Epidermolysis bullosa (EB) is characterized by blistering of the skin and mucosal erosions caused by hemidesmosomal abnormalities. EB is divided into 3 major subgroups depending on the particular location of tissue separation: EB simplex, dystrophic EB, and junctional EB. Junctional EB (JEB) can further be broken down into Herlitz, non-Herlitz, and JEB with pyloric atresia (Carmi syndrome) depending on genetic and histologic testing. When extensive, management of a patient with EB can be challenging due to not only cutaneous but also extracutaneous manifestations as well. Families and health care teams are often faced with difficult decisions in their infant’s best interest. We report a case of a preterm neonate with Carmi syndrome and unique findings on immunofluorescence studies. The patient’s course was complicated by multisystem involvement and ultimately death. A multidisciplinary approach was crucial in the light of diagnostic, therapeutic, and ethical challenges.
Epidermolysis bullosa (EB) is an inherited, autosomal recessive, bullous disease, characterized by mucosal erosions and skin blisters. Numerous subtypes of EB are described and are divided into three major groups: EB simplex (EBS), dystrophic EB (DEB), and junctional EB (JEB). Junctional EB is further divided into three subgroups: Herlitz, non-Herlitz, and JEB with pyloric atresia (JEB-PA) also known as Carmi syndrome. JEB has a proven familial predisposition and is caused by mutations in the ITGA6, ITGB4, LAMA3, LAMB3, LAMC2, and COL17A1 genes [
A 30-week gestation male was born via vaginal delivery to a G2P2 mother in a nonconsanguineous marriage with appropriate prenatal care and an unremarkable prenatal course. The premature delivery was precipitated by placental abruption and preterm onset of labor. The mother received two doses of antenatal steroids prior to delivery. Apgar scores were 8 and 9 at 1 and 5 minutes of life, respectively. On examination, the baby was noted to have bilateral microtia along with extensive truncal and appendicular epidermolytic lesions (Figure
Cutaneous involvement of the neonate. (a) Involvement of the left wrist and hand. (b) Absence of skin on the nasal bridge and neck. Microtia also notable. (c) Involvement of the right forearm and elbow. (d) Circumferential epidermolytic lesions on right ankle.
The infant was started on prophylactic ampicillin and gentamicin given his prematurity and open skin wounds. Aquaphor barrier cream and soft silicone dressings were applied, and the patient was placed in reverse isolation. He was placed in a 34°C temperature-controlled incubator without humidity, as heat and humidity can exacerbate blistering. Dermatology, plastic surgery, wound care, and genetics services were consulted upon the patient’s admission.
On the first day of life, he had numerous desaturation episodes likely secondary to prematurity in conjunction with sloughing of the respiratory epithelium. He was intubated and placed on mechanical ventilation support. High gastric output was noted without abdominal distension, and a combined chest and abdominal X-ray showed mild gaseous distension of the stomach with no free intra-abdominal air (Figure
Radiographic imaging consistent with pyloric atresia. (a) Abdominal X-ray showing gaseous distension of the stomach with no free intra-abdominal air. (b) Fluoroscopic abdominal X-ray showing total gastric outlet obstruction with no contrast entering the duodenum.
Surgical repair was tentatively scheduled with concerns around the adequacy of postoperative healing. A screening renal ultrasound showed a right multicystic and dysplastic kidney. On the second day of life, a skin biopsy of the left upper extremity was obtained by dermatology. Renal function was followed closely, and medication dosage was renally dose adjusted. Gentamicin was switched to cefotaxime to avoid nephrotoxic side effects. By the sixth day of life, the patient’s creatinine had increased to 1.6 mg/dL. On day of life 7, a decision was made to discontinue ampicillin and cefotaxime after blood cultures remained negative. Bacitracin ointment was started topically. After 12 hours without antibiotics, the patient was febrile to 38.4°C; after blood and urine cultures were sent, piperacillin-tazobactam and oxacillin were started. The white blood cell count was noted to be 13.4·109/L with 18% neutrophils and 14% bands. During the urinary bladder catheterization, red discoloration of the urine was noted. The blood and urine cultures had no growth at 48 hours.
