A TALE OF 3 PARAPARESIS CASES!!!!!


I've been given these 3 cases to solve in an attempt to understand the topic of "patient’s clinical data analysis" to develop my competency in reading and comprehending clinical data including history, clinical findings, investigations and come up with a diagnosis and treatment plan. 
                                
                                               CASE : 1

You can find the entire real patient clinical problem in this link here..

Following is my analysis of this patient problems

Chief complaints are -
1. Weakness of bilateral lower limbs since 5 days with tingling & numbness 
2. Vomiting 5 days back 3-4 episodes, non-projectile, non-bilious, food particles as content 
3. Gluteal abscess since 5 months
4. Scrotal abscess since 20 days

WEAKNESS OF LOWER LIMBS 

- Sudden onset , 5 days ago , associated with tingling & numbness , h/o sudden fall when got up for urination 
This weakness can be attributed to either vascular / neural / muscular causes. To know which is causing let’s analyse
a) Vascular cause - There is h/o sudden fall which may be indication of vascular cause (in brain like ischemia , infarcts etc., or can be PVD ) . Here in this case there are no signs pertaining to the PVD (like varicosities , Claudication , atrophy etc.,) so it can be ruled out. But to know the brain involvement we should do an MRI
b) Neural cause - Weakness can also arise due to any nervous system abnormality and to rule out we must have a thorough examination of the patient regarding nervous system which is given below
c) Muscular cause - Weakness can be due to myopathies but there are no evidence of it...

The following are the results of nervous system examination;
Cns conscious
speech-normal
cranial nerves intact.
MOTOR SYSTEM 
                         Right.         Left
Bulk:               normal.      Normal
Tone: ul.        normal.       Normal
           LL.       hypotonia    hypotonia
Power          rt.          lt
         ul.        5/5.      5/5
         LL.       2/5.      0/5
Reflexes.  
   Superficial reflexes
                       Right.           Left
Corneal.        P                   P
Conjunctival P.                  P
Abdominal.   P.                  P
Plantar          Extensor   Extensor
    Deep tendon reflexes 
                     Right.             Left
Biceps.        2+                  1+
Triceps.       2+                   1+
Supinator.    3+                   2+
Knee             3+                  2+
Ankle.           3+                  2+
jaw jerk.        1+.                1+
ankle clonus present.     absent
Primitive reflex -absent
Involuntary movements - absent 
 
SENSORY SYSTEM - normal

CEREBELLUM
titubation - absent
Nystagmus- absent
Intensional tremors - absent
Pendular knee jerk - absent 
Coordination test -normal

MENINGIAL SIGNS
Neck stiffness - negative
Kernigns sign - negative
Brudzinkis sign - negative

So from the above results it is clearly seen there is increased DTR in the Supinator(C6) ,  knee(L4) & ankle(S1) which suggests there is UMN lesion above the C6  level ...
So now it is evident that the weakness is due to the neural cause which is  UMN lesion above the C6 level i.e, anywhere between cerebral cortex upto the level of C6...

Investigations done are  MRI & X-ray which showed the following;
- There are significant enhancement representing meningeal enhancement or exudates
- Multiple nodules in pulmonary spices suggesting Pulmonary Kochs and disseminated TB

So based on MRI we can tell that the UMN lesion is in the brain but where exactly in brain??? 
For this we have to know about some anatomy of brain...., we all know that the motor functions of the body are controlled by the Primary Motor Cortex area in the frontal lobe along the precentral gyrus....



And there neurological map dedicated to motor functions of different body parts called MOTOR HOMUNCULUS in the primary motor cortex area...


Since our patient had weakness of legs there should be lesion at the leg area of the Motor Homunculus....
Let’s see where the leg area is present......


So the leg area will be in the medial side of the each hemisphere corresponding to the longitudinal groove where the falx cerebi descends down vertically....
Here in the patient the MRI features are also seen at the same regions....so we got the exact location of the UMN lesion...

Based on the X- ray there are findings of TB , but he had no complains of TB in the past and there are no classical symptoms of TB at present too...So may be it is asymptomatic tb or a healed tb ???? And he had h/o multiple sex partners...so the possibility of HIV shouldn’t be excluded!!!!!

