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    Filmography by Year by Job by Ratings by Votes by Genre by Keyword Personal Details Biography Other Works Publicity Listings Official Sites Contact Info IMDbPro Did You Know?

    Share this page:. The Female Gaze! Worthy Women of Porn. Do you have a demo reel? Add it to your IMDbPage.

    How Much Have You Seen? How much of Britt Morgan's work have you seen? Known For. The Young and the Wrestling Pretty Penelope. Cheeks 4: A Backstreet Affair Caroline.

    Watch out for this band. Her wistful tunes, rippling guitar and subdued, plaintive vocals got support from Gavin Peterson's steady drums and Ashton Jenicek's atmospheric synthesizer.

    Gain the Confidence to learn any of Your Favorite Songs using The SONG System? Learning proper sitting and hand positioning takes the struggle out of playing guitar and builds a solid foundation that will last you a lifetime.

    If you've tried to play before but became discouraged by the struggle, I can help! Throughout this course, I coach you through reading the notes on all six strings ONE string at a time.

    Chords make up a large part of guitar playing. Throughout this course, I'll show you proper fingerings for popular chords, and how to recall and set them down quickly.

    Beginning students will save a lot of time by learning chords the right way! I love music so much, and need more activities that are relaxing. When we spoke on the phone, your program seemed like a perfect fit.

    The scheduled coaching calls, weekly classes, and practical application were all very positive for my learning style.

    I fell behind, but was able to pick it back up when it worked for me. Even with a little time away, I feel much further along playing guitar than ever.

    It [Guitar Success Academy] taught me everything I need to know to be successful, gave me a platform to work with moving forward, [and got me] playing my first ever song on a guitar any musical instrument, really.

    Having access to past classes via video is very helpful when you need to revisit a topic or just see it again with a fresh perspective. The coaching calls are very helpful for specific questions and tips, and to hear where others are succeeding or struggling….

    I can't thank you enough for your kind and gentle way of supporting me as a beginner. I can get a little a LOT in my own way and frustrated with the early steps of learning a new skill.

    Your flexible and encouraging approach made it so much easier to keep trying. You are clearly doing what you were put on this earth to do and I'm grateful for you.

    She uses an effective combination of video lectures and demonstrations, homework, handouts, external resources, video coaching sessions, and social media interaction to keep her students engaged and moving forward.

    When I started the GSA program, I had been trying to teach myself using online videos, which were helpful, but didn't provide me with the focus, direction, and perspective I needed.

    I was pleasantly surprised to discover that playing finger-style was within my reach, even as a beginner. I feel that GSA has provided me with a very solid foundation on which to build my skills with practice.

    The opportunity to sign up for the Guitar Success Academy came up and I decided to give it a try as the next step in my journey.

    So glad I did. Ana has a great program that set forth a road map for students and got me back in gear on my journey.

    She is kind, patient, and explains thoroughly and clear. I couldn't ask for a better teacher. She is very accommodating with my busy schedule and values my time.

    She is always willing to answer the questions I have and is an overall very good guitarist. She is very kind and better that any music teacher I have ever had.

    I would very much recommend Ana if you are looking for a music teacher that is kind and works around you.

    Her lessons are fun and she not only able to show you how to play the guitar but also teaches you to read basic music.

    Placing a given tumor into one of these categories depends on well-defined histological features: size, lymphovascular invasion , mitotic counts, Ki labelling index, invasion of adjacent organs, presence of metastases and whether they produce hormones.

    Traditionally, neuroendocrine tumors have been classified by their anatomic site of origin. NETs can arise in many different areas of the body, and are most often located in the intestine , pancreas or the lungs.

    The various kinds of cells that can give rise to NETs are present in endocrine glands and are also diffusely distributed throughout the body, most commonly Kulchitsky cells or similar enterochromaffin-like cells , that are relatively more common in the gastrointestinal and pulmonary systems.

    NETs include certain tumors of the gastrointestinal tract and of the pancreatic islet cells , [1] certain thymus and lung tumors, and medullary carcinoma of the parafollicular cells of the thyroid.

    Within the broad category of neuroendocrine tumors there are many different tumor types: [7] this outline is presented to facilitate retrieving information.

    Neuroendocrine tumors are uncommon in many of these areas, and frequently represent only a very small proportion of the tumors or cancers at these locations.

