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小儿原发性弥漫性软脑膜黑色素瘤病:病例报告及文献复习

Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature.

作者信息

Xu Xinke, Zheng Yaqi, Li Junliang, Wang Fenghua, Li Fangcheng

机构信息

Department of Neurosurgery.

Department of Operating Room.

出版信息

Medicine (Baltimore). 2020 Feb;99(8):e19178. doi: 10.1097/MD.0000000000019178.

Abstract

RATIONALE

Primary melanocytic tumors of central nerve system (CNS) are rare, primary diffuse leptomeningeal melanomatosis (PDLM), a subtype of malignant melanomas of CNS, is extremely rare,especially in pediatrics. As the clinical manifestation of PDLM is not characteristic, It is often misdiagnosed as tubercular meningitis and hemorrhage.

PATIENT CONCERNS

A 13-year-old boy was admitted to our department with symptoms of recurrent headache and vomiting twice. As the brain imaging revealed a lesion located in the left temporal lobe mimicked hemorrhage, so there was a misdiagnosis of hemorrhage in first hospitalization. He was admitted again for the recurrence of the headache and vomiting. Detailed physical examination showed multiple melanin changes in the skin of the whole body which were ignored in last hospitalization. Brain imaging showed the significantly enlarged lesion in the left temporal lobe and several smaller lesions in the left parietal lobe and cerebellum which indicated metastasis.

DIAGNOSIS

According to the history,physical examination and the radiological finding, the patient was diagnosed with malignant melanoma of central never system possibly.

INTERVENTIONS

The patient underwent left temporal and parietal lesions total resection with a craniotomy.

OUTCOMES

The diagnosis of PDLM was established according to pathological characteristics and the negative finding of positron emission tomography (PET)-computed tomography (CT) outside CNS. The patient got no further treatment for economic reasons and experienced the progression and died 5 months after operation.

LESSONS

PDLM is extremely rare in CNS, as the clinical manifestation, radiological changes are not special, early diagnosis is difficult. The confirmed diagnosis is established by leptomeningeal biospy or surgical tissue. PET-CT can help differential diagnosis with metastastic leptomeningeal melanomas. The prognosis is dismal due to the inefficiency of chemotherapy or radiotherapy.

摘要

理论依据

中枢神经系统(CNS)原发性黑素细胞肿瘤较为罕见,原发性弥漫性软脑膜黑素瘤病(PDLM)是CNS恶性黑色素瘤的一种亚型,极为罕见,尤其是在儿科患者中。由于PDLM的临床表现不具有特异性,常被误诊为结核性脑膜炎和出血。

患者情况

一名13岁男孩因反复头痛、呕吐两次入院。脑部影像学检查显示左颞叶有一类似出血的病变,因此首次住院时被误诊为出血。因头痛和呕吐复发再次入院。详细体格检查发现全身皮肤有多处黑色素沉着改变,上次住院时被忽略。脑部影像学检查显示左颞叶病变明显增大,左顶叶和小脑有几个较小病变,提示转移。

诊断

根据病史、体格检查和影像学检查结果,患者可能被诊断为中枢神经系统恶性黑色素瘤。

干预措施

患者接受了开颅手术,切除左颞叶和顶叶病变。

结果

根据病理特征及中枢神经系统外正电子发射断层扫描(PET)-计算机断层扫描(CT)检查结果阴性,确诊为PDLM。患者因经济原因未接受进一步治疗,术后5个月病情进展死亡。

经验教训

PDLM在中枢神经系统中极为罕见,由于临床表现和影像学改变不具有特异性,早期诊断困难。确诊需依靠软脑膜活检或手术组织病理检查。PET-CT有助于与转移性软脑膜黑色素瘤进行鉴别诊断。由于化疗或放疗效果不佳,预后较差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c5a/7034675/e6ea43b30765/medi-99-e19178-g001.jpg

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