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Related Concept Videos

The Parathyroid Glands00:59

The Parathyroid Glands

The two pairs of parathyroid glands embedded within the posterior surface of the thyroid gland are restricted by a dense capsule around them. These glands comprise two distinct cell populations—parathyroid oxyphil and parathyroid principal cells- pivotal in calcium homeostasis.
Oxyphil cells, whose functions remain elusive, emerge during late puberty, adding a layer of complexity to the parathyroid gland's intricacies. In contrast, principal parathyroid cells undertake a vital role by producing...
Hyperthyroidism II: Pathophysiology01:27

Hyperthyroidism II: Pathophysiology

Hyperthyroidism is a hypermetabolic state caused by elevated levels of thyroid hormones, triiodothyronine (T3) and thyroxine (T4). It results from dysregulation at the thyroid, pituitary, or immune system level and affects multiple organ systems.PathophysiologyThe most common cause of hyperthyroidism is Graves’ disease, an autoimmune disorder in which antibodies, specifically thyroid-stimulating antibodies (TSAb), a subtype of TSH receptor antibodies (TRAb), bind to and activate TSH receptors...
Hyperthyroidism I: Introduction01:25

Hyperthyroidism I: Introduction

Hyperthyroidism is a type of thyrotoxicosis characterized by the thyroid gland's overproduction of the thyroid hormones triiodothyronine (T3) and thyroxine (T4). This hormone excess increases the basal metabolic rate and enhances sensitivity to catecholamines.DiagnosisDiagnosis is based on clinical features and biochemical testing. It typically shows suppressed thyroid-stimulating hormone (TSH) levels below 0.4 mIU/L, with elevated free T3 and/or T4. Additional tests, including thyroid...
Graves Disease II: Pathophysiology01:24

Graves Disease II: Pathophysiology

Graves’ disease is an autoimmune disorder characterized by the production of thyroid-stimulating immunoglobulins (TSI) that activate TSH receptors, leading to excessive synthesis and release of thyroid hormones (T3 and T4) and resulting in hyperthyroidism.Among all causes of hyperthyroidism, Graves’ disease is the most common and can happen at any age, though it is more frequent in women. It produces a hypermetabolic state with features such as weight loss, tachycardia, tremor, and heat...
Hypothyroidism II: Pathophysiology01:23

Hypothyroidism II: Pathophysiology

Hypothyroidism is a disorder characterized by insufficient production of thyroid hormones, which regulate metabolism, energy balance, and multiple organ systems.TypesHypothyroidism is classified based on the level of dysfunction. Primary hypothyroidism results from intrinsic thyroid gland dysfunction, causing reduced hormone production despite normal or increased stimulation. Secondary hypothyroidism arises from inadequate thyroid-stimulating hormone (TSH) secretion by the pituitary. Tertiary...
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...

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Related Experiment Video

Updated: May 16, 2026

Establishment of a Simple and Effective Rat Model for Intraoperative Parathyroid Gland Imaging
07:12

Establishment of a Simple and Effective Rat Model for Intraoperative Parathyroid Gland Imaging

Published on: August 17, 2022

Primary hyperparathyroidism having multiple Brown tumors mimicking malignancy.

Ekram Ullah1, Mehtab Ahmad, Syed Asmat Ali

  • 1Department of Radiodiagnosis, Jawaharlal Nehru Medical College, A.M.U. Aligarh, Uttar Pradesh, India.

Indian Journal of Endocrinology and Metabolism
|December 11, 2012
PubMed
Summary

Primary hyperparathyroidism can cause rare bone lesions called Brown tumors, which may mimic cancer. This case highlights the importance of considering hyperparathyroidism in differential diagnoses for lytic bone lesions.

Keywords:
Brown tumorsendocrine systemexpansile lesionsprimary hyperparathyroidism

Related Experiment Videos

Last Updated: May 16, 2026

Establishment of a Simple and Effective Rat Model for Intraoperative Parathyroid Gland Imaging
07:12

Establishment of a Simple and Effective Rat Model for Intraoperative Parathyroid Gland Imaging

Published on: August 17, 2022

Area of Science:

  • Endocrinology
  • Oncology
  • Skeletal Biology

Background:

  • Primary hyperparathyroidism involves excessive parathormone secretion, leading to bone resorption and potential skeletal complications.
  • Brown tumors are rare fibrotic, cystic bony changes associated with hyperparathyroidism, occurring in less than 2% of patients.
  • These lesions can present as multiple, lytic, expansile masses, posing diagnostic challenges.

Observation:

  • A 23-year-old Indian woman presented with multiple lytic expansile bone lesions.
  • Initial clinical suspicion leaned towards malignancy or fibrous dysplasia due to the nature of the lesions.
  • The patient's evaluation ultimately revealed primary hyperparathyroidism as the underlying cause.

Findings:

  • The presented case demonstrates a rare manifestation of primary hyperparathyroidism.
  • Multiple Brown tumors, initially suspected as malignant neoplasms, were diagnosed.
  • The differential diagnosis of lytic bone lesions must include endocrine disorders.

Implications:

  • This case underscores the critical need for comprehensive differential diagnosis in patients with unexplained lytic bone lesions.
  • Recognizing rare skeletal manifestations of endocrine diseases like primary hyperparathyroidism is crucial for accurate diagnosis and treatment.
  • Early identification can prevent misdiagnosis and ensure appropriate management of hyperparathyroidism and its skeletal sequelae.