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Research Article | Volume 11 Issue 4 (None, 2025) | Pages 637 - 642
Clinicopathological Study of Pleural Effusion in A Tertiary Care Hospital
 ,
1
Assistant Professor: Department of Pathology, Kamineni Academy of Medical Sciences and Research Centre, L. B. Nagar, Hyderabad, Telangana 500068
2
Assistant Professor: Department of General medicine, Institute of Medical Sciences, Narketpalle, Telangana 508254.
Under a Creative Commons license
Open Access
Received
March 10, 2025
Revised
April 11, 2025
Accepted
April 8, 2025
Published
April 27, 2025
Abstract

Background: Pleural effusion is an excess fluid that accumulates between two pleural layers.There are two types of effusions including Transudative and Exudative effusion.Common causes of exudative effusion include tuberculosis, parapneumonic effusion, viral infections, and malignancy. Pleural fluid analysis and cytology are the mainstays for diagnosing various pulmonary diseases.  Aim of the study: A clinicopathological study of pleural effusion in a tertiary care hospital. Material and Methods: Prospective study was conducted in the department of General medicine at TRR medical college for duration of 1 year i.e. from March 2021 to Feb 2022. Results: In the present study Tuberculosis was commonly reported accounting 38.4%(25/65) , Pneumonia 30.7% (20/65), Empyema, Pancreatitis, Liver cirrhosis and Malignancy 7.6%(5/65). Purulent 76.8%(50/65), Hemorrhagic 15.3%(10/65) and Straw colored 7.6% (5/65) . Conclusion: Aetiological evaluation of pleural effusion is very important for management of the disease. This is important because management is different for different cases. Pleural fluid analysis can be considered as gold standard in evaluation of pleural effusion

Keywords
INTRODUCTION

Pleural effusion (PE) is an abnormal collection of fluid in the pleural space. The etiological spectrum of pleural effusion depends on the geographical region and the local incidence of different diseases that cause pleural effusions. In the developed countries, the common causes of pleural effusion in adult are cardiac failure, malignancy and pneumonia .1 Whereas, in developing countries tuberculosis and par pneumonic effusions are more. 2,3

Pleural effusion is a common finding among patients presenting with cardiopulmonary symptoms. A systemic approach to the investigations is needed due to the extensive differential diagnosis. Pleural effusions can be transudative or exudative.4 In cases with transudative pleural effusion, the diagnosis is usually made without much difficulties, but exudative pleural effusion requires careful differential diagnosis that includes parapneumonic effusion, tuberculosis (TB), and

metastatic cancers which are found to be the cases in large number of patients.

If metastatic cancer leads to hypoalbuminemia (e.g., due to liver metastasis causing liver failure or nephrotic syndrome), it may cause transudative effusion due to decreased oncotic pressure.

Light's criteria are frequently used to distinguish between exudative effusion and transudative effusion, the two types of pleural effusions.1 If any one of the following conditions is met, the pleural fluid is exudative: pleural fluid protein/serum protein ratio >0.5; pleural fluid lactate dehydrogenase/serum LDH ratio >0.6; or pleural fluid LDH level >2/3 the upper limit.

MATERIALS AND METHODS

Prospective study was conducted in the department of General medicine at TRR medical college for duration of 1 year i.e. from March 2021 to Feb 2022. Ethical permission was taken from Institutional ethical committee. Written consent was obtained from all the study participants

 

Sample size: 65

Inclusion criteria

  • Age 10-60 years
  • Patients with clinically or radiologically documented pleural effusion.

 

Exclusion criteria

  • Age <10 years and more than 60 years
  • Patients with hydropneumothorax and trauma chest
  • Past history of thoracocentesis

 

Methodology

The demographic data collected included age, sex, and address.  A detailed history was obtained inlcuding  chief complaints, history of presenting illness, and significant history including the drug history. A through physical examination was done. Investigations such as complete hemogram, random blood sugar, renal function tests, serum albumin, chest-X-ray, and pleural fluid analysis and cytology were carried out in all the cases.

Pleural fluid analysis on neubar chamber: Total Leucocyte Count

LIGHT et al.s criteria were used to distinguish exudative from transudative effusions. Predominant pleural fluid cell types were defined based on British Thoracic Society guidelines.

Pleural fluid cytology

The International System (TIS) for reporting serous fluid cytopathology was proposed by the International Academy of Cytology and the American Society of Cytopathology.6,

 

 

Table 1:Diagnostic categories of TIS for reporting serous effusion cytopathology8

Diagnostic categories and definitions

I. Nondiagnostic (ND)

  Specimens with insufficient cellular elements for a cytologic interpretation

II. Negative for malignancy (NFM)

  Specimens with cellular changes completely lacking evidence of mesothelial or nonmesothelial malignancy

III. Atypia of undetermined significance (AUS)

  Specimens showing limited cellular (nuclear) and/or architectural atypia (e.g., papillary clusters or pseudoglandular formations)

IV. Suspicious for malignancy (SFM)

  Specimens showing features suspicious but not definitively diagnostic for malignancy

