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CLINICAL NOTE Facial Cutaneous Mucormycosis in a Full-term Infant Sandeep P. Dave, MD; Richard J. Vivero, AB; Soham Roy, MD, FAAP ucormycosis is a rare and potentially fatal fungal infection that most commonly affects the immunocompromised population. Although originally described by Pal- 1(p573) tauf in 1885 (D. G. Finn as cited by Vessely et al and A. M. Marchevsky as 2(p1607) M cited by Oh and Notrica ), it was not until 1955 that Harris (as cited by Ves- 1(p573) sely et al ) reported the first case of a mucormycosis survivor. In recent years, the number of immunosuppressed patients has increased partly owing to the widespread implementation of or- gan transplantation and the increasing prevalence of human immunodeficiency virus infection. Consequently, the incidence of mucormycosis has also increased, especially in pediatric patients. In the setting of immunocompromise, a high index of suspicion is required to accurately diagnose and treat this potentially lethal infection in a timely fashion. To our knowledge, we report the first case of facial cutaneous mucormycosis in an infant, who also represents the first reported neonate or infant to survive a cutaneous mucormycosis infection of the head and neck. After an uncomplicated liver, partial gas-
JAMA Otolaryngology - Head & Neck Surgery – American Medical Association
Published: Feb 1, 2008
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