Hypertension: Pathology review

Hypertension: Pathology review

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Sepsis
Infective endocarditis: Clinical
Endocarditis: Pathology review
Endocarditis
Fever of unknown origin: Clinical
Salmonella typhi (typhoid fever)
Plasmodium species (Malaria)
Schistosomes
Zinc deficiency and protein-energy malnutrition: Pathology review
Hypophosphatemia
Hyponatremia
Hyponatremia: Clinical
Hypertriglyceridemia
Hypertensive disorders of pregnancy: Clinical
Preeclampsia & eclampsia
Gestational hypertension
Gestational diabetes
Contraception: Clinical
Preterm labor
Erectile dysfunction
PDE5 inhibitors
Fallopian tube and uterus histology
Endometriosis
Chlamydia trachomatis
Neisseria gonorrhoeae
Treponema pallidum (Syphilis)
Congenital syphilis
Sexually transmitted infections: Clinical
HIV (AIDS)
Herpes simplex virus
Human papillomavirus
Endometrial hyperplasia
Endometrial cancer
Endometrial hyperplasia and cancer: Clinical
Ovarian cysts and tumors: Pathology review
Cervical cancer
Cervical cancer: Clinical
Cervical cancer: Pathology review
Ectopic pregnancy
Endometritis
Pelvic inflammatory disease
Ovarian germ cell tumors
Ovarian cysts, cancer, and other adnexal masses: Clinical
Sexual dysfunctions: Clinical
Anatomy clinical correlates: Wrist and hand
Placenta previa
Placental abruption
Vaginal versus cesarean delivery: Clinical
Antepartum hemorrhage: Clinical
Postpartum hemorrhage
Postpartum hemorrhage: Clinical
Urinary incontinence
Stages of labor
Shock
Shock: Clinical
Shock: Pathology review
Opioid agonists, mixed agonist-antagonists and partial agonists
Opioid use disorder
Opioid antagonists
Syncope: Clinical
Hypertension: Clinical
Hypertension
Hypertension: Pathology review
Local anesthetics
Ventricular arrhythmias: Pathology review
Supraventricular arrhythmias: Pathology review
Wolff-Parkinson-White syndrome
Ventricular fibrillation
Class II antiarrhythmics: Beta blockers
Class III antiarrhythmics: Potassium channel blockers
Class IV antiarrhythmics: Calcium channel blockers and others
Atrial fibrillation
Atrial flutter
Ventricular tachycardia
Premature ventricular contraction
Heart failure
Heart failure: Pathology review
Heart failure: Clinical
Nephrotic syndromes: Pathology review
Nephritic and nephrotic syndromes: Clinical
Nephritic syndromes: Pathology review
Frank-Starling relationship
Aortic dissection
Aortic dissections and aneurysms: Pathology review
Aortic aneurysms and dissections: Clinical
Pericarditis and pericardial effusion
Atherosclerosis and arteriosclerosis: Pathology review
Angina pectoris
Leg ulcers: Clinical
Chronic venous insufficiency
Ischemic stroke
Stroke: Clinical
ECG cardiac hypertrophy and enlargement
Hypertrophic cardiomyopathy
Cardiomyopathies: Pathology review
Cardiomyopathies: Clinical
Dilated cardiomyopathy
Restrictive cardiomyopathy
Long QT syndrome and Torsade de pointes
Brugada syndrome
Action potentials in pacemaker cells
Asthma
Asthma: Clinical
Pneumonia
Pneumonia: Clinical
Pneumonia: Pathology review
Streptococcus pneumoniae
Pneumocystis jirovecii (Pneumocystis pneumonia)
Reading a chest X-ray
Mycobacterium tuberculosis (Tuberculosis)
Tuberculosis: Pathology review
Upper respiratory tract infection
General anesthetics
Lung cancer
Lung cancer: Clinical
Lung cancer and mesothelioma: Pathology review
Chronic obstructive pulmonary disease (COPD): Clinical
Sleep apnea
Apnea, hypoventilation and pulmonary hypertension: Pathology review
Sleep disorders: Clinical
Sleep
Narcolepsy (NORD)
Clinical Skills: BiPAP and CPAP
Restrictive lung diseases
Restrictive lung diseases: Pathology review
Diffuse parenchymal lung disease: Clinical
Idiopathic pulmonary fibrosis
Hypersensitivity pneumonitis
Sarcoidosis
Acetaminophen (Paracetamol)
Paracetamol toxicity
Non-steroidal anti-inflammatory drugs
Respiratory alkalosis
Metabolic and respiratory alkalosis: Clinical
Metabolic and respiratory acidosis: Clinical
