Delmar Forum Senior
Topics: 22 Posts: 132
| | 07/07/03 - 02:51 AM  
 
   
 
|   #1 |
:arrow: ABDOMINAL AORTIC ANEURYSM (AAA): About 20% will have a history of aortic aneurysm. ABETALIPOPROTEINAEMIA rare recessive disorder inability to produce LDL chylomicron formation is defective characteristic features to age 2 -steatorrhoea, failure to thrive -low serum lipids, acanthocytosis later childhood -ataxia, intention tremor, nystagmus -athetosis, muscle weakness, dec. reflexes -IQ normal but emotionally labile -some develop retinitis pigmentosa ABNORMAL P WAVES-criteria right atrial abnormality (p pulmonale) >2.6mm tall in an inferior lead left atrial abnormality/hypertrophy >0.12s wide with notch >=0.04s wide ACANTHOSIS NIGRICANS-associations (velvety brown thickness, pigmentation wartiness and tendency to papilloma formation in the axilla, groins +mucocutaneous junctions e.g. angles of mouth) GI malignancy esp. gastric Ca lung Diabetes Mellitus with insulin receptor abnormalities. ACANTHOSIS NIGRICANS: CAUSES: gastrointestinal carcinoma (stomach, pancreas), lymphoma, acromegaly, diabetes mellitus and other endocrinopathies. ACCOMODATION, FAILURE OF PUPIL CONSTRICTION causes -poor technique -Parkinson's disease (+failed convergance) -upper brain stem lesion -diphtheria ACEi INDUCED ANGIOEDEMA Occurs in 0.1-0.2% of patients. 60% occur within the first week of therapy (range: hours -years). Most commonly involves the face. Class phenomenon. Mechanism unknown ? biochemical ?immunological. REFERENCES: 1) Angioedema in relation to treatment with ACEi. BMJ.1992:304(6832):941-946. 2) Angioedema after substituting lisinopril for captopril. Ann. Int. Med. 1992;116(5):426-427. 3) Severe angioedema after long-term use of an ACEi. Ann.Int.Med.1990;112(4):312-313. ACETYLATION-drugs affected by slow acetylators isoniazid-inc. neuropathy,dec. hepatitis,LE hydralazine-LE procainamide-LE phenelzine dapsone acetlyated outside liver. no diff in slow acetylators -some sulphonamides -paraaminobenzoic acid -paraaminosalicylic acid ACHONDROPLASIA autosomal dominant one of the commonest forms of inherited dwarfism physeal dysplasia - thin zone of cartilage cells, diminished columnar arrangement short thick bones spinal length almost always normal features - short limbs, normal trunk, large head, saddle nose, exagerrated lumbar lordosis normal mental and sexual development, spinal problems homozygotes - neonatal death (Harrisons) ACNE ROSACEA (Har 13th 279,293)_ Erythema,telangectasia,pustules affecting the central face. Rare under 30yrs. F>M. May lead to rhinophyma formation. Treatment: Oral tetracycline, topical metronidazole ACOUSTIC NEUROMA: - occuring at the cerebellopontine angle may present with hearing loss (VIII), facial weakness (VII), or an absent corneal reflex (V). The main differential is a meningioma. ACROMEGALY GH excess leads to bony+soft tissue overgrowth_Prevalence = 38/million. Incidence = 3/million/yr (M=F)_AETIOLOGY: 99% pituitary adenoma. 1% ectopic production of GHRH eg bronchial carcinoid tumours._SIGNS: 1) FACE: Coarsening of facial features (100%), enlarged tongue (macroglosia), enlarged lower jaw (prognathism), splaying of the teeth (70%), deep/husky/ resonant voice (laryngeal hypertrophy+ sinus enlargement), frontal bossing, hirsuitism, nasal polyps (15%)._2) EYES: Bitemporal hemianopia, Abnormal fundi ( optic atrophy, papilloedema, angioid streaks, diabetic or hypertensive changes)._3) THYROID: Goiter is common (IGF-I stimulation of thyroid cell growth). 3-7% of patients are hyperthyroid._4) AXILLA: Skin tags (60%), Acanthosis nigricans, oily skin._5) UPPER LIMBS: Proximal myopathy, thickened ulna nerve, carpal tunnel syndrome (50%). Spade like hands with doughy consistence, sweaty (95%). Arthralgia (90%)_6) CARDIAC: Signs of cardiomegaly (90%) and CHF. Hypertension (33%)_7) ABDOMEN: Organomegaly (liver, kidneys, spleen). Inguinal hernias (33%). Colonic polyps (correlate with skin tags). Incresed incidence of bowel cancer._8) TESTICLES: Hypogonadism. (33% impotent)._9) LOWER LIMBS: Proximal myopathy, arthritis (OA, pseudogout), foot drop (peroneal nerve entrapment), heel pad thickening. 10) OTHER ASSOCIATED DISORDERS: Obstructive sleep apnoea in 38% (hypersomnolence), Intracranial aneurysms (< 10%), Glucose intolerance (30-50%), Diabetes (10%). Hyperprolactinaemia (15%), Hypopituitarism (10%), Increased bone density, elevated serum phosphate (50%), hypercalciuria in 50% (predisposes to stones). DIAGNOSIS:_1) X-RAY: Pituitary fossa enlarged in 90-95%. Heel pad thickness > 22mm in 95%._2) FASTING GH LEVELS: Usually elevated (20x normal) but may be normal in up to 10% of cases. GH is secreted in a pulsatile fashion with increased frequency._2) GH LEVEL FOLLOWING GLUCOSE: GH measured 60-120min after 100g glucose . In acromegaly there is failure to suppress GH to < 2ug/l which is the normal response (with acromegaly usually > 10ug/l)._3) SERUM SOMATOMEDIN-C (IGF-1) LEVELS: Increased, also increased in puberty and pregnancy._ TREATMENT: _1) TRANSSPHENOIDAL SURGERY: - The primary therapy curative in 60-70%. 