Hypercalcemia

597,448views

00:00 / 00:00

Hypercalcemia

V

V

Familial hypercholesterolemia
Multiple endocrine neoplasia
Neurofibromatosis
Tuberous sclerosis
von Hippel-Lindau disease
Albinism
Cystic fibrosis
Gaucher disease (NORD)
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
Hemochromatosis
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Krabbe disease
Leukodystrophy
Niemann-Pick disease types A and B (NORD)
Fabry disease (NORD)
Tay-Sachs disease (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Phenylketonuria (NORD)
Cystinuria (NORD)
Aromatic L-amino acid decarboxylase deficiency (NORD)
Sickle cell disease (NORD)
Spinocerebellar ataxia (NORD)
IgA nephropathy (NORD)
Focal segmental glomerulosclerosis (NORD)
Muscular dystrophies and mitochondrial myopathies: Pathology review
Wiskott-Aldrich syndrome
Muscular dystrophy
Hemophilia
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Alport syndrome
Alpha-thalassemia
Beta-thalassemia
Congenital adrenal hyperplasia
Primary adrenal insufficiency
Waterhouse-Friderichsen syndrome
Hyperaldosteronism
Cushing syndrome
Conn syndrome
Thyroglossal duct cyst
Hyperthyroidism
Graves disease
Thyroid eye disease (NORD)
Toxic multinodular goiter
Thyroid storm
Hypothyroidism
Hashimoto thyroiditis
Riedel thyroiditis
Thyroid cancer
Hypocalcemia
Hypercalcemia
Hyperparathyroidism
Hypoparathyroidism
Diabetes mellitus
Diabetic retinopathy
Diabetic nephropathy
Hyperpituitarism
Pituitary adenoma
Hyperprolactinemia
Prolactinoma
Gigantism
Acromegaly
Hypopituitarism
Pituitary apoplexy
Sheehan syndrome
Hypoprolactinemia
Constitutional growth delay
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Precocious puberty
Delayed puberty
Premature ovarian failure
Polycystic ovary syndrome
Androgen insensitivity syndrome
Kallmann syndrome
5-alpha-reductase deficiency
Multiple endocrine neoplasia
Pancreatic neuroendocrine neoplasms
Zollinger-Ellison syndrome
Carcinoid syndrome
Pheochromocytoma
Neuroblastoma
Myelodysplastic syndromes
Nephrotic syndromes: Pathology review
Reye syndrome
Tourette syndrome
Fragile X syndrome
Valvular heart disease: Pathology review
Sleep apnea
HIV (AIDS)
Heart blocks: Pathology review
Malabsorption syndromes: Pathology review
Tuberculosis: Pathology review
Hypothyroidism: Pathology review
Inflammatory bowel disease: Pathology review
Osteoporosis medications
Osteoarthritis
Acute pancreatitis
Major depressive disorder
Bipolar and related disorders
Generalized anxiety disorder
Panic disorder
Obsessive-compulsive disorder
Body dysmorphic disorder
Post-traumatic stress disorder
Physical and sexual abuse
Schizoaffective disorder
Schizophreniform disorder
Delusional disorder
Schizophrenia
Delirium
Amnesia
Dissociative disorders
Anorexia nervosa
Bulimia nervosa
Factitious disorder
Somatic symptom disorder
Attention deficit hyperactivity disorder
Tourette syndrome
Autism spectrum disorder
Rett syndrome
Neuroleptic malignant syndrome
Skin cancer: Clinical
Spina bifida
Amenorrhea: Clinical
Cervical cancer: Clinical
Seizures: Clinical
Leukemia: Clinical
Headaches: Clinical
Portal hypertension
Cirrhosis
Cirrhosis: Pathology review
Kawasaki disease
Lymphedema
Truncus arteriosus
Transposition of the great vessels
Total anomalous pulmonary venous return
Hypoplastic left heart syndrome
Patent ductus arteriosus
Ventricular septal defect
Coarctation of the aorta
Atrial septal defect
Tricuspid valve disease
Pulmonary valve disease
Mitral valve disease
Aortic valve disease
Dilated cardiomyopathy
Restrictive cardiomyopathy
Hypertrophic cardiomyopathy
Cor pulmonale
Acyanotic congenital heart defects: Pathology review
Cyanotic congenital heart defects: Pathology review
Valvular heart disease: Pathology review
Prinzmetal angina
Aneurysms
Acute leukemia
Acute pyelonephritis
Acute kidney injury: Clinical
Poliovirus
Renal tubular acidosis

Assessments

Flashcards

0 / 17 complete

USMLE® Step 1 questions

0 / 3 complete

High Yield Notes

6 pages

Flashcards

Hypercalcemia

0 of 17 complete

Questions

USMLE® Step 1 style questions USMLE

0 of 3 complete

A 67-year-old male comes to his outpatient provider’s office for evaluation of fatigue and diffuse muscle aches. His symptoms started about a year ago and have been progressing over time. He also reports having bowel movement once a week with hard, pellet-like stool formation. Past medical history is significant for insulin-dependent diabetes mellitus type 2 and end-stage renal disease. He underwent a kidney transplant two months ago. His medications include insulin and sirolimus. The patient has a 35-pack-year smoking history but is no longer smoking. In the office, his temperature is 37.6°C (99.7°F), pulse is 68/min, respirations are 14/min and blood pressure is 115/74 mmHg. Laboratory testing reveals the following results:

 
 Laboratory value  Result 
 Serum chemistry 
 Serum calcium  11.2 mmol/L 
 Serum phosphate  2.4 mmol/L 
 Parathyroid hormone 560 pg/mL 
  *Normal range: 10-55 pg/mL  

Which of the following is the most likely cause of the patient’s presentation? 

