Metastasis to the Ovaries from Transitional Cell Carcinoma of the Bladder and Renal Pelvis: a Report of Two Cases
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Bladder Cancer Early Detection, Diagnosis, and Staging Detection and Diagnosis
cancer.org | 1.800.227.2345 Bladder Cancer Early Detection, Diagnosis, and Staging Detection and Diagnosis Finding cancer early, when it's small and hasn't spread, often allows for more treatment options. Some early cancers may have signs and symptoms that can be noticed, but that's not always the case. ● Can Bladder Cancer Be Found Early? ● Bladder Cancer Signs and Symptoms ● Tests for Bladder Cancer Stages and Outlook (Prognosis) After a cancer diagnosis, staging provides important information about the extent (amount) of cancer in the body and the likely response to treatment. ● Bladder Cancer Stages ● Survival Rates for Bladder Cancer Questions to Ask About Bladder Cancer Here are some questions you can ask your cancer care team to help you better understand your cancer diagnosis and treatment options. ● Questions To Ask About Bladder Cancer 1 ____________________________________________________________________________________American Cancer Society cancer.org | 1.800.227.2345 Can Bladder Cancer Be Found Early? Bladder cancer can sometimes be found early -- when it's small and hasn't spread beyond the bladder. Finding it early improves your chances that treatment will work. Screening for bladder cancer Screening is the use of tests or exams to look for a disease in people who have no symptoms. At this time, no major professional organizations recommend routine screening of the general public for bladder cancer. This is because no screening test has been shown to lower the risk of dying from bladder cancer in people who are at average risk. Some providers may recommend bladder cancer tests for people at very high risk, such as: ● People who had bladder cancer before ● People who had certain birth defects of the bladder ● People exposed to certain chemicals at work Tests that might be used to look for bladder cancer Tests for bladder cancer look for different substances and/or cancer cells in the urine. -
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BCG LIVE (FOR INTRAVESICAL USE) TICE® BCG WARNING TICE® BCG contains live, attenuated mycobacteria. Because of the potential risk for transmission, it should be prepared, handled, and disposed of as a biohazard material (see PRECAUTIONS and DOSAGE AND ADMINISTRATION). BCG infections have been reported in health care workers, primarily from exposures resulting from accidental needle sticks or skin lacerations during the preparation of BCG for administration. Nosocomial infections have been reported in patients receiving parenteral drugs that were prepared in areas in which BCG was reconstituted. BCG is capable of dissemination when administered by the intravesical route, and serious infections, including fatal infections, have been reported in patients receiving intravesical BCG (see WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS). DESCRIPTION TICE® BCG for intravesical use, is an attenuated, live culture preparation of the Bacillus of Calmette and Guerin (BCG) strain of Mycobacterium bovis.1 The TICE® strain was developed at the University of Illinois from a strain originated at the Pasteur Institute. The medium in which the BCG organism is grown for preparation of the freeze-dried cake is composed of the following ingredients: glycerin, asparagine, citric acid, potassium phosphate, magnesium sulfate, and iron ammonium citrate. The final preparation prior to freeze drying also contains lactose. The freeze-dried BCG preparation is delivered in glass vials, each containing 1 to 8 x 108 colony forming units (CFU) of TICE® BCG which is equivalent to approximately 50 mg wet weight. Determination of in- vitro potency is achieved through colony counts derived from a serial dilution assay. A single dose consists of 1 reconstituted vial (see DOSAGE AND ADMINISTRATION). -
Primary Melanoma of the Bladder at Puerperium
