The Lymphoma Hub is an open-access online resource, dedicated to providing balanced, credible, and up-to-date medical education in lymphoma and CLL. Our aim is to enhance knowledge in lymphoma and CLL, through the multichannel dissemination of global advances related to their classification, diagnosis, treatment, and management.
The Lymphoma Hub shares new data, evidence-based articles, therapy approvals, expert opinions, and international congress coverage to treatment teams and researchers around the world.
Jó napot! Köszönöm a videót. Nekem korábban is volt ilyen problémám, a Demyxil segített megoldani. Krém formájában kapható. Budapesten élek, ide rendeltem a weboldalról. Ajánlom a terméket! Most időnként használom a láb bőrének puhaságáért.
Hi Everyone My mom has a swollen lymph node in her neck. We went to doctor before 6 months. They told it was normal. After 6 months the node went small, but still we showed to doctor. Went through a CT scan and biopsy. Biopsy told it might be hodgkin's lymphoma. Then, she had 2 biopsy in the same area and the result came as same, where it tolds, it might be hodgkin's lymphoma. Then, in pet scan nodes can be seen on her body somewhere. So doctor come to an conclusion it was hodgkin's lymphoma. On biopsy, they recommended excision biopsy or IHC test. Doctors doesn't performed it. She neither has any symptoms or swollen nodes anywhere outside. Also the node on the neck got disappeared. have few doubts. Please clarify me In first biopsy - Moderate cellular smear shows scatterd population of mononucleated and binucletaed cells with prominent nucleoli admixed with eosinophils in a lymphoid background. Second biopsy: RBC series shows microlytic hypochromic RBC exhibiting mild amisocytosis and WBC series shows Normal in count with Neutrophilic pryondrance. Please tell me what does it mean and why the doctors not confirmed it as hodgkin's lymphoma, they only suggested hodgkin's lymphoma. No excisional biopsy and IHC test were taken. CT scan shows Normal. Also the swollen node on her neck got reduced in this mean time. Is this because of back to back biopsy done on her node reduced that or any other reason? She got none of the symptoms with the disease where this is happening for over 6 months except the foundings in the PET scan and the suggestive biopsy results. Doctors are not giving enough information. So, please clarify my doubts.
I was diagnosed with double hit in 2015 at age 52. I did one round of hyper c-vad and five rounds of dose adjusted R-EPOCH. I also did two intrathecal methotrexate.
@@Lisa-zs2iygood luck to you and your husband. The dose adjusted R-EPOCH was rough to take. The Rituxan , a monoclonal antibody was very effective for me and I was not bothered by it. Don’t hesitate to reach out to me if you have any questions . I also combined a lot of lifestyle enhancements…diet, exercise, relaxation. See book titled Anti Cancer, a new way of life by Dr Sirvan Schreiber
I know the Medical Industrial Complex is heralding CAR-T; but, as a patient, the $500k "miracle" treatment w/a 6 month wait list having 40% disease progression already after just 12 months is NOT exciting. She ignores PFS for p53 mutated (me)- I think it was median 7mo. This is definetely not going to save my life.
Well done. I enjoyed this. When I was diagnosed with FL my bone marrow was "95% infected with Lymphoma." I began B & R the next day. 31 months (after completion of the 6 (2 day) X 28 day cycles) a CT Scan showed enlarged Lymph nodes in the Inguinal area. 15 months later I have progression on both sides of the diaphragm, misting of the mesentery and am "on watch and wait." What I haven't been able to find is a chart showing POD 24 - only showing POD 24, month by month AND month by month after the 24. In my case is 31 months much better than POD 24? Is it the same as 48 months? Is there a progression in degree of seriousness between 24 and 48. Or is 24 really a "turning point" and everything later than that is "party time at my place!" Just wondering...
Dr. Epperla, thank you! I really enjoyed the talk and your assessments. I felt like I was in your office and you were my doctor! I have just been found to have relapsed FL. When initially diagnosed with FL 5(ish) years ago my bone marrow was "95% infected with lymphoma." I began a modified B & R treatment the next day. I am excited about how much new information and options there are even after just 5 years.
