408. Van Wyk-Grumbach syndrome is primary hypothyroidism associated with precocious puberty and galactorrhea.
409. Vater - ampulla is location where common bile duct enters the duodenum; described by German anatomist Vater (1684-1751).
410. Vater - ampulla is location where common bile duct enters the duodenum; described by German anatomist Vater (1684-1751).
411. Vincent’s infection is acute necrotizing ulcerative gingivitis - occurring in patients with decreased resistance to infection - from concurrent infection with the symbiotic bacteria Fusobacterium fusiforme and Borrelia vincentii.
412. Virchow’s node is supraclavicular adenopathy associated with a malignancy - often on left side - associated with stomach cancer among other neoplasms but also GI and pelvic malignancies in general. First described by Virchow in 1848 - more cases added by Troisier in 1886; referred to as Troisier’s node in France.
413. Voight - lines of is boundaries which delimit distribution area of main cutaneous nerves; seen in black and Asian skin and rarely in white subjects.
414. Volkmann contracture is sequelae of compartment syndrome post-supracondylar fracture of humerus dut to brachial artery compression where there is contraction of forearm flexors.
415. Von Braun-Fernwald’s sign is Piskacek’s sign.
416. Von Graefe sign is in Graves’s disease - lag of the upper eyelid as it follows the rotation of the eyeball downward.
417. Von Meyenburg complexes is close to or within portal tracts - small clusters of modestly dilated bile ducts embedded in a fibrous - sometimes hyalinized stroma; contain inspissated bile concrements and may communicate with the biliary tree; common and usually without clinical significance.
418. Von Recklinghausen’s disease is generalized neurofibromatosis.
419. Von Willebrand factor is vWF bridges collagen and platelets and favors platelet aggregation - ensuring platelet and vessel wall interactions; glycoprotein Ib-IX major receptor for vWF; vWF also serves as carrier for factor VIII; made in endothelial cells and megakaryocytes.
420. Von Willebrand’s disease is deficiency in von Willebrand factor; frequency of 1% - most common inherited disorder of bleeding; type 1 and 3 reduced quantity of vWF; type 2 qualitative defects in vWF.Kussmaul’s respiration is hyperpnea - associated with acidosis - especially DKA but also in uremia.
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