What is the difference between reactive leukocytosis and myeloproliferative disorders in a 57-year-old female with severe abdominal pain? - #30191
Subject: Evaluation for Persistent Neutrophilic Leukocytosis with Left Shift/Basophilia – Reactive Process vs Myeloproliferative Disorder Patient Details: 57-year-old female, previously leading a normal active life with no known prior hematological malignancy or chronic systemic illness apart from occasional treatment for diabetes mellitus and hypertension. Past thyroid dysfunction was present many years ago but reportedly normalized later. Weight has remained stable around 70 kg for a long duration. No prior history of chronic fever, recurrent infections, appetite loss, weight loss, abnormal bleeding/bruising, recurrent hospitalizations, lymph node swelling, or known splenomegaly. History of Present Illness: Current illness started suddenly around 2–3 days prior to admission with first-time severe bilateral lower abdominal/groin pain (both iliac/kokh regions), associated with lower back/flank pain and mild breathing discomfort/heaviness. Fever (~100–100.1°F) also appeared for the first time during the same period. Subsequently patient developed marked weakness, dizziness, abdominal tenderness on touch and intermittent fever. No significant urinary burning, retention or major lower urinary tract symptoms were initially reported. BP remained largely stable during admission and patient remained conscious/oriented. Urine Examination: Urine routine microscopy revealed: - Protein ++ - Pus cells: 30–40/hpf - RBCs: 3–4/hpf - Acidic urine - Specific gravity: 1.010 - Urine sugar: Nil Findings were suggestive of urinary tract/kidney inflammatory process. Radiology: Ultrasound whole abdomen showed: - Grade 1 fatty liver - Multiple tiny right renal concretions - 3.1 mm left renal calculus - No significant hydronephrosis or major obstruction reported Hematology/CBC Findings: Initial CBC: - TLC approximately 50,950/cu mm - Neutrophils: 82.9% - ANC: ~42,240 - Hemoglobin: ~10 g/dL - Platelets: previously ~9.39 lakh/cu mm - ESR initially ~35 mm/hr Latest CBC/Hematology: - Hemoglobin: 9.2 g/dL - RBC count: 4.16 million/cu mm - Hematocrit: 30.5% - MCV: 73.3 fL - MCH: 22.1 pg - MCHC: 30.2 g/dL - RDW-CV: 18.3% - TLC: 50,400/cu mm - Neutrophils: 71% - Lymphocytes: 13% - Monocytes: 4% - Eosinophils: 1% - Basophils: 4% - Metamyelocytes: 4% - Promyelocytes: 3% - Platelet count: 5.98 lakh/cu mm - ESR: 62 mm/hr Peripheral Blood Smear (PBS): - Predominantly microcytic hypochromic RBCs with anisocytosis - TLC raised on smear - DLC shows left shift with basophilia - Platelets mildly raised with small platelet clumps - Impression: Microcytic hypochromic anemia with neutrophilic leukocytosis - Advice on report: close hematological follow-up with repeat PBS after control of inflammation/infection to rule out possibility of myeloproliferative disorder Biochemistry: - Serum Creatinine: 0.61–0.66 mg/dL - Serum Urea: 24 mg/dL - SGOT(AST): 22 U/L - SGPT(ALT): 14 U/L - CRP Quantitative: 0.8 mg/L (normal) - Mildly elevated alkaline phosphatase and direct bilirubin noted earlier Viral Markers: - HBsAg: Non-reactive - Anti-HCV: Non-reactive - HIV: Non-reactive Metabolic Findings: During illness, stress hyperglycemia was noted with glucometer readings approximately 235–300+. Current Management: Patient is admitted and receiving antibiotics, hydration, supportive care, antipyretics and symptomatic treatment. Current/recent medications include IV antibiotics initially, followed by Farotuf 200, Dolo 650, Febuxostat 40 mg, Esosan LSR and hydration/electrolyte support. Further Workup: Bone marrow aspiration, bone marrow biopsy and BCR-ABL quantitative testing have now been advised/performed to evaluate persistent neutrophilic leukocytosis with left shift and basophilia. Clinical Query: Kindly review whether the overall presentation appears more consistent with severe reactive leukocytosis/leukemoid reaction secondary to infection/inflammation versus chronic myeloproliferative neoplasm/CML or related hematological disorder, and advise regarding further evaluation and management.
