MRCPUK Part 1 Syllabus
MRCPUK Part 1 Syllabus
MRCPUK Part 1 Syllabus
Part 1
Compiled and
edited by the
MRCP(UK)
Syllabus
Part 1
Examining Board
and
Federation of
Royal Colleges of
Physicians of the UK
by the MRCP(UK)
Central Office
1
MRCPUK Part 1 Syllabus
MRCPUK
Part 1
Syllabus
The MRCP (UK) Part 1 Examination for the Membership of the Royal Colleges
of Physicians of the United Kingdom was introduced in October 1968. Since
then there have been major developments in the study of medical education
and the certification of competence worldwide. These developments have
had an impact both on generic and specialist training. The Royal Colleges of
Physicians are committed to the academic development of medical
education and as part of that commitment are publishing a raft of
publications covering various aspects of the MRCP (UK) Examination. The
Syllabus for the MRCP (UK) Part 1 Examination is a key element in the Royal
Colleges' on-going commitment to candidates and their tutors.
This Syllabus covers those areas of knowledge tested in the MRCP (UK) Part 1
Examination. We believe that a thorough knowledge of common and
important disorders is essential and that candidates should also have an
understanding of basic sciences relevant to medical practice so that not only
can physicians in training develop their full clinical and academic potential
but also achieve success in the Examination.
I
The current Examination employs multiple true/false MCQs to test a large
body of core knowledge which is at a level appropriate for this stage in a
young physician's professional development.
Our hope is that this Syllabus will assist candidates and their tutors in
knowing the extent of knowledge required to pass the Examination.
Although each diet will not test every area of knowledge detailed in the
Syllabus, the Examination should be viewed as a representative sample of
the items of knowledge set out in the following pages. The Syllabus should
be used in conjunction with the MRCP (UK) Part 1 Examination papers which
are being published simultaneously.
This Syllabus could not have been produced without the considerable input
of the following past and present members of the MRCP (UK) Part 1
Examining Board, though the Medical Secretary and Chairman of the Board
bear prime responsibility for the edited script:
II
In addition, the comments of Kate Horne and Jim Benson, both of Central
Office, are acknowledged gratefully. Barbara Reeves prepared the
manuscript for press notwithstanding multiple revisions. John Reid of Metro
Press was a constant source of assistance as this series of books on the MRCP
(UK) was produced. Kenneth Cochran and John Thomson generously assisted
with proof reading.
November 1999
III
C ONTENTS
Introduction 1
Entry requirements 1
Purpose and academic aims 2
Content of the Examination 3
Assessment of a candidate's performance 4
Quality of the Examination 4
Syllabus 4
Genetics 5
Cell, molecular and membrane biology 5
Anatomy 6
Physiology, biochemistry and metabolism 6
Immunology 7
Immunology and immunological tests 7
Clinical conditions 7
Management 9
Infectious diseases and tropical medicine 10
Microbiology 10
Immunology of infectious diseases 10
Pathophysiology 10
Epidemiology 10
Treatment 11
Specific infections 11
Statistics, epidemiology and evidence-based medicine 13
Descriptive statistics 13
Graphical techniques 13
Inferential techniques 14
Evidence-based medicine 14
Clinical trials 14
Clinical haematology 15
Iron metabolism 15
Megaloblastic anaemias 15
Haemolytic anaemias 15
Other anaemias 16
Polycythaemia and myeloproliferative disorders 16
White cell disorders 16
Disorders of haemostasis 16
Clinical pharmacology, therapeutics and clinical toxicology 17
Pharmacology 17
Clinical pharmacokinetics 17
V
Monitoring drug therapy 17
Adverse drug reactions 18
Drug interactions 18
Pharmacogenetics 18
Therapeutics for specific patient groups 18
Clinical toxicology 19
Criteria for selecting drugs in a therapeutic class 19
Drug formulations and routes of administration 20
Rheumatology 21
Clinical science 21
Clinical conditions 22
Investigations 23
Management 23
Cardiology 24
Anatomy and physiology 24
