Is congenital melanocytic naevus a link between Hirayama disease and moyamoya pattern: a new syndrome or a co-incidence?
BMJ Case Rep
; 20162016 Jan 08.
Article
em En
| MEDLINE
| ID: mdl-26746830
A 22-year-old man presented with a history of progressive weakness and wasting of the right hand and forearm for 12â
months followed by similar symptoms in the left upper limb for the past 5â
months. He also gave a history of episodes of loss of consciousness for the past 5â
years with a frequency of one per 3â
months. On examination, there were melanocytic naevi-one large lesion in the nape of the neck and multiple satellite lesions. On investigation, the cervical cord MRI was normal. The brain MRI and angiography showed a moyamoya pattern. Thus, this patient had congenital melanocytic naevi with Hirayama disease and moyamoya pattern. He was treated with extracranial-intracranial bypass for moyamoya disease. During 6-month follow-up, he has been stable. Although moyamoya syndrome has been associated with several systemic diseases and conditions, the coexistence of a moyamoya pattern with Hirayama disease and melanocytic naevi has not been described so far.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Atrofias Musculares Espinais da Infância
/
Doença de Moyamoya
/
Nevo Pigmentado
Tipo de estudo:
Etiology_studies
/
Incidence_studies
/
Risk_factors_studies
Limite:
Adult
/
Humans
/
Male
Idioma:
En
Ano de publicação:
2016
Tipo de documento:
Article