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Results:

Patient demonstrated functional improvements with inten-

sive therapies, and required less assistance in ambulation and activ-

ities of daily living. Environmental adjustments to therapies were

required, including working in smaller gym with fewer people and

distractions as patient expressed fear of falling during ambulation and

felt more secure with familiar therapists in smaller group settings.

Another barrier faced involved behavior as patient at times was un-

willing to give maximal effort in therapies and expressed desires to be

home. Limitations to other distractions such as phone usage were

required for complete participation in therapies; parents of patient

were supportive in this.

Discussion:

Patients with Down Syndrome are more susceptible to

immunologic diseases including autoimmune endocrinopathies, type 1

diabetes mellitus, and acute lymphoblastic leukemia. It has been

speculated this is due to genes on the trisomic chromosome 21. This is

the first documented case of polyneuropathy with a possible auto-

immune etiology.

Conclusions:

Down Syndrome may predispose patients to autoimmune

polyneuropathy. These patients benefit from modified inpatient

rehabilitation to account for intellectual disability and behavioral

challenges.

Level of Evidence:

Level V

Poster 366:

Acute Disseminated Encephalomyelitis Mimicking

Cocaine Induced Cerebral Ischemia

Wade O. Johnson, DO (NY Presby Hosp/Columbia/Cornell, New York,

NY, United States), Danielle Bousquet, PT, Emily Lyons, MS OTR/L,

Chichang David Lin, MD

Disclosures:

Wade Johnson: I Have No Relevant Financial Relation-

ships To Disclose

Case/Program Description:

Acute disseminated encephalomyelitis

(ADEM) is a rare condition most commonly seen in children that is

often preceded by a viral or bacterial infection. Common presenting

symptoms include headache, fever, altered mental status, motor and

sensory deficits, and oculomotor deficits.

Setting:

Inpatient Rehabilitation Unit.

Results:

A 52-year-old man presented to acute care hospital with

complaints of dizziness, diplopia, and imbalance with multiple falls

for 1 week. During admission, symptoms progressed prompting MRI

revealing multifocal regions of patchy T2 hyperintensity consistent

ischemic foci prompting diagnosis of stroke in setting of cocaine use

and hypertension. Patient was admitted to acute rehabilitation with

functional level of total assist for all ADLs and ambulation, and

remained at those functional levels despite treatment with anti-

platelet and conventional stroke rehabilitative therapies. On day

29, patient developed acute flaccid paralysis of LUE. Repeat MRI

revealed progression of T2 hyperintensities throughout the brain, as

well as edge enhancing lesions consistent with active demyelin-

ation. Patient was managed with IV steroid, followed by oral steroid

taper with rapid improvement in clinical status. Workup also

revealed urinary tract infection which was successfully treated with

IV and oral antibiotics.

Discussion:

Patient’s presenting symptoms, and risk factors of prior

cocaine use and hypertension led to initial diagnosis of stroke during

acute hospitalization. Episode of acute left arm weakness is being

attributed to development of UTI which prompted further workup

allowing new diagnosis of ADEM. Upon receiving treatment for ADEM,

patient showed rapid improvement clinically, and eventually func-

tionally with targeted therapy.

Conclusions:

Multifocal hyper-intensities on neuroimaging, as seen in

cocaine induced vasculitis may appear ischemic, but share many

similarities to demyelinating disease. While rare, it is important to

consider a demyelinating process such as ADEM in young patients with

presumptive diagnosis of stroke displaying waxing and waning neuro-

logical signs and making minimal functional gains in acute

rehabilitation.

Level of Evidence:

Level V

Poster 367:

A Rare Case of Acute Disseminated Encephalomyelitis

(ADEM) in an Adult Patient with Cystic Fibrosis: A

Case Report

Simon M. Willis, MD (WA Hosp Cntr/Georgetown Univ, Washington,

District of Columbia, United States), Michele Anderson, BSc,

Camilo Castillo, MD

Disclosures:

Simon Willis: I Have No Relevant Financial Relationships

To Disclose

Case/Program Description:

A 26-year-old man with a history of cystic

fibrosis who developed acute back pain with leg numbness and

weakness presented with an inability to stand or ambulate after res-

olution of fever and cough with antibiotic treatment.

Setting:

Inpatient academic center.

Results:

At an outside hospital a lumbar puncture was performed

showing cerebrospinal fluid with 1500 red blood cells, 1071 white

blood cells, glucose of 54, protein of 188, and negative cultures.

Magnetic resonance imaging (MRI) revealed symmetrical abnormal

central cord signal after which he was transferred to the university

hospital for management of presumed ADEM. Upon transfer he was

placed on decadron and broad-spectrum antibiotics. Seven treat-

ments of plasmapheresis were completed with minimal improve-

ment of lower extremity mobility, however repeat MRI

demonstrated an interval resolution of hyperintense cord signals

from his brain down to the T1 level. He was admitted to our

inpatient spinal cord injury unit with an L1 ASIA C equivalent level

of insult. Upon discharge from acute inpatient rehabilitation he

was walking more than 30 feet with a rolling walker with minimal

to moderate assistance.

Discussion:

ADEM is a rare demyelinating condition that predomi-

nantly affects the white matter of the brain and spinal cord. It is

usually immune mediated and generally provoked by an identifiable

febrile prodromal illness, commonly a viral infection. More than 80% of

cases occur in children less than 10 years of age with less than 3%

occurring in adulthood. Patients with cystic fibrosis have an increased

likelihood of contracting both viral and bacterial infections increasing

their risk of developing ADEM.

Conclusions:

Patients with cystic fibrosis with acute development of

polyfocal neurologic deficits require prompt neurologic assessment

and screening for acute demyelinating syndromes with a high suspicion

reserved for ADEM. Although most recover completely, patients should

be followed linearly as some may develop secondary pathological

residua.

Level of Evidence:

Level V

Poster 368:

Retroperitoneal Hematoma Causing Right Hip Pain

Status Post Recombinant Tissue Plasminogen

Activator (rt-PA) Administration for Acute Ischemic

Stroke: A Case Report

Simon M. Willis, MD (WA Hosp Cntr/Georgetown Univ, Washington,

District of Columbia, United States), Rachna Malhotra, DO

Disclosures:

Simon Willis: I Have No Relevant Financial Relationships

To Disclose

Case/Program Description:

A 66-year-old woman who received re-

combinant tissue plasminogen activator (rt-PA) administration after a

S248

Abstracts / PM R 9 (2017) S131-S290