Pathophysiology and pathology 24
Cell biology 25
Clinical pharmacology 25
Clinical cardiology 25
Respiratory medicine 27
Anatomy and physiology 27
Pathophysiology and pathology 27
Cell biology and genetics 28
Clinical pharmacology 28
Clinical conditions 28
Neurology 30
Neuroanatomy 30
Neurophysiology 30
Neurogenetics 30
Cell biology 31
Neuropharmacology 31
Neuropathology 31
Clinical neurology 31
Psychiatry 33
Mental state 33
Aetiological factors in psychiatric illness 33
Investigations 33
Syndromes of psychiatric disorder and their treatment 33
VI
Psychiatric aspects of physical disease 34
Mental retardation 34
Gastroenterology 35
Clinical science 35
Clinical nutrition 35
Disorders of the mouth, tongue and salivary glands 36
Disorders of the oesophagus and stomach 36
Functional disorders 36
Disorders of the small intestine 37
Disorders of the liver, biliary tree and pancreas 37
The acute abdomen 38
Inflammatory bowel diseases 38
Colorectal disorders 38
Endocrinology 40
Thyroid 40
Hypothalamus/Pituitary 40
Adrenal 41
Ovary 41
Testis 42
Growth 42
Parathyroid/bone 42
Diabetes mellitus 43
Disorders of lipid metabolism 43
Nephrology 44
Physiology 44
Molecular biology and genetics 44
Glomerular and tubular disorders 44
Infections of the kidney 45
Calculus formation within the urinary tract 45
Acute and chronic renal failure 46
Hypertension and renal problems in pregnancy 46
Drugs and the kidney 46
Renal replacement therapy 46
Dermatology 47
Basic science 47
Clinical dermatology 47
Investigation 48
Drugs and therapy 48
VII
I NTRODUCTION
There are three Royal Colleges of Physicians in the United Kingdom: the Royal
College of Physicians of Edinburgh, the Royal College of Physicians and
Surgeons of Glasgow and the Royal College of Physicians of London. All three
Colleges share a common Membership Examination; Part 1 was introduced in
October 1968. Since January 1971, the Royal College of Physicians of Ireland
has used the MRCP(UK) Part 1 Examination as the first part of its
examination leading to Membership of the Royal College of Physicians of
Ireland. In addition, the School of Postgraduate Medical Studies in Singapore
uses the MRCP(UK) Part 1 Examination paper as Part 1 of its Master of
Medicine (Singapore) degree.
E NTRY REQUIREMENTS
To meet the entry requirements for the Part 1 Examination, you must hold
an acceptable medical qualification. You will not be admitted to the
Examination before the expiry of 18 months from the date of your
graduation. Further details are given in the Regulations.
1
P URPOSE AND ACADEMIC AIMS
It is important that you develop skills and acquire professional habits which
will enable you to keep abreast of current medical knowledge and new
developments. Preparation for the Examination will help you to develop such
skills and professional habits. Hence, reading the medical literature and
attending relevant medical meetings should be a normal part of your
professional life.
2
C ONTENT OF THE EXAMINATION
As a general guide you will wish to know that there are some 14 clinical
science MCQs in the Part 1 Examination and these are made up as follows:
Genetics 1-2
Cell, molecular and membrane biology 2-3
Anatomy 2
Physiology, biochemistry and metabolism 5-6
Immunology 2-3
Statistics, epidemiology and evidence-based medicine 1
3
ASSESSMENT OF A CANDIDATE ’ S PERFORMANCE
Your answer sheet is machine read and it is therefore imperative that you
adhere strictly to the Examination instructions in completing your answer
sheet.
The MRCP(UK) Part 1 Examining Board considers each question prior to its
appearance in the paper and subsequently reviews each question’s
performance. In addition to the final scores obtained by the candidates, the
MRCP(UK) Part 1 Examining Board will also note the mean score for the
Examination and the mean scores for, and the discriminatory power of, the
questions that comprise the paper. A detailed analysis of the responses to
each item (including a separate index of discrimination for every item), and a
coefficient indicating the internal reliability of the Examination as a whole
are also considered by the Board to ensure the quality of the Examination is
maintained.