    Neuroendocrine lesions are graded histologically according to markers of cellular proliferation, rather than cellular polymorphism. The following grading scheme is currently recommended for all gastroenteropancreatic neuroendocrine neoplasms by the World Health Organization : [35].

    If mitotic count and Ki are discordant, the figure which gives the highest grade is used. G1 and G2 neuroendocrine neoplasms are called neuroendocrine tumors NETs — formerly called carcinoid tumours.

    G3 neoplasms are called neuroendocrine carcinomas NECs. It has been proposed that the current G3 category be further separated into histologically well-differentiated and poorly-differentiated neoplasms to better reflect prognosis.

    Currently there is no one staging system for all neuroendocrine neoplasms. Well differentiated lesions generally have their own staging system based on anatomical location, whereas poorly differentiated and mixed lesions are staged as carcinomas of that location.

    For example, gastric NEC and mixed adenoneuroendocrine cancers are staged as a primary carcinoma of the stomach. Conceptually, there are two main types of NET within the gastroenteropancreatic neuroendocrine tumors GEP-NET category: those which arise from the gastrointestinal GI system and those that arise from the pancreas.

    In usage, the term "carcinoid" has often been applied to both, although sometimes it is restrictively applied to NETs of GI origin as herein , or alternatively to those tumors which secrete functional hormones or polypeptides associated with clinical symptoms, as discussed.

    Carcinoids most commonly affect the small bowel, particularly the ileum, and are the most common malignancy of the appendix. Many carcinoids are asymptomatic and are discovered only upon surgery for unrelated causes.

    These coincidental carcinoids are common; one study found that one person in ten has them. A carcinoid crisis with profound flushing, bronchospasm, tachycardia, and widely and rapidly fluctuating blood pressure [1] can occur if large amounts of hormone are acutely secreted, [48] which is occasionally triggered by factors such as diet, [48] alcohol, [48] surgery [1] [48] chemotherapy, [48] embolization therapy or radiofrequency ablation.

    Chronic exposure to high levels of serotonin causes thickening of the heart valves , particularly the tricuspid and the pulmonic valves, and over a long period can lead to congestive heart failure.

    Many other hormones can be secreted by some of these tumors, most commonly growth hormone that can cause acromegaly , or cortisol, that can cause Cushing's syndrome.

    Occasionally, haemorrhage or the effects of tumor bulk are the presenting symptoms. Bowel obstruction can occur, sometimes due to fibrosing effects of NET secretory products [46] with an intense desmoplastic reaction at the tumor site, or of the mesentery.

    Pancreatic neuroendocrine tumors PanNETs are often referred to as "islet cell tumors", [50] [51] or "pancreatic endocrine tumors" [2].

    The PanNET denomination is in line with current WHO guidelines. Historically, PanNETs have also been referred to by a variety of terms, and are still often called "islet cell tumors" or "pancreatic endocrine tumors".

    PanNETs are quite distinct from the usual form of pancreatic cancer , adenocarcinoma, which arises in the exocrine pancreas.

    Well or intermediately differentiated PanNETs are sometimes called islet cell tumors; neuroendocrine cancer NEC synonymous with islet cell carcinoma is more aggressive.

    In addition to the two main categories of GEP-NET, there are rarer forms of neuroendocrine tumors that arise anywhere in the body, including within the lung , thymus and parathyroid.

    Bronchial carcinoid can cause airway obstruction, pneumonia , pleurisy , difficulty with breathing, cough, and hemoptysis , or may be associated with weakness, nausea, weight loss, night sweats, neuralgia, and Cushing's syndrome.

    Some are asymptomatic. Animal neuroendocrine tumors include neuroendocrine cancer of the liver in dogs, and devil facial tumor disease in Tasmanian devils.

    Most pancreatic NETs are sporadic. Given these associations, recommendations in NET include family history evaluation, evaluation for second tumors, and in selected circumstances testing for germline mutations such as for MEN1.

    NETs are believed to arise from various neuroendocrine cells whose normal function is to serve at the neuroendocrine interface.

    Neuroendocrine cells are present not only in endocrine glands throughout the body that produce hormones , but are found in all body tissues. Symptoms from secreted hormones may prompt measurement of the corresponding hormones in the blood or their associated urinary products, for initial diagnosis or to assess the interval change in the tumor.