ISSN: 2469-5742 Rubio et al. Int Arch Urol Complic 2020, 6:073 DOI: 10.23937/2469-5742/1510073 Volume 6 | Issue 1 International Archives of Open Access Urology and Complications CASE REPORT Primary Melanoma of the Bladder at Puerperium: Case Report Rubio Galisteo JM1*, Gomez Gomez E1, Valero Rosa J1, Salguero Segura J1, Pineda Reyes B2, Gonzalez T3, Barbudo Merino J4, Ruiz Garcia JM1 and Requena Tapia MJ1 1Urology Department, Hospital Universitario Reina Sofia, Spain 2Ginecology Department, Hospital Universitario Reina Sofia, Spain 3 Check for Pathological Anatomy Department, Hospital Universitario Reina Sofia, Spain updates 4Emergency Department, Hospital Universitario Reina Sofia, Spain *Corresponding author: Rubio Galisteo JM, Urology Department, Hospital Universitario Reina Sofía, Av Menendez Pidal S/N, UGC Urología, Córdoba, CP: 14004, Spain, Tel: +3460-004-5566 of urinary bladder in a 39-years-old postpartum wom- Abstract an. Primary malignant melanoma of the urinary bladder is a sporadic disease and very little described in the literature. Case Presentation A 39-years-old female at the end of her pregnancy without previous history of skin disease was presented with hema- A healthy 39-years-old female is presented at the turia after cesarean and with constitutional syndrome. After end of her first pregnancy. The patient gives a history of the study, the patient was diagnosed with metastatic blad- 10 kg lost at the last months, and urinary tract infection der melanoma. Other locations of primary injury were ruled out. The patient died a month and a half after the diagnosis. treated with antibiotics with a urine culture positive to E. -
Renal Transitional Cell Carcinoma: Case Report from the Regional Hospital Buea, Cameroon and Review of Literature Enow Orock GE1*, Eyongeta DE2 and Weledji PE3
Enow Orock, Int J Surg Res Pract 2014, 1:1 International Journal of ISSN: 2378-3397 Surgery Research and Practice Case Report : Open Access Renal Transitional Cell Carcinoma: Case report from the Regional Hospital Buea, Cameroon and Review of Literature Enow Orock GE1*, Eyongeta DE2 and Weledji PE3 1Pathology Unit, Regional Hospital Buea, Cameroon 2Urology Unit, Regional Hospital Limbe, Cameroon 3Surgical Unit, Regional Hospital Buea, Cameroon *Corresponding author: Enow Orock George, Pathology Unit, Regional Hospital Buea, South West Region, Cameroon, Tel: (237) 77716045, E-mail: [email protected] Abstract United States in 2009. Primary renal pelvis and ureteric malignancies, on the other hand, are much less common with an estimated 2,270 Although transitional cell carcinoma is the most common tumour of the renal pelvis, we report the first histologically-confirmed case in cases diagnosed and 790 deaths in 2009 [6]. Worldwide statistics our service in a period of about twenty years. The patient is a mid- vary with the highest incidence found in the Balkans where urothelial aged female African, with no apparent risks for the disease. She cancers account for 40% of all renal cancers and are bilateral in 10% presented with the classical sign of the disease (hematuria) and of cases [7]. We report a first histologically-confirmed case of renal was treated by nephrouretectomy for a pT3N0MX grade II renal pelvic transitional cell carcinoma in 20 years of practice in a mid-aged pelvic tumour. She is reporting well one year after surgery. The case African woman. highlights not only the peculiar diagnosis but also illustrates the diagnostic and management challenges posed by this and similar Case Report diseases in a low- resource setting like ours. -
Primary Renal Carcinoid Tumor: a Radiologic Review
Radiology Case Reports Volume 9, Issue 2, 2014 Primary renal carcinoid tumor: A radiologic review Leslie Lamb, MD, Msc, Bsc; Wael Shaban, MBBCH, MD, PhD Carcinoid tumor is the classic famous anonym of neuroendocrine neoplasms. Primary renal carcinoid tumors are extremely rare, first described by Resnick and colleagues in 1966, with fewer than a total of 100 cases reported in the literature. Thus, given the paucity of cases, the clinical and histological behav- ior is not well understood, impairing the ability to predict prognosis. Computed tomography and (occa- sionally) octreotide studies are used in the diagnosis and followup of these rare entites. A review of 85 cases in the literature shows that no distinctive imaging features differentiate them from other primary renal masses. The lesions tend to demonstrate a hypodense appearance and do not usually enhance in the arterial phases, but can occasionally calcify. Octreotide scans do not seem to help in the diagnosis; however, they are more commonly used in the postoperative followup. In addition, we report a new case of primary renal carcinoid in a horseshoe kidney. Case report Imaging findings 40-year-old male initially presented to a community hos- pital with a 20-lb weight loss over a few months. In retro- CT of the abdomen and pelvis, done in the portal ve- spect, the patient recalled mild left-flank discomfort and nous phase, demonstrated a solid, hypodense, 4.5-cm renal fatigue, but denied any hematuria. Blood work revealed an mass containing calcifications, located in the posterior as- elevated serum glucose, and he was diagnosed with type 2 pect of the medial diabetes. -
