Differential Diagnosis Flashcards

1
Q

DDx of Enlarged epitrochlear lymph nodes

A
  • Sarcoidosis
  • Rheumatoid arthritis
  • Leprosy
  • Secondary Syphyllis
  • Melanoma
  • Lymphoma
  • HIV
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

DDx of Tall Stature

A
  • Gigantism
  • Ehler’s syndrome
  • Marfan syndrome
  • Klinefelter’s syndrome
  • Acromegaly
  • Familial tall stature
  • Haemocysturia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

CLUBBING

A

Clubbing of fingers is staged according to its severity :
STAGE I - increased sponginess of the nail fold.
STAGE II - obliteration of the angle between the nail and the nail fold.
STAGE III - increased convexity of the nail in both directions longitudinally and transversely. Schamroth’s window test
STAGE IV - Bulbous swelling of the distal end of the finger.
Stage V- hypertrophic osteoarthrophathy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Exophthalmus (Bulging of the eyes)

A

Hyperthyroidism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Clubbing of alimentary canal

A

-malabsorption syndrome,
-cirrhosis of the liver
-hepatoma or hepatocellular carcinoma
-ulcerative colitis causes inflammation or ulcers of the git
-Crohn’s disease refers to form of inflammatory bowel disease that causes inflammation of a part of the git
- abdominal Tuberculosis
-GI lymphomas
-celiac sprue or disease
MCHUC2GA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

DDX of Xanthelasma

A
  • Chronic cholestasis in primary biliary cirrhosis
  • Dyslipidemia
    -hypertriglyceridemia
  • hyperlipidemia
    -paraproteinemia
  • myeloma
  • lymphoid malignancy
    CDH2PML
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Skin, nails and hands in git

A
  • Spider naevi small telangiectatic superficial blood vessels on the chest and face
  • Leukonychia (Chronic liver disease)
    Palmar erythema on the thenar and hypothenar eminences
  • Bruising
  • Dupuytren’s contracture can occur in the absence of liver disease mainly occurs in chronic liver disease
  • Scratch marks particularly in cholestatic liver disease, obstructive jaundice
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Endocrine due to excess oestrogens

A
  • Gynaecomastia
  • Testicular atrophy
  • Loss of axillary and pubic hair
  • painful sex due to lack of vagina lubrication
  • irregular or absent period
  • hot flushes
  • breast tenderness
  • infertility in males
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Other stigmata in git

A
  • Parotid swelling particularly in alcohol
  • Hepatic fetor characteristic sweet smell from the mouth related liver disease smelling breath
  • Hepatic flap a sign of encephalopathy and advanced diseased
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

1) looks Younger than stated age

2) looks Older than stated age

A
1) Hypopituitarism
Endomyocardial fibrosis
Cystic fibrosis
Juvenile Diabetes Mellitus (Type 1)
Sickle cell disease

2) Pituitary rumor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Anarsaca

 Causes
liver failure (cirrhosis)
kidney failure
right-sided heart failure
severe malnutrition, especially in cases of a protein deficiency
allergic reactions
A
  • Skin that will show simple after you press a finger onto it for several seconds
  • skin that looks shiny and stretched
  • swollen face thereby impairing one’s vision since it will be difficult to open the eyes
  • liver is difficult to palpate due to large amount of ascites present but if palpable the liver is enlarged
  • Elevated jugular venous pressure
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Marfan syndrome in relation to CVS
This is a connective tissue disorder
The most common of these problems affects the aorta, the main blood vessel carrying blood from the heart to the rest of the body. Heart valves can also have problems.

A
  • Aortic dilation
  • Dissecting aorta
  • Mitral valve prolapse
  • Aortic regurgitation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

People with Marfan syndrome are tall and thin with long arms, legs, fingers and toes

A

Pain areas: in the back due to dissection aorta
Heart: mitral valve prolapse or murmur, aortic regurgitation
Mouth: abnormally raised roof of the mouth or crowded teeth
Visual: blurred vision or nearsightedness
Chest: bulging chest or sunken chest
Also common: disproportionately long arms and legs, fatigue, flat feet, joint hypermobility syndrome, pneumothorax, scoliosis, small pupil, spider fingers, stretch marks, or tall and slender build

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Risk of heart defects in Turner syndrome which affects only females and is related to a missing or partially missing X chromosome

A

The risk of congenital heart defects such as
bicuspid aortic valves,
aortic coarctation,
septal defect increased.
aortic dissection at a young age is increased, as is the risk of hypertension, ischemic heart disease, and stroke