S YLLABUS
No syllabus can be comprehensive. Hence, this Syllabus is indicative of those
areas of knowledge with which you are expected to be familiar, but is not
intended to be exhaustive or to exclude other items of knowledge which are
of similar relevance. You can expect, however, that the majority of questions
will test knowledge in the broad areas specified.
4
G ENETICS
You should have an understanding of the structure and function of
chromosomes and genes and a knowledge of the principles of inheritance of
chromosomal and genetic disorders.
• Inherited diseases
• Chromosome structure
• Common chromosome abnormalities
5
A NATOMY
Clinically relevant anatomy will be tested, including neuroanatomy.
It is essential that you understand the structure and function of the different
organs which make up the body and how these organs interact, such as
through hormonal and neural influences. You should know the broad
principles of metabolism such as the production of energy and the pathways
of carbohydrate, protein and lipid metabolism, but a detailed knowledge of
the chemical processes in the steps of the metabolic pathways is not
necessary. You should have an understanding of the principles of nutrition,
water, electrolyte and acid-base balance. Knowledge of the physiology and
biochemistry of each organ system is examined under that specialty.
6
I MMUNOLOGY
Although a detailed knowledge of basic immunology and immunological
diseases is not required, you should have a sound working knowledge of the
principles of immunomechanisms.
Clinical conditions
You should be able to answer questions on the various immunodeficiency
syndromes.
7
Examples of question topics might include:
• Mechanisms of immunodeficiency
• Antibody immunodeficiency disorders
• T-cell immunodeficiency disorders
• Combined antibody and cellular immunodeficiency disorders
• Phagocytic dysfunction diseases
• Complement deficiencies
You should know the main clinical characteristics and immediate
management of acute allergic emergencies.
• Anaphylaxis
• Angio-oedema
• Urticaria
You should be familiar with immunology as applied to other medical
diseases.
8
Management
You should be able to answer questions on the principles of
immunosuppressive therapy including major indications and side-effects.
You should know about the principles of immunisation and be familiar with
vaccines currently in use.
9
I NFECTIOUS DISEASES AND TROPICAL MEDICINE
Microbiology
You should understand the major taxonomy of bacteria in terms of
Gram-staining and aerobic/anaerobic metabolism. Virus classification is
not important except for members and characteristics of the herpes group.
Virus replication with reference to retroviruses should be understood. Major
pathogenic protozoa and helminths should be known.
• Opportunistic infections
• Immunisation policy
Pathophysiology
You should have a basic understanding of:
• Septic shock
• ARDS
• Role of cytokines in infection
Epidemiology
You should have knowledge of the principles of epidemiology relevant to
infectious diseases.
10
Examples of question topics might include:
Treatment
You should know the broad indications for, and major adverse effects of,
commonly employed antimicrobial agents.
• B-lactams
• Tetracyclines
• Macrolides
• Aminoglycosides
• Quinolines
• Trimethoprim
• Metronidazole
• Antituberculous drugs
• Antimalarial drugs
• Antiviral agents
Specific infections
Knowledge of the characteristics, recognition, prevention, eradication and
pathological effects of all commonly encountered bacteria, viruses, rickettsia,
fungi, protozoa, parasites and toxins, including an understanding of the
principles of infection control, will be required. Special attention to
differential diagnosis, appropriate investigations and awareness of when
presumptive therapy is indicated is essential.
