SlideShare a Scribd company logo
CASE DISCUSSION
DR MALIKA THARANI
PG TRAINEE
MEDICAL 1
HISTORY
 45 years old male ,Married k/c of CIDP? , works in garment factory, resident
of orangi town, shifted from neurology ward presented with c/o
 Pedal edema for 1 month
 Facial swelling for 4 days
 Abdominal distension for 3 days
 Rash on both legs for 2 days
HOPC
 A/c to my patient he was in usual state of health till one month back when he
noticed swelling of his both feet which gradually increase to involve the
shins ,it was not associated with fever, pain or redness. for 4 days he noticed
swelling of the face and abdominal swelling which has increased progressively
and associated with generalized abdominal pain that is mild to moderate in
intensity ,dull aching in nature, not radiating anywhere, with no aggravating
or relieving factors, not associated with nausea or vomiting.
 He developed rash on both legs for 2 days which are small, reddish ,painless
on both shins, not associated with itching. no such rashes on any other site
and no bleeding from any other site.
HOPC
 There is no current or previous hx of melena, hematemesis, altered
sensorium. No hx of chest pain, shortness of breath, orthopnea ,PND.NO hx of
hematuria, frothy urine, burning micturition, urinary frequency, urgency or
Dec urine output.
SYSTEMIC INQUIRY
 General: generalized weakness and Fatigue is present
 Abd: unremarkable.
 CVS: unremarkable
 Resp: unremarkable
 CNS: weakness and numbness of both legs is present with no tingling or
paresthesia, no hx of vertigo, dizziness, headache, blackouts, seizures or diplopia
 GU: unremarkable
 MSK: no hx of joint pain, oral ulcers, photosensitivity, dry eyes, dry mouth,
dysphagia, Raynaud's phenomenon or psychosis
 Endocrine: no hx of heat or cold intolerance, palpitations, tremors or dryness of
skin.
PERSONAL HX
 No hx of weigh loss
 Appetite is normal
 Sleep is normal
 Bladders habits are normal
 Bowel habits are normal
 He is Gutka addict
PAST HX
 Pt has hx of b/l lower limb weakness 2.5 years back which was gradual
progressive and ascending .he become unable to walk and even do his daily
activities, he left his job due to this weakness, no urinary or fecal
incontinence at that time. it extended to involved the upper limbs within the
period of 1 year and at that time MRI cervical and dorsal spine (screening)
was done which showed disc degeneration at C5 C6 C7 D7 D8 levels, EMG-
NCVs were done which showed CHRONIC SENSORY MOTOR AXONAL
POLYNEUROPATHY, 5 sessions of plasmapheresis were done at that time and he
was started on Imuran and steroids( which he took for 5 months and then left)
after this treatment his weakness improved, he become able to carry out his
daily activities but still walk with support.
 This weakness again increased for 2 months and then the patient presented in
neurology
PAST HX
 Pt has hx hemorrhoids for that he took hakeemi medications for 1 month.
 There is no past surgical or blood transfusion history.
FAMILY HX
 NO hx of tuberculosis in family
 No chronic illness in family
NUTRIONAL HX
 Good intake of green vegetables and chicken
 Takes red meat once a week
SOCIOECONOMIC HX
 Lives in well ventilated house
 No pets at home
EXAMINATION
GENERAL PHYSICAL EXAMINATION
 Middle aged male with normal built and average height lying on bed
comfortably, he is well oriented to time place and person with vitals of
 BP 130/70mm oh hg
 Pulse 87beats/min regular and good volume
 Temp A/F
 RR 20 breaths/min
 RBS 100mg/dl
 So2 96% on RA
GENERAL PHYSICAL EXAMINATION
 SUBVITALS
 Anemia present
 Jaundice absent
 Clubbing absent
 Koilonychias/leukonychia absent
 Dehydration absent
 Edema present ( B/l up to shins and periorbital puffiness )
 Thyroid Not palpable
 Lymph nodes Not palpable
 JVP Not raised
GENERAL PHYSICAL EXAMINATION
 SUBVITALS
 Oral ulcers Not present
 Palmar erythema Not present
 Spider nevi Not present
 Flapping Tremors Not present
 Petechial rash on distal half of both shins ( small 2-3mm in diameter non blanching)
ABDOMINAL EXAMINATION
 INSPECTION: Abdomen was distended, moving with respiration. Umbilicus was
central with everted margins. No visible pulsations, stria, scars or prominent
veins.
 PALPATION: Abdomen was tense, non tender, no visceromegaly appreciated.
 PERCUSSION: fluid thrill was positive.
