Department of Neurology, King Fahad Hospital of the University, Imam Abdulrahman Bin Faisal University, Damman, Saudi Arabia
*Corresponding Author’s e-mail: danah.aljaafari@gmail.com

 طور متعلق ابخلزل السفلي يف ُمَتاَلزَِمُة غيَّان-ابريه يف غضون األربعة
وعشرين ساعة األوىل ما بعد الوالدة

تقرير حالة

دانة اجلعفري و نعمان ا�سحاق

abstract: Guillain-Barré syndrome (GBS) is a heterogeneous disorder with a diverse clinical presentation 
ranging from weakness of certain body regions to tetraparesis with autonomic dysfunction and respiratory failure. 
Paraparetic GBS is a variant of GBS which is characterised by weakness limited to the lower limbs only. It is crucial to 
identify such topographical presentations, as a delay in diagnosis can lead to delayed initiation of specific treatment, 
which can negatively impact the outcome. We report a 29-year-old female patient who presented to the King Fahd 
Hospital of the University, Al Khobar, Saudi Arabia, in 2017 with rapid onset asymmetrical weakness of lower 
extremities associated with bladder dysfunction during the immediate postpartum period. The weakness spared 
cranial nerves and arms and imaging studies of the spine was unremarkable. Cerebrospinal fluid investigations 
showed cyto-albuminologic dissociation and nerve conduction studies showed features of demyelination. The 
patient was diagnosed with a paraparetic variant of GBS and treated with intravenous immunoglobulin. She had 
almost recovered completely at the two–month follow-up.

Keywords: Paraparesis; Guillain-Barré Syndrome; Demyelination; Postpartum Period; Case Report; Saudi Arabia.

امللخ�ص: ُمَتاَلِزَمُة غيَّان-باريه هي ا�سطراب متغاير املن�ساأ، ويجيء ب�سور �رسيرية متنوعة، ترتاوح بني �سعف يف اأجزاء معينة من اجل�سم اإىل 
خزل رباعي يرتافق مع خلل وظيفي اتونومي )م�ستقل( وف�سل تنف�سي. وُيعد اخلزل ال�سفلي طورا من اأطوار ُمَتاَلِزَمة غيَّان-باريه يت�سف ب�سعف 
يقت�رس على الطرفني ال�سفليني فقط. ومن املهم اال�ستعراف على مظاهره الطبوغرافية، اإذ اأن التاأخري يف الت�سخي�ص قد يف�سي اإىل تاأخري يف بدء 
العالج املحدد، وهذا من �ساأنه اأن يوؤثر على النتيجة. ويف هذا التقرير نقدم حالة مري�سة عمرها 29 عاما جاءت مل�ست�سفى امللك فهد بجامعة 
اخلرب يف اململكة العربية ال�سعودية يف عام 2017م وهي ت�سكو من �سعف ع�سلي المتناظر يف طرفيها ال�سفليني حدث �رسيعا مرتافقا مع 
اختالل يف وظيفة املثانة يف غ�سون الفرتة التالية مبا�رسة للو�سع. ومل يحدث ذلك ال�سعف يف االأع�ساب القحفية وال يف اليدين، وال يف العمود 
الفقري )حيث اأظهرت الت�سوير اال�سعاعي �سالمته(. واأظهر فح�ص ال�سائل الدماغي النخاعي تفارقا خلويا البيوميني املن�ساأ. واأثبتت درا�سات 
التو�سيل الع�سبي بع�ص مظاهر زوال امليالني. ومت ت�سخي�ص حالة املري�سة على اأنها طور متعلق باخلزل ال�سفلي يف ُمَتاَلِزَمة غيَّان- باريه، 

وعوجلت باحلق الوريدي بغلوبيولني مناعي. و�سفيت املري�سة ب�سورة �سبه كاملة عند فح�سها بعد �سهرين من العالج.
الكلمات املفتاحية: اخلزل ال�سفلي؛ ُمَتاَلِزَمة غيَّان-باريه؛ زوال امليالني؛ الفرتة التالية للو�سع؛ تقرير حالة؛ اململكة العربية ال�سعودية.

