Pathology
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [9]
Pathology is the study and diagnosis of disease through examination of organs, tissues, cells and bodily fluids. The term encompasses both the medical specialty which uses tissues and body fluids to obtain clinically useful information, as well as the related scientific study of disease processes.
History
The histories of both experimental and medical pathology can be traced to the earliest application of the scientific method to the field of medicine, a development which occurred in Western Europe during the Italian Renaissance.[1] Most early pathologists were also practicing physicians or surgeons. Like other medical fields, pathology has become more specialized with time, and most pathologists today do not practice in other areas of medicine.
Origins of pathology
The concept of studying disease through the methodical dissection and examination of diseased bodies, organs, and tissues may seem obvious today, but there are few if any recorded examples of true autopsies performed prior to the Renaissance. The first physician known to have repeatedly used anatomic dissection to determine cause of death was an Italian, Antonio Benivieni (1443-1502).[1] Perhaps the most famous early gross pathologist was Giovanni Morgagni (1682-1771). His magnum opus, De Sedibus et Causis Morborum per Anatomem Indagatis, published in 1761, describes the findings of over 600 partial and complete autopsies, organised anatomically and methodically correlated with the symptoms exhibited by the patients prior to their demise. Although the study of normal anatomy was already well advanced at this date, De Sedibus was one of the first treatises specifically devoted to the corrolation of diseased anatomy with clinical illness.[2][3] By the late 1800s, an exhaustive body of literature had been produced on the gross anatomical findings characteristic of known diseases. The extent of gross pathology research in this period can be epitomized by the work of the Viennese pathologist (originally from Hradec Kralove in the Czech Rep.) Carl Rokitansky (1804-1878), who is said to have performed 20,000 autopsies, and supervised an additional 60,000, in his lifetime .[1][4]
Origins of microscopic pathology
Rudolf Virchow (1821-1902) is generally recognized to be the father of microscopic pathology. While the compound microscope had been invented approximately 150 years prior, Virchow was one of the first prominent physicians to emphasize the study of manifestations of disease which were visible only at the cellular level.[1][5] A student of Virchow's, Julius Cohnheim (1839-1884) combined histology techniques with experimental manipulations to study inflammation, making him one of the earliest experimental pathologists.[1] Cohnheim also pioneered the use of the frozen section; a version of this technique is widely employed by modern pathologists to render diagnoses and provide other clinical information intraoperatively.[6]
Modern experimental pathology
As new research techniques, such as electron microscopy, immunohistochemistry, and molecular biology have expanded the means by which biomedical scientists can study disease, the definition and boundaries of investigative pathology have become less distinct. In the broadest sense, nearly all research which links manifestations of disease to identifiable processes in cells, tissues, or organs can be considered experimental pathology.[7]
Pathology as a science
Pathology is a broad and complex scientific field which seeks to understand the mechanisms of injury to cells and tissues, as well as the body's means of responding to and repairing injury. Disease processes may be incited or exacerbated by a variety of external and internal influences, including trauma, infection, poisoning, loss of blood flow, autoimmunity, inherited or acquired genetic damage, or errors of development. One common theme in pathology is the way in which the body's responses to injury, while evolved to protect health, can also contribute in some ways to disease processes.[8] Elucidation of general principles underlying pathologic processes, such as cellular adaptation to injury, cell death, inflammation, tissue repair, and neoplasia, creates a conceptual framework with which to analyze and understand specific human diseases.
Adaptation to injury
Cells and tissues may respond to injury and stress by specific mechanisms, which may vary according to the cell types and nature of the injury. In the short term, cells may activate specific genetic programs to protect their vital proteins and organelles from heat shock or hypoxia, and may activate DNA repair pathways to repair damage to chromosomes from radiation or chemicals. Hyperplasia is a long-term adaptive response of cell division and multiplication, which can increase the ability of a tissue to compensate for an injury. For example, repeated irritation to the skin can cause a protective thickening due to hyperplasia of the epidermis. Hypertrophy is an increase in the size of cells in a tissue in response to stress, an example being hypertrophy of muscle cells in the heart in response to increased resistance to blood flow as a result of narrowing of the heart's outflow valve. Metaplasia occurs when repeated damage to the cellular lining of an organ triggers its replacement by a different cell type.[8]
Cell death
Necrosis is the irreversible destruction of cells as a result of severe injury in a setting where the cell is unable to activate the needed metabolic pathways for survival or orderly degeneration. This is often due to external pathologic factors, such as toxins or loss of oxygen supply. Milder stresses may lead to a process called reversible cell injury, which mimics the cell swelling and vacuolization seen early in the necrotic process, but in which the cell is able to adapt and survive. In necrosis, the components of degenerating cells leak out, potentially contributing to inflammation and further damage. Apoptosis, in contrast, is a regulated, orderly degeneration of the cell which occurs in the settings of both injury and normal physiological processes.[8]
Inflammation
Inflammation is a particularly important and complex reaction to tissue injury, and is particularly important in fighting infection. Acute inflammation is generally a non-specific response triggered by the injured tissue cells themselves, as well as specialized cells of the innate immune system and previously developed adaptive immune mechanisms. A localized acute inflammatory response triggers vascular changes in the injured area, recruits pathogen-fighting neutrophils, and begins the process of developing a new adaptive immune response. Chronic inflammation occurs when the acute response fails to entirely clear the inciting factor. While chronic inflammation can lay a positive role in containing a continuing infectious hazard, it can also lead to progressive tissue damage, as well as predisposing (in some cases) to the development of cancer.[8]
Tissue repair
Tissue repair, as seen in wound healing, is triggered by inflammation. The process may proceed even before the resolution of a precipitating insult, through the formation of granulation tissue. Healing involves the proliferation of connective tissue cells and blood vessel-forming cells as a result of hormonal growth signals. While healing is a critical adaptive response, an aberrent healing response can lead to progressive fibrosis, contractures, or other changes which can compromise function.[8]
Neoplasia
Neoplasia, or "new growth," is a proliferation of cells which is independent of any physiological process. The most familiar examples of neoplasia are benign tumors and cancers. Neoplasia results from genetic changes which cause cells to activate genetic programs inappropriately. Dysplasia is an early sign of a neoplastic process in a tissue, and is marked by persistence of immature, poorly differentiated cell forms. Interestingly, there are many similarities in the gene pathways activated in cancer cells, and those activated in cells involved in wound healing and inflammation.[8]
Pathology as a medical specialty
Physicians who practice pathology diagnose and characterize disease in living patients by examining biopsies and other specimens. For example, the vast majority of cancer diagnoses are made or confirmed by a pathologist. Pathologists may also conduct autopsies to investigate causes of death. The medical practice of pathology grew out the tradition of investigative pathology, and many of the academic leaders in pathology today are accomplished in both basic science research and diagnostic practice. However, as with other specialties in medicine, most modern physician-pathologists are employed in full-time practice, and do not perform original research.