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

DDx of anemia caused by not having enough Hb and oxygen in you RBC you turn pale

A
Hookworm infestation
Malaria
Lead poisoning 
Systemic lupus erythematous
Thalassemia syndrome: less Hb than normal 
Sickle cell anemia
Unstable haemoglobins
Hypersplenism
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Peripheral cyanosis
CR DMed PC2VS

A
  • Cold exposure
  • Raynaud’s phenomenon: This condition causes small blood vessels to narrow in response to cold or stress, leading to cyanosis primarily in the fingers and toes.
  • DVT
  • medications such as beta blockers
  • Peripheral Artery disease: buildup of plaque in the peripheral arteries can decrease blood flow to the extremities, causing cyanosis.
  • congestive heart failure Although this condition primarily causes central cyanosis due to poor oxygenation of blood in the lungs, it can also lead to peripheral cyanosis, especially if there is accompanying peripheral vasoconstriction or cold exposure.
  • COPD
  • venous insufficiency: Inability of the veins to adequately return blood to the heart can lead to blood pooling in the extremities, resulting in cyanosis.
    Shock
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Temperature and moisture

A

Cold and sweaty-anxiety, ď‚®Cold and dry-raynauds phenomenomen,congestive heart failureď‚®Hot and sweaty-hyperthyroidismď‚®Dry coarse skin-hypothyrodism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

1) Older nodes( tender papules found on the pulp of the finger)
2) Janeway lesions( non tender erythematous macules found on the palm of the hand)

A

1) - Infective endocarditis
- Systemic lupus erythematous
- typhoid fever
- gonococcal infections
- haemolytic anaemia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Glasgow Coma Scale
Talks about the level of consciousness of the individual when he or she gets a traumatic brain injury
Divided into Motor, Vision and Verbal

A
Eye opening scores
See the list below:
4: Spontaneously
3: To verbal command
2: To pain
1: No response

Motor scores

6: Obeys command
5: Localizes pain
4: Flexion withdrawal
3: Flexion abnormal (decorticate)
2: Extension (decerebrate)
1: No response

Verbal Response

  1. Well oriented to time and place and person
  2. Confused conversation
  3. Inappropriate words
  4. Incomprehensible sounds like groans, grunts
  5. Absence of speech
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

DDx of unconsciousness

A

Neurologic ::- Meningitis

  • Encephalitis
  • head trauma
  • stroke
  • epilepsy
  • orthostatic or postural hypertension
  • brain hypoxia
  • tetralogy of fallot
  • endomyocardial fibrosis

Metabolic: - low blood sugar

  • low blood pressure
  • dehydration
  • drug poisoning
  • alcohol intoxication
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