Paraparetic Variant of Guillain-Barré Syndrome in 
First 24 Hours of Postpartum Period

A case report
*Danah Aljaafari and Noman Ishaque

Sultan Qaboos University Med J, May 2020, Vol. 20, Iss. 2, pp. e227–230, Epub. 28 Jun 20
Submitted 19 Sep 19
Revisions Req. 19 Nov & 30 Dec 19; Revisions Recd. 8 Dec 19 & 2 Jan 20
Accepted 19 Jan 20

acute ataxic variant, facial diplegia with paraesthesic 
variant, acute pandysautonomia and the paraparetic 
variant of GBS.3–7 

This report describes a case of rapid onset 
asymmetric paraparesis with predominant involve- 
ment of distal muscles with areflexia during the 
immediate postpartum period after complete recovery 
from epidural anaesthesia. This case highlights the 
importance of considering paraparetic variant of GBS 
when a patient complains of paraparesis. Failure to do 
so can lead to delay in diagnosis and consequent delay 
in initiation of specific treatment that can negatively 
impact outcome. 

Guillain-barré syndrome (gbs) is an acute polyradiculoneuropathy characterised by flaccid weakness associated with decreased 
reflexes and cytoalbuminologic dissociation in the 
cerebrospinal fluid (CSF).1 It is a heterogeneous dis- 
order with diverse clinical presentation ranging from 
weakness limited to certain regions of the body to 
tetraparesis with autonomic dysfunction and respiratory 
failure.2 Symptoms that are restricted to certain body 
parts are termed ‘GBS variants’ or ‘topographical 
variants’. These include Miller Fisher syndrome, 
Bickerstaff brainstem encephalitis, pharyngeal cervical 
brachial variant, multiple cranial neuropathy variant, 

This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License.

https://doi.org/10.18295/squmj.2020.20.02.015

case report

https://creativecommons.org/licenses/by-nd/4.0/


Paraparetic Variant of Guillain-Barré Syndrome in First 24 Hours of Postpartum Period 
A case report

e228 | SQU Medical Journal, May 2020, Volume 20, Issue 2

Case Report

A 29-year-old female patient presented to the King 
Fahd Hospital of the University, Al Khobar, Saudi 
Arabia, in 2017 with weakness in her lower extremities. 
She had no known chronic illnesses and was admitted 
to the hospital for delivery at 38 weeks of pregnancy. 
She had a history of two Caesarean sections and had 
given birth to a total of three children. Her family 
history was unremarkable and she did not have any 
allergies. At the time of admission, she was taking 
multivitamins. Her routine blood workup at the time 
of admission was within normal limits. She delivered 
a healthy baby girl through an uneventful Caesarean 
section under epidural anaesthesia, which was given at 
lumbar (L) 4/L5 level using 10 mg of bupivicaine (0.3%) 
and 2.5 mL of fentanyl. Her post-delivery recovery was 

uneventful and she regained full strength of her lower 
extremities as well as bladder function. The following 
morning, she complained of weakness in her lower 
extremities. The weakness started from her feet and 
worsened over time. Within a few hours, the weakness 
had progressed to the extent that she was not able to 
stand or walk unaided. It was associated with urinary 
retention. There was no fever or pain in the back or 
lower extremities and her arms were also unaffected. 
She had had an upper respiratory tract infection one 
week prior to admission. However, there was no 
history of recent immunisation or gastrointestinal 
infection. 

Upon physical examination, she was found to 
have a good build and was able to lie comfortably 
on the bed with a urinary catheter in place. Her vital 
signs were stable, her higher mental functions were 
intact and her extraocular movements were perfect. 
She had normal speech and facial symmetry. Her gag 
reflex was intact and the power of her neck flexion was 
normal. Motor examination of her upper extremities 
was unremarkable for bulk, tone, power and reflexes. 
A bulk of her lower extremities was normal but both 
lower extremities were flaccid. On the Modified 
Research Council (MRC) scale, the power of her left 
hip flexion was 3/5 and the power of her right hip 
flexion was 2/5. Her left hip extension was 4/5 and 
her right hip extension was 3/5. Her knee flexion 
was 3/5 on the left side and 2/5 on the right side. The 
knee extension was 2/5 on both sides, whereas the 
plantar flexion and dorsiflexion was 0/5 bilaterally. 
Deep tendon reflexes could not be elicited even with 
reinforcement in lower extremities. The plantar reflex 
was equivocal bilaterally. All sensory modalities were 
found to be intact and the saddle anaesthesia as well as 

 
Figure 1: Imaging of the spine of a 29-year-old female 
patient with a paraparetic variant of Guillain-Barré 
syndrome. A: Computed tomography scan of the 
lumbosacral spine showing an absence of hyperdense 
signals. B & C: Magnetic resonance imaging (MRI) 
scans of the lumbosacral spine (B) on the day of 
symptom onset and (C) one week later showing no 
acute infarction or herniated disc. D: MRI of the whole 
spine was grossly unremarkable.