11
Examples of question topics might include:
• Septicaemia
• Meningitis and encephalitis
• Endocarditis
• Pneumonia (community-acquired, hospital-acquired, lung abscess,
empyema)
• Tuberculosis
• PUO (appropriate investigations, when empirical therapy might be
indicated)
• Soft-tissue infection and osteomyelitis
• Streptococcal infection, rheumatic fever, nephritis
• Intra-abdominal sepsis
• Food-poisoning (especially salmonellosis, campylo-bacter, verocytotoxin
producing E coli)
• Tropical infections (especially malaria, bilharzia, amoebiasis, filariasis,
leishmaniasis, hookworm and viral haemorrhagic fevers)
• Viral hepatitis
• HIV/AIDS (course of typical infection; CD4 count and HIV viral load as
markers of progression; main opportunistic infections including
Pneumocystis pneumonia, CNS toxoplasmosis, cryptococcal meningitis,
tuberculosis)
• Glandular fever syndrome and its differentiation from HIV
seroconversion illness
• Spirochaetosis - syphilis, leptospirosis, borrelia
• Toxic shock syndrome and staphylococcal infections
12
S TATISTICS , EPIDEMIOLOGY AND
EVIDENCE - BASED MEDICINE
You should have a basic understanding of the usage and limitations of the
common statistical tests used in reporting the results of research in clinical
journals. The following lists of terms should give some idea of the range of
terms and techniques which you should understand, all of which can be
found regularly in journals such as The Lancet, British Medical Journal and
New England Journal of Medicine.
You are not expected to have any knowledge of computer packages for
carrying out statistical calculations. You may be expected to carry out simple
calculations that do not require the use of a calculator. You are not expected
to memorise formulae for statistical tests, but should understand their
conceptual basis.
The following lists are not intended to be inclusive but as illustrative of the
type of knowledge that you need to possess.
Descriptive statistics
Examples of question topics might include:
• Histogram
• Box-plot
• Scattergram
13
Inferential techniques
Examples of question topics might include:
• Null hypothesis
• Alternative hypothesis
• Parametric and non-parametric tests
• Normal distribution
• Type 1 and Type 2 errors
• False positive and false negative
• Statistical power
• One and two-tailed tests
• Statistical significance, P value
• T-test
• Mann-Whitney and Wilcoxon test
• Chi-square test for 2 x 2 contingency table
• Correlation (Pearson's and Spearman's)
• Linear regression
• Study design
Evidence-based medicine
You are expected to have an understanding of evidence-based medicine and
an ability to apply this understanding in the management of patients.
Clinical trials
Examples of question topics might include:
14
C LINICAL HAEMATOLOGY
Iron metabolism
You should have an understanding of:
Megaloblastic anaemias
You should understand the physiology of vitamin B12 and folic acid and the
mechanisms and investigation of deficiencies and their management.
• B12 deficiency
• Folate deficiency
Haemolytic anaemias
You should understand:
15
• Molecular pathology of thalassaemia and common
haemoglobinopathies
• Causes of haemolysis
• Diagnosis of haemolytic anaemia
Other anaemias
Examples of question topics might include:
• Physiology of leucocytes
• Leucocytosis and leucopenia
• Acute and chronic leukaemias, including diagnosis, management and
prognosis
• Lymphoproliferative diseases including Hodgkin's disease, non-Hodgkin’s
lymphomas, and plasma cell dyscrasias
Disorders of haemostasis
You should possess knowledge of:
16
C LINICAL PHARMACOLOGY, THERAPEUTICS AND
CLINICAL TOXICOLOGY
You are expected to have a good knowledge and understanding of the
principles of clinical pharmacology, therapeutics and clinical toxicology.
Pharmacology
You should understand the:
Clinical pharmacokinetics
You should understand the principles that underlie:
17
Emphasis will be given to the areas of clinical practice and therapeutics
where the narrow therapeutic range of particular pharmacokinetic
properties of the drug make this approach important.
Drug interactions
You should have an understanding of the epidemiology of adverse drug
interactions, and of the mechanisms by which interactions may occur. You
should also have a knowledge of common drug interactions and their clinical
consequences.
Pharmacogenetics
You should understand the principles of pharmacogenetics and its
importance in determining variations in response to drugs in man, both in
terms of efficacy and toxicity. You should have knowledge of the clinical
consequences of the common pharmacogenetic variations relevant to
clinical practice.