DDx of clubbing cvs

A

~~~
- cyanotic congenital disease:
.Tetralogy of fallot
. Transposition of the great vessels
. Truncus arteriosus
. Tricuspid atresia
. Total anomalous pulmonary venous return
- atrial myxoma
- Infective endocarditis
- endomyocardial fibrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Where will you see wasting

A
  • Dorsal interrossei
  • wasting of the thernar and hypotherna eminences
  • head of the humerus
  • biceps
  • triceps
  • prominent temporalis muscle
  • prominent zygomatic bone
  • prominent intercostal spaces
  • sunken supraclavicular fossa
  • bony pelivic landmark
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

DDx of generalized wasting

A

External
Malignancy via release of cytokines to cause Cachexia
- infection such as TB, HIV
By yourself
- anorexia nervousa
-malabsorption
- liver disease due to not able to absorb nutrients
- chronic kidney disease due to breakdown of protein muscle
- post gastroectomy syndrome
Hormones
- Addison disease decreased production of hormone levels
- thyrotoxicosis since body burns more energy while it is at rest

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

DDx of bilateral Anosmia ( loss of sense of smell)

11

A
- COVID-19
Head
- upper respiratory tract infection
- tumors of ethmoid bone
- head trauma
- subfrontal meningioma
Done by you
- smoking
-old age
Dx
- Parkinson’s disease
- Huntington’s disease: genetic dx in which nerve cell in the brain breakdown over time 
- multiple sclerosis: immune system eats away protective covering of nerves 
- Kallman syndrome delayed puberty
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Unilateral anosmia

2

A
  • subfrontal meningioma

- mucous blocked nostril

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Shortening of the metacarpals of the ring and little finger

A

Pseudohypoparathytoidism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Hyperthyroidism

A
  • agitated individuals

- hot and sweaty palms

28
Q

Hypopiturusm

A
  • seen in individuals who look smallish for their age

- underproduction of melanin

29
Q

Risk factor for obstructive sleep apnea

A
  • obesity
  • to dollar and adenoid enlargement in children
  • male gender
  • middle aged
  • smoking
  • excess alcohol
  • usage of sedating drugs
30
Q

Causes of daytime sleepiness

A
  • obstructive sleep apnea
  • sleep disturbance due to anxiety, depression
  • narcolepsy
  • hypothyroidism
  • medication
31
Q

Nocturnal choking or gasping

A
  • GERD
  • nocturnal asthma
  • heart failure
32
Q

What are the causes of cachexia in the elderly patient

A

-Infection: Tuberculosis, HIV
- uraemia
- Diabetes mellitus
- thyrotoxicosis
- malignancy: phaechromocytoma
- malnutrition
- malabsorption
- post gastroectomy syndrome
- M3T2D

33
Q

Presentation of a young girl with cachexia

A
  • thyrotoxicosis
  • diabetes mellitus
  • malnutrition
  • malabsorption
  • anorexia nervosa
  • Addison’s disease
  • Infectious disease: HIV, tuberculosis
  • phaechromocytoma
  • uremia
    M2A2T2D
34
Q

Addison’s disease also known as adrenal insufficiency

A
  • It is a disorder that occurs when the adrenal glands don’t make enough of certain hormones. These include cortisol, sometimes called the “stress hormone,
  • symptoms are fatigue, muscle weakness, loss of appetite, weight loss, and abdominal pain. Adrenal insufficiency can be caused by autoimmune disease or suddenly stopping steroid medicines used to treat other conditions, among other causes.
  • diagnosis of adrenal insufficiency with blood tests. Other tests, such as computed tomography (CT) scans and magnetic resonance imaging (MRI)
  • treat adrenal insufficiency with medicines that replace the hormones your body isn’t making.
35
Q

If the patient has goiter what will you want to know from the history

A
  • heat or cold intolerance
  • appetite
  • weight loss
36
Q

Tall stature- tall, lean, thin

A

Ddx: Marfan syndrome
The patient is tall, lean and thin. Extremities are long, face is narrow and elongated with arachno-
dactyly (long, elongated fingers

What else will you want to examine
- : I want to examine the eyes (dislocated lens), heart (aortic regurgitation), high-arched palate, arm span and height.

37
Q

Presentation of a tall and obese patient

A
  • I want to see gynaecomastia, testis (atrophy), secondary sex characteritcs
    and voice. This may be a case of Klinefelter’s syndrome
38
Q

Causes of tall stature

A

-Familial, constitutional
- Gigantism (GH produced in excess)
- Marfan syndrome
- Kinelfelter syndrome
- Eunuchoidism (androgen deficiency- an abnormal condition in males, characterized by lack of fully developed reproductive organs and the manifestation of certain female sex characteristics, as high voice or lack of facial and body hair, resulting from the absence of a normal production of male sex hormones.)
