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Common Symptoms/Complaints in Family Medicine Medicine and Skin Dr Edmond CW Chan Medicine  Dizziness  A 69 yo woman who has no children and her husband has married again 2 years ago and he has migrated to USA. She has 5 years history of NIDDM and HT and now on Diamrion 80mg BD and Natrilix 2.5mg om  She complained severe dizziness for few days. Reviewed the has history, she has repeatedly attended to A&E for dizziness in recent 2 years. What questions will you ask?  Definitioin of dizziness  Vertigo  Posture:  Tinnitus: which ear?  Balance  Severity:  Associated symptoms: N, Vomiting, pallor, sweating chest pain, palpitation, neurological symtoms  Drugs hx  psychosocial Physical examination  Cardiovascular system: BP: supine and erect(S:20;D:10) both arms Pulse: regular or irregular heart murmur, carotid bruit CNS: muscle power and tone, gait eyes movement, Nystagmus cranial nerves V, VIII ( corneal reflex) cerebellar signs  Features of cervical spondolysis  Otoscope: ear wax chronic otitis media  Hearing test: Rinne’s test and Weber’s test  Other systems to look for any primary tumor ( probably brain secondary) Further investigations  CBP  Na, K, H’stix, glucose and HbA1c  Head tilt test: starting from sitting position to hyperextend the neck when lying supine and turned the head to one side Vertigo and nystagmus adaptation  ECG  Caloric test  Others like X-ray, CT brain, MRI, autonomic functional test etc if indicated Differential diagnosis      Vertigo: Benign positional vertigo Vestibular neuronitis (without tinnitus or deafness) Acute labyrinthitis (hearing loss) Meniere’s syndrome (vertigo, tinnitus, sensorineural deafness, recurrent episodes)  Acoustic neuroma  Brain stem migraine  Multiple sclerosis Differential diagnosis          Pseudovertigo: Drugs Anaemia Perimenopausal syndrome Postural hypotension Cardiac arrhythmias Complete partial seizure Brain secondary Psychosocial Vestibular neuronitis  Usually a viral infection of vestibular nerve causing a prolonged attack of vertigo lasting for several days  Can be severe enough for asking admission  Precedes with some URI symptoms (viral infection)  Without tinnitus or hearing loss  Abrupt onset with nausea, vomiting, dizziness and vertigo  May take 6 week or so to subside  Nystagmus present because of involving the vestibular system  DDx: Acute labyrinthitis Tx: Stemetil 1 tab tds or im if severe beware of extra-pyramidal side effects relieved by benadryl diphenhydramine Meniere’s syndrome  Usually over diagnosed  30-50 aged group  Paroxysmal attacks of vertigo, tinnitus, nausea and vomiting, sweating and pallor, sensorineural deafness  Abrupt onset  Lasts 30 mins to several hours  Variable interval between attacks, recurrent episodes  Nystagmus (usually opposite to the affect ear)      Treatment: explanation and advice on stress management Avoid coffee and smoking Low salt diet Drug: cyclizine 50mg tds Betahistine (Serc 8-16mg tds)  Refer to ENT for persistent Meniere’s syndrome for any surgical treatment such as operative decompression of the saccus endolymphaticus or labyrinthectimy Benign positional vertigo  All age group  Recurs periodically for several days  Brief and subsides rapidly (changing position or adaptation)  Not associated with nausea, vomiting or deafness  Treatment: explanation and reassurance avoidance measures Palpitation  A 46 yo woman, single, working as accounting manager, chronic smoker with BMI >28 has history of thyrotoxicosis 20 yrs ago and has been put on Carbimazole but stopped for more than 5 yrs because of normal TFT. She has complained occasional palpitation for recent few months. Previously she has experienced chest discomfort but did not seek for any medical help. What questions will you ask?  For discussion Physical examination  General appearance: Xanthoma/Xanthelasma/arcus senilis BMI Goitre Anxiety/depressed sweating, pallor  CVS: BP pulse: rate, volume and regularity JVP heart murmurs, mid-systolic click carotid bruit Any signs of thyrotoxicosis Any signs of infection Further investigation  For discussion Differential diagnosis  Sinus tachycadia: fever anaemia perimenopausal Thyrotoxicosis Phaeochromocytoma Carcinoid syndrome Porphyria Anxiety/Depression (effort syndrome) Drugs, tea, coffee, alcohol, cigarette smoking  Paroxysmal bradycardia: Sick sinus syndrome heart blocks  Paroxysmal tachycardia: supraventricular (narrow QRS)— Atrial ectopics SVT Atrial flutter Atrial fibrillation Wolff-Parkinson-White syndrome Ventricular (wide QRS)— Ventricular ectopics Ventricular tachycardia Ventricular fibrillation Note: It is important to look for the underlying cause of each arrhythmia and the provoking factors Supraventricular tachycardia:  Rate: 150-220/min  Sudden onset  Passing copious urine after an attack (ANP)  Predisposing factors: thyrotoxicosis, WPW  Treatment: carotid sinus message (no carotid bruit) valsalva maneuver immersion face to water drink a glass of ice water Verapamil/Diltiazem (monitor BP) DC cardioversion (haemodynamically unstable) Wolff-Parkinson-White syndrome  Risk of sudden death  Congenital abnormality with bundle of Kent  Can present with SVT or AF  EPS and radiofrequency ablation of the abnormal pathway Atrial fibrillation  Common causes of AF: IHD Thyrotoxicosis Valvular lesions like ASD, mitral valve disease Alcohol-related heart disease impaired ventricular function Idiopathic AF  Acute or chronic?  Sinus rhythm converted or ventricular rate control ?  Chemically converted or DC cardioversion?  