International Journal of Medical and Pharmaceutical Research
2026, Volume-7, Issue 3 : 107-112
Research Article
The Pivotal Role of the Peripheral Blood Smear in the Initial Diagnosis of Various Leukemia
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Received
April 2, 2026
Accepted
May 1, 2026
Published
May 8, 2026
Abstract

Background: Peripheral blood smear (PBS) examination remains a cornerstone in the initial evaluation of hematological disorders. Despite advances in immunophenotyping and molecular diagnostics, PBS continues to provide rapid and valuable morphological insights, especially in resource-limited settings.

Aim: To evaluate the role of peripheral blood smear in the early diagnosis and classification of various leukemias.

Materials and Methods: A retrospective observational study was conducted on in P.D.U. Government Hospital, Rajkot. The study period was taken between 1st August 2025 to 31st March 2026. Between this time period we found 55 cases of leukemia. Clinical details, hematological parameters, and peripheral smear findings were analyzed and correlated.

Results: Acute Myeloid Leukemia (30.91%) was the most common subtype followed by Chronic Myeloid Leukemia (20%). Pallor was the most frequent presenting feature. Peripheral smear findings such as blasts, smudge cells, and basophilia were instrumental in initial diagnosis.

Conclusion: Peripheral blood smear remains a rapid, cost-effective, and indispensable diagnostic tool that aids in early detection and classification of leukemias.

Keywords
INTRODUCTION

Leukemia comprises a diverse group of clonal hematopoietic malignancies characterized by abnormal proliferation of white blood cells in the bone marrow and peripheral circulation. These disorders are broadly classified into acute and chronic leukemias, each with distinct clinical behavior, prognosis, and management strategies.

 

Early and accurate diagnosis is critical, as many leukemias—particularly acute leukemias—require urgent intervention. While modern diagnostic modalities such as flow cytometry, cytogenetics, and molecular studies have significantly improved classification and prognostication, they may not always be immediately available, particularly in resource-constrained settings.

 

In such scenarios, peripheral blood smear examination serves as the first and often most informative diagnostic tool. It provides immediate morphological details, including identification of blasts, assessment of cell lineage, and detection of characteristic features such as Auer rods, smudge cells, and basophilia.

 

Moreover, PBS allows correlation with clinical findings and can guide further investigations. Its role is especially crucial in initial suspicion, triaging patients, and initiating early management.

 

The present study was undertaken to evaluate the diagnostic utility of peripheral blood smear in various leukemias and to correlate morphological findings with clinical and demographic parameters.

 

MATERIALS AND METHODS

This retrospective observational study was conducted on 55 cases of leukemia. Study Design we chose is of retrospective descriptive study.Study Setting conducted in a tertiary care center, P.D.U. Government Hospital, Rajkot. Study Duration was from 1st August 2025 to 31st March 2026.

 

Data Collection

The following parameters were recorded:

  • Age and gender
  • Clinical presentation
  • Hematological parameters
  • Peripheral smear findings

 

Peripheral Smear Examination

  • Blood samples collected in EDTA vials
  • Smears prepared using standard
  • Stained with Leishman stain and Field Stain.
  • Examined under light microscopy.

 

RESULTS

A total of 55 cases were analyzed.

Table 1: Distribution of Leukemia Types

Diagnosis

No. Of Cases

Percentage

Acute myeloid Leukemia

17

30.91%

Acute Lymphoid Leukemia

10

18.18%

Chronic myeloid Leukemia

11

20%

Chronic lymphoid Leukemia

10

18.18%

Acute BlasticLeukemia

06

10.91%

Lymphoma leukemia

01

1.82%

Total

55

100%

 

The most common leukemia observed was AML (30.91%), followed by CML (20%). Acute leukemias constituted a larger proportion compared to chronic leukemias, indicating a higher burden of aggressive disease presentation.

 

Table 2: Gender Distribution Of various Leukemia

Diagnosis

Male

Female

Total

Acute myeloid Leukemia

09

08

17

Acute Lymphoid Leukemia

07

03

10

Chronic myeloid Leukemia

07

04

11

Chronic lymphoid Leukemia

08

02

10

Acute BlasticLeukemia

02

04

06

Lymphoma leukemia

00

01

01

Total

33

22

55

 

There was a clear male predominance (60%) compared to females (40%). This trend was consistent across most leukemia subtypes, suggesting possible gender-related susceptibility or healthcare access differences.

 

Table 3: Age Distribution Of various Leukemia

Age

(Years)

AML

ALL

CML

CLL

Acute Blastic Leukemia

Lymphoma Leukemia

Total

<10

01

06

00

00

02

00

09

11-20

02

02

00

00

01

00

05

21-30

02

02

05

00

02

00

11

31-40

05

00

02

02

01

00

11

41-50

03

00

02

04

00

00

09

51-60

00

00

01

01

00

00

02

61-70

02

00

00

01

00

00

03

>70

02

00

01

02

00

01

05

ALL was predominantly seen in children (<10 years). AML showed a wider age distribution. CML was more frequent in young to middle-aged adults. CLL was mainly observed in older age groups. This reflects known epidemiological patterns of leukemia distribution.