Possible diagnosis :  I am thinking that , it is late onset paraparesis developing after a variable period in patient with healed tb which got disseminated to various regions!!!!!
  • Dissemination of TB to the vertebral column probably at lumbar level forming a cold abscess there, which spread to the gluteal & scrotal region forming abscess there too...
  • Dissemination of TB to the brain particularly to the falx cerebri region affecting the motor homunculus mainly the leg area causing weakness of the lower limbs....
Further investigations recommended are -
1. Sputum microscopy 
2. Broncho alveolar lovage
3. CBNAAT & Gene Expert
4. Culture of the abscess 
5. As there is h/o multiple sex partners HIV testing must be done....since there is close relation between HIV & TB....

Treatment given :
T.ATT 3 tabs/day fdc
T.Benadon 40mg/od
T.pregabalin 75mg/po/h/s
OINT.MEGAHEAL FOR LOCAL APPLICATION
SITZ BATH WITH BETADINE TID
FREQUENT CHANGE OF POSITION


                                                         CASE : 2

You can find the entire real patient clinical problem in this link here..


Following is my analysis of this patient problems

Mainly he came with the chief complains of
1. Weakness of both lower limbs since 20 days
2. Bilateral edema of lower limbs

WEAKNESS OF LOWER LIMBS

It started in the proximal region initially 2yrs back which is insidious in onset & gradually progressed to distal region....It has been associated with the difficulty in wearing and holding chappals ...

So let’s analyse this weakness in lower limbs.....this can be attributed to either Vascular or Neural or Muscular system abnormalities!!!!
a) Vascular cause - Here we didn’t see any sign of PVD like varicosities , claudication , atrophy so it can be ruled out...
b) Neural cause - To know this we must have a thorough nervous system examination.....and the following are results....
patient is conscious, coherent, coperative 
patient well oriented to time, place and person
higher mental functions= normal
Cranial nerves- intact
Motor system-
       tone - normal
       power -  4-/5 in both lower limbs
        reflexes absent in both lower limbs
sensory system-normal
No meningeal signs
No cerebellar signs

From the above results....there is no evidence of hyper reflexes or spasticity....but there is absent of reflexes which leads us to think about the LMN involvement....
So it can be any where from the Anterior horn cell to the Neuromuscular junction....broadly at the peripheral nerve or at the NMJ...
To know whether it is peripheral nerve related; we must do nerve conduction test which showed normal
To know whether it is NMJ related; we must do electromyography which again showed normal...
So the neural cause also ruled out...and we left with muscular cause!!!!

c) Muscular cause - To know this we have to examine creatine kinase levels & do muscle biopsy...
And the results came out as ; there is increased creatine kinase levels and biopsy of Quadriceps Femoris showed no evidence of polymyosis but suggestive of dystrophy...
So let’s rule out all muscular causes...;the various aetiology can be as follows
- Inflammatory : which can be ruled out as there no evidence of inflammation like signs and antibodies 
- Metabolic : which can be ruled out as there is no evidence of glycogen storage disorders etc.,
- Endocrine : can also be ruled out as there are no thyroid abnormalities &TFT is normal 
- Drug induced : no h/o drugs intake so can be ruled out
- Dystrophies : it is more likely to be because there is proximal muscle weakness first and also the biopsy showed fat cells , necrotising and regenerative muscle fibre....

So what type of Dystrophy is causing this???....there are mostly 3 common types of dystrophies like Myotonic , Duchene’s , Becker’s....
- Myotonic dystrophy can be ruled out as it will starts with facial muscle weakness and mostly sparing proximal muscles
- Duchene’s Muscular dystrophy can be ruled out as it presents in the early life at 3 to 5 yrs & these persons usually wheelchair bound in adolescence or die in their late teens due to severe pulmonary infections 
- So , Becker’s Muscular dystrophy is most likely to be the diagnosis....

It is a X-linked recessive disease presenting at 5 to 15 yrs of age with weakness in the muscle due to reduced Dystrophin which is a protein connecting cytoskeleton of muscle to extra cellular membrane providing strength & stability to muscle. It presents with; muscle weakness , pseudo hypertrophy of calf muscles due to infiltration of fat cells , use of Gower’s manoeuvre to get up from floor 

Therapeutic options : 

There is no specific cure for Becker’s muscular dystrophy. We may prescribe steroids to help the individual able to walk for as long as possible (as it increases the production of protein Utrophin a close resemble of Dystrophin). Physiotherapy may be helpful to maintain the strength if the muscle. There should be repeated monitoring of cardiac parameters because it is the main cause of mortality...
Presently new strategies like Using stem cells for repairing damaged muscle fibres , Insertion of new Dystrophin genes etc., are being experimented...

