额区巨大原发性顶突癌:临床表现、组织病理学特征和外科治疗。

Dragana Petrović Popović, Marijan Novaković, Milan Stojičić, Dimitrije Brašanac, Mirjana Petrović-Elbaz
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引用次数: 0

摘要

原发性皮肤顶泌癌是汗腺癌的一种亚型,是一种极为罕见的恶性肿瘤。即使对病理学家来说,区分顶泌癌和乳腺癌转移也很困难。大多数发生在腋窝等顶泌腺密度高的区域,很少发生在头皮和眼睑,但也可能发生在皮肤的其他地方。头皮原发性皮肤顶泌癌是一种罕见的恶性肿瘤,在文献中最常以病例报告或小病例系列的形式报道。据我们所知,文献中尚未描述额区原发性皮肤顶泌癌的巨大形式。原发性皮肤顶泌癌的治疗尚无既定方案。我们报告一例巨大的原发性皮肤顶泌癌,局限于额区。通过显微镜和免疫组织化学分析进行活检,确定了原发性皮肤顶泌癌的确切诊断。对于继发性缺损,我们选择了广泛的手术切除和重建,并采用大面积的局部移位皮瓣和厚皮片移植。原发性皮肤顶泌癌是一种非常罕见的恶性肿瘤,其巨大的形态尚未被描述。手术治疗为患者提供了无瘤状态、满意的美学外观和生活质量。
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Giant Primary Apocrine Carcinoma of the Frontal Region: Clinical Presentation, Histopathological Features, and Surgical Treatment.

Primary cutaneous apocrine carcinoma (PCAC), a subtype of sweat gland carcinoma, is an extremely rare malignant neoplasm. Distinguishing an apocrine carcinoma from a breast carcinoma metastasis is difficult even for a pathologist. Most arise in regions of high apocrine gland density like the axilla, and rarely on the scalp and eyelid, but they can occur elsewhere on the skin. Primary cutaneous apocrine carcinoma of the scalp is a rare malignancy most often reported in the literature as case reports or small case series. The giant form of primary cutaneous apocrine carcinoma in the frontal region has not been described in the literature, to the best of our knowledge. There are no established protocols for treatment of primary cutaneous apocrine carcinoma. We report a case of a giant primary cutaneous apocrine carcinoma localized in the frontal region. A definitive diagnosis of a primary cutaneous apocrine carcinoma was established by biopsy with microscopic and immunohistochemical analysis. Wide surgical excision and reconstruction with large local transposition flap and split thickness skin grafts for secondary defect were our therapy of choice. Primary cutaneous apocrine carcinoma is a very rare malignancy, and the giant form has not yet been described. Surgical treatment provided the patient with tumor-free status as well as satisfactory aesthetical appearance and quality of life.

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