Pathology is a unique medical specialty in that pathologists typically do not see patients directly, but rather serve as consultants to other physicians (often referred to as "clinicians" within the pathology community). However, in the United States and in many other countries, pathologists receive the same doctorate training, and undergo the same medical licensure process as other physicians. Pathology is a diverse field, and the organization of subspecialties within pathology vary between nations.
Anatomical Pathology
Anatomical pathologists diagnose disease and gain other clinically significant information through the examination of tissues and cells. This generally involves gross and microscopic visual examination of tissues, with special stains and immunohistochemistry employed to visualize specific proteins and other substances in and around cells. More recently, anatomical pathologists have begun to employ molecular biology techniques to gain additional clinical information from these same specimens. Anatomic pathologists serve as the definitive diagnosticians for most cancers, as well as numerous other diseases.
- Surgical pathology is the most significant and time-consuming area of practice for most anatomical pathologists. Surgical pathology involves the gross and microscopic examination of surgical specimens, as well as biopsies submitted by non-surgeons such as general internists, medical subspecialists, dermatologists, and interventional radiologists.
- Cytopathology is concerned with the microscopic examination of whole, individual cells obtained from smears or fine needle aspirates.
- Molecular pathology refers to the use of nucleic acid-based techniques, such as in-situ hybridization, reverse-transcriptase polymerase chain reaction, and nucleic acid microarrays for specialised diagnostic studies of disease in tissues and cells.
- Autopsies are used to provide definitive evidence of the disease processes contributing to a person's death.
- Forensic pathology receive specialized training in determining the cause of death and other legally relevant information from the bodies of persons who died in a non-medical or potentially criminal circumstances.
Clinical pathology
Clinical pathology, also known as laboratory medicine, is the medical specialty concerned with diagnosing diseases based on the analysis of body fluids, such as plasma, urine, stool, respiratory or mucosal secretions, inflammatory exudates, and pleural, pericardial, peritoneal, synovial, or cerebrospinal fluid. The practice of clinical pathology is centered around the clinical laboratory. In modern clinical laboratories, many routine studies are largely automated. The clinical pathologist is responsible for overseeing the work of laboratory technicians, performing quality assurance to assure the validity of test results, performing interpretations of more complex studies, and serving as a consultant to clinicians so that the most appropriate studies can be performed for the diagnosis or assessment of an individual patient's condition. In some areas, non-pathologists, such as other physicians or Ph.D.'s may run clinical labs and perform functions within those specific labs which are similar to the role of a board-certified clinical pathologist.
Sub-specialties within clinical pathology include the following:
- Clinical chemistry (A board-certifiable subspecialty, chemical pathology, in the U.S.)
- Hematology and Flow cytometry (Part of a board-certifiable subspecialty, hematology, in the U.S.)
- Blood banking/Transfusion medicine (A board-certifiable subspecialty in the U.S.)
- Medical microbiology (A board-certifiable subspecialty in the U.S.)
- Medical cytogenetics
- Immunology
- Molecular genetic pathology (A board-certifiable subspecialty in the U.S.)
Dental pathology
In the United States, subspecialty-trained doctors of dental surgery (D.D.S), rather than medical doctors, can be certified by a professional board to practice dental pathology.
Training of medical pathologists
Pathology in the United States
In the United States, pathologists are medical doctors (M.D.) or doctors of osteopathic medicine (D.O.), that have completed a four-year undergraduate program, four years of medical school training, and three to four years of postgraduate training in the form of a pathology residency. Training may be within two primary specialties, as recognized by the American Board of Pathology: Anatomic Pathology, and Clinical Pathology, each of which requires separate board certification. Many pathologists seek a broad-based training and become certified in both fields. These skills are complementary in many hospital-based private practice settings, since the day-to-day work of many clinical laboratories only requires the intermittent attention of a physician. Thus, pathologists are able to spend much of their time evaluating anatomic pathology cases, while remaining available to cover any special issues which might arise in the clinical laboratories. Pathologists may pursue specialised fellowship training within one or more sub-specialties of either anatomic or clinical pathology. Some of these sub-specialities permit additional board certification, while others do not.[9]
Pathology in the United Kingdom
In the UK pathologists are medical doctors registered with the UK General Medical Council. They will have completed an undergraduate medical education which in most countries lasts 4-6 years. The training to become a pathologist is under the oversight of the Royal College of Pathologists. Typically a one year training attachment is followed by an aptitude test. This is followed by further specialist training in surgical pathology, cytopathology, and post mortem pathology. There are two examinations run by the Royal College of Pathologists termed Part 1 and Part 2. The Part 2 examination is designed to test competence to work as an independent practitioner in pathology and is typically taken after 5 years specialist training. All post-graduate medical training and education in the UK is overseen by the Postgraduate Medical Education and Training Board. It is possible to take a specialist part 2 examination in paediatric pathology or neuropathology. It is possible to take a special diploma in dermatopathology or cytopathology, recognising additional specialist training and expertise.
