International Journal of Medical and Pharmaceutical Research
2025, Volume-6, Issue-5 : 322-325 doi: 10.5281/zenodo.17140781
Research Article
Clinico-Pathological and Imaging Correlation in Benign Breast Lumps Among Reproductive-Age Females: Focus on Fibroadenoma Management
 ,
 ,
Received
Aug. 14, 2025
Accepted
Aug. 31, 2025
Published
Sept. 15, 2025
Abstract

Background: Benign breast diseases (BBDs) are more prevalent than malignant conditions in reproductive-age women. Fibroadenoma is the most common BBD.[1]

Objectives: To analyze clinical, pathological, and imaging features of BBDs with a focus on management strategies for fibroadenoma.

Methods: A prospective observational study of 100 female patients aged 15–49 presenting with breast lumps was conducted. Clinical evaluation, imaging (USG/mammography), and histopathology (FNAC/core biopsy) were performed.

Results: Fibrocystic disease (37%) and fibroadenoma (33%) were the most common BBDs. There was a strong clinico-radiological and pathological correlation [2,3]. Conservative management of fibroadenoma was successful in most cases, with 76% showing reduction in lump size over six months.

Conclusion: Triple assessment is essential for accurate diagnosis of BBDs. [4,5] Fibroadenoma in young women can often be managed conservatively with close follow-up.

Keywords
INTRODUCTION

Benign breast diseases (BBDs) encompass a spectrum of non-malignant disorders.[6] Fibroadenomas, traditionally regarded as tumors, are now recognized as hyperplastic lobular growths.[7] Accurate diagnosis using clinical exam, imaging, and cytology allows for effective conservative management and avoids unnecessary surgery.[8]

 

METHODS

  • Study Design: Prospective observational study
  • Setting: Medical College & Hospital, Kolkata (2019–2020)
  • Sample: 100 women (age 15–49) with benign breast lumps
  • Tools: Clinical examination, USG/mammography, FNAC/core biopsy
  • Inclusion/Exclusion: Excluded malignancy, trauma, pregnancy, abscess
  • Statistical Analysis: Pearson correlation, chi-square test, descriptive statistics

 

 

 

RESULTS

Figure 1; Age distribution of Benign breast disease

 

Table 1: Distribution of Benign Breast Diseases (N=100)

Diagnosis

Number (n)

Percentage (%)

Mean Age (years)

Age Range (years)

Fibrocystic Disease

37

37.0

34.0

22-42

Fibroadenoma

33

33.0

25.7

16-42

Duct Ectasia

6

6.0

27.4

21-30

Granulomatous Mastitis

5

5.0

26.4

19-38

Phyllodes Tumor

4

4.0

31.25

22-40

Lipoma

3

3.0

36.0

28-42

Normal Study

3

3.0

-

-

Others*

9

9.0

-

-

*Others include: Galactocele (2), Hemangioma (2), Duct Papilloma (2), Neurofibroma (2), Sebaceous Cyst (1)

 

Table 2: Diagnostic Correlation Analysis

Correlation Parameters

Pearson Coefficient (r)

P-value

Statistical Significance

Clinical vs Radiological Diagnosis

0.98

<0.0001

Highly Significant

Clinical vs Pathological Diagnosis

0.98

<0.001

Highly Significant

 

 

Table 3: Fibroadenoma Management Outcomes (N=33)

Parameter

Conservative (n=22)

Surgical (n=11)

Statistical Test

P-value

Treatment Distribution

66.66%

33.33%

-

-

Size Reduction at 6 months

16/21 (76.19%)

N/A (excised)

-

-

Pain Relief at 6 months

12/21 (57.14%)

7/10 (70%)

χ² = 1.4053

0.704

 

The age distribution of benign breast diseases (Figure 1) showed a predominance in the second and third decades of life, with fibroadenomas more common in younger women and fibrocystic changes occurring at slightly older ages.

 

Among the 100 patients studied, fibrocystic disease (37%) and fibroadenoma (33%) were the most frequent diagnoses, while less common conditions included duct ectasia, granulomatous mastitis, phyllodes tumor, and lipoma; rare entities such as galactocele, hemangioma, duct papilloma, neurofibroma, and sebaceous cyst were also documented (Table 1).

 

Diagnostic accuracy was excellent, with near-perfect correlation between clinical, radiological, and pathological findings (r = 0.98, p < 0.001), confirming the reliability of triple assessment in benign breast disease evaluation (Table 2).

Focusing on fibroadenoma management, two-thirds of patients were treated conservatively and one-third surgically; notably, 76% of conservatively managed cases demonstrated significant lump size reduction over six months, and pain relief was comparable between groups without statistical significance (p = 0.704), reinforcing conservative management as a safe and effective approach in selected patients (Table 3).