- homocystinuria

39
Q

Causes of short stature

A
  • Familial or constitutional
  • Genetic such as Down syndrome, Turner’s syndrome, Chstic fibrosis, Achondroplasia
  • Endocrine such as Cretinism, juvenile hypothyroidism, hypopituitarism
  • Any chronic disease from childhood such as renal, cardiac, nutritional
40
Q

Causes of pallor

A
  • Anaemia (commonest) from G6PD, SCD, malnutrition
    -hypovolemia
  • shock
  • hypoxia in conditions such as copd, emphysema or living at high altitude. This is a condition in which the body or a region of the body is deprived of adequate oxygen supply.
  • cold exposure causes vasoconstriction
  • vasovagal response
  • ## certain medications such as beta blockers
41
Q

Causes of carotenemia

A
  • Excess intake of carotene contains foods ( carrot, mango, tomato)
  • hypothyroidism (due to impaired metabolism of carotene by the liver)
42
Q

Jaundice basic info

A
  • It is a clinical condition characterized by yellow discolouration of skin and mucous membrane
    due to excess bilirubin in the blood. Clinically, jaundice is seen when serum bilirubin is .3 mg/dL. If it is ,2.5 mg/dL, called subclinical (or anicteric hepatitis). Jaundice should be seen in natural daylight. Bilirubin has strong affinity for elastic tissue, sclera contains plenty of elastic tissue (also in the skin). So, it is seen in sclera.
  • three types of jaundice:
    . Prehepatic phase: predominately unconjugated hyperbilirubinemia
    . Hepatic phase: both unconjugated hyperbilirubinemia and conjugated hyperbilirubinemia
    . Posthepatic or obstructive jaundice: predominately conjugated hyperbilirubinemia
43
Q

Causes of jaundice

A

Prehepatic jaundice:
- excess production of bilirubin due to excess breakdown of RBC ( haemolytic anaemia)
- reduced hepatic uptake of bilirubin or impaired conjugation:
. Gilbert syndrome there is a mild reduction of UDP glucuronyltransferase enzyme thereby preventing unconjugated bilirubin from being converted to conjugated bilirubin. Predisposing factor stress but has a good prognosis
. Criggler Najjar syndrome: absent UGT enzyme hence highhhh unconjugated bilirubin
. Drugs such as sulphonamides, rifampicin, penicillin
. Physiological jaundice of bewborn

Hepatic jaundice:

Viral hepatitis due to A, B, C, D, E, other virus such as EBV, CMV, Yellow fever, dengue,
2. Drugs—Antitubercular drugs (rifampicin, pyrazinamide, INH), Phenothiazines
(chlorpromazine, haloperidol), Cyclosporine, Alcohol.
3. Metabolic—Wilson’s disease, haemochromatosis.
4. Autoimmune hepatitis.
5. Inherited disorders (Dubin–Johnson syndrome, Rotor syndrome).
Dubin* Johnson :unexcretable bilirubin in the liver hence high conjugated bilirubin. Hence, causes a dark liver
Rotor: mild bilirubinexcretion so not as serious as Dubin*

Post hepatic or obstructive jaundice:

Extrahepatic:
• Choledocholithiasis.
• Carcinoma of head of pancreas.
• Cholangiocarcinoma.
• Periampullary carcinoma.
• Extrahepatic biliary atresia.
• Round worm in common bile duct.
• Biliary stricture (due to trauma, sclerosing cholangitis).
2. Intrahepatic:
• Primary biliary cirrhosis (PBC).
• Primary sclerosing cholangitis.
• Viral hepatitis (causes transient intrahepatic cholestasis).

44
Q

Values for conjugated and unconjugated bilirubin

A
  • Conjugated bilirubin: 0-0.4 mg/ dl
  • Unconjugated bilirubin: 0.2-1.2 mg/dl
45
Q

What are the types of congenital non-haemolytic hyperbilirubinaemia?

A
  • Gilbert’s syndrome (unconjugated)
  • Crigler Najarr Syndrome (unconjugated)
  • Dubin- Johnson syndrome (conjugated)
  • Rotor’s syndrome (conjugated)
46
Q

History taking in a patient presenting with jaundice

A

Hepatitis:
- anorexia, nausea, vomiting (indicates viral or drug induced hepatitis)
- History of contact with jaundiced patient or sexual exposure.
• History of injection, infusion or blood transfusion, I/V drug abuse, tattooing or surgery
(HBV or HCV).
• History of travelling abroad (hepatitis B).
- history of alcohol or any drugs
Other causes:
- Colour of the stool (yellowish, pale, dark), itching indicates obstructive jaundice.
• Family history of jaundice, consanguinity of marriage among parents, associated with pallor
(indicates hereditary haemolytic anaemia, in prehepatic jaundice).
Associated history of high fever, urinary complain (indicates leptospirosis).
• Recurrent jaundice associated with any neurological abnormality (indicates Wilson’s
disease).
• Associated abdominal pain and fluctuating jaundice (indicates bile duct stricture or stone).

47
Q

What are the common features of different types of jaundice? How to investigate?

A