 ASCULTATION: Gut sounds audible. No renal hepatic or aortic bruit present
CENTRAL NERVOUS SYSTEM EXAMINATION
 GCS 15/15
 SOMI absent
 Pupils BERL
 Higher Mental functions intact
 Speech normal
 Cerebellar function and Cranial nerves intact
 Gait – unable to walk/walk with support
 Fundus normal
CENTRAL NERVOUS SYSTEM EXAMINATION
 SENSORY SYSTEM
 Proprioception was impaired in lower limbs
 Vibration was impaired in lower limbs
 Pinprick was impaired in lower limbs ( glove and stocking type of sensory loss)
CENTRAL NERVOUS SYSTEM EXAMINATION
 MOTOR SYSTEM
UPPER LIMB LOWER LIMB
RIGHT LEFT RIGHT LEFT
BULK N N BULK N N
TONE N N TONE DEC DEC
POWER +4/5 +4/5 POWER
(proximal)
+4/5 +4/5
DISTAL +3/5 +3/5
ANKLE 1/5 1/5
REFLEXES A A REFLEXES A A
PLANTARS MUTE MUTE
RESPIRATORY SYSTEM EXAMINATION
 INSPECTION: Normal shaped chest with abdominothoracic respiration. No
prominent striae, pulsations or scar marks, moving equally with respiration.
 PALPATION: Trachea central. Apex beat palpated in 5th ICS medial to
midclavicular line. Normal chest expansion.
 PERCUSSION: Resonant percussion note throughout lung fields except on the
b/l mid to lower zones ( DULL on b/l mid to lower lower zones)
 AUSCULTATION: Coarse crepitations on b/l mid zones with increased vocal
resonance. Absent breath sounds at both lower zones with decreased vocal
resonance.
CARDIOVASCULAR EXAMINATION
 PERIPHERAL PULSES: Palpable and good volume.
 INSPECTION: No scar marks, pigmentation, pulsations or prominent vessels
 PALPATION: Apex beat palpated in 5th intercostal space medial to
midclavicular line, normal in character. No parasternal heave or thrill
present.
 AUSCULTATION: S1 + S2 audible. No Murmur Appreciated
CASE SUMMARY
 45 years old male ,Married k/c of CIDP? , works in garment factory, resident
of orangi town, shifted from neurology ward presented with c/o Pedal edema
for 1 month, Facial swelling for 4 days, Abdominal distension for 3 days, Rash
on both legs for 2 days.
 generalized weakness, Fatigue. Weakness and numbness of both legs.
 He is gutka addict.
 Pt has past hx of b/l lower and upper limb weakness 2.5 years back .got
plasmapheresis done one year back, and took steroids and Imuran for 6
months then left, increasing weakness for 2 months.
 Pt has hx hemorrhoids for that he took Hakimi medications for 1 month.
CASE SUMMARY
 Pt is anemic with periorbital puffiness and bilateral pitting edema and
petechie on both shins.
 Abdomen was distended with everted umbilicus, tense , fluid thrill was
positive.
 On CNS exam tone and power was decreased in both lower limbs, reflexes
were absent in all four limbs , planters bilaterally mute, proprioception and
vibration, pinprick were impaired , glove and stocking type of sensory
impairment.
 On chest exam pt has bilateral coarse crepitation on mid zones with increased
VR consistent with consolidation and absent breath sounds with dec VR on
lower zones consistent with pleural effusion.
DIFFERENTIAL DIAGNOSIS
 Disseminated tuberculosis
 Nephrotic syndrome
 Serositis sec to connective tissue disease
 Decompensated liver disease
 Hypothyroidism
 Congestive cardiac failure
 CIDP may occurs with these conditions
 Chronic hepatitis
 Diabetes
 Infection with the bacterium Campylobacter jejune
 HIV/AIDS
 Immune system disorders due to cancer
 Inflammatory bowel disease
 Systemic lupus erythematosus
 Cancer of the lymph system
 Overactive thyroid
 Side effects of medicines to treat cancer or HIV
 paraprotenemias
INVESTIGATIONS
HB 8.3
HCT 27.9
MCV 93
WBC 4.0
N 37.5
L 50.8
E 1.3
Monocytes 10.1
B 0.3
plat 68
 PERIPHEAL FILM
ANISOCYTOSIS, POIKILOCYTOSIS,
POLYCHROMASIA ? CAUSE
PLATELETS LOW ON FILM
OCCASIONAL ATYPICAL LYMPHOCYTES
SEEN? VIRAL INFECTION
ESR 115
CRP 64.6
Retic count 2.80%
 NUTRIONAL PROFILE
 S.iron 28mcg/dl
 Ferritin 108 ng/ml
 TIBC 233mcg/dl
 T.sat 12%
 Vit B12 >2000
BUN 13
Cr 1
Na 135
k 3.2
CL 108
Ca 7.9
Mg 1.8
phos 3.6
Corrected Ca 9.4
T.bili 1.1
SGPT 13
ALK ph 142
T.pro 7.1
Albumin 2.1
globulin 5
A/G ratio 0.42
PT 14.2
APTT 34.2
INR 1.36
 Dengue Ns1 antigen was not detected
 MP Mp(ICT) were not seen
 HbsAg and AntiHCV on ICT and CMIA are Non-reactive
 Hep B core antibody negative
 HIV Non-reactive
 URINE DR
 Color yellow
 Appearance slightly turbid
 PH 5
 Sp gravity 1.021
 Protein 0.25g/l (+1)
 Glucose negative
 Ketones negative
 Red cells >20
 Pus cells>20
 Casts nil
 Multiple UDR repeated shows protein trace
 CULTURES
 UCS on 24th
may shows growth of E.coli.