Advanced cardiac life support (ACLS): Clinical
Respiratory acidosis
Pancoast tumor
Congenital cytomegalovirus (NORD)
Congenital TORCH infections: Pathology review
Alport syndrome
Pediatric ear, nose, and throat conditions: Clinical
Turner syndrome
Down syndrome (Trisomy 21)
Developmental milestones: Clinical
Neonatal sepsis
Auditory transduction and pathways
Muscular dystrophy
Cerebral palsy
Respiratory syncytial virus
Respiratory distress syndrome: Pathology review
Newborn management: Clinical
Neonatal respiratory distress syndrome
Appendicitis
Appendicitis: Clinical
Appendicitis: Pathology review
Meckel diverticulum
Neonatal jaundice: Clinical
Hirschsprung disease
Congenital gastrointestinal disorders: Pathology review
Pediatric allergies: Clinical
Pediatric constipation: Clinical
Pediatric vomiting: Clinical
Febrile seizure
Rotator cuff tear
Carpal tunnel syndrome
Achilles tendon rupture
Patellar tendon rupture
Anterior cruciate ligament injury
Spinal disc herniation
Sciatica
Degenerative disc disease
Compartment syndrome
Osteomyelitis
Bone tumors
Osteoporosis
Osteomalacia and rickets
Osteoarthritis
Rheumatoid arthritis
Gout
Psoriatic arthritis
Ankylosing spondylitis
Septic arthritis
Bursitis
Polymyositis
Dermatomyositis
Myasthenia gravis
Lambert-Eaton myasthenic syndrome
Sjogren syndrome
Systemic lupus erythematosus
Raynaud phenomenon
Platelet plug formation (primary hemostasis)
Coagulation (secondary hemostasis)
Role of Vitamin K in coagulation
Clot retraction and fibrinolysis
Anticoagulants: Heparin
Anticoagulants: Warfarin
Anticoagulants: Direct factor inhibitors
Sensitivity and specificity
Positive and negative predictive value
Sickle cell disease (NORD)
Sickle cell disease: Clinical
Cystic fibrosis
Cystic fibrosis: Pathology review
Cystic fibrosis: Clinical
Phenylketonuria (NORD)
Non-corticosteroid immunosuppressants and immunotherapies
Glucocorticoids
Child abuse: Clinical
Abdominal hernias
Hernias: Clinical
Inguinal hernia
Femoral hernia
Volvulus
Varicocele
Nutcracker syndrome
Testicular tumors: Pathology review
Testicular torsion
Intestinal atresia
Tracheoesophageal fistula
Necrotizing enterocolitis
Diabetes mellitus
Diabetes mellitus: Clinical
Diabetes mellitus: Pathology review
Gestational diabetes
Hypoglycemics: Insulin secretagogues
Insulins
Diabetic nephropathy
Diabetic retinopathy
Diabetes insipidus
Insulin
Diabetes insipidus and SIADH: Pathology review
Pituitary gland histology
Anatomy of the thyroid and parathyroid glands
Thyroid and parathyroid gland histology
Pituitary tumors: Pathology review
Pituitary adenomas and pituitary hyperfunction: Clinical
Pituitary adenoma
Hyperprolactinemia
Prolactinoma
Cushing syndrome
Cushing syndrome: Clinical
Cushing syndrome and Cushing disease: Pathology review
Acromegaly
Gigantism
Hypopituitarism
Hypopituitarism: Clinical
Hypopituitarism: Pathology review
Hyperpituitarism
Pituitary apoplexy
Adrenal gland histology
Primary adrenal insufficiency
Adrenal insufficiency: Clinical
Adrenal insufficiency: Pathology review
Thyroid nodules and thyroid cancer: Clinical
Thyroid nodules and thyroid cancer: Pathology review
Thyroid cancer
Hashimoto thyroiditis
Thyroid storm
Thyroid hormones
Hypothyroidism and thyroiditis: Clinical
Hyperthyroidism
Hyperthyroidism: Pathology review
Hyperthyroidism: Clinical
Hyperthyroidism medications
Hypothyroidism
Hypothyroidism medications
Hypothyroidism: Pathology review
Toxic multinodular goiter
Graves disease
Cortisol
Renin-angiotensin-aldosterone system
Conn syndrome
Waterhouse-Friderichsen syndrome
Adrenal masses and tumors: Clinical
Adrenal masses: Pathology review
Skin cancer
Skin cancer: Pathology review
Skin cancer: Clinical
Sarcoptes scabiei (Scabies)
Anti-mite and louse medications
Psoriasis
Psoriatic arthritis
Eczematous rashes: Clinical
Atopic dermatitis
Contact dermatitis
Seborrhoeic dermatitis
Keratitis
Miscellaneous antifungal medications
Azoles