When did you first notice the abdominal and groin pain?:
- 4-7 daysHow would you rate the severity of your abdominal pain?:
- Very severeHave you experienced any other symptoms along with the abdominal pain?:
- FeverHow has your energy level been since the onset of symptoms?:
- Significantly decreasedDo you have any history of blood disorders or family history of hematological diseases?:
- No, neitherWhat medications are you currently taking for your diabetes and hypertension?:
- Oral medicationsHave you noticed any changes in your appetite or weight recently?:
- Stable weightHave you had any recent infections or illnesses before this episode?:
- No recent illnesses100% Anonymously
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Doctors' responses
The key distinction between reactive leukocytosis and myeloproliferative disorders, like chronic myelogenous leukemia (CML), involves understanding the underlying cause of increased white blood cells. Reactive leukocytosis typically occurs in response to factors like infections, inflammation, or stress, while myeloproliferative disorders are blood cancers characterized by clonal proliferation of blood cells. In your case, the severe abdominal pain, presence of infection indicators such as pus cells in urine, and elevated inflammatory markers like ESR, support a reactive process. Neutrophilic leukocytosis with left shift and basophilia, likely points towards an infection or inflammation-triggered response. The presence of microcytic hypochromic anemia on the peripheral smear, coupled with normal creatinine and liver function, could further support an acute phase reaction rather than a primary hematological disorder. The markedly elevated TLC and platelet count along with metamyelocytes and promyelocytes presence do raise suspicion of a myeloproliferative disorder. The decision to perform a bone marrow biopsy and BCR-ABL testing rightly aims to differentiate these conditions. A monoclonal hematological issue (like CML) might also present with Philadelphia chromosome positivity, hence the relevance of BCR-ABL testing. Further evaluation should blend the outcomes of these tests with clinical stability; serial CBC follow-up after controlling for potential infectious triggers will also be crucial. If a reactive process is confirmed, continuing antibiotics and supportive treatments should see improvement; if a myeloproliferative disorder is diagnosed, hematological consultation for targeted therapy based on genetic findings will be needed. Basically, if the bone marrow results reveal CML features or significant myeloid hyperplasia without secondary causes, specific treatments like tyrosine kinase inhibitors would be crucial. Thus, a clear picture should soon emerge with ongoing investigations.
Thank you so much for such a detailed, balanced, and clear explanation. It has given us a lot of clarity and reassurance regarding the current line of treatment. I wanted to share a quick update regarding her latest clinical status and the recent ultrasound report: Ultrasound Update: A fresh ultrasound was done which confirms that the 3.1 mm kidney stone has successfully passed. Both kidneys are now completely normal with no calculi or hydronephrosis. Organ Enlargement: The ultrasound did show an enlarged spleen measuring 13.4 cm, along with mild hepatomegaly/fatty liver grade 1 (liver measuring 16.8 cm). Current Symptoms: Her severe abdominal colic pain has subsided significantly (as the stone has passed), but she is still experiencing regular fever spikes and severe weakness. Current Medications: To treat the heavy UTI (30-40 pus cells), she is currently on a course of antibiotics (Loxof, Nitrofurantoin, and Fosfomycin). Along with this, her primary doctor has started her on Tab Hydroxyurea (Hydrozest) as a bridging therapy to control the markedly elevated WBC count. We are currently continuing with this treatment and waiting for the final Bone Marrow Biopsy and BCR-ABL test results to differentiate between a reactive leukemoid response and CML. I will share the final reports with you as soon as we receive them. Thank you once again for your valuable time and guidance. Warm regards.
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