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proximal muscle weakness
Stretch marks (classically purple abdominal striae
Hirsutism
depression
osteoporosis
insulin resistance, polyuria,
dyslipidemia
weight gain- central obesity, moon facies
secondary HTN
hyper - cortisol / cushing
symptom not seen in primary hypercortisolism
hyper pigmentation; seen in secondary
labs; cushing
BMP; Na, K, metabolic alkalosis
Blood glucose
serum cholestrol and triglycerides
urine free cortisol
low dose dexamethasone
serum cortisol
plasma ACTH level
CT/ MRI; adrenal or pituitary
why is cortisol checked at night
In healthy individuals, cortisol levels are low at night.
In Cushing's syndrome, this diurnal rhythm is lost, and cortisol remains inappropriately elevated at night.
"Cushing disease" refers specifically to
secondary hypercortisolism that results from excessive production of ACTH by pituitary adenomas.
Rx of cushing disease
Control hypertension (e.g., ACE inhibitors, calcium channel blockers)
Treat hyperglycemia (e.g., insulin, metformin)
Prevent/treat infections (risk ↑ due to immunosuppression)
Electrolyte correction: hypokalemia common in ectopic ACTH syndrome → give K⁺ and spironolactone
Osteoporosis treatment: bisphosphonates, calcium, vitamin D
first line(ACTH-independent) - adrenalectomy + steorid replacement
Cushing disease (ACTH-producing pituitary adenoma) - Bilateral adrenalectomy
Ectopic ACTH production; Common sources: small cell lung cancer, carcinoid tumors Locate and resect the tumor
Ketoconazole, Pasireotide, osilodrostate
causes of cushing
most common - prolonged glucorticoid therapy
adrenal adenoma, carrcinoma (primary/ acth independent)
pitutary adenoma; cushing disease
ectopic acth; paraneiplastic syndrome, small cell lung caricnoma, lung endocrine tumor, pheocromocytoma
what causes bilateral adrenal ATROPHY in cushing
excess glucocorticoid use
primary hypercortisolism casues
atrophy of contralateral gland
cushing disease/secondary causes
bilateral adrenal HYPERPLASIA
hypocortisolism is called
hypercortisolism is called
addisons
cushing
causes of addison
1. Autoimmune destruction
2. Infection (TB)
2. adrneal hemorrage; (Waterhouse-Friderichsen syndrome), sepsis, DIC
4. Mets to adrenal gland
5. adrenalectomy
6. sudden discontinuation of chronic glucocorticoid therapy
7. hypopituitaryism
symptoms of addison
Hypoaldosteronism
Hypotension
Salt craving
hypocorti; weigh loss, fatigue, GI issues, orthostatic hypotension
elevated ACTH > hyperpigementation
adrenal gland secretes
aldosterone,
cortisol,
epinephrine, norepinephrine
androgen
labs; addison
BMP
Na ↓, K ↑,
blood glucose; Hypoglycemia
morning cortisol
morning ACTH
short ACTH stimulation test
plasma renin (high cause aldost is low)
CXR; TB
MRI; pituitary
CT/MRI; adrenial gland
Rx. addison
Primary adrenal insufficiency: Replace
Glucocorticoids (e.g., hydrocortisone)
Mineralocorticoids (e.g., fludrocortisone)
± Androgens (e.g., DHEA, if needed)
100mg IV bolus of hydrocortisone is the first line for glucocorticoid replacement. not available, dexamethasone
intravenous saline & glucose
(fluid replacement) - then maintenance hydrocortisone & adequate saline intake oral
Secondary/Tertiary adrenal insufficiency: Replace
Glucocorticoids only
Stress-dose steroids: Increase glucocorticoids during illness/surgery to prevent adrenal crisis
