Below is a summary of my thyroid ultrasound and fine needle aspiration report. I do have a family history of papillary and follicular ca (aunt) and my mother had a partial thyroidectomy as a teenager for unknown dx--limited follow up. I am curious as to what you would recommend as a next step? We are hoping to become pregnant shortly (almost 38 yrs old) and I want to make sure that this is not something that I need to worry about prior to that. Initial ultrasound done d/t fam hx...no palpable nodules or thyroid related symptoms
US: Rt lobe: 3 nodules, 2 upper pole (10x7x7, 10x9x6) solid heterogenous, some calcifications, 1 mid pole (9x7x5) Lt. lobe nl
Bx - upper pole nodule, essentially no follicular cells, colloid and histiocytes "raising possibility of goiter"; population of smaller cells w/ nuclear atypia "question degenerating epithelial cells transforming into histiocytes but difficult to determine"; no overt malignancy but recommend close follow up and re-biopsy.
labs: calcitonin 2, TSH 0.888, Free T4 0.88, negative thyroid antibodies
Do I need to be on synthroid suppression therapy? Do I need to wait on becoming pregnant? How soon should I consider a repeat biopsy...of the same nodule or of a different nodule? Should I consider a lobectomy? These are all options that my primary care physician as raised.
Thank you very much for your input