Clinical Eponyms
Q-R

 

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This list is available for the Palm Pilot at Andrew Yee's website.

Queckenstedt’s maneuver
Applying pressure on the internal jugular vein to dilate cranial veins and increase incranial pressure; can be used to see if there’s block in CSF flow by at lumbar puncture pressures in response
Quellung reaction
Swelling of bacterial capsule when exposed to antibody; used for diagnosis of S. pneumoniae, H. influ type B, N. meningitidis groups A and C
Queyrat, erythroplasia of
Carcinoma in situ of the glans penis Auguste Queyrat, French dermatologist, born 1872
Quincke’s sign
In aortic regurgitation, capillary pulsations detected by pressing a glass slide on the patient’s lip or by transmitting a light through the patient’s fingertips; of questionable utility since seen in normal people
Rabson-Mendenhall syndrome
Congenital syndrome characterized by insulin resistance, acanthosis nigricans, and growth retardation; associated with developmental abnormalities of bones and teeth, PCOD, genitomegaly, and pineal gland hyperplasia; associated with mutation in insulin receptor
raccoon eyes
Bilateral black eyes in basilar skull fracture
Radovici's sign
To determine if a patient has increased intracranial pressure, stroke the thenar eminence of the hand and watch for ipsilateral contractions of the muscles of the chin. (The reflex is listed in Stedman's Medical Dictionary as the palmomental reflex: unilateral (sometimes bilateral) contraction of the mentalis or orbicularis oris muscles caused by a brisk scratch made on the palm of the ipsilateral hand. Synonym: palm-chin reflex.)
Ramsay Hunt syndrome
Herpes zoster infection of the geniculate ganglion; facial nerve involvement (ear, palate, pharynx, or neck); pain and vesicles appear in external auditory canal, and patients lose their sense of taste in anterior 2/3 of tongue while developing ipsilateral facial palsy
Randle cycle
Glucose-free fatty acid cycle; inverse relationship between glucose and free fatty acid use
Ranke complex
Combination of Ghon lesion and involved lymph nodes in tuberculosis
Rapoport-Luebering shunt
In red blood cells, pathway converting 1,3-diphosphoglyceric acid to 2,3-DPG and then to 3-phosphoglyceric acid; enzyme is diphosphoglycerate synthetase; 2,3-DPG reduces affinity of hemoglobin for oxygen; 2,3-DPG rises with alkalosis and decreases with acidosis, result of effect of pH on enzyme
Rasmussen’s encephalitis
Progressive childhood disease characterized by severe epilepsy, hemiplegia, dementia, and inflammation of the brain potentially from autoantibodies to GluR3 antigen
Rathke’s pouch
A diverticulum involved in development of pituitary gland, vestigial remnants lead to craniopharyngioma
Rebuck skin window
Dermal abrasion technique for testing tissue penetration of neutrophils, scraping forearm, then putting coverslip over it, checking glass for neutrophils
Reed-Sternberg cells
In Hodgkin’s lymphoma, giant macrophage-like cells with two nuclei
refeeding syndrome
Hypokalemia, hypomagnesemia, and hypophosphatemia after refeeding a starved patient
Refsum’s disease
AR; phytanic acid accumulates as a result of an absence of the enzyme -phytanic acid -hydroxylase involved in its catabolism; give patient’s large amounts of nicotinic acid or triparanol, chemicals that inhibit lipid synthesis; dryness and scaling similar to the appearance of icthyosis develop, associated with neuropathy
Reichert’s cartilage
Branchial arch 2
Reid index
Comparing the relative thickness of the mucous glands with the total thickness of the airway wall; increased in patients with chronic bronchitis (normally < 0.4)
Reinke crystals
In 25% of Leydig cell tumors, intracytoplasmic rod-shaped crystalloids
Reinke’s edema
Vocal cord polyposis in female smokers, 50s-70s
Reitan trail test
Timed connect-the-number test for detecing alterations in mental status; time>60s pathologic in all age groups
Reiter’s syndrome
