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鼻腔黏膜恶性黑色素瘤放疗后一年复发

Mucosal Malignant Melanoma of Nasal Cavity Recurring a Year After Radiotherapy.

作者信息

Çomunoğlu Cem, Kuzey Gamze Mocan, Inançli Mete, Baba Füsun, Özkayalar Hanife

机构信息

Department of Pathology, Yakın Doğu University, Faculty of Medicine, LEFKOŞA, TURKİSH REPUBLIC of NORTHERN CYPRUS.

出版信息

Turk Patoloji Derg. 2017;33(1):66-69. doi: 10.5146/tjpath.2013.01218.

Abstract

OBJECTIVE

Sinonasal mucosal malignant melanoma is a rare entity. In this report we present a nasal mucosal malignant melanoma case with its histopathological and clinical features.

CASE REPORT

An 88-year-old female patient presented with epistaxis a month ago. Examination revealed a polypoid mass lesion of right nasal cavity originating from the middle concha. Her medical history revealed that she had been found to have a mass lesion in the right nasal cavity 15 months ago. She then underwent a punch biopsy from that lesion. A definitive histopathological diagnosis was not made but it was declared that the lesion had been a malignant epithelial tumor. The patient then had radiotherapy and the lesion showed complete regression. One year after completion of radiotherapy, the lesion recurred. Her last PET-CT showed multiple metastatic foci. Endoscopic excisional biopsy was performed for her recurrent lesion. Fragmented tumoral tissues were measured as 3,6x3x0,5 cm. Macroscopically the tumor was brownish in color. Histopathologically the tumor consisted of spindled and epitheloid cells. Immunohistochemically the tumor cells displayed positivity for S-100, HMB-45 and Melan-A. Findings were consistent with malignant melanoma.

DISCUSSION

Mucosal malignant melanomas have a poor prognosis despite chemotherapy and radiotherapy. Five-year survival for sinonasal melanoma is reported to be lower than 35%. Sinonasal melanomas show a high recurrence rate. The immunohistochemical markers showing high specificity for malignant melanoma such as S-100, HMB-45 and Melan-A are used in order to reach a correct diagnosis. In our case the tumor showed recurrence and multiple metastases 1 year after completion of radiotherapy. For this recurrent tumor, chemotherapy and radiotherapy have been planned.

摘要

目的

鼻窦黏膜恶性黑色素瘤是一种罕见的疾病。在本报告中,我们呈现了一例鼻腔黏膜恶性黑色素瘤病例及其组织病理学和临床特征。

病例报告

一名88岁女性患者于1个月前出现鼻出血。检查发现右侧鼻腔有一个息肉样肿块病变,起源于中鼻甲。她的病史显示,15个月前她被发现右侧鼻腔有一个肿块病变。随后她对该病变进行了穿刺活检。未做出明确的组织病理学诊断,但宣布该病变为恶性上皮肿瘤。患者随后接受了放疗,病变显示完全消退。放疗结束1年后,病变复发。她最后一次的PET-CT显示有多个转移灶。对其复发病变进行了内镜切除活检。切除的肿瘤组织碎片大小为3.6×3×0.5厘米。肉眼可见肿瘤呈褐色。组织病理学上,肿瘤由梭形细胞和上皮样细胞组成。免疫组织化学检查显示肿瘤细胞对S-100、HMB-45和Melan-A呈阳性。结果符合恶性黑色素瘤。

讨论

尽管进行了化疗和放疗,黏膜恶性黑色素瘤的预后仍然很差。据报道,鼻窦黑色素瘤的5年生存率低于35%。鼻窦黑色素瘤的复发率很高。为了做出正确诊断,使用了对恶性黑色素瘤具有高特异性的免疫组织化学标志物,如S-100、HMB-45和Melan-A。在我们的病例中,肿瘤在放疗结束1年后出现复发和多处转移。对于这个复发性肿瘤,已计划进行化疗和放疗。

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