Questions

USMLE® Step 1 style questions USMLE

0 of 3 complete

Start
A 55-year-old woman comes to the clinic for a hypertension follow up. She was diagnosed with hypertension 6 months ago and was prescribed a low-sodium diet and exercise. Medical history is significant for diabetes mellitus type 2 that is currently managed with metformin. She has been smoking 1 pack of cigarettes daily for 20 years. Family history is significant for osteoporosis in her mother and diabetes mellitus in her father. Temperature is 37.0 °C (98.6 °F), pulse is 80/min, and blood pressure is 152/95 mmHg. Urinalysis reveals microalbuminuria. DXA scan shows normal bone mineral density. A decision is made to add a pharmacological antihypertensive medication that works by inhibiting the production of angiotensin II. Which of the following types of medications was provided to this patient? 

Transcript

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Anthony is a 40 year old male with a history of type 2 diabetes mellitus presenting to a family medicine clinic for his annual health check-up. His blood pressure measurement is 145 over 95 millimeters of mercury, and his BMI is 32. On further history, he explains that his job as a truck driver has prevented him from exercising regularly. His father had a history of hypertension and passed away from a stroke. A follow-up appointment showed a blood pressure of 150 over 90. Alicia is a 30 year old female who came in because she’s concerned that she might be pregnant. Her pregnancy test is negative, however, her blood pressure is 170 over 90. On her second appointment, her blood pressure remains elevated. She is placed on lisinopril. A couple of days later, she presents with decreased urine output, and an elevated blood urea nitrogen and creatinine. Finally, Vikander is a 62 year old-male with a history of hypertension. He complains of headache, altered mental status, and visual changes. On further history, he mentions he is “sick of all the medications he has to take”. Fundoscopic examination reveals a swollen optic disk, and his blood pressure is 200 over 120.

Okay so all three people present with hypertension. Now normal blood pressure is less than 120 systolic over 80 diastolic. According to the recent 2017 American Heart Association and American College of Cardiology guidelines, hypertension is currently defined as a blood pressure over 130 systolic and 80 diastolic. Now, typically, both systolic and diastolic pressures tend to rise or fall together, but that’s not always the case. Sometimes, you can have systolic or diastolic hypertension. This is referred to as isolated systolic hypertension or isolated diastolic hypertension.

Okay, just because you see an elevated blood pressure on the exam, it does not mean that individual has hypertension. The blood pressure must be persistently elevated in order to define it as hypertension. So on your exam, remember that the diagnosis requires at least 2 separate readings on 2 separate visits. The reason for this is because of the phenomenon of “white coat hypertension”. This is hypertension on physical exam that occurs because of anxiety experienced by the individual.

Hypertension is classified into primary, or essential hypertension, and secondary hypertension. Primary hypertension occurs without a known secondary cause, and accounts for 90 percent of cases. The pathophysiology of primary hypertension is thought to be related to decreased renal sodium excretion. Reduced sodium excretion increases plasma volume, increasing the stroke volume, and as a result the systolic blood pressure. Also, the increased plasma volume causes decreased renin release from the juxtaglomerular apparatus, producing what’s called low-renin hypertension, and this can be high yield. Additionally, decreased sodium excretion promotes vasoconstriction of the peripheral arterioles, increasing the systemic vascular resistance, which increases diastolic blood pressure.

Okay, so risk factors for primary hypertension include age, physical inactivity, obesity, diabetes mellitus, smoking, family history of hypertension, as well as excess salt or alcohol consumption. It’s thought that in type II diabetes, high levels of insulin promote renal sodium retention.

Okay, before diagnosing an individual with primary hypertension, the causes of secondary hypertension must be ruled out. Your exams will often try to clue you towards this by mentioning that the individuals were on multiple antihypertensives and they didn’t work, or by having a relatively young individual with hypertension. The best approach is to look at different organ systems, starting with the adrenal gland. Important causes include primary hyperaldosteronism, or Conn syndrome, Cushing syndrome and tumors like pheochromocytoma and neuroblastoma. Clues in the question stem will help you identify which one it is. Hypokalemia, metabolic alkalosis and an increase in the aldosterone-to-renin ratio indicate Conn syndrome. Abdominal striae, supraclavicular fat pads, truncal obesity, and hyperglycemia point towards Cushing syndrome. Paroxysmal hypertension, that is hypertension that comes and goes, associated with headaches, palpitations and sweating indicate a pheochromocytoma. Neuroblastomas are common in children, and present with an abdominal mass.