 Multiple UCS and BLOOD C/S shows NO GROWH.
 HbA1C
 4.7
 Urinary ACR
 CHEST XRAY
 CHEST XRAY
 U/S ABDOMEN
 Liver is Enlarged in size 17.5cm with irregular margins and coarse echotexture.NO
focal mass. Intrahepatic biliary ducts ae not dilated. Portal vein normal
0.8cm,nomal flow, normal phasicity and velocity.
 Thick walled gallbladder.
 Normal Pancreas
 Spleen enlarged measuring 14cm.homogenous parenchyma, no focal mass, splenic
vein normal.
 Gross abdominopelvic ascites.
 Bilateral minimal pleural effusion.
 Repeated ultrasound after one month shows thick walled urinary blader with
internal echoes suggestive of cystitis. otherwise same findings
ASCITIC FLUID STUDIES
SAAG 0.54
 GASTIC ASPIRATE FOR AFB AND GENE XPERT
 NOT DETECTED
 THYROID PROFILE
 TSH 6.22 ( 0.4-4.5)
 fT3 2.07 (2.1-4.4)
 fT4 1.06 ( 0.8 – 2.7)
 Anti thyroid Peroxidase antibodies Negative
ECHO
 ECG :NSR
ANA PROFILE
 ANA POSITIVE
 Spindle pole pattern (SLE , Sjogren syndrome)
 1/160 (titer)
 ASMA NEGATIVE
 AMA NEGATIVE
 ANTI DsDNA (igG) NEGATIVE
 Serum C3 and C4 within normal ranges
 Rheumatoid factor Negative
ENA PROFILE
EMG-NCVs
 Chronic sensorimotor demyelinating polyneuropathy
CT CHEST AND ABDOMEN WITH
CONTRAST
 CONCLUSION
 Gross ascites with omental thickening and bilateral minimal non tapable pleural
effusion with basal collapse consolidation likely due to infective etiology raising the
possibility of tuberculosis.
 Ascitic tap for D/R and gene expert is advised for confirmation.
 Bony changes in right glenoid cavity are likely due to aggressive etiology could be
osteomyelitis in suspected case of tuberculosis. Would recommend MRI for proper
evaluation and characterization of the lesion.
ASCITIC FLUID STUDIES
 AFB SMEAR and GENE XPERT not detected
 AFB Culture is negative.(prelim report)
 C/S shows No growth.
 ADA levels : 20 ( normal upto 30)
 Cytology shows Proteinaceous background along with lymphocytes,
histiocytes and some Reactive mesothelial cells.
 Tumor markers
 CA 19-9 19.32 ( <37)
 CEA 1.81 (<3)
 AFP 1.34 (<8.2)
 MESENTIC LYMPH NODE
 OMENTAL BIOPSY
FINAL DIANOSIS
TREATMENT GIVEN IN WARD
 Inj Lasix 40mg iv BD initially then SOS
 Inj Neurobion iv OD for 7 days
 Tab folic Acid 5mg OD
 Inj tanzo 4.5 gm iv TDS
 Inj flagyl 500mh iv TDS
 Inj N/S @60cc/hr
 Tab HCQ 200mg BD started one week back
Table 18.22-1. Classification criteria for primary Sjögren syndrome according to ACR/EULAR guidelines
Clinical inclusion criteria (ocular and oral symptoms; ≥1 positive response to the following questions):
1) Have you had daily, persistent, troublesome dry eyes for >3 months?