Chemotherapy does not call the cancer stem cells - just the "daughter cells". So, it often comes back with a vengeance as the immune system is really harmed by chemotherapy. Causing "shrinkage" does not stop cancers from continuing to grow.
Being great full to Dr osaye from all time till all time I hope you find what your heart desires just as you have put a smile on many of our faces with just your hands and herbal’s More grace to you work doctor thanks so much for the medication,it did fight the (Els) and nailed it…
I haven’t been so greatful for so much things before, but for the fact that the herpes virus almost took a part of my life and I thought it was the end not believing that someday Gods plan In my life is permanent and I had the opportunity to get to Dr osaye,and im so happy that i have finally been cured thank you so much dr..
Instead of predicting survival in patients with relapsed diffuse large B-cell lymphoma, why not predict reactions to R-CHOP so the recipe is tailored to the patient instead of waiting until AFTER administration when the damage is done? With a survival of 20% with T Cells (from the patient's POV it's a failure of 80%), coming up with a new measurement of survival is a distinction without a difference.
Trust and honesty is something that will always lead you straight to what’s right,firstly I was afraid to trust the doctor not knowing he was the one God sent to heal my virus,I was diagnosed with ectopic lymphoid structure (ELS), and I’ve been battling with this virus and just decided to take a step and order the medication from Dr osaye,now I can finally testify and say thank you doctor from the deepest of my heart..
can someone please tell doctors to learn fuckjing English before they decide to lecture in English!!?? I'd have understood his Italian better for Davinci's sake!!>/??>.?.?>?
Here is my story (so far): I have primary Sjögren’s syndrome and recently discovered cherry angiomas all over, with a new band on my upper back (which is called the Sign of Leser Trelat) and bilateral, partially indurated, arcuate-form erythematous, hypopigmented, and slightly atrophic patches on face with cigarette paper skin and some scaling, with new telangiectasiae, as well as FMF-looking patch on the lower back- all extremely pruritic. They recently came about with a surge of hormones (peri-menopause). I went to a dermatologist who had looked at the photos I’d sent ahead of time to my PCP and had already decided when I got to her office that I was working myself up before she even saw me because she told me in office with an attitude that I took as patronizing (which really hurt my feelings, by the way), gave a quick glance at my back with a gentle swipe of her hand and pat on my shoulder. She then glanced momentarily (and not with a dermatoscope) at my face and dismissively informed me that she wasn’t worried and that I looked “fine”. I have a family history of cancer (few different types- melanoma being one of them), however, along with having red hair, green eyes and freckles. I insisted on biopsies (unfortunately, she failed to recognize the follicular patch, and did not take a punch of it, but took one nearby, instead); she sent the biopsies (3 in total) to a pathologist who was not a dermatopathologist. The dermatologist did not mention that FMF was in the differential to the pathologist, even though I told her that FMF is a concern Interestingly enough, I also have a patch of spiky skin near my left elbow and many subcutaneous nodules on my arms, trunk and thighs (some tethered and painful, all of which were also not examined and were just as quickly dismissed by the doctor because my mother has them, as well). Prior to these (extremely pruritic) cherry angiomas and various patches, I’d also been found to have a Bartholin gland cyst, axillary cyst, acrochordons, and velvety, intertriginous patches (that I suspect to be AN, but that were also immediately dismissed by the doctor, as they do not appear to be hyperpigmented). In addition to the small moles and cherry angiomas in a band across my back, there are several small, pruritic, erythematous papules on my chest, face and back, with symmetrical, confetti-type of vitiligo on my face, chest and arms. Both eyebrows have been losing hair over the lateral/superior aspect- also highly pruritic. I get a photosensitive rash on my face, arms and chest (with systemic symptoms). The malar rash has always spared the nasolabial folds prior to experiencing the telangiectasiae there. The 3” follicular patch on my back has perilesional halos. CBC showed a small decrease in lymphocytes, anemia (chronic), low levels of zinc and vitamin D, but on the whole, WNLs (with the exception of a weakly positive ANA and +SS-A), along