Non-human pathology
Veterinary pathologists are veterinary practitioners who specialise in the diagnosis and characterization of veterinary diseases through the examination of animal tissue and body fluids. Veterinary pathologists are veterinarians with advanced training (board certification or Ph.D.) in either diagnostic pathology or research into the biological processes underlying disease (pathobiology). Diagnostic veterinary pathologists are further subcategorized as either anatomical pathologists or clinical pathologists. Clinical pathologists examine specimens such as blood, excretions or biopsy material to diagnose disease in living animals. Anatomical pathologists utilize post mortem examinations of dead animals to arrive at a diagnosis. Post mortem examinations entail a necropsy (an animal autopsy), histopathologic (microscopic) study of tissue specimens collected at the necropsy and sometimes specialized studies (radiographic, toxicologic, etc.)
Plant pathologists are specialized scientists who investigate the causes of diseases in plants.
References
- ↑ 1.0 1.1 1.2 1.3 1.4 [1] History of Pathology, at the USC School of Dentistry
- ↑ [2] A History of Medicine from the Biblioteca Centrale dell'Area Biomedica
- ↑ [3] Founders of Modern Medicine: Giovanni Battista Morgagni. Medical Library and Historical Journal. 1903 October; 1(4): 270–277.
- ↑ [4] Karl von Rokitansky at Whonamedit.com
- ↑ [5] Rudolf Virchow at Whonamedit.com
- ↑ [6] Jewish Encyclopedia entry on Julius Cohnheim
- ↑ [7] Mission of the American Society for Investigative Pathology
- ↑ 8.0 8.1 8.2 8.3 8.4 8.5 Ramzi Cotran, Vinay Kumar, Tucker Collins (1999). Robbins Pathologic Basis of Disease, Sixth Edition. W.B. Saunders. ISBN 072167335X.
- ↑ [8] Homepage of the American Board of Pathology
See also
External links
- American Society for Investigative Pathology
- American Society of Cytopathology
- British Neuropathological Society
- Case Records of the Massachusetts General Hospital - Clinicopathological Conference
- College of American Pathologists
- Immunohistochemistry protocols and troubleshooting
- Pathological Society of Great Britain and Ireland
- Royal College of Pathologists (UK)
- Sullivan Nicolaides Pathology - Leading Australian Pathology Laboratory.
- United States and Canadian Academy of Pathology
- WebPath: The Internet Pathology Laboratory for Medical Education
- What is a Pathologist? - a perspective from UK pathologist Fraser Charlton.
- Royal College of Pathologists (UK)
- HistoPathology Atlas
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Major subtopics of biology |
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| Anatomy - Astrobiology - Biochemistry - Bioinformatics - Botany - Cell biology - Ecology - Developmental biology - Evolutionary biology - Genetics - Genomics - Marine biology - Human biology - Microbiology - Molecular biology - Origin of life - Paleontology - Parasitology - Pathology - Physiology - Taxonomy - Zoology |
Endocrine pathology: endocrine diseases (E00-35, 240-259) | |
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| Thyroid | Hypothyroidism (Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre, Myxedema) - Hyperthyroidism (Graves disease, Toxic multinodular goitre, Teratoma with thyroid tissue or Struma ovarii) - Thyroiditis (De Quervain's thyroiditis, Hashimoto's thyroiditis, Riedel's thyroiditis) - Euthyroid sick syndrome |
| Pancreas | Diabetes mellitus (type 1, type 2, coma, angiopathy, ketoacidosis, nephropathy, neuropathy, retinopathy) - Hypoglycemia - Hyperinsulinism - Zollinger-Ellison syndrome - insulin receptor (Rabson-Mendenhall syndrome) |
| Parathyroid | Hypoparathyroidism (Pseudohypoparathyroidism) - Hyperparathyroidism (Primary, Secondary, Tertiary) |
| Pituitary | Hyperpituitarism (Acromegaly, Hyperprolactinaemia, SIADH) - Hypopituitarism (Simmonds' disease/Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes insipidus) - Adiposogenital dystrophy - Empty sella syndrome |
| Adrenal | Cushing's syndrome (Nelson's syndrome, Pseudo-Cushing's syndrome) - CAH (Lipoid, 3β, 11β, 17α, 21α) - Hyperaldosteronism (Conn syndrome, Bartter syndrome) - Adrenal insufficiency (Addison's disease) - Hypoaldosteronism |
| Gonads | ovarian dysfunction (Polycystic ovary syndrome, Premature ovarian failure) - testicular dysfunction (5-alpha-reductase deficiency) - testosterone biosynthesis (17-beta-hydroxysteroid dehydrogenase deficiency) - general (Hypogonadism, Delayed puberty, Precocious puberty) |
| Other | Androgen insensitivity syndrome - Autoimmune polyendocrine syndrome - Carcinoid syndrome - Gigantism - Short stature (Laron syndrome, Psychogenic dwarfism) - Multiple endocrine neoplasia (1, 2) - Progeria - Woodhouse-Sakati syndrome |
Nutritional pathology (E40-68, 260-269) | |
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| Malnutrition | Kwashiorkor - Marasmus - Catabolysis |
| Avitaminosis | B vitamins: B1: Beriberi/Wernicke's encephalopathy, B2: Ariboflavinosis, B3: Pellagra, B6: Pyridoxine deficiency, B7: Biotin deficiency, B9: Folate deficiency, B12: Vitamin B12 deficiency other vitamins: A: Vitamin A deficiency/Bitot's spots, C: Scurvy, D: Rickets/Osteomalacia |
