Thymus Cancer Early Detection, Diagnosis, and Staging Detection and Diagnosis
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Radical Transsternal Thymectomy David Park Mason, MD
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Radical Transsternal Thymectomy David Park Mason, MD bnormalities of the thymus comprise more than half of generalized enlargement of the thymic gland caused by dif- Athe lesions found in the anterior mediastinal compart- fuse thymocyte proliferation. Thymic hyperplasia is an im- ment in adults. Greater than 95% of the tumors of the thymus munologic condition.10 In children, thymic hyperplasia can are thymomas that originate from thymic epithelial cells. be associated with a variety of endocrine disorders including They generally present as an incidental radiographic finding. hyperthyroidism. In adults, thymic hyperplasia has been as- They are of surgical importance both as isolated entities as sociated with thymoma as well as many immune dysfunction well as in association with myasthenia gravis (MG). Surgical syndromes—the most notable being myasthenia gravis. Re- excision is the cornerstone of therapy for thymoma.1 In ad- moval of the thymus gland, by a variety of surgical ap- dition, thymectomy is an integral component of the manage- proaches, appears to influence the immune dysfunction ob- ment of myasthenia gravis. served in myasthenia gravis.7 The mechanism of this Ludwig Rehn performed the first thymic operation in 1896, a influence, and the relative benefit of removing all residual or transcervical exothymopexy for a patient with an enlarged thy- ectopic thymic tissue, is unclear. 2 mus causing episodes of suffocation. He pulled the enlarged The most frequent asymptomatic indication for thymec- thymus out of the mediastinum and performed a pexy of the tomy is thymoma. -
Lung Anatomy
Lung anatomy Breathing Breathing is an automatic and usually subconscious process which is controlled by the brain. The brain will determine how much oxygen we require and how fast we need to breathe in order to supply our vital organs (brain, heart, kidneys, liver, stomach and bowel), as well as our muscles and joints, with enough oxygen to carry out our normal daily activities. In order for breathing to be effective we need to use our lungs, breathing muscles and blood system efficiently. This leaflet should help you to better understand the process of breathing and how we get the much needed oxygen into our bodies. The lungs You have two lungs, one in the right side and one in the left side of your chest. The right lung is bigger than the left due to the position of the heart (which is positioned in the left side of the chest). Source: Pulmonary Rehabilitation Reference No: 66354-1 Issue date: 13/2/20 Review date: 13/2/23 Page 1 of 5 Both lungs are covered by 2 thin layers of tissue called the pleura. The pleura stop the surface of the lungs rubbing together as we breathe in and out. The lungs are protected by the ribcage. The airways Within the lungs there is a vast network of airways (tubes) which help to transport the oxygen into the lungs and the carbon dioxide out. These tubes branch into smaller and smaller tubes the further they go into the lungs. Page 2 of 5 Trachea (windpipe): This tube connects your nose and mouth to your lungs. -
Rare APC Promoter 1B Variants in Gastric Cancer Kindreds Unselected
PostScript with familial adenomatous polyposis.3 However, the prevalence of APC promoter Gut: first published as 10.1136/gutjnl-2020-321990 on 7 September 2020. Downloaded from variants in molecularly undiagnosed GC kindreds unselected for fundic gland polyp- osis is unknown. To investigate the contribution of APC promoter variants to GC predisposition in families lacking causal germline vari- ants CDH1, which account for 19%–40% of HDGC, we performed multigene sequencing in 259 individuals from 254 families ascertained on the basis of personal and/or family history of GC (table 1). This included 174 individuals meeting Inter- national Gastric Cancer Linkage Consor- tium criteria for HDGC and one meeting criteria for FIGC.4 The majority (76.8%) of individuals had a personal history of GC, with 85.4% diffuse GC and median age of diagnosis of 42 years (range 9–87). Six additional individuals were potential obli- gate carriers for GC predisposition. The APC promoter 1B was analysed by next- Rare APC promoter 1B variants generation sequencing (n=232) or Sanger in gastric cancer kindreds sequencing (n=27) in all index cases. unselected for fundic We identified a pathogenic variant (APC gland polyposis c.