with many other signs and symptoms of pSS (laundry list of stuff, including unstable angina, previous SCAD episode, HTN and TIAs, ). One other very interesting finding was that increasing my vitamin D intake (50,000 units a week), which my neurologist prescribed due to vit. D deficiency, seemed to slightly alleviate the pruritus. I felt completely dismissed by my dermatologist and left her a very upsetting message (which I feel badly about now) when she only diagnosed me with rosacea (because they found one single mite- and as you know, these are normal flora in small amounts). I did not even look at the slides myself; as soon as I saw her comments, I’d decided to dismiss her as my provider). In addition to the many systemic signs and symptoms of pSS I’ve had, I also regularly experience dry cough, chronic pancreatic pain, renal colic due to nephrocalcinosis, BPPV, night sweats, extreme fatigue, polyneuropathy, polyarthralgia, nausea, bone pain, neurological decline, extreme pruritus and burning back pain. I have had 19 doctors so far (specialists, not including my PCP) and have had to fight tooth and nail for every test I’ve had. No diagnosis, and no treatment so far. I’m in pain all the time and cannot work due to the widespread pain and fatigue, along with hypersensitivity to everything (as soon as I get stressed out- physically or emotionally), I get hives and puffy eyes and am just miserable. I’m not the type to be anxious or depressed, but after all of these tests and knowing deep down something is very wrong. Having pSS complicates everything but none of my doctors are knowledgeable about the syndrome and have all- except my neurologist and nephrologist- have dismissed me promptly. I’m desperate to find a doctor who is experienced and knowledgeable and can help!
Praying for you! With your doctor’s help, increase your vitamin D intake (get your doctor to do a study to see if you are deficient- studies show an inverse relationship between vitamin D deficiency and MF).
@@SongOfSongsOneTwelve oh wow! Thank you for letting me know. I didn’t know this. I’m going to have to do light therapy and I have white spots all over my body mixed with this acne looking stuff.
@@SongOfSongsOneTwelve also, There isn’t much information on this cancer. Thankfully I’m going to have treatment at Duke. My dermatologist didn’t know too much about this rare disease
@@priscillaroldan If you look at Dr. Clay Cockerell’s dermatopathology teaching series on T cell lymphoma (ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-D84RLj1nUish.htmle), he says a lot about the disease, but there are studies on vitamin D and Mycosis fungoides. I’ll try to leave a link, but YT keeps censoring my comments.
I was a patient diagnosed with Peripheral T cell NHL in the year 2014. Location of the infected lymph node was Right Groin, which enlarged to lower abdomen. Peripheral T cell NHL diagnosed after excision biopsy. I got 7 Cycle CHOP and Radiotherapy. In September 2020 a PET-CT Scan done after I notice sever itching problem. PET scan showed an 70x51x70mm sized Anterior Mediastinal Mass with SUV max 11. Thoracic surgeon refused to operate the mass. A core biopsy and histochemistry done. Which shows an Intermediate grade Diffuse large B cell Lymphoma. CD20, BCL6 & MUM1 are positive. BCL2, CD3, CD5 & CD10 Negative. Bone marrow aspiration suggesting "Reactive marrow with myeloid hyperplasia and excess of lymphocytes. Before all these diagnosis I only faced itching problem. First symptom noticed in beginning of August 2019. Last 24-26th October I suddenly faced swallowing face. An echocardiogram of the heart on 27th October showing small amount of fluid build up around my heart. LDH lifted to 366. My oncologists immediately suggest chemotherapy. The new chemo protocol is R-GCEOP. 1st Cycle started on 27th October and spited into 3 days. Rituximab, Cyclophosphamide, Gemcitabine, Etoposide, Vincristine, prednisone given. After 1st cycle chemo, face swallowing and itching removed significantly. We took part in a research project which involved a two day trip to Florida to the ALS Disease Centre, We had the opportunity to meet with Dr Odia, A highly recommended herbalist with scientific medicine. There is a lot to say about Dr Odia. I began healing herbs from Dr Odia, MD, who specializes in internal and pulmonary herbal medicine at ( drodiaherbalistcenter@gmail.com). I would encourage anyone to seek a second opinion especially if they’ve been told there’s no hope. It’s also crucial to learn as much as you can about your diagnosis. Seek options. Find out about what’s out there that could help. Contact Dr Odia via: facebook.com/DrOdiathenaturopathic/ WhatsApp +17278553511.. He has a cure for Encephalitis, Herpes and cancer.