Table 1: Motor nerve conduction study results of a 29-year-old female patient with a paraparetic variant of Guillain-
Barré syndrome
Nerve test 
location

Latency in ms Amplitude in mV Conduction velocity in m/s

First 
study

Second 
study

Third 
study

First 
study

Second 
study

Third 
study

First 
study

Second 
study

Third 
study

Left peroneal nerve

Fibula head 4.2 10.3 10.5 7.0 5.5 5.7 - - -

Popliteal fossa 6.2 20.1 15.7 6.1 1.0 1.9 45 26 30

Left tibial nerve

Ankle 3.3 13.5 18.4 23 20.0 21.5 - - -

Popliteal fossa 7.0 18.0 17.9 18.2 5.2 10.8 41 30 27.6

Right peroneal nerve

Ankle 6.0 11.7 13.9 5.8 4.5 6.6 - - -

Fibula head 8.0 12.8 15.5 5.3 1.3 2.6 39 21 26

Right tibial nerve

Ankle 4.3 6.4 19.3 18.2 16.3 19.5 - - -

Popliteal fossa 8.6 10.3 11.5 12.9 6.4 9.7 43 27 25



Danah Aljaafari and Noman Ishaque

Case Report | e229

a sensory level were also absent. Signs of any cerebellar 
dysfunction were absent in the arms and could not be 
examined in lower extremities. The rest of the systemic 
examination was unremarkable. 

Laboratory investigations including serum elec- 
trolyte, potassium, magnesium and phosphate levels 
as well as the coagulation profile, were within normal 
limits. The C-reactive protein level was 0.9 mg/dL 
(normal range: 0.05–0.3 mg/dL). A computed tomo- 
graphy scan of the lumbosacral spine was immediately 
performed which excluded an epidural haematoma 
[Figure 1A]. In addition, a magnetic resonance imaging 
scan of the entire spine did not show any findings 
suggestive of transverse myelitis, herniated intervert- 
ebral disc, spinal cord compression from a haematoma, 
spinal cord infraction, demyelinating disorder, a tumour, 
arteriovenous malformation or arachnoiditis of an 
infective or chemical nature [Figure 1B–D]. As imaging 
did not reveal any aetiology of her symptoms, a lumbar 
puncture was performed. CSF studies showed a protein 
level of 270 mg/dL (normal range: 15–45 mg/dL) 
and a white blood cell count of 22 k/µL (normal range: 0–5 
k/µL) with 92% lymphocytes (normal range: 40–80%). 
Next, the nerve conduction studies (NCS) were 
performed on the first day of the symptoms’ onset 
and repeated after one and two weeks [Tables 1–3]. 
This showed a prolongation of F-wave latencies, 
significant delay in distal latencies and decreased 
conduction velocities with conduction block and 
temporal dispersion. Sensory NCS were normal. NCS 
of her arms were also normal. Features of NCS were 
suggestive of a demyelinating disorder. 

A diagnosis of the paraparetic variant of GBS 
was made based on the rapid onset of areflexic 
paraparesis, cytoalbuminologic dissociation in CSF, 
demyelinating features on the NCS and absence of any 
other explanation of her symptoms on the remainder 
of investigations, including imaging. The patient 
was administered intravenous immunoglobulin for 

five days. She started to regain power in her lower 
extremities after one week and was able to move with 
support after two weeks. She had almost completely 
recovered, was able to walk unaided and could return 
to her daily activities after two months.

Discussion

GBS is an acute polyradiculoneuropathy that has diverse 
clinical presentations, findings on electrophysiological 
tests and outcome. GBS is an acute peripheral neuro- 
pathy that is thought to be due to an autoimmune 
reaction triggered by a vaccination or surgical proc- 
edure or a preceding infection, mainly respiratory or 
gastrointestinal.2 This immunopathogenesis is mainly 
controlled by four factors: (1) antiganglioside anti- 
bodies which can be detected in the serum of approx- 
imately half of GBS patients; (2) molecular mimicry 
and cross-reactivity to nerve gangliosides as in campy- 
lobacter-associated GBS cases; (3) complement activation 
that causes a neurotoxic effect; and (4) the charact- 
eristic of the patient themselves such as their immune 
status and genetic polymorphisms.8 Clinical presentation 
is the primary diagnostic criterion along with electro- 
physiologic studies and CSF analysis. In addition to 
the typical clinical presentation, many atypical clinical 
presentations of GBS have been described.3–7 It is 
crucial to identify these variants of GBS as early 
diagnosis of such cases can lead to earlier initiation 
of specific treatment and monitoring and thus, better 
outcomes.