Sick day rule: Double/triple glucocorticoid dose during stress/illnes
complication; addison
adrneal crisis
chronic fatigue
electrolyte distrubance
inferitlity adn menstrual irregularities
Fatigue, decreased physical activity,
cold intolerance, decreased sweating,
hair loss (Queen Anne sign),
brittle nails, cold dry skin,
weight gain despite poor appetite, constipation,
bradycardia,
puffy appearance
hoarse voice,
Hypo-thyroidism
Labs; hypothyoridism
Thyroid function test;
TSH, Free T4 and T3
Anti-thyroid antibodies (for autoimmune causes):
· Anti-thyroid peroxidase (anti-TPO) - hashimoto
· Anti-thyroglobulin antibodies - hashimoto
Lipid profile CBC
BMP
Creatine kinase:
Prolactin
Serum cortisol
Imaging; Thyroid ultrasound , nuclear medicine thyroid scan
Complications of hypothyroidism
myxedema coma,
primary thyroid lymphoma,
Rx; hypothyroidism
Levothyroxine
Overtreatment can lead to symptoms of thyrotoxicosis; heat intolerance, tremors, Tachycardia; arrhythmias, Weight loss
Drugs that reduce levothyroxine absorption include PPIs, calcium salts, ferrous sulfate, and bile acid sequestrants
differential; hypothyroidism
Euthyroid sick syndrome, Goiter, Myxedema coma, Anemia, Riedel thyroiditis, Subacute thyroiditis
causes of hypothroidism
autoimmune (hashi)
postopartum
viral infection, de quervein
iatrogenic,
pituitary
hypothalamic
Heat intolerance,
excessive sweating,
weight loss despite increased appetite, frequent bowel movements,
pretibial myxedema,
onycholysis,
thyroid acropachy,
lid lag, lid retraction,
exophthalmos
tachycardia
atrial fibrillation
fine tremor, proximal muscle weakness (hyperthyroid myopathy),
gynecomastia, decreased libido, glucose intolerance, anxiety, restlessness, insomnia, hyperreflexia.
hyper thyroidism
Labs; hyper thyroidism
- Thyroid Function Tests
o TSH ↓ in primary hyperthyroidism
o Free T4 and Free T3 ↑
o Thyroid-stimulating immunoglobulin (TSI) - specific for Graves
o TSH receptor antibodies (TRAb) - confirms Graves disease
o Anti-TPO antibodies - positive in autoimmune thyroid disease
o Thyroglobulin levels - helps detect thyroiditis or exogenous hormone use
- CBC, Fasting glucose/HbA1c Serum cholesterol
- ECG - tachyarrhythmia or atrial fibrillation
- Imaging; thyroid ultrasound, radioactive iodine uptake scan, Nuclear medicine thyroid scan
Rx, hyperthyroidism
All symptomatic patients
> First-line: Propranolol (for hyperadrenergic symptoms)
> If contraindicated; Verapamil or Diltiazem
Antithyroid Drugs
Most patients: Methimazole
Thyroid storm / 1st trimester pregnancy: Propylthiouracil (PTU)
Radioactive Iodine Ablation (RAIA); Toxic MNG, toxic adenoma
> Graves / toxic MNG: Near-total or total thyroidectomy
> Toxic adenoma: Lobectomy
causes of hyperthyroidism
1. Graves disease - most common cause overall (autoimmune)
2. Toxic multinodular goiter
3. Toxic adenoma
4. Subacute thyroiditis (De Quervain) - painful, post-viral,
5. Silent/postpartum thyroiditis - painless, transient
6. Excess iodine
7. exogenous thyroid hormone intake
8. Struma ovarii - rare ovarian teratoma
9. TSH-secreting pituitary adenoma
10. Hypothalamic TRH-producing tumors -
complications of hyperthyroidism
atrial fibrillation
thyroid storm
eye complications / graves opthalmopathy
Diffuse bilateral reticulonodular shadowing in both lungs
Miliary Tuberculosis:
Differentials for Miliary TB