• The elderly
• Pregnancy and breast feeding
• Patients with renal disease
• Patients with hepatic disease
You should understand that the altered physiology in these patient groups
may affect the pharmacokinetics and pharmacodynamics of drugs. You
18
should know the principles underlying drug choice, in pregnancy and breast
feeding, and have an understanding of the teratogenic effects of drugs that
may be used in pregnancy. In the case of renal and hepatic disease it is also
necessary for you to have an understanding of drugs that may produce
toxicity of these organs and whose use is particularly affected by disease of
these organs.
Clinical toxicology
You should understand the principles of management of patients who have
been poisoned with drugs or other toxic substances. This should include
assessment, recognition of common symptom patterns, principles of
removal of toxic substances, and their antidotes where these approaches
may be appropriate.
• Paracetamol poisoning
• Salicylate poisoning
• Tricyclic antidepressant poisoning
• Lithium poisoning
• Iron poisoning
• Digoxin poisoning
• Intoxication due to drugs of abuse
Criteria for selecting drugs in a therapeutic class
You should understand the criteria that may be used to select a drug from
among drugs in a popular therapeutic class. This would include:
19
Drug formulations and routes of administration
You should be aware of the various formulations of medicines available, and
of the routes by which medicines may be administered. You should also
understand the advantages and disadvantages of various routes and
preparations. From this knowledge, you would be expected to be able to
select the most appropriate formulation and route of drug administration in
common clinical scenarios.
20
R HEUMATOLOGY
Detailed knowledge of all the rheumatic conditions is not required. However,
you should have a sound working knowledge of the basic principles of the
common musculoskeletal conditions.
• Inflammatory arthritis
• Back pain
• Periarticular disorders
• Osteoarthritis
• Connective tissue diseases
• Bone diseases
Clinical science
Basic physiology, biochemistry, anatomy and pathology relating to
musculoskeletal disease should be known.
• Physiology of pain
• Physiology of inflammation
• Urate metabolism
• Bone metabolism
• Applied anatomy, particularly of cervical and lumbar nerve roots, and of
peripheral nerves commonly involved in disease
• Rheumatoid arthritis
• Osteoarthritis
• Connective tissue diseases
• Bone diseases
21
Clinical conditions
You should know the relative prevalence and major associations of the
common rheumatological conditions.
• Age
• Gender
• Genetic influences
• Constitutional influences
• Environmental influences
• Occupational influences
You should be able to answer questions on the symptoms and signs of the
rheumatic diseases.
• Sarcoidosis
• Erythema nodosum
• Infections and arthritis (e.g. Parvovirus B 19)
22
Investigations
You should have knowledge of the investigations relevant to the diagnosis
and assessment of rheumatic diseases.
Management
You should be able to answer questions on the management of acute
rheumatological emergencies.
• Septic arthritis
• Osteomyelitis
• Temporal arteritis
• Acute spinal cord compression
You should be able to answer questions on the management of rheumatic
diseases.
23
CARDIOLOGY
• Thrombosis
• Infarction
• Atherogenesis
• Hypertrophy
• Heart failure
• Cardiomyopathies
• Dysrhythmias
• Hypertension
24
Cell biology
You do not need detailed specialised knowledge of cell biology as only topics
of proven clinical relevance will be tested.
• Excitation-contraction process
• Molecular and cellular aspects of hypertrophy of the myocardium and of
vascular smooth muscle
Clinical pharmacology
You should know the indications for drug therapy in cardiac disease and
understand the actions, interactions and side effects of the drugs used. The
emphasis will often be on new drugs or on novel applications or newly
observed side effects of established drugs. Details of drug dosage are asked
only rarely.
Clinical cardiology
You must know the clinical features and management of the cardiac
disorders encountered in hospital practice by the general physician, though
detailed specialist knowledge is not expected. You should have knowledge
of risk factors.