 

DISCUSSION

This prospective study of 100 reproductive-age women with benign breast lumps highlights important epidemiological and clinical patterns within the Indian context. Fibrocystic disease (37%) and fibroadenoma (33%) were the two most frequent entities. While some studies report fibroadenoma as the predominant lesion (42%) [9,10], others, such as Memon et al., observed a higher prevalence of fibrocystic disease (66.3%). [11] Our findings therefore align more closely with regional variations where fibrocystic changes are more frequent in slightly older women, whereas fibroadenomas predominate in younger patients. The mean age of fibroadenoma cases in our cohort (25.7 years) matched well with classical descriptions by Haagensen, who noted that the majority occur between 16–30 years. [12]

 

Similarly, fibrocystic disease presented predominantly in the fourth decade, in keeping with the ANDI classification. [13] Clinical presentation trends were also consistent, with mastalgia being a common symptom in fibrocystic disease, while fibroadenomas were mostly painless, as reported by Hughes et al. [14]

Diagnostic accuracy was excellent, with near-perfect correlation between clinical, radiological, and pathological assessments (r = 0.98, p < 0.001). This reinforces the established role of triple assessment as the gold standard for breast lump evaluation, as supported by prior studies. [9,10]

 

Management outcomes for fibroadenoma provide an important contribution to existing literature. Conservative management was offered to two-thirds of patients, with 76% showing spontaneous size reduction over six months. These findings support earlier recommendations by Cant et al. [6] and Greenberg et al. [15] advocating non-operative management in selected cases.

 

The comparable pain relief in conservative and surgical groups, without significant statistical difference, further challenges the need for routine excision in all fibroadenomas. Overall, our results validate established diagnostic approaches while adding quantitative evidence for the efficacy of conservative fibroadenoma management in an Indian tertiary care setting. With appropriate patient selection and systematic follow-up, non-operative strategies can reduce unnecessary surgical burden while maintaining favourable outcomes.

 

CONCLUSION

This study provides valuable addition to the literature on benign breast diseases in reproductive-age women, particularly in the Indian context. The findings largely corroborate existing knowledge while providing new insights into conservative management outcomes. The excellent diagnostic correlations validate current assessment protocols, while the successful conservative management outcomes support evidence-based practice evolution.

 

The results suggest that with appropriate patient selection and systematic follow-up, conservative management of fibroadenomas can achieve favourable outcomes, potentially reduce healthcare burden while maintain quality of care. This evidence contributes to the growing body of literature supporting personalized, risk-stratified approaches to benign breast disease management.

 

Study Limitations

  • Small sample size (n=100)
  • Single-center study
  • Non-blinded, non-randomized design
  • Observer bias potential
  • Only fibroadenoma cases followed up systematically

 

Conflict of Interest

None

Ethical Approval

Approved by Institutional Ethics Committee. Informed consent obtained ref no MC/KOL/IEC/NON_SPON/318/02-2019

 

REFERENCES

  1. Khan YS, Sajjad H. Anatomy, Thorax, Mammary Gland. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2020. PMID: 30855831
  2. Pandya S, Moore RG. Breast development and anatomy. Clin Obstet Gynecol. 2011 Mar;54(1):91–5. doi:10.1097/GRF.0b013e318207ffe9
  3. Haagensen CD. Diseases of the Breast. 3rd ed. Philadelphia: Saunders; 1986.
  4. Love SM, Barsky SH. Position Paper: The Nashville Classification of Benign Breast Disorders. Surg Clin North Am. 1990 Aug;70(4):853–71. doi:10.1016/S0039-6109(16)45463-6
  5. Page DL, Dupont WD, Rogers LW, Rados MS. Atypical hyperplastic lesions of the female breast: a long-term follow-up study. Cancer. 1985 Jun 1;55(11):2698–708. doi:10.1002/1097-0142(19850601)55:11<2698::aid-cncr2820551124>3.0.co;2-u
  6. Cant PJ, Madden MV, Close PM, Dixon JM. Management of discrete benign breast lumps by general surgeons in Southeast Scotland. BMJ. 1987 Nov 7;295(6609):1211–2. doi:10.1136/bmj.295.6609.1211
  7. Kataria K, Dhar A, Bhatnagar D. Benign breast diseases: recent advances and management. ISRN Obstet Gynecol. 2013;2013:1–5. doi:10.5402/2013/740291
  8. Sangma MBM, Panda K, Dasiah S. A clinical study of benign breast disease in a teaching hospital of North-East India. J Clin Diagn Res. 2013 Mar;7(3):503–6. doi:10.7860/JCDR/2013/4910.2800
  9. Brajesh Kumar, Nitish Khandelwal, AK Paliwal, Manashi Ghosh. Clinico-radiological-pathological study of benign breast diseases. Int J Contemp Med Res. 2018;5(12):L1-L4.
  10. Malik MAN, et al. Benign breast diseases: clinical, radiological and pathological correlation.
  11. Memon A, Parveen S, Sangrarasi AK, et al. Changing pattern of benign breast lumps in young females. Pak J Med Sci. 2007.
  12. Haagensen CD. Diseases of the Breast. 3rd ed. Philadelphia: WB Saunders; 1986.
  13. Hughes LE, Mansel RE, Webster DJT. Aberrations of normal development and involution (ANDI): A new perspective on pathogenesis of benign breast disorders. Lancet. 1987.
  14. Kataria K, Dhar A, Srivastava A, et al. Current understanding and management of mastalgia. Indian J Surg. 2014;76(3):217–222.
  15. Greenberg R, Skornick Y, Kaplan O. Management of breast fibroadenomas. J Gen Intern Med. 1998;13:640–645.
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