Toxic multinodular goiter

Toxic multinodular goiter

M2 Digestive & Endocrine

M2 Digestive & Endocrine

Anatomy of the abdominal viscera: Blood supply of the foregut, midgut and hindgut
Gastroesophageal reflux disease (GERD): Clinical
Gastroesophageal reflux disease (GERD)
Inflammatory bowel disease: Pathology review
Inflammatory bowel disease: Clinical
Helicobacter pylori
Esophageal cancer
Esophageal disorders: Clinical
Gastric cancer
Peptic ulcers and stomach cancer: Clinical
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Lymphomas: Pathology review
Colorectal cancer
Colorectal cancer: Clinical
Colorectal polyps and cancer: Pathology review
Anal conditions: Clinical
Meckel diverticulum
Zollinger-Ellison syndrome
Colorectal polyps
Familial adenomatous polyposis
Juvenile polyposis syndrome
Diverticular disease: Pathology review
Diverticular disease: Clinical
Diverticulosis and diverticulitis
Small bowel ischemia and infarction
Gastrointestinal bleeding: Clinical
Gastrointestinal bleeding: Pathology review
Ovarian sex-cord stromal tumors
Neurofibromatosis
Li-Fraumeni syndrome
Anatomy of the abdominal viscera: Pancreas and spleen
Anatomy of the abdominal viscera: Liver, biliary ducts and gallbladder
Gastric motility
Development of the gastrointestinal system
Elimination disorders: Clinical
Pediatric constipation: Clinical
Laxatives and cathartics
Hirschsprung disease
Bowel obstruction
Abdominal pain: Clinical
Peritonitis
Hernias: Clinical
Abdominal hernias
Gallstones
Gallstone ileus
Gallbladder disorders: Pathology review
Primary sclerosing cholangitis
Biliary atresia
Acute pancreatitis
Pancreatic secretion
Pancreatic cancer
Chronic pancreatitis
Pancreatitis: Pathology review
Pancreatitis: Clinical
Pancreatic pseudocyst
Gallbladder carcinoma
Acute cholecystitis
Chronic cholecystitis
Viral hepatitis
Non-alcoholic fatty liver disease
Chewing and swallowing
Carbohydrates and sugars
Fats and lipids
Proteins
Vitamins and minerals
Diarrhea: Clinical
Irritable bowel syndrome
Campylobacter jejuni
Clostridium difficile (Pseudomembranous colitis)
Clostridium botulinum (Botulism)
Escherichia coli
Salmonella (non-typhoidal)
Salmonella typhi (typhoid fever)
Shigella
Staphylococcus aureus
Vibrio cholerae (Cholera)
Yersinia enterocolitica
Mycobacterium avium complex (NORD)
Adenovirus
Norovirus
Rotavirus
Cytomegalovirus infection after transplant (NORD)
Cryptosporidium
Entamoeba histolytica (Amebiasis)
Giardia lamblia
Anisakis
Enterobius vermicularis (Pinworm)
Trichuris trichiura (Whipworm)
Ascaris lumbricoides
Ancylostoma duodenale and Necator americanus
Strongyloides stercoralis
Diphyllobothrium latum
Malabsorption syndromes: Pathology review
Malabsorption: Clinical
Tropical sprue
Whipple's disease
Antidiarrheals
Diabetes mellitus: Pathology review
Diabetes mellitus
Ketone body metabolism
Sleep apnea
Sleep disorders: Clinical
Pituitary gland histology
Adrenal gland histology
Congenital adrenal hyperplasia
Anatomy of the thyroid and parathyroid glands
Hyperthyroidism
Hyperthyroidism: Pathology review
Hyperthyroidism: Clinical
Hypothyroidism
Hypothyroidism: Pathology review
Hypothyroidism and thyroiditis: Clinical
Congenital adrenal hyperplasia: Clinical
Cushing syndrome
Cushing syndrome and Cushing disease: Pathology review
Cushing syndrome: Clinical
Graves disease
Hashimoto thyroiditis
Riedel thyroiditis
Thyroid cancer
Adrenal insufficiency: Pathology review
Adrenal cortical carcinoma
Pheochromocytoma
Adrenal masses: Pathology review
Sheehan syndrome
von Hippel-Lindau disease
Multiple endocrine neoplasia
Thyroid hormones
Thyroid nodules and thyroid cancer: Clinical
Toxic multinodular goiter
Subacute granulomatous thyroiditis
Cirrhosis
Viral hepatitis: Clinical
Autoimmune hepatitis
Primary biliary cholangitis
Hepatitis A and Hepatitis E virus
Hepatitis C virus
Hepatitis D virus
Hepatitis medications
Leptospira
Rickettsia rickettsii (Rocky Mountain spotted fever) and other Rickettsia species
Brucella
Coxiella burnetii (Q fever)
Echinococcus granulosus (Hydatid disease)
Hepatocellular adenoma
Hemochromatosis
Wilson disease
Alpha 1-antitrypsin deficiency
Gaucher disease (NORD)
Cholestatic liver disease
Alcohol-associated liver disease
Benign liver tumors
Portal hypertension

Transcript

Watch video only

In toxic multinodular goiter, also called Plummer’s disease, ‘toxic’ refers to something harmful, ‘nodular’ refers to little lumps or nodules of tissue, and ‘goiter’ refers to a large thyroid gland.