In 1916, Reiter described a triad of arthritis, urethritis, and conjunctivitis; 80% possess HLA-B27; associated with Shigella flexneri; ReA develops in 20% of exposed B27+ individuals; subset of reactive arthritis; triad present in 1/3 of patients; incidence estimated as 3.5/100K in males under age of 50; balanitis circinata (penis) and keratoderma blenorrhagica
Bertin, renal columns of
The spaces between adjacent pyramids where cortical tissue extends into
Renshaw cells
Inhibitory cells in the ventral horn of the spinal cord
Retzius, space of
The preperitoneal space anterior to the bladder
Retzius, veins of
Numerous small veins in the retroperitoneum that connect the retroperitoneal viscera to the posterior abdominal wall; dilated in portal hypertension
Reye’s syndrome
Rare disease characterized by fatty change in liver and encephalopathy that in its most severe forms may be fatal; associated with VZV and influenza virus B in children given aspirin
Reynold’s pentad
Charcot’s triad plus altered mental status and shock in cholangitis
Richter syndrome
The evolution of chronic lymphocytic leukemia to a large cell lymphoma with high fever, weight loss, enlarging lymph nodes, and hepatosplenomegaly
Riedel’s lobe
In some persons, especially those with a lanky build, the liver tends to be somewhat elongated so that its right lobe is easily palpable as it projects downward toward the iliac crest; such elongation, called Riedel’s lobe
Riedel’s thyroiditis
Unknown etiology, marked by glandular atrophy, hypothyroidism, and replacement of the thyroid by fibrous tissue with adhesion to surrounding structures
Riggler’s sign
See wall of bowel in perforation
Riley-Day syndrome
Hereditary sensory and autonomic neuropathy type III (familial dysautonomia), recessive disorder that commences in infancy and is characterized by conspicuous autonomic dysfunction (absent tearing, labile temperature, and blood pressure), and accompanied by absent taste sensation, absent funfigform papillae on tongue, impaired pain and temperature sensation, and areflexia; occurs among Ashkenazi
Rinne test
Sensorineural loss, AC>BC conduct loss, BC>AC
Ritter’s disease
Staph scaled skin syndrome
Roger’s disease
Small congenital VSD defect <0.5 cm in diameter (most are muscular); Henri L. Roger, French physician, 1809-1891
Rokitansky-Aschoff sinuses
Small outpouchings of the gallbladder mucosa that may penetrate into and through the muscle wall; prominence in the settings of inflammation and gallstone formation (e.g. chronic cholecystitis) suggests that they are acquired herniations
Romaña’s sign
In the first week of Chagas disease, unilateral periorbital edema and swelling of the eyelid associated with reduviid bug of eye
Romberg test
Patient stands feet together, eyes open and then closes both eyes for 20 to 30 sec without support; positive test with eyes open suggestive of cerebellar ataxia; with eyes closed suggestive of impaired proprioception
Rosenbach’s sign
In aortic regurgitation, hepatic pulsations
Rosenbach’s sign
In thyrotoxicosis, tremor of the closed eyelids
Rosenthal fibers
Inclusions that develop in astrocytes in chronic reactive and neoplastic proliferations; abundant in Alexander’s disease
Roth’s spots
In bacterial endocarditis and other retinal hemorrhagic conditions, a round white spot surrounded by hemorrhage (secondary to microemboli in endocarditis)
Rotor’s syndrome
Poorly defined defects in hepatic uptake and storage of bilirubin; resembles Dubin-Johnson syndrome, but liver pigment missing
Rotter’s lymph nodes
Lymph nodes between the pectoralis minor and pectoralis major
Rovsing’s sign
Pain in the right lower quadrant during left-sided pressure suggests appendicitis; so does right lower quadrant pain on quick withdrawal (referred rebound tenderness)
Ruffini’s corpuscles
Sensory receptors for heat
Russel bodies
Endoplasmic reticulum of plasma cells engaged in active synthesis of immunoglobulins may become hugely distended, producing large, homogenous eosinophilic inclusions called Russell bodies
Russell’s sign
Lanugo, dry skin, hand calluses, associated with purging and bulimia
Russell viper venom time
Sensitive screening tests for lupus anticoagulant activity

 

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From Andrew Yee, Harvard Med '00