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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
Full text How to cite this article

Language: Spanish
References: 14
Page: 1-6
PDF size: 277.94 Kb.


Key words:

HaNDL, migraine, headache, lymphocytic pleocytosis.

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.


REFERENCES

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Rev Clin Esc Med. 2018;8