CJA
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Résumé de cet Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a scholarly reply
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Alsuwaida, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Alsuwaida, K.
Canadian Journal of Anesthesia 49:880-882 (2002)
© Canadian Anesthesiologists' Society, 2002

Neuroanesthesia and Intensive Care

Primary cutaneous mucormycosis complicating the use of adhesive tape to secure the endotracheal tube

[La mucormycose cutanée primaire nuit à l’usage de ruban adhésif utilisé pour assurer l’immobilité du tube endotrachéal]

Kerrayem Alsuwaida, MD FRCPC

From the University Health Network, University of Toronto, Toronto, Ontario, Canada.

Dr. Kerrayem Alsuwaida, University Health Network, University of Toronto, CCRW3-884, 101 College Street, Toronto, Ontario M5G 1L7, Canada. E-mail: alsuwaida{at}sprint.ca

Purpose: To report a rare case of primary cutaneous mucormycosis (PCM), complicating securing of the endotracheal tube with adhesive tape.

Clinical features: A 39-yr-old woman with systemic lupus erythematosus (SLE) developed four annular, punched out ulcers with a necrotic centre and elevated border in a linear distribution over the left cheek, under the tape securing the endotracheal tube. A tissue biopsy revealed broad, branching, nonseptate hyphae found in epidermis and dermis consistent with mucormycosis, best demonstrated with silver staining. Cultures were positive for Rhizopus species. Treatment with iv amphotericin B was successful.

Conclusion: Because of the rarity of the disease and the difficulty of culturing the causative organism, diagnosis of mucormycosis is often elusive. Tissue biopsy and microscopic visualization of nonseptate hyphae with right-angled branching are the only methods for making the diagnosis. Skin biopsy of new ulcerative or plaque-like lesions should be obtained in immunocompromised patients. Early diagnosis and prompt treatment are critical for favourable outcomes in PCM.




This article has been cited by other articles:


Home page
Clin. Microbiol. Rev.Home page
B. Spellberg, J. Edwards Jr., and A. Ibrahim
Novel Perspectives on Mucormycosis: Pathophysiology, Presentation, and Management
Clin. Microbiol. Rev., July 1, 2005; 18(3): 556 - 569.
[Abstract] [Full Text] [PDF]


Home page
CMAJHome page
A. Mater, G. Al-Sulaiti, D. L. Johnston, and R. Slinger
A 4-year-old child with leukemia and an enlarging arm lesion
Can. Med. Assoc. J., February 1, 2005; 172(3): 332 - 332.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 by the Canadian Anesthesiologists' Society.