2018, Number 3
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Rev Clin Esc Med 2018; 8 (3)
Síndrome de HaNDL: cefalea con pleocitosis linfocitaria
Porras MK, García BR, Zúñiga SR, Pérez R
Language: Spanish
References: 14
Page: 1-6
PDF size: 277.94 Kb.
ABSTRACT
A male of 32 years, without any previous diagnosed
disease, asked for attention at the Emergency Room
because of headache. In addition, he had visual aura,
numbness of both arms, and a cerebrospinal fluid
analysis that showed: intracranial hypertension
and lymphocytic pleocystosis. Additional studies
were performed in order to exclude: structural,
vascular, inflammatory, infectious causes. He
received symptomatic treatment, showing clinical
and cerebrospinal fluid analysis showing resolution.
Therefore, in retrospective HaNDL syndrome is
diagnosed.
This entity is uncommon or underdiagnosed,
meanwhile, it has a good prognosis in comparison
with its differential diagnosis. An appropriate
comprehension and identification of it would avoid
iatrogenic lesions.
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