| Mineral deficiency | Zinc deficiency - Iron deficiency - Magnesium deficiency - Chromium deficiency |
| Hyperalimentation | Obesity - Vitamin poisoning (Hypervitaminosis A, Hypervitaminosis D, Hypervitaminosis E) |
Metabolic pathology / Inborn error of metabolism (E70-90, 270-279) | |
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| Amino acid | Aromatic (Phenylketonuria, Alkaptonuria, Ochronosis, Tyrosinemia, Albinism, Histidinemia) - Branched chain (Maple syrup urine disease, Propionic acidemia, Methylmalonic acidemia, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency) - Transport (Cystinuria, Cystinosis, Hartnup disease, Fanconi syndrome, Oculocerebrorenal syndrome) - Sulfur (Homocystinuria, Cystathioninuria) - Urea cycle disorder (N-Acetylglutamate synthase deficiency, Carbamoyl phosphate synthetase I deficiency, Ornithine transcarbamylase deficiency, Citrullinemia, Argininosuccinic aciduria, Hyperammonemia) - Glutaric acidemia type 1 - Sarcosinemia |
| Carbohydrate | Lactose intolerance - Glycogen storage disease (type I, type II, type III, type IV, type V, type VI, type VII) - fructose metabolism (Fructose intolerance, Fructose bisphosphatase deficiency, Essential fructosuria) - galactose metabolism (Galactosemia, Galactose-1-phosphate uridylyltransferase galactosemia, Galactokinase deficiency) - other intestinal carbohydrate absorption (Glucose-galactose malabsorption, Sucrose intolerance) - pyruvate metabolism and gluconeogenesis (PCD, PDHA) - Pentosuria - Renal glycosuria |
| Lipid storage | Sphingolipidoses/Gangliosidoses: GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease) - GM1 gangliosidoses - Mucolipidosis type IV - Gaucher's disease - Niemann-Pick disease - Farber disease - Fabry's disease - Metachromatic leukodystrophy - Krabbe disease Neuronal ceroid lipofuscinosis (Batten disease) - Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman disease) |
| Other lipid | Lipoprotein/lipidemias: Hyperlipidemia - Hypercholesterolemia - Familial hypercholesterolemia - Xanthoma - Combined hyperlipidemia - Lecithin cholesterol acyltransferase deficiency - Tangier disease - Abetalipoproteinemia Fatty acid: Adrenoleukodystrophy - Carnitine (Primary, I, II) |
| Mineral | Cu Wilson's disease/Menkes disease - Fe Haemochromatosis - Zn Acrodermatitis enteropathica - PO43− Hypophosphatemia/Hypophosphatasia - Mg2+ Hypermagnesemia/Hypomagnesemia - Ca2+ Hypercalcaemia/Hypocalcaemia/Disorders of calcium metabolism |
| Fluid, electrolyte and acid-base balance | Electrolyte disturbance - Na+ Hypernatremia/Hyponatremia - Acidosis (Metabolic, Respiratory, Lactic) - Alkalosis (Metabolic, Respiratory) - Mixed disorder of acid-base balance - H2O Dehydration/Hypervolemia - K+ Hypokalemia/Hyperkalemia - Cl− Hyperchloremia/Hypochloremia |
| Purine and pyrimidine | Hyperuricemia - Lesch-Nyhan syndrome - Xanthinuria |
| Porphyrin | Acute intermittent, Gunther's, Cutanea tarda, Erythropoietic, Hepatoerythropoietic, Hereditary copro-, Variegate |
| Bilirubin | Unconjugated (Gilbert's syndrome, Crigler-Najjar syndrome) - Conjugated (Dubin-Johnson syndrome, Rotor syndrome) |
| Glycosaminoglycan | Mucopolysaccharidosis - 1:Hurler/Hunter - 3:Sanfilippo - 4:Morquio - 6:Maroteaux-Lamy - 7:Sly |
| Glycoprotein | Mucolipidosis - I-cell disease - Pseudo-Hurler polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis |
| Other | Alpha 1-antitrypsin deficiency - Cystic fibrosis - Amyloidosis (Familial Mediterranean fever) - Acatalasia |
WHO ICD-10 mental and behavioural disorders (F · 290–319) | |
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| Neurological/symptomatic | Dementia (Alzheimer's disease, multi-infarct dementia, Pick's disease, Creutzfeldt-Jakob disease, Huntington's disease, Parkinson's disease, AIDS dementia complex, Frontotemporal dementia) · Delirium · Post-concussion syndrome |
| Psychoactive substance | Intoxication (drunkenness) · Physical dependence (alcohol dependence, opioid dependency, cocaine dependence) · Withdrawal (benzodiazepine withdrawal, delirium tremens) · </br> Amnesic: (Korsakoff's syndrome) |
| Psychotic disorder | Schizophrenia (disorganized schizophrenia) · Schizotypal personality disorder · Delusional disorder · Folie à deux · Schizoaffective disorder |
| Mood (affective) | Mania · Bipolar disorder · Clinical depression · Cyclothymia · Dysthymia |
| Neurotic, stress-related and somatoform | Agoraphobia · Anxiety disorder · Panic disorder · Generalized anxiety disorder · Social Anxiety Disorder · OCD · Acute stress reaction · PTSD · Adjustment disorder · Conversion disorder (Ganser syndrome) · Somatoform disorder · Somatization disorder · Neurasthenia |
| Physiological/physical behavioural | Eating disorder (anorexia nervosa, bulimia nervosa) · Sleep disorder (dyssomnia, insomnia, hypersomnia, parasomnia, night terror, nightmare) · </br>Sexual dysfunction (erectile dysfunction, premature ejaculation, vaginismus, dyspareunia, hypersexuality) · Postpartum depression |
