Chiari malformation type 1 presenting as unilateral progressive foot drop: a case report and review of literature

Foot drop is a disabling neurological condition which requires careful evaluation to identify the cause. Differential diagnosis for foot drop is broad however, mostly involve disorders of the peripheral nervous system. Here, we present an extremely rare central cause of foot drop in a child, which if not recognized early, could lead to multiple complications.

A 6-year-old girl presented with progressively worsening difficulty in walking and left sided foot droop for1-monthduration. There was no pain, paresthesia or sensory symptoms in limbs and she did not complain of headache or backache. There was no history of trauma. She is the second child of non-consanguineous parents and had an uncomplicated birth and perinatal period. She was apparently well except for frequently relapsing nephrotic syndrome for which she was on 5 mg of prednisolone and 60 mg of levimasole on alternative days. Her last (fourth) relapse was six months ago.

On examination she was averagely built for her age. Nervous system examination revealed wasting of anterior compartment of the left leg and reduced muscle power in distal muscle groups on the left side - 0/5 in dorsiflexors and 3/5 in plantar flexors. Muscle power in proximal muscles of the left lower limb, all muscle groups in the right lower limb and both upper limbs were normal (5/5). Left knee jerk was diminished and left ankle jerk and left plantar response were absent. Sensory loss was noted in L4 and L5 dermatomes on the left side. Superficial abdominal reflex was present on the right side however was absent on the left side which pointed towards a central cause for foot drop. All other systems including blood pressure were clinically normal.

Basic investigation including full blood count, erythrocyte sedimentation rate and C-reactive protein were unremarkable and rheumatoid factor and antinuclear antibodies were negative. Nerve conduction studies revealed normal distal amplitude, latency and velocities in common fibular nerve (tested at extensor digitorum brevis) in the left (amplitude 3.3 mV; latency 2.8 ms; velocity 59 m/s) and right (amplitude 2.9 mV; latency 3.1 ms) sides and tibial nerve (tested at abductor hallucis)in the left side(amplitude 20.8 mV; latency 4.2 ms). Sural nerve sensory response was normal. Electromyography (EMG) at left tibialis anterior revealed fibrillations and scanty motor unit potentials (MUP). EMG of left medial gastrocnemius and right tibialis anterior were normal. These results suggested prompt imaging of the spine. MRI of the lumbosacral spine was arranged and was later expanded to whole spine and brain. This revealed a holocord syrinx extending from the cervicomedullary junction to conus medullaris (Fig. 1A and B) and Chiari malformation type 1 without bony deformities (Fig. 2).

The patient was referred to the neuro-surgical team and is awaiting surgery which will include suboccipital craniectomy, C1 laminectomy and duroplasty decompressing foramen magnum. Neuro-rehabilitation was commenced and an ankle foot orthosis was offered for the foot drop.

Identification of the exact cause is the most important component of the management of foot drop. Causes are diverse, consists of a broad range of pathologies however, lesions in the peripheral nervous system which include, common peroneal neuropathy, L5 radiculopathy, lumbosacral plexopathy, hereditary neuropathies, mononeuritis multiplex and anterior horn cell diseases predominate. Rarely, central lesions including brain tumours and tuberculomas can cause foot drop. In this report we have described an extremely rare presentation of a central lesion-Chiari malformation type 1- presenting as unilateral foot drop.

Chiari malformations refer to a spectrum of congenital hind brain abnormalities affecting structural relationships between the cerebellum, brain stem, the upper cervical cord and the bony cranial base [1]. Chiari malformation type 1 is the most common form which usually presents with recurrent headache, neck pain, urinary frequency, and progressive lower-extremity spasticity during adolescence or adulthood. It is characterized by displacement of cerebellar tonsils below the level of the foramen magnum which results in impaction of the foramen magnum, compression of the cervicomedullary junction by the herniating tonsils and interruption of the cerebrospinal fluid (CSF) through the region [2, 3]. Disordered CSF flow may result in syringomyelia which usually presents with ‘central cord symptoms’ - numbness followed by the development of atrophy and weakness in the upper extremities. It can have a combination of upper motor and lower motor neuron lesion feature [4, 5].

Our patient did not demonstrate any of the usual presenting symptoms or signs of Chiari malformation type 1 or syringomyelia. Instead, the only presenting clinical features were abnormality in gait and progressive unilateral foot drop. The initial clinical examination and nerve conduction test suggested a lumbar spine pathology however ipsilateral absence of superficial abdominal reflexes suggested a lesion at the thoracic level or above. MRI scan revealed the diagnosis of holocord syrinx with underlying Chiari malformation type 1.

Chiari malformation type 1 and associated holocord syrinx presenting as foot drop is extremely rare and only few case reports are found in the literature (Table 1). The limited number of patients who had presented with foot drop demonstrates variable physical signs and has marked diversity in neurophysiological abnormalities suggesting variable sites of involvement.

Early diagnosis of Chiari malformation type-1 is pivotal as prognosis after the surgery depends on the extent of the neurological deficit prior to the surgery. Our patient is awaiting surgery and has an excellent prognosis [6, 7]. In conclusion, this case highlights the importance of considering broad differential diagnosis for foot drop and value of the complete neurological examination including superficial reflexes in arriving at a diagnosis.