Anticoagulant?  Risks: disease itself and the treatment Chest Pain  A 40 yo man, chronic smoker and social drinker who is working in the construction site. He has history of epigastric pain with PPU and patch repair done 5 years ago. Incidentally AXR found a small radio-opaque asymptomatic gallstone. He complained sudden onset of chest discomfort for few hours during duty and then run to your clinic for medical help.  DDX and immediate treatment? What questions will you ask?  Site: retrosternal, epigastric, superficial  Onset: acute, progressive, crescendo, chronic  Quality: crushing, tight, heavy  Duration: Angina-few mins, Infaration >30mins  Radiation: jaw, shoulders: angina/infarction back: dissecting aneurysm/PPU/acute pancreatitis dermatome: shingles  Aggravating factors: supine– reflux oesopagitis exercise, emotion, large meal, sexual intercourseangina inspiration—acute pericarditis  Relieving factors: rest, TNG —angina/oesophageal spasm leaning forward– acute pericarditis antacid, standing up, belching --GRED  Associated symptoms: SOB, palpitation, headache, fatigue, sweating, ankle swelling, nausea and profound vomiting  Risk factors: smoking, alcohol, occupation, lifestyle, obesity  Family history: lipid, Marfan’s  Medication: TNG, Antacid, OCP  Life events and worries: cardiac neurosis Physical examination  For discussion  General appearance: P/E  CVS:  Chest:  Abd:  Others: Further investigation  For discussion: Differential diagnosis Consider anatomically from the skin to deep inside and the referral pain           Skin infection or inflammation Costochondritis/ Ribs fracture IHD (Angina/MI) Acute pericarditis Dissecting thoracic aorta Pneumothorax Reflux oesophagitis/oesophageal spasm Peptic ulcers Gallstones diseases, pancreatits, shingles Cardiac neurosis/Effort syndrome Pectoris angina  Sudden onset of retrosternal chest pain radiating to the jaw or left shoulder lasting 3-5mins only and relieving by rest and TNG, aggravated by exertion.  Risk factors found  P/E unremarkable  ECG: no change at rest  Further investigation like TMT and echo  TNG and risk factors modification Myocardial infaraction  Sudden onset of restrosternal chest pain at rest lasting more than 15 mins associated with distress and not relieved by TNG  Beware the painless presentation in DM  ECG: ST elevation, T wave inverted and pathological Q-wave  Elevated CE: CK, AST, LDH CK-MB, Troponin I/T  Echo: EF, akinesia, valvular lesions  Medical treatment: Streptokinase Symptoms control: Morphine, nitrates Aspirin Beta-blockers  Risk factors modifications  ? Primary PTCA  CABG  Cardiac rehabilitation Common skin problem in FM  Diagnosis in dermatology mainly based on  Clinical history  Morphology  Distribution  Further investigation Dermatology terms  Macule: skin colour change without elevation  Papule: palpable elevation <5mm  Nodule: palpable mass >5mm  Plaque: palpable plateau-like elevation >2cm  Vesicle: small blister <5mm of clear fluid within or below the epidermis  Bulla: larger vesicle >5mm  Pustule: visible collection of free pus in a blister  Wheal: an area of dermal odema  Crust: dried serum and exudate  Excoriations: lesions caused by scratching that results in loss of the epidermis  Erosion: superficial break in the epidermis not extending into the dermis  Ulcer: extending into the dermis  Lichenification: chronic thickening of the skin with increased skin markings Eczema/Dermatitis  3 hallmarks:  1) pruritus  2) ill defined border of the lesions  3) epidermal elements: Acute, subacute– papules, vesicles, weeping Chronic– lichenification, xerosis, scaling  Endogenous vs exogenous Atopic eczema        Chronic, relapsing, pruritic disorder 10% population, Strong genetic predisposition: Associated with asthma, hay fever, allergic rhinitis Elevated serum IgE in 80% Infantile type: 1-6 months Itchy scaly weeping lesions over the face, trunk, extensor of elbows and knees  Remit between 2-5 yo (50 % by 5 yo) Actopic eczema:  Childhood type :  Lichenification at antecubital, popliteal fossa, nape of neck around adolescence (80% by 10 yo)  Adult type:  Poor prognosis  Bad prognostic factors: strong family hx, onset after 2yo, social & maternal deprivation, discoid type, extensor area, associated with ichthyosis Treatment:  General:  Explanation and reasuurance  Avoid soap or detergents  Avoid irritating woolen clothing  Avoid sudden temperature & humidity change  Removal of common allergens (house dust mite)        Emollients: (use adequately and frequently) Aqueous cream, emulsifying ointment Urea cream (also as humectant) Topical steroids: Avoid potent one Oral antihistamines: piriton, clarityn Topical /systemic antibiotics: aureomycin, fucidin, bactroban, cloxacillin, macrolides, quinolones  Tar onitment or bath Tinea  Common superficial fungal infection  Incidence high in summer  Individual susceptibility  Chronic itchy erythematous scaly lesions with active margin  Cause agents: trichophyton, microsporum, epidermatphyton  Diagnosis: clinical picture, skin scarping, Wood’s lamp (tinea capitis)  Tinea capitis: scalp  Tinea pedis: feet, toe web  Tinea manuum: hand  Tinea unguium: nail  Tinea crutis: groin  Tinea corporis: trunk  Tinea faciale: face  Treatment:  Topical: Imidazole, Allylamine, Whitfield onitment, tolnaftate  Systemic: Griseofulvin Imidazole (ketoconazole, miconazole) Triazole (itraconazole, fluconazole) Allylamine (terbinafine)  Usually use for longer term and beware the LFT
 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                            