case


Hello everyone I'm a medical intern.This blog is to share my experiences and cases I came across during this period

This is an online E log book to post and discuss our patient's de-identified health data posted after taking informed consent where we discuss patient-centered clinical problems through series of discussions among the community of experts without letting the patient move to distant places to different doctors with an aim to solve their clinical problems with the collective best evidence input from them. This online platform also reflects my patient-centered learning portfolio.
This is a case of 22yr old male with Cushings syndrome
Case history:
A 22 year old male resident of devarkonda came with Chief complaints of distension of abdomen and facial puffiness since 8months 
HOPI
He was apparently asymptomatic 1.5years back then developed red itchy ring like lesions over the thighs for which he applied clobeta GM for 7months intermittently he also took raktha shodini syrup (ayurvedic patanjali)400ml
 then (October 2019)his lesions increased and blood was oozing from them and he also noticed that he is gaining weight (from 50kgs to 70kgs)  then the patient went to kamineni LB nagar  in October and he was diagnosed with tinea incognito and he was prescribed antifungals
Xyzal tablets
 Ebermet cream 
Sebafin cream
He had fever after 5 days  which was high grade and associated with chills and rigors for 2 days and joint pains for which he was prescribed  antoxid cefixim for 1 week     
At a review after 1 month for his allergy he was prescribed  itraconazole and ketoconazole during follow  up in December

Patient didn't give any history of oral steroid intake
No history of constipation or loose stools ,fever cough, abdominal pain, no history of hair loss or thinning ,no history of hypertension, diabetes mellitus ,thyroid, coronary artery disease, epilepsy no history of body pains, delayed wound healing no history of pedal edema, emotional lability ,anorexia ,easy fatigability ,no h/o decreased vision, no h/o weakness, no h/o acne
Personal history
The patient is having a good appetite mix diet adequate sleep and bladder movements regular and no addictions

General examination
Pt is conscious coherent cooperative obese and moderately nourished 
No pallor, icterus , cyanosis,clubbing,lymphadenopathy and  pedal edema
Distended abdomen with purple striae present


Facial puffiness present
BP 120/80mm of hg
Pulse 82bpm regular
Temp afebrile 
RR 20 cpm
Systemic examination:
 CVS: s1 S2 heard no murmurs

Respiratory system: bilateral air entry present normal vesicular breath sounds heard

Per abdomen soft nontender distension of abdomen present
CNS no abnormality detected

Investigations

Cortisol after ACTH stimulation


Diagnosis: drug induced (topical steroids) Cushings syndrome with suppressed hpa axis 

Treatment:
Injection ACTH 0.4 ml IM at 7:00 a.m.
Serum cortisol level check at 8 a.m. and serum cortisol turned out to be 0.35 so patient was started on tab.hydrocortisone 5mg 2tablets in the morning 7am 1tablet at 12pm 1tablet at 5pm for 20days followed by gradual tapering off the dose 
Tab.pantop 40mg OD PO
Tab.MVT OD 
Monitor BP pr RR
Inform SOS
Advice at discharge.                                   
Tab.hydrocortisone 5mg for 20days PO(2tabs 7am-1tab 12pm-1tab 5pm)
Tab.MVT PO OD
Tab.pantop 40mg OD PO
Follow up after 20days and dermatologist opinion for tinea incognito

And his serum cortisol on 28th February when he came for a follow up 


Itraconazole increased methylprednisolone concentrations markedly with enhanced suppression of endogenous cortisol secretion, but had no effect on prednisolone pharmacokinetics. The pharmacokinetic interaction between methylprednisolone and itraconazole is probably related to inhibition of hepatic CYP3A4 activity by itraconazole
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2014476/


Reversible adrenal insufficiency occurred in one among eight patients receiving high-dose itraconazole (600 mg day−1) for a mean duration of 5.5 months [39]. In our study, the baseline profile of cortisol during the itraconazole phase was not determined. However, the cortisol concentrations at 08.00 h t0 did not differ during the itraconazole phase compared with drug free values. Thus we postulate that the secretion of cortisol was maintained after 4 days of itraconazole administration. It seems reasonable to consider that suppression of endogenous cortisol is related only to the effect of the corticosteroid.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2014476/

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