0
JAMA Clinical Challenge |

Appearance of a Rapidly Expanding Facial Eschar in a Severely Injured Trauma Patient FREE

Michael R. Christy, MD; Sachin M. Shridharani, MD
[+] Author Affiliations

Author Affiliations: The R Adams Cowley Shock Trauma Center and Division of Plastic, Reconstructive and Maxillofacial Surgery, University of Maryland, Baltimore.


JAMA. 2012;307(10):1080-1081. doi:10.1001/jama.2012.288.
Text Size: A A A
Published online

A 21-year-old woman presents to the trauma resuscitation unit via helicopter transport following a motor vehicle crash. She was an unrestrained driver involved in a front-end collision and had a prolonged extrication from the vehicle. At the scene, she was unresponsive and underwent emergency intubation. She sustained multiple severe traumatic injuries including a ruptured spleen requiring abdominal exploration and splenectomy, atlanto-occipital dislocation requiring halo placement, bilateral pelvic fractures requiring pelvic binder, and left lower extremity crush injury with multiple open fractures ultimately requiring a left hemipelvectomy. She underwent 38 operative interventions in a 3-week period.

The plastic surgery department is consulted 14 days after the initial crash to evaluate a 4 × 4-cm left cheek wound measuring 2.5 cm deep with exposed zygomaticus major muscle (Figure 1A). In the ensuing 48 hours, the wound rapidly progresses and develops a necrotic eschar (Figure 1B).

Place holder to copy figure label and caption
Grahic Jump Location

Figure 1. A, 4 × 4-cm left cheek wound with exposed zygomaticus major muscle. B, Cheek wound after wide local debridement 48 hours after the original procedure.

  • A. Do nothing; the wound will resolve and granulate over time

  • B. Obtain a biopsy of the lesion

  • C. Perform surgical debridement in the operating room

  • D. Prescribe intravenous antibiotics

Cutaneous mucormycosis

C. Perform surgical debridement in the operating room

The key clinical feature in this case is making the diagnosis of rapidly spreading cutaneous fungal infection. The presence of fuzzy, nonsuppurative necrosis in a critically ill patient should raise the possibility of mucormycosis. Rapidly spreading necrotic soft tissue infections are an indication for emergency surgical debridement.

Mucormycosis primarily affects patients who are undergoing immunosuppressive therapy, have hematologic malignancies, or have diabetes mellitus.1 The most common clinical presentation is rhinocerebral infection in a patient with diabetes.2 Mucormycosis is not common in trauma patients who have no other risk factors. Mucormycosis can manifest as a superficial or deep infection or can appear as pustules, blisters, nodules, necrotic ulcerations, echthyma gangrenosum–like lesions, or necrotizing cellulitis. A skin biopsy is required for diagnosis. Cultures and fungal stains of wound swabs are not sensitive and may give misleading microbiological results.3

Prevention of disseminated infection is of primary concern in patients presenting with cutaneous mucormycosis. There have been occasional case reports of dissemination of the cutaneous form to the lungs, causing severe pulmonary involvement.4 Prevention of disseminated disease can be accomplished by wide local excision of the lesion with primary or secondary skin grafting and intravenous administration of amphotericin B.57

Pathology of the lesion from the initial debridement revealed invasion of nonseptate hyphae into the epidermal vasculature leading to thrombosis of the involved vessel (Figure 2A). The patient was treated with wide debridement of the wound. Doing nothing would result in rapid progression of the infection and likely development of fungal sepsis. Prescribing oral antibiotics would have no effect on the fungus. Although secondary infection can be a concern with cutaneous mucormycosis, antibiotics were not clinically indicated in this case as evidenced by the lack of surrounding cellulitis and purulent fluid drainage. Obtaining a biopsy would provide relevant information; however, this would not occur in a timely manner.

Place holder to copy figure label and caption
Grahic Jump Location

Figure 2. A, Biopsy of the initial lesion showing dark pink nonseptate fungal hyphae (arrowhead)(periodic acid–Schiff, original magnification ×600). B, Angioinvasive fungal hyphae (arrowhead)(periodic acid–Schiff, original magnification ×400).

Amphotericin B was initiated for presumed mucormycosis, and the patient underwent daily surgical debridement, but her course deteriorated. Prior to developing significant metabolic acidosis, control of the cutaneous facial mucormycosis was obtained.

Over the next 7 days the patient was taken back to the operating room every 24 hours for aggressive management of her injuries and abdominal exploration. Disseminated mucormycosis was noted on intra-abdominal exploration. In addition, the right lower extremity and left hemipelvectomy site also became infected with mucormycosis. Subsequently, the patient required increased ventilatory support and high-dose vasopressor therapy for profound sepsis. A discussion was held with the family regarding the patient's critical condition and her continued deterioration despite maximum operative and medical therapy. The family decided to withdraw life support, and the patient died.

Conflict of Interest Disclosures: The authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest and none were reported.

Additional Contributions: We thank the patient's family for providing permission to publish her information.

