First of all greetings to everyone.
I have been reading this forum for last couple of days (for hours on end) and I am really glad I found a place with so much knowledge, compassion and courage.
English is not my first language, so I will try to give my best with medical terminology.
I live in small country in Europe where the health care options and standards are not so high as in USA or some other bigger countries, and people especially in my family have bitter experiences with medical professionals, so sadly often they chose to avoid them at all cost
Yesterday after MRI we found out that my father aged 78 (no other chronic illness, still working and active) most likely has prostate cancer, and judging by the results it doesn't seem to be one of the less aggressive ones
Short story:
03/2022 - having trouble urinating, primary doctor orders urinary cultures and PSA, urinary test comes positive and he is treated with antibiotics, PSA is 9 and there is a suggestion to visit urologist, which feeling better my father declines.
10/2022 - he is again having huge problems with urinating, he visits primary doctor again, this time urinary culture is negative, he still get antibiotics
12/2022 - still having problems after antibiotics I force him to visit private urologist(he still doesnt wanna visit hospital), he does DRE which was fine, and ultrasound of prostate which reveals big prostate (150ml), he orders PSA which is 23 now, he recommends MRI/biopsy
02/2022 - I finally make him visit hospital urologist, PSA is 31 now. Urologist orders prostate biopsy in two months. I ask him to order him for MRI which he refuses claiming it wont give us conclusive evidence of anything and he will still have to do biopsy, he gets pills for BPH in meantime (Dutasteride/tamsulozinklorid)
03/2022 - his PSA is 41 now, having been reading alot I still think MRI is useful to do before biopsy, so I drive him 200 miles to other town where we do MRI 3T scan and I get worst possible news
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MRI RESULTS :
Findings and Opinion:
A standard mpMRI of the prostate was performed using T1 and T2 sequences, multiparametric analysis, pre-contrast and dynamic post-contrast sequences, and diffusion imaging in a patient with an elevated PSA value of 41. The prostate is enlarged, with dimensions of 6.6x5.6x8 cm (APxLLxCC, 146 cc, PSA density=0.16 ng/mL/mL). The transitional zone of the prostate is hypertrophic, with BPH nodules and degenerative changes, and the peripheral zone is laterally reduced in width, with visible prostatic calculi apically.
The posterior part of the prostate is infiltrated by a PI-RADS 5 lesion measuring 7x5.6x8 cm, which infiltrates the spermatic cord, seminal vesicles, the posterior part of the prostate's predominantly peripheral zone, the initial part of the urethra, the MRF, and the mesorectal space up to the rectum, which it is inseparable from, and which is probably infiltrated. The lesion also impresses upon the posterior wall of the urinary bladder and the peritoneal fold. The neurovascular bundles are infiltrated.
Lymph nodes adjacent to the common iliac vessels are up to 1.2 cm in diameter, with the left external lymph node up to 1.5 cm, while the inguinal lymph nodes are not enlarged. The urinary bladder is poorly distended. No free intraperitoneal fluid is detected. Small focal lesions are visible in the pelvic bones, and bone scintigraphy is recommended.
Conclusion:
A permagna PI-RADS 5 lesion is seen in the posterior part of the prostate.
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I then call urologist again, and present him with MRI findings.
He is not pleased that we did MRI on our own accord and claims he still need to do biopsy to coniform cancer (which I understand), but I also believe MRI could be useful to target suspicious area...
He tell me that after biopsy there will be bone scans and CT/PET scan, and then the treatment will begin with probably combination of hormone therapy and radiation.
He reassures me that this is still treatable, and you can live with this condition, and that I shouldn't write my father off (I was very distressed at that moment).
I now know we should have reacted sooner where it would more manageable but as I said my parents harbor big distrust to medical community which they will have to change now.
I blame myself allot also, not taking things in my hands before and not forcing him to go through with exams, I will have to wear this cross with me now. I feel like I failed my father, and he was nothing but a good unselfish person his whole life, giving everything to others and not caring for himself and his own needs.
So my questions would be, is 1 month to wait for biopsy too much (considering his big and quickly raising PSA)?
Is there hope for my father to be with us at least few more years ?
I really need some positive outlook/news, and maybe some tips during this grim road ahead of him.