23 yr old with pancytopenia/ CBBLE UDHC SIMILAR CASES 

 






   CBBLE UDHC SIMILAR CASES 



This is an online e log book to discuss our patient de-identified health data shared after taking his / her / guardians signed informed consent. Here we discuss our individual patients problems through series of inputs from available global online community of experts with an aim to solve those patients clinical problem with collective current best evident based input.




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I have been given this case to solve in an attempt to understand the topic of " patient clinical data analysis" to develop my competency in reading and comprehending clinical data including history, clinical findings, investigations and come up with diagnosis and treatment plan.



CHIEF COMPLAINTS:

   Pt. Presented to OPD with yellowish discolouration of eyes since 15 days, fever, abdominal discomfort and shortness of breath on exertion since 1 week.  1 episode of Blood in stools 2 days back

HOPI : 

Pt. Was apparently asymptomatic 3 yrs back then he developed fever for which he went to a hospital and on investigations he had hb of 4gm% so packed red blood cell transfusion was done and he was told by an attender that he had b12 deficiency for which he was given b12 Injections. His hb then improved to 12 gm% 

There were no similar complaints from past 3 years until 15 days back after which he developed yellowish discolouration of eyes, so he went to RMP and he was told he had jaundice for which he used a herbal medication for a week. After a week he developed high grade fever associated with chills and rigor, shortness of breath on exertion which was insidious in onset and gradually progressive and intermittent abdominal pain which was of squeezing type associated with nausea. No vomiting, hematemesis, malaena. 

2 days back, he had an episode of Blood in stools with a burning sensation while passing stools. 

PAST HISTORY: 

Had Blood transfusion 3 yrs back.

Not a known case of DM/ HTN/ epilepsy/ asthma/ TB

PERSONAL HISTORY

Diet- veg 

Appetite- reduced.

Sleep- adequate. 

Bowel and bladder- bloody stools 

Addictions- beer ( 1 to 2 beer/ 2 weeks ) 

Micturition: Normal 

No allergies. 


FAMILY HISTORY: 

No significant family history. 


GENERAL EXAMINATION:: 

PALLOR- present


             HYPERPIGMENTATION OF KNUCKLES


Icterus- present 

Cyanosis: absent 

Clubbing - absent

Lymphadenopathy: absent 

Oedema- absent 


VITALS :- 

Temperature 98.6f 

Pulse rate- 72 beats per minute

Respiratory rate- 20 breaths per minute.

B.P - 110/ 70mm hg

Spo2 - 99% at room air

GRBS - 92gm% 


Systemic examination: 


CVS:- S1 and S2 are heard, elevated jvp.




RS:- No dyspnoea,  wheeze , NVBS+

P/A - no tenderness. 

CNS EXAMINATION: 

Pt. Was conscious coherent and co-operative  

Speech : Normal 

No signs of meningeal irritation.

Cranial nerves, Sensory system, motor system are normal. 

 


                           INVESTIGATIONS 


1.    

Hb- 2.1 gm% 

TLC- 3100 (DECREASED)

MCV- 106.9 ( INCREASED)

MCH- 36.2( increased)

Rbc count- 0.58 million/ cumm ( DECREASED)

RDW- 00 ( DECREASED) 

Smear shows:- 

Macrocytic normochromic with macrovalocytes, microcytes, tear drop cells , target cells fragmented forms


2.    

LDH- 3054 IU/L ( Normal range- 230-460) 


3.  

Mildly Dilated right atrium, Left atrium, and right ventricle. 

IVC- Dilated


4. Ultrasound

Grade 1 Hepatosplenomegaly

5. LFT. 

              

Elevated total bilurubin-2.68 mg/dl(0-1mg/dl)

Elevated direct bilurubin-   0.38mg/dl(0-0.02)

TOTAL PROTEINS ARE DECREASED-5.9gm/dl( (6.4-8.3gm/dl) 


6. RFT

Creatinine- 0.8mg/dl( 0.9-1.3mg/dl) 

7. Reticulocyte count- Normal 


8 

9.  


10. 


11.  


Provisional diagnosis: 

Pancytopenia secondary to megaloblastic anemia.

Treatment:-

Inject methylcobalamine

Tab paracetamol 


Discussion: 

-Celiac disease (CD) is an immune-mediated enteropathy triggered by the ingestion of gluten.

- Anemia has frequently been reported as the only manifestation or the most frequent extra-intestinal symptom of CD. 

-The cause of the Vitamin B12 deficiency in CD may include decreased gastric acid, bacterial overgrowth, autoimmune gastritis, decreased efficiency of mixing with transfer factors in the intestine, or perhaps subtle dysfunction of the distal small intestine. Recent studies suggested that 8-41% of previously untreated subjects with CD were deficient in Vitamin B12

- CD-already an under-recognized disorder in India-should be considered not only in the differential diagnosis of iron deficiency but also in anemia of chronic disease. We should obtain a small-bowel biopsy in all patients with nutritional anemia .












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