Prabhu RM, Patel R. Mucormycosis and entomophthoramycosis: a review of the clinical manifestations, diagnosis and treatment.  Clin Microbiol Infect. 2004;10(suppl 1)  31-47
PubMed   |  Link to Article
Ketenci I, Unlü Y, Kaya H,  et al.  Rhinocerebral mucormycosis: experience in 14 patients.  J Laryngol Otol. 2011;125(8):e3
PubMed   |  Link to Article
Losee JE, Selber J, Vega S, Hall C, Scott G, Serletti JM. Primary cutaneous mucormycosis: guide to surgical management.  Ann Plast Surg. 2002;49(4):385-390
PubMed   |  Link to Article
Van Sickels N, Hoffman J, Stuke L, Kempe K. Survival of a patient with trauma-induced mucormycosis using an aggressive surgical and medical approach.  J Trauma. 2011;70(2):507-509
PubMed   |  Link to Article
Veliath AJ, Rao R, Prabhu MR, Aurora AL. Cutaneous phycomycosis (mucormycosis) with fatal pulmonary dissemination.  Arch Dermatol. 1976;112(4):509-512
PubMed   |  Link to Article
Ashkenazi-Hoffnung L, Bilavsky E, Avitzur Y, Amir J. Successful treatment of cutaneous zygomycosis with intravenous amphotericin B followed by oral posaconazole in a multivisceral transplant recipient.  Transplantation. 2010;90(10):1133-1135
PubMed   |  Link to Article
Lin CT, Lee JC, Chan DC, Yu JC, Hsieh CB. Successful treatment of mucormycosis infection after liver transplantation: report of a case and review of the literature.  Z Gastroenterol. 2011;49(4):449-451
PubMed   |  Link to Article

Figures

Place holder to copy figure label and caption
Grahic Jump Location

Figure 1. A, 4 × 4-cm left cheek wound with exposed zygomaticus major muscle. B, Cheek wound after wide local debridement 48 hours after the original procedure.

Place holder to copy figure label and caption
Grahic Jump Location

Figure 2. A, Biopsy of the initial lesion showing dark pink nonseptate fungal hyphae (arrowhead)(periodic acid–Schiff, original magnification ×600). B, Angioinvasive fungal hyphae (arrowhead)(periodic acid–Schiff, original magnification ×400).

Tables

Interactive Graphics

Video

Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

Use interactive graphics and maps to view and sort country-specific infant and early dhildhood mortality and growth failure data and their association with maternal

References

Prabhu RM, Patel R. Mucormycosis and entomophthoramycosis: a review of the clinical manifestations, diagnosis and treatment.  Clin Microbiol Infect. 2004;10(suppl 1)  31-47
PubMed   |  Link to Article
Ketenci I, Unlü Y, Kaya H,  et al.  Rhinocerebral mucormycosis: experience in 14 patients.  J Laryngol Otol. 2011;125(8):e3
PubMed   |  Link to Article
Losee JE, Selber J, Vega S, Hall C, Scott G, Serletti JM. Primary cutaneous mucormycosis: guide to surgical management.  Ann Plast Surg. 2002;49(4):385-390
PubMed   |  Link to Article
Van Sickels N, Hoffman J, Stuke L, Kempe K. Survival of a patient with trauma-induced mucormycosis using an aggressive surgical and medical approach.  J Trauma. 2011;70(2):507-509
PubMed   |  Link to Article
Veliath AJ, Rao R, Prabhu MR, Aurora AL. Cutaneous phycomycosis (mucormycosis) with fatal pulmonary dissemination.  Arch Dermatol. 1976;112(4):509-512
PubMed   |  Link to Article
Ashkenazi-Hoffnung L, Bilavsky E, Avitzur Y, Amir J. Successful treatment of cutaneous zygomycosis with intravenous amphotericin B followed by oral posaconazole in a multivisceral transplant recipient.  Transplantation. 2010;90(10):1133-1135
PubMed   |  Link to Article
Lin CT, Lee JC, Chan DC, Yu JC, Hsieh CB. Successful treatment of mucormycosis infection after liver transplantation: report of a case and review of the literature.  Z Gastroenterol. 2011;49(4):449-451
PubMed   |  Link to Article
CME
Accreditation Information
The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
Note: You must get at least of the answers correct to pass this quiz.
You have not filled in all the answers to complete this quiz
The following questions were not answered:
Sorry, you have unsuccessfully completed this CME quiz with a score of
The following questions were not answered correctly:
Commitment to Change (optional):
Indicate what change(s) you will implement in your practice, if any, based on this CME course.
Your quiz results:
The filled radio buttons indicate your responses. The preferred responses are highlighted
For CME Course: A Proposed Model for Initial Assessment and Management of Acute Heart Failure Syndromes
Indicate what changes(s) you will implement in your practice, if any, based on this CME course.
NOTE:
Citing articles are presented as examples only. In non-demo SCM6 implementation, integration with CrossRef’s “Cited By” API will populate this tab (http://www.crossref.org/citedby.html).
Submit a Response

Some tools below are only available to our subscribers or users with an online account.

Related Content

Customize your page view by dragging & repositioning the boxes below.

Articles Related By Topic
Related Topics
PubMed Articles