In 2001, I had classical gallbladder pain and ultrasound revealed while the gallbladder did have some small stone, the pain was from a large mass on my liver. After a CT scan, then a CT guided biopsy and subsequently a surgical biopsy (when the gallbladder was removed) pathologists were unable to differentiate and diagnose the tumor. I subsequently had the tumor and the left lobe of my liver removed. Local pathologists were still unable to diagnose but thought it was carcinoma. They did send a specimen to the Armed Forces Institute pathologists who determined that it was an angiomyolipoma - a tumor usually found on the kidneys. In 2004, my brother (my only sibling) had abdominal pain and it was discovered he had a kidney tumor. They removed the kidney and the tumor turned out to be a angiomyolipoma.
My questions are:
1) What type of follow-up should I have? Ultrasound? How often? I have read that these tumors sometimes re-occur and may then be cancerous.
2) My bother's surgeon told him that our children (now in their early 30's) should be screened sometime. Is this a
hereditaryHereditary amyloidosis
Pseudohypoparathyroidism tumor? And if not, what casued both of us to have it?
3) Why was it so difficult for the pathologists to determine what my tunor was? It took over a month to get results and the wait was very stressful.