This past December I got a bad cold which eventually turned into pneumonia by the middle of the month. I had
feverAllergic rhinitis
Coccidioidomycosis
Febrile seizures
Fever
Fever blister
Fever blisters and canker sores
Herpes labialis (oral herpes simplex)
Histoplasmosis
Malaria
Rheumatic fever
Scarlet fever, body aches, and extreme coughing
spasmsCoronary artery spasm
Croup
Eyelid twitch
Facial tics
Hand or foot spasms
Urge incontinence
Vascular spasm for more than two weeks. I coughed up every
colorColor blindness
Color blindness tests
Color vision test in the rainbow and at times so hard that my lungs hurt. After 3 rounds of antibiotic, I started to feel better. I had chest X-rays done before, during and after the pneumonia. Unfortunately, the final follow-up film showed a place in the bottom right section of my lung that would not
clearClear by design
Clear eyes
Clear eyes acr
Clear eyes clr
Clear-atadine
Clear-atadine children's up. A CT Scan was ordered and what was thought to be a mass was discovered. More antibiotic and a needle biopsy were then scheduled. Another CT Scan was done just before the needle biopsy and, based on that, I was told that it had shrunk and that there appeared to be no need for the biopsy. A month later after another CT Scan I was told that the mass/nodule had not changed – no bigger or smaller – and that the biopsy was back on. The result of the biopsy was no cancer cells present. However, they did find some
atypicalAtypical pneumonia cells. I was sent to a pulmonologist who said that the
atypicalAtypical pneumonia cells along with the shape of the nodule (partly smooth and round with some little rounded nobs on one side) made him feel that the FNA was inconclusive. He ordered a bronchoscopy which also came back without any cancer cells. However, he also said he didn’t feel he was able to really get to the nodule as it was so far down in the right lobe. I am now scheduled to meet with a thoractic surgeon to discuss yet another biopsy via microsurgery (VATS?).
I am a 51 year old female with a history of ovarian cancer (early detection, Stage 1, Type 2 tumor, no lymph nodes involved, surgery November 2001). I have not had a hint of recurrence in the 4.5 years since my surgery and chemo treatments and my CA 125 tests and bi-yearly exams have been excellent. My question is, does this seem related to the pneumonia in any way to you? The earlier Xrays done just before the pneumonia developed showed nothing where the nodule now is – it only showed up during the follow-up X-rays after the pneumonia and coughing fits had progressed. This has been going on for over two months and I am pretty close to going insane with worry at this point. Any insight is greatly appreciated.
I saw the surgeon today and have decided to have this thing removed through VATs surgery. The other option was to wait and watch it - which, in a sense, made me feel a bit better that he would consider that since it at least implied that he wasn't thinking of it as an emergency at this point. I will go in this coming Tuesday (May 16th) with 5-6 days in the hospital and about about 2 weeks recovery at home. One thing I do know is that God has his hand on this - it's the only possible explanation for how I'm getting through it.