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Clinical Eponyms M-N |
| A-B | C-D | E-F | G-H | I-J | K-L | M-N | O-P | Q-R | S-T | U-V | W-Z |
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This list is available for the Palm Pilot at Andrew Yee's website.
MacCallums plaques |
Irregular thickenings, usually in the left atrium, from subendocardial lesions, usually exacerbated by regurgitant jets | ||||||||||||
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Macewen’s sign |
In hydrocephalus before closure of sutures, cracked pot sound when percussing over dilated ventricles | ||||||||||||
Machado-Joseph disease |
Spinocerebellar ataxia 3, named for affected families of Azorean origin, autosomal dominant disorder cause by a CAG expansion in gene on 14q, onset after age 40, associated with diabetes | ||||||||||||
Maffuccis syndrome |
Endochondromatosis associated with soft tissue hemangiomas; associated with ovarian carcinomas and brain gliomas; essentially Olliers disease with hemangiomas | ||||||||||||
Magendie, foramen of |
Midline foramen exiting out of fourth ventricle | ||||||||||||
Mallory body |
"Alcoholic hyalin," an eosinophilic intracytoplasmic inclusion in liver cells that is characteristic of alcoholic liver disease but seen in many other conditions as well (e.g., primary biliary cirrhosis, Wilsons disease, chronic cholestatic syndromes, focal nodular hyperplasia, and hepatocellular carcinoma); inclusions composed largely of intermediate filaments of prekeratin | ||||||||||||
Mallory-Weiss tears |
Small defects in gastroesophageal junction, from violent retching and beef with alcoholic gastritis, can bleed like crazy, 87% occur below gastroesophageal junction; bleeding stops 90% without intervention | ||||||||||||
Malta fever |
Brucellosis | ||||||||||||
Maltese cross |
Fat droplets in urine | ||||||||||||
Marchiafava Bignami syndrome |
Seen in malnourished alcoholics, necrosis of corpus callosum and subcortical white matter leading acutely to chronically to dementia, spasticity, dysarthria, gait disorder, and coma | ||||||||||||
Marcus Gunn pupil |
Afferent pupillary defect, pupil dilates instead of constricts because of optic nerve defect | ||||||||||||
Marie-Strümpell disease |
Refers to ankylosing spondylitis in Europe | ||||||||||||
Marjolin's ulcer |
Squamous cell carcinoma ulceration overlying chronic osteomyelitis or burn scar | ||||||||||||
Markle sign |
Jar tenderness in abdomen from heel drop as a localizing sign of peritoneal irritation; described in 1973 | ||||||||||||
Marshall syndrome |
Dominantly inherited chondrodysplasias characterized by midfacial hypoplasia, high myopia, and sensorineural hearing deficit, from mutation in COL11A1; similar to Stickler syndrome | ||||||||||||
Marshall-Smith syndrome |
Accelerated skeletal maturation, failure to thrive, and dysmorphic facial features with death in early infancy or childhood from pulmonary infections | ||||||||||||
May-Hegglin anomaly |
Neutrophils with large pale blue inclusions resembling Döhle bodies, giant platelets (30-80 fL v. 7-10 in nl); rare AD asymptomatic trait | ||||||||||||
Mayer's reflex |
Adduction of the thumb in response to flexion of the MCP joint of the ring finger in a person with a relaxed hand - a normal finding | ||||||||||||
Mayer-Rokitansky-Küster-Hauser syndrome |
Absence of vagina from abnormality of müllerian development | ||||||||||||
Mayne’s sign |
In aortic regurgitation, decrease in diatolic pressure of 15 mm Hg when arm is held above the head; of questionable utility since observed in 65% of normal people | ||||||||||||
Mayo, vein of |
Vein overlying pylorus | ||||||||||||
Mazzotti reaction |
Reaction to proteins released by dying onchocerca, including fevers, rashes, ocular damage, joint and muscle pain, and lymphangitis as well as hypotension, pyrexia, respiratory distress, and prostration | ||||||||||||
McArdles syndrome |
