Principles MCQs Flashcards
On a blood test, an increase in what cell indicates acute infection?
A – Polymorph
B – Monocyte
C – Histiocyte
D – Monomorph
E – Lymphocyte
A - Polymorph
Polymorph is another name for neutrophil which relates to its polymorphous nucleus (typically 4 or 5 lobes). A monocyte is the name given to macrophages that are still in the blood stream. We call them macrophages when they reach the tissues. A histiocyte is an umbrella term for types of macrophages. A monocyte is therefore a kind of histiocyte. There is no such thing as a monomorph. Lymphocytes are a cell of chronic inflammation.
Suppuration tends not to involve:
A – Necrosis
B – Phagocytosis
C – Abscess formation
D – Lymphocytes
E - Neutrophils
D - Lymphocytes
Suppuration is one of the outcomes of acute inflammation and broadly means the formation of pus. Necrotic debris is a main constituent of pus some of which will undergo phagocytosis by neutrophils. Lymphocytes are a cell of chronic inflammation. It should be noted that there is often some overlap between the outcomes of acute inflammation and that a degree of restitution, suppuration and chronic inflammation often coexist.
Granulomas are not associated with:
A – Cancer
B – Lymphoma
C – Bacterial infection
D – Foreign material
E – Autoimmune disease
F – Viral infection
F - Viral infection
Granulomas are an aggregate of epithelioid histiocytes. Epithelioid is a term that means the macrophages look more like epithelial cells which in this context just means they are bigger and rounder. Granulomatous inflammation is relatively uncommon but is associated with several important disease processes many of which are rare but important not to miss.
Causes of granulomatous inflammation include
Tuberculosis and any other mycobacterial infection – this is one of the most important differential diagnoses and should always be kept at the back of your mind when someone mentions granuloma. Remember if it is a granuloma with caseating necrosis the diagnosis is TB until proven otherwise. Other infections frequently cause granulomatous responses but these are often fungal or parasitic. Viral infections do not typically cause granulomatous inflammation.
Foreign material is difficult to digest and phagocytose (like mycobacterium) and it often elicits a granulomatous response. Suture material after surgery is often associated with granulomas, as are inhaled agents and some illicit drugs.
Some autoimmune diseases show altered immune responses and result in granulomatous inflammation. Sarcoidosis is a multi-system disorder of unknown aetiology that is, however, likely to have an autoimmune basis. It is charactersied by the formation of well-formed granulomas. As it is a multi-system disorder it can result in granulomatous inflammation in any organ.
The final important point to remember is that some malignancies (lymphoma and carcinomas) can be associated with a granulomatous response.
An autopsy on a 4 year old is performed. The father of the child claims that the boy fell off a climbing frame injuring his leg and then banging his head. He states that the injury occurred that morning. Which pathological feature in the bone would suggest that this is not true.
A – The presence of neutrophils
B – The presence of blood clot
C – The presence of fibroblasts
D – Vascular dilatation
E – High levels of complement at the injury site
C - The presence of fibroblasts
This is a slightly contrived question but does highlight to some extent why understanding the process of inflammation and healing is important. You should recall that one of the first changes in acute inflammation are the vascular changes. The vessels dilate and the rate of flow slows down allowing white cells to drift to the edges of the vessel. If there is significant vascular damage then a blood clot will form as a result of initiation of the coagulation cascade. Hopefully you now know that neutrophils are associated with acute inflammation and therefore the presence of neutrophils occurs early. Fibroblasts are a later feature at a point when the initial acute inflammation has died down. Immigration of fibroblasts into the damaged tissue is the first step towards forming granulation tissue and then either resolution or restitution of the site of injury.
