Case report: Fever- pneumonia- lymphadenectasis- osteolytic- subcutaneous nodule: Disseminated chromoblastomycosis caused by phialophora.
Administration, Intravenous
Administration, Oral
Adult
Antifungal Agents
/ therapeutic use
Chromoblastomycosis
/ complications
Drug Therapy, Combination
Fever
/ drug therapy
Humans
Lung
/ diagnostic imaging
Lymph Nodes
/ diagnostic imaging
Male
Osteolysis
/ diagnosis
Phialophora
/ isolation & purification
Pneumonia
/ diagnosis
Positron Emission Tomography Computed Tomography
Tibia
/ diagnostic imaging
Treatment Outcome
Chromoblastomycosis
Lymphadenectasis
Osteolytic
Phialophora
Pneumonia
Journal
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy
ISSN: 1437-7780
Titre abrégé: J Infect Chemother
Pays: Netherlands
ID NLM: 9608375
Informations de publication
Date de publication:
Dec 2019
Dec 2019
Historique:
received:
30
01
2019
revised:
05
04
2019
accepted:
07
05
2019
pubmed:
24
6
2019
medline:
31
3
2020
entrez:
24
6
2019
Statut:
ppublish
Résumé
Chromoblastomycosis (CBM) is a chronic cutaneous and subcutaneous fungal infection caused by certain dematiaceous fungi (usually Fonsecaea, Phialophora, or Cladophialophora). Histologically, CBM is characterized by the presence of medlar bodies. However, the diagnosis is difficult because of the rarity of these pathognomonic presentations and the wide variety of presentations. Treatment of these infections is challenging as it lacks standardization. Herein, we report a case of chromoblastomycosis caused by Phialophora, in a 42-year-old immunocompetent male agriculturist from the humid and subtropical region of southern China. He had a 3-month history of pneumonia with intermittent fever, coughing, and expectoration. The infection subsequently spread to the bone and lymph nodes forming deep lesions and eventually resulting in osteolysis and lymphadenectasis. These subcutaneous nodules were observed after 9 months. Antifungal treatment was administered for 20 months leading to clinical improvement before the patient was lost to follow-up. This case is unique because such deep lesions are rare in immunocompetent individuals and because the initial onset was associated with pneumonia.
Identifiants
pubmed: 31229375
pii: S1341-321X(19)30135-7
doi: 10.1016/j.jiac.2019.05.002
pii:
doi:
Substances chimiques
Antifungal Agents
0
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1031-1036Informations de copyright
Copyright © 2019 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.