Atypical Pneumonia
Pulmonary edema
ARDS
clinical features of miliary TB
non specific
Lymphadenopathy
Hepatosplenomegaly
Low-grade fever with night sweats
Weight loss
Decreased appetite
Malaise
examination findings; TB
Consolidation: dullness on percussion, crackles
Cavitation: hyperresonance on percussion, amphoric breath sounds
lab; TB
Sputum AFB smear (Ziehl-Neelsen stain)
Sputum culture for Mycobacterium tuberculosis
Nucleic acid amplification test
CBC
ESR/CRP
LFTs
HIV test
Chest XRYA,
CT chest
PCR
Spine X-ray / MRI Spine; Pott's disease (vertebral TB)
biposy in sever cases
Rx. TB
2 months; RIPE
4 months; RI
Adjuvant treatment: pyridoxine to prevent vitamin B6 deficiency
RIPE for TB
RIPE": Rifampin, Isoniazid, Pyrazinamide, and Ethambutol
Complications; TB
ARDS
Empyema
Pneumothorax
Disseminated tuberculosis infection (including tubercular meningitis)
Bronchiectasis
Aspergilloma
Hemoptysis
Mediastinal shift to the opposite side
Depressed diaphragm on affected side
Hyperlucent (dark) hemithorax on the affected side
no bronchovascular markings
Tension Pneumothorax
Rx. pneumothorax
Immediate Needle Decompression; 2nd / 5th intercostal space, midclavicular line
Chest Tube (Tube Thoracostomy); 4th or 5th intercostal space, mid-axillary line
Oxygen supplementation
IV fluids if hypotensive
Monitor vitals and repeat chest X-ray to confirm lung re-expansion
complications; penumothorax
Complete pulmonary collapse → respiratory failure
Tension pneumothorax → cardiac failure
Hemothorax
Pneumomediastinum
Pneumoperitoneum
examinations findings; pneumothorax
Reduced or absent breath sounds
Hyperresonant percussion
Decreased tactile fremitus
Reduced chest expansion
Distended neck veins
Bilateral hilar lymphadenopathy is seen
Sarcoidosis (classic cause)
Tuberculosis
Lymphoma
Fungal infections (e.g., histoplasmosis)
Silicosis
Other granulomatous diseases
labs; sarcoidosis
CBC and differential
ESR, CRP
CMP (including calcium levels)
Urinalysis
Serum ACE levels
Chest X-ray
High-resolution CT (HRCT)
Pulmonary function tests (PFTs)
Bronchoalveolar lavage (BAL)
Tissue biopsy (gold standard)
first line treatment; sarcoidosis
Observation: For asymptomatic or mild cases, especially Stage I.
Corticosteroids: First-line for symptomatic or progressive disease.
Supportive care: Treat organ-specific complications (e.g., supplemental oxygen for lung involvement).
What is the most common causative organism of lobar pneumonia?
Streptococcus pneumoniae.
pathophysiological stages of lobar pneumonia.
Congestion, red hepatization, gray hepatization, resolution.
Homogeneous consolidation confined to one or more lobes with air bronchograms.
chest X-ray findings in lobar pneumonia.
lab; pneumonia
CBC (leukocytosis)
CRP
ESR
Serum procalcitonin (PCT)
Blood cultures
Sputum culture and Gram stain
Imaging
Chest X-ray (posteroanterior and lateral)
Chest CT (usually without contrast)
Bronchoscopy (for suspected mass, pathohistology, inconclusive CT, poor treatment response)
how to decide for hospitalization of pneumonia
CURB 65
CURB 65
Confusion (disorientation, impaired consciousness)
Serum Urea > 7 mmol/L or BUN > 20 mg/dL
Respiratory rate ≥ 30/min
Blood pressure: systolic BP ≤ 90 mm Hg or diastolic BP ≤ 60 mm Hg
Age ≥ 65 years
CURB-65 score 0 or 1: The patient may be treated as an outpatient.
CURB-65 score ≥ 2: Hospitalization is indicated.