| Adult personality and behaviour | Personality disorder · Passive-aggressive behavior · Kleptomania · Trichotillomania · Voyeurism · Factitious disorder · Munchausen syndrome · Ego-dystonic sexual orientation |
| Mental retardation | Mental retardation |
| Psychological development (developmental disorder) | Specific: speech and language (expressive language disorder, aphasia, expressive aphasia, receptive aphasia, Landau-Kleffner syndrome, lisp) · Scholastic skills (dyslexia, dysgraphia, Gerstmann syndrome) · Motor function (developmental dyspraxia) Pervasive: Autism · Rett syndrome · Asperger syndrome |
| Behavioural and emotional, childhood and adolescence onset | ADHD · Conduct disorder · Oppositional defiant disorder · Separation anxiety disorder · Selective mutism · Reactive attachment disorder · Tic disorder · Tourette syndrome · Speech (stuttering · cluttering) |
Pathology of the nervous system, primarily CNS (G00-G47, 320-349) | |
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| Inflammatory diseases of the CNS | Meningitis (Arachnoiditis) - Encephalitis - Myelitis - Encephalomyelitis (Acute disseminated) - Tropical spastic paraparesis |
| Systemic atrophies primarily affecting the CNS | Huntington's
Spinocerebellar ataxia (Friedreich's ataxia, Ataxia telangiectasia, Hereditary spastic paraplegia) Spinal muscular atrophy: Werdnig-Hoffman - Kugelberg-Welander - Fazio Londe - MND (ALS, PMA, PBP, PP, PLS) |
| Extrapyramidal and movement disorders | Parkinson's disease - Neuroleptic malignant syndrome - Postencephalitic parkinsonism - Pantothenate kinase-associated neurodegeneration - Progressive supranuclear palsy - Striatonigral degeneration
Dystonia/Dyskinesia (Spasmodic torticollis, Meige's, Blepharospasm) Essential tremor - Myoclonus - Lafora Chorea (Choreoathetosis) - Restless legs - Stiff person |
| Other degenerative / demyelinating diseases | Alzheimer's - Pick's - Alpers' - Dementia with Lewy bodies - Leigh's demyelinating: Multiple sclerosis - Devic's - Central pontine myelinolysis - Transverse myelitis |
| Seizure/epilepsy | Focal (Simple partial, Complex partial) - Generalised (Tonic-clonic, Absence, Atonic, Benign familial neonatal) Lennox-Gastaut - West - Epilepsia partialis continua - Status epilepticus (Complex partial status epilepticus) |
| Headache | Migraine (Familial hemiplegic) - Cluster - Vascular - Tension |
| Vascular | Transient ischemic attack (Amaurosis fugax, Transient global amnesia) Cerebrovascular disease (MCA, ACA, PCA, Foville's, Millard-Gubler, Lateral medullary, Weber's, Lacunar stroke) |
| Sleep disorders | Insomnia - Hypersomnia - Sleep apnea (Ondine's curse) - Narcolepsy - Cataplexy - Kleine-Levin - Circadian rhythm sleep - Delayed sleep phase - Advanced sleep phase |
| Other | Intracranial hypertension: Hydrocephalus (Normal pressure) - Idiopathic intracranial hypertension Encephalopathy - Brain herniation - Cerebral edema - Reye's - Syringomyelia - Syringobulbia - Spinal cord compression |
Nervous system pathology, primarily PNS (G50-G99, 350-359) | |
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| Nerve, nerve root and plexus disorders (neuropathy, radiculopathy, plexopathy) | cranial nerve: V (Trigeminal neuralgia) - VII (Facial nerve paralysis, Bell's palsy, Melkersson-Rosenthal syndrome, Central seven) - XI (Accessory nerve disorder)
nerve root and plexus: Brachial plexus lesion - Thoracic outlet syndrome - Phantom limb mononeuropathy: upper limb (Carpal tunnel syndrome, Ulnar nerve entrapment, Radial neuropathy) - Causalgia - lower limb (Meralgia paraesthetica, Tarsal tunnel syndrome, Morton's neuroma) - Mononeuritis multiplex |
| Polyneuropathies and other disorders of the PNS | hereditary and idiopathic (Charcot-Marie-Tooth disease, Dejerine Sottas syndrome, Refsum's disease, Morvan's syndrome) Guillain-Barré syndrome - Alcoholic polyneuropathy |
| Diseases of myoneural junction | autoimmune: Myasthenia gravis - Lambert-Eaton myasthenic syndrome |
| Diseases of muscle (myopathy) | Muscular dystrophy
myotonic (Myotonic dystrophy, Myotonia congenita, Thomsen disease, Neuromyotonia, Paramyotonia congenita) congenital myopathy (Centronuclear myopathy, Nemaline myopathy, Central core disease) periodic paralysis: Hypokalemic - Hyperkalemic |
| Autonomic | Familial dysautonomia - Horner's syndrome - Multiple system atrophy (Shy-Drager syndrome, Olivopontocerebellar atrophy) |
Cerebral palsy and other paralytic syndromes (G80-G83, 342-344) | |
|---|---|
| Paresis and plegia NOS | Paralysis - Quadriplegia - Triplegia - Hemiplegia/Hemiparesis - Paraplegia/Diplegia - Monoplegia |
| Flaccid vs. spastic | Flaccid paralysis - Spastic diplegia - Spastic paraplegia |
| Specific types | Cerebral palsy - Cauda equina syndrome - Locked-In syndrome |
Eye disease - pathology of the eye (H00-H59, 360-379) | |||||||||||||
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| Adnexa | eyelid: inflammation (Stye, Chalazion, Blepharitis) - Entropion - Ectropion - Lagophthalmos - Blepharochalasis - Ptosis - Blepharophimosis - Xanthelasma - Trichiasis
