What is DRESS Syndrome?

DRESS (drug reaction with eosinophilia and systemic symptoms) is a poorly understood syndrome that has an unknown prevalence in the pediatric population because it is often missed by doctors. 

Symptoms include fever, an itchy rash covering over half the body, enlarged lymph nodes, and inflammation of the liver. A blood test reveals increased white blood cells, "atypical lymphocytes" (abnormally large and irregular lymphocytes because they are infected with the virus), and elevated eosinophils. 

What causes it? There have been links to both herpesvirus (including oral and genital herpes, epstein barr virus and roseola virus) and a couple months after starting certain anti-seizure medications. Bad cases will involve >90% of the skin and affect multiple organs such as the kidneys, and there may be involvement of the mucosal lining of the mouth and lips which can mimic life threatening drug and infectious reactions known as Stevens Johnson Syndrome and Toxic Epidermal Necrolysis.

It is very difficult to avoid getting this syndrome, as it is unknown why some patients get it and others do not. It can take months to fully recover from DRESS syndrome. The treatment, if caused by a medication, is to stop that medication. Most patients get IV or topical steroids to calm the immune system. 

Most often, pediatric rashes are harmless. In rare cases such as this, however, some detective work is required to make a swift and proper diagnosis.

Death From Simple Infections: Disorders of Neutrophils

White blood cells (WBC) are made in our bone marrow and are absolutely imperative to fight infection. Without WBCs, we would succumb to even the most benign viruses and bacteria (i.e. germs) in our environment and die at a very early age. Once WBCs are made, they are released into the blood to mix with the RBCs (cells that carry oxygen) and circulate around our body. Stem cells in the bone marrow give rise to multiple WBC types, namely lymphocytes (T cells and B cells), neutrophils, basophils, eosinophils, and monocytes. Each type of WBC has a specific function. Eosinophils, for example, are important when fighting parasitic infectious. Many people are familiar with the Human Immunodeficiency virus (HIV), a disorder of T cells which impairs the body's ability to fight life-threatening bacterial and fungal infections. Neutrophils play a major function in our first line of defense against bacteria and fungi, and problems with them can carry grave consequences.

Neutrophils are typically first to the scene of an infection or traumatic injury. They are very quick, and their lifespan is only a few days. They follow chemical trails left behind by inflammation and, when they arrive, they suck bacteria into the center of their cell where some sanitizing then takes place- trapped bacteria are basically bathed in hydrogen peroxide. Two things can go wrong in this fight against the bacteria: either the neutrophils fail to work correctly, or the numbers of neutrophils are far too low to overpower invaders. Mildly low levels lead to oral/vaginal/rectal ulcers, ear infections, and skin abscesses. Severely low levels lead to overwhelming infection and death.

Disorders of the FUNCTION of neutrophils:
Congenital Leukocyte Adhesion Deficiency 1. Neutrophil movement is affected, so they are slow and fail to arrive to the scene of the infection. Newborn infants have delayed separation of their umbilical cord or infection where the cord meets the belly (omphalitis)

Chronic Granulomatous Disease. The release of the hydrogen peroxide inside the cell ("respiratory burst") doesn't work properly. Children need lifetime antibiotics (bactrim)

Hyperimmunoglobulin E Syndrome. The neutrophils don't follow the chemical trail to the site of infection like they are supposed to. Levels of an immune globulin called IgE are very high, and children have recurrent "cold" (non-red, non-tender) staph abscesses.

Chediak-Higashi Syndrome. There is a problem bringing the bacteria into the cell to sanitize them. Children also have albinism and their condition is worsened by infection with Epstein-Barr virus (EBV)


Disorders of the NUMBER of neutrophils:
External factors. Neutropenia caused by viruses (some viruses "shock" the stem cells and cause them to stop functioning for a period of time) or cancer chemotherapy

Autoimmune disorders. Neonatal Isoimmune Neutropenia occurs briefly in infants, whereby their mothers release antibodies that cross the placenta and attack their neutrophils. The disorder will resolve in less than 3 months. After 3 months, the baby can make their own antibodies against neutrophils leading to autoimmune neutropenia of infancy or chronic benign neutropenia.

Genetic syndromes. Shwachman-Diamond and Kostman Syndrome are characterized by low levels of neutrophils. Another interesting disorder is termed cyclic neutropenia, characterized by 3 day periods of neutropenia occurring every 21 days.

New Antibody Discovered Highly Effective Against HIV

A recent article in the Journal of Immunology highlighted a groundbreaking discovery in the fight against the human immunodeficiency virus (HIV). Funded by the National Institute of Health (NIH) and the National Institute of Allergy and Infectious Diseases (NIAID), Dr. Mark Connors and his team discovered an antibody named N6 that appeared to neutralize over 98 percent of the HIV isolates tested. What is particularly promising was the ability to eradicate even the known resistant strains.

