Introduction: Amyloid goiter is a very rare manifestation of amyloidosis, can occur as a result of either primary or secondary
amyloidosis of unknown etiology, leading in an increase in the size of the thyroid gland and compressive symptoms, depending on
deposit location and severity. Case presentation: We report a case of 17-year-old patient who came with a one year history of
enlarging painless neck and face swelling, presented to the Endocrine department in Tadawi international Poly Clinics in Abha
City, Aseer Area, South of Kingdom Saudi Arabia. An enlarged thyroid gland with mediastinal involvement was discovered on
ultrasound. The patient was diagnosed with primary amyloidosis involving only the thyroid gland, which was confirmed by
histopathology. The multinodular appearance was compatible with a diagnosis of multinodular goiter. Discussion and conclusion:
Amyloid Goiter is an extremely uncommon condition. Many previous studies revealed that a strong index of suspicion is expected
in individuals with enlarged thyroid glands and a history of persistent inflammatory processes or plasma cell disorders. Fine needle
aspiration cytology/biopsy (FNAC/B) should be undertaken to rule out thyroid cancer. Thyroidectomy is required for a variety of
reasons; such as confirmed diagnosis cases.
Keywords: Amyloidosis, Thyroid, Ultrasound, Male, Goiter, KSA