-191T>C) in an obligate carrier meeting clinical criteria for HDGC (figure 1). The index case (III-8) was diagnosed with pros- Although multiple demographic, environ- tate cancer at the age of 73, following mental and genetic factors contribute to a diagnosis of GC in two children. IV-2 gastric cancer (GC) risk, familial clustering initially presented with lower abdominal occurs in around 10%–15% of cases.1 pain, distension and ascites at 37 years A strong genetic predisposition under- of age. -
Of the Pediatric Mediastinum
MRI of the Pediatric Mediastinum Dianna M. E. Bardo, MD Director of Body MR & Co-Director of the 3D Innovation Lab Disclosures Consultant & Speakers Bureau – honoraria Koninklijke Philips Healthcare N V Author – royalties Thieme Publishing Springer Publishing Mediastinum - Anatomy Superior Mediastinum thoracic inlet to thoracic plane thoracic plane to diaphragm Inferior Mediastinum lateral – pleural surface anterior – sternum posterior – vertebral bodies Mediastinum - Anatomy Anterior T4 Mediastinum pericardium to sternum Middle Mediastinum pericardial sac Posterior Mediastinum vertebral bodies to pericardium lateral – pleural surface superior – thoracic inlet inferior - diaphragm Mediastinum – MR Challenges Motion Cardiac ECG – gating/triggering Breathing Respiratory navigation Artifacts Intubation – LMA Surgical / Interventional materials Mediastinum – MR Sequences ECG gated/triggered sequences SSFP – black blood SE – IR – GRE Non- ECG gated/triggered sequences mDIXON (W, F, IP, OP), eTHRIVE, turbo SE, STIR, DWI Respiratory – triggered, radially acquired T2W MultiVane, BLADE, PROPELLER Mediastinum – MR Sequences MRA / MRV REACT – non Gd enhanced Gd enhanced sequences THRIVE, mDIXON, mDIXON XD Mediastinum – Contents Superior Mediastinum PVT Left BATTLE: Phrenic nerve Vagus nerve Structures at the level of the sternal angle Thoracic duct Left recurrent laryngeal nerve (not the right) CLAPTRAP Brachiocephalic veins Cardiac plexus Aortic arch (and its 3 branches) Ligamentum arteriosum Thymus Aortic arch (inner concavity) Trachea Pulmonary -
C O N F E R E N C E 7 18 October 2017
Joint Pathology Center Veterinary Pathology Services WEDNESDAY SLIDE CONFERENCE 2017-2018 C o n f e r e n c e 7 18 October 2017 CASE I: F1753191 (JPC 4101076). veterinarian revealed a regenerative anemia, stress leukogram and hypoproteinemia Signalment: 9-year-old, female intact, Rock characterized by hypoalbuminemia and the Alpine goat, Capra aegagrus hircus, goat was treated with ivermectin. caprine. Bloodwork at CSU revealed hyperglycemia and elevated creatinine, creatine kinase and History: A 9-year-old, female intact Rock aspartate aminotransferase levels. A fecal Alpine goat presented to Colorado State floatation revealed heavy loads of coccidia, University Veterinary Teaching Hospital strongyles and Trichuris spp. During a nine two months prior to necropsy with a three- day hospitalization, the doe was treated with day history of hyporexia and lethargy which intravenous fluids, kaopectate, thiamine, had progressed to lateral recumbency and fenbendazole, sulfadimethoxine, oxy- complete anorexia. The referring tetracycline and multiple blood transfusions. veterinarian had previously diagnosed the After significant improvement of her clinical doe with louse infestation, endoparasites and signs and bloodwork, including partial a heart murmur. Bloodwork by the referring resolution of the dermatitis, the doe was Haired skin goat. The skin was dry, alopecia, and covered with hyperkeratotic crusts and ulcers. (Photo courtesy of: Colorado State University, Microbiology, Immunology, and Pathology Department, College of Veterinary Medicine and Biomedical Sciences, http://csucvmbs.colostate.edu/academics/mip/Pages/default.aspx) 1 discharged. exfoliating epithelial crusts which were often tangled within scant remaining hairs. Two months later, the goat presented with a This lesion most severely affected the skin one month history of progressive scaling and over the epaxials, the ventral abdomen and ulceration over the withers, dew claws, and teats, coronary bands and dew claws. -
