小儿非典型Spitz肿瘤1例报告。

Q4 Medicine
Joseph H Kelly, Linze Christensen, Marcus L Frohm
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引用次数: 0

摘要

Spitzoid肿瘤是一种黑色素细胞病变的集合,通过一组独特的组织学和分子特征区别于传统的痣或黑色素瘤。Spitz痣、Spitz样黑色素细胞瘤、非典型Spitz肿瘤(ast)和Spitz样黑色素瘤等Spitz样增生从良性到恶性不等。形态学本身是一种不充分的预后工具,但免疫组织化学(IHC)染色证明对风险分层是有用的。ast很少转移到区域淋巴结之外,治疗包括广泛的局部切除(WLE),根据组织分子特征,有或没有前哨淋巴结(SNL)活检。切缘为阴性的ast的WLE通常是可治愈的,在儿科病例中具有良好的长期生存率和接近零的死亡率。病例:一名12岁的男孩向他们的儿科医生提出了一个良好的儿童检查,没有相关症状。检查发现一个5 × 4毫米的椭圆形凸起的红色丘疹,伴有不对称的棕色/黑色变色。他被转到皮肤科做评估。5个月后,病变扩大到11 x 6毫米,覆盖粉红色/黑色外壳。刮胡子活检显示非典型的spitzo样黑色素细胞增生,但没有明显的PRAME或BRAF染色。进一步评估时,ALK染色未显示黑色素细胞。这些免疫组化结果与非典型Spitz肿瘤最一致。行5 mm边缘WLE,边缘未见残余黑素细胞增生。结论:本病例突出了ast在儿科患者的临床、诊断和管理方面的挑战。虽然恶性的可能性是不确定的,但在WLE后,ast通常有良好的预后和阴性的边缘。在本例中,PRAME和BRAF的IHC染色有助于支持推迟SNL活检的决定。这个病例强调了形态学和分子分析对评估风险和指导管理的重要性。对分子生物标志物的进一步研究可能会改善儿科ast患者的风险分层和优化治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atypical Spitz Tumor in a Pediatric Patient: A Case Report.

Introduction: Spitzoid neoplasms are a collection of melanocytic lesions distinguished from conventional nevi or melanoma by a unique set of histological and molecular features. These spitzoid proliferations - Spitz nevi, spitzoid melanocytoma, atypical Spitz tumors (ASTs), and spitzoid melanoma - range from benign to malignant. Morphology alone has been an insufficient prognostic tool, but immunohistochemical (IHC) stains prove useful for risk stratification. ASTs rarely metastasize beyond regional lymph nodes and treatment includes wide local excision (WLE) with or without sentinel lymph node (SNL) biopsy depending on histomolecular features. WLE of ASTs with negative margins is typically curative with excellent long-term survival and mortality rates close to zero in pediatric cases.

Case: A 12-year-old male presented to their pediatrician for a well child check without pertinent symptoms. Examination revealed a 5 x 4 mm elliptical, raised, red papule with asymmetric brown/black discoloration. He was referred to dermatology for evaluation. Five months later the lesion had grown to 11 x 6 mm covered with a pink/black crust. A shave biopsy displayed atypical spitzoid melanocytic proliferation but lacked significant staining with PRAME or BRAF. An ALK stain did not highlight the melanocytes upon further evaluation. These IHC findings are most consistent with an atypical Spitz tumor. A WLE with 5 mm margins was performed and margins revealed no residual melanocytic proliferation.

Conclusion: This case highlights the clinical, diagnostic, and management challenges of ASTs in pediatric patients. Although malignant potential is uncertain, ASTs often have an excellent prognosis with negative margins following WLE. In this case, IHC staining for PRAME and BRAF helped support the decision to defer SNL biopsy. This case underscores the importance of morphologic and molecular analysis to assess risk and guide management. Further research into molecular biomarkers may improve risk stratification and optimize treatment strategies for ASTs in pediatric patients.

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