Cargando…
Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature
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 misdiagnose...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034675/ https://www.ncbi.nlm.nih.gov/pubmed/32080099 http://dx.doi.org/10.1097/MD.0000000000019178 |
_version_ | 1783499920285630464 |
---|---|
author | Xu, Xinke Zheng, Yaqi Li, Junliang Wang, Fenghua Li, Fangcheng |
author_facet | Xu, Xinke Zheng, Yaqi Li, Junliang Wang, Fenghua Li, Fangcheng |
author_sort | Xu, Xinke |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7034675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-70346752020-03-10 Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature Xu, Xinke Zheng, Yaqi Li, Junliang Wang, Fenghua Li, Fangcheng Medicine (Baltimore) 6200 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. Wolters Kluwer Health 2020-02-21 /pmc/articles/PMC7034675/ /pubmed/32080099 http://dx.doi.org/10.1097/MD.0000000000019178 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 6200 Xu, Xinke Zheng, Yaqi Li, Junliang Wang, Fenghua Li, Fangcheng Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature |
title | Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature |
title_full | Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature |
title_fullStr | Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature |
title_full_unstemmed | Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature |
title_short | Pediatric primary diffuse leptomeningeal melanomatosis: Case report and review of the literature |
title_sort | pediatric primary diffuse leptomeningeal melanomatosis: case report and review of the literature |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034675/ https://www.ncbi.nlm.nih.gov/pubmed/32080099 http://dx.doi.org/10.1097/MD.0000000000019178 |
work_keys_str_mv | AT xuxinke pediatricprimarydiffuseleptomeningealmelanomatosiscasereportandreviewoftheliterature AT zhengyaqi pediatricprimarydiffuseleptomeningealmelanomatosiscasereportandreviewoftheliterature AT lijunliang pediatricprimarydiffuseleptomeningealmelanomatosiscasereportandreviewoftheliterature AT wangfenghua pediatricprimarydiffuseleptomeningealmelanomatosiscasereportandreviewoftheliterature AT lifangcheng pediatricprimarydiffuseleptomeningealmelanomatosiscasereportandreviewoftheliterature |