Fibroadenoma with pseudo angiomatous stromal hyperplasia and hamartoma of the breast: a case report

Authors

  • Qazi N. Ahmed Department of Surgery, IIMSR, Jalna, Maharashtra, India
  • Syed O. Chand Department of Surgery, IIMSR, Jalna, Maharashtra, India
  • Riyaj S. Patel Department of Surgery, IIMSR, Jalna, Maharashtra, India
  • Hingora M. Saquib drqazinihalahmed@gmail.com

DOI:

https://doi.org/10.18203/2320-6012.ijrms20252042

Keywords:

Fibroadenoma, Pseudoangiomatous stromal hyperplasia , Hamartoma, Bloody nipple discharge

Abstract

Pseudo angiomatous stromal hyperplasia (PASH) is an uncommon benign proliferative lesion of the breast stroma, characterized histologically by interanastomosing slit-like spaces within a dense collagenous background, mimicking vascular channels but lacking true endothelial lining. It was first described in 1986 by Vuitch, Rosen, and Erlandson, who reported nine cases of breast masses simulating vascular tumors, composed of proliferative mammary stromal tissue. Although PASH is often an incidental microscopic finding in breast biopsies, it can occasionally present as a palpable mass, particularly in premenopausal women, likely influenced by hormonal factors such as estrogen and progesterone. Fibroadenomas and hamartomas are also common benign breast entities, each with distinct histopathological features. However, the coexistence of PASH, fibroadenoma, and hamartoma within a single lesion is exceedingly rare, and its presentation with bloody nipple discharge, a symptom more often associated with intraductal carcinoma or papilloma, makes diagnosis particularly challenging. Accurately distinguishing benign from malignant lesions requires a multimodal approach, integrating clinical examination, radiologic imaging and core needle biopsy. Lesions that are classified as B3 on histopathology-including cellular fibroadenomas, papillomas with atypia, or complex sclerosing lesions-typically mandate complete surgical excision to rule out associated malignancy. This case report underscores the diagnostic complexities associated with overlapping benign breast lesions and highlights the importance of comprehensive evaluation and interdisciplinary collaboration in guiding management. Further prospective studies are warranted to optimize early detection strategies and decision-making in cases involving lesions with uncertain or mixed histology. This case emphasizes the need for a multidisciplinary approach, combining clinical, radiological, and pathological evaluations to accurately diagnose complex presentations. Recognizing rare benign lesions can prevent overtreatment and alleviate patient anxiety.

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References

Jaunoo S, Thrush S, Dunn P. Pseudoangiomatous stromal hyperplasia (PASH): a brief review. Int J Surg. 2011;9:20–2. DOI: https://doi.org/10.1016/j.ijsu.2010.09.005

Bowman E, Oprea G, Okoli J, Gundry K, Rizzo M, Gabram-Mendola S, Manne U, Smith G, Pambuccian S, Bumpers HL. Pseudoangiomatous stromal hyperplasia (PASH) of the breast: a series of 24 patients. Breast J. 2012;18:242–7. DOI: https://doi.org/10.1111/j.1524-4741.2012.01230.x

Anderson C, Ricci A Jr, Pedersen CA, Cartun RW. Immunocytochemical analysis of estrogen and progesterone receptors in benign stromal lesions of the breast. Evidence for hormonal etiology in pseudoangiomatous hyperplasia of mammary stroma. Am J Surg Pathol. 1991;15:145–9. DOI: https://doi.org/10.1097/00000478-199102000-00007

Powell CM, Cranor ML, Rosen PP. Pseudoangiomatous stromal hyperplasia (PASH). A mammary stromal tumor with myofibroblastic differentiation. Am J Surg Pathol. 1995;19:270–7. DOI: https://doi.org/10.1097/00000478-199503000-00004

Zanella M, Falconieri G, Lamovec J, Bittesini L. Pseudoangiomatous hyperplasia of the mammary stroma: true entity or phenotype. Pathol Res Pract. 1998;194:535–40. DOI: https://doi.org/10.1016/S0344-0338(98)80042-3

Ajmal M, Khan M, Van Fossen K. Breast fibroadenoma. In: StatPearls. Treasure Island (FL): StatPearls Publishing. 2022.

Sevim Y, Kocaay AF, Eker T, Celasin H, Karabork A, Erden E, Genc V. Breast hamartoma: a clinicopathologic analysis of 27 cases and a literature review. Clinics (Sao Paulo). 2014;69:515–23. DOI: https://doi.org/10.6061/clinics/2014(08)03

Polger MR, Denison CM, Lester S, Meyer JE. Pseudoangiomatous stromal hyperplasia: mammographic and sonographic appearances. AJR Am J Roentgenol. 1996;166:349–52. DOI: https://doi.org/10.2214/ajr.166.2.8553945

Tahmasebi S, Zadeh AKR, Zangouri V, Akrami M, Johari MG, Talei A. Pseudoangiomatous stromal hyperplasia of the breast: a case report. Clin Case Rep. 2022;10:5387. DOI: https://doi.org/10.1002/ccr3.6221

Ibrahim S. Bailey & Love’s Short Practice of Surgery. Malaysian Orthopaed J. 2019;13(2):63.

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Published

2025-06-27

How to Cite

Ahmed, Q. N., Chand, S. O., Patel, R. S., & Saquib, H. M. (2025). Fibroadenoma with pseudo angiomatous stromal hyperplasia and hamartoma of the breast: a case report. International Journal of Research in Medical Sciences, 13(7), 3023–3026. https://doi.org/10.18203/2320-6012.ijrms20252042

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Section

Case Reports