AssessmentsCoagulation disorders: Pathology review
USMLE® Step 1 style questions USMLE
A 3-week-old boy presents to the emergency department due to worsening vomiting at home. The vomiting began suddenly today, and the patient has been more sleepy than usual. He was born full-term at home to a mother who has a history of epilepsy but is otherwise healthy. The patient has not received any vaccines since the mother is concerned they will increase his risk of developing “behavioral disorders.” Temperature is 37.0°C (98.6°F), pulse is 190/min, respirations are 52/min, and blood pressure is 104/54 mmHg. On physical examination the infant begins seizing with tonic-clonic movements in the upper and lower extremities. He is noted to have a bulging anterior fontanelle and downward displacement of the eyes. No pain is elicited with flexion of the neck. Point of care glucose is 60 mg/dL. Which of the following best describes the etiology of this patient’s clinical presentation?
At the hematology ward, there’s Braden, a 5 year old male, who developed prolonged bleeding after circumcision.
His mother is worried because he has a history of recurrent hemarthrosis after minor falls.
Family history reveals a relative of his mother who suffered from bleeding diathesis.
Now, there’s also a 3 day old preterm baby, called Harlow, who is bleeding severely from the umbilicus.
Her mother states that she did not get the standard care after delivery. CBC, PT and PTT are ordered for both patients.
They both have normal platelet count.
Now, Braden has normal PT but elevated PTT, while Harlow has both PT and PTT elevated.
Both Braden and Harlow are suffering from a hemostasis disorder.
Hemostasis disorders, also known as bleeding disorders, can be broadly divided into three groups.
The second group includes problems with secondary hemostasis, which is making a strong fibrin clot through activation of the intrinsic, extrinsic and common coagulation pathways, and so they’re known as coagulation disorders.
So, let’s look at hemophilia first.
They are a group of inherited bleeding disorders caused by deficiencies in various coagulation factors.
Hemophilia A and B are X-linked recessive disorders so a high yield fact is that they almost exclusively affect males while females are carriers.
A big hint for hemophilia is a family history of a maternal relative with a bleeding disorder.
Hemophilia C on the other hand is an autosomal recessive disorder, meaning it can affect both males and females, leading to a deficiency in factor XI.
Vitamin K acts as a cofactor to an enzyme found in the liver called gamma glutamyl carboxylase, which converts the non-functional forms of coagulation factors II, VII, IX, and X into their functional forms.
So without vitamin K, the loss of factor VII means that the extrinsic pathway won’t function; and without factor IX, the intrinsic pathway won’t function; and without factor X and II, the common pathway won’t function.
So, it’s easy to see that vitamin K deficiency can occur in malabsorption syndromes like cystic fibrosis and celiac disease, or with prolonged use of broad-spectrum antibiotics that kill intestinal microbial flora such as fluoroquinolones and cephalosporins.
That’s why every newborn gets an intramuscular injection of vitamin K.
Whatever the cause, coagulation problems share some common symptoms and these are high yield!
People with these disorders can get large bruises after very minor trauma, and this is called easy bruising.
They also suffer from ecchymoses, which is discoloration caused by bleeding under the skin, deep tissue hematomas, hemarthrosis, which is bleeding inside the joint space, posterior epistaxis, which causes a severe nosebleed, GI bleeding, urinary bleeding, and persistent bleeding after surgical procedures.
The severity of the symptoms depends on the severity of the underlying mutation. Having 5 to 40% of normal factor activity is mild, 1 to 5% is moderate, and less than 1% is severe.
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