Resolution of injury and inflammation of the skin is more likely if there is:
A – Vascular disease
B – Persistence of the injury
C – Damage of the basement membrane
D – A poor nutritional state
E – Loss of the superficial layers of the epidermis
E - Loss of the superficial layers of the epidermis
We discussed the features of injury that are likely to favour complete healing or resolution.Healing tissue requires a supply of oxygen to produce ATP. ATP is the energy currency of all cells and cells in healing tissues will require lots of energy and therefore a good supply. Similarly, people in a poor nutritional state are less likely to be able to supply the correct building blocks in the form of protein, carbohydrate etc. that will be required for tissue to heal.
Persistence of the injury will continue to stimulate the same response that initiated the acute inflammation in the first place.
Epithelial tissues lie on a basement membrane. This provides them with a structure from which to grow. You may think of it as being analogous to having a scaffold in place to within which to build a house around. Without the scaffold in place it is difficult to completely build/repair the house. Therefore superficial injuries where the basement membrane remains intact heal well. This is relevant to traumatic injuries but is also important when we consider damage to the epidermis as a result of burns. 1st degree burns are only superficial. 2nd degree burns involve the dermis and have therefore disrupted the basement membrane. 3rd degree burns go even deeper and often into underlying connective tissue or fat.
Located along the length of the testis at its posterioir aspect; its contents move in a superior to inferior direction.
A - Deep inguinal ring
B - Ejaculatory duct
C - Epididymis
D - Penile Urethra
E - Seminal vesicle
F - Seminiferous tubules
G - Spermatic cord
H - Tunica vaginalis
I - Ureter
J - Vas deferens
C - Epididymis
This structure is located at the posterior aspect of the testis. Sperm pass from the seminiferous tubules to the epididymis and then pass within the epididymis (in a superior to inferior direction) into the vas deferens which is the continuation of the epididymis at the inferior pole of the testis.
Is sectioned (cut) and ligated (tied off) in a common male sterilisation procedure
A - Deep inguinal ring
B - Ejaculatory duct
C - Epididymis
D - Penile Urethra
E - Seminal vesicle
F - Seminiferous tubules
G - Spermatic cord
H - Tunica vaginalis
I - Ureter
J - Vas deferens
J - Vas deferens
The procedure is called a vasectomy, the derivation of this word: vas (vas deferens), ectomy (to cut out) (although note the vas deferens is not usually completely removed during this procedure). Although in theory, if any part of the route that sperm take from formation to ejaculation was completely interrupted (blocked or cut), it would render a male sterile, it is the vas deferens which is the easiest to access to achieve this. The vas is cut and ligated within the scrotum and a vasectomy can be carried out under local anaesthetic.
Drains semen into prostatic urethra
A - Deep inguinal ring
B - Ejaculatory duct
C - Epididymis
D - Penile Urethra
E - Seminal vesicle
F - Seminiferous tubules
G - Spermatic cord
H - Tunica vaginalis
I - Ureter
J - Vas deferens
B - Ejaculatory duct
The Ejaculatory duct is formed from the vas deferens and the duct from the seminal vesicle joining together. The ejaculatory duct is located at the posteroinferior aspect of the bladder and it drains its contents (semen) into the prostatic urethra.
Describe an encircling of skeletal muscle.
A - External anal sphincter
B - Filiform papillae
C - Kidney
D - Internal anal sphincter
E - Lacteal
F - Major duodenal papilla
G - Mesentery
H - Pyloric sphincter
I - Rugae
J - Splenic flexure
A - External anal sphincter
Through this structure digestive enzymes enter the GI tract.
A - External anal sphincter
B - Filiform papillae
C - Kidney
D - Internal anal sphincter
E - Lacteal
F - Major duodenal papilla
G - Mesentery
H - Pyloric sphincter
I - Rugae
J - Splenic flexure
F - Major duodenal papilla
Is usually located in the flank/lumbar region.
A - External anal sphincter
B - Filiform papillae
C - Kidney
D - Internal anal sphincter
E - Lacteal
F - Major duodenal papilla
G - Mesentery
H - Pyloric sphincter
I - Rugae
J - Splenic flexure
C - Kidney
Is part of the axial skeleton and articulates with a cervical vertebra.