2) Do you have a recurrent sensation of sand or gravel in your eyes?
3) Do you use tear substitutes >3 times a day?
4) Have you had a daily feeling of dry mouth for >3 months?
5) Do you frequently drink liquids to aid in swallowing dry food?
Or suspicion of Sjögren syndrome based on ESSDAIa
Clinical exclusion criteria: History of head and neck radiation therapy, active HCV infection (confirmed by PCR), AIDS, sarcoidosis,
amyloidosis, graft-versus-host disease, IgG4-related disease
Classification criteria (histopathology, autoantibodies, ocular signs) Points
Diagnosis of focal lymphocytic sialadenitis in a labial salivary
glandb
with a focus score count >1 foci/4 mm2
3
Anti-Ro/SSA antibody positive 3
Ocular staining scorec
≥5 or van Bijsterveld scored
≥4 in ≥1 eye 1
Schirmer test ≤5 mm/5 minutes in ≥1 eye 1
Unstimulated whole saliva flow rate ≤0.1 mL/minf
1
Interpretation:
Patients with a total score ≥4 points meet the criteria for primary Sjogren syndrome (sensitivity, 96%; specificity, 95%)
 Workup for sjogren syndrome
 CBC
 ESR
 ANA
 Anti-Ro/Anti-La
 RF
 Schirmer test
 SPEP
 Staining (Rose Bengal and lissamine green staining)
 Salivary testing (sialometry)
 Protein profiling ( tear proteomics)
 Sialography and scintigraphy
 Minor salivary gland biopsy with histology
PH 7.512
PCo2 27.6
PO2 88.7
So4 98.4
Hco3 24.3
ABE -0.7
Na 133
k 4.4
Cl 104
A.G 5
 ABGs
THANKYOU

More Related Content

PPTX
28 years Male with Quadriparesis Final-1.pptx
PPT
A 18 years old male presented with bilateral leg swelling & generalized weakn...
PPTX
TB Myeloradiculopathy
PPTX
dr AMNA DALEEL PPT 2024.pptx PGR FCPS PART
PPTX
CNS case presentation for medicine postgraduates
PPT
HIV (AIDS) with Disseminated TB with HIVAN.ppt
PPTX
Medicine- Spinal Cord System- Case discussion.pptx
PPTX
SYRINGOMYELIA WITH RARE FINDINGS
28 years Male with Quadriparesis Final-1.pptx
A 18 years old male presented with bilateral leg swelling & generalized weakn...
TB Myeloradiculopathy
dr AMNA DALEEL PPT 2024.pptx PGR FCPS PART
CNS case presentation for medicine postgraduates
HIV (AIDS) with Disseminated TB with HIVAN.ppt
Medicine- Spinal Cord System- Case discussion.pptx
SYRINGOMYELIA WITH RARE FINDINGS

Similar to CASE PRESENTATION unknown serositis and multiple other things (20)

PPTX
Neurology Long Case MND.pptx
PPTX
Dr Jasir - Quadriplegia-1., hypokalemic pptx
PPTX
case presentation on neuroleptic malignant syndrome.pptx
PPTX
Mixed connective tissue disorder (case)
PPTX
PPTX
Neuroloy Long Case presentation.pptx
PPTX
a case presentation of polymyositis
PDF
Clinical materials for medicine V
DOCX
Case report of Rhumatoid arthritis
PPTX
chronic liver disease
PPTX
Case Discussion in Medicine
PPTX
Hypercoagulability presentation
PPTX
Mohamed Osman.pptx
PPTX
Paraplegia
PPTX
Dengue leading to Guillian barre syndrom
PPTX
Clinical Club M5- CIDP.pptx- a case of lower limb weakness
PDF
Approach to myositis and clinical presentation
PPTX
Case Discussion demyelinating diseases Central nervous system.pptx
PDF
PPTX
case presentation : castleman's disease
Neurology Long Case MND.pptx
Dr Jasir - Quadriplegia-1., hypokalemic pptx
case presentation on neuroleptic malignant syndrome.pptx
Mixed connective tissue disorder (case)
Neuroloy Long Case presentation.pptx
a case presentation of polymyositis
Clinical materials for medicine V
Case report of Rhumatoid arthritis
chronic liver disease
Case Discussion in Medicine
Hypercoagulability presentation
Mohamed Osman.pptx
Paraplegia
Dengue leading to Guillian barre syndrom
Clinical Club M5- CIDP.pptx- a case of lower limb weakness
Approach to myositis and clinical presentation
Case Discussion demyelinating diseases Central nervous system.pptx
case presentation : castleman's disease
Ad

Recently uploaded (20)

PPTX
Gastroschisis- Clinical Overview 18112311
PPTX
Neurotransmitter, Types of neurotransmitters,Neurotransmitter function, Neur...