To date, the discovery of a vaccine has been difficult due to the rapidly changing structure of the proteins on the surface of the virus. The N6 antibody, however, is particularly adept at binding a more consistent portion of the virus called the CD4 binding site, which allows it to attach to human cells.

The N6 antibody joins the ranks of the VRC01 antibody, which was discovered in 2010 and is in clinical trials, but it's effectiveness is far greater. This may translate to a vaccine that will finally prevent HIV from evading our immune system, saving countless lives and cutting healthcare costs. 

What happens in the NICU?

The Neonatal Intensive Care Unit (NICU), in contrast to the newborn nursery, is a highly specialized unit with skilled staff prepared to handle the most dangerous postnatal complications of sick or premature infants. Babies can be found in incubators known as isolettes, which control their temperatures. The  average gestational age (GA) at birth is between 38 and 42 weeks, and an infant delivered before 37 weeks is considered to be "premature". The last trimester (12 weeks) in the womb is an important time for the baby's growth, and underdeveloped organs are vulnerable. The NICU staff, led by a neonatologist, monitors around the clock to identify and manage any problems. Here are a few of the most common:

Apnea: when a baby, typically less than 35 weeks GA, stops breathing momentarily for OVER 20 seconds. This can be central (the brain needs help reminding the baby to breathe, which is treated with caffeine) or obstructive (managed with suctioning and repositioning).

Bronchopulmonary Dysplasia (BPD): when the baby's lungs do not have a change to fully develop, they will need help to breathe until their lungs mature. This may include supplemental oxygen using either a nasal cannula, CPAP, or mechanical ventilation. Typically, OB/GYN doctors help prevent this by giving steroids (betamethasone) to mothers within 24 hours of their delivery if between 24-34 weeks GA. After delivery of a preterm infant, the neonatologist may provide further protection by coating the newborn's lungs in a material called surfactant. BPD is diagnosed if any newborn requires 28 or more days of oxygen support, and is further classified as mild, moderate, or severe depending on how much oxygen he or she is on at 36 weeks GA.

Polycythemia or Anemia: when the baby's hematocrit (ratio of red cells in the blood) is greater than 65% or below 30%, respectively. Anemia of prematurity occurs in the second month of life.

Patent Ductus Arteriosis: persistence of a connection between the right sided chamber of the heart and the aorta, which normally closes at birth. Characterized by tachypnea (fast breathing), cardiac murmur, and a low mean arterial pressure (MAP). Diagnosed with an echocardiogram.

Retinopathy of Prematurity: poor formation of the blood vessels of the eyes, occurs in most infants less than 28 weeks GA, screened for by an ophthalmologist if the baby is <30 weeks GA.

Necrotizing Enterocolitis: when the baby's bowel becomes overwhelmed with bacteria, leading to air in the walls of the intestines and can lead to perforation. Usually occurs in very preterm infants and is characterized by poor feeding, abdominal distension, and bloody stools.

Intraventricular Hemorrhage: when there is bleeding into spaces within the baby's brain known as the ventricles. Usually occurring within the first 3 days of birth and in very premature infants (<1500 grams) who have not fully developed their brains yet.


Problems in full term newborns (>37 weeks) that may require a NICU stay include hypoglycemia, poor feeding, poor tone, meconium aspiration syndrome, transient tachypnea of the newborn, infection, hyperbilirubinemia, and anatomical/chromosomal abnormalities.

A Swollen Pediatric Joint

A 6 year old girl with a swollen right knee in the absence of trauma, fever, rash or lymphadenopathy. Symptoms are worse in the early morning, and improve throughout the day. She also complains of eye pain. What is the diagnosis?

Juvenile Idiopathic Arthritis (oligoarticular type)


Arthritis in children is not uncommon. When encountered by pediatricians, it is characterized into one of three subtypes: systemic, oligoarticular, and polyarticular.

• The oligoarticular type is the most common. Usually occuring around 5 years old, it is seen in the large joints (but not the hips) and is known for it's casual but unique association with uveitis (irritation of the eye) and a positive ANA (an antibody in the blood). If left untreated, this uveitis can lead to glaucoma when they are older.

• The polyarticular type is the second most common, and usually affects the large and small joints on both sides symmetrically. Older children with bloodwork that is rheumatoid factor positive are likely to progress to arthritis as adults.

• The systemic type is often easiest to recognize, as an adolescent will often present with fever, a salmon-colored rash, and lymphadenopathy. Many different joints can be affected, and treatment requires disease-modifying drugs (DMARDs). Untreated systemic JIA can progress to a dangerous condition known as macrophage activating syndrome. 

The disease is manageable when caught early, and is typically managed by a specialist known as a rheumatologist. An early step is be sure the swelling isn't the result of an athletic injury or fall. The pediatrician will be sure to rule out more serious causes such as a septic (infected) joint.