Medicine case
Hello all , I’m an intern and here is a case history of one of our patients who got admitted .
This is to complete my log book as a part of my internship duty.
Edit:I was not there in the op so i collected the hirtory part from my co- intern and i had to type the discharge letter so i added extra points about the examination and investigations part . So we both helped each other.
Edit:I was not there in the op so i collected the hirtory part from my co- intern and i had to type the discharge letter so i added extra points about the examination and investigations part . So we both helped each other.
11/04/2020
A 47 year old female presented to OPD with complaints of
Difficulty in breathing since 10 days not aggravated or relieved with positional or diurnal variation
palpitations since 10 days which were short lasting
Bilateral pitting type of edema of lower extremities since 10 days
No h/o pain or warmth at the local sites of edema , no color change
No h/o facial puffiness or abdominal distention.
Bp : 130/90 mmhg
Pulse: 88 bpm
Temp: afebrile
She is a known hypertensive pt since 20 years .she is on medication tab . Telmisartan 20mg daily
H/o filariasis in rt lower limb since 15 years and is using medication DEC 100 mg for 2 weeks in a year.
ON EXAMINATION
Pt was c/c
Temperature:96.5 F
Bp:130/90mm Hg
Pulse:84 bpm
Spo2: 99%
CVS: S1 S2 heard
RESPIRATORY SYSTEM: normal vesicular breath sounds
P/A: shape of the abdomen: obese
No free fluid ,scars ,sinuses
Hernial orifices normal
No tenderness
Liver is palpable 2-3 cms
Spleen is palpable- 4 cms
Bowel sounds present
CNS: HMF intact
Speech normalk
Sensory system normal
INVESTIGATIONS
Hemogram: On presentation she had hb-4.5 gm/dl .After 1 st blood transfusion On12/05/20 hb:6.2 gm/dl
Total count:14,200 cells/cumm
Pcv:18.3 vol
Rbc:1.96 millions/cumm
Platelet: 1.01 lakhs/cumm
After 2 ndblood tranfusion
On 15/05/20 hb: 9gm/dl
Pcv:28.6 vol%
Mchc:31.3%
Rdw-cv 19.5%
Serum iron- 40ug/dl
Serum ferritin- 109ng/ml
Rft: urea- 10mg/dl
Sodium-139mEq/l
Potassium-4.1mEq/l
Chloride-104mEq/l
Lft:Total bilirubin-1.28mg/dl
Direct bilirubin-0.52mg/dl
SGOT-24IU/L
SGPT-12IU/L
Alkaline phosphate- 118IU/L
Total proteins - 5.7gm/dl
Albumin-3.7gm/dl
Smear:
RBC:hypochromic with anisopoikilocytosis comprising
normocytes ,macrocytes ,tear drop cells,Schistocytes
,polychromasia and nucleated rbcs 2-3 / 100 wbc
WBC: normal count with hypersegmented neutrophils and mild shift to left
Platelets: adequate
No parasites
Impression: normocytic hypochromic anemia with
hypersegmented neutrophils
-? Megaloblastic anemia
-? Hemolytic anemia
Osmotic fragility-lysis starts at 0.45%
Completes at 0.33%
Stool culture: no pus cells,no rbcs, no parasitic forms of ova / cyst seen
Stool for occult blood: positive
USG abdomen-splenomegaly
Fibroid uterus
Right hydrosalpinx
2d echo: mild dilated R.A/ R.V
PROCEDURE LEARNT: BONE MARROW ASPIRATION ( site- sternum) done on 13/05/20
First consent was taken from the patient. Then the patient was given a test dose of xylocaine. After half and hour at the level of 2 nd intercoastal space 10ml xylocaine was
given then marrow was aspirated .
Report: reactive marrow with erythroid
DIAGNOSIS:
?megaloblastic anemia
?hemolytic anemia
TREATMENT GIVEN:
Planned for 2 prbc blood transfusion
Inj. Vitcofol 2cc/im/od (D 3/5)
T.livogen 150mg/po/od for 1 month
T.MVT/po/od
Inj methylcobalamine 1 amp/im/od 500 mcg for 5 days (D1/5)
ADVICE AT DISCHARGE:
Inj. Hydroxocobalamin 1000 mcg for 3 days. Followed with weekly once for 1 month. Later on monthly once for 2 months
T. MVT po od for 1 week
TOPIC LEARNT TODAY:SUBARACHNOID HEMORRHAGE
etiology:
Rupture of aneursyms( most common)
Trauma
Av malformations
Vasculitis
Intracranial arterial dissections
Amyloid angiopathy
Bleeding diathesis
Drug use( cocaine and amphetamines)
Clinical features:
Sudden severe headche (thunderclap headache) described as the “worst headache of my life”
Headache associated with loss of consciousness , seizure, nausea and vomiting
Investigations :
1)Plain ct head: clot demonstrated within 24 hours of the bleed
2)Lumber puncture: elevated opening pressure and a uniformly blood stained CSF . Xanthrochromia represents hb degradation products suggestive of SAH
3)Angiogram: nature and location of lesion
4)CT or angiography
Treatment:
1 )admit in icu
2)bed rest ,stool softeners,adequate analgesia
3)DVT prophylaxis
4)discontinue all anticoagulants and antiplatelet agents
5)reduction of intracranial pressure- head end elevation, mannitol,loop diuretics, use of iv steroids(dexamethasone)
6)reduction of bp- labetalol infusion
7)prevetion of vasospasm- nimodipine
8)seizure prophylaxis
9)treatment of aneurysm and av malformations: placement of a clip across the neck of aneurysm or endovascular techniques with coil placement
Complications
1)rebleeding
2)vasospasm
3)hydrocephalus
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