Spindle cells Cell types - Connecive tissue: fibroblasts/ fibrocytes *collagen* - Bone: Osteocytes/ osteoblasts - Cartilage: Chonodroblasts/ chondrocytes - Muscle: Myocytes Morphology - Nucleus: basophilic, medium sized, ovoid or elongate, well defined, pale to moderate density - Cytoplasm: pink (eosinophilic), elongated Behaviour - Individual cells, but can form sheets, or structures such as tendons, muscles, bone. - Often associated with extracellular matrixes (collagen, bone, cartilage) Round cells *immune cells* Cell types - Lymphocytes - Plasma cells, - Granulocytes - monocytes/ macrophages - Mast cells Morphology - Nucleus: varies with cell type, basophilic, well defined - Cytoplasm: round, other features vary with cell type Behaviour or arrangement - Individual cells - Can lie against each other but don’t form structures Steps: 1. Look at the general structure (architecture) with low power - What is this tissue (given) - List the structural elements - Take note of the arrangement of the elements, to see whether they are all in their normal place 2. List and take notes of constituent elements and non-constituent elements Structures Liver Stained in pink (connective tissue) - Hepatic lobule (central vein and portal triad, portal triad includes hepatic portal vein, bile duct and hepatic artery) - Blood vessels (with RBCs) Cancer: Liver cancer Microscopy (normal) Intestine - Skin - Epithelial layer (simple columnar epithelium) Connective tissue Smooth muscle tissues Capillaries (with RBCs) Epidermis Dermis Hair follicles Blood vessels Sweat gland Sebaceous (Exocrine) glands → secrete oil or waxy matter Skin cancer: Lung - Alveolar sacs Alveoli (simple squamous) Bronchi Cancer: Lung cancer (adenocarcinoma) - Hypertrophic tumor cells (increased in size) - The infiltration of various inflammatory cells can be prominent and occaisional hisiocytic multinucleated giant cells can be present in areas with degradation of normal structures. Muscle Each skeletal muscle fiber is a single cylindrical muscle cell. An individual skeletal muscle may be made up of hundreds, or even thousands, of muscle fibers bundled together and wrapped in a connective tissue covering. Each muscle is surrounded by a connective tissue sheath called the epimysium. Cardiac muscle appears striated like the skeletal muscle due to arrangement of contractile proteins. Cardiac muscle fibers are long cylindrical cells with one or two nuclei. The nuclei are centrally situated like that of smooth muscle Smooth muscle fibers are long, spindle-shaped (fusiform) cells. Note the single and centrally placed nucleus in each smooth muscle cell. The absence of striation is also characteristic of the smooth muscle cells (skeletal) Lymph node Cancer: Lymphoma CT Tumour cell Characteristics of malignant neoplasms include: ● More rapid increase in size ● Less differentiation (or lack of differentiation, called anaplasia) ● Tendency to invade surrounding tissues ● Ability to metastasize to distant tissues Cytologic features of malignant neoplasms include: ● Increased nuclear size (with increased nuclear/cytoplasmic ratio--N/C ratio). ● Variation in nuclear or cell size (pleomorphism). ● Lack of differentiation (anaplasia). ● Increased nuclear DNA content with subsequent dark staining on H and E slides (hyperchromatism). ● Prominent nucleoli or irregular chomatin distribution within nuclei. ● Mitoses (especially irregular or bizarre mitoses). Answer format: Describe: (1-2 short paragraphs) 1. Architecture of the tissue - what type of tissue it is - what types of cell make up this tissue - spindle, round, epithelial [squamous/ cuboidal/ columnar; simple/ stratified/ pseudostratified] - any CT? spaces? - whether the cells are forming any particular structure (e.g. vessels, tube, glands) a. Constituent elements of the normal tissue - Cellular (parenchyma) constituents e.g. nucleus and cytoplasm - Morphology : size, shape, colour [medium to high power] - Behaviour: orientation, location, grouped/individual [ medium power] - Non cellular (stroma) constituents e.g. connective tissue, bone, cartilage, spaces - Morphology (how do they look like): shape, colour - Behaviour: location, loose/dense, regular/irregular, reticular b. Non constituent elements (those do not belong to the normal tissue) - Cellular (parenchyma) constituents e.g. nucleus and cytoplasm - morphology : size, shape, colour - Behaviour: orientation, location, grouped/individual - Non cellular (stroma) constituents e.g. connective tissue, bone, cartilage - Morphology (how do they look like): shape, colour - Behaviour: location, loose/dense, regular/irregular, reticular Interpretation (1 simple paragraph) - Explain the features that lead to your conclusion (from the above structures you described) - State whether it is controlled or u ncontrolled growth (if it’s uncontrolled, is it benign or malignant?) a. Malignant: - Invasive, Spread-out (metastasis), (locally into “where”, e.g. alveolar spaces/ lymphatic tissue) - Pleomorphic (cell alteration → loss of specialisation), causing n ecrosis - Any mitotic figures? b. Benign: no pleomorphism (structure differentiation retained), no metastasis - Give a summary of the important features of the lesion (state out the features of the lesion; one word each) 1. Severity → mild/ marked/ severe 2. Time-course → peracute/ acute/ chronic → determined by the exudate and type of WBCs present - Peracute: transudate (not much protein contents but water → not much pink staining) - Acute: Usually haemorrhage and oedema and neutrophils are often predominant - Chronic: Cells dominate in the exudate, fluid is limited (cellular events > vascular events) 3. Distribution → focal/ multifocal/ diffuse/ widespread/ portal/ centrilobular/ follicular/ cortical etc 4. Site (anatomical site) 5. Lesion - Benign: - oma - Malignant: - sarcoma (spindle cells), - carcinoma (epithelial cells) e.g. lung - Disorder of Growth - Uncontrolled (disturbing archietecture and filling no function) - Malignant: pleiomorphic, invasive (locally into alveolar spaces/ into lymphatic vessels) → Causing necrosis (likely by thrombosis) - Epithelial cells: forming groups and sheets E.g. Haemangioma (benign growth at blood vessel) Description The section shows a piece of skin, showing epidermis, dermis and subcutis. [ description of architecture] - In the subcutis there is a roughly ovoid, well demarcated mass. - The epidermis and dermis towards the edges of the specimen show stratum corneum, granulosum, spinosum and basal in normal arrangement, as well as adnexal structures such as hair follicles and sweat glands. - Towards the center of the specimen, overlying the subcutaneous mass, the epidermis and dermis are thinner, and there is an absence of adnexal structures. - - The subcutaneous mass has a well defined border and appears to consist of a tightly packed collection of thin walled cavities. - These contain red blood cells, and/ or pink amorphous material. [non constituents] - The cavities are lined by a single layer of cells with an extremely flattened nucleus and cytoplasm [non constituents], resembling the endothelial cells that line normal blood vessels. Underlying this (between the cavity- like structures) is a fine network of eosinophilic fibres and occasional spindle cells (connective tissue). Overall, the mass resembles a proliferation of thin-walled blood vessels of varying size but uniform in structure and cell morphology, containing red blood cells and plasma. No mitotic figures are visible. Interpretation This is a proliferation of vascular endothelium. - It serves no apparent purpose and is localised (therefore unlikely to be a controlled proliferation). There is no evidence of pleiomorphism, high mitotic rate or invasion, and the cells are well differentiated and forming well defined structures. - Benign neoplasm of vascular endothelium- subcutaneous haemangioma E.g. Kidney (Malignant) Description General architecture The slide shows a section of kidney. It is normal in general shape and approximately 1/3 of its mass appears normal in structure, with renal pelvis, renal medulla containing collecting ducts, and the cortex containing glomeruli and convoluted tubules. The remaining 2/3 appears as widespread, multifocal to coalescing basophilic areas. Constituent elements The convoluted tubules appear normal, being lined with well defined, simple cuboidal epithelium and being separated by minimal connective tissue. The glomeruli appear well defined, consisting of a tuft of capilaries in an empty space (bowman’s capsule). The collecting ducts appear empty, and are lined with a low cuboidal epithelium Non-constituent elements In the basophilic portion of the slide, there is a dense infiltrate of cells pushing between and displacing the renal tubules and glomeruli. The infiltrate consists of a mixture of round cells. Some have small dense round nuclei and scant cytoplasm (lymphocytes), others have similar nuclei but with a moderate amount of cytoplasm (plasma cells), and many have a large ovoid nucleus and a large amount of cytoplasm (macrophages). Scattered throughout are cells with multiple round nuclei and abundant pink cytoplasm (giant cells). In clusters, multifocally and in some cases involving the glomerulus, there are groups of cells with a dense multi-lobed nucleus and a moderate amount of cytoplasm (neutrophils). Interpretation - Widespread infiltration of the renal interstitium (connective tissue), also involving the glomeruli, by a mixed inflammatory infiltrate consisting of neutrophils, lymphocytes, plasma cells, and macrophages and giant cells. - Severe, widespread, chronic, pyogranulomatous interstitial glomerulo-nephritis. (or you could just say - severe, widespread, chronic active inflammation of the interstitium and glomeruli of the kidney)