Urothelial Carcinoma of Bladder and Upper Tract
Urothelial Carcinoma of Bladder and Upper Tract Page 1 of 18 Disclaimer: This algorithm has been developed for MD Anderson using a multidisciplinary approach considering circumstances particular to MD Anderson’s specific patient population, services and structure, and clinical information. This is not intended to replace the independent medical or professional judgment of physicians or other health care providers in the context of individual clinical circumstances to determine a patient's care. This algorithm should not be used to treat pregnant women. Note: Consider Clinical Trials as treatment options for eligible patients. CLINICAL INITIAL INITIAL INITIAL SCREEN PRESENTATION EVALUATION DIAGNOSIS STAGING Negative for Treat as indicated3 bladder cancer Less than T2 See Page 2-3 ● Hematuria ● History and physical ● Transurethral resection (TUR) ● Recurrent unexplained 1 ● Office cystoscopy ● Exam under anesthesia (EUA) urinary tract infection Positive for ● Imaging: CT urogram or ● Consider single dose peri- ● Other unexplained bladder cancer 4 intravenous urogram (IVU) operative chemotherapy lower urinary tract 2 ● Lifestyle risk assessment instillation symptoms T2-4 See Page 4 (muscle invasion) Positive for See Page 6 upper tract tumor 1 Consider urinary cytology or other MD Anderson approved genitourinary biomarkers 2 See Physical Activity, Nutrition, and Tobacco Cessation algorithms; ongoing reassessment of lifestyle risks should be a part of routine clinical practice 3 If persistant microhematuria, recommend repeat of history and physical, office cystoscopy, imaging (CT urogram or IVU) in 2-3 years 4 Refer to Principles of Intravesical Treatment on Page 8 Department of Clinical Effectiveness V9 Approved by The Executive Committee of the Medical Staff on 07/21/2020 Urothelial Carcinoma of Bladder and Upper Tract Page 2 of 18 Disclaimer: This algorithm has been developed for MD Anderson using a multidisciplinary approach considering circumstances particular to MD Anderson’s specific patient population, services and structure, and clinical information. -
Solitary Duodenal Metastasis from Renal Cell Carcinoma with Metachronous Pancreatic Neuroendocrine Tumor: Review of Literature with a Case Discussion
Published online: 2021-05-24 Practitioner Section Solitary Duodenal Metastasis from Renal Cell Carcinoma with Metachronous Pancreatic Neuroendocrine Tumor: Review of Literature with a Case Discussion Abstract Saphalta Baghmar, Renal cell cancinoma (RCC) is a unique malignancy with features of late recurrences, metastasis S M Shasthry1, to any organ, and frequent association with second malignancy. It most commonly metastasizes Rajesh Singla, to the lungs, bones, liver, renal fossa, and brain although metastases can occur anywhere. RCC 2 metastatic to the duodenum is especially rare, with only few cases reported in the literature. Herein, Yashwant Patidar , 3 we review literature of all the reported cases of solitary duodenal metastasis from RCC and cases Chhagan B Bihari , of neuroendocrine tumor (NET) as synchronous/metachronous malignancy with RCC. Along with S K Sarin1 this, we have described a unique case of an 84‑year‑old man who had recurrence of RCC as solitary Departments of Medical duodenal metastasis after 37 years of radical nephrectomy and metachronous pancreatic NET. Oncology, 1Hepatology, 2Radiology and 3Pathology, Keywords: Late recurrence, pancreatic neuroendocrine tumor, renal cell carcinoma, second Institute of Liver and Biliary malignancy, solitary duodenal metastasis Sciences, New Delhi, India Introduction Case Presentation Renal cell carcinoma (RCC) is unique An 84‑year‑old man with a medical history to have many unusual features such as notable for hypertension and RCC, 37 years metastasis to almost every organ in the body, postright radical nephrectomy status, late recurrences, and frequent association presented to his primary care physician with second malignancy. The most common with fatigue. When found to be anemic, sites of metastasis are the lung, lymph he was treated with iron supplementation nodes, liver, bone, adrenal glands, kidney, and blood transfusions. -