2) RADIATION: - Given post-op if not cured, cures 50% but can take up to 5 yrs. (Defn. of cure = normal GTT) 3) SOMATOSTATIN (octreotide):- Used while awaiting cure from radiotherapy. 80% of cases have a reduction in GH levels , in 50% the reduction is in the cure range (<5ug/l). In 70% the IGF-1 levels return to normal, Tumour shrinkage occurs in 37%, clinical improvement occurs in 70%, Gallstones occur in 20%. _ ACROMEGALY-features osteoporosis inc. renal mass, thickened heel pad inc. depth of frontal sinuses 90% have enlarged sella turcica inc. body hair + hirsuitism in females impotence in males, sweatiness nerve entrapment, rarely sensory polyneuropathy (nerve thickening) somatomedin levels raised in acromegalics prolactin raised in 25% can be caused by carcinoids clinical response to somatostatin paradoxically -TRH causes an inc. in GH -raised glc causes an inc. in GH -dopaminergic drugs cause dec. in GH MEN I ACUTE CORTICAL NECROSIS-causes abruptio placentae eclampsia septic abortion acute pyelonephritis any cause of prolonged + intense ischaemia N.B. rare, 1-2% of all patients with apparent acute tubular necrosis ACUTE DISSEMINATING ENCEPHALOMYELITIS: Monophasic illness which may follow infection (Measles, mumps, influenza, EBV) or vaccination (small pox, rabies). Severity and onset is variable. Motor and/or sensory findings may be present. Cerebellar signs common. Protein and lymphocytes may be raised in the CSF. Recovery may not be complete, particularly in those severely affected. Treatment is with IV methylprednisolone 1g daily for 3 days followed by a 3 week tapering course of prednisone. ACUTE GONOCOCCAL INFECTION - Rx amoxycillin 3g stat + probenecid 1g or Trobicin 2g (M) 4g (F) IM stat give doxycycline 100mg bd for 10 days for simultaneous chlamydia infection complex infection salpingitis/epidydimitis amoxycillin 500mg tds 5-7 days surveillance swabs at 2 and 7 days following Rx (SHC, Hamilton) ACUTE HEPATITIS-drug induced (NB not sex hormones) methyl dopa isoniazid halothane ketoconazole nitrofurantoin phenothiazines-cholestatic hepatitis dantrolene subacute picture -amiodarone -perhexiline -verapamil ACUTE INTERMITTANT PORPHYRIA-drugs main precipitants -barbiturates -sulphonamides -griseofulvin others -phenytoin -dichloralphenazone -meprobamate -glutethamide -imipramine -ergot preperations safe -sedatives other than barbiturates -opiates -penicillin, tetracycline, chloraphenicol -streptomycin -prochlorperazine -digoxin -corticosteroids ACUTE INTERMITTENT PORPHYRIA-features autosomal dominant expressed more in girls most common in Sweden attacks common in late pregnancy + puerperium acute attacks characterised by colicky abdo pain 95%,muscle aches 50% psychological symptoms 50% vomiting80%,constipation75%,diarrhoea10% SIADH, peripheral neuropathy 66% dec. tendon jerks 50% inc. BP+HR, siezures 10% proteinuria 10% many precipitating factors urinary porphobilinogen excretion raised between attacks ACUTE LEUKAEMIA-increased risk with Down's, Kleinfelter's ataxia telangiectasia Fanconi's anaemia Hodgkin's disease
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| smitha Forum Elite
Topics: 53 Posts: 236
| | 07/07/03 - 03:08 AM  
 
   
 
|   #2 |
Thanq delmar..... Good luck to u too.........hope u too r the anxious individual like me & many,waiting for ur step2 to get done...... 
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| werefrenz Forum Newbie
Topics: 0 Posts: 4
| | 07/20/03 - 11:58 AM  
 
   
 
|   #3 |
that was very informative. but shorter posts eg. one for each diagnosis would be better for viewer of the forum. (it will earn you more points too). anyway, good work, mate.
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| Delmar Forum Senior
Topics: 22 Posts: 132
| | 07/23/03 - 03:08 AM  
 
   
 
|   #4 |
as u said, informative and collective together. no need to scatter info just to gain some points LOL, whats the use of those points in the 1st place? do they add to my score hehehheehe we'r here primarly to share buddy not to earn points
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| | 11/29/03 - 10:29 AM  
 
   
 
|   #5 |
sorry but lowered and not elevated glucose causes an increase of groth hormone
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