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Subcutaneous Fat Necrosis of the Newborn




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Author: Amy J Theos, MD, Director of Pediatric Dermatology, Assistant Professor, Department of Dermatology, University of Alabama at Birmingham

Amy J Theos is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, and Society for Pediatric Dermatology

Coauthor(s): Craig A Elmets, MD, Director of Dermatology, Departments of Dermatology, Pathology, and Environmental Health Sciences; Professor, The Kirklin Clinic, University of Alabama at Birmingham

Editors: Daniel Mark Siegel, MD, MS, Director, Procedural Dermatology Fellowship Program, Clinical Professor of Dermatology, Department of Dermatology, State University of New York Downstate; Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University School of Medicine; Consulting Staff, Mountain View Dermatology, PA; Van Perry, MD, Assistant Professor, Department of Medicine, Division of Dermatology, University of Texas Health Science Center; Joel M Gelfand, MD, MSCE, Medical Director, Clinical Studies Unit, Assistant Professor, Department of Dermatology, Associate Scholar, Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania; Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center

Author and Editor Disclosure

Synonyms and related keywords: sclerema neonatorum, SN, skinbound disease, skin-bound disease, subcutaneous fat disorder, neonatal subcutaneous fat disorder, neonatal subcutaneous fat disease

Background

The classic description of sclerema neonatorum (SN) is credited to Underwood, who described it in 1784 and appropriately termed it "skinbound disease." In 1817, Alibert introduced the term sclerema, derived from the Greek word skleros, meaning hard. Sclerema neonatorum is a disorder of the subcutaneous fat in debilitated neonates and is considered best as a sign of a potentially fatal underlying disease process and not a specific disease entity.1 A thorough review of the nomenclature, clinical findings, histological features, differential diagnosis, and management of sclerema neonatorum was published in 2008.2

The Medscape Pediatric Dermatology Resource Center may be of interest.

Pathophysiology

In an infant, fat has a higher saturated-to-unsaturated fatty acid ratio compared to adult fat and thus, a higher melting point. Prematurity, hypothermia, shock, and metabolic abnormalities have been postulated to further increase this ratio, possibly as a result of enzymatic alteration allowing precipitation of fatty acid crystals within the lipocytes. This condition has been suggested to result in the dramatic clinical findings in affected skin. X-ray diffraction techniques have confirmed that infants with sclerema neonatorum have an increase in saturated fats and that the crystals within the fat cells are composed of triglycerides.3

Frequency

United States

The exact incidence of sclerema neonatorum is unknown. All studies describe sclerema neonatorum as extremely rare. The number of reported cases in recent years has declined, probably as a result of better neonatal care.

Mortality/Morbidity

Because sclerema neonatorum invariably is associated with serious underlying disease, the mortality rate is high. In different series, the reported mortality rates range from 67-88%, with death occurring hours to days after onset. If the underlying disease is treated successfully, the skin softens and returns to normal.

Race

No racial predilection has been reported.

Sex

Sclerema neonatorum shows a slight male predominance, with an estimated male-to-female ratio of 1.5:1.4

Age

Sclerema neonatorum is a disease confined to the newborn period. Sclerema neonatorum can present at birth, but onset within the first week of life is more common. The oldest reported infant presented with Pseudomonas septicemia at age 106 days.



History

Half the infants affected by sclerema neonatorum are premature, and the others are full term but have a serious underlying illness. They are often of low birth weight (<2500 g) and have cyanosis and low Apgar scores.5 In one series, 75% of the mothers were healthy, while 25% had preeclampsia, placenta previa, or infection. Labor is usually normal, and delivery is spontaneous and nontraumatic.

Physical

Physical findings of sclerema neonatorum appear suddenly, first on the thighs and buttocks and then, spreading rapidly, often affecting all parts of the body except the palms, soles, and genitalia. The involved skin is pale, waxy, and firm to palpation. The skin cannot be pitted or pinched up because it is bound to the underlying tissues. The affected infant often displays flexion contractures at the elbows, knees, and hips; temperature instability; restricted respiration; difficulty in feeding; and decreased spontaneous movement.

Causes

Associated underlying conditions include pneumonia, septicemia, hypothermia, metabolic acidosis, respiratory distress syndrome, congenital heart defects, gastroenteritis, and intestinal obstruction.6 Two case reports have described sclerema neonatorum that developed after therapeutic hypothermia initiated for neonatal asphyxia.7, 8



Hutchinson-Gilford Progeria
Scleredema
Subcutaneous Fat Necrosis of the Newborn

Other Problems to be Considered

Congenital lymphedema (Milroy disease)
Neonatal cold injury
Restrictive dermopathy
Scleroderma



Lab Studies

Laboratory abnormalities associated with sclerema neonatorum correlate with the underlying disease process. Hypoglycemia, metabolic acidosis, respiratory alkalosis, hyperkalemia, hypocalcemia, and elevated blood urea are common, albeit nonspecific, findings. A complete sepsis workup should be initiated in all infants with sclerema neonatorum.