PPTX
post stroke aphasia rehabilitation physician
PPTX
Chapter-1-The-Human-Body-Orientation-Edited-55-slides.pptx
PDF
Deadly Stampede at Yaounde’s Olembe Stadium Forensic.pdf
PPT
Management of Acute Kidney Injury at LAUTECH
PPT
Breast Cancer management for medicsl student.ppt
PPTX
15.MENINGITIS AND ENCEPHALITIS-elias.pptx
PDF
Therapeutic Potential of Citrus Flavonoids in Metabolic Inflammation and Ins...
PPT
genitourinary-cancers_1.ppt Nursing care of clients with GU cancer
PDF
NEET PG 2025 | 200 High-Yield Recall Topics Across All Subjects
PPTX
JUVENILE NASOPHARYNGEAL ANGIOFIBROMA.pptx
PPTX
Note on Abortion.pptx for the student note
PPTX
Respiratory drugs, drugs acting on the respi system
PPTX
surgery guide for USMLE step 2-part 1.pptx
PPT
1b - INTRODUCTION TO EPIDEMIOLOGY (comm med).ppt
PPTX
NEET PG 2025: Memory-Based Recall Questions Compiled by Dr. Shivankan Kakkar, MD
PDF
Khadir.pdf Acacia catechu drug Ayurvedic medicine
PPTX
DENTAL CARIES FOR DENTISTRY STUDENT.pptx
PDF
Handout_ NURS 220 Topic 10-Abnormal Pregnancy.pdf
Gastroschisis- Clinical Overview 18112311
Neurotransmitter, Types of neurotransmitters,Neurotransmitter function, Neur...
post stroke aphasia rehabilitation physician
Chapter-1-The-Human-Body-Orientation-Edited-55-slides.pptx
Deadly Stampede at Yaounde’s Olembe Stadium Forensic.pdf
Management of Acute Kidney Injury at LAUTECH
Breast Cancer management for medicsl student.ppt
15.MENINGITIS AND ENCEPHALITIS-elias.pptx
Therapeutic Potential of Citrus Flavonoids in Metabolic Inflammation and Ins...
genitourinary-cancers_1.ppt Nursing care of clients with GU cancer
NEET PG 2025 | 200 High-Yield Recall Topics Across All Subjects
JUVENILE NASOPHARYNGEAL ANGIOFIBROMA.pptx
Note on Abortion.pptx for the student note
Respiratory drugs, drugs acting on the respi system
surgery guide for USMLE step 2-part 1.pptx
1b - INTRODUCTION TO EPIDEMIOLOGY (comm med).ppt
NEET PG 2025: Memory-Based Recall Questions Compiled by Dr. Shivankan Kakkar, MD
Khadir.pdf Acacia catechu drug Ayurvedic medicine
DENTAL CARIES FOR DENTISTRY STUDENT.pptx
Handout_ NURS 220 Topic 10-Abnormal Pregnancy.pdf
Ad

CASE PRESENTATION unknown serositis and multiple other things

  • 1. CASE DISCUSSION DR MALIKA THARANI PG TRAINEE MEDICAL 1
  • 2. HISTORY  45 years old male ,Married k/c of CIDP? , works in garment factory, resident of orangi town, shifted from neurology ward presented with c/o  Pedal edema for 1 month  Facial swelling for 4 days  Abdominal distension for 3 days  Rash on both legs for 2 days
  • 3. HOPC  A/c to my patient he was in usual state of health till one month back when he noticed swelling of his both feet which gradually increase to involve the shins ,it was not associated with fever, pain or redness. for 4 days he noticed swelling of the face and abdominal swelling which has increased progressively and associated with generalized abdominal pain that is mild to moderate in intensity ,dull aching in nature, not radiating anywhere, with no aggravating or relieving factors, not associated with nausea or vomiting.  He developed rash on both legs for 2 days which are small, reddish ,painless on both shins, not associated with itching. no such rashes on any other site and no bleeding from any other site.
  • 4. HOPC  There is no current or previous hx of melena, hematemesis, altered sensorium. No hx of chest pain, shortness of breath, orthopnea ,PND.NO hx of hematuria, frothy urine, burning micturition, urinary frequency, urgency or Dec urine output.
