50 results
Thyroid Goiter in Severe Hypothyroidism on Neck Physical Examination

TSH 124. Hashimoto’s, lost to care and thyroid
moves up with swallowing ... #PhysicalExam #clinical ... Hypothyroidism #endocrinology
Thyroid Goiter on Physical Exam

Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
goiter moves with swallowing ... iodine #deficiency #endocrinology ... #clinical #video
Retrosternal Thyroid Goiter on Physical Exam

Note the movement with swallowing, indicating a thyroid mass.

#Retrosternal #Thyroid #Goiter
movement with swallowing ... #PhysicalExam #clinical ... #video #endocrinology
Adrenal Insufficiency Differential Diagnosis Algorithm
Clinical suspicion: Weakness, fatigue, nausea, musculoskeletal pain, dizziness, volume depletion, abdominal pain,
Adrenal Insufficiency ... Diagnosis Algorithm Clinical ... ACTH - Primary adrenal ... ACTH - Secondary adrenal ... Diagnosis #Algorithm #endocrinology
Adrenal Insufficiency Diagnosis Algorithm
Clinical features: 
 - Weight loss, anorexia, Weakness, fatigue, GI distress
 - Hypotension,
Adrenal Insufficiency ... Diagnosis Algorithm Clinical ... seen in PRIMARY adrenal ... suggestive of adrenal ... Stimulation #StimTest #Endocrinology
Benign Adrenal Mass - Differential Diagnosis Algorithm
Hyperplasia - Often Bilateral
 • Congenital Adrenal Hyperplasia
 • ACTH
Benign Adrenal Mass ... • Congenital Adrenal ... High Plasma E2 +Clinical ... Diagnosis #Algorithm #Endocrinology
Hoffmann's Sign

Hoffman's sign means upper motor neuron injury.  The Hoffmann's reflex test itself involves loosely
fingernail downward, allowing ... Positive #Abnormal #clinical ... #video #neurology
Malignant Adrenal Mass - Differential Diagnosis Algorithm
Suggestive of Malignancy: Inhomogenous Density, Delay in CT Contrast Washout
Malignant Adrenal ... Syndrome, Congenital Adrenal ... High Plasma E2 + Clinical ... Often Bilateral) Adrenal ... Diagnosis #Algorithm #Endocrinology
Hoffmann's Reflex on Physical Exam
The Hoffmann's reflex itself involves loosely holding the middle finger and flicking
fingernail downward, allowing ... #PhysicalExam #clinical ... #neurology #UMN
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... 21-OHD in the adrenal ... as "congenital adrenal ... pathophysiology #genetics #endocrinology