Incidence and Familial Risk of Pleural Mesothelioma in Sweden: a National Cohort Study
ERJ Express. Published on May 12, 2016 as doi: 10.1183/13993003.00091-2016 ORIGINAL ARTICLE IN PRESS | CORRECTED PROOF Incidence and familial risk of pleural mesothelioma in Sweden: a national cohort study Jianguang Ji1, Jan Sundquist1,2 and Kristina Sundquist1,2 Affiliations: 1Center for Primary Health Care Research, Lund University, Malmö, Sweden. 2Stanford Prevention Research Center, Stanford University School of Medicine, Stanford, CA, USA. Correspondence: Jianguang Ji, Center for Primary Health Care Research, Lund University, CRC, Jan Waldenstroms gata 35, 205 02 Malmö, Sweden. E-mail: [email protected] ABSTRACT Familial clustering of pleural mesothelioma was reported previously, but none of the reports quantified the familial risk of mesothelioma or the association with other cancers. The contributions of shared environmental or genetic factors to the aggregation of mesothelioma were unknown. We used a number of Swedish registers, including the Swedish Multigeneration Register and the Swedish Cancer Register, to examine the familial risk of mesothelioma in offspring. Standardised incidence ratios (SIRs) were used to calculate the risk. Age standardised incidence rates of mesothelioma were calculated from the Swedish Cancer Registry. The incidence of mesothelioma reached its peak rate in 2000 and decreased thereafter. Risk of mesothelioma was significantly increased when parents or siblings were diagnosed with mesothelioma, with SIRs of 3.88 (95% CI 1.01–10.04) and 12.37 (95% CI 5.89–22.84), respectively. Mesothelioma was associated with kidney (SIR 2.13, 95% CI 1.16–3.59) and bladder cancers (SIR 2.09, 95% CI 1.32–3.14) in siblings. No association was found between spouses. -
Multilingual Cancer Glossary French | Français A
Multilingual Cancer Glossary French | Français www.petermac.org/multilingualglossary email: [email protected] www.petermac.org/cancersurvivorship The Multilingual Cancer Glossary has been developed Disclaimer to provide language professionals working in the The information contained within this booklet is given cancer field with access to accurate and culturally as a guide to help support patients, carers, families and and linguistically appropriate cancer terminology. The consumers understand their healthand support their glossary addresses the known risk of mistranslation of health decision making process. cancer specific terms in resources in languages other than English. The information given is not fully comprehensive, nor is it intended to be used to diagnose, treat, cure or prevent Acknowledgements any medical conditions. If you require medical assistance This project is a Cancer Australia Supporting people please contact your local doctor or call Peter Mac on with cancer Grant initiative, funded by the Australian 03 8559 5000. Government. To the maximum extent permitted by law, Peter The Australian Cancer Survivorship Centre, A Richard Pratt Mac and its employees, volunteers and agents legacy would like to thank and acknowledge all parties are not liable to any person in contract, tort who contributed to the development of the glossary. (including negligence or breach of statutory duty) or We particularly thank members of the project steering otherwise for any direct or indirect loss, damage, committee and working group, language professionals cost or expense arising out of or in connection with and community organisations for their insights and that person relying on or using any information or assistance. advice provided in this booklet or incorporated into it by reference. -
Primary Malignant Melanoma of the Urinary Bladder
