I’m 34, 10 months ago I gave birth to a beautiful baby girl but was unable to breastfeed due to inverted nipples. My left nipple is fully inverted and my right nipple is partially inverted. I developed mastitis in my right breast which was treated and went away.
After a couple of months I developed a hard lump next to my areola which I saw a GP about, they told me to come back if it was still there after 3 months, which it was so I went back and got a referral to the breast clinic. I saw a dr and had an ultrasound and to my delight they told me it didn’t look suspicious and they would see me in another 3 months for another ultrasound if it was still there.
In the time between ultrasound appointments my right breast began leaking what I think is milk and blood, my nipple swelled and burst several times and now leaks fluid on a daily basis and hurts a lot. The lump is still there, you can easily feel it, its about 3cm long.
I went back to the clinic last week and they did another ultrasound and took 3 core biopsies from my right breast. The dr said he suspects it’s a papilloma and ultrasounded my left breast and said he thinks it’s the same thing on that side too and may be what’s causing the nipple retraction. He also mentioned they normally like to surgically remove papillomas. He also kept asking me if I was ok and if I understood everything, which has left me feeling like it could be more serious than originally thought.
Like us all, I’ve done sone reading online and can see that while in the majority of cases papillomas are benign tumors it’s not always the case, and if there are multiples then your chances of developing BC in the future increase.
I’m now worried that even if my results come back benign (please!) I’ll have to have surgery anyway. I don’t have much in the way of breasts as it is (don’t fill an A cup) and don’t like the idea of a general anaesthesia.
Dr also said they would most likely want to take more biopsies from the left breast.
Should I be worried they took 3 biopsies?
Does anyone have any idea how much marginal tissue they take?
Should I be worried about future papillomas even if they remove these ones?
I’m also not sure exactly how they will contact me with the results, the slip of paper says an outpatient appointment and it’ll take a week to process, i’m assuming a letter in the post, or do you get a phone call? Does anyone know how the NHS get back to you ?
Sorry for the essay (and TMI) good to order events and thoughts. What are your experiences with biopsies and results? Xx