Adaptive Immune Systems
Immunology 101 (for the Non-Immunologist) Abhinav Deol, MD Assistant Professor of Oncology Wayne State University/ Karmanos Cancer Institute, Detroit MI Presentation originally prepared and presented by Stephen Shiao MD, PhD Department of Radiation Oncology Cedars-Sinai Medical Center Disclosures Bristol-Myers Squibb – Contracted Research What is the immune system? A network of proteins, cells, tissues and organs all coordinated for one purpose: to defend one organism from another It is an infinitely adaptable system to combat the complex and endless variety of pathogens it must address Outline Structure of the immune system Anatomy of an immune response Role of the immune system in disease: infection, cancer and autoimmunity Organs of the Immune System Major organs of the immune system 1. Bone marrow – production of immune cells 2. Thymus – education of immune cells 3. Lymph Nodes – where an immune response is produced 4. Spleen – dual role for immune responses (especially antibody production) and cell recycling Origins of the Immune System B-Cell B-Cell Self-Renewing Common Progenitor Natural Killer Lymphoid Cell Progenitor Thymic T-Cell Selection Hematopoetic T-Cell Stem Cell Progenitor Dendritic Cell Myeloid Progenitor Granulocyte/M Macrophage onocyte Progenitor The Immune Response: The Art of War “Know your enemy and know yourself and you can fight a hundred battles without disaster.” -Sun Tzu, The Art of War Immunity: Two Systems and Their Key Players Adaptive Immunity Innate Immunity Dendritic cells (DC) B cells Phagocytes (Macrophages, Neutrophils) Natural Killer (NK) Cells T cells Dendritic Cells: “Commanders-in-Chief” • Function: Serve as the gateway between the innate and adaptive immune systems. -
Lung Microbiome Participation in Local Immune Response Regulation in Respiratory Diseases
microorganisms Review Lung Microbiome Participation in Local Immune Response Regulation in Respiratory Diseases Juan Alberto Lira-Lucio 1 , Ramcés Falfán-Valencia 1 , Alejandra Ramírez-Venegas 2, Ivette Buendía-Roldán 3 , Jorge Rojas-Serrano 4 , Mayra Mejía 4 and Gloria Pérez-Rubio 1,* 1 HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico; [email protected] (J.A.L.-L.); [email protected] (R.F.-V.) 2 Tobacco Smoking and COPD Research Department, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico; [email protected] 3 Translational Research Laboratory on Aging and Pulmonary Fibrosis, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico; [email protected] 4 Interstitial Lung Disease and Rheumatology Unit, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico; [email protected] (J.R.-S.); [email protected] (M.M.) * Correspondence: [email protected]; Tel.: +52-55-5487-1700 (ext. 5152) Received: 11 June 2020; Accepted: 7 July 2020; Published: 16 July 2020 Abstract: The lung microbiome composition has critical implications in the regulation of innate and adaptive immune responses. Next-generation sequencing techniques have revolutionized the understanding of pulmonary physiology and pathology. Currently, it is clear that the lung is not a sterile place; therefore, the investigation of the participation of the pulmonary microbiome in the presentation, severity, and prognosis of multiple pathologies, such as asthma, chronic obstructive pulmonary disease, and interstitial lung diseases, contributes to a better understanding of the pathophysiology. Dysregulation of microbiota components in the microbiome–host interaction is associated with multiple lung pathologies, severity, and prognosis, making microbiome study a useful tool for the identification of potential therapeutic strategies. -
Cells, Tissues and Organs of the Immune System