Histologic Findings

Despite the striking clinical presentation, histologic findings of sclerema neonatorum are subtle. The most consistent findings are edema, a thickening of the subcutaneous fibrous septa, and a radial array of fine, needlelike clefts in the fat cells. Autopsy studies have identified identical needle-shaped crystals in adipocytes of visceral fat in patients with sclerema neonatorum.9 In the subcutaneous fat, inflammation is sparse and, when present, consists of lymphocytes, histiocytes, and multinucleated giant cells. In contrast to subcutaneous fat necrosis of the newborn, no granulomatous inflammation exists.



Medical Care

Recognition and the prompt institution of therapy specific for the underlying disease are mandatory. Careful monitoring, correction of electrolyte abnormalities, respiratory support, correction of hypovolemia, and control of hypothermia are important in sclerema neonatorum patients.

  • Antibiotics: Some authors advocate the prompt institution of prophylactic broad-spectrum antibiotic therapy for possible associated sepsis.
  • Systemic steroids: The value of systemic steroids is controversial. No controlled studies have demonstrated improved survival with the use of systemic steroids in sclerema neonatorum, although they are often used.5
  • Exchange transfusions: A randomized controlled trial demonstrated a significant survival benefit in septic neonates with sclerema neonatorum who were treated with exchange transfusion.10

Consultations

  • Infants with sclerema neonatorum are best cared for in a neonatal intensive care unit by an intensivist.
  • Depending on the underlying illness (eg, sepsis), consultation to the appropriate specialists should be made.



Medical therapy of the skin is not beneficial; successful treatment of the underlying disorder improves the skin.



Complications

Unless the underlying disease is identified and treated, the course of sclerema neonatorum is one of rapid deterioration in the general health of the infant and, ultimately, death.

Prognosis

If the infant survives and the underlying condition is treated successfully, the condition of the skin may return to normal.



Medical/Legal Pitfalls

Sclerema neonatorum is a sign of underlying disease; therefore, failure to identify sclerema neonatorum and diagnose the underlying condition may put patients at risk for the complications and mortality of that disease.



  1. Warwick WJ, Ruttenberg HD, Quie PG. Sclerema neonatorum--a sign, not a disease. JAMA. Jun 1 1963;184:680-3. [Medline].
  2. Zeb A, Darmstadt GL. Sclerema neonatorum: a review of nomenclature, clinical presentation, histological features, differential diagnoses and management. J Perinatol. Jul 2008;28(7):453-60. [Medline].
  3. Kellum RE, Ray TL, Brown GR. Sclerema neonatorum. Report of a case and analysis of subcutaneous and epidermal-dermal lipids by chromatographic methods. Arch Dermatol. Apr 1968;97(4):372-80. [Medline].
  4. Bwibo NO, Anderson BT. Sclerema neonatorum (a study of 16 cases in the special care unit, Mulago Hospital, Kampala). East Afr Med J. Jan 1970;47(1):50-5. [Medline].
  5. Milunsky A, Levin SE. Sclerema neonatorum: a clinical study of 79 cases. S Afr Med J. Jul 2 1966;40(27):638-41. [Medline].
  6. Fretzin DF, Arias AM. Sclerema neonatorum and subcutaneous fat necrosis of the newborn. Pediatr Dermatol. Aug 1987;4(2):112-22. [Medline].
  7. Battin M, Harding J, Gunn A. Sclerema Neonatorum following hypothermia. J Paediatr Child Health. Oct 2002;38(5):533-4. [Medline].
  8. Navarini-Meury S, Schneider J, Bührer C. Sclerema neonatorum after therapeutic whole-body hypothermia. Arch Dis Child Fetal Neonatal Ed. Jul 2007;92(4):F307. [Medline].
  9. Torrelo A, Hernández A. Panniculitis in children. Dermatol Clin. Oct 2008;26(4):491-500. [Medline].
  10. Sadana S, Mathur NB, Thakur A. Exchange transfusion in septic neonates with sclerema: effect on immunoglobulin and complement levels. Indian Pediatr. Jan 1997;34(1):20-5. [Medline].

Sclerema Neonatorum excerpt

Article Last Updated: Oct 21, 2008