Ahire Priya P, Gandhi Ami S, Jaiswal Yogesh, Binorkar Ashwini, Joshi Pritesh N, Sukumaran Gayathri
General Surgery, Grant Government Medical College and Sir JJ Group of Hospitals, Mumbai, IND.
Plastic and Reconstructive Surgery, Grant Government Medical College and Sir JJ Group of Hospitals, Mumbai, IND.
Cureus. 2024 Nov 18;16(11):e73896. doi: 10.7759/cureus.73896. eCollection 2024 Nov.
Hamartomas are rare, benign pseudotumors consisting of a mixture of ducts, lobules, fibrous stroma, and adipose tissue. Despite their benign nature, these lesions can present significant clinical challenges and may be underrecognized. A 48-year-old female presented with a progressively enlarging lump in the right breast over eight years. The lump, measuring 42 x 45 cm, displaced the nipple-areola complex and exhibited a bosselated, variegated consistency. Magnetic resonance imaging revealed a well-defined, lobulated lesion (15.3 x 21 x 26 cm) involving the right breast parenchyma and skin surface. Histopathology from core biopsies showed predominantly fibrocollagenous tissue with mild atypia. The patient underwent wide local excision and reconstruction with a latissimus dorsi myocutaneous flap. Postoperative histopathology confirmed a well-encapsulated mammary hamartoma (29 x 25 x 11.5 cm, 6 kg) with no malignant features. Hamartomas are usually benign and can be challenging to diagnose due to their complex, disorganized architecture. Imaging modalities such as mammography, ultrasound, and MRI are essential for diagnosis, while histopathological examination confirms the nature of the lesion. Surgical excision remains the definitive treatment, addressing both functional and cosmetic concerns. Although malignancy is rare, precise diagnosis and thorough surgical management are critical. This case is the largest breast hamartoma documented in the literature to our best knowledge, providing significant insights into its clinical presentation and management.
错构瘤是一种罕见的良性假瘤,由导管、小叶、纤维基质和脂肪组织混合组成。尽管它们本质上是良性的,但这些病变可能带来重大的临床挑战,且可能未得到充分认识。一名48岁女性在八年时间里右乳出现一个逐渐增大的肿块。该肿块大小为42×45厘米,使乳头乳晕复合体移位,质地呈分叶状、不均匀。磁共振成像显示一个边界清晰的分叶状病变(15.3×21×26厘米),累及右乳实质和皮肤表面。粗针活检的组织病理学显示主要为纤维胶原组织,有轻度异型性。患者接受了广泛局部切除,并采用背阔肌肌皮瓣进行重建。术后组织病理学证实为一个包膜完整的乳腺错构瘤(29×25×11.5厘米,6千克),无恶性特征。错构瘤通常是良性的,由于其结构复杂、紊乱,诊断可能具有挑战性。乳腺X线摄影、超声和磁共振成像等影像学检查手段对诊断至关重要,而组织病理学检查可确认病变性质。手术切除仍然是 definitive 治疗方法,可解决功能和美观方面的问题。尽管恶性情况罕见,但精确诊断和彻底的手术管理至关重要。据我们所知,本病例是文献记载中最大的乳腺错构瘤,为其临床表现和管理提供了重要见解。