Immune Cells and Organs Bonnie Hylander, Ph.D. Aug 29, 2014 Dept of Immunology [email protected] Immune system Purpose/function? • First line of defense= epithelial integrity= skin, mucosal surfaces • Defense against pathogens – Inside cells= kill the infected cell (Viruses) – Systemic= kill- Bacteria, Fungi, Parasites • Two phases of response – Handle the acute infection, keep it from spreading – Prevent future infections We didn’t know…. • What triggers innate immunity- • What mediates communication between innate and adaptive immunity- Bruce A. Beutler Jules A. Hoffmann Ralph M. Steinman Jules A. Hoffmann Bruce A. Beutler Ralph M. Steinman 1996 (fruit flies) 1998 (mice) 1973 Discovered receptor proteins that can Discovered dendritic recognize bacteria and other microorganisms cells “the conductors of as they enter the body, and activate the first the immune system”. line of defense in the immune system, known DC’s activate T-cells as innate immunity. The Immune System “Although the lymphoid system consists of various separate tissues and organs, it functions as a single entity. This is mainly because its principal cellular constituents, lymphocytes, are intrinsically mobile and continuously recirculate in large number between the blood and the lymph by way of the secondary lymphoid tissues… where antigens and antigen-presenting cells are selectively localized.” -Masayuki, Nat Rev Immuno. May 2004 Not all who wander are lost….. Tolkien Lord of the Rings …..some are searching Overview of the Immune System Immune System • Cells – Innate response- several cell types – Adaptive (specific) response- lymphocytes • Organs – Primary where lymphocytes develop/mature – Secondary where mature lymphocytes and antigen presenting cells interact to initiate a specific immune response • Circulatory system- blood • Lymphatic system- lymph Cells= Leukocytes= white blood cells Plasma- with anticoagulant Granulocytes Serum- after coagulation 1. -
The Future: Surgical Advances in MEN1 Therapeutic Approaches And
2410 S M Sadowski et al. Advances in surgical 24:10 T243–T260 Thematic Review management of MEN1 The future: surgical advances in MEN1 therapeutic approaches and management strategies S M Sadowski1, G Cadiot2, E Dansin3, P Goudet4 and F Triponez1 1Thoracic and Endocrine Surgery and Faculty of Medicine, University Hospitals of Geneva, Geneva, Switzerland 2Gastroenterology and Hepatology, University Hospital of Reims, Reims, France 3 Oncology, Oscar Lambret Cancer Center, University of Lille, Lille, France Correspondence 4 Endocrine Surgery, University Hospital of Dijon, and INSERM, U866, Epidemiology and Clinical Research in Digestive should be addressed Oncology Team, and INSERM, CIC1432, Clinical Epidemiology Unit, University Hospital of Dijon, Clinical Investigation to F Triponez Centre, Clinical Epidemiology/Clinical Trials Unit, Dijon, France Email [email protected] Abstract Multiple endocrine neoplasia type 1 (MEN1) is a hereditary autosomal dominant Key Words disorder associated with numerous neuroendocrine tumors (NETs). Recent advances in f multiple endocrine the management of MEN1 have led to a decrease in mortality due to excess hormones; neoplasia type 1 (MEN1) however, they have also led to an increase in mortality from malignancy, particularly f neuro-endocrine tumors (NET) NETs. The main challenges are to localize these tumors, to select those that need f thymic NET therapy because of the risk of aggressive behavior and to select the appropriate therapy f pancreatico-gastro-intestinal associated with minimal morbidity. This must be applied to a hereditary disease with a NET Endocrine-Related Cancer Endocrine-Related high risk of recurrence. The overall aim of management in MEN1 is to ensure that the f lung NET patient remains disease- and symptom-free for as long as possible and maintains a good quality of life. -
The Peripheral Nervous System
The Peripheral Nervous System Dr. Ali Ebneshahidi Peripheral Nervous System (PNS) – Consists of 12 pairs of cranial nerves and 31 pairs of spinal nerves. – Serves as a critical link between the body and the central nervous system. – peripheral nerves contain an outermost layer of fibrous connective tissue called epineurium which surrounds a thinner layer of fibrous connective tissue called perineurium (surrounds the bundles of nerve or fascicles). Individual nerve fibers within the nerve are surrounded by loose connective tissue called endoneurium. Cranial Nerves Cranial nerves are direct extensions of the brain. Only Nerve I (olfactory) originates from the cerebrum, the remaining 11 pairs originate from the brain stem. Nerve I (Olfactory)- for the sense of smell (sensory). Nerve II (Optic)- for the sense of vision (sensory). Nerve III (Oculomotor)- for controlling muscles and accessory structures of the eyes ( primarily motor). Nerve IV (Trochlear)- for controlling muscles of the eyes (primarily motor). Nerve V (Trigeminal)- for controlling muscles of the eyes, upper