Rx. pneumonia
Outpatient (no comorbidities)
Amoxicillin or doxycycline or macrolide (e.g., azithromycin)
Outpatient (with comorbidities)
Amoxicillin-clavulanate + macrolide
OR respiratory fluoroquinolone (e.g., levofloxacin)
Inpatient (non-ICU)
IV ceftriaxone or cefotaxime + azithromycin
OR respiratory fluoroquinolone
ICU
Ceftriaxone + azithromycin or fluoroquinolone
Consider coverage for MRSA or Pseudomonas if risk factors
Oxygen therapy, 45 sitting degree postion , parentral antipyertics, analgesics, antibiotics acc to type of
Bronchodilators if wheezing antimucolytics (inccase of SOB exces sputum, mucolytics)
most common cause of atypical pneumonia in young adults?
Mycoplasma pneumoniae
first-line treatment for atypical pneumonia?
Macrolides (e.g., azithromycin) or doxycycline
Cavity with air fluid level
Lung abscess
Tuberculosis (especially reactivation TB)
Necrotizing pneumonia (due to Klebsiella, S. aureus, Pseudomonas)
Fungal infections (e.g., Aspergillus, Histoplasma)
Malignancy
causes of lung abscess
anaerobic bacterial infection
aspiration
bronchial obstruction
immunosupression
fungal infection
recent/unresolved pneumonia
Rx. lung abscess
Empiric Antibiotic Therapy
no risk factors for MRSA:; Ceftriaxone + Metronidazole
If MRSA suspected: Vancomycin
nterventional Therapy; Percutaneous drainage, Surgical resection
chest xray findings; pleural effusion
Large Homongenous (since its big ) opacity in the middle and lower lobes of right lobe
Blunted costophrenic border in the right side
Silhouette sign
meniscus sign
labs; pleural effusion
Serum protein LDH
blood culture
xray
ct
pleural fluid analyisis via thoracocentesis
how to differentiate pleural effusion type
lights criteria
Light's criteria
Pleural Effusion is likely EXUDATIVE if atleast ONE of the following exists:
1. Pleural Protein : Serum Protein > 0.5
2. Pleural LDH : Serum LDH > 0.6
3. Pleural LDH is > 2/3 the upper limits of normal for serum
Transudative causes of pleural effusion:
Congestive heart failure
Hepatic cirrhosis
Nephrotic syndrome
Protein-losing enteropathy
Chronic kidney disease (Na+ retention)
Exudative causes of pleural effusion
infection. *parapneumonic)
empyema
malignancy
PE
Autoimune disease; sle
trauma
pancreatitis
Rx; pleural effusion
Treatment of the underlying cause [6]
Acute congestive heart failure: loop diuretics
thoracocentesis
low glucose (less than 60) pleural effusion
MEAT has low glucose: Malignancy, Empyema, Arthritis (rheumatoid pleurisy), and Tuberculosis
causes of Cloudy, milky effusion
Chylothorax
Pseudochylothorax
causes of purulent effusion
Parapneumonic effusion
Empyema
•Pleural fluid lymphocytosis suggests
TB, sarcoidosis or malignancy.
•Neutrophil dominant effusions are associated with
empyema or pulmonary embolism.
how to classify effusion/ascites based on LDH
LDH less than 225 U/L = transudate
LDH > 225U/ L = exudate
Serum ascitic albumin gradient (SAAG);
measures portal pressure to determine if ascites is due to portal hypertension ;
SAAG = (serum albumin) – (ascitic fluid albumin)
Diagnostic tools for ascites include
ultrasound, paracentesis, ascitic fluid analysis, fluid culture
Aspirated ascitic fluid ; clinically detectable until there are at least -- mL of fluid present.
500
Clinical features; ascites
{Abdominal distension, discomfort, Weight gain, Shortness of breath, Reduced appetite
Rx. ascities
aspirate, gram stain, culture, empiric, broad-spectrum antibiotics immediately after peritoneal fluid is obtained, till culture results become available
Diuretics
Monotherapy with spironolactone
Combination therapy with spironolactone PLUS furosemide
paracentesis