  • 5. SYSTEMIC INQUIRY  General: generalized weakness and Fatigue is present  Abd: unremarkable.  CVS: unremarkable  Resp: unremarkable  CNS: weakness and numbness of both legs is present with no tingling or paresthesia, no hx of vertigo, dizziness, headache, blackouts, seizures or diplopia  GU: unremarkable  MSK: no hx of joint pain, oral ulcers, photosensitivity, dry eyes, dry mouth, dysphagia, Raynaud's phenomenon or psychosis  Endocrine: no hx of heat or cold intolerance, palpitations, tremors or dryness of skin.
  • 6. PERSONAL HX  No hx of weigh loss  Appetite is normal  Sleep is normal  Bladders habits are normal  Bowel habits are normal  He is Gutka addict
  • 7. PAST HX  Pt has hx of b/l lower limb weakness 2.5 years back which was gradual progressive and ascending .he become unable to walk and even do his daily activities, he left his job due to this weakness, no urinary or fecal incontinence at that time. it extended to involved the upper limbs within the period of 1 year and at that time MRI cervical and dorsal spine (screening) was done which showed disc degeneration at C5 C6 C7 D7 D8 levels, EMG- NCVs were done which showed CHRONIC SENSORY MOTOR AXONAL POLYNEUROPATHY, 5 sessions of plasmapheresis were done at that time and he was started on Imuran and steroids( which he took for 5 months and then left) after this treatment his weakness improved, he become able to carry out his daily activities but still walk with support.  This weakness again increased for 2 months and then the patient presented in neurology
  • 8. PAST HX  Pt has hx hemorrhoids for that he took hakeemi medications for 1 month.  There is no past surgical or blood transfusion history.
  • 9. FAMILY HX  NO hx of tuberculosis in family  No chronic illness in family
  • 10. NUTRIONAL HX  Good intake of green vegetables and chicken  Takes red meat once a week
  • 11. SOCIOECONOMIC HX  Lives in well ventilated house  No pets at home
  • 13. GENERAL PHYSICAL EXAMINATION  Middle aged male with normal built and average height lying on bed comfortably, he is well oriented to time place and person with vitals of  BP 130/70mm oh hg  Pulse 87beats/min regular and good volume  Temp A/F  RR 20 breaths/min  RBS 100mg/dl  So2 96% on RA
  • 14. GENERAL PHYSICAL EXAMINATION  SUBVITALS  Anemia present  Jaundice absent  Clubbing absent  Koilonychias/leukonychia absent  Dehydration absent  Edema present ( B/l up to shins and periorbital puffiness )  Thyroid Not palpable  Lymph nodes Not palpable  JVP Not raised
  • 15. GENERAL PHYSICAL EXAMINATION  SUBVITALS  Oral ulcers Not present  Palmar erythema Not present  Spider nevi Not present  Flapping Tremors Not present  Petechial rash on distal half of both shins ( small 2-3mm in diameter non blanching)
  • 16. ABDOMINAL EXAMINATION  INSPECTION: Abdomen was distended, moving with respiration. Umbilicus was central with everted margins. No visible pulsations, stria, scars or prominent veins.  PALPATION: Abdomen was tense, non tender, no visceromegaly appreciated.  PERCUSSION: fluid thrill was positive.  ASCULTATION: Gut sounds audible. No renal hepatic or aortic bruit present
  • 17. CENTRAL NERVOUS SYSTEM EXAMINATION  GCS 15/15  SOMI absent  Pupils BERL  Higher Mental functions intact  Speech normal  Cerebellar function and Cranial nerves intact  Gait – unable to walk/walk with support  Fundus normal
  • 18. CENTRAL NERVOUS SYSTEM EXAMINATION  SENSORY SYSTEM  Proprioception was impaired in lower limbs  Vibration was impaired in lower limbs  Pinprick was impaired in lower limbs ( glove and stocking type of sensory loss)
  • 19. CENTRAL NERVOUS SYSTEM EXAMINATION  MOTOR SYSTEM UPPER LIMB LOWER LIMB RIGHT LEFT RIGHT LEFT BULK N N BULK N N TONE N N TONE DEC DEC POWER +4/5 +4/5 POWER (proximal) +4/5 +4/5 DISTAL +3/5 +3/5 ANKLE 1/5 1/5 REFLEXES A A REFLEXES A A PLANTARS MUTE MUTE
  • 20. RESPIRATORY SYSTEM EXAMINATION  INSPECTION: Normal shaped chest with abdominothoracic respiration. No prominent striae, pulsations or scar marks, moving equally with respiration.  PALPATION: Trachea central. Apex beat palpated in 5th ICS medial to midclavicular line. Normal chest expansion.  PERCUSSION: Resonant percussion note throughout lung fields except on the b/l mid to lower zones ( DULL on b/l mid to lower lower zones)  AUSCULTATION: Coarse crepitations on b/l mid zones with increased vocal resonance. Absent breath sounds at both lower zones with decreased vocal resonance.