Glycogen storage disease V, deficiency in muscle phosphorylase, with consequent glycogen accumulation in skeletal muscle, produces painful muscle cramps and muscle weakness following exercise | ||||||||||||
McBurneys point |
One-third the distance from the ASIS to the umbilicus | ||||||||||||
McBurneys sign |
Tenderness at McBurneys point in appendicitis | ||||||||||||
McCune-Albright syndrome |
Triad of irregular café au lait spots, fibrous dysplasia of long bones with cysts, and precocious puberty | ||||||||||||
McMurray's sign |
An audible click heard when rotating the tibia on the femur, indicating meniscal injury | ||||||||||||
McRoberts’s maneuver |
Flexion of legs onto maternal abdomen for shoulder dystocia, causeing a significant cephalad rotation of the symphysis pubis and subsequent flattening of the sacrum. | ||||||||||||
Means-Lerman scratch |
In hyperdynamic heart (as in hyperthyroidism), a systolic scratch occasionally heard in the second left intercostal space during expiration, presumed to be secondary to rubbing together of normal pleural and pericardial surfaces | ||||||||||||
Meckel scan |
99Tc pertechnetate scan that selectively tags acid secreting cells (gastric mucosa); it is used most often for unexplained bleeding in infants and young adults | ||||||||||||
Meckels cartilage |
Branchial arch 1 | ||||||||||||
Meckels diverticulum |
Persistence of vitelline duct, contains all 3 layers of bowel (mucosa, submucosa, muscularis propria), antimesenteric, present in 2% of population, usually within 30 cm of ileocecal valve; the five 2s: 2" long, 2 feet from ileocecal valve, 2% of population, commonly persists in first 2 years of life, may have 2 types of epithelia | ||||||||||||
Meckel-Gruber syndrome |
Sloping forehead, posterior encephalocele, polydactyly, and polycystic kidneys | ||||||||||||
Meess lines |
Horizontal white bands of the nails seen in chronic arsenical poisoning, and occasionally in leprosy; R.A. Mees, 20th century Dutch physician | ||||||||||||
Meige’s syndrome |
Blepharospasm with facial dystonia and lip smacking | ||||||||||||
Meigss syndrome |
Unusual combination of hydrothorax, ascites, and ovarian fibroma | ||||||||||||
Meissners plexus |
Submucous plexus; innervates glandular epithelium, muscularis mucosa, intestinal endocrine cells, and submucosal blood vessels | ||||||||||||
MELAS |
Mitochondrial encephalopathy with acidosis and stroke, onset in childhood, stroke-like episodes with hemiparesis, hemianopia, or cortical blindness; full expression of the disease leads to death often before age 20; 80-90% have point mutation in leucine tRNA in mtDNA | ||||||||||||
Mendelsons syndrome |
Chemical pneumonitis after aspiration of gastric contents | ||||||||||||
Ménétriers disease |
Giant cerebriform enlargement of the rugal folds of the gastric mucosa, results from profound hyperplasia of the surface mucous cells with accompanying glandular atrophy, most often encountered in men (3:1), 40s-60s, sometimes in children, may produce epigastric discomfort, weight loss, and sometimes bleeding related to superficial rugal erosions, gastric secretions mostly mucous, little HCl, may be sufficient protein loss to produce hypoalbuminemia | ||||||||||||
Ménieres disease |
1. fluctuating sensorineural loss, classically involving the low frequencies; 2. Vertiginous episodes; 3. Aural pressure; 4. Tinnitus that is most frequently described roaring; pathologic changes are said to consist of a dilation of the endolymphatic system that leads to a degeneration of the delicate vestibular and cochlear hair cells | ||||||||||||
Menkes disease |
X-linked, problem in the distribution of copper in the body, amount of copper and ceruloplasmin in serum reduced, excess of copper in intestinal mucosa, muscle, spleen, and kidney; usually fatal by age 3 | ||||||||||||
MERRF |
Myoclonic epilepsy and ragged red fibers, syndrome of mitochondrial myopathy, myoclonus, generalized seizures, intellectual deficits, ataxia, and hearing loss; extraocular movements normal; associated with point mutations in lysine tRNA in mtDNA | ||||||||||||