A - Acromial end of clavicle
B - Hyoid
C - Illium
D - Ischium
E - Mandible
F - Manubrium of sternum
G - Occipital bone
H - Rib 1
I - Rib 11
J - Sacrum
G - Occipital bone
It is located in the neurocranium and articulates with C1 (the atlas) at the atlantooccipital joint.
Does not articulate with any other bones
A - Acromial end of clavicle
B - Hyoid
C - Illium
D - Ischium
E - Mandible
F - Manubrium of sternum
G - Occipital bone
H - Rib 1
I - Rib 11
J - Sacrum
B - Hyoid
This bone is located in the anterior part of the neck, at the level of C3. This bone is described as “floating” as it is suspended by muscles that connect it to other bones and cartilage: the mandible, a part of the temporal bone (the styloid process), the thyroid cartilage (of the larynx), the manubrium of the sternum and the scapula.
Forms a component of the pelvic outlet
A - Acromial end of clavicle
B - Hyoid
C - Illium
D - Ischium
E - Mandible
F - Manubrium of sternum
G - Occipital bone
H - Rib 1
I - Rib 11
J - Sacrum
D - Ischium
More specifically, it is the ischiopubic ramus (a specific part of the ischium) that forms the anterolateral aspect of the pelvic outlet, along with the coccyx posteriorly, the pubic symphysis anteriorly, the ischial tuberosities posterolaterally and the sacrotuberous ligament posterolaterally.
Is part of a fibrous joint
A - Acromioclavicular joint
B - Atlanto-occipital joint
C - Distal radioulnar joint
D - Facet joint
E - Hip joint
F - Interosseus membrane
G -Knee joint
H - Shoulder joint
I - Temporomandibular joint
J - Wrist joint
F - Interosseus membrane
This is the fibrous sheet that connects 2 bones, e.g. the radius and ulna, or the tibia and fibula. The joint thus formed between the membrane and the bones is a type of fibrous joint known as a syndesmosis (fibrous sheet).
A joint between C1 and a bone of the neurocranium
A - Acromioclavicular joint
B - Atlanto-occipital joint
C - Distal radioulnar joint
D - Facet joint
E - Hip joint
F - Interosseus membrane
G -Knee joint
H - Shoulder joint
I - Temporomandibular joint
J - Wrist joint
B - Atlanto-occipital joint
C1 is the 1 st cervical vertebrae, also known as the atlas, and the occipital bone is the bone that forms the posterior aspect of the neurocranium.
A joint in which there is normally approximately 180° of flexion
A - Acromioclavicular joint
B - Atlanto-occipital joint
C - Distal radioulnar joint
D - Facet joint
E - Hip joint
F - Interosseus membrane
G -Knee joint
H - Shoulder joint
I - Temporomandibular joint
J - Wrist joint
H - Shoulder joint
180 degrees of flexion from the anatomical position is a large movement, so the answer is likely to be a joint that is highly mobile. That rules out A, D & F. Flexion does not occur at the distal radioulnar joint or the TMJ so that rules out C&I. At the remaining joints, flexion does occur however not 180 degrees (even though you have not been given values for the movements at the other joints, you can work this out just by undertaking the movements). The hip (as indicated in the lecture) has approx. 135 degrees of flexion. The knee joint approximately the same. The wrist joint will have a normal range of flexion less than that, approx. 90 degrees. You were asked in the learning objectives just to know the values for normal range of movements occurring at the shoulder, hip and knee joints.
Site of production of ribosomes
A - Communicating junctions (gap junctions)
B - Desmosomes
C - Golgi apparatus
D - Microtubules
E - Mitochondria
F - Nucleolus
G - Occluding junctions (tight junctions)
H - Ribosomes
I - Rough endoplasmic reticulum
J - Smooth endoplasmic reticulum
F - Nucleolus
Ribosomes become associated to the rough endoplasmic reticulum in large numbers, indeed causing the ‘rough’ nature of the RER, however they are produced within the nucleus in the special region called the nucleolus, which typically appears as a dark ‘spot’ within the nucleus in both light micrographs and electron micrographs.