  • 21. CARDIOVASCULAR EXAMINATION  PERIPHERAL PULSES: Palpable and good volume.  INSPECTION: No scar marks, pigmentation, pulsations or prominent vessels  PALPATION: Apex beat palpated in 5th intercostal space medial to midclavicular line, normal in character. No parasternal heave or thrill present.  AUSCULTATION: S1 + S2 audible. No Murmur Appreciated
  • 22. CASE SUMMARY  45 years old male ,Married k/c of CIDP? , works in garment factory, resident of orangi town, shifted from neurology ward presented with c/o Pedal edema for 1 month, Facial swelling for 4 days, Abdominal distension for 3 days, Rash on both legs for 2 days.  generalized weakness, Fatigue. Weakness and numbness of both legs.  He is gutka addict.  Pt has past hx of b/l lower and upper limb weakness 2.5 years back .got plasmapheresis done one year back, and took steroids and Imuran for 6 months then left, increasing weakness for 2 months.  Pt has hx hemorrhoids for that he took Hakimi medications for 1 month.
  • 23. CASE SUMMARY  Pt is anemic with periorbital puffiness and bilateral pitting edema and petechie on both shins.  Abdomen was distended with everted umbilicus, tense , fluid thrill was positive.  On CNS exam tone and power was decreased in both lower limbs, reflexes were absent in all four limbs , planters bilaterally mute, proprioception and vibration, pinprick were impaired , glove and stocking type of sensory impairment.  On chest exam pt has bilateral coarse crepitation on mid zones with increased VR consistent with consolidation and absent breath sounds with dec VR on lower zones consistent with pleural effusion.
  • 24. DIFFERENTIAL DIAGNOSIS  Disseminated tuberculosis  Nephrotic syndrome  Serositis sec to connective tissue disease  Decompensated liver disease  Hypothyroidism  Congestive cardiac failure
  • 25.  CIDP may occurs with these conditions  Chronic hepatitis  Diabetes  Infection with the bacterium Campylobacter jejune  HIV/AIDS  Immune system disorders due to cancer  Inflammatory bowel disease  Systemic lupus erythematosus  Cancer of the lymph system  Overactive thyroid  Side effects of medicines to treat cancer or HIV  paraprotenemias
  • 27. HB 8.3 HCT 27.9 MCV 93 WBC 4.0 N 37.5 L 50.8 E 1.3 Monocytes 10.1 B 0.3 plat 68  PERIPHEAL FILM ANISOCYTOSIS, POIKILOCYTOSIS, POLYCHROMASIA ? CAUSE PLATELETS LOW ON FILM OCCASIONAL ATYPICAL LYMPHOCYTES SEEN? VIRAL INFECTION ESR 115 CRP 64.6 Retic count 2.80%
  • 28.  NUTRIONAL PROFILE  S.iron 28mcg/dl  Ferritin 108 ng/ml  TIBC 233mcg/dl  T.sat 12%  Vit B12 >2000
  • 29. BUN 13 Cr 1 Na 135 k 3.2 CL 108 Ca 7.9 Mg 1.8 phos 3.6 Corrected Ca 9.4 T.bili 1.1 SGPT 13 ALK ph 142 T.pro 7.1 Albumin 2.1 globulin 5 A/G ratio 0.42 PT 14.2 APTT 34.2 INR 1.36
  • 30.  Dengue Ns1 antigen was not detected  MP Mp(ICT) were not seen  HbsAg and AntiHCV on ICT and CMIA are Non-reactive  Hep B core antibody negative  HIV Non-reactive
  • 31.  URINE DR  Color yellow  Appearance slightly turbid  PH 5  Sp gravity 1.021  Protein 0.25g/l (+1)  Glucose negative  Ketones negative  Red cells >20  Pus cells>20  Casts nil  Multiple UDR repeated shows protein trace
  • 32.  CULTURES  UCS on 24th may shows growth of E.coli.  Multiple UCS and BLOOD C/S shows NO GROWH.  HbA1C  4.7
  • 36.  U/S ABDOMEN  Liver is Enlarged in size 17.5cm with irregular margins and coarse echotexture.NO focal mass. Intrahepatic biliary ducts ae not dilated. Portal vein normal 0.8cm,nomal flow, normal phasicity and velocity.  Thick walled gallbladder.  Normal Pancreas  Spleen enlarged measuring 14cm.homogenous parenchyma, no focal mass, splenic vein normal.  Gross abdominopelvic ascites.  Bilateral minimal pleural effusion.  Repeated ultrasound after one month shows thick walled urinary blader with internal echoes suggestive of cystitis. otherwise same findings