Features of prehepatic jaundice—
• Usually in hereditary haemolytic anaemia. There is triad of anaemia, jaundice and splenomegaly. Other features—frontal and parietal bossing, mongoloid facies, gnathopathy
• Other features are according to the causes of haemolytic anaemia—malaria, autoimmune haemolytic anaemia

Features of hepatocellular jaundice—
• Anorexia, nausea, vomiting, weakness.
• Stool is yellow (but may be dark or clay coloured in later stage due to intrahepatic cholestasis).
• Liver is enlarged and tender.
Features of obstructive jaundice—Dark stools
• Itching of whole body.
• May be abdominal pain, mass in the epigastrium.
• Other features depend upon cause (xanthelasma or xanthoma in PBC).
• Bleeding tendency (due to deficiency of Vitamin K, resulting in deficiency in Vitamin K dependent
clotting factors— II, VII, IX, X).
• Bone pain (due to osteomalacia).

Investigations in jaundice:
1. Liver function tests such as serum bilirubin, SGPT, SGOT, alkaline phosphatase, prothrombin time.
2. USG of hepatobiliary system.
3. Viral markers:
• For A—anti-HAV IgM.
• For E—anti-HEV IgM.
• For B—HBsAg, HBeAg, anti-HBc.
• For C—anti-HCV.
4. Other investigation should be done according to the suspicion of cause. Such as:
• For haemolytic anaemia—Hb electrophoresis
• In obstructive jaundice—ERCP, MRCP.
• CT scan of whole abdomen.
Treatment:
1. General measures: See in the respective chapters. 2. Specific: According to the cause.

48
Q

Causes of fluctuating jaundice

A

Prehepatic:
Haemolytic jaundice.
• Wilson disease.
• Gilbert’s syndrome.

Posthepatic:
Choledocholithiasis.
• Choledochal cyst.
• Sometimes in primary sclerosing cholangitis.
Benign recurrent intrahepatic cholestasis (BRIC).
• Recurrent pancreatitis.

49
Q

Causes of progressive jaundice

A

Hepatic: Acute viral hepatitis
Post hepatic:
• Carcinoma of the head of the pancreas.
• Cholangiocarcinoma.
• Primary biliary cirrhosis.
• Primary sclerosing cholangitis.

50
Q

Causes of recurrent jaundice

A

Congenital hyperbilirubinaemia (e.g., Gilbert syndrome).
• Recurrent benign cholestasis.

51
Q

Causes of palpable gall bladder with jaundice

A

Carcinoma of head of pancreas.
• Carcinoma of ampulla of Vater.
• Stone in common bile duct.
• Pressure from outside on bile duct (lymphoma and secondaries).
• Cholangiocarcinoma.
• Sclerosing cholangitis.

52
Q

Causes of palpable gallbladder without jaundice

A

Mucocoele.
• Empyema.
• Occasionally, carcinoma of the gall bladder.

53
Q

Causes of painless progressive jaundice without gall bladder enlargement

A

Carcinoma of head of the pancreas.

54
Q

Causes of jaundice with itching

A

Obstructive jaundice
• Primary biliary cirrhosis.

55
Q

Causes of abdominal pain with fluctuating jaundice:

A

• Stone in CBD or stricture.
• Pancreatitis.

56
Q

Differential diagnosis of proximal muscle weakness

A
  • thyrotoxicosis
  • Cushing’s syndrome
57
Q

Malar rash

A
  • mitral disease
58
Q

Butterfly rash

A

Systemic lupus erythematous

59
Q

Subcutaneous nodules

A
  • rheumatoid
  • neurofibromatosis
60
Q

Subcutaneous nodules

A
  • neurofibromatosis
  • rheumatoid
61
Q

Yellow skin

A
  • jaundice
  • carotinemia
  • pernicious anaemia
  • uraemia
62
Q

Ddx of cyanosis

A

Lung: inadequate oxygen transfer eg if there is a luminal obstruction- asthma, copd, pneumonia, PE, pulmonary oedema. Corrected by increasing oxygen levels
Congenital heart diseases: truncus arteriosus, tricuspid atresia, tetralogy of Fallot, total anomalous pulmonary venous return, VSD with Eisenmenger syndrome
Methaemoglobinemia RX: oxygen therapy, Vit C

63
Q

Iron deficiency anaemia stigmata

A
  • koilynychia
  • stomatitis
64
Q

Haemolytic anaemia

A

Anaemia with jaundice, shortness of breath, dark urine, rapid heart rate

Under normal circumstances, red blood cells live for about 120 days in the bloodstream. In hemolytic anemia, however, these cells are removed or destroyed in the bloodstream, the liver, or the spleen more quickly than the bone marrow can replace them.
2 types intrinsic hemolytic anaemia: sickle cell anaemia, thalassemia, spherocytosis, G6PD
Extrinsic hemolytic anaemia: These occur when the body’s immune system mistakenly destroys normal red blood cells. Examples include autoimmune hemolytic anemia and drug-induced hemolytic anemia, infection related hemolytic anaemia

65
Q

Drugs that can cause G6PD

A
  • camphor balls
  • anti malarial drugs: primaquine, chloroquine
  • sulfa drugs: sulfamethoxazole
  • dapsone
  • nitrofurantoin
  • quinidine and quinine
    Methylene blue RX for methaemoglobinemia
66
Q

Psychological Ddx of chest pain

A
  • painc disorder: dull constricting ache with SOB, lightheadedness, recent unusual stress, recurrent episodes in healthy people