Friday, January 3, 2020

Meckel's diverticulum

 

Meckel's diverticulum

Meckel diverticulum is the most common congenital anomaly of the GI tract and is caused by the incomplete obliteration of the omphalomesenteric duct during the 7th wk of gestation.

Meckel diverticulum has been conveniently referred to by the “rule of 2s,”:

  • Occurs in 2% of the population.
  • Appears within 2 feet (50-75 cm) of the ileocecal valve.
  • approximately 2 inches in length
  • Approximately 2% to 4% of patients develop complications over the course of their lives.
  • Typically presents before age 2 years.
  • Two-thirds of patients with MD have 2 types of heterotopic mucosa (gastric and pancreatic), although colonic heterotopic mucosa has also been reported.
  •  Is twice as likely to be symptomatic in boys than girls

Meckel diverticulum is typically lined by ileal mucosa.

Clinical presentations:

The majority are asymptomatic.

It is often found incidentally on imaging studies.

Hematochezia:

  • Cause of bleeding is ectopic gastric mucosa (acid-secreting mucosa)
  • Intermittent painless rectal bleeding (hematochezia) occurs suddenly and tends to be massive in younger patients.
  • Bleeding occurs without prior warning and usually spontaneously subsides.
  • The color of the stool is typically described as brick colored or currant jelly colored.
  • Bleeding can cause significant anemia but is usually self-limited (resolves without intervention) because of contraction of the splanchnic vessels, as patients become hypovolemic.
  • Bleeding from a Meckel diverticulum can also be less dramatic, with melanotic stools.

It should be suspected in children with recurrent or atypical intussusception, a patient with symptoms of appendicitis after their appendix has been removed, and patients with an unclear source of GI bleeding.

Tuesday, January 1, 2019

Periumbilical necrotizing fasciitis in the newborn

 Periumbilical necrotizing fasciitis in the newborn

Neonatal necrotizing fasciitis is a rare complication of omphalitis.

Necrotizing fasciitis starts initially as periumbilical cellulitis and rapidly spreads to the subcutaneous tissues, with the overlying skin appearing edematous with purplish blue discoloration.

Necrotizing fasciitis may also present with bullae, crepitus and peau d’orange appearance.

Necrotizing fasciitis should be recognized early and treated aggressively by debridement, broad-spectrum antibiotics, and supportive care.

In addition to debridement of the involved abdominal wall, it is important to resect the umbilical vein, both umbilical arteries, and any urachal remnant that is present, as these may be involved in the necrotizing infection (even if they look normal).

Reported mortality rates are as high as 60 to 85 percent.

References:

  1. Cilley R. Disorders of the umbilicus. In: Pediatric Surgery, Grosfeld J, O'Neill J, Coran A, Fonkalsrud E (Eds), Mosby Inc., Philadelphia 2006.
  2. Pomeranz A. Anomalies, abnormalities, and care of the umbilicus. Pediatr Clin North Am 2004; 51:819.

 

Thursday, January 18, 2018

Refeeding Syndrome

Refeeding Syndrome

Refeeding syndrome occurs in response to reintroduction of nutrition (whether enterally or parenterally) in the malnourished patient.

Rapid electrolyte and fluid Intracellular shifts in response to the surge of insulin brought on by the presence of nutrients which can lead to numerous medical complications and may progress to life-threatening outcomes, including Coma heart failure, and sudden death.

The hallmark biochemical feature of refeeding syndrome is hypophosphatemia. However, the syndrome is complex and may also feature abnormal sodium and fluid balance; changes in glucose, protein, and fat metabolism; thiamine deficiency; hypokalaemia; and hypomagnesaemia.

Pathogenesis (Howdoes refeeding syndrome develop?) 

Clinical Signs and Symptoms of Refeeding Syndrome

Patient populations at risk for refeeding syndrome  

Prevention and management of refeeding syndrome