and lower jaws and tear glands (mixed). Nerve VI (Abducens)- for controlling muscles that move the eye (primarily motor). Nerve VII (Facial) – for the sense of taste and controlling facial muscles, tear glands and salivary glands (mixed). Nerve VIII (Vestibulocochlear)- for the senses of hearing and equilibrium (sensory). Nerve IX (Glossopharyngeal)- for controlling muscles in the pharynx and to control salivary glands (mixed). Nerve X (Vagus)- for controlling muscles used in speech, swallowing, and the digestive tract, and controls cardiac and smooth muscles (mixed). Nerve XI (Accessory)- for controlling muscles of soft palate, pharynx and larynx (primarily motor). Nerve XII (Hypoglossal) for controlling muscles that move the tongue ( primarily motor). -
Peripheral Nervous System
Peripheral Nervous System Nervous system consists of CNS = brain and spinal cord ~90% (90 Bil) of all neurons in body are in CNS PNS = Cranial nerves and spinal nerves ~10% (10 Bil) of all neurons in body are in PNS PNS is our link to the outside world without it CNS us useless sensory deprivation hallucinations sensory (afferent) neurons ~2-3M; 6-8x’s more sensory than motor fibers motor (efferent) neurons ~350,000 efferent fibers somatic motor neurons autonomic motor neurons these neurons are bundled into nerves difference between nerve and neuron: neuron = individual nerve cell nerve = bundle of axons outside CNS surrounded by layers of connective tissue CNS PNS Axons Tracts Nerves Cell Bodies Nuclei Ganglia Nerves consist of either sensory or motor neurons or a combination of both (=mixed nerves) mixed nerves often carry both somatic and autonomic motor fibers ganglia examples: dorsal root ganglia = cell bodies of sensory neurons autonomic chain ganglia = cell bodies, dendrites & synapses of autonomic motor neurons PNS consists of 43 pairs of nerves branching from the CNS: 12 pairs of cranial nerves 31 pairs of spinal nerves Cranial Nerves 12 pairs of cranial nerves 1 structurally originate from: cerebrum: I, II midbrain: III, IV pons: V, VI, VII,VIII (pons/medulla border) medulla: IX, X, XI, XII functionally: some are sensory only: I. Olfactory [sense of smell] II. Optic [sense of sight] VIII. Vestibulocochlear [senses of hearing and balance] -injury causes deafness some are motor only: III. Oculomotor IV. Trochlear [eye movements] VI. Abducens -injury to VI causes eye to turn inward some are mixed nerves: V. -
Manatee Anatomy and Physiology
Manatee Anatomy and Physiology Grade level: Elementary 5 Subject Area: Biology, Anatomy and Physiology, Marine Biology Duration: Teach: 15 minutes, Activity: 20 minutes, Discussion: 20 minutes. Setting: Classroom Next Generation Sunshine State Standards: Reading: LAFS.5.RI Reading standards for Information text Cluster 3 LAFS.5.RI.3 Writing: LA.B.2.1, LA.B.1.2 Speaking and Listening: Cluster 2 LAFS.5.SL.Z Presentation of Knowledge and Ideas Science: Body of Knowledge Life Science: SC.5.L.14, SC.5.L.15, SC.5.L.17, Body of Knowledge Nature of Science Supporting Idea 1: SC.5.N.1 Practice of Science, Supporting Idea 2:SC.5.N.2 Characteristics of Scientific Knowledge Earth Systems and Patterns: 7SC.E.E.7 Statewide Science Assessment Prompt: How might humans help manatees survive? Objectives: Students will learn about manatee bodies and explain some anatomical and physiological differences between manatees, humans and other animals. Materials: Handouts of basic manatee anatomy, dolphin anatomy & human anatomy, crayons or markers, coloring direction sheet, question worksheet, Quiz sheet Vocabulary: Mammal, endangered species, habitat, conservation, vibrissae, nares, blowhole, flipper, herbivore, omnivore, carnivore. Background/Preparation: Handouts of manatee, dolphin, and human anatomy. Fact sheets comparing and contrasting specific and unique anatomical aspects of each species. Basic manatee fact sheet highlighting personality, limited habitat, endangered status and conservation efforts. Teachers can review the manatee fact sheets, and select points of interest they would most like to incorporate into a lesson. This activity may fit best into the week where the human anatomy lessons are addressed. Teachers can present the information via traditional lecture, group discussion, question and answer session, or doing the coloring activity as the lesson points are addressed, etc.