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一名9岁患者耳后汗腺腺瘤恶变成为汗腺癌:病例报告

Malignant Transformation of Retroauricular Hidradenoma in Hidradenocarcinoma in a Nine-Year-Old Patient: A Case Report.

作者信息

Zorro Sara, Matias Rafael, Sousa Cátia, Aguiar Artur

机构信息

Radiation Oncology, Instituto Português de Oncologia do Porto, Porto, PRT.

Pediatric Oncology, Instituto Português de Oncologia do Porto, Porto, PRT.

出版信息

Cureus. 2023 Apr 5;15(4):e37160. doi: 10.7759/cureus.37160. eCollection 2023 Apr.

Abstract

Hidradenocarcinoma, a rare malignant entity that derives from sweat glands, is especially rare in the pediatric population. The treatment of choice is surgery. Radiation therapy is used only in selected patients. Chemotherapy is not used extensively because its effectiveness has not been demonstrated yet. This case report describes a nine-year-old female patient who presented in 2018 with a vegetative lesion in the right parietal region. After excisional surgery, pathology confirmed that the lesion was a benign hidradenoma. However, the lesion recurred six months later, and subsequent surgery revealed nodular hidradenoma with positive margins. In July 2019, a new heterogenous lesion appeared in the right retroauricular region, which was surgically removed. The pathology report found possible malignant characteristics, and the patient was referred to our hospital where she was diagnosed with poorly differentiated right retroauricular carcinoma with infiltrative and perineural permeation, along with homolateral lymph node metastasis. It was histologically compatible with a hidradenocarcinoma. The patient underwent a wide-margin excision and homolateral total cervical lymphadenectomy, followed by adjuvant radiotherapy. The last follow-up MRI was negative for disease recurrence or metastasis; however, a slow-growing node on the left jugular chain (level II) was noted. The patient is on regular follow-ups to monitor disease status and treatment-related adverse events. This case highlights the challenges of diagnosing and treating hidradenocarcinoma, a rare malignancy that requires aggressive management with a multidisciplinary approach. More robust clinical evidence is needed to define the best treatment approach for these aggressive tumors.

摘要

汗腺癌是一种起源于汗腺的罕见恶性肿瘤,在儿科人群中尤为罕见。首选治疗方法是手术。放射治疗仅用于特定患者。化疗尚未广泛应用,因为其有效性尚未得到证实。本病例报告描述了一名9岁女性患者,她于2018年出现右顶叶区的赘生性病变。切除手术后,病理证实该病变为良性汗腺腺瘤。然而,病变在6个月后复发,随后的手术显示为切缘阳性的结节性汗腺腺瘤。2019年7月,右耳后区域出现一个新的异质性病变,手术切除。病理报告发现可能的恶性特征,患者被转诊至我院,在我院被诊断为右耳后低分化癌,伴有浸润和神经周围浸润,以及同侧淋巴结转移。组织学上与汗腺癌相符。患者接受了广泛切缘切除和同侧全颈淋巴结清扫术,随后进行辅助放疗。最后一次随访MRI显示疾病无复发或转移;然而,在左颈静脉链(II区)发现一个生长缓慢的淋巴结。患者正在定期随访,以监测疾病状态和治疗相关的不良事件。本病例突出了汗腺癌诊断和治疗的挑战,这是一种罕见的恶性肿瘤,需要采用多学科方法进行积极管理。需要更有力的临床证据来确定这些侵袭性肿瘤的最佳治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1b1/10161949/6b7d400e5620/cureus-0015-00000037160-i01.jpg

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