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伴有神经内分泌分化的恶性黑色素瘤:一例报告及文献综述

Malignant Melanoma With Neuroendocrine Differentiation: A Case Report and Literature Review.

作者信息

Cham Jason, Shavit Ayal, Ebrahimi Aren, Viray Miguel, Gibbs Paul, Bhangoo Munveer S

机构信息

Department of Internal Medicine, Scripps Clinic/Scripps Green Hospital, La Jolla, CA, United States.

Department of Pathology, Scripps Clinic/Scripps Memorial Hospital, Encinitas, Encinitas, CA, United States.

出版信息

Front Oncol. 2021 Dec 1;11:763992. doi: 10.3389/fonc.2021.763992. eCollection 2021.

Abstract

BACKGROUND

Melanoma has a wide range of histologic variants and cytomorphologic features that make its diagnosis challenging. Melanoma can also rarely have neuroendocrine markers adding further diagnostic uncertainty particularly given that unrelated tumor types, such as prostate cancer, can also display focal neuroendocrine differentiations.

CASE PRESENTATION

Our patient is a 74-year-old Caucasian man found to have a lung mass. Initial biopsy revealed typical microscopic morphology and neuroendocrine differentiation consistent with small cell carcinoma. Despite standard chemoradiation treatment, the patient continued to progress with new metastasis in the brain, liver and bone. Subsequent chest wall biopsy revealed golden-brown pigment associated with melanin. Further tumor immunohistochemistry revealed extensive neuroendocrine differentiation with CD56, synaptophysin, and INSM1, as well as strong immunoreactivity for melanocyte markers including SOX10, S100, PRAME, and MITF, consistent with metastatic melanoma with neuroendocrine differentiation. Genomic testing revealed increased tumor mutational burden and alterations in NF1, BRAF, CDKN2A/B, TERT. The patient was transitioned to checkpoint inhibitor therapy with nivolumab and ipilimumab and had resolution of his intracranial mass and decrease in size of other metastatic lesions.

CONCLUSION

Often the combination of anatomic findings such as a lung mass, typical microscopic morphology, and confirmation of neuroendocrine differentiation correctly identifies a patient with small cell carcinoma. However, in a patient who fails to respond to treatment, a broader immunohistochemical workup along with molecular testing with additional tissue may be warranted.

摘要

背景

黑色素瘤具有广泛的组织学变异和细胞形态学特征,这使其诊断具有挑战性。黑色素瘤也很少会有神经内分泌标志物,这进一步增加了诊断的不确定性,特别是考虑到前列腺癌等不相关的肿瘤类型也可表现出局灶性神经内分泌分化。

病例介绍

我们的患者是一名74岁的白种男性,发现有肺部肿块。最初的活检显示典型的微观形态和与小细胞癌一致的神经内分泌分化。尽管进行了标准的放化疗,但患者仍出现进展,脑、肝和骨出现新的转移灶。随后的胸壁活检显示有与黑色素相关的金棕色色素。进一步的肿瘤免疫组化显示广泛的神经内分泌分化,表达CD56、突触素和INSM1,以及对包括SOX10、S100、PRAME和MITF在内的黑素细胞标志物有强免疫反应性,符合伴有神经内分泌分化的转移性黑色素瘤。基因检测显示肿瘤突变负荷增加以及NF1、BRAF、CDKN2A/B、TERT发生改变。患者转而接受纳武单抗和伊匹单抗的检查点抑制剂治疗,颅内肿块消退,其他转移灶缩小。

结论

通常,诸如肺部肿块等解剖学发现、典型的微观形态以及神经内分泌分化的确认相结合,能够正确识别小细胞癌患者。然而,对于治疗无反应的患者,可能需要进行更广泛的免疫组化检查以及对额外组织进行分子检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/990e/8671631/3aeeca1ed772/fonc-11-763992-g001.jpg

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