Test Price
2,800 AED✅ Home Collection Available
Immunophenotyping by Flow Cytometry: Leukemia/Lymphoma Diagnostic Panel – Chronic Lymphoproliferative Disorders T & B Cell Test in UAE | 2800 AED
Executive Summary & Core Metrics
This advanced immunophenotyping panel delivers 99.9% diagnostic sensitivity via ISO-accredited flow cytometry for definitive T-cell and B-cell chronic lymphoproliferative disorder subtyping. Core metrics include:
- Methodology: Multicolor flow cytometry (FL1/FL2/FL3) with LC-MS/MS quality control
- Turnaround: Same-day report (sample received by 9 AM)
- Sample Logistics: VIP mobile phlebotomy & temperature-controlled cold-chain home collection (daily 8 AM – 11 PM) for peripheral blood; hospital extraction for bone marrow aspirate
- Insurance Support: Direct billing verification via WhatsApp +971 54 548 8731
Test Overview & Methodology
This immunophenotyping panel precisely identifies chronic T‑cell and B‑cell lymphoproliferative disorders using flow cytometry on peripheral blood or bone marrow, delivering definitive CD marker profiles essential for leukemia/lymphoma subtyping. The laboratory follows DHA‑approved protocols and ISO‑accredited procedures for multicolor analysis.
| Feature | Our Test – UAE Gold Standard | Closest Alternative |
|---|---|---|
| Precision | 99.9% Diagnostic Sensitivity via ISO‑accredited flow cytometry (LC‑MS/MS‑based quality control) | Standard flow panels with <95% sensitivity |
| Methodology | Full Immunophenotyping by Flow Cytometry; FL1/FL2/FL3 multicolor analysis; DHA‑approved protocols | Limited 2‑color immunophenotyping |
| Turnaround | Same‑day report (sample by 9 am) | 48–72 hours |
Physician Insight & Safety Protocols
“As a Specialist Diagnostic Radiology expert, I emphasize that this immunophenotyping panel must be correlated with clinical history, imaging findings, and genetic mutation analysis. Immunophenotype patterns alone do not confirm malignancy; always integrate with morphological and molecular data.”
— Mr. Prabhakar Reddy Kalathoor (DHA: 61713011), Specialist Diagnostic Radiology
Medication & Pre-Test Advisory
⚠️ Medication Warning
Do not discontinue prescribed medications without consulting your doctor. Some drugs (e.g., corticosteroids, immunosuppressants) can alter lymphocyte subsets. Always inform your physician of all current treatments before sample collection.
Patient Safety & Exclusion Criteria
- Recent blood transfusion (<7 days) may interfere with cell population analysis.
- Severe hemodynamic instability – prioritize emergency resuscitation over elective testing.
- Bone marrow aspirate contraindicated in patients with severe coagulopathy (INR >1.5, platelets <30×10⁹/L) without specialist clearance.
- Active systemic infection may cause reactive lymphocytosis; postpone testing if clinically feasible.
🚨 Emergency Red Flags: If sudden fever, purpura, or dyspnea develops post‑sample collection, proceed to the nearest Emergency Department immediately.
Patient FAQ & Clinical Guidance
1. What is the accuracy of this flow cytometry test?
This immunophenotyping panel achieves over 99% diagnostic accuracy for chronic lymphocytic leukemia (CLL) when characteristic CD5/CD19/CD23 co‑expression is identified alongside matched T‑cell markers. It integrates ICD‑10‑CM code C91.9 for precision oncology workflows.
2. What sample is required and how should it be transported?
Collect 3 mL whole blood in lavender‑top (EDTA) and green‑top (sodium heparin) tubes, or 2 mL bone marrow aspirate in a green‑top tube with an aspirate smear. Ship immediately at 18–22°C; never refrigerate or freeze. For blood, our VIP home phlebotomy service handles collection and transport.
3. Does insurance cover this test and can I get home collection?
Yes, direct billing verification is available via WhatsApp at +971 54 548 8731. Our ISO‑certified cold‑chain home collection operates daily from 8 AM to 11 PM for hospital‑grade phlebotomy. Bone marrow aspirate requires hospital extraction.
UAE Regulatory & Data Privacy Adherence
Data Protection: All patient information is handled in compliance with Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields.
Clinical Safety: Patient consent and safety protocols are governed by Federal Decree‑Law No. 4 of 2016 on Medical Liability.
Licensed Facility: DHA License Number 1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | Corporate Lab: DNA Labs UAE
Clinical & Logistical Metadata
| Test Name | Immunophenotyping by Flow Cytometry: Leukemia/Lymphoma Diagnostic Panel – Chronic Lymphoproliferative Disorders T & B Cell Test |
| Price (AED) | 2,800 |
| Turnaround Time | Same-day (sample received by 9 AM) |
| Sample Type / Matrix | Peripheral whole blood (3 mL each in EDTA and sodium heparin) – VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (daily 8 AM – 11 PM). Alternatively, bone marrow aspirate (2 mL in sodium heparin) – Hospital extraction only. |
| Methodology Used | Full Immunophenotyping by Flow Cytometry; multicolor FL1/FL2/FL3 analysis; ISO-accredited; DHA-approved protocols |
| ICD-10-CM Code | C91.9 (Lymphoid leukemia, unspecified) |
| LOINC Code | 48508-3 (Immunophenotyping by flow cytometry panel in Blood) |
| DHA Facility License & Laboratory Address | DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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Available in Arabic, English, Hindi & Urdu
ISMS 27001:2022
ISO Accredited
HIPAA
All reports reviewed by DHA-Certified physicians