lacrimal system: Dacryoadenitis - Epiphora - Dacryocystitis orbit: Exophthalmos - Enophthalmos | ||||||||||||
| Eyeball |
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| Optic nerve and visual pathways | Optic neuritis - Papilledema - Optic atrophy - Leber's hereditary optic neuropathy - Dominant optic atrophy - Optic disc drusen - Glaucoma - Toxic and nutritional optic neuropathy - Anterior ischemic optic neuropathy | ||||||||||||
| Ocular muscles, binocular movement, accommodation and refraction | Paralytic strabismus: Ophthalmoparesis - Progressive external ophthalmoplegia - Palsy (III, IV, VI) - Kearns-Sayre syndrome
Other strabismus: Esotropia/Exotropia - Hypertropia - Heterophoria (Esophoria, Exophoria) - Brown's syndrome - Duane syndrome | ||||||||||||
| Visual disturbances and blindness | Amblyopia - Leber's congenital amaurosis - Subjective (Asthenopia, Hemeralopia, Photophobia, Scintillating scotoma) - Diplopia - Scotoma - Anopsia (Binasal hemianopsia, Bitemporal hemianopsia, Homonymous hemianopsia, Quadrantanopia) - Color blindness (Achromatopsia, Dichromacy, Monochromacy) - Nyctalopia (Oguchi disease) - Blindness/Low vision | ||||||||||||
| Pupil | Anisocoria - Argyll Robertson pupil - Marcus Gunn pupil/Marcus Gunn phenomenon - Adie syndrome - Miosis - Mydriasis - Cycloplegia | ||||||||||||
| Infectious diseases | Trachoma - Onchocerciasis | ||||||||||||
| Other | Nystagmus - Glaucoma/Ocular hypertension - Floater - Leber's hereditary optic neuropathy - Red eye - Keratomycosis - Xerophthalmia - Phthisis bulbi | ||||||||||||
| See also congenital | |||||||||||||
Diseases of the ear and mastoid process (H60-H99, 380-389) | |
|---|---|
| External ear | Otitis externa |
| Middle ear and mastoid | Otitis media - Mastoiditis (Bezold's abscess) - Cholesteatoma - Perforated eardrum |
| Inner ear | Otosclerosis - Balance disorder - Ménière's disease - Benign paroxysmal positional vertigo - Vestibular neuronitis - Vertigo - Labyrinthitis - Perilymph fistula |
| Hearing impairment | Conductive hearing loss - Sensorineural hearing loss - Presbycusis |
| Other | Tinnitus - Hyperacusis |
| See also congenital | |
Circulatory system pathology (I, 390-459) | |
|---|---|
| Hypertension | Hypertensive heart disease - Hypertensive nephropathy - Secondary hypertension (Renovascular hypertension) |
| Ischaemic heart disease | Angina pectoris (Prinzmetal's angina) - Myocardial infarction (heart attack) - Dressler's syndrome |
| Pulmonary circulation | Pulmonary embolism - Cor pulmonale |
| Pericardium | Pericarditis - Pericardial effusion - Cardiac tamponade |
| Endocardium/heart valves | Endocarditis - mitral valve (regurgitation, prolapse, stenosis) - aortic valve (stenosis, insufficiency) - pulmonary valve (stenosis, insufficiency) - tricuspid valve (stenosis, insufficiency) |
| Myocardium | Myocarditis - Cardiomyopathy (Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Loeffler endocarditis, Restrictive cardiomyopathy) - Arrhythmogenic right ventricular dysplasia |
| Electrical conduction system of the heart | Heart block: AV block (First degree, Second degree, Third degree) - Bundle branch block (Left, Right) - Bifascicular block - Trifascicular block Pre-excitation syndrome (Wolff-Parkinson-White, Lown-Ganong-Levine) - Long QT syndrome - Adams-Stokes syndrome - Cardiac arrest - Sudden cardiac death Arrhythmia: Paroxysmal tachycardia (Supraventricular, AV nodal reentrant, Ventricular) - Atrial flutter - Atrial fibrillation (Familial) - Ventricular fibrillation - Premature contraction (Atrial, Ventricular) - Ectopic pacemaker - Sick sinus syndrome |
| Other heart conditions | Heart failure - Cardiovascular disease - Cardiomegaly - Ventricular hypertrophy (Left, Right) |
| Cerebrovascular diseases | Stroke - Transient ischemic attack - Intracranial hemorrhage/cerebral hemorrhage: Extra-axial hemorrhage (Epidural hemorrhage, Subdural hemorrhage, Subarachnoid hemorrhage) Intra-axial hematoma (Intraventricular hemorrhages, Intraparenchymal hemorrhage) - Anterior spinal artery syndrome - Binswanger's disease - Moyamoya disease |
| Arteries, arterioles and capillaries | Atherosclerosis (Renal artery stenosis) - Aortic dissection/Aortic aneurysm (Abdominal aortic aneurysm) - Aneurysm - Raynaud's phenomenon/Raynaud's disease - Buerger's disease - Vasculitis/Arteritis (Aortitis) - Intermittent claudication - Arteriovenous fistula - Hereditary hemorrhagic telangiectasia - Spider angioma - Dissection (Carotid artery, Vertebral artery) |
| Veins, lymphatic vessels and lymph nodes | Thrombosis/Phlebitis/Thrombophlebitis (Deep vein thrombosis, May-Thurner syndrome, Portal vein thrombosis, Venous thrombosis, Budd-Chiari syndrome, Renal vein thrombosis, Paget-Schroetter disease) - Varicose veins / Portacaval anastomosis (Hemorrhoid, Esophageal varices, Varicocele, Gastric varices, Caput medusae) - Superior vena cava syndrome - Lymph (Lymphadenitis, Lymphedema, Lymphangitis) |
| Other | Hypotension (Orthostatic hypotension) - Rheumatic fever |
| See also congenital (Q20-Q28, 745-747) | |