V. Malignant (MAL)

  Specimens include those with definitive findings and/or supportive studies indicating mesothelial or nonmesothelial malignancies

DISCUSSION

Table 1: Age distribution

Age distribution

No. of cases

Percentage

10-20

02

3.07

21-30

10

15.3

31-40

15

23.0

41-50

28

43.0

51-60

10

15.3

Total

65

99.9%

Gender distribution

 

 

Females

45

69.2%

males

20

30.7%

Symptom

 

 

Fever

60

92.3%

cough

50

76.9%

Breathlessness

45

69.2%

chest pain

40

61.5%

Side of distribution

 

 

Right side

50

76.9%

left side

15

23%

Comorbidities

 

 

Hypertension 

22

33.8%

Coronary artery disease

21

32.3%

Diabetes mellitus 

11

16.9%

Rheumatoid arthritis 

6

9.2%

Pancreatitis

6

9.2%

 

In the present study age distribution varied from 10 - 60 years . Majority noted among 41-50 years constituting 43% (28/65)  and 23% (15/65) among 31-40 years , 15.3%(10/65) among 21-30 years and 51-60 years .3.0% (2/65).

 

Females were predominant constituting  69.2% (45/65) and Males accounting 30.7%(20/65).

Fever  was predominant symptom constituting  92.3% (60/65) ,followed  by cough 76.9% (50/65), Breathlessness 69.2% (45/65), and chest pain 61.5%(40/65).

 Right side 76.9%(50/65) was more common compared to Left side 23.0%(15/65)

Hypertension  and Coronary artery disease  constituting  33.8%(22/65) and 32.3%(21/65). Diabetes mellitus  16.9%(11/65),Rheumatoid arthritis  9.2% (6/65) and  Pancreatitis 9.2% (6/65).

 

Table-2: Distribution of Nature of effusion

Nature of effusion 

 

No. of cases

Percentage

Exudative

40

61.5

Transudative

25

38.4

Total

65

99.9%

Type Plueral fluid

 

 

Purulent

50

76.8%

Hemorrhagic

10

15.3%

Straw colored

5

7.6%

 

In the present study Exudative  61.5%(40/65) and Transudative  38.4%(25/65). Purulent 76.8%( 50/65) , Hemorrhagic  15.3%(10/65) and Straw colored 7.6%(5/65) .

Table-3:  Distribution of Clinical diagnosis

Clinical diagnosis

 

No. of cases

Percentage

Tuberculosis

25

38.4

Empyema

05

7.6

Malignancy

05

7.6

Acute Pancreatitis

05

7.6

Pneumonia

20

30.7

Liver cirrhosis

05

7.6

Total

65

99.9%

 

In the present study Tb was commonly reported accounting 38.4%(25/65) , Pneumonia  30.7% ( 20/65), Empyema , Pancreatitis ,Liver cirrhosis and Malignancy 7.6%(5/65)

Figure-1:  Bar diagram showing Distribution of Clinical diagnosis

 

Table-4: DLC  on Nuebar chamber

DLC

Mean +SD

Lymphocytes

42.9+10.3

Nuetrophils

58.3+20.9

In our study lymphocytes mean was 42.9+10.3 and Nuetrophils58.3+20.9

Table-5: Distribution of Cytological diagnosis

Cytological diagnosis

No. of cases

Percentage

I.Nondiagnostic (ND)

-

-

II.Negative for malignancy (NFM)

60

92.4

III. Atypia of undetermined significance (AUS)

-

-

IV. Suspicious for malignancy (SFM)

05

7.6

V. Malignant (MAL)

 

 

Total

65

99.9%

 

In our study No malignant cells noted in 92.4% cases and Malignant cells seen. In 7.6% cases.

DISCUSSION

In the present study age distribution varied from 10 - 60 years . Majority noted among 41-50 years constituting 43% (28/65)  and 23% (15/65) among 31-40 years , 15.3%(10/65) among 21-30 years and 51-60 years .3.0% (2/65).In Shashikanth et al9  study  mean age was 38.10 years. In Saurabh et al10  study mean age was 53.32 ± 9.15 years.

 

In the present study Females were predominant constituting  69.2% (45/65) and Males accounting 30.7%(20/65).Where as in Saurabh et al 10, Arif et al11  and Shashikanth et al study9  with Male gender were more common with (67.86%) , (66.9%) and 70 (70%).

 

In the present study Right side 76.9%(50/65) was more common compared to Left side 23.0%(15/65)/.Similar findings were noted with  Arif et al 11.Saurabh  al10  and Shashikanth et al9  study 46.9% ,58.93% and 41.07%.

 

In the present study Chest pain  was predominant symptom Fever constituting  92.3% (60/65) ,followed by cough 76.9% (50/65), Breathlessness 69.2% (45/65), Fever 61.5%(40/65). In Arif et al11 study  majority of pleural patients presented with chest pain (78.5%) followed by cough (50.7%), fever (46.1%) and breathlessness (32.2%).In Shashikanth et al9 study  fever (53%) and breathlessness (45%) were most common symptoms, followed by, cough, chest pain, and abdominal pain .In Ranganathan et al12 study fever and cough are the most common seen 64 and 76 percentage respectively, followed by chest pain (44) and breathlessness (42%).In Saurabh et al  11 study cough (78.57%), chest pain (67.86%), decreased appetite (64.29%), fever (62.50%), breathlessness (58.93%), weight loss (21.43%) and joint pain (16.07%).