25
Examples of question topics might include:
26
R ESPIRATORY MEDICINE
• Asthma
• Alveolitis
• Tuberculosis
You should possess knowledge of humoral and cellular immunodeficiency
states and sequelae.
27
The microbiology of acute and chronic respiratory infections should be
known.
• Asthma
• Cystic fibrosis
• Alpha 1 antitrypsin deficiency
The role and value of gene therapy should be understood.
Clinical pharmacology
The indications for, and mechanisms of action of, drugs used in respiratory
disease together with their interactions and side effects should be known.
Important respiratory complications of other drugs, e.g., NSAIDs and beta
blockers should also be understood.
Clinical conditions
The clinical features, investigation and management of respiratory disease
likely to be encountered by a general physician must be known.
• Pleural effusion
• Chest pain
• Haemoptysis
• Breathlessness
28
The impact of systemic disease on the respiratory system should be known.
• Vasculitis
• Neuromuscular diseases
• HIV infection
Knowledge of occupational lung disease, particularly asthma,
pneumoconiosis, and asbestos related disease is required.
You should know the indications for, and problems of, lung transplantation.
Exclusions
Knowledge of detailed pulmonary mechanics, oncology drug regimens, drug
therapy of environmental mycobacterial infection, inhalation drug kinetics
and detailed histological descriptions is not required.
29
N EUROLOGY
Neuroanatomy
You are not expected to have detailed knowledge of neuroanatomy.
Questions with an anatomical bias will be confined to circumstances where
an understanding of anatomical structure is of critical importance in
appreciating the localisation of a particular neurological problem.
Neurogenetics
You are expected to have knowledge of recent advances in the
understanding of the genetic basis for various neurological disorders.
30
Cell biology
Questions in this area will relate to advances in the cellular mechanisms of
certain neurological disease processes which have provided better
understanding of disease mechanisms and which might, in the future, lead
to more rational therapy.
• The genesis of tissue damage in stroke and the role of certain excitatory
neurotransmitters
• The role of the dopaminergic system in various extrapyramidal disorders
• The role of other neurotransmitters in certain diseases, for example, in
Alzheimer's disease
Neuropharmacology
You are expected to have some knowledge of new drug developments in
neurology, as well as the established drug therapies.
Clinical neurology
Questions in the field of clinical neurology will test your knowledge of the
more common disorders. There will be emphasis on clinical features which
have been shown to be of diagnostic value. The choice of subject matter will
be influenced by areas of recent advance, particularly those which have
31
either led to better definition of disease entities, or have led to their
improved management.
32
P SYCHIATRY
Mental state
You should understand the conduct and scope of a mental state
examination.
You are expected to be familiar with the features of abnormal mental states
and particularly those that present commonly to physicians and to Accident
and Emergency Departments.
• Genetic factors
• Environmental factors
• Life events
Investigations
You should be familiar with the potential value of, and indications for,
common investigations used in psychiatric illness including:
• Psychometric testing
• EEG
• Brain imaging
Syndromes of psychiatric disorder and their treatment
You should have knowledge of:
33
• Self-harm, attempted suicide, suicide
• Substance misuse (including alcohol dependence)
• Eating disorders
• Obsessive compulsive disorder
• Abnormal illness behaviour
• Syndromes associated with medically explained physical symptoms
(including somatization and somatoform syndrome)
34
G ASTROENTEROLOGY
Clinical science
You should understand the:
• Calorific requirements
• Body water distribution
• Derivation of the body mass index
• Protein calorie malnutrition
35
• Essential dietary constituents
• Vitamin requirements
• Pathogenesis and management of obesity
Disorders of the mouth, tongue and salivary glands
You should have an understanding of:
• Achalasia
• Carcinomas
• Peptic ulceration
• Gastritis
• Gastrointestinal haemorrhage
Examples of question topics might include:
36
Examples of question topics might include:
37
The acute abdomen
You should have knowledge of:
• Crohn's disease
• Ulcerative colitis
• Infective gastroenteritis
• Parasitic and protozoal gut infections
Examples of question topics might include:
Colorectal disorders
You should have knowledge of:
• Polyps
• Carcinomas
• Diverticular disease
• Anorectal disorders
38
Examples of question topics might include:
39
E NDOCRINOLOGY
Although you are not expected to have a detailed knowledge of
biochemistry, it is anticipated that you will have an insight into the
mechanisms of hormone action and the importance of receptors and
substances involved in control of intracellular metabolism. You should have
a knowledge of the clinically relevant anatomical aspects of this specialty.
