Garlet Bruno Bisognin, Zogbi Luciano, Lima Juliana Piveta de, Favalli Paulo Pereira de Souza, Krahe Frederico Diefenthaeler
Department of Surgery, Federal University of Rio Grande (FURG), Visconde de Paranaguá Street, No. 102, 96203-900, Rio Grande, Brazil.
Postgraduate Program in Nursing, Federal University of Rio Grande (PPGEnf - FURG), Visconde de Paranaguá Street, No. 102, 96203-900, Rio Grande, Brazil.
Int J Surg Case Rep. 2019;60:25-29. doi: 10.1016/j.ijscr.2019.05.032. Epub 2019 Jun 5.
Phyllodes tumors are biphasic fibroepithelial tumors that account for fewer than 1% of mammary tumors. They usually appear in middle-aged women, with an average size of 4-7 cm and rapid growth.
A 25-year-old woman sought care after excision of recurrent nodules in the right breast, with a diagnosis of borderline phyllodes tumor. She had no new lesions on physical examination. Imaging studies revealed an anechoic collection and nodular areas in a previous surgical site, correlated with pathology. Immuno-histochemical examination was positive for vimentin, calponin, Ki-67 and estrogen receptor. Systemic staging did not show metastases. Skin-reducing mastectomy was performed on the right side, followed by reconstruction and left reduction mammaplasty for symmetry. At 8-month follow-up, there was no relapse of the lesions on clinical and ultrasonographic examinations.
Phyllodes tumors are rare neoplasms characterized by rapid growth, occurring in women between 35-55 years of age. They are classified as benign, borderline and malignant, according to histological parameters. There are reports of genetic mutations in TP53 associated with malignant phyllodes tumor. On immunohistochemistry, there is a greater tendency to malignancy in tumors with Ki-67 and estrogen receptor expression. Imaging methods may aid in diagnosis, which is only definitive after excision and histopathological analysis of the tumor. These tumors have high local recurrence rates and possibility of metastases, closely related to histology.
Phyllodes tumors are a great challenge to the surgeon. Treatment is surgical, with wide excision; radiotherapy and chemotherapy are controversial.
叶状肿瘤是一种双相性纤维上皮性肿瘤,占乳腺肿瘤的比例不到1%。它们通常出现在中年女性中,平均大小为4 - 7厘米,生长迅速。
一名25岁女性在右乳复发性结节切除术后寻求治疗,诊断为交界性叶状肿瘤。体格检查未发现新的病变。影像学检查显示先前手术部位有一无回声区和结节状区域,与病理结果相符。免疫组化检查波形蛋白、钙调蛋白、Ki-67和雌激素受体呈阳性。全身分期未显示转移。右侧行皮肤缩减乳房切除术,随后进行乳房重建及左侧乳房缩小整形术以保持对称。随访8个月时,临床和超声检查未发现病变复发。
叶状肿瘤是罕见的肿瘤,其特点是生长迅速,多见于35至55岁的女性。根据组织学参数,它们被分为良性、交界性和恶性。有报道称TP53基因突变与恶性叶状肿瘤有关。免疫组化显示,Ki-67和雌激素受体表达的肿瘤有更高的恶变倾向。影像学方法有助于诊断,但只有在肿瘤切除并进行组织病理学分析后才能确诊。这些肿瘤局部复发率高,有转移的可能,与组织学密切相关。
叶状肿瘤对外科医生来说是一个巨大的挑战。治疗以手术为主,需广泛切除;放疗和化疗存在争议。