Paediatrics videos & books

2022-06-22 18:02:54 62) While working in the emergency department in the winter, you examine a 3-week-old female infant. The baby is accompanied by her mother and father. They report that the baby has been congested for the past 24 hours. The parents have been taking the infant’s temperature rectally and report that it has been normal. The infant was a born at 35 weeks’ gestation and was delivered by caesarian due to preeclampsia. On examination, you see a well-appearing infant with a respiratory rate (RR) of 46 and a heart rate (HR) of 112. The TMs are normal and the lung fields are clear to auscultation. The mother relates that she has had a “cold” for the past few days. The father reports that he smokes, but only outside. As part of your evaluation you perform a nasopharyngeal swab for RSV antigen, which comes back positive. The best course of action for this infant is which of the following? Open / Comment

2022-06-17 11:51:02 Children with tuberous sclerosis (tuberous sclerosis complex, TSC) can develop nasolabial fold angiofibromas (commonly referred to adenoma sebaceum). These can be mistaken for acne in an adolescent and is seen in over 80% of adolescents with TSC. Other cutaneous findings include peri- and subungual fibromas, ash leaf spots (hypomelanocytic macules), and shagreen patches. Skin findings are seen in 75% of cases of tuberous sclerosis. Tuberous sclerosis can also have CNS cortical defects and “tubers,” which may be foci of seizure activity. The “tubers” have a classic periventricular distribution. Mental retardation is very common in varying degrees. Sturge-Weber syndrome (also known as leptomeningeal angiomatosis) is a port wine stain, typically with V1 or V2 distribution, with an underlying leptomeningeal blood vessel dysplasia. These dysplastic vessels will typically result in an underlying cortical atrophy. This cortical atrophy can be a nidus for seizures and can be seen on a CT scan of the head. Neurofibromatosis, type 1 is polymorphous neurocutaneous syndrome. The most common findings are café au lait spots, which may be present at birth and worsen during puberty.Beckwith-Wiedemann syndrome and CHARGE association are discussed further in explanations 44 and 45. Open / Comment

2022-06-16 11:49:59 61) A mildly mentally retarded 9-year-old girl is brought to your office for acne. On examination, she does not actually have acne but has small flesh colored papules along her nasolabial fold. Her past history is significant for having had a first (afebrile)… Open / Comment

2022-06-16 11:49:04 61) A mildly mentally retarded 9-year-old girl is brought to your office for acne. On examination, she does not actually have acne but has small flesh colored papules along her nasolabial fold. Her past history is significant for having had a first (afebrile) seizure last year. The mother reminds you that she has a faint birthmark on her hip that is pale and becomes more prominent in the summer, when the child’s skin tans. Examination of this area reveals a 5-cm oval patch that is hypopigmented. Which condition would she most likely have? Open / Comment

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2022-06-09 12:12:01 HUS is, as the name implies, the combination of a microangiopathic hemolytic anemia and acute renal failure. It is commonly associated with E. coli O157/H7 gastroenteritis. HUS is one of the most common causes of acquired renal failure in children. Open / Comment

2022-06-08 12:11:03 60) A 4-year-old child is brought to your office because of a sudden onset of irritability, weakness, and pallor. The mother tells you that both of her children have been experiencing episodes of vomiting and diarrhea. Your physical examination reveals a blood… Open / Comment

2022-06-08 12:10:01 60) A 4-year-old child is brought to your office because of a sudden onset of irritability, weakness, and pallor. The mother tells you that both of her children have been experiencing episodes of vomiting and diarrhea. Your physical examination reveals a blood pressure of 115/80, dry mucus membranes, petechiae, and diffuse abdominal pain. The following laboratory work is obtained: Urinalysis: microscopic hematuria and proteinuria Blood urea nitrogen (BUN)/creatinine (Cr): 20/1.0 mg/dL Hemoglobin: 7 g/dL Peripheral blood smear: fragmented RBCs Prothrombin time (PT), partial thromboplastin time (PTT): normal Coombs’ test: negative
What is the most likely diagnosis? Open / Comment

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