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450 AED

✅ Home Collection Available

Immunohistochemistry CD138 (Syndecan-1) Test in UAE – 450 AED – DNA Labs UAE

Executive Summary & Core Metrics

  • Accuracy Guarantee: 99.9% diagnostic sensitivity via ISO 9001:2015 accredited processing and validated immunohistochemistry protocols.
  • Specimen Logistics: Secure Medical Courier Solid Tissue Specimen Retrieval for FFPE blocks, tissue biopsies, and surgical pathology cuts; temperature-controlled chain of custody maintained at every stage.
  • Clinical Guidance: Complimentary telephonic post-test clinical correlation session with a DHA-licensed consultant to interpret CD138 findings in the context of morphology and ancillary markers.
  • Insurance Verification: Direct billing confirmation available via WhatsApp at +971 54 548 8731 prior to sample submission.

Test Overview & Methodology

The CD138 (Syndecan-1) immunohistochemistry test is a tissue-based assay that specifically stains plasma cells and their malignant counterparts. This assay is essential for distinguishing plasma cell neoplasms such as multiple myeloma and plasmacytoma from other lymphomas, carcinomas, or reactive plasma cell proliferations. The test is performed on formalin-fixed paraffin-embedded (FFPE) tissue sections using validated monoclonal antibody clones targeting the syndecan-1 epitope, with automated staining platforms ensuring consistent, reproducible results. Interpretation integrates CD138 positivity with morphological features, kappa/lambda light chain restriction patterns, and a panel of complementary markers including MUM1, CD38, and CD56 to achieve a definitive diagnosis.

Feature DNA Labs UAE CD138 IHC Service Standard Laboratory IHC Offering
Diagnostic Precision 99.9% sensitivity with validated, calibrated antibody clones and automated staining platforms; full internal quality control per ISO 15189 standards Variable sensitivity (90–95%); manual interpretation without standardized antibody validation
Methodology Immunohistochemistry (IHC) with syndecan-1 specific detection; full FFPE compatibility; automated platform ensures uniform staining across all slides Generic IHC panels often lacking CD138 specificity; manual protocol variability between runs
Turnaround Time FFPE block: 5 working days | Small tissue biopsy: 5 days | Large complex tissue: 7 days Typically 7–10 days without expedited handling protocols
Patient Support Complimentary post-test clinical interpretation call; direct insurance verification via WhatsApp; dedicated patient coordinator Limited or no interpretive support; no insurance liaison service

Physician Insight & Safety Protocols

"A clearly positive CD138 stain identifies plasma cell lineage; when correlated with morphological features, clinical presentation, and serum protein electrophoresis data, the result guides the diagnosis toward multiple myeloma, solitary plasmacytoma, or lymphoplasmacytic lymphoma. Negative staining does not entirely exclude a plasma cell neoplasm — inadequate tissue sampling, necrosis, or antigen masking can produce false-negative results. In such cases, repeat biopsy or complementary markers including MUM1 and CD38 should be considered. Accurate interpretation depends on a complete clinical picture; therefore, providing the full histopathology report, biopsy site details, and relevant laboratory values is essential."

— Mr. Prabhakar Reddy Kalathoor, Specialist Diagnostic Radiology, DHA Registration ID: 61713011

⚠️ Clinical Advisory – Exclusion Criteria & Emergency Red Flags

  • Exclusion Criteria: Inadequate, necrotic, or poorly fixed tissue specimens; samples submitted without an accompanying histopathology report and complete clinical history cannot be processed. Tissue blocks lacking clear patient identification will be rejected.
  • Consent Requirement for Minors: Parental or legal guardian consent is mandatory for patients under 18 years of age in accordance with Federal Decree-Law No. 4 of 2016 on Medical Liability; no test will proceed without documented written authorisation.
  • Medication Advisory: Do not discontinue any prescribed medication without consulting your treating physician. This diagnostic test provides tissue-level information and does not replace a comprehensive clinical evaluation or treatment decision.
  • Emergency Red Flags: Seek immediate medical attention if you experience new or worsening bone pain, progressive fatigue, unexplained fever, or signs of hypercalcemia including nausea, vomiting, confusion, or excessive thirst during the diagnostic period — these may indicate an aggressive plasma cell disorder requiring urgent intervention.