Metzer index |
MCV/RBC ratio; >13 iron def, < 13 thalassemia | ||||||||||||
Meyers loop |
A portion of the optic radiations subserving vision from the superior field coursing rostrally within the temporal lobe before heading caudally to the primary visual cortex; lesions produce contralateral upper quadrantanopia (pie in the sky) | ||||||||||||
Meynert, basalis nucleus of |
Degenerates in Alzheimers; uses ACh | ||||||||||||
Mikuliczs syndrome |
Bilateral inflammatory enlargement of the parotid, submaxillary, and sublingual, and lacrimal glands and xerostomia, secondary to sarcoid, leukemia, lymphoma, etc. | ||||||||||||
Milkmans fractures |
In osteomalacia, radiolucent narrow lines that lie either at right angles or obliquely to the cortical outlines of bones and often transect them; bilateral and symmetric, found at the axillary margins of the scapula, lower ribs, neck of the proximal femurs, and posterior regions of the proximal ulnas; related either to stress fractures or to mechanical erosion by penetrating nutrient arteries; aka Loosers zones | ||||||||||||
Millard-Gubler syndrome |
Ventral pontine injury causing symptoms similar to Fouville’s syndrome except lateral rectus weakness only, instead of gaze palsy | ||||||||||||
Miller Fisher syndrome |
Variant of Guillain-Barré where cranial nerves are affected, leading to triad of ataxia, areflexia and ophthalmoplegia, cross-reacting antibodies to GQ1b ganglioside have been found | ||||||||||||
Mirrizis syndrome |
Extrinsic obstruction of the common bile duct from a cystic duct gallstone | ||||||||||||
mitral facies |
Malar flush with pinched and blue facies in mitral stenosis | ||||||||||||
Mobitz type I AV block |
Wenckebach pattern, second degree block with intermittent conduction failure resulting in progressive PR prolongation before dropped beat; may be seen in ischemic heart disease, digitalis, beta blockers, calcium channel blockers, inferior wall MI | ||||||||||||
Mobitz type II AV block |
Second degree block with intermittent conduction failure with sudden non-conducted sinus P wave without progressive prolongation of PR interval; not seen with digitalis excess or inferior wall MI generally but may be seen with anterior wall MI | ||||||||||||
Möbius syndrome |
Congenital facial paralysis with or without limb defects associated with misoprostol use | ||||||||||||
Modigliani syndrome |
Thyroid in normal position but people with long curving necks enhance prominence and palpation of thyroid | ||||||||||||
Mönckebergs arteriosclerosis |
Ring-like calcifications within the media of medium-sized to small muscular arteries (femoral, tibial, radial, and ulnar arteries, genital arteries), occurs almost exclusively in individuals over 50 years old; doesnt narrow lumen, distinct from atherosclerosis | ||||||||||||
Mondors disease |
Thrombophlebitis of superficial breast veins | ||||||||||||
Monges disease |
Chronic mountain sickness, loss of high altitude tolerance after prolonged exposure, characterized by extreme polycythemia, exaggerated hypoxemia, and reduced mental and physical capacity; relieved by descent | ||||||||||||
Monro, foramina of |
Connects each of the lateral ventricles with the third ventricle | ||||||||||||
Monro-Kellie doctrine |
cranial cavity is a closed rigid box, change in the amount of intracranial blood can occur only through changes in CSF quanitity | ||||||||||||
Monsels solution |
Ferric subsulfate | ||||||||||||
Monteggia fracture |
Fracture of the proximal third of the ulna with a dislocation of radial head | ||||||||||||
Montgomery, glands of |
Sebaceous glands of areola | ||||||||||||
Mooren corneal ulcers |
Chronic, painful ulcers, involves circumference of peripheral cornea and may progress to vision loss; associated with hep C | ||||||||||||
Morgagni's hernia |
Anterior parasternal diaphragmatic hernia, right more common than left | ||||||||||||
Morrisons pouch |
Hepatorenal recess; the most posterior cavity in the peritoneal cavity | ||||||||||||