The paraparetic variant of GBS is a typical forme 
fruste of this disorder where weakness is mainly 
limited to the legs. It was first described by Ropper in 
1986 as paraparesis with normal power and reflexes in 
the arms.3 Pokalkar et al. also identified a paraparetic 
variant of GBS and described it as a variant of GBS 
with an isolated weakness of the lower limbs with 

Table 2: Sensory nerve conduction study results of a 29-year-old female patient with a paraparetic variant of Guillain-
Barré syndrome

Sensory 
nerve test 
location

Onset latency in ms Peak latency in ms Amplitude in µV Conduction velocity in 
m/s

First 
study 

Second 
study

Third 
study

First 
study

Second 
study

Third 
study

First 
study

Second 
study

Third 
study

First 
study

Second 
study

Third 
study

Right sural 
nerve in 
the ankle

2.3 1.8 2.6 3.2 2.1 3.6 12.5 10.2 9.7 52 50 56

Table 3: F-wave study results of a 29-year-old female patient with a paraparetic variant of Guillain-Barré syndrome
Nerve test location Motor distal latency in ms F-wave latency in ms

First study Second study Third study First study Second study Third study

Right peroneal nerve 3.2 5.5 7.5 NR 59.0 63.1

NR = not recordable



Paraparetic Variant of Guillain-Barré Syndrome in First 24 Hours of Postpartum Period 
A case report

e230 | SQU Medical Journal, May 2020, Volume 20, Issue 2

minimal or no paraesthesia or sensory loss.5 They 
found that 7% of their study population with GBS had 
a paraparetic variant characterised by symmetrical 
areflexic weakness of the lower extremities without 
sensory loss. However, one-third of those patients 
showed clinical or electrophysiologic involvement of 
the upper extremities. NCS in those patients showed 
axonopathy in 59% and demyelinating features in 
33%.5 Van Den Berg et al. found that 8% of their study 
population with GBS had a paraparetic variant.9 
Those patients with a paraparetic variant of GBS had 
mild disease, less cranial nerve involvement and less 
respiratory failure compared to the GBS patients with 
quadriparesis. They also identified a delay between 
symptom onset and initiation of treatment and a lower 
likelihood of receiving specific treatment (88% with 
paraparesis versus 97% with quadriparesis; P = 0.014). 

Bladder involvement was seen in 14% of Van Den 
Berg et al.’s cases, as was seen in the current case.9 
The asymmetrical weakness and predominantly distal 
distribution in the current case were associated with 
areflexia and bladder dysfunction, which resembled 
cauda equina syndrome, while the classic GBS is 
considered to present with a symmetrical distribution 
of weakness with more gradual onset and infrequent 
involvement of the bladder. The current patient had a 
similar cell count in their CSF as 16% of Van Den Berg 
et al.’s cases (CSF cell count range: 10–50).9 Data from 
imaging was available only for 30% of their patients and 
there was no explanation for paraparesis on imaging 
which is similar to the current case. NCS studies in 
Van Den Berg et al.’s study showed demyelinating 
features as the most common finding in almost half 
of their patients; this finding is similar to the current 
case.9 One patient in their cohort had clinical and 
electrophysiologic abnormalities limited to the lower 
extremities, as was the case in the current patient. A 
total of 98% of their patients could walk unaided at six 
months.9 

There are very few reported cases of the para- 
paretic variant of GBS with findings restricted to the 
lower extremities.10,11 Kimachi et al. reported the case 
of an elderly female patient who developed progressive, 
symmetrical lower limb weakness after an upper 
respiratory tract infection sparing the arms and cranial 
nerves.10 Similarly, the limb weakness in the current 
patient was also preceded by an upper respiratory tract 
infection. CSF showed cytoalbuminologic dissociation 
and NCS showed axonal type features.10 Nagashima et 
al. reported the case of an older female patient who 
developed weakness of the lower extremities three 
weeks after an episode of fever and diarrhoea.11 The 
weakness was restricted to the lower extremities with 

intact sensation. The NCS showed findings of an axonal 
variety.11 Compared to other cases, the current patient 
was younger and experienced rapid onset asymmetrical 
paraparesis and demyelinating features on NCS. In the 
current case, the diagnosis is supported by antecedent 
upper respiratory tract infection, areflexic flaccid 
paraparesis, cytoalbuminologic dissociation in CSF, 
demyelinating features on NCS, normal spine imaging 
and a monophasic course of illness.