  • 38.  GASTIC ASPIRATE FOR AFB AND GENE XPERT  NOT DETECTED
  • 39.  THYROID PROFILE  TSH 6.22 ( 0.4-4.5)  fT3 2.07 (2.1-4.4)  fT4 1.06 ( 0.8 – 2.7)  Anti thyroid Peroxidase antibodies Negative
  • 41. ANA PROFILE  ANA POSITIVE  Spindle pole pattern (SLE , Sjogren syndrome)  1/160 (titer)  ASMA NEGATIVE  AMA NEGATIVE  ANTI DsDNA (igG) NEGATIVE  Serum C3 and C4 within normal ranges  Rheumatoid factor Negative
  • 43. EMG-NCVs  Chronic sensorimotor demyelinating polyneuropathy
  • 44. CT CHEST AND ABDOMEN WITH CONTRAST  CONCLUSION  Gross ascites with omental thickening and bilateral minimal non tapable pleural effusion with basal collapse consolidation likely due to infective etiology raising the possibility of tuberculosis.  Ascitic tap for D/R and gene expert is advised for confirmation.  Bony changes in right glenoid cavity are likely due to aggressive etiology could be osteomyelitis in suspected case of tuberculosis. Would recommend MRI for proper evaluation and characterization of the lesion.
  • 45. ASCITIC FLUID STUDIES  AFB SMEAR and GENE XPERT not detected  AFB Culture is negative.(prelim report)  C/S shows No growth.  ADA levels : 20 ( normal upto 30)  Cytology shows Proteinaceous background along with lymphocytes, histiocytes and some Reactive mesothelial cells.
  • 46.  Tumor markers  CA 19-9 19.32 ( <37)  CEA 1.81 (<3)  AFP 1.34 (<8.2)
  • 47.  MESENTIC LYMPH NODE  OMENTAL BIOPSY
  • 49. TREATMENT GIVEN IN WARD  Inj Lasix 40mg iv BD initially then SOS  Inj Neurobion iv OD for 7 days  Tab folic Acid 5mg OD  Inj tanzo 4.5 gm iv TDS  Inj flagyl 500mh iv TDS  Inj N/S @60cc/hr  Tab HCQ 200mg BD started one week back
  • 50. Table 18.22-1. Classification criteria for primary Sjögren syndrome according to ACR/EULAR guidelines Clinical inclusion criteria (ocular and oral symptoms; ≥1 positive response to the following questions): 1) Have you had daily, persistent, troublesome dry eyes for >3 months? 2) Do you have a recurrent sensation of sand or gravel in your eyes? 3) Do you use tear substitutes >3 times a day? 4) Have you had a daily feeling of dry mouth for >3 months? 5) Do you frequently drink liquids to aid in swallowing dry food? Or suspicion of Sjögren syndrome based on ESSDAIa Clinical exclusion criteria: History of head and neck radiation therapy, active HCV infection (confirmed by PCR), AIDS, sarcoidosis, amyloidosis, graft-versus-host disease, IgG4-related disease Classification criteria (histopathology, autoantibodies, ocular signs) Points Diagnosis of focal lymphocytic sialadenitis in a labial salivary glandb with a focus score count >1 foci/4 mm2 3 Anti-Ro/SSA antibody positive 3 Ocular staining scorec ≥5 or van Bijsterveld scored ≥4 in ≥1 eye 1 Schirmer test ≤5 mm/5 minutes in ≥1 eye 1 Unstimulated whole saliva flow rate ≤0.1 mL/minf 1 Interpretation: Patients with a total score ≥4 points meet the criteria for primary Sjogren syndrome (sensitivity, 96%; specificity, 95%)
  • 51.  Workup for sjogren syndrome  CBC  ESR  ANA  Anti-Ro/Anti-La  RF  Schirmer test  SPEP  Staining (Rose Bengal and lissamine green staining)  Salivary testing (sialometry)  Protein profiling ( tear proteomics)  Sialography and scintigraphy  Minor salivary gland biopsy with histology
  • 52. PH 7.512 PCo2 27.6 PO2 88.7 So4 98.4 Hco3 24.3 ABE -0.7 Na 133 k 4.4 Cl 104 A.G 5  ABGs

Editor's Notes

  • #27: Polychromasia means that the bone marrow is releasing immature cells