Open Access Case Report DOI: 10.7759/cureus.14067 Primary Malignant Melanoma of the Urinary Bladder Elizabeth Snajdar 1 , Andrina R. Ajo 2 , Katie Rosen 1 , Roy Miller 1 , Safi Mohammed 1 , Craig Gordon 3 , John C. Pui 4 , Gregory McIntosh 5 1. Department of Urology, McLaren Macomb Hospital, Macomb, USA 2. College of Natural Science, Michigan State University, East Lansing, USA 3. Department of Hematology and Oncology, Beaumont Hospital, Farmington Hills, USA 4. Department of Pathology, Beaumont Hospital, Farmington Hills, USA 5. Department of Urology, Michigan Institute of Urology, Macomb, USA Corresponding author: Elizabeth Snajdar, [email protected] Abstract There are only 30 reported cases of primary malignant melanoma of the bladder in the literature so far. Of those, 17 cases were reported as deceased within three years of presentation. Our case reported here is that of a 78-year-old female who presented with a new-onset incontinence and intermittent hematuria. She had no evidence of primary melanoma anywhere else in her body. The patient was treated with cystectomy and ileal conduit with plans for adjuvant chemotherapy. Unfortunately, the patient succumbed to her disease with diffuse metastatic involvement within 16 months of presentation. Categories: Dermatology, Pathology, Urology Keywords: cystectomy, melanoma, primary malignant melanoma, extracutaneous melanoma, bladder cancer, transurethral resection of bladder tumor Introduction Melanoma of the skin had an incidence of roughly 23% of all new US cancer diagnoses in 2017 [1]. While the majority of melanomas are cutaneous lesions of the skin, only 4-5% of melanomas are extracutaneous [2]. One extracutaneous lesion, primary malignant melanoma (PMM) of the bladder, represents less than 0.2% of all melanomas [2-5], making this malignancy extremely rare. -
HCC/RCC Referral Form
Date Shipment Needed: Ship To: Patient Prescriber Nursing needed; Training needed ►All the supplies including syringes and needles will be dispensed if needed. HEPATOCELLULAR CARCINOMA (HCC) Phone: 866.892.1580 • Fax: 866.892.2363 RENAL CELL CARCINOMA (RCC) REFERRAL FORM PATIENT INFORMATION Patient Name: DOB: Sex: M F Weight: lbs. kg. SSN: Phone: Allergies: Address: City: State: Zip: Emergency Contact: Phone: Please attach demographic information PRESCRIBER INFORMATION Prescriber: NPI: DEA: State Lic: Supervising Physician: Practice Name: Address: City: State: Zip: Phone: Fax: Key Office Contact: Phone: DIAGNOSIS INFORMATION / MEDICAL ASSESMENT Primary Diagnosis: C22.0 Hepatocellular Carcinoma (HCC) C22.2; C22.7; C22.8; C64.9 Renal Cell Carcinoma (RCC) Other________________________________ . Has patient been treated previously for this condition? Yes No Medication(s): __________________________________________________________________ . Cancer Stage: Stage 0 Stage I Stage II Stage III Stage IV Other: ______________________________________________________________________ . Is patient currently on therapy? Yes No Medication(s): ____________________________________________________________________________________ . Will patient stop taking the above medication(s) before starting the new medication? Yes No If yes: _________________________________________________ . How long should patient wait before starting the new medication? ________________________________________________________________________________ . Other medications patient is -
Second Malignant Neoplasms Among Long-Term Survivors of Ovarian Cancer
(CANCER RESEARCH 56. 1564-1570. April 1. I996| Second Malignant Neoplasms among Long-Term Survivors of Ovarian Cancer Lois B. Travis,1 Rochelle E. Curtis, John D. Boice, Jr., Charles E. Platz, Benjamin F. Hankey, and Joseph F. Fraumeni, Jr. Division of Cancer Epidemu>l(}g\ and Genetics [L. B. T.. R. E. C., J. D. B., J. F. F.¡,und Cancer Statistics Branch, Sun-eillancc Program, Division of Cancer Prevention and Control ¡B.F. H.I, National Cancer Institute, National Institutes of Health. Bethesda. Maryland 20892: and Department of Pathology, University of Iowa, Iowa City, Iowa 1C. E. P.I ABSTRACT registries of the SEER2 program of the National Cancer Institute (197.1-1992) or to the CTR (1935-1972).' In addition to Connecticut. SEER areas include Second malignant neoplasms were evaluated among 32,251 women with Hawaii. Iowa. New Mexico, Utah, and the metropolitan regions of Atlanta ovarian cancer, including 4,402 10-year survivors, within the nine popu (1975-1992), Detroit, San Francisco and Oakland, and Seattle and Puget lation-based registries of the Surveillance, Epidemiology, and End Results Sound (1974-1992). which together constitute -10% of the U.S. population. Program of the National Cancer Institute (1973-1992) and the Connect Information routinely collected by all SEER registries includes patient demo icut Tumor Registry (1935-1972). Overall, 1,296 second cancers occurred graphic data, tumor histology, and vital status. Active tracing of all living against 1,014 expected (observed/expected (O/E), 1.28; 95% confidence patients involving patient or physician contact and data linkage with files that interval (Cl), 1.21-1.35].