de Andrés Gómez Alejandra, Navarro Moratalla Carla, Villalba Ferrer Francisco, Sabater Marco Vicente, García-Vilanova Andrés, Fuster Diana Carlos, Medrano González Jose, Palao Errando Jesús
University GeneralHospital of Valencia, Av. De les Tres Creus, 2, 46014 València, Spain.
University GeneralHospital of Valencia, Av. De les Tres Creus, 2, 46014 València, Spain.
Int J Surg Case Rep. 2015;15:81-4. doi: 10.1016/j.ijscr.2015.08.017. Epub 2015 Aug 18.
Eccrine spiradenomas are rare adnexal tumours of the skin that originate in the sweat glands. There are only three cases, including ours, diagnosed as malignant transformation in the breast.
We present a case of an asymptomatic 48 year old woman in whom the lesion was detected on the basis of breast cancer prevention programme. The metastatic study detection and the sentinel lymph node biopsy were negative so wide excision of the mass was performed with no further treatment. After 32 months of follow-up, there is no evidence of recurrent or metastatic disease in our patient.
The lesions usually show a typical history of a long-standing unchanged cutaneous solitary nodule that becomes enlarged. The imaging findings of breast eccrine spiradenomas have not been clearly demonstrated. Diagnosis is based in histopathological findings of malignant focus. A large list of uncommon dermatological skin malignancies and breast benign lesions can mimic malignant eccrine spiradenomas (MES); therefore, determination of inmunophenotype allows narrowing differential diagnosis. Distant metastases portend an ominous prognosis. The mainstay of treatment is surgical removal with wide excision margins. Radiation and hyperthermic chemotherapy can also be administered to prevent focal recurrence. Due to the high risk of developing metastases, close follow up of these patients for early detection of recurrence should be carried out.
Eccrine spiradenomas are rare adnexal tumours of the skin. Intraparenquimatous breast location is especially infrequent. Diagnosis is based on histopathological examination. MES metastasizes (40%), so a close follow up is recommended.
小汗腺螺旋腺瘤是一种罕见的起源于汗腺的皮肤附属器肿瘤。包括我们的病例在内,仅有三例被诊断为乳腺恶性转化。
我们报告一例48岁无症状女性病例,该病变是在乳腺癌预防项目中被发现的。转移研究检测和前哨淋巴结活检均为阴性,因此对肿块进行了广泛切除,未进行进一步治疗。经过32个月的随访,我们的患者没有复发或转移疾病的证据。
病变通常表现为长期不变的皮肤孤立结节,随后增大。乳腺小汗腺螺旋腺瘤的影像学表现尚未明确显示。诊断基于恶性病灶的组织病理学发现。大量不常见的皮肤恶性肿瘤和乳腺良性病变可模仿恶性小汗腺螺旋腺瘤(MES);因此,免疫表型的测定有助于缩小鉴别诊断范围。远处转移预示预后不良。治疗的主要方法是手术切除,切缘要广泛。也可进行放疗和热化疗以预防局部复发。由于发生转移的风险高,应对这些患者进行密切随访以早期发现复发。
小汗腺螺旋腺瘤是罕见的皮肤附属器肿瘤。乳腺实质内的位置尤其罕见。诊断基于组织病理学检查。MES会发生转移(40%),因此建议密切随访。