Spread of electrical excitation directly from cell to cell
A - Communicating junctions (gap junctions)
B - Desmosomes
C - Golgi apparatus
D - Microtubules
E - Mitochondria
F - Nucleolus
G - Occluding junctions (tight junctions)
H - Ribosomes
I - Rough endoplasmic reticulum
J - Smooth endoplasmic reticulum
A - Communicating junctions (gap junctions)
Only one of these choices provides a direct celltocell link between two cells which would allow direct spread of electrical excitation. That is the communicating, or gap, junctions, which consists of aligned pores in the adjacent membranes. Occluding junctions are sites of membrane contact, but do not provide direct communication, and although desmosomes involve contact between cells in the form of proteins inserted across the membrane, this interaction occurs in the extracellular space.
Site where lipids are synthesised
A - Communicating junctions (gap junctions)
B - Desmosomes
C - Golgi apparatus
D - Microtubules
E - Mitochondria
F - Nucleolus
G - Occluding junctions (tight junctions)
H - Ribosomes
I - Rough endoplasmic reticulum
J - Smooth endoplasmic reticulum
J - Smooth endoplasmic reticulum
The principal site of lipid synthesis is the smooth endoplasmic reticulum. Most cells have relatively little of this, however in some cells, for example those producing steroid hormones, it is found in abundance. By contrast, the rough ER is the main site of synthesis for proteins destined for secretion, incorporation into the lumen of organelles, or incorporation into membranes.
An avascular, typically polarised tissue that forms cohesive sheets, covering surfaces and lining cavities
A - Bone
B - Dense irregular connective tissue
C - Dense regular connective tissue
D - Epithelium
E - Glandular tissue
F - Loose connective tissue
G - Nervous tissue
H - Skeletal muscle
I - Smooth muscle
D - Epithelium
This is basically the definition of an epithelium. Most glandular tissue is epithelial in nature, however it would not fit the definition of ‘covering surfaces’ and ‘lining cavities’.
Composed of very long elongated cells with each cell having multiple nuclei
A - Bone
B - Dense irregular connective tissue
C - Dense regular connective tissue
D - Epithelium
E - Glandular tissue
F - Loose connective tissue
G - Nervous tissue
H - Skeletal muscle
I - Smooth muscle
H - Skeletal muscle
Only skeletal muscle fulfils this. Certainly many neurons can be considered very elongated as they have long processes (typically axons), however neurons do not have multiple nuclei per cell.
Composed mainly of packed, extracellular bundles of collagen fibres which are arranged in random directions
A - Bone
B - Dense irregular connective tissue
C - Dense regular connective tissue
D - Epithelium
E - Glandular tissue
F - Loose connective tissue
G - Nervous tissue
H - Skeletal muscle
I - Smooth muscle
B - Dense irregular connective tissue
Only connective tissue consists mainly of extracellular space and indeed fibres, thus we need to consider the different forms of connective tissue listed. The words that are key here are ‘packed’ which indicate a dense connective tissue, rather than a loose one, and ‘random directions’ which defines a dense irregular connective tissue.
These cells appear striated, are branched and have a single nucleus that is located near their centre
A - Astrocytes
B - Cardiac muscle fibres
C - Chondrocytes
D - Mast cells
E - Microglial cells
F - Mucous cells
G - Oligodendrocytes
H - Osteocytes
I - Skeletal muscle fibres
B - Cardiac muscle fibres
If we just consider ‘striated’, there are only two cell types that we have discussed which are striated, skeletal muscle cells and cardiac muscle cells. However only cardiac muscle cells are branched (skeletal muscle cells are long ‘tubelike’ structures which do not branch) and have a single, central nucleus (skeletal muscle cells have many, many nuclei, which are located adjacent to the cell membrane).