So toxic multinodular goiter is a condition where the thyroid gland enlarges and is filled with lots of little nodules of tissue - each of which produce so much thyroid hormone that it becomes harmful to the body

Normally, the hypothalamus, which is located at the base of the brain, detects low blood levels of thyroid hormones and releases thyrotropin-releasing hormone into the hypophyseal portal system - which is a network of capillaries linking the hypothalamus to the anterior pituitary.

The anterior pituitary then releases thyroid-stimulating hormone, also called thyrotropin or simply TSH.

TSH stimulates the thyroid gland which is a gland located in the neck that looks like two thumbs hooked together in the shape of a “V”.

The thyroid gland is made up of thousands of follicles, which are small spheres lined with follicular cells.

Follicular cells convert thyroglobulin, a protein found in follicles, into two iodine-containing hormones, triiodothyronine or T3, and thyroxine or T4.

Once released from the thyroid gland, these hormones enter the blood and bind to circulating plasma proteins.

Only a small amount of T3 and T4 will travel unbound in the blood, and these two hormones get picked up by nearly every cell in the body.

Once inside the cell T­4 is mostly converted into T3, and it can exert its effect. T3 speeds up the basal metabolic rate.

So as an example, they might produce more proteins and burn up more energy in the form of sugars and fats.

It’s as if the cells are in a bit of frenzy.

T3 increases cardiac output, stimulates bone resorption - thinning out the bones, and activates the sympathetic nervous system, the part of the nervous system responsible for our ‘fight-or-flight’ response.

Thyroid hormone is important - and the occasional increase is like getting a boost to fight off a hungry predator or to stay warm during a snowstorm! 

Toxic multinodular goiter usually starts with a chronic lack of dietary iodine, and follicular cells need iodine to make T3 and T4.

With less iodine around, each follicular cell makes less thyroid hormone, and as a whole, the level of thyroid hormone goes down.

In response to low levels of thyroid hormones, the anterior pituitary releases TSH.

The high levels of TSH cause thyroid hypertrophy - the build up in thyroid tissue - and hyperplasia - increased numbers of follicular cells.

But, here’s the thing - some parts of the thyroid gland are more responsive to TSH than others, so the growth ends up being uneven throughout the thyroid.

So the most responsive follicular cells start to grow quickly and develop into a nodule, and the rest of the gland looks basically the same.

Typically, multinodular goiter starts with a single nodule and over years multiple nodules start to appear.

This strategy works for a while and the thyroid is considered a non-toxic multinodular goiter.

In other words, having more follicular cells makes up for the fact that each follicular cell makes less thyroid hormone - so the thyroid enters a balanced or euthyroid state.

Key Takeaways

Toxic multinodular goiter (TMNG) is a condition characterized by the growth of multiple nodules in the thyroid gland, which can cause the gland to become enlarged and produce too much thyroid hormone. The excess thyroid hormone production can lead to symptoms of hyperthyroidism, including weight loss, rapid heart rate, tremors, and heat intolerance.

TMNG typically develops after prolonged iodine deficiency, which causes hypertrophy and hyperplasia of the thyroid gland. Continued follicular cell division can lead to a genetic mutation of the TSH receptor turning a non-toxic multinodular goiter into a toxic multinodular goiter.

Symptoms include an enlarged thyroid as well as the typical symptoms of hyperthyroidism like weight loss, a rapid heart rate, and hyperactivity. The treatment for TMNG involves medications like beta-blockers and radioactive iodine, or surgery to remove part or all of the thyroid gland.

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. "Harrison's Endocrinology, 4E" McGraw-Hill Education / Medical (2016)
  6. "Large Multinodular Toxic Goiter: Is Surgery Always Necessary?" Case Reports in Endocrinology (2016)
  7. "Clinical outcomes after estimated versus calculated activity of radioiodine for the treatment of hyperthyroidism: systematic review and meta-analysis" European Journal of Endocrinology (2009)
  8. "Molecular Pathogenesis of Euthyroid and Toxic Multinodular Goiter" Endocrine Reviews (2004)