Malignant melanoma with bone metastases in a child: a case report and review of literature.

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Annals of Medicine and Surgery Pub Date : 2025-01-09 eCollection Date: 2025-01-01 DOI:10.1097/MS9.0000000000002767
Neda Ashayeri, Parya Khani, Ghasem Miri-Aliabad, Masoumeh Jafari, Ali Pajouhi
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Abstract

Introduction and importance: Melanoma is the fifth most common cancer diagnosed in the US in 2022. While its incidence increased from 1980 to 2017, it rarely happens in children. Its diagnosis and treatment are challenging in pediatric patients due to its rarity and different presentations compared to adults.

Case presentation: An 11.5-year-old boy with a complaint of back pain was admitted to the hospital. Initial examinations were normal; however, due to continued pain and symptoms (e.g., inability to walk, knee pain and ankle ecchymosis, weight loss, vomiting, nausea, and dyspnea), further examinations were performed. Biopsy, nuclear scan, computed tomography (CT) scan, and immunohistochemistry (IHC) confirmed the malignant melanoma diagnosis with bone and lung metastasis. Single-agent treatment with nivolumab was initiated after the diagnosis confirmation with no specific complication. The patient's parents decided to continue the treatment in their city of residence to reduce costs. However, the treatment was not continued, and unfortunately, the patient has passed away.

Clinical discussion: Melanoma is rare in children, making its diagnosis challenging. There are no specific guidelines for treating melanoma in pediatric patients, especially in children under 12, with ongoing debate on the most suitable treatment and follow-up options for these patients. It is important to fully examine resected legions for malignancy.

Conclusion: The study highlights the difficulties in diagnosing and treating malignant melanoma in children, considering its rarity and unusual signs and symptoms compared to adults. Specific guidelines are needed for diagnosing and treating malignant melanoma in pediatric patients.

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儿童恶性黑色素瘤伴骨转移1例报告及文献复习。
简介和重要性:黑色素瘤是2022年美国诊断出的第五大常见癌症。虽然其发病率从1980年到2017年有所增加,但很少发生在儿童身上。由于其罕见且与成人相比表现不同,儿科患者的诊断和治疗具有挑战性。病例介绍:一名11.5岁的男孩因背部疼痛被送往医院。初步检查正常;然而,由于持续的疼痛和症状(如无法行走、膝盖疼痛和踝关节淤斑、体重减轻、呕吐、恶心和呼吸困难),我们进行了进一步的检查。活检,核扫描,计算机断层扫描(CT)和免疫组织化学(IHC)证实恶性黑色素瘤诊断为骨和肺转移。确诊后开始使用纳武单抗单药治疗,无特异性并发症。患者的父母决定在他们居住的城市继续治疗,以减少费用。然而,治疗没有继续,不幸的是,病人已经去世了。临床讨论:黑色素瘤在儿童中很少见,使得其诊断具有挑战性。目前还没有针对儿科患者,特别是12岁以下儿童治疗黑色素瘤的具体指南,关于这些患者最合适的治疗方法和随访选择的争论仍在继续。充分检查切除的军团是否有恶性肿瘤是很重要的。结论:该研究强调了诊断和治疗儿童恶性黑色素瘤的困难,考虑到与成人相比,其罕见和不寻常的体征和症状。儿科患者恶性黑色素瘤的诊断和治疗需要具体的指导方针。
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Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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5.90%
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