Patient FAQ & Clinical Guidance

1. What does the CD138 IHC test detect and why is it important?

The CD138 immunohistochemistry test detects syndecan-1, a transmembrane heparan sulfate proteoglycan that is strongly expressed on the surface of normal and neoplastic plasma cells. This marker is the gold standard for confirming plasma cell lineage in tissue biopsies. A positive result, when integrated with morphology and clinical data, supports the diagnosis of multiple myeloma, plasmacytoma, or lymphoplasmacytic lymphoma. The test is also used to quantify plasma cell burden in bone marrow trephine biopsies, assess minimal residual disease, and differentiate plasma cell neoplasms from B-cell lymphomas or metastatic carcinomas that may mimic plasma cell morphology.

2. How do I prepare for sample collection and what materials must I provide?

No fasting or special preparation is required on your part. For FFPE block submission, please ensure the block is clearly labelled with the patient name and unique identifier, and provide the original histopathology report along with details of the biopsy site, date of collection, and relevant clinical history. If you are submitting tissue slides, confirm that they are unstained and of adequate thickness. Our Secure Medical Courier Solid Tissue Specimen Retrieval service will collect the materials from your location using temperature-controlled packaging; simply contact our team to arrange the pickup at a time convenient for you.

3. When will my results be ready and how do I interpret the findings?

Results are delivered within 5 to 7 working days depending on tissue complexity and the number of additional markers requested. You will receive a secure digital pathology report that details CD138 positivity, staining intensity, and the percentage of positive plasma cells. A complimentary telephone consultation with a DHA-licensed clinical specialist is included to explain the findings and their diagnostic implications. We strongly recommend that you discuss the final report with your treating haematologist or oncologist, who will integrate the IHC result with your serum protein electrophoresis, immunofixation, imaging studies, and overall clinical context.

4. Can I proceed with this test if I am on medication or have a concurrent infection?

Yes, but you must inform the laboratory of any current medications, recent infections, or known autoimmune conditions at the time of sample submission. Certain medications and inflammatory states can transiently alter plasma cell distribution in the bone marrow or soft tissue, potentially affecting interpretation. The pathologist will note these factors in the report. Do not stop or modify any prescribed treatment without explicit guidance from your physician. If you have an active infection with fever, your doctor may advise deferring the biopsy until the infection resolves to avoid confounding the diagnostic picture.

5. What is the difference between CD138 IHC and serum-based tests like serum protein electrophoresis?

CD138 immunohistochemistry is a tissue-based assay that visualises plasma cells directly within their native microenvironment, providing spatial and morphological context. Serum protein electrophoresis and immunofixation are blood-based tests that detect monoclonal immunoglobulins or free light chains secreted by plasma cells into the circulation. The two approaches are complementary: tissue IHC confirms the presence and lineage of the plasma cell infiltrate, while serum studies quantify the systemic burden of monoclonal protein. For a complete diagnostic workup of suspected plasma cell disorders, both tissue and serum evaluations are typically required.

UAE Regulatory & Data Privacy Adherence

  • Data Protection: All patient data is processed in full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL). Personal health information is encrypted, access-controlled, and used solely for diagnostic purposes.
  • Health Information Governance: The laboratory operates under Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields, ensuring secure electronic health data exchange, audit logging, and patient consent management.
  • Clinical Safety & Consent: All invasive specimen collection procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability, which governs patient consent, medical record keeping, and professional accountability in diagnostic practice.
  • Accreditation: DNA Labs UAE is ISO 9001:2015 certified (Cert: INT/EGQ/2509DA/3139) and operates under DHA regulatory oversight to ensure the highest standards of laboratory quality and diagnostic reliability.

Clinical & Logistical Metadata

Test Name Immunohistochemistry CD138 (Syndecan-1)
Price (AED) 450
Turnaround Time 5–7 working days depending on tissue complexity and additional marker requirements
Sample Type / Matrix Archival Tissue Specimen – Secure Medical Courier Solid Tissue Specimen Retrieval (FFPE block, tissue biopsy, surgical pathology cuts); hospital extraction only for bone marrow core biopsies
Methodology Used Immunohistochemistry (IHC) with validated syndecan-1 specific monoclonal antibodies, automated staining platform, full FFPE compatibility, internal and external quality control
ICD-10-CM Code C90.00 (Multiple myeloma not having achieved remission), C90.02 (Multiple myeloma in relapse), C90.20 (Plasmacytoma not having achieved remission)
LOINC Code 94495-4 (CD138 [Immune stain] in Tissue by Immunohistochemistry)
DHA Facility License & Laboratory Address DHA Facility License Number: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE

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