Mucha-Habermann disease |
Pityriasis lichenoides et varioliformis acuta, scattered necrotic papules and vesicles that can resemble insect bites but usually are more generalized and symmetric | ||||||||||||
Muehrckes nails |
Paired narrow horizontal white bands that are immobile as nail grows; seen in hypoalbuminemia, nephrotic syndrome | ||||||||||||
Müllers maneuver |
Reverse Valsalva | ||||||||||||
Müllers sign |
In aortic regurgitation, systolic pulsations of the uvula | ||||||||||||
Müller-Lyer illusion |
The two horizontal lines stuff with arrows | ||||||||||||
Munchausen’s syndrome |
Factitious disorder, eponym given by Asher in 1951 after Baron Karl Munchausen (1720-1797), retired German cavalry officer with a reputation for preposterous stories about his activities as a soldier, hunter | ||||||||||||
Munros microabscesses |
In psoriasis, when neutrophils form small aggregates within the parakeratotic stratum corneum | ||||||||||||
Murphys sign |
A sharp increase in tenderness with a sudden stop in inspiratory effort, sign of acute cholecystitis, 27% sensitive | ||||||||||||
Myersons sign |
Persistent blinking with glabellar stuff | ||||||||||||
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Nägeles rule |
Means of estimating date of delivery by counting back 3 months from the first day of the last menstrual period and adding seven days; full term 38 weeks after fertilization, 40 weeks after LNMP | ||||||||||||
Nardi test |
Narcotic-indcued stimulation or spasm reproducing the abdominal pain and amylase elevation of relapsing pancreatitis (for inferring sphincteric disease in any pancreatic or biliary ductal system without a gallbladder), presumably accurate in the diagnosis of peri-sphincteric disease | ||||||||||||
Naxos disease |
Initially described on Greek island of Naxos, synrome of arrhythmogenic right ventricular cardiomyopathy, non-epidermolytic palmoplantar keratoderma, and woolly hair, due to deletion in plakoglobin, a constituent protein in adherens and desmosomal junctions | ||||||||||||
Negri bodies |
In rabies virus-infected brain neurons, eosinophilic cytoplasmic inclusions | ||||||||||||
Nelsons syndrome |
Enlargement of a pituitary adenoma in a patient with Cushings disease whose adrenals have been removed from loss of feedback inhibition of cortisol | ||||||||||||
nerve endings |
FREE includes Merkel cell associated: found in the epidermis as small aggregates called tactile corpuscles (Merkel cell has neural crest and squamous properties); ENCAPSULATED includes Meissners: asymmetrical, lamellated; Pacinian: symmetrical, lamellated; Ruffini: no lamellation | ||||||||||||
Niemann-Pick disease |
Unifying feature, lysosomal accumulation of sphingomyelin and cholesterol, type A&B (*deficiency of sphingomyelin-cleaving enzyme sphingomyelinase*) and type C&D (enzyme normal or nearly normal, defect in esterification and transport); type A, 75-80% of all cases, extensive neurologic involvement, marked visceral accumulations of sphingomyelin, and progressive wasting and early death within the first 3 years of life); half have cherry red spot in macula as in Tay-Sachs | ||||||||||||
Nikolskys sign |
A peculiar vulnerability of the skin in pemphigus vulgaris; the apparently normal epidermis may be separated at the basal layer and rubbed off when pressed with a sliding motion | ||||||||||||
Nissl bodies |
In neurons, rough ER | ||||||||||||
Nissl stain |
Stains cell bodies dye binds to acid groups, in particular the RNAs of the ribosomes located within the cell body; Franz Nissl, German medical student at time | ||||||||||||
Norwalk virus |
Outbreak in a school in Norwalk, Ohio in 1969 | ||||||||||||
Nothnagel’s syndrome |
Injury to superior cerebellar peduncle causing ipsilateral oculomotor palsy and contralateral cerebellar ataxia | ||||||||||||
| A-B | C-D | E-F | G-H | I-J | K-L | M-N | O-P | Q-R | S-T | U-V | W-Z |
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From Andrew Yee, Harvard Med '00