Pathology of respiratory system (J, 460-519), respiratory diseases | |||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Upper RT (including URTIs, Common cold) |
| ||||||||||||||||||||||
| Lower RT/lung disease (including LRTIs) |
| ||||||||||||||||||||||
| Pleural cavity/ mediastinum |
| ||||||||||||||||||||||
| Other/general | Respiratory failure · Influenza · SARS · Idiopathic pulmonary haemosiderosis · Pulmonary alveolar proteinosis | ||||||||||||||||||||||
| see also congenital, neoplasia | |||||||||||||||||||||||
Oral Pathology: Stomatognathic disease (K00-K14, 520-529) | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Teeth |
| ||||||||||||
| Other Hard, Soft and Periapical Tissues | Gingivitis - Periodontitis - Ulcer | ||||||||||||
| Dentofacial Anomalies | Gnathitis - Micrognathism - Prognathism - Retrognathism Malocclusion - Temporomandibular joint disorder | ||||||||||||
| Maxillomandibular anomalies | Ameloblastoma - Cherubism - Congenital epulis - Odontogenic keratocyst - Torus mandibularis - Torus palatinus | ||||||||||||
| Salivary glands | Sialadenitis - Drooling/sialorrhea - Benign lymphoepithelial lesion - Necrotizing sialometaplasia - Ranula - Sialolithiasis - Xerostomia | ||||||||||||
| Lip and Oral mucosa | Cheilitis (Angular cheilitis) - Erythroplakia - Leukoplakia (Hairy leukoplakia) - White sponge nevus | ||||||||||||
| Tongue | Glossitis (Geographic tongue) - Fissured tongue - Glossodynia - Black hairy tongue | ||||||||||||
| Other | Stomatitis (Aphthous ulcer) Velopharyngeal inadequacy | ||||||||||||
| see also neoplasia | |||||||||||||
Digestive system - Digestive disease - Gastroenterology (primarily K20-K93, 530-579) | |||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Upper GI tract |
| ||||||||||||||
| Intestinal |
| ||||||||||||||
| Accessory |
| ||||||||||||||
| Hernia | Diaphragmatic: Congenital diaphragmatic - Hiatus
Abdominal hernia: Inguinal (Indirect, Direct) - Umbilical - Incisional - Femoral Obturator hernia | ||||||||||||||
| Peritoneal | Peritonitis (Spontaneous bacterial peritonitis) - Hemoperitoneum - Pneumoperitoneum | ||||||||||||||
| GI bleeding | Upper (Hematemesis, Melena) - Lower (Hematochezia) | ||||||||||||||
| See also congenital, neoplasia | |||||||||||||||
Diseases of the skin and subcutaneous tissue (integumentary system) (L, 680-709) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Infections |
| ||||||||
| Bullous disorders | acantholysis (Pemphigus, Transient acantholytic dermatosis) · Pemphigoid (Bullous, Cicatricial, Gestational) · Dermatitis herpetiformis | ||||||||
| Inflammatory |
| ||||||||
| Radiation-related disorders | Sunburn · actinic rays (Actinic keratosis, Actinic cheilitis) · Polymorphous light eruption (Acne aestivalis) · Radiodermatitis · Erythema ab igne | ||||||||
| Pigmentation disorder | hypopigmentation (Albinism, Vitiligo) · hyperpigmentation (Melasma, Freckle, Café au lait spot, Lentigo/Liver spot, Acanthosis nigricans, Acral acanthotic anomaly) | ||||||||
| Other skin | keratosis/hyperkeratosis (Seborrheic keratosis, Callus) · other epidermal thickening (Ichthyosis acquisita, Palmoplantar keratoderma)
skin ulcer (Pyoderma gangrenosum, Bedsore) Cutaneous Markers of Internal Malignancy (Florid cutaneous papillomatosis, acanthosis nigricans, sign of Leser-Trelat) atrophic (Lichen sclerosus, Acrodermatitis chronica atrophicans) necrobiosis (Granuloma annulare, Necrobiosis lipoidica) · other granuloma (Granuloma faciale, Pyogenic granuloma) cutaneous vasculitis (Livedoid vasculitis, Erythema elevatum diutinum) | ||||||||
| Connective tissues | collagen disease: Keloid localized connective tissue disorders: Lupus erythematosus (Discoid lupus erythematosus, Subacute cutaneous lupus erythematosus) · Scleroderma/Morphea · Linear scleroderma · Calcinosis cutis · Sclerodactyly · Ainhum | ||||||||
| see also congenital, neoplasia | |||||||||
Diseases of the musculoskeletal system and connective tissue (M, 710-739) | |
|---|---|
| Arthropathies | Arthritis (Septic arthritis, Reactive arthritis, Rheumatoid arthritis, Psoriatic arthritis, Felty's syndrome, Juvenile idiopathic arthritis, Still's disease) - crystal (Gout, Chondrocalcinosis) - Osteoarthritis (Heberden's node, Bouchard's nodes)
acquired deformities of fingers and toes (Boutonniere deformity, Bunion, Hallux rigidus, Hallux varus, Hammer toe) - other acquired deformities of limbs (Valgus deformity, Varus deformity, Wrist drop, Foot drop, Flat feet, Club foot, Unequal leg length, Winged scapula) patella (Luxating patella, Chondromalacia patellae) Protrusio acetabuli - Hemarthrosis - Arthralgia - Osteophyte |
| Systemic connective tissue disorders | Polyarteritis nodosa - Churg-Strauss syndrome - Kawasaki disease - Hypersensitivity vasculitis - Goodpasture's syndrome - Wegener's granulomatosis - Arteritis (Takayasu's arteritis, Temporal arteritis) - Microscopic polyangiitis - Systemic lupus erythematosus (Drug-induced) - Dermatomyositis (Juvenile dermatomyositis) - Polymyositis - Scleroderma - Sjögren's syndrome - Behçet's disease - Polymyalgia rheumatica - Eosinophilic fasciitis - Hypermobility |
