Introduction: The syringomyelia is a condition characterized by a fusiform cavity filled with fluid inside
the spinal cord¹ that can even spread to other parts of the nervous system. Among the most common
symptoms is the loss of temperature and pain sensibility (mainly in the upper limbs)¹ without loss of
mechanical sensibility, besides other symptoms, as paresis and paresthesia, which depends of the cavity
spreading. Referring to its etiology, it can be primary (congenital conditions, as malformations) or
secondary (acquired conditions, as tumors or trauma). The treatment is surgical and consists of spinal
cord decompression in order to reduce the symptoms.
Case report: Female patient, 31 years old, was admitted to the emergency referring difficulty to walk,
lower limbs paresis, posteriorly upper limbs paresis, dysphonia, dysphagia and muscle pain. The physical
examination shown lesions in the left upper limb and hands muscles atrophy. The neurologic examination
identified dysarthria, impairment of the cranial nerves V (hypoesthesia in the right face), IX, X (deviation
of the uvula to the left) and XII (deviation in the left side of the tongue), upper and lower limbs paresis,
decrease in mechanical and pain sensibility in upper limbs, hyporeflexia in upper limbs and hyperreflexia
in lower limbs. The magnetic resonance imaging shown extend syringomyelia affecting the thoracic spinal
cord (images 1 and 2) and the cervical spinal cord, with small component to the medulla Discussion: The reported case presents the classic symptoms of a cervical syringomyelia: loss of
temperature and pain sensibility without loss of mechanical sensibility (in this case, the patient presents
loss of mechanical sensibility because of the extensive impairment of the cervical spinal cord). It leads to
classic conditions, as the lesions in the upper limbs, caused by the loss of some sensibility components.
The medulla and lower spinal cord impairment are the responsible for the additional symptoms, as paresis
and paresthesia, damage to cranial nerves and even the lower limbs hyperreflexia (upper neuron
syndrome) and upper limbs hyporeflexia (lower neuron syndrome).
Conclusion: Considering the extension of the cavity, since the inferior portion of the medulla until the
thoracic spinal cord, the reported case is even more complex than a cervical syringomyelia case. Thus, the
patient presents the classic and non-classic symptoms. Considering this, it is important to report and to
know more about the subject, in order to get more specific diagnostics in these cases.

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ROBBINS & COTRAN. Patologia: bases patológicas das doenças. 8 ed. Rio de Janeiro: Elservier, 2010.

GONIK, Renato et al. Siringomielia: revisão da literatura e relato de caso; Arquivo de Neuropsiquiatria.

São Paulo, 48(3): 376-384, 1990.

WILLIAMS, Bernard. On the pathogenesis of syringomyelia: a review. Journal of the Royal Society of

Medicine. Smethwick, v. 73. November 1980.

SILVA, José A. G. et al. Posterior fossa descompression with tonsillectomy in 104 cases of basilar

impression, Chiari malformation and/or syringomyelia. Arq Neuropsiquiatr. São Paulo, 69(5): 817-823,


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