Sunday 10 December 2017

DERMATOLOGY SPOTTER





Q. What is the diagnosis?( Clue: Xlinked dominant disease)
1) Becker disease
2) Incontinenta Pigmenti
3) Ichthyosis
4) Pemphigus vulgaris








Ans: 2) Incontinenta Pigmenti.

Incontinentia pigmenti is a complex developmental syndrome due to an X-linked dominant
trait that is usually lethal in males; 95% of cases are females.Vesicular, verrucous, and pigmented
skin lesions are usually seen.


Q). 34 years old female after sun exposure, what is the diagnosis?
1) Acne
2) Solar eczema
3) polymorphic light eruption
4) SLE







Ans: 3) Polymorphic light eruption.                                                                                                            
 This is a common intermittent skin reaction to UV exposure, which may represent a delayed type
hypersensitivity response to UV-induced cutaneous antigens. PLE presents with
an itchy, non-scarring, symmetrical papular rash
on light-exposed sites  within hours or days of significant sun exposure in young female usually below 30 years of age.
Large and small papules, papulopustules, and vesicles can occur. The eruption is transient, and resolves within several days, but it may persist if exposure continues.
Cutaneous lupus should be considered as differential diagnosis, and a minority of patients with PLE may subsequently develop lupus after several years .


Q). Skin eruption in a 26 year old male after scarlet fever.what is the diagnosis?
1) TSS
2)SSSS
3) Septic shock
4) Lyells syndrome





Ans: 1) TSS.


Scarlet fever (scarlatina) is an acute infection with a toxin-producing strain of Streptococcus pyogenes. Complications caused by the toxin or bacterial invasion include meningitis,
osteomyelitis, rheumatic fever, and glomerulonephritis

Saturday 8 July 2017

HAEMATOLOGY






Q. A 23-year-old woman is hospitalised with severe anorexia nervosa. Her FBC shows WBC 3.5 × 109/l, neutrophil count 1.1 × 109/l, Hb 100 g/l, MCV 104 fl and platelet count 70 × 109/l. Blood film shows occasional acanthocytes. Neutrophils show normal segmentation. Her prothrombin time (PT) is slightly increased.The most likely diagnosis is:
a Aplastic anaemia
b Folic acid deficiency
c Haematological features of anorexia nervosa
d Hepatic steatosis
e Vitamin B12 deficiency

Ans: c. Haematological features of anorexia nervosa.
The haematological abnormalities are all attributable to anorexia nervosa per se and can be related to bone marrow hypocellularity and gelatinous transformation




Q. A 23-year-old African man who presents with an epileptiform convulsion and fever is found to have a microangiopathic haemolytic anaemia, thrombocytopenia and acute kidney injury. The micro-organism you would test for is:
a Escherichia coli O104:H4
b Escherichia coli O157:H7
c Hepatitis B
d Human herpesvirus 8
e Human immunodeficiency virus
  
Ans: e.Human immunodeficiency virus.
Escherichia coli O157:H7 is the usual cause of haemolytic uraemic syndrome while Escherichia coli O104:H4 was responsible for a German outbreak of this syndrome in 2011. However this patient has features suggesting a diagnosis of thrombotic thrombocytopenic purpura (TTP).1,2 It is important that all patients presenting with TTP are tested for human
immunodeficiency virus (HIV) since TTP may be the presenting feature of HIV infection. Some patients with HIV infection and TTP have a low ADAMTS13 and an ADAMTS13 antibody whereas others do not have an ADAMTS13 deficiency. Those who are deficient require plasma exchange as well as highly active anti-retroviral therapy.


Q. An 18-year-old medical student is permitted to perform an unsupervised venepuncture on a febrile Indian patient and suffers a needle prick injury. He is anxious that he may have contracted human immunodeficiency virus (HIV) infection. Assuming that the patient is infected, transmission is most likely for:
a Dengue fever
b Hepatitis B
c Hepatitis C
d Human immunodeficiency virus (HIV)
e Leishmaniasis

Ans: . b Hepatitis B.
The infection most readily transmitted by needle prick injury is hepatitis B with reported transmission rates of 7−30%, followed by hepatitis C (reported rates 0−7%) then HIV (about 0.5%). Occasional examples of transmission of dengue fever have been reported.


Q. A 33-year-old woman with systemic lupus erythematosus who has developed livedo reticularis suffers an unprovoked deep vein thrombosisin her left leg. Her coagulation screen shows a PT of 16 s (12–14) and an APTT of 40 s (26–33.5). The test most strongly indicative of your suspected diagnosis would be?
a Anti-β2 glycoprotein 1 antibodies
b Antibodies to the phosphatidylserine–prothrombin complex
c Anti-cardiolipin antibodies
d Anti-prothrombin antibodies
e Lupus anticoagulant


Ans: e Lupus anticoagulant.
The clinical picture suggests the antiphospholipid syndrome. Livedo reticularisand venous thrombosis are among the more common features of this syndrome. Guidelines for diagnosis include, as laboratory criteria, the presence of anti-β2 glycoprotein 1 antibodies, anti-cardiolipin antibodies or the lupus anticoagulant, in each case the abnormality to be
demonstrated on at least two occasions, 12 weeks apart.1 Of these abnormalities, the lupus anticoagulant is the one that most strongly correlates with thrombosis and with fetal loss.

IMAGE DIAGNOSIS

Q). What is the diagnosis?


 





Ans: Psoriasis.



 Q.) What is the diagnosis?(Clue: Target Lesion)
 


Ans: Erythema Multiforme.
Q). What is the diagnosis?

 



Ans: Mongolion Spot.


Q.) What is the diagnosis?





Ans: Necrobiosis lipoidica diabeticorum.