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原发性阴道恶性黑色素瘤:一例难以诊断的罕见疾病病例报告。

Primary malignant melanoma of the vagina: A case report of a rare disease that is difficult to diagnose.

作者信息

Park Soyoung, Park Jung-Woo, Rha Seo-Hee, Kim Sujin

机构信息

Department of Obstetrics and Gynecology, Dong-A University, College of Medicine, Busan, Republic of Korea.

Department of Pathology, Dong-A University College of Medicine, Busan, Republic of Korea.

出版信息

Medicine (Baltimore). 2025 Jan 10;104(2):e41259. doi: 10.1097/MD.0000000000041259.

Abstract

RATIONALE

Malignant melanoma is a rare cancer that accounts for approximately 1% of all cancers. Primary malignant melanoma of the female genital tract accounts for approximately 3% to 7% of all malignant melanomas, and 0.3% to 0.8% of all melanomas in women. It affects postmenopausal women ages 60 to 80 years. Various hormonal factors, including puberty, pregnancy, menopause, oral contraceptive use, and human papillomavirus infection are associated with primary malignant melanoma of the vagina.

PATIENT CONCERNS

Symptoms often include vaginal bleeding, discharge, and pain; however, it can also present as pigmented or nonpigmented lesions, making diagnosis challenging.

DIAGNOSES

Diagnosis involves detailed history, physical examination, and imaging (CT, MRI, and positron emission tomography). Immunohistochemical staining for markers, such as human melanoma black-45 and Melan-A, is crucial for confirmation. The diagnosis was made through careful physical examination, imaging studies, and immunohistochemistry.

INTERVENTIONS

The treatment includes wide local excision, radical surgery, radiotherapy, chemotherapy, and immunotherapy. The prognosis of primary malignant melanoma of the vagina is usually poor owing to late diagnosis, and the 5-year survival rate is 5% to 25%.

OUTCOMES AND LESSONS

To consider the possibility of primary malignant melanoma of vagina, postmenopausal women, particularly those who with human papillomavirus infection, should be performed thorough examination regardless of symptoms of vaginal bleeding or discharge.

摘要

理论依据

恶性黑色素瘤是一种罕见的癌症,约占所有癌症的1%。女性生殖道原发性恶性黑色素瘤约占所有恶性黑色素瘤的3%至7%,占女性所有黑色素瘤的0.3%至0.8%。它影响60至80岁的绝经后女性。包括青春期、怀孕、绝经、口服避孕药使用和人乳头瘤病毒感染在内的各种激素因素与阴道原发性恶性黑色素瘤有关。

患者关注问题

症状通常包括阴道出血、分泌物和疼痛;然而,它也可能表现为色素沉着或无色素沉着的病变,这使得诊断具有挑战性。

诊断

诊断包括详细的病史、体格检查和影像学检查(CT、MRI和正电子发射断层扫描)。对人黑色素瘤黑色素-45和黑色素A等标志物进行免疫组织化学染色对于确诊至关重要。通过仔细的体格检查、影像学研究和免疫组织化学做出了诊断。

干预措施

治疗包括广泛局部切除、根治性手术、放疗、化疗和免疫治疗。由于诊断较晚,阴道原发性恶性黑色素瘤的预后通常较差,5年生存率为5%至25%。

结果与经验教训

为了考虑阴道原发性恶性黑色素瘤的可能性,绝经后女性,尤其是那些有人乳头瘤病毒感染的女性,无论有无阴道出血或分泌物症状,都应进行全面检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6228/11729272/0b5bc89075cf/medi-104-e41259-g001.jpg

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