| Dorsopathies | Kyphosis - Lordosis - Scoliosis - Scheuermann's disease - Spondylolysis - Torticollis - Spondylolisthesis - Spondylopathies (Ankylosing spondylitis, Spondylosis, Spinal stenosis) - Schmorl's nodes - Degenerative disc disease - Coccydynia - Back pain (Radiculopathy, Neck pain, Sciatica, Low back pain) |
| Soft tissue disorders | muscle: Myositis - Myositis ossificans (Fibrodysplasia ossificans progressiva)
synovium and tendon: Synovitis/Tenosynovitis (Calcific tendinitis, Stenosing tenosynovitis, Trigger finger, DeQuervain's syndrome) - Irritable hip - Ganglion cyst bursa: bursitis (Olecranon, Prepatellar, Trochanteric) - Baker's cyst fibroblastic disorders (Dupuytren's contracture, Plantar fasciitis, Nodular fasciitis, Necrotizing fasciitis, Fasciitis, Fibromatosis) shoulder lesions: Adhesive capsulitis - Rotator cuff tear - Subacromial bursitis enthesis: enthesopathies (Iliotibial band syndrome, Achilles tendinitis, Patellar tendinitis, Golfer's elbow, Tennis elbow, Metatarsalgia, Bone spur, Tendinitis) other, NEC: Muscle weakness - Rheumatism - Myalgia - Neuralgia - Neuritis - Panniculitis - Fibromyalgia |
| Osteopathies | disorders of bone density and structure: Osteoporosis - Osteomalacia - continuity of bone (Pseudarthrosis, Stress fracture) - Monostotic fibrous dysplasia - Skeletal fluorosis - Aneurysmal bone cyst - Hyperostosis - Osteosclerosis Osteomyelitis - Avascular necrosis - Paget's disease of bone - Algoneurodystrophy - Osteolysis - Infantile cortical hyperostosis |
| Chondropathies | Juvenile osteochondrosis (Legg-Calvé-Perthes syndrome, Osgood-Schlatter disease, Köhler disease, Sever's disease) - Osteochondritis - Tietze's syndrome |
| See also congenital conditions (Q65-Q79, 754-756) | |
Urinary system · Pathology · Urologic disease / Uropathy (N00-N39, 580-599) | |||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Abdominal |
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| Pelvic |
| ||||||||||||||||||||||||||||||||||||||||||
| Any/all | Obstructive uropathy · Urinary tract infection · Retroperitoneal fibrosis · Urolithiasis (Kidney stone, Renal colic) | ||||||||||||||||||||||||||||||||||||||||||
| See also congenital, neoplasia, symptoms/signs | |||||||||||||||||||||||||||||||||||||||||||
Diseases of the pelvis and genitals (N40-N99, 600-629) | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Female |
| ||||||||||||||||
| Male |
| ||||||||||||||||
| See also congenital, neoplasia | |||||||||||||||||
Pathology of pregnancy, childbirth and the puerperium (O, 630-676) | |
|---|---|
| Pregnancy with abortive outcome | Ectopic pregnancy - Hydatidiform mole - Miscarriage |
| Oedema, proteinuria and hypertensive disorders | Pregnancy-induced hypertension - Pre-eclampsia - Eclampsia - Gestational diabetes |
| Other, predominantly related to pregnancy | Hyperemesis gravidarum - Gestational pemphigoid - Intrahepatic cholestasis of pregnancy |
| Maternal care related to the fetus and amniotic cavity and possible delivery problems | Polyhydramnios - Oligohydramnios - Chorioamnionitis - Premature rupture of membranes - Amniotic band syndrome - Placenta praevia - Braxton Hicks contractions - Antepartum haemorrhage - Placental abruption |
| Complications of labour and delivery | Premature birth - Postmature birth - Cephalopelvic disproportion - Dystocia (Shoulder dystocia) - Fetal distress - Vasa praevia - Uterine rupture - hemorrhage - Placenta accreta - Umbilical cord prolapse - Amniotic fluid embolism |
| Maternal complications in the weeks after childbirth | Puerperal fever - Peripartum cardiomyopathy - Postpartum thyroiditis - Galactorrhea - Postpartum depression |
| Complications related to the fetus | Fetal intervention - Fetal surgery |
| Other | Maternal death |
Certain conditions originating in the perinatal period (P, 760-779) | |
|---|---|
| Maternal factors and complications | Umbilical cord prolapse - Nuchal cord - Chorioamnionitis |
| Length of gestation and fetal growth | Small for gestational age - Large for gestational age - Premature birth - Postmature birth |
| Birth trauma | Cephalhematoma - Brachial plexus lesion (Erb's palsy, Klumpke paralysis) |
| Respiratory | Intrauterine hypoxia - Infant respiratory distress syndrome - Transient tachypnea of the newborn - Meconium aspiration syndrome - pleural disease (Pneumothorax, Pneumomediastinum) - Wilson-Mikity syndrome - Bronchopulmonary dysplasia |
| Cardiovascular | Pneumopericardium - Persistent fetal circulation |
| Haemorrhagic and haematological/ hematologic disease | Haemorrhagic disease of the newborn - Hemolytic disease of the newborn - Rh disease - Hydrops fetalis - Hyperbilirubinemia (Kernicterus, Neonatal jaundice) |
| Digestive system | Ileus - Necrotizing enterocolitis |
| Integument and temperature regulation | Erythema toxicum |
| Other disorders | Periventricular leukomalacia - Gray baby syndrome - muscle tone (Congenital hypertonia, Congenital hypotonia) - Perinatal infection (Congenital rubella syndrome) - Velamentous cord insertion - Omphalitis |
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