatment, and evaluates patients with swelling or pain.
Test Parameters: 1. Histopathology Review (9-15 Blocks)
Pretest Condition: No fasting required. Collect tissue. Report history of swelling, pain, or cancer symptoms.
Specimen: Tissue (FFPE, 0.5-2 cma³). Transport in a biohazard container.
Sample Stability at Room Temperature: 7 days
Sample Stability at Refrigeration: Not refrigerated
Sample Stability at Frozen: Not frozen
Medical History: Document swelling, pain, weight loss, or family history of cancer. Include current medications, especially chemotherapy.
Consent: Written consent required, detailing the tests purpose, cancer implications, and risks of biopsy.
Procedural Considerations: Uses histopathology to review 9-15 tissue blocks. Results are available in 3-5 days, supporting clinical decisions. Performed in laboratories, often for complex cancer diagnosis.
Factors Affecting Result Accuracy: Improper tissue fixation or low tissue quality can affect results. Insufficient block number may limit diagnosis.
Clinical Significance: Abnormal histopathology confirms cancer, guiding treatment (e.g., surgery, chemotherapy). Normal results may require further testing.
Specialist Consultation: Consult an oncologist or pathologist for result interpretation and treatment planning.
Additional Supporting Tests: Immunohistochemistry, molecular profiling, or imaging (e.g., PET-CT) to confirm cancer diagnosis.
Test Limitations: Limited to 15 blocks; complex cancers may require more extensive review. Clinical correlation is needed.
References: CAP Pathology Guidelines, 2023; Archives of Pathology, Fitzgibbons PL, 2022.

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