BRS Pathology by Arthur S. Schneider MD, Philip A. Szanto MD

By Arthur S. Schneider MD, Philip A. Szanto MD

This revised 5th version is a superb pathology evaluate for college kids getting ready for the USMLE Step 1 and direction examinations. Written within the well known Board evaluate Series define layout, this article covers common and uncomplicated pathology, significant suggestions of affliction procedures, and systemic pathology that surveys the central problems of every organ method via concise descriptions and full-color illustrations. USMLE-style questions on the finish of every bankruptcy emphasize board-relevant details and make allowance for self-testing to verify strengths and discover parts of weak point. Plus, the excellent examination on the finish of the booklet is a smart prep software for the particular exam!

You also will discover:
- Full-color layout, illustrations, and tables summarize info for handy review
- Over 450 USMLE-style questions, solutions, and rationales either electronically and in print to augment your pathology evaluate
- Key subject icons aid concentration your learn
- Correlation containers emphasize connections among pathology and scientific medication
- A loose better half web site with entry to the book, photograph financial institution, and an interactive query financial institution that includes the entire questions from the booklet for enticing, powerful try preparation!

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BRS Pathology

This revised 5th version is a wonderful pathology overview for college students getting ready for the USMLE Step 1 and direction examinations. Written within the well known Board overview sequence define layout, this article covers basic and easy pathology, significant techniques of affliction approaches, and systemic pathology that surveys the valuable problems of every organ method via concise descriptions and full-color illustrations.

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Extra resources for BRS Pathology

Sample text

Immunologic injury 6. Tissue death. Inflammatory changes occur in viable tissue adjacent to necrotic areas. II. Acute Inflammation A. Adhesion molecules 1. General considerations a. Adhesion molecules play an important role in acute inflammation. b. They are divided into three families: selectins, immunoglobulin (Ig)-family adhesion proteins, and integrins. 2. Selectins a. These molecules are induced by the cytokines interleukin-1 (IL-1) and tumor ­necrosis factor (TNF). L-selectins are expressed on neutrophils and bind to endothelial mucin-like molecules such as GlyCam-1.

C5a is chemotactic, mediates the release of histamine from platelet-dense granules, induces the expression of leukocyte adhesion molecules, and activates the lipoxygenase pathway of arachidonic acid metabolism. (2) C3b is an opsonin. (3) C5b-9, the membrane attack complex, is a lytic agent for bacteria and other cells. Nitric oxide (formerly known as endothelium-derived relaxing factor) (1) This is produced by endothelial cells. (2) It stimulates relaxation of smooth muscle, thus playing a role in controlling vascular tone.

Methylene tetrahydrofolate reductase mutation (MTHFR C677T) (1) This results in a moderate increase in serum homocysteine, which is associated with both arterial and venous thrombosis. The increased homocysteine can be reduced by dietary supplementation with folic acid and vitamins B6 (pyridoxine) and B12 (cobalamin). (2) This is also associated with an increased risk of neural tube defects and possibly a number of diverse neoplasms. e. Increased levels of factor VIII, factor IX, factor XI, or fibrinogen are also associated with increased venous thrombosis.

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