External References

First Aid

2024

2023

2022

2021

Abdominal pain

hypercalcemia p. 609

Anxiety

hypercalcemia and p. 609

Bladder cancer

hypercalcemia and p. 219

Breast cancer

hypercalcemia and p. 219

Familial hypocalciuric hypercalcemia p. 342

Hypercalcemia p. 609

acute pancreatitis and p. 404

adult T-cell lymphoma p. 435

bisphosphonates for p. 495

calcium carbonate in p. 406

diabetes insipidus p. 349

granulomatous diseases and p. NaN

hyperparathyroidism p. 342

loop diuretics for p. 624

lung cancer p. 703

paraneoplastic syndrome p. 219

PTH-independent p. 348

sarcoidosis and p. 695

succinylcholine p. 565

teriparatide p. 496

thiazides as cause p. 627

Williams syndrome p. 62

Lung cancer p. NaN

hypercalcemia and p. 219

Lymphoma

hypercalcemia and p. 219

Ovarian cancer

hypercalcemia and p. 219

PTH-independent hypercalcemia p. 348

Renal cell carcinomas p. 617

hypercalcemia and p. 219

Squamous cell carcinomas

hypercalcemia and p. 219

Transcript

Watch video only

With hypercalcemia, hyper -means over and -calc- refers to calcium, and -emia refers to the blood, so hypercalcemia means higher than normal calcium levels in the blood, generally over 10.5 mg/dL.

Now, calcium exists as an ion with a double positive charge - Ca2+ - and it’s the most abundant metal in the human body.

So I know what you’re thinking - yeah, we’re all pretty much cyborgs,- Cool, huh?

So about 99% of that calcium is in our bones in the form of calcium phosphate, also called hydroxyapatite.

The last 1% is split so that the majority, about 0.99% is extracellular - which means in the blood and in the interstitial space between cells, and 0.01% is intracellular or inside cells.

High levels of intracellular calcium causes cells to die.

In fact, that’s exactly what happens during apoptosis, also known as programmed cell death.

For that reason, cells end up spending a lot of energy just keeping their intracellular calcium levels low.

Now, calcium gets into the cell through two types of channels, or cell doors, within the cell membrane.

The first type are ligand-gated channels, which are what most cells use to let calcium in, and are primarily controlled by hormones or neurotransmitters.

The second type are voltage-gated channels, which are mostly found in muscle and nerve cells and are primarily controlled by changes in the electrical membrane potential.

So calcium flows in through these channels, and to prevent calcium levels from rising too high, cells kick excess calcium right back out with ATP-dependent calcium pumps as well as Na+-Ca2+ exchangers.

In addition, most of the intracellular calcium is stored within organelles like the mitochondria and smooth endoplasmic reticulum and is released selectively just when it's needed.

Now, the majority of the extracellular calcium is split almost equally between two groups - calcium that is diffusible and calcium that is not diffusible.

Diffusible calcium is separated into two subcategories: free-ionized calcium, which is involved in all sorts of cellular processes like neuronal action potentials, contraction of skeletal, smooth, and cardiac muscle, hormone secretion, and blood coagulation, all of which are tightly regulated by enzymes and hormones.

The other category is complexed calcium, which is where the positively charged calcium is ionically linked to tiny negatively charged molecules like oxalate, which is a small anions that’s normally found in our blood in small amounts.

The complexed calcium forms a molecule that’s electrically neutral and small enough to cross cell membranes, but, unlike free-ionized calcium is not useful for cellular processes.

Finally, though, there’s the non-diffusible calcium which is bound to negatively charged proteins like albumin and globulin, and the resulting protein-calcium complex is too large and charged to cross membranes, leaving this calcium also uninvolved in cellular processes.

When the body’s levels of extracellular calcium change, it’s detected by a surface receptor in parathyroid cells called the calcium-sensing receptor.

This affects the amount of parathyroid hormone that gets released by the parathyroid gland.

The parathyroid hormone gets the bones to release calcium, and gets the kidneys to reabsorb more calcium so it's not lost in the urine and synthesize calcitriol also known as active vitamin D.

Active vitamin D then goes on to increase calcium absorption in the gastrointestinal tract.

All together, these effects help to keep the extracellular levels of calcium within a very narrow range, between 8.5 to 10 mg/dl.

Sometimes, though, total calcium levels in the blood, which includes both diffusible and non-diffusible - blood can vary a bit, depending on the blood's pH and protein levels.

This happens because albumin has acidic amino acids, like glutamate and aspartate, which have some carboxyl groups that are in the form of COO- or COOH.

Overall the balance of COOi and COOH changes based on the pH of the blood.

Now, when there’s a low pH, or acidosis, there are plenty of protons or H+ ions floating around, and a lot of those COO- groups pick up a proton and become COOH.

More COOH groups make albumin more positively charged, and since calcium is positively charged, these two repel each other, and this decreases bound calcium and increases the proportion of free ionized calcium in blood.

So as more protons bind albumin, more free ionized calcium builds up in the blood, and so even though total levels calcium are the same, there’s less bound calcium and more ionized calcium, which remember is important for cellular processes and can lead to symptoms of hypercalcemia.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  5. "Calcium block of Na <sup>+</sup> channels and its effect on closing rate" Proceedings of the National Academy of Sciences (1999)
  6. "The diagnosis and management of hypercalcaemia" BMJ (2015)
  7. "Osborn waves in a hypothermic patient" Journal of Community Hospital Internal Medicine Perspectives (2012)