I was a patient diagnosed with Peripheral T cell NHL in the year 2014. Location of the infected lymph node was Right Groin, which enlarged to lower abdomen. Peripheral T cell NHL diagnosed after excision biopsy. I got 7 Cycle CHOP and Radiotherapy. In September 2020 a PET-CT Scan done after I notice sever itching problem. PET scan showed an 70x51x70mm sized Anterior Mediastinal Mass with SUV max 11. Thoracic surgeon refused to operate the mass. A core biopsy and histochemistry done. Which shows an Intermediate grade Diffuse large B cell Lymphoma. CD20, BCL6 & MUM1 are positive. BCL2, CD3, CD5 & CD10 Negative. Bone marrow aspiration suggesting "Reactive marrow with myeloid hyperplasia and excess of lymphocytes. Before all these diagnosis I only faced itching problem. First symptom noticed in beginning of August 2019. Last 24-26th October I suddenly faced swallowing face. An echocardiogram of the heart on 27th October showing small amount of fluid buildup around my heart. LDH lifted to 366. My oncologists immediately suggest chemotherapy. The new chemo protocol is R-GCEOP. 1st Cycle started on 27th October and spited into 3 days. Rituximab, Cyclophosphamide, Gemcitabine, Etoposide, Vincristine, prednisone given. After 1st cycle chemo, face swallowing and itching removed significantly. We took part in a research project which involved a two day trip to Florida to the ALS Disease Centre, We had the opportunity to meet with Dr Odia, A highly recommended herbalist with scientific medicine. There is a lot to say about Dr Odia. I began healing herbs from Dr Odia, MD, who specializes in internal and pulmonary herbal medicine at ( facebook.com/DrOdiathenaturopathic/ ). I would encourage anyone to seek a second opinion especially if they’ve been told there’s no hope. It’s also crucial to learn as much as you can about your diagnosis. Seek options. Find out about what’s out there that could help. Contact Dr Odia via WhatsApp +17278553511.. He has a cure for Encephalitis, Herpes and cancer.
I was a patient diagnosed with Peripheral T cell NHL in the year 2014. Location of the infected lymph node was Right Groin, which enlarged to lower abdomen. Peripheral T cell NHL diagnosed after excision biopsy. I got 7 Cycle CHOP and Radiotherapy. In September 2020 a PET-CT Scan done after I notice sever itching problem. PET scan showed an 70x51x70mm sized Anterior Mediastinal Mass with SUV max 11. Thoracic surgeon refused to operate the mass. A core biopsy and histochemistry done. Which shows an Intermediate grade Diffuse large B cell Lymphoma. CD20, BCL6 & MUM1 are positive. BCL2, CD3, CD5 & CD10 Negative. Bone marrow aspiration suggesting "Reactive marrow with myeloid hyperplasia and excess of lymphocytes. Before all these diagnosis I only faced itching problem. First symptom noticed in beginning of August 2019. Last 24-26th October I suddenly faced swallowing face. An echocardiogram of the heart on 27th October showing small amount of fluid buildup around my heart. LDH lifted to 366. My oncologists immediately suggest chemotherapy. The new chemo protocol is R-GCEOP. 1st Cycle started on 27th October and spited into 3 days. Rituximab, Cyclophosphamide, Gemcitabine, Etoposide, Vincristine, prednisone given. After 1st cycle chemo, face swallowing and itching removed significantly. We took part in a research project which involved a two day trip to Florida to the ALS Disease Centre, We had the opportunity to meet with Dr Odia, A highly recommended herbalist with scientific medicine. There is a lot to say about Dr Odia. I began healing herbs from Dr Odia, MD, who specializes in internal and pulmonary herbal medicine at ( Dr Odia Herbalist Home on Facebook). I would encourage anyone to seek a second opinion especially if they’ve been told there’s no hope. It’s also crucial to learn as much as you can about your diagnosis. Seek options. Find out about what’s out there that could help. Contact Dr Odia via: facebook.com/DrOdiathenaturopathic/ WhatsApp +17278553511.. He has a cure for Encephalitis, Herpes and cancer.