 

Table 4: Clinical Presentation

Presenting

Feature

AML

ALL

CML

CLL

Acute BlasticLeukemia

Lymphoma Leukemia

Total

Fever

01

01

01

00

00

00

03

Weakness

02

02

01

02

02

00

09

Pallor

11

04

00

00

04

00

19

Bleeding

02

00

00

00

00

00

02

Spleenomegaly

01

00

09

00

00

01

10

Lymphadenopathy

00

03

00

08

00

00

11

Total

17

10

11

10

06

01

55


Pallor (34.5%) was the most common presenting feature, reflecting underlying anemia. Lymphadenopathy and splenomegaly were also frequent findings, particularly in CLL and CML respectively. Bleeding manifestations were less common but clinically significant.

 

Table 5: CML cases distribution according to Phases

CML phase

No. Of Cases

Percentage

Chronic Phase

08

80%

Accelerated Phase

00

00%

Blast crisis Phase

02

20%

Total

10

100%


Majority of CML cases (80%) were diagnosed in the chronic phase, indicating early detection in most patients. However, presence of blast crisis cases highlights delayed presentation in a subset.

 

Table 6: AML Subclassification

AML subclass

No. Of Cases

Acute PromyelocyticLeukemia

02

Acute MyelomonocyticLeukemia

01

AML M0

06

AML M2

08

Total

17


AML M2 was the most common subtype, followed by AML M0. Presence of APML cases is clinically significant due to its distinct treatment and prognosis.

 

Table 7: Peripheral Smear Findings

Key Peripheral Smear Finding

No. Of Cases

Blast

23

Auer rods

02

Smudge cells

10

Left shift

00

Basophillia

08

Total

43


Blasts were the most frequent finding (23 cases), confirming their central role in diagnosing acute leukemias. Smudge cells were characteristic of CLL, while basophilia was strongly associated with CML. Auer rods, though less frequent, provided definitive evidence of myeloid lineage.

 

Image:1: Acute lymphoblastic leukemia: Blasts having high N:C ratio. 1-2 inconspicous nucleoli are seen. (Field stain,40x)

 

Image:2: Acute promyelocytic leukemia. Many promyeolocytes with auer rods are seen. Fggot cells are also seen. (Field stain,100x)

 

Image:3: Acute myelomonocytic leukemia. Many monoblasta having reniform nuclei and cytoplasmic vacuolation are see. Myeloblasta are also present. (Field stain,100x)

 

Image:4: Chronic myeloid leukemia. Myelomonocytic buldge is seen. (Field stain,100x)

 

Image:5: Chronic lymphocytic leukemia. Many mature lymphocytes are seen. (Field stain,40x)

 

DISCUSSION

The present study reinforces the critical role of peripheral blood smear in the initial diagnosis of leukemias.

 

The predominance of AML observed in this study aligns with multiple regional studies, where AML is frequently reported as the most common adult leukemia. The relatively high proportion of acute leukemias emphasizes the need for rapid diagnostic methods, as delays can significantly impact patient outcomes.

 

Male predominance noted in this study has been consistently reported in hematological malignancies. While the exact reason remains unclear, genetic, environmental, and occupational factors may contribute.

 

The age distribution findings were also in agreement with established patterns. ALL showed a clear predilection for pediatric age groups, whereas CLL was predominantly seen in elderly individuals. CML affected a relatively younger population in this study compared to Western data, which is a known trend in developing countries.

 

Clinical presentation in leukemia is often nonspecific. Pallor being the most common symptom reflects anemia due to marrow infiltration. Lymphadenopathy and splenomegaly are important clinical clues that help narrow the differential diagnosis.

 

Peripheral smear findings played a decisive role in diagnosis. Blasts enabled identification of acute leukemias. Auer rods confirmed myeloid origin.Smudge cells were highly suggestive of CLL.Basophilia strongly pointed toward CML.

These morphological features not only aid in diagnosis but also help prioritize further confirmatory tests such as bone marrow examination and immunophenotyping.

 

In resource-limited settings, where advanced diagnostics may be delayed, PBS serves as an invaluable frontline tool. It enables early clinical decision-making and initiation of supportive therapy.

 

CONCLUSION

Peripheral blood smear examination continues to be an indispensable diagnostic modality in hematology.It is rapid, cost-effective, and widely accessible.Provides crucial morphological insights.It enables early diagnosis and classification of leukemias. Guides further diagnostic and therapeutic interventions

 

Even in the era of advanced technologies, PBS remains a cornerstone in the initial evaluation of leukemia.

 

REFERENCES

  1. Bain BJ. Blood Cells: A Practical Guide.
  2. Hoffbrand AV, Moss PAH. Essential Haematology.
  3. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues.
  4. Greer JP. Wintrobe’s Clinical Hematology.
  5. Dacie JV, Lewis SM. Practical Haematology.
  6. Tefferi A. Primary leukemias: clinical review.
  7. Lichtman MA. Leukemia overview and classification.
  8. Swerdlow SH. WHO hematologic malignancy classification updates.
  9. Arber DA et al. AML classification and diagnosis guidelines.
  10. Hallek M. Chronic lymphocytic leukemia: diagnosis and treatment.

 

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