Severe dermatophytosis in solid organ transplant recipients: A French retrospective series and literature review. Issue 1 (25th January 2018)
- Record Type:
- Journal Article
- Title:
- Severe dermatophytosis in solid organ transplant recipients: A French retrospective series and literature review. Issue 1 (25th January 2018)
- Main Title:
- Severe dermatophytosis in solid organ transplant recipients: A French retrospective series and literature review
- Authors:
- Rouzaud, Claire
Chosidow, Olivier
Brocard, Anabelle
Fraitag, Sylvie
Scemla, Anne
Anglicheau, Dany
Bouaziz, Jean‐David
Dupin, Nicolas
Bougnoux, Marie‐Elisabeth
Hay, Roderick
Lortholary, Olivier
Lanternier, Fanny - Other Names:
- Alanio A. investigator.
Angoulvant A. investigator.
Aubert H. investigator.
Bouteille B. investigator.
Botterel F. investigator.
Carlotti A. investigator.
Cassagnau E. investigator.
Deschamps L. investigator.
Doffoel‐Hantz V. investigator.
Franck F. investigator.
François H. investigator.
Guillaudeau A. investigator.
Houzé S. investigator.
Lazure T. investigator.
Longvert C. investigator.
Morio F. investigator.
Oro S. investigator.
Ortonne N. investigator.
Poirier P. investigator.
Vignon Pennamen M‐D. investigator. - Abstract:
- Abstract: Objective: Severe dermatophytosis is described in immunocompromised patients with defective cellular immunity. We report here a large series and a literature review of severe dermatophytosis in solid‐organ transplant (SOT) recipients. Method: The data main source was a national French retrospective study of severe dermatophytosis in SOT recipients between 2010 and 2016. Inclusion criteria were the presence of dermatophytes in skin culture and 1 severity criteria: dermal invasion by dermatophytes (invasive dermatophytosis) or involvement of at least two body sites or >10% of body surface area (extensive dermatophytosis). Results: A total of 12 patients were included (8 men, median age of 56 years [range: 33‐71]). Of the 12 patients, 10 underwent kidney transplantation. The median time from transplantation to severe dermatophytosis diagnosis was 16 months [range: 2‐94]. Clinical signs of superficial dermatophytosis were present in 8/12 patients before the emergence of severe dermatophytosis. Nine patients had invasive forms and three extensive ones, and nodules of the lower extremities were found in eight. Trichophyton rubrum was isolated in 11 cases. First‐line treatment was terbinafine (7/12), posaconazole (3/12), or topical treatment alone (2/12). Immunosuppressive therapy was reduced in 3 patients because of associated infections. Complete response was obtained for 3/3 and 5/9 patients with extensive or invasive forms, respectively, after a median treatment'sAbstract: Objective: Severe dermatophytosis is described in immunocompromised patients with defective cellular immunity. We report here a large series and a literature review of severe dermatophytosis in solid‐organ transplant (SOT) recipients. Method: The data main source was a national French retrospective study of severe dermatophytosis in SOT recipients between 2010 and 2016. Inclusion criteria were the presence of dermatophytes in skin culture and 1 severity criteria: dermal invasion by dermatophytes (invasive dermatophytosis) or involvement of at least two body sites or >10% of body surface area (extensive dermatophytosis). Results: A total of 12 patients were included (8 men, median age of 56 years [range: 33‐71]). Of the 12 patients, 10 underwent kidney transplantation. The median time from transplantation to severe dermatophytosis diagnosis was 16 months [range: 2‐94]. Clinical signs of superficial dermatophytosis were present in 8/12 patients before the emergence of severe dermatophytosis. Nine patients had invasive forms and three extensive ones, and nodules of the lower extremities were found in eight. Trichophyton rubrum was isolated in 11 cases. First‐line treatment was terbinafine (7/12), posaconazole (3/12), or topical treatment alone (2/12). Immunosuppressive therapy was reduced in 3 patients because of associated infections. Complete response was obtained for 3/3 and 5/9 patients with extensive or invasive forms, respectively, after a median treatment's duration of 2.5 [range: 1.5‐5] months and 7.5 months [range: 4‐12]. Unrelated deaths (n = 2) and graft function impairment (n = 3) occurred. Conclusion: Severe dermatophytosis is a late complication in SOT recipients presenting with lower limb nodules, which might be prevented by prompt treatment of superficial dermatophytosis. … (more)
- Is Part Of:
- Transplant infectious disease. Volume 20:Issue 1(2018)
- Journal:
- Transplant infectious disease
- Issue:
- Volume 20:Issue 1(2018)
- Issue Display:
- Volume 20, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 20
- Issue:
- 1
- Issue Sort Value:
- 2018-0020-0001-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-01-25
- Subjects:
- deep dermatophytosis -- dermatophytosis -- immunosuppression -- Majocchi's granuloma -- Solid‐organ transplant -- Trichophyton rubrum
Transplantation of organs, tissues, etc -- Complications -- Periodicals
Communicable diseases -- Periodicals
Infection -- Periodicals
617.01 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=mid ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/tid.12799 ↗
- Languages:
- English
- ISSNs:
- 1398-2273
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9024.988700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5825.xml