Pseudoangiomatous stromal hyperplasia of the breast presenting as gigantomastia
case report
Keywords:
breast neoplasms, breast implantation, lactation, mastectomy, pathologyAbstract
Pseudoangiomatous stromal hyperplasia (PASH) of the breast is a benign condition generally seen as an incidental finding of biopsies for other causes. In some rare cases, it can evolve with expressive growth of breast tissue, leading to large breasts. The present study presents a case report of a patient who started with breast hypertrophy during lactation, evolving with gigantomastia, and arrived at the office 3 years after gestation with breasts of 6.2 and 4.3 kg and growth of accessory breast and axillary lymph nodes. The patient was emaciated, with bodily pain and psychological distress. Computed tomography was performed with the finding of diffuse retroglandular nodules and axillary and mediastinal lymph node enlargement, without being able to rule out the lymphoproliferative process. Then, core biopsies were made in several places on the breast whose pathological examination revealed PASH samples. Bilateral mastectomy was performed as a surgical treatment, with resection of the left accessory breast and left axillary lymph node, and breast reconstruction, with placement of silicone prostheses and graft of the areola-papillary complex, together with a plastic surgeon. She evolved in the postoperative period with good healing of the surgical wound, weight gain, necrosis of the areola-papillary complex and with severe psychiatric disorder, which was treated appropriately by psychiatrists, with remission of symptoms. This case report presents a rare evolution of PASH with gigantomastia, bringing intense physical and psychological distress to the patient, whose treatment chosen was total surgical resection of the breast tissue and aesthetic reconstruction.
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References
Vuitch MF, Rosen PP, Erlandson RA. Pseudoangiomatous hyperplasia of mammary stroma. Hum Pathol. 1986;17(2):185‑91. https://doi.org/10.1016/s0046-8177(86)80292-1
Smilg P. Pseudoangiomatous stromal hyperplasia: Presentation and management – a clinical perspective. SA J Radiol. 2018;22(2):1366. https://dx.doi.org/10.4102%2Fsajr.v22i2.1366
Raj SD, Sahani VG, Adrada BE, Scoggins ME, Albarracin CT, Woodtichartpreecha P, et al. Pseudoangiomatous Stromal Hyperplasia of the Breast: Multimodality Review With Pathologic Correlation. Curr Probl Diagn Radiol. 2017;46(2):130-5. http://doi.org/10.1067/j.cpradiol.2016.01.005
Yoon KH, Koo B, Lee KB, Lee H, Lee J, Kim JY, et al. Optimal treatment of pseudoangiomatous stromal hyperplasia
of the breast. Asian J Surg. 2020;43(7):735-41. https://doi.org/10.1016/j.asjsur.2019.09.0085 Pseudoangiomatous stromal hyperplasia of the breast presenting as gigantomastia: case report Mastology 2020;30:e20200062
Powell CM, Cranor ML, Rosen PP. Pseudoangiomatous Stromal Hyperplasia (PASH). Am J Surg Pathol. 1995;19(3):270‑7. https://doi.org/10.1097/00000478-199503000-00004
Hoda SA, Brogi E, Koerner FC, Rosen PP. Rosen’s Breast Pathology. 4th ed. Philadelphia: Wolters Kluwer Health/Lippincott Williams Wilkins; 2014. 1379 p.
Bourke AG, Tiang S, Harvey N, McClure R. Pseudoangiomatous stromal hyperplasia causing massive breast enlargement. BMJ Case Rep. 2015;2015:bcr2014204343. https://doi.org/10.1136/bcr-2014-204343
Nascimento TC, Djahjah MC, Carneiro AHPC, Oliveira AC de, Marchiori E. Pseudoangiomatous stromal hyperplasia presenting as a tumor. Radiol Bras. 2019;52(2):128-9. https://doi.org/10.1590/0100-3984.2017.0135
Krawczyk N, Fehm T, Ruckhäberle E, Mohrmann S, Riemer J, Braunstein S, et al. Bilateral Diffuse Pseudoangiomatous Stromal Hyperplasia (PASH) Causing Gigantomastia in a 33-Year-Old Pregnant Woman: Case Report. Breast Care. 2016;11(5):356-8. https://doi.org/10.1159/000450867
Virk RK, Khan A. Pseudoangiomatous Stromal Hyperplasia: An Overview. Arch Pathol Lab Med. 2010;134(7):1070-4. https://doi.org/10.1043/2008-0686-RS.1
Prichard RS, O’Neill CJ, O’Hara JL, Atmore BB, Hassall M. Pseudoangiomatous stromal hyperplasia of the breast: an unusual pathology necessitating bilateral mastectomy during pregnancy. ANZ J Surg. 2011;81(4):304-5. https://doi.org/10.1111/j.1445-2197.2011.05688.x
Tsuda B, Kumaki N, Ishida R, Sakaeda E, Ishii S, Mizuno M, et al. Rare finding of bilateral pseudoangiomatous stromal hyperplasia of the breast: A case report. Tokai J Exp Clin Med. 2019;44(4):73-9.
Polger MR, Denison CM, Lester S, Meyer JE. Pseudoangiomatous stromal hyperplasia: mammographic and sonographic appearances. Am J Roentgenol. 1996;166(2):349-52. https://doi.org/10.2214/ajr.166.2.8553945
Amorim HLE, Torres AF, Macedo Filho MAA, Paz AR, Pereira GCG. Análise dos achados ecográficos em nódulos de hiperplasia pseudoangiomatosa do estroma mamário diagnosticados por core biópsia. Rev Bras Mastol. 2011;21(2):66‑9.
Soares AB, Queiroga RC, Soares BR, Maximiano AMC, Cardoso IF, Leal PR. Reconstrução mamária imediata após ressecção de hiperplasia estromal pseudoangiomatosa em adolescente de 13 anos. Rev Bras Mastol. 2011;21(3):127-30.
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Copyright (c) 2020 Juliana Pontes Farias, Humberto Espínola Guedes Neto, Ariano Brilhante Pegado Suassuna, Rafael Chaves Claudino de Queiroga, Arthur Antonino da Silva Nunes, Adriano de Lima Quirino, Thaíse Lopes Medeiros

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