On the eighth day of life, the pathology report using immunofluorescence mapping showed an absence of
Immunofluorescence staining. (a) Absence of
Simultaneously, the infant’s renal function continued to worsen with serum creatinine levels rising to 2.0 mg/dL and serum sodium decreasing to 131 mEq/L, so the nephrology team was consulted. They recommended increasing total fluid intake due to possible prerenal factors contributing to the acute kidney injury in light of insensible water losses due to JEB. The following day, the serum sodium decreased further to 122 mEq/L, so fluids were restricted which showed improvement in the sodium level. On day of life 10, while still on antibiotics, the patient was again febrile to 38.7°C. Two wound cultures were obtained, another blood culture was sent, and labs showed WBCs of 29.7·109/L with 50% neutrophils and 8% bands. The blood culture was again negative at 48 hours. One of the wound cultures grew coagulase negative
A multidisciplinary meeting took place involving the mother and her partner, the attending neonatologist, geneticist, nephrologist, palliative care, and ancillary staff. After gleaning the mother’s understanding of her infant’s condition, the medical team clarified the grave prognosis of Carmi syndrome compounded by renal failure. After a discussion of goals of care, a range of compassionate options was presented to the family. One possibility was aggressive medical management including possible dialysis and surgical correction of the infant’s pyloric atresia. Due to the extent of blistering, the uncertainties of meaningful wound healing from a dialysis catheter placement, surgical skin incisions, intestinal re-anastomosis, and the potential increased risk of infection were presented to the family. Other options included a redirection of care towards comfort: limiting aggressive medical interventions with the understanding that the infant may not survive. In our specific case, when presented with a range of compassionate options, this family held the best interests of their child at the core of their decision-making, valuing comfort. The medical team, respecting this decision as well as upholding principles of nonmaleficence agreed to comfort care. The family opted for palliative care with compassionate extubation allowing them to hold the infant. Skin care, intravenous fluids, and pain medication were continued for comfort. Once the extended family was at the bedside, the infant’s respiratory support was removed and the baby died 48 hours later, on day of life 17.
Swinburne and Kohler first described the association between PA and EB in 1967 at the 13th Annual Pediatric Pathology Society in England and published the corresponding paper in 1968 [
Prenatally, JEB-PA can present with polyhydramnios or fetal gastric dilation as seen on ultrasound. For pregnancies at risk, prenatal diagnosis can be established by examining DNA from chorionic villi or amniotic fluid cells or by using monoclonal antibodies. Additionally, direct skin biopsies can be obtained via fetoscopy or ultrasound guidance to confirm the diagnosis [
Clinical features may be apparent at birth or may appear later. The skin may show localized or extensive areas of peeling or blistering with little or no trauma. Significant oral and mucous membrane involvement is common. Additional features of EB-PA may include fusion of the skin between the fingers and toes, nail dystrophy, scarring alopecia, contractures, and dilated cardiomyopathy. PA is usually suspected when neonates develop recurrent non-bilious vomiting and abdominal distension.
Diagnosis is usually suspected based on clinical findings of skin blistering and gastric outlet obstruction. The most precise means of diagnosing inherited EB involves the assessment of a combination of ultrastructural and antigenic features by transmission electron microscopy, immunofluorescence antigenic mapping, and EB-related monoclonal antibody studies. Molecular genetics are available but not necessary for diagnostic confirmation. Depending on the level of basement membrane cleavage, three major varieties of EB have been identified: simplex EB (epidermolytic), junctional EB (lucidolytic), and dystrophic EB (dermolytic). All three types of EB have been described to coexist with congenital PA. As previously mentioned, JEB is further broken down into 3 main categories: JEB Herlitz (JEB-H), JEB non-Herlitz (JEB-nH), and JEB with pyloric atresia (JEB-PA). JEB-H is the most severe with widespread lesions and death early in the neonatal period, associated with absent laminin-332 (formerly laminin-5) on immunofluorescence (IF) studies. JEB-nH can be broken down into generalized and localized depending on the amount of lucidolytic and extracutaneous involvement. Generalized JEB-nH stains incompletely with laminin-322 and type XVII collagen. Localized JEB-nH stains incompletely with type XVII collagen. Lastly, JEB-PA stains with absent or severely decreased
JEB subtypes and the protein abnormalities.
Uniquely, our patient had absent
Uroepithelium similar to other epithelialized structures may be affected by EB, as seen in our patient [
There is no definitive treatment for JEB-PA. If a prenatal diagnosis is established, a caesarean section should be considered to reduce trauma during delivery. Postnatally, the patient should be immediately placed in contact isolation. Dressings and ointments should be used to cover open blisters with wound care or plastic surgery consultation. Ointments can also be used to cover gloves and medical equipment to avoid skin damage, and specialized tape should be considered when securing vascular access devices. Environmental humidity and heat need to be closely regulated. Supportive measures including antibiotics, adequate hydration, and nutritional support enhance care. Prevention of secondary complications such as growth delay, anemia, zinc deficiency, osteopenia/osteoporosis, and scarring of skin and mucosal surfaces are best addressed in a multidisciplinary fashion. A timely plain abdominal radiograph needs to be performed in all babies with EB to exclude PA. Surgical intervention may be indicated to correct PA. While the surgical management for PA is straightforward, poor wound healing with possible infections, protein loss, and failure to thrive complicate the severe lucidolytic skin lesions, often leading to death. Previously, this has led to the recommendation that surgical treatment be withheld in patients with EB-PA [
In many cases, the course of JEB-PA is relentless and fatal despite surgical correction of concomitant PA. The prognosis of this disease is poor due to prematurity, extensive skin blistering with fluid and electrolyte imbalance, respiratory morbidities, malnutrition, sepsis, and associated significant renal and genitourinary disease. Of the 100 reported cases as of 2018, 94 included survival status and of those 70 died (74.5%) with median time of death 30 days of age [
With this case, we presented a severe generalized form of JEB-PA with unique histopathology: absent
The authors declare that there are no conflicts of interest regarding the publication of this article. Only TDH and HS were directly involved in the care of this patient.