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一名患有巨大先天性痣且未检测到原发性黑色素瘤的患者出现孤立性黑色素瘤转移:病例报告及文献综述

Isolated melanoma metastasis in a patient with large congenital nevus without detectable primary melanoma: a case report and review of literature.

作者信息

Pabianek Marta, Jatczak-Grochala Ilona, Lesiak Aleksandra, Narbutt Joanna, Siekierko Aleksandra, Stasikowska-Kanicka Olga, Ciążyńska Magdalena

机构信息

Chemotherapy Unit and One-Day Chemotherapy Unit, Specialist Oncology Hospital NU-MED, Tomaszów Mazowiecki, Poland.

Department of Proliferative Diseases, Nicolaus Copernicus Multidisciplinary Centre for Oncology and Traumatology, Łódź, Poland.

出版信息

Front Med (Lausanne). 2024 Oct 15;11:1427982. doi: 10.3389/fmed.2024.1427982. eCollection 2024.

Abstract

Giant congenital pigmented nevi constitute an extremely diverse group of skin lesions with varying morphologies. These nevi are often associated with many clinical implications, such as increased risk of melanoma and the presence of neurocutaneous melanosis, with melanoma being the primary concern. We present a rare case of a 62-year-old patient with a giant congenital birthmark who reported to the oncology department due to a tumor in the lower abdomen detected during an ultrasound examination. A biopsy of the lesion showed the presence of melanoma metastasis. Four independent dermatologists performed a dermoscopic examination of the patient's skin and mucous membranes. In the PET/CT examination, apart from the previously described change in the lower abdomen, no metabolically active foci with features of malignant growth were found. The patient underwent surgical removal of the lesion in the lower abdomen. The postoperative histopathological examination confirmed the presence of metastasis of melanoma in the subcutaneous tissue of the abdomen with no connection to the epidermis. The mutation was not found in the molecular test. For stage IV R0 melanoma with distant metastasis, with stage T0N0M1a, the only adjuvant treatment option following radical resection is nivolumab. After a rheumatological consultation, the patient was qualified for adjuvant treatment with nivolumab.

摘要

巨大先天性色素痣是一组形态各异、极为多样的皮肤病变。这些痣常伴有许多临床问题,如黑色素瘤风险增加以及神经皮肤黑素沉着症的存在,其中黑色素瘤是主要关注点。我们报告一例罕见病例,一名62岁患有巨大先天性胎记的患者,因超声检查发现下腹部有肿瘤而前往肿瘤科就诊。病变活检显示存在黑色素瘤转移。四名独立的皮肤科医生对患者的皮肤和黏膜进行了皮肤镜检查。在PET/CT检查中,除了先前描述的下腹部病变外,未发现具有恶性生长特征的代谢活跃病灶。患者接受了下腹部病变的手术切除。术后组织病理学检查证实腹部皮下组织存在黑色素瘤转移,与表皮无关联。分子检测未发现该突变。对于伴有远处转移的IV期R0黑色素瘤,T0N0M1a期,根治性切除后唯一的辅助治疗选择是纳武单抗。经过风湿科会诊,该患者符合纳武单抗辅助治疗的条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63d0/11518708/293166004201/fmed-11-1427982-g001.jpg

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