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17岁女孩腋窝副乳腺纤维腺瘤:病例报告

Fibroadenoma in Axillary Supernumerary Breast in a 17-Year-Old Girl: Case Report.

作者信息

Surd Adrian, Mironescu Aurel, Gocan Horatiu

机构信息

Pediatric Surgery Specialist, Department of Pediatric Surgery, Emergency Children's Hospital, Cluj-Napoca, Romania.

Professor of Pediatric Surgery, Childrens Hospital, Brasov, Romania.

出版信息

J Pediatr Adolesc Gynecol. 2016 Oct;29(5):e79-e81. doi: 10.1016/j.jpag.2016.04.008. Epub 2016 May 13.

Abstract

BACKGROUND

Supernumerary breast or polymastia is a well documented anomaly of the breast, and commonly presents along the embryonic milk line extending between the axilla and groin. However, cases of polymastia have been recorded in the face, vulva, and perineum. The clinical significance of these anomalies include their susceptibility to inflammatory and malignant changes, and their association with other congenital anomalies of the urinary and cardiovascular systems.

CASE

In this article we report a case of fibroadenoma that developed in the supernumerary breast of the right axilla in a 17-year-old girl. It is uncommon to find such palpable masses in young patients. Clinical and sonographic examination of both breasts revealed no abnormalities and no lymph nodes were detected in the axillae or the neck. No associated urologic or cardiovascular abnormalities were found, and the histopathological examination of the excisional biopsy samples showed a well-defined, capsulated intracanalicular type of fibroadenoma similar to that of eutopic mammary tissue.

SUMMARY AND CONCLUSION

In this report, we describe a rare case of fibroadenoma in an accessory breast in a young woman. There are a fewer than 40 reports in the world about this subject, of which differential diagnoses include: cancer in axillary supernumerary breast, hidradenitis, axillary lymphadenomegaly, lipomas, anexial cutaneous neoplasia, cysts, and phylloides tumor. The combination of clinical examination, ultrasound, and cytology leads to adequate treatment, especially surgical. The diagnosis could be confused because of findings from cytology. In this case, because of the clinical and sonographic findings and multiple differential diagnosis, only the histopathological study was used to confirm the diagnosis. Despite its high sensitivity, cytology has low specificity and could create false positive results. However, atypical lesions can be seen in fibroadenomas, especially in younger patients, pregnant patients, and in patients who use hormonal contraception. Although there are a few reports, our case report is similar to current medical registers and, after surgical treatment, our patient had an excellent prognosis.

摘要

背景

多乳症或副乳腺是一种有充分文献记载的乳腺异常,通常出现在沿腋窝和腹股沟之间延伸的胚胎乳线上。然而,也有在面部、外阴和会阴出现多乳症的病例记录。这些异常的临床意义包括它们易发生炎症和恶性变化,以及与泌尿和心血管系统其他先天性异常的关联。

病例

在本文中,我们报告了一名17岁女孩右腋窝副乳腺发生纤维腺瘤的病例。在年轻患者中发现这种可触及的肿块并不常见。对双侧乳房进行临床和超声检查均未发现异常,腋窝和颈部未检测到淋巴结。未发现相关的泌尿系统或心血管异常,切除活检样本的组织病理学检查显示为界限清楚、有包膜的管内型纤维腺瘤,与正常乳腺组织相似。

总结与结论

在本报告中,我们描述了一名年轻女性副乳腺中罕见的纤维腺瘤病例。关于这一主题,世界上的报道少于40例,其鉴别诊断包括:腋窝副乳腺癌症、汗腺炎、腋窝淋巴结肿大、脂肪瘤、附件皮肤肿瘤、囊肿和叶状肿瘤。临床检查、超声和细胞学检查相结合可实现充分治疗,尤其是手术治疗。由于细胞学检查结果,诊断可能会混淆。在本病例中,由于临床和超声检查结果以及多种鉴别诊断,仅通过组织病理学研究来确诊。尽管细胞学检查敏感性高,但特异性低,可能产生假阳性结果。然而,纤维腺瘤中可见非典型病变,尤其是在年轻患者、孕妇和使用激素避孕的患者中。虽然报道较少,但我们的病例报告与当前医学记录相似,手术治疗后,我们的患者预后良好。

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