Treatment taken :

T Prednisolone 15mg po od
T Pantop 40mg bbf
T Met xl 12.5mg od
Cap Becosules od
T Chymerol forte od
T Taxim 200mg bd
T Vit c od
T Ultracet sos
                                  
                   
                                                       CASE : 3

You can find the entire real patient clinical problem in this link here..


Following is my analysis of the patient problems 

1. Difficulty in walking since 1 month
2. Bilateral lower limb weakness since 1 month
3. Pain in lower limb calf muscles since 1 month
4. Fever since 1 week

DIFFICULTY IN WALKING & WEAKNESS IN LOWER LIMBS

It is of sudden onset since 1 month in the both legs below knee near the calf associated with difficulty in standing from sitting position, climbing stairs, holding chappals...

So this can be attributed to any abnormality in Bone / Muscle / Vascular / Nervous....let's decode them...

a) Bone related - there is no h/o trauma or fracture , no h/o osteoarthritis or rheumatoid arthritis....so we can rule out this...
b) Muscle related - if it is so there should be increased creatine kinase levels....but no evidence of it and no h/o muscle hypertrophy or wasting...so we can rule out this too..
c) Vascular related - there is no h/o varicosities, claudication , atrophy...so it can also be ruled out...
d) Nervous related - to know about this we must have a through nervous system examination....which is given below;
cranial nerves- intact
MOTOR SYSTEM 
                                              Right.         Left
Bulk:    inspection       decreased.     decreased
             palpation.       decreased.     decreased
Measurements  U/l   28.5cm.   28.5cm
                                  L/L 37 cm    37 cm
Tone:               ul.            normal.         Normal
                         LL.         hypotonia.      hypotonia
Power              UL.                5/5.              5/5
               iliopsoas                3/5.              3/5
   adductor femoris            4/5.               4/5
       gluteus medius             3/5.               3/5
   gluteus maximus            3/5.               3/5
              hamstrings            3/5.               3/5
quadriceps femoris            3/5.               3/5
tibialis anterior.                   3/5.               3/5
tibialis posterior.                 3/5.               3/5
peroneii.                                3/5.               3/5
gastronemius.                     4/5.               4/5
extensor -
         digitorum longus.       3/5.               3/5
flexor digitorum longus      3/5.               3/5

Reflexes.  
   Superficial reflexes
                       Right.           Left
Corneal.            P                  P
Conjunctival    P.                  P
Abdominal.      +               +
Plantar            mute           mute
cremasteric.    +                +

    Deep tendon reflexes 
                     Right.             Left
Biceps.          P.                     ---
Triceps.         ---.                   ---
Supinator.     ---                    ---
Knee              ---                    ---
Ankle.            ---                    ---
 
SENSORY SYSTEM 
                                    RIGHT.           LEFT
SPINOTHALAMIC 
             crude touch.   N.                   N
                 pain.             N.                   N
            temperature.   N.                   N
post:
             fine touch.      N.                   N
             vibration.        N.                   N
     position sensor.    N.                   N
 cortical 
 2 point discrimination  N.                   N
tactile localisation.        N.                   N

CEREBELLUM
titubation - absent
ataxia - absent
hypotonia.                present            present

From the above it is clear that there is no hyper reflexes, spasticity...so UMN lesion can be ruled out....and we left with LMN lesion which can be in the peripheral nerve or at the NMJ...
The electromyography showed normal so NMJ involvement is ruled out...and we left with the peripheral nerve....to know that we have to do nerve conduction studies which showed that
“BILATERAL COMMON PERONEAL & SURAL AXONAL NEUROPATHY”

So from above it is evident that axonal degeneration is causing all his symptoms...
From the h/o the patient is alcoholic...so which can cause deficiency of vitamins B1,3,6 and lead to peripheral neuropathy. Due to these metabolic disturbances there can be accumulation of fructose and sorbitol in Schwann cell which can lead to axonal degeneration....But rule out other causes a Sural nerve biopsy is indicated and the results are awaited...

The other problems like pain & fever can also be attributed to this because of the inflammation in the nerves...

Other examination revealed that the patient is having scabies with the lesion (burrows) in the web spaces and with positive h/o among his contacts....

Treatment underwent : 
1)T.PCM 650mg/ TID
2)INJ.NEOMOL 100ml/ IV INFUSION IF TEMPERATURE >101F
3)PERMETHRIN 5% LOTION OVERNIGHT APPLICATION ALL OVER BODY EXCEPT FACE

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