Thyroid
Since thyroid disease is common you are expected to have a broad
knowledge of the mechanisms of thyroid disease, its clinical presentation
and treatment.
40
Examples of question topics might include:
Adrenal
A detailed knowledge of mechanisms of steroid biosynthesis is not required,
but you are expected to have some knowledge of those parts which are
clinically important.
Ovary
You are expected to be conversant with the physiology of ovarian function
and with the conditions presenting to a physician.
41
Testis
You are not expected to have a detailed knowledge of the urological
investigation of infertility but some concept of relevant investigations and of
the endocrine aspects of testicular function is required.
Growth
Growth is a very important topic in relation to general medicine as well as
endocrinology.
42
• Hyperparathyroidism, both primary and secondary
• The differentiation of primary, secondary and pseudo-hypoparathyroidism
• The prophylaxis and treatment of osteoporosis
• Calcitonin and its role in metabolism
Diabetes mellitus
You are expected to have detailed knowledge of this very common condition.
43
N EPHROLOGY
Physiology
You should have knowledge of:
• Polycystic kidney
• Alport’s syndrome
• Hypophosphataemic rickets
You should have an understanding of inflammatory injury of the kidney
mediated by various cytokines and growth factors.
• Diabetes mellitus
• SLE
• Hypertensive nephrosclerosis
• Vasculitis
• Amyloidosis
44
Knowledge of interstitial nephritis (especially those cases with reversible
aetiology such as drugs , heavy metals and analgesics) is expected.
• Reflux nephropathy
• Prostatic hypertrophy
You should be aware of other infections that could affect the kidney by direct
invasion or by immune-complex deposition.
Examples of question topics might include infection of the urinary tract with:
• Mycobacteria
• HIV
• CMV
• HBV
• HCV
Calculus formation within the urinary tract
You should possess a knowledge of metabolic disorders predisposing to
45
stone formation, their investigation, prevention and treatment.
• Idiopathic hypercalciuria
• Primary hyperparathyroidism
• Cystinuria
• Hyperoxaluria
Acute and chronic renal failure
A knowledge of the management of acute and chronic renal failure and of
the disturbed physiology involved is expected. You should be familiar with
pathophysiological changes and non-dialytic treatment in different stages of
progressive renal failure.
46
D ERMATOLOGY
Basic science
You will be expected to have a working knowledge of the structure and
function of the epidermis and dermis.
Clinical dermatology
Many diseases affecting internal organs will present with skin signs or
symptoms. You are expected to be able to recognise the cutaneous
symptoms and signs of systemic diseases.
• Itch
• Hyperpigmentation
• Generalised erythema
• Loss of hair
• Increased hair growth
• Common patterns of nail dystrophy such as clubbing
• Erythema nodosum
47
• Erythema multiforme
• Purpura
• Ulceration
• Vasculitis
A knowledge of the clinical features of the following skin diseases is
required:
• Psoriasis
• Eczema
• Urticaria
• Superficial fungal infections (dermatophytosis, pityriasis versicolor)
• Common skin cancers such as melanoma
• Vitiligo and alopecia areata
• Pemphigus and pemphigold
• Cutaneous herpes virus infections (herpes simplex, varicella zoster)
• Cutaneous staphylococcal and streptococcal infections
• Leprosy
Investigation
You should know the principles but not details of dermatological
investigation such as patch testing.
48
The publication of this Syllabus for the MRCP (UK) Part 1
pass the Examination. Although each diet will not test every