Conclusion

This case highlights that the paraparetic variant of 
GBS should be considered as one of the differential 
diagnoses of cauda equina syndrome, if there is no 
alternative aetiology. Early recognition of GBS is of 
vital importance with respect to the patient’s outcome.

References
1. Yuki N, Hartung HP. Guillain-Barré syndrome. N Engl J Med 

2012; 366:2294–304. https://doi.org/10.1056/NEJMra1114525.

2. Benamer HT, Bredan A. Guillain-Barré syndrome in Arab 
countries: a systematic review. J Neurol Sci. 2014 Aug 15; 
343:221–3.

3. Ropper AH. Unusual clinical variants and signs in Guillain-Barré 
syndrome. Arch Neurol 1986; 43:1150–2. https://doi.org/10.10 
01/archneur.1986.00520110044012.

4. Ropper AH. Further regional variants of acute immune poly- 
neuropathy. Bifacial weakness or sixth nerve paresis with pare- 
sthesias, lumbar polyradiculopathy, and ataxia with pharyngeal-
cervical-brachial weakness. Arch Neurol 1994; 51:671–5. 
https://doi.org/10.1001/archneur.1994.00540190051014.

5. Pokalkar D, Narisetty V, Polusani R, Kamera S, Poosarla SSL. A 
study on topographic variants of Guillain-Barré syndrome in a 
tertiary care hospital in South India. IAIM 2015; 2:32–8. 

6. Hiew FL, Ramlan R, Viswanathan S, Puvanarajah S. Guillain-Barré 
syndrome, variants & forms fruste: Reclassification with new 
criteria. Clin Neurol Neurosurg 2017; 158:114–18. https://doi.
org/10.1016/j.clineuro.2017.05.006.

7. Wakerley BR, Yuki N. Mimics and chameleons in Guillain-
Barré and Miller Fisher syndromes. Pract Neurol 2015; 15:90–9. 
https://doi.org/10.1136/practneurol-2014-000937.

8. van Doorn PA, Ruts L, Jacobs BC. Clinical features, patho- 
genesis, and treatment of Guillain-Barré syndrome. Lancet 
Neurol 2008; 7:939–50. https://doi.org/10.1016/S1474-4422(08) 
70215-1.

9. Van den Berg B, Fokke C, Drenthen J, van Doorn PA, Jacobs BC. 
Paraparetic Guillain-Barré syndrome. Neurology 2014 Jun 3; 
82:1984–9. https://doi.org/10.1212/WNL.0000000000000481.

10. Kimachi T, Yuki N, Kokubun N, Yamaguchi S, Wakerley BR. 
Paraparetic Guillain-Barré syndrome: Nondemyelinating rever- 
sible conduction failure restricted to the lower limbs. Muscle 
Nerve 2017; 55:281–5. https://doi.org/10.1002/mus.25242.

11. Nagashima T, Kokubun N, Shahrizaila N, Funakoshi K, Hirata K, 
Yuki N. Paraparetic Guillain-Barré syndrome: Extending the axonal 
spectrum. Neurol Clin Neurosci 2013; 1:224–6. https://doi.org/10.1 
111/ncn3.59.

https://doi.org/10.1056/NEJMra1114525
https://doi.org/10.1001/archneur.1986.00520110044012
https://doi.org/10.1001/archneur.1986.00520110044012
https://doi.org/10.1001/archneur.1994.00540190051014
https://doi.org/10.1016/j.clineuro.2017.05.006
https://doi.org/10.1016/j.clineuro.2017.05.006
https://doi.org/10.1136/practneurol-2014-000937
https://doi.org/10.1016/S1474-4422%2808%2970215-1
https://doi.org/10.1016/S1474-4422%2808%2970215-1
https://doi.org/10.1212/WNL.0000000000000481
https://doi.org/10.1002/mus.25242
https://doi.org/10.1111/ncn3.59
https://doi.org/10.1111/ncn3.59