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Reading File
Patient: Mullaji Mobeen Ali Ali, 56-year-old Indian male, Al-Naim Polyclinic, Hofuf. Samples were reported on 10-11-2026. Pages 1 and 2 of 3 were provided, so page 3 is missing.
Topics covered by a full review
  1. Anemia work-up (CBC red cell indices)
  2. Hyperglycemia and diabetes (RBS 310)
  3. Kidney function (creatinine 1.38)
  4. White cell differential (neutrophilia)
  5. Lipid profile and cardiovascular risk
  6. Liver enzyme, missing data and suggested next tests
  7. Overall summary and likely unifying diagnosis
High-level overview
  • Abnormal results
    • Hb is 10.0 g/dL (low), RBC 3.82 (low), HCT 33.9% (low) and MCHC 29.6 (low). MCV is 88.7 fL (normal) and MCH is 26.3 pg (borderline).
    • This is a mild normocytic anemia with a tendency to hypochromia. Possible causes are anemia of chronic disease or CKD, early or mixed iron deficiency, or blood loss.
    • Random blood sugar is 310 mg/dL (high). In a 56-year-old this strongly suggests uncontrolled or undiagnosed diabetes. It needs HbA1c and a fasting glucose to confirm.
    • Creatinine is 1.38 mg/dL (high). My estimate of eGFR is about 60 mL/min/1.73 m² (CKD-EPI 2021), which is borderline. Diabetic kidney disease is possible, but you'd need repeat testing over at least 3 months, a urine albumin-to-creatinine ratio and urinalysis to confirm CKD.
    • Neutrophils are 80.6% (high) and lymphocytes 15.8% (low). The total WBC is 10.62, at the top of normal. Causes include infection (for example urinary or foot), physiologic stress, steroids or hyperglycemia.
  • Normal results
    • Platelets are 317, MCV, monocytes and eosinophils are normal, and the total WBC is normal.
    • Cholesterol is 130, LDL 62 and triglycerides 116. These are excellent and suggest he may already be on a statin.
    • SGPT (ALT) is 13 U/L, so there is no hepatocellular injury.
  • Overall picture: The most likely story is hyperglycemia with early renal impairment and a mild anemia that may be related to it. Possible infection or stress is a secondary concern. There is no clinical history, medication list or symptoms, so this is a lab interpretation only and not a diagnosis.
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