Next is the kidney. Renal artery stenosis, also called renovascular disease is usually caused by an atherosclerotic plaque occluding the renal artery, especially in 60 to 70 year old males. Less commonly, it can be caused by fibromuscular dysplasia, especially in 20 to 30 year old females. This classically causes the “string of beads” appearance of the renal artery. Regardless of the cause, renal artery stenosis decreases renal perfusion. This makes your body think it’s in a hypotensive state. So in response, the renin-angiotensin-aldosterone system, or RAAS, is activated, resulting in vasoconstriction and increased renal sodium and water reabsorption, and eventually hypertension. Decreased renal perfusion causes the affected kidney to shrink, and histologically, there will be glomerular tubulointerstitial atrophy and fibrosis.

A high yield fact to remember for your exams is that unilateral renal artery stenosis does not cause CKD because the contralateral kidney is functioning normally, and in fact it hypertrophies to compensate. However, bilateral renal artery stenosis results in CKD because both kidneys are affected. Also, it’s important to not give ACE inhibitors to people with bilateral renal artery stenosis. This is because angiotensin II constricts the efferent arteriole in the glomerulus, which maintains the GFR. If an ACE inhibitor is given, the efferent arterioles dilate, causing a drop in the GFR.

Okay, renal parenchymal diseases like diabetic nephropathy, glomerulonephritis or polycystic kidney disease can also cause hypertension by retaining sodium.

Moving on, Coarctation of the aorta is also an important cause of hypertension, especially in children. And the mechanism is quite similar to renal artery stenosis, since renal perfusion is decreased, just that the obstruction is more proximal. Speaking of the aorta, aging causes the amount of elastin in the arterial wall to decrease, and the amount of collagen to increase, producing a stiff, non-compliant aorta. This manifests in elderly adults as isolated systolic hypertension, which means an elevated systolic blood pressure, but a normal diastolic.

Moving on, both hyperthyroidism and hypothyroidism can cause hypertension. Hyperthyroidism increases the cardiac output, causing an elevated systolic blood pressure. For some reason, hypothyroidism increases renal retention of sodium, and interestingly causes an isolated elevation of the diastolic blood pressure. The adjacent parathyroid glands are also potential suspects, because primary hyperparathyroidism causes hypercalcemia which increases vasoconstriction of the peripheral arterioles, resulting in an increased total peripheral vascular resistance.

Alright, if the person presents with hypertension, bradycardia and an irregular respiratory pattern, think of an increased intracranial pressure, which triggers a reflex that results in the Cushing’s triad. In pregnancy, it’s crucial to consider preeclampsia and eclampsia.

Finally, always be aware of what medications the individual is taking. Estrogen-containing oral contraceptives are common causes of hypertension, especially in young women. Estrogen works by increasing the synthesis of angiotensinogen in the liver, which is ultimately converted to angiotensin one and two. Cocaine is another potential drug that can cause hypertension by increasing sympathetic activity. Additionally, in people take monoamine-oxidase inhibitors, ingestion of tyramine-containing foods like cheese and wine may initiate an acute hypertension. Remember that sometimes the exam might not mention the medication but simply state that the person has a history of atypical or drug-resistant depression, which is an indication for MAOIs.

Alright, chronic hypertension can result in multiple complications affecting different organ systems. Let’s start with the heart. Hypertension increases the afterload, that is the resistance the heart has to pump against. In response, the left ventricle hypertrophies to overcome that resistance. Concentric hypertrophy increases the myocardial oxygen demand, which means the heart needs more coronary blood supply than usual. Also, concentric hypertrophy makes the heart stiff, which limits diastolic relaxation. This is why heart failure from hypertension is a diastolic heart failure, so the ejection fraction will actually be normal. Hypertension is also a risk factor for atherosclerosis, so there’s an increased risk of coronary artery disease, which is the most common cause of death from hypertension. Aortic dissection is another important complication, and hypertension is the most important risk factor contributing to it.

Sources

  1. "Rapid Review Pathology" Elsevier (2018)
  2. "Fundamentals of Pathology" H.A. Sattar (2017)
  3. "Williams Textbook of Endocrinology" W B Saunders Company (2008)
  4. "Pharmacotherapy for hypertension in adults aged 18 to 59 years" Cochrane Database Syst Rev (2017)
  5. "Hypertensive crisis" Cardiol Rev (2010)