 

In the present study Tb was commonly reported accounting 38.4%(25/65) , Pneumonia  30.7% ( 20/65), Empyema , Pancreatitis ,Liver cirrhosis and Malignancy 7.6%(5/65). In Souruabh et al10 study Tuberculosis (58.93%) was most common cause of exudative pleural effusion followed by empyema (8.93%), malignant (5.36%), pancreatitis (5.36%), rheumatic arthritis (3.57%) and para pneumonic (1.79%). Undiagnosed cases were 16.07%.In Arif et al11  study tuberculosis (64.6%) was the most common followed by  Para pneumonic (14.6% and malignancy (11.5%)

 

In the present study Exudative 61.5%(40/65) and Transudative 38.4%(25/65). .Similar findings were noted with  Arif et al 11 and Shashikanth et al 9 study with 90.8% and 66% .

 

In the present study Purulent 76.8%( 50/65) , Hemorrhagic  15.3%(10/65) and Straw colored 7.6%(5/65). In Souraubh et al10 study pleural fluid Appearance was Straw colored (55.36 %) in majority cases and purulent in 5 cases .only (8.93 %). In Ranganathan et al12 study majority of the patients with tuberculous pleural had yellowish and turbid fluid, while malignant pleural effusion had hemorrhagic fluid.

 

In our study Predominant Neutrophilia  seen in 46.1% cases where as in Ranganathan et al12, Souraubh et al10 study  and Kaushal et al study113 shows predominant lymphocytosis .

CONCLUSION

Etiological evaluation of pleural effusion is very important for management of the disease. Among patients of exudative pleural effusion male gender, right sided effusion, tuberculosis, straw coloured pleural fluid, raised TLC were common findings. Knowledge of the etiological pattern of exudative pleural effusion helps

physicians to plan diagnostic tests, and to provide appropriate treatment to reduce mortality and morbidity rates resulting from Plueral effusion  complication .

REFERENCES
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  2. Afful B et al. The characteristics and causes of pleural effusions 3. in Kumasi Ghana-a prospective study. Tropical Doctor, 2008; 38: 219-220.
  3. Jamaluddin, Rakesh Kumar, Mehre Darakhshan Mehdi, Md. Faiyaz Alam. “Study of Etiological and Clinical Profile of Pleural Effusion in a Teritary Care Hospital in Kosi Region of Bihar”. Journal of Evidence based Medicine and Healthcare; Volume 2, Issue 47, November 12, 2015; Page: 8330-8334.
  4. Keshmiri M, Hashemzadeh M. Use of cholesterol in differentiating of exudative and transudative pleural effusions. Med J Islamic Repub Iran 1997;2:187-9.
  5. Pinto D, Chandra A, Crothers BA, Kurtycz DFI, Schmitt F. The international system for reporting serous fluid cytopathology-diagnostic categories and clinical management. J Am Soc Cytopathol. 2020 Nov-Dec;9(6):469-477.
  6. Hou T, Landon G, Stewart J, Roy-Chowdhuri S. The value of a tiered cytology diagnostic reporting system in assessing the risk of malignancy in indeterminate serous effusions. Cancer Cytopathol 2021;129(1):75-82 
  7. Zhu YL, Ren WH, Wang Q, Jin HZ, Guo YY, Lin DM. A retrospective analysis of serous effusions based on the newly proposed international system for reporting serous fluid cytopathology: a report of 3633 cases in an oncological center. Diagn Pathol 2022;17(1):56 
  8. Wang M, Chandra A, Cai G. The International System for Reporting Serous Fluid Cytopathology—An Updated Review. J Clin Transl Pathol. 2023;3(4):160-177.
  9. Shashikant A, Archana G. A study of clincoetiological profile of patients with pleural effusion. J Dent Med Sci IOSR 2017; 16:23-7.
  10. Saurabh Borgaonkar, Sachin Muralidhar Kate: Clinical and etiological study of exudative pleural effusion in patients at a tertiary care center .MedPulse International Journal of Medicine, 2021:Volume 20, Issue 3, pp 173-177.
  11. Mohd Arif Siddiqui: Clinical And Etiological Profile of Patients With Pleural Effusion: A Retrospective Cross-Sectional Study in North India: Indian Journal Of Applied Research: May 2016, Volume 6, Issue 5, pp-285-287.
  12. Ranganatha M, Nagabhushana S, Ranjith Kumar GK3 , Virupakshappa: Study of etiology of pleural effusion in the district hospital, Shimoga , Indian Journal of Immunology and Respiratory Medicine, April-June 2017;2(2):54-57.
  13. Kaushal MB, Krupal PM. Pleural Effusion: A Two Year Prospective Study in Western India. Sch. J App Med Sci. 2015;3(8A):2790-793.
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