Department of Otorhinolaryngology - Head & Neck Surgery, Medical University of Graz, Graz, Austria.
Department of Dermatology and Venereology, Medical University of Graz, Graz, Austria.
J Dermatol. 2023 May;50(5):700-704. doi: 10.1111/1346-8138.16716. Epub 2023 Jan 18.
Trichoblastic carcinosarcoma is a seldom biphasic adnexal tumor with malignant epithelial and mesenchymal components. The authors report the first tumor on the neck developed from preexistent trichoblastoma showing aggressive, recurrent behavior. An 82-year-old man presented with a solitary 3-cm exophytic lesion. Histology verified the diagnosis of trichoblastic carcinosarcoma. Four years earlier, a trichoblastic carcinoma arising in a preexisting trichoblastoma was excised at the same location. Despite successful surgical treatments, three local recurrences within 4 years were diagnosed. After the second relapse, the patient agreed on adjuvant radiation. Twelve months later, another relapse was excised in toto. In the last surgical specimen, only the mesenchymal component was found. Copy number variation analysis of the preexisting tumor and two recurrences revealed the same entity and additional chromosomal aberrations in the recurrences. Adnexal carcinosarcomas are seldom, yet presumably underdiagnosed biphasic tumors with aggressive growth potential. They should have adequate preoperative clarification with wide tumor excision, as radiosensitivity seems to be of limited effect.
毛母质癌肉瘤是一种罕见的具有恶性上皮和间叶成分的附属器双相性肿瘤。作者报告了首例源自先前存在的毛母质瘤的颈部肿瘤,表现出侵袭性、复发性的行为。一位 82 岁男性出现单发 3cm 外生性病变。组织学证实了毛母质癌肉瘤的诊断。4 年前,同一部位切除了一个源自先前存在的毛母质瘤的毛母质癌。尽管进行了成功的手术治疗,但在 4 年内诊断出 3 次局部复发。第二次复发后,患者同意接受辅助放疗。12 个月后,再次完全切除了另一次复发。在最后一次手术标本中,仅发现了间叶成分。对先前存在的肿瘤和两次复发进行拷贝数变异分析显示,两者为同一实体,并在复发中发现了额外的染色体异常。附属器癌肉瘤少见,但可能被低估的具有侵袭性生长潜能的双相性肿瘤。应在术前充分明确诊断,并进行广泛的肿瘤切除,因为放射敏感性的效果似乎有限。