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原发性恶性黑色素瘤,颈椎内不典型表现:病例报告。

Primary malignant melanoma, an atypical presentation in the cervical spine: a case report.

机构信息

Department of Surgery, Neurosurgery, College of Medicine, Makerere University, Kampala, Uganda.

Faculty of Medicine, Université Catholique du Graben, Butembo, Democratic Republic of the Congo.

出版信息

J Med Case Rep. 2023 Dec 17;17(1):548. doi: 10.1186/s13256-023-04290-5.

Abstract

BACKGROUND

Few studies have documented the occurrence of melanoma in the cervical spine. Of all malignant melanoma cases, 1% are primary melanoma of the central nervous system, which makes it extremely uncommon and nonspecific. We aim to report a case of the uncommon presentation of primary melanoma in the cervical spine.

CASE PRESENTATION

The patient was a 59-year-old Muganda male who presented with a 2-year history of anterior neck swelling as well as severe pain and a tingling sensation in the left shoulder and arm, which worsened in the recent 6 months. He developed weakness and paresthesia in the upper left arm and progressive gait disturbance of the left leg. A physical examination revealed masses in the left cervical and right submandibular region. Additionally, the upper and lower left extremities revealed hemiparesis and hemihypoesthesia. A magnetic resonance imaging scan showed a hyperintense lesion on TIWI and another hypointense lesion on T2WI, originating from the cervical spine and involving the vertebral bodies and paravertebral soft tissues. The patient underwent surgery, a black tumor was extracted, and histology revealed the tumor to be malignant melanoma. The patient died within 1 month after the diagnosis and surgery.

CONCLUSION

This case is presented to highlight the significance and challenges associated with making a pre- and postoperative diagnosis of primary cervical melanoma with atypical radiological characteristics. Patients with extradural lesions that show hyperintensity on T1-weighted images and hypointensity on T2-weighted images should have spinal melanoma examined as a possible differential diagnosis.

摘要

背景

鲜有研究记录过颈椎黑色素瘤的发病情况。在所有恶性黑色素瘤病例中,有 1%为中枢神经系统原发性黑色素瘤,这使其极其罕见且无特异性。我们旨在报告一例颈椎原发性黑色素瘤的罕见表现病例。

病例介绍

患者为 59 岁男性,Muganda 族,2 年前出现颈前肿块,伴有左侧肩部和手臂剧烈疼痛及刺痛感,近 6 个月来症状加重。他出现左上臂无力和感觉异常,并逐渐出现左下肢步态不稳。体格检查发现左侧颈部和右侧颌下区有肿块。此外,上下肢左侧偏瘫和感觉减退。磁共振成像扫描显示 T1WI 上呈高信号病变,T2WI 上呈另一个低信号病变,源于颈椎并累及椎体和椎旁软组织。患者接受了手术,切除了一个黑色肿瘤,组织学显示为恶性黑色素瘤。诊断和手术后 1 个月内患者死亡。

结论

本病例旨在强调对具有非典型影像学特征的原发性颈椎黑色素瘤进行术前和术后诊断的重要性和挑战。对于 T1 加权图像上呈高信号、T2 加权图像上呈低信号的硬膜外病变患者,应将脊髓黑色素瘤作为可能的鉴别诊断进行检查。

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