Dergiler / European Journal of Breast Health / 2019 / Cilt: 15 - Sayı: 3

Our 20-Year Institutional Experience with Surgical Approach for Breast Hamartomas

Sayfa
171–175
Yayın Tarihi
2022-10-18
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Therefore, careful diagnosis and appropriate management including surgery are required.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Objective: Hamartomas are rare, slowly-growing breast tumours.
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Temel Bulgular & Veri:Clinical, radiological and histopathological examination together increase thediagnostic accuracy.
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Sonuç & Katkı:Therefore, careful diagnosis and appropriate management including surgery are required.
🔬Tür:Araştırma Makalesi
📍Kapsam:2015 Verileri
⚙️Değişkenler:Alan Parametreleri

Abstract

Objective: Hamartomas are rare, slowly-growing breast tumours. Clinical, radiological and histopathological examination together increase thediagnostic accuracy. To evaluate the clinicopathologic features of hamartomas and outline our clinical approach to hamartomas in our 20-year experience at our Breast Clinic.Materials and Methods: Between 1995 and 2015, 24 cases were retrospectively analyzed with a diagnosis of breast hamartoma at our BreastClinic followed by excisional biopsy. Data was obtained on patient demographics, clinical examination, radiological findings and histopathologicalsubtypes.Results: Of 1338 benign breast tumours excised from January 1995 to January 2015, 24 (1.8%) were identified as breast hamartoma. Median ageof patients was 42 (range, 13-70), whereas the median tumour size was 5 cm (1-10 cm). On preoperative imaging, hamartoma was most commonlymisdiagnosed as fibroadenoma. Pathological examination of the 24 biopsy specimens revealed 3 cases with pseudoangiomatous stromal hyperplasia,and another hamartoma associated with a radial scar within the centre of the lesion. Of those, one patient was diagnosed with malignant phylloidestumour in the same breast. At a median follow-up 58.4 months, none of the patients recurred or developed malignancy.Conclusion: Hamartomas can often be missed by clinicians, due to its benign nature which is poorly understood. Despite their slow growth, hamartomas can reach large sizes and can cause breast asymmetry. Although it is rare, hamartoma can be seen along with malignancy, as it is formed fromsimilar components of breast tissue. Therefore, careful diagnosis and appropriate management including surgery are required.

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Bu Makaleye Atıf Yap

ÖNDER, S., MÜSLÜMANOĞLU, M., ACUNAŞ, G., İĞCİ, A., TÜKENMEZ, M., ÖZMEN, V., TÜRKYILMAZ, Z., AYDIN, T., YILMAZ, R., ÖZKURT, E., DİNÇAĞ, A., CABİOĞLU, N. (2022). Our 20-Year Institutional Experience with Surgical Approach for Breast Hamartomas. European Journal of Breast Health, Cilt: 15 - Sayı: 3, 171–175. https://ajindex.com/articles/510787

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Kaynakça (6)

  1. Pyrm P. Pseudoadenome, Adenome und Mastome der weiblichen Brustdrüse; Studien für die Entstehung umschriebener adenom-ähnlicher Herde in der Mamma und für die Nachahmung der Brustdrüsengewebes durch echte Adenome und Fibroadenome. Beitr Pathol Anat Pathol 1928; 81: 221
  2. Arrigoni MG, Dockerty MB, Judd ES. The identification and treatment of mammary hamartoma. Surg Gynecol Obstet 1971; 133: 577-582. (PMID: 5096305
  3. Daya D, Trus T, D'Souza TJ, Minuk T, Yemen B. Hamartoma of the breast, an underrecognized breast lesion: A clinicopathologic and radiologic study of cases. Am J Clin Pathol 1995; 103: 685-689. (PMID: 7785651) [CrossRef] 4. Cheng CY, Long SJ, Wu MS, Pan ST. Breast adenolipoma-a variant hamartoma. Journal of Medicine and Health 2014; 3: 109-115
  4. Charpin C, Mathoulin MP, Andrac L, Barberis J, Boulat J, Sarradour B, Bonnier P, Piana L. Reappraisal of breasthamartomas. A morphological study of 41 cases. Pathol Res Pract 1994; 190: 362-371. (PMID: 8078805) [CrossRef] 6. Fisher CJ, Hanby AM, Robinson L, Millis RR. Mammary hamartomareview of 35 cases. Histopathol 1992; 20: 99-106. (PMID: 1559675) [CrossRef] 7. Dragoumis D, Assamaki A, Tsiftsoglou A. Hamartoma of the breast. An uncommon benign tumor. Am J Case Rep 2008; 9: 101-104
  5. Sanal HT, Ersoz N, Altinel O, Unal E, Can C. Giant hamartoma of the breast. Breast J 2006; 12: 84-85. (PMID: 16409596) [CrossRef] 9. Wu CY, Lin SH, Tu SH, Huang CS, Jeng CM. Hamartoma of the Breast. Chin J Radiol 2003; 28: 143-148
  6. Sevim Y, Kocaay AF, Eker T, Celasin H, Karabork A, Erden E, Genç V. Breast hamaroma: A clinicopathologic of 27 cases and a literature review. Clinics 2014; 69: 515-523. (PMID: 25141109) [CrossRef] 11. Tse GM, Law BK, Ma TK, Chan AB, Pang LM, Chu WC, Cheung HS. Hamartoma of the breast: a clinicopathological review. J Clin Pathol 2002; 55: 951-954. (PMID: 12461066) [CrossRef] 12. Riveros M, Cubilla A, Perotta F, Solalinde V. Hamartoma of the breast. J Surg Oncol 1989; 42: 197-200. (PMID: 2811385) [CrossRef] 13. Amir RA, Sheikh SS, Breast hamartoma: A report of 14 cases of an underrecognized and under-reported entity. Int J Surg Case Rep 2016; 22: 1-4. (PMID: 27002389) [CrossRef] 14. Kemp TL, Kilgore MR, Javid SH. Invasive ductal carcinoma a rising within a large mammary hamartoma. Breast J 2015; 21: 196-197. (PMID: 25613435) [CrossRef] 15. Lambert J, Jerjir N, Casselman J, Steyaert L. Invasive lobuler carsinoma arising in a hamartoma of the breast: A case report. Clin Breast Cancer 20