In chronic obstructive pulmonary disease, there is increased risk ofrespiratory
tract infection with all of the following pathogens, except: Strep/ pneumonia
H. influenza
Atypical mycobacteria
Moraxxela cataralis
Legionella pneumonia
Actions of PTH include all of the following,except: Increase bone resoption
Increase net acid excretion
Increased calcium absorption from GI tract
Increased calcium reabsorption in the kidney
Increased phosphate excretion
effect of serum osmolarity of a patient with the following labs: Na+ 125 mmol/l, glucose
108 mg/dL and BUN of 140 mg/dL is: Serum osmolarity= 2 x[Na+] + Glucose/18 + Urea/2.8 = 2x15+108/18+140/2.8= 250+ 6 + 50 = 306
Actions of PTH include all of the following,except: Increase bone resoption
Increase net acid excretion
Increased calcium absorption from GI tract
Increased calcium reabsorption in the kidney
Increased phosphate excretion
Answer: C (this is a function of vitamin D). So, PTH acts indirectly to increase calcium absorption from GI tract by increasing the synthesis of vitamin D.
The effect of serum osmolarity of a patient with the following labs: Na+ 125mmol/l, glucose 108 mg/dL and BUN of 140 mg/dLis:
Serum osmolarity= 2 x[Na+] + Glucose/18 + Urea/2.8 = 2x15+108/18+140/2.8= 250+ 6 + 50 = 306
Syndrome of inappropriate ADH secretion is characterized by all of the following, except: Urine osmolarity more than 100
Hypoosmolarity of the serum
Urine Na+ more than 40
Normovolemia and hyperuricemia
All of the following factors increase distal tubular secretion of K+, except: Increased serum K+.
All of the following electrolyte and acid-base disturbances may be seen in a patient with diabetic ketoacidosis upon presentation,except: Hyponatremia
Normal anion gap metabolic acidosis
Hyperkalemia
Hyperphosphatemia
Increased urea
Answer: B (DKA causes high anion gap metabolic acidosis)
All of the following are causes of high turnover bone disease in chronicrenal failure,except: Aluminum toxicity
Decreased vitamin D hydroxylation
Metabolic acidosis
Hyperpohsphatemia
Increased parathyroid hormones
All of the following are true about chronic myeloid leukemia (CML),except: It is a disease of middle aged which could present with constitutional symptoms
The laboratory finding usually show leukocytosis, with left shift and high leucocyte alkaline phosphatase.
It is characterized by specific transloation between chromsomes 9, 22 (Philadelphia chromosome)
Possible treatment for CML include; imtinib ??? and allogenic BMT
CML could transfer to AML or ALL Answer: B (low Luecocyte alkaline phosphatase).
All of the following are true about myeloproliferative disorders,except: In polycythemia vera, the serum erythropoietin level is high.
In essential thrombocytosis, the bone marrow biospy usually show hypercellular marrow with increased megakaryocytes
Massive splenomegaly in CML and myelofibrosis
The adrenal glands, one iscorrect: The zona reticularis is the most important area in the cortex during embryogenesis
There is no relation between the adrenal cortex and the adrenal medullar regarding catecholamine synthesis Wrong! Cortisol increases catecholamine sysnthesis.
Phechromocytoma is associated with high blood pressure and hyperkalemia
Atrophy of the glnads is a late sign of autoimmune adrenalitisi
Zona fasiculata is the place for adrenal androgen synthesis
In Cushing syndrome, one iscorrect: Significant hypokealima is associated with Cushign diseas
Loss of diurnal variation of serum cortiosol is found in cushing syndrome
Proimal myopathy is a rare feature of Cushing syndrome
Glucose intolerance in Cushing syndrome is related to suppression of insulin release
In Addison disease, one iscorrect: Hyperpigmention of the gums and skin is secondary to the increased release of prolactin hormone…
Postural dizziness is a common feature in the history of a paitient with Addison disease
Normokaleima is the rule unlcess there is recurrent vomiting
The ACTH level is normal in the later stage of disease
Hemorrhage into the adrenals is the most common cause Ans: B???
Extra info: Schmitdt syndrome: Primary adrenal insufficiency + Hypothryoidism (and often type 1 DM).
A 17 year old pregnant lady was referred for evaluation of anemia. As a child, she was hospitalized with pneumonia and visited ER twice with abdominal pain. Two years ago, she was found anemia and iron was recommended, but intermittently taken. The examination was unremarkable except for a palpable spleen tip. The Hb was 10 with ferritin 105 and saturation 18%. The peripheral smear revealed slight hypochrmoasiaand target cells, but no sickle forms. Hb electrophoresis results were HbA 26%, HbF 5%, and HbS 69%. Which of the following is the most likelydiagnosis: ?
?
?
?
?
Answer: B? B-Thalassemia minor + Sickle cell trait
A 65-year-old man with progressive pancytopenia is referred for evaluation. On examination, there is splenomegaly. Bone marrow aspirate demonstrated no dysplasia but decreased cellularity. Which diagnosis is mostlikely: Aplastic anemia