    Secretory activity of the tumor cells is sometimes dissimilar to the tissue immunoreactivity to particular hormones. Given the diverse secretory activity of NETs there are many other potential markers, but a limited panel is usually sufficient for clinical purposes.

    Newer markers include N-terminally truncated variant of Hsp70 is present in NETs but absent in normal pancreatic islets. Neuroendocrine secretory protein, a member of the chromogranin family, is seen in pancreatic endocrine tumors but not intestinal NETs.

    For morphological imaging, CT-scans , MRIs , sonography ultrasound , and endoscopy including endoscopic ultrasound are commonly used.

    Multiphase CT and MRI are typically used both for diagnostics and for evaluation of therapy. The multiphase CT should be performed before and after an intravenous injection of an iodine-based contrast agent, both in the late arterial phase and in the portal venous phase triple-phase study.

    While MRI is generally superior to CT, both for detection of the primary tumor and for evaluation of metastases, CECT is more widely available, even at academic institutions.

    Therefore, multiphase CT is often the modality of choice. Advances in nuclear medicine imaging, also known as molecular imaging, has improved diagnostic and treatment paradigms in patients with neuroendocrine tumors.

    This is because of its ability to not only identify sites of disease but also characterize them. Neuronedocrine tumours express somatostatin receptors providing a unique target for imaging.

    Octreotide is a synthetic modifications of somatostatin with a longer half-life. Somatostatin receptor imaging can now be performed with positron emission tomography PET which offers higher resolution, three-dimensional and more rapid imaging.

    Gallium receptor PET -CT is much more accurate than an OctreoScan. Imaging with fluorine fluorodeoxyglucose FDG PET may be valuable to image some neuroendocrine tumors.

    Tumors that grow more quickly use more sugar. Using this scan, the aggressiveness of the tumor can be assessed. Functional imaging with Gallium-labelled somatostatin analog and 18F-FDG PET tracers ensures better staging and prognostication of neuroendocrine neoplasms.

    The combination of somatostatin receptor and FDG PET imaging is able to quantify somatostatin receptor cell surface SSTR expression and glycolytic metabolism, respectively.

    This is enabling better selection of the most appropriate therapy for an individual patient. Neuroendocrine tumors, despite differing embryological origin, have common phenotypic characteristics.

    NETs show tissue immunoreactivity for markers of neuroendocrine differentiation pan-neuroendocrine tissue markers and may secrete various peptides and hormones.

    There is a lengthy list of potential markers in neuroendocrine tumors; several reviews provide assistance in understanding these markers.

    Neuron-specific enolase NSE is less specific. NETs are often small, yellow or tan masses, often located in the submucosa or more deeply intramurally, and they can be very firm due to an accompanying intense desmoplastic reaction.

    The overlying mucosa may be either intact or ulcerated. Some GEP-NETs invade deeply to involve the mesentery.

    The cells may align variously in islands, glands or sheets. High power examination shows bland cytopathology.

    Electron microscopy can identify secretory granules. There is usually minimal pleomorphism but less commonly there can be anaplasia , mitotic activity, and necrosis.

    Some neuroendocrine tumor cells possess especially strong hormone receptors , such as somatostatin receptors and uptake hormones strongly.

    This avidity can assist in diagnosis and may make some tumors vulnerable to hormone targeted therapies.

    NETs from a particular anatomical origin often show similar behavior as a group, such as the foregut which conceptually includes pancreas, and even thymus, airway and lung NETs , midgut and hindgut ; individual tumors within these sites can differ from these group benchmarks:.

    Several issues help define appropriate treatment of a neuroendocrine tumor, including its location, invasiveness, hormone secretion, and metastasis.

    Treatments may be aimed at curing the disease or at relieving symptoms palliation. Observation may be feasible for non-functioning low grade neuroendocrine tumors.

    If the tumor is locally advanced or has metastasized, but is nonetheless slowly growing, treatment that relieves symptoms may often be preferred over immediate challenging surgeries.

    Intermediate and high grade tumors noncarcinoids are usually best treated by various early interventions active therapy rather than observation wait-and-see approach.

    Treatments have improved over the past several decades, and outcomes are improving. Detailed guidelines for managing neuroendocrine tumors are available from ESMO , [70] NCCN [71] and a UK panel.

    Even if the tumor has advanced and metastasized, making curative surgery infeasible, surgery often has a role in neuroendocrine cancers for palliation of symptoms and possibly increased lifespan.

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