21 year old female with anemia. July 04, 2023

21 year old female came to gm op with chief complaints of easy fatiguability ,light headedness since 7 years 

C/o sob since 7 years ( sometimes ) 

No c/o Fever, burning micturation,vomitings, loose stools 

No c/o involuntary movements or tingling sensation or numbness . 

HISTORY OF PRESENTING ILLNESS:

Patient was apparently asymptomatic 20 years back then she developed fever , edema over the fronto parietal region and irritability she was admitted in the hospital treated ( her hospital stay was around 10 days and she was discharged )

At the age of 3 years she had an episode of giddiness and was unconscious, she was again admitted in the hospital and then they were told that she had low levels of hemoglobin and she underwent blood transfusion.

At 15 years of age she was taken to the hospital for weakness, giddiness , she was admitted in the hospital and had second episode ofblood transfusion, her hemoglobin level improved to 9 after blood transfusion.

Few months after blood transfusion she started feeling weak and again went to the hospital , then her blood hemoglobin went down to 4 . 

Since 3 to 4 months she complains of joint pains 

Since 20 days she has allergy over her palms ,she has itching all over her hands relieved after taking medication at local hospital.

Since 20 days anasarca ( intermittently ) 

Resolved by its own . Last episode 2 days back 

From 10 years of age she started noticing hyperpigmentation patches on her body which was slowly progressive to current stage .(neurofibromatosis ) 


Past history: history of trauma to head at the age of 10 while playing under a tree .

Daily routine: 

Childhood 

During the days she felt alright:

She wakes up at 6 Am ,does all the house hold work , she helps her mother and has breakfast at 8 Am and goes to school by walk (around 2 km ) , and comes back in the evening around 5 (by walk ) and plays with her friends and has dinner at 8 pm and goes to sleep by 10 pm 

During summer holidays she went to work in the field ( cotton farms and chilli farms ) 

From morning 10 Am to evening 5 pm .

She studied till intermediate and didn’t go any further to college because of illness. 

After progression of her illness she didn’t go to work in the fields , she helped her mother in all the household activities.

PAST History:

She is not a known case of DM, HTN, CVA, CAD, asthma, epilepsy.

FAMILY HISTORY:

Her sister has low value of hemoglobin (hb -6 gm/dl),but her sister doesn’t complain of any weakness.

Her mother has neurofibromatosis 
GENERAL EXAMINATION: 
Patient is conscious, coherent and co-operative.

Mooderately built and moderately nourished.

Pallor - present 

Icterus - Absent

Cyanosis - Absent

 Clubbing - Absent 

No lymphadenopathy

Pedal edema- absent

Vitals : 

Temperature - 98.2 F 

Blood Pressure - 120/80mm hg 

Pulse Rate - 82 bpm

Respiratory Rate - 16 cpm



SYSTEMIC EXAMINATION: 

PER ABDOMINAL EXAMINATION:

INSPECTION-

Shape of abdomen : flat

Umbilicus : inverted 

All quadrants of abdomen move with respiration 

No visible peristalsis, pulsations, sinuses, engorged veins, hernial sites 



PALPATION-

Abdomen soft

No local rise of temperature 

No tenderness

Inspectors findings are confirmed 

organomegaly - moderate splenomegaly 



PERCUSSION:

Resonant note heard over all quadrants.



AUSCULTATION:

Bowel sounds heard  



CVS EXAMINATION:

INSPECTION

The chest wall is bilaterally symmetrical

No dilated veins, scars or sinuses are seen

Apical impulse not visible



PALPATION:

Apex beat localised 

AUSCULTATION:

S1 and S2 heard

No Murmurs 

RS EXAMINATION:

INSPECTION: 

Shape of chest: bilaterally symmetrical

Expansion of chest: Equal on both sides

Position of trachea: Central

No visible scars, sinuses, pulsations
PALPATION:

Inspectory findings confirmed

No tenderness, local rise of temperature

Normal expansion of chest on both sides in all areas

Position of trachea: Central

Vocal fremitus: resonant note felt

PERCUSSION:

Resonant note heard over all areas
AUSCULTATION:

BAE positive

Vocal resonance: resonant in all areas

CNS :No focal neurological deficit.
Provisional diagnosis:


Iron deficiency Anemia secondary to ? Blood loss ? Thalassemia minor k/c/o neurofibromatosis.



Investigations:

ECG 




2d echo :

Trivial TR/AR/MR 

No RWMA , NO AS/MS 

Good LV systolic function, No diastolic dysfunction.





4/7/2023 investigations 

Hemogram :

Hb-6.4

TlC- 11200

N /L/E/M -35,19,41,5

PCV-25.9 

MCV- 56.9

MCH-14.1

MCHC-24.7 

RDW-27.2

Smear: 

MICROCYTIC HYPOCHROMIC FEW PENCIL FORMS AND TARGET CELLS SEEN 

WBC :normal limit with eosinophilia 

Plt - adequate 

BGT :A positive 

RETICULOCYTE : 1.5 

BLOOD UREA -18

SERUM CREATININE:0.6

Na - 140 

K -4.7

Cl-102

LFT :

Total bilirubin: 0.49

Direct bilirubin:0.15

AST-14 

ALT-10 

ALP-128 

TP:6.7 

ALBUMIN: 4.35 

A/g :1.85 

Serology: negative.

Ultrasound 5/7/2023

Mild splenomegaly .

Serum ferritin :73.5 ng/ml

Stool for occult blood - negative 

8-7-2023

HBA -98.4%



HBA2-1.6%

TIBC-394 ug/dl 

TRANSFERRIN SATURATION -8%

UIBC-363.9ug/dl 

IRON -30ug/dl 

Hemogram 10. -7-23

Hb-6.8 

TLC -7500 

N -30 ,L-25 ,E-40 ,M-5 , B-0 

PCV-27.3 

MCV-59

MCHC -24.9 

MCH-14.7 


DISCHARGE SUMMARY:

Diagnosis:
 IRON DEFICIENCY ANEMIA SECONDARY TO BLOOD LOSS ,NUTRITIONAL LOSS K/C/O NEUROFIBROMATOSIS

 Case History and Clinical Findings :
C/O EASY FATIGUABILITY SINCE 7 YRS C/O SOB SINCE 7YRS
HOPI:
 PT WAS APPARENTLY ASYMPTOMATIC 7 YRS AGO SINCE THEN HAS EASY FATIGUABILITY ,LIGHT HEADEDNESS , SOB GRADE 3 ,INSIDIOUS IN ONSET ,GRADUALLY PROGRESSIVE ,ORTHOPNEA PRESENT SOMETIMES C/O OCCASIONAL PALPITATIONS , C/O CONSTIPATION NO C/O FEVER ,BURNING MICTURITION ,VOMITINGS,LOOSE STOOLS NO C/O INVOLUNTARY MOVEMENTS,TINGLING SENSATION AND NUMBNESS H/O GENERALISED ITCHING 15 DAYS BACK H/O ANASARCA 15 DAYS BACK H/O BLOOD TRANSFUSION 3 YRS BACK AND WHEN SHE WAS 9 YRS OLD H/O NEUROFIBROMATOSIS NOT A K/C/O DM,HTN,SEIZURES,ASTHMA,TB
 PERSONAL HISTORY
Diet
 : MIXED APPETITE :
 NORMAL BOWEL AND BLADDER
 : REGULAR
 ADDICTIONS : NONE SLEEP: ADEQUATE

 GENERAL EXAMINATION PATIENT IS CONSCIOUS /COHERENT/CO OPERATIVE PALLOR PRESENT NO ICTERUS,CYANOSIS,CLUBBING,LYMPHADENOPATHY,OEDEMA VITALS TEMP : AFEBRILE PR : 84 BPM RR: 18 CPM BP : 140/90 MMHG

 SYSTEMIC EXAMINATION

 CVS : S1,S2 HEARD ,NO MURMURS 
RS: BLAE PRESENT 
P/A : SOFT,NON TENDER 
CNS: NO FOCAL NEUROLOGICAL DEFICITS

 OPHTHALMOLOGY REFERRAL ON 6/7/23 RIGHT EYE : REFRACTION - 4.50 SPH ,0.50 CYL X40* -6/9 IRIS SHOWS LISCH NODULES LEFT EYE : REFRACTION - 4.50 SPH ,0.50 CYL X 60 * - 6/9 ,LIDS - UL PUS POINT PRESENT IRIS SHOWS LISCH NODULES FUNDUS STUDY IS NORMAL ADVICE USE SPECTACLES FOR REFRACTION ERROR


 Investigation 2D ECHO WAS DONE ON 4/7/23 WHICH SHOWED EF : 62% ; IVC 0.6 COLLAPSING ; RVSP : 36 mmHg TRIVIAL TR/MR/AR NO RWMA, NO AS/MS GOOD LV SYSTOLIC FUNCTION
NO DIASTOLIC DYSFUNCTION ,NO PAH/PE USG DONE ON 5/7 MILD SPLENOMEGALY 13 CM INCREASE SIZE ON 4/7
 BLOOD GROUP : A POSITIVE RETICULOCYTE COUNT : 1.5 % HEMOGRAM HB: 6.4 GM/DL TLC : 11,200 CELLS /CUMM N/L/E/M/B : 35//19/41/05/00 PCV : 25.9 VOL% RBC COUNT : 4.55 MILLIONS/CUMM PLATELET COUNT : 4.26 LAKHS/CUMM PERIPHERAL SMEAR : RBS SHOWS MICROCYTIC HYPOCHROMIC WITH FEW PENCIL FORMS AND TARGET CELLS WBC SHOWS WITHIN NORMAL LIMITS WITH EOSINOPHILIA PLATELET ADEQUATE LFT T.B : 0.49MG/DL D.B : 0.15 MG/DL SGOT: 14 IU/L SGPT: 10 IU/L ALP :128 IU/L T.P: 6.7 GM/DL ALBUMIN :4.35 GM/DL A/G RATIO : 1.85 HBS AG RAPID : NEGATIVE ANTI HCV ANTIBODIES RAPID : NEGATIVE
SERUM CREATININE : 0.6 MG/DL SERUM ELECTROLYTES : SODIUM/POTASSIUM / CHLORIDE/CALCIUM IONIZED : 140/4.7/102/1.06 BLOOD UREA : 18 MG/DL CUE ALBUMIN ,SUGARS NIL PUS CELLS ; 2 TO 3 STOOL FOR OCCULT BLOOD : NEGATIVE FERRITIN : 73.5 NG/ML ON 6/7 PERIPHERAL SMEAR RBC : ANISOPOIKILOCYTOSIS WITH HYPOCHROMASIA PREDOMINANTLY MICROCYTES FEW TEAR DROP CELLS INCREASED IN COUNT WITH EOSINOPHILIA PLATELET ADEQUATE IMP- MICROCYTIC HYPOCHROMIC ANEMIA WITH EOSINOPHILIA ON 8/7 HEMOGLOBIN ELECTROPHORESIS Hb A : 98.4% Hb A2 : 1.6 % IRON STUDIES TIBC : 394 UG/DL TRANSFERRIN SAT : 8% UIBC : 363.99 UG/DL PHOTOMETRY : 30 UG/DL 

Treatment Given(Enter only Generic Name) 1.INJ IRON SUCROSE 200MG IN 100ML NS IV/OD OVER 30 TO 40 MIN GIVEN ON 4/7 ,5/7 , 7/7 ,9/7/23 2.TAB .OROFER XT PO/OD

Advice at Discharge
 1.TAB.OROFER XT PO/OD [X-1-X] FOR 30 DAYS 
2.TAB.LIMCEE PO/OD [X-1-X] FOR 30 DAYS 3.TAB.MVT PO